John Blangero
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American human geneticist
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#6670
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#1671
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Genetics
#417
World Rank
#483
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#181
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Biology
John Blangero's Degrees
- PhD Genetics University of Texas Health Science Center at Houston
- Bachelors Biology University of Texas at Austin
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Why Is John Blangero Influential?
(Suggest an Edit or Addition)According to Wikipedia, John Blangero is an American human geneticist who ranks in the top 3000 researchers in the world in terms of scholarly citations. His research has been highly funded by the National Institutes of Health where he is reported to have obtained more than $64 million in direct funding for genetic studies of common diseases such as cardiovascular disease, diabetes, and psychiatric diseases. He is a professor in the Department of Human Genetics at the University of Texas Rio Grande Valley School of Medicine in Brownsville, Texas, where he is also Director of the Genomics Computing Center at the South Texas Diabetes and Obesity Institute. In addition, he serves as director of the San Antonio Family Heart Study, and played a major role in organizing the construction of the 11,000-processor computer cluster MEDUSA, which he and his collaborators use for genetic research at UTRGV. Before joining UTRGV, he worked at the Southwest Foundation for Biomedical Research. His research has included a project focused on studying the function and structure of the human brain, for which he collaborated with David Glahn of Yale University. He has also studied the genetic and environmental causes of diabetes and fatty liver disease among the Mexican American population in South Texas.
John Blangero's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Multipoint quantitative-trait linkage analysis in general pedigrees. (1998) (3112)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
- New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
- A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants (2015) (1024)
- Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies (2010) (984)
- The genetic architecture of type 2 diabetes (2016) (927)
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) (785)
- A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
- Common genetic variants influence human subcortical brain structures (2015) (731)
- Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome. (2000) (665)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) (646)
- Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes (2007) (536)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
- An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. (1998) (497)
- Large upward bias in estimation of locus-specific effects from genomewide scans. (2001) (491)
- A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 (1997) (456)
- The transcriptional landscape of age in human peripheral blood (2015) (450)
- Genetic control over the resting brain (2010) (447)
- Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico (2013) (419)
- Loss-of-function mutations in SLC30A8 protect against type 2 diabetes (2014) (405)
- Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. (2000) (389)
- Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans. The San Antonio Family Heart Study. (1996) (376)
- A comprehensive linkage analysis for myocardial infarction and its related risk factors (2002) (357)
- The genetic architecture of the human cerebral cortex (2018) (355)
- Bivariate quantitative trait linkage analysis: Pleiotropy versus co‐incident linkages (1997) (354)
- Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia. (2000) (347)
- Genetic variation in selenoprotein S influences inflammatory response (2005) (347)
- Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans. (1999) (340)
- Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group (2013) (328)
- Long-term neural and physiological phenotyping of a single human (2015) (324)
- The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. (2001) (324)
- Genetic contribution of the endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels. (1997) (314)
- Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. (1999) (311)
- Detection of differential gene flow from patterns of quantitative variation. (1990) (306)
- Fractional anisotropy of water diffusion in cerebral white matter across the lifespan (2012) (305)
- Plasma lipid profiling in a large population-based cohort[S] (2013) (295)
- Hemoglobin concentration of high-altitude Tibetans and Bolivian Aymara. (1998) (272)
- Chemerin is associated with metabolic syndrome phenotypes in a Mexican-American population. (2009) (271)
- Genetic determinants of hemostasis phenotypes in Spanish families. (2000) (269)
- Endophenotypes as quantitative risk factors for psychiatric disease: rationale and study design. (2001) (268)
- Neuroimaging endophenotypes: Strategies for finding genes influencing brain structure and function (2007) (259)
- Variance component methods for detecting complex trait loci. (2001) (244)
- Heritability of age at menarche in girls from the Fels Longitudinal Study. (2005) (244)
- New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
- Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. I. Likelihood formulation and simulation results. (1999) (240)
- Novel genetic loci associated with hippocampal volume (2017) (238)
- Modern human origins (1994) (232)
- Plasma Lipid Profiling Shows Similar Associations with Prediabetes and Type 2 Diabetes (2013) (229)
- Multipoint oligogenic linkage analysis of quantitative traits (1997) (224)
- Brain charts for the human lifespan (2021) (224)
- Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia. (2007) (223)
- The functional connectivity of the human caudate: An application of meta-analytic connectivity modeling with behavioral filtering (2012) (223)
- Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 (2011) (221)
- Factors of insulin resistance syndrome--related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic mexican-americans. (2002) (214)
- Chemerin, a novel adipokine in the regulation of angiogenesis. (2010) (208)
- Genetic analysis of the IRS. Pleiotropic effects of genes influencing insulin levels on lipoprotein and obesity measures. (1996) (206)
- Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. (1999) (198)
- A variance component approach to dichotomous trait linkage analysis using a threshold model (1997) (194)
- Amygdalar and hippocampal substrates of anxious temperament differ in their heritability (2010) (194)
- Ventilation and hypoxic ventilatory response of Tibetan and Aymara high altitude natives. (1997) (193)
- Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time. (2000) (192)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association (2016) (192)
- Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes (2020) (184)
- High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes (2012) (175)
- Quantitative trait loci analysis of human event-related brain potentials: P3 voltage. (1998) (174)
- Genetic Analysis Workshop 17 mini-exome simulation (2011) (173)
- Genetic and environmental factors influencing the human factor H plasma levels (2004) (171)
- Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration (2013) (171)
- A single nucleotide polymorphism in MGEA5 encoding O-GlcNAc-selective N-acetyl-beta-D glucosaminidase is associated with type 2 diabetes in Mexican Americans. (2005) (163)
- Robust LOD scores for variance component‐based linkage analysis (2000) (163)
- Genetics of microstructure of cerebral white matter using diffusion tensor imaging (2010) (161)
- Meta‐Analysis of Genome‐wide Linkage Studies in BMI and Obesity (2007) (159)
- A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans. (2001) (158)
- Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
- Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (153)
- Genetic drift and gene flow in post-famine Ireland. (1997) (151)
- Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations (2019) (151)
- Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
- Anxiety proneness linked to epistatic loci in genome scan of human personality traits. (1998) (148)
- Measuring and comparing brain cortical surface area and other areal quantities (2012) (147)
- Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
- Arguments for the sake of endophenotypes: Examining common misconceptions about the use of endophenotypes in psychiatric genetics (2014) (144)
- Normal variation in leptin levels in associated with polymorphisms in the proopiomelanocortin gene, POMC. (1999) (138)
- Anthropometric variation and the genetic structure of the Jirels of Nepal. (1989) (137)
- Power of variance component linkage analysis to detect quantitative trait loci. (1999) (136)
- Amplitude of visual P3 event-related potential as a phenotypic marker for a predisposition to alcoholism: preliminary results from the COGA Project. Collaborative Study on the Genetics of Alcoholism. (1998) (135)
- Fractional anisotropy of cerebral white matter and thickness of cortical gray matter across the lifespan (2011) (133)
- Quantitative variation in obesity-related traits and insulin precursors linked to the OB gene region on human chromosome 7. (1996) (132)
- Future of genetics of mood disorders research (2002) (131)
- Genetic Epidemiological Approaches to the Search for Osteoporosis Genes (2000) (131)
- On the genetic architecture of cortical folding and brain volume in primates (2010) (130)
- The baboon as a nonhuman primate model for the study of the genetics of obesity. (2003) (129)
- Serum leptin concentration, body composition, and gonadal hormones during puberty (1999) (128)
- Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene (2012) (128)
- The relationship of soluble ICAM-1, VCAM-1, P-selectin and E-selectin to cardiovascular disease risk factors in healthy men and women (2001) (126)
- Genes on chromosomes 1 and 13 have significant effects on Ascaris infection (2002) (124)
- Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis. (2000) (123)
- Haplotypes of Transcription Factor 7–Like 2 (TCF7L2) Gene and Its Upstream Region Are Associated With Type 2 Diabetes and Age of Onset in Mexican Americans (2007) (122)
- Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2016) (120)
- Novel epigenetic determinants of type 2 diabetes in Mexican-American families. (2015) (117)
- The quantitative trait locus on chromosome 2 for serum leptin levels is confirmed in African-Americans. (1999) (117)
- Genetic and environmental influences on infant weight and weight change: The Fels longitudinal study (2007) (117)
- A major susceptibility locus influencing plasma triglyceride concentrations is located on chromosome 15q in Mexican Americans. (2000) (116)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (115)
- Genetic basis of variation in carotid artery wall thickness. (1996) (115)
- A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project. (2005) (112)
- Major gene with sex‐specific effects influences fat mass in Mexican Americans (1995) (111)
- A paired sibling analysis of the beta-3 adrenergic receptor and obesity in Mexican Americans. (1998) (111)
- Genetic analysis of susceptibility to infection with Ascaris lumbricoides. (1999) (108)
- A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. (2006) (108)
- Linkage of high-density lipoprotein–cholesterol concentrations to a locus on chromosome 9p in Mexican Americans (2002) (108)
- Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes (2010) (107)
- A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. (2002) (107)
- Localization and identification of human quantitative trait loci: king harvest has surely come. (2004) (107)
- Obesity, central adiposity and cardiometabolic risk factors in children and adolescents: a family‐based study (2014) (106)
- Plasma HDL cholesterol, triglycerides, and adiposity. A quantitative genetic test of the conjoint trait hypothesis in the San Antonio Family Heart Study. (1995) (105)
- Human pedigree-based quantitative-trait-locus mapping: localization of two genes influencing HDL-cholesterol metabolism. (1999) (104)
- Novel Loci Associated with Usual Sleep Duration: The CHARGE Consortium Genome-Wide Association Study (2014) (104)
- The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness. (2010) (102)
- The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations (2009) (102)
- Quantitative Trait Loci on Chromosomes 2p, 4p, and 13q Influence Bone Mineral Density of the Forearm and Hip in Mexican Americans (2003) (102)
- Major gene for percent of oxygen saturation of arterial hemoglobin in Tibetan highlanders. (1994) (101)
- Adjudicating neurocognitive endophenotypes for schizophrenia (2007) (101)
- Evidence of a novel quantitative-trait locus for obesity on chromosome 4p in Mexican Americans. (2004) (101)
- Heritability of brain volume, surface area and shape: An MRI study in an extended pedigree of baboons (2007) (101)
- Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation (2016) (100)
- Multivariate segregation analysis using the mixed model (1991) (99)
- The Pro12Ala variant of peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) is associated with measures of obesity in Mexican Americans (2000) (99)
- Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus (2015) (98)
- Testing the Hypothesis of Accelerated Cerebral White Matter Aging in Schizophrenia and Major Depression (2013) (98)
- Novel family‐based approaches to genetic risk in thrombosis (2003) (96)
- A quantitative trait locus influencing BMI maps to the region of the beta-3 adrenergic receptor. (1999) (95)
- Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins (2011) (94)
- A transcriptional profile of the decidua in preeclampsia. (2011) (94)
- A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels. (2007) (94)
- A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1) (2013) (93)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
- Interactions Between Variants in the β3-Adrenergic Receptor and Peroxisome Proliferator–Activated Receptor-γ2 Genes and Obesity (2001) (90)
- SORCS1: A Novel Human Type 2 Diabetes Susceptibility Gene Suggested by the Mouse (2007) (90)
- A genome search identifies major quantitative trait loci on human chromosomes 3 and 4 that influence cholesterol concentrations in small LDL particles. (1999) (90)
- Exposure to Schistosoma mansoni infection in a rural area in Brazil. II: Household risk factors (2001) (89)
- Genetics of primary cerebral gyrification: Heritability of length, depth and area of primary sulci in an extended pedigree of Papio baboons (2010) (89)
- Non-crossover gene conversions show strong GC bias and unexpected clustering in humans (2014) (89)
- Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes (2011) (89)
- A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility. (2003) (89)
- Genetics of atherosclerosis risk factors in Mexican Americans. (2009) (86)
- Genome scan for determinants of serum uric acid variability. (2007) (86)
- Smoking behavior is under the influence of a major quantitative trait locus on human chromosome 5q (1999) (86)
- Determinants of variation in human serum paraoxonase activity (2009) (85)
- Percent of oxygen saturation of arterial hemoglobin among Bolivian Aymara at 3,900-4,000 m. (1999) (85)
- Meta‐analysis of genome‐wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women (2013) (84)
- Searching for genes underlying normal variation in human adiposity (2001) (83)
- Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project (2003) (82)
- The mitochondrial rhomboid protease PSARL is a new candidate gene for type 2 diabetes (2005) (81)
- Heritability of event-related brain potentials in families with a history of alcoholism. (1999) (80)
- Variance component methods for analysis of complex phenotypes. (2010) (79)
- Quantitative trait locus mapping using human pedigrees. (2000) (79)
- Quantitative genetic analysis of arterial oxygen saturation in Tibetan highlanders. (1997) (79)
- Evidence that multiple genetic variants of MC4R play a functional role in the regulation of energy expenditure and appetite in Hispanic children. (2010) (77)
- Genetic differentiation between baboon subspecies: Relevance for biomedical research (1990) (76)
- Plasma Lipidomic Profile Signature of Hypertension in Mexican American Families: Specific Role of Diacylglycerols (2013) (76)
- Intergenerational neural mediators of early-life anxious temperament (2015) (75)
- Evidence for linkage of regions on chromosomes 6 and 11 to plasma glucose concentrations in Mexican Americans. (1996) (75)
- Neurocognitive Endophenotypes in a Multiplex Multigenerational Family Study of Schizophrenia (2007) (75)
- Serum leptin levels are independently correlated with two measures of HDL. (1997) (73)
- Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. (2019) (73)
- Genome-wide linkage analyses of type 2 diabetes in Mexican Americans: the San Antonio Family Diabetes/Gallbladder Study. (2005) (72)
- Genetic Basis of Variation in Carotid Artery Plaque in the San Antonio Family Heart Study (2002) (72)
- Comparison of variance components and sibpair‐based approaches to quantitative trait linkage analysis in unselected samples (1999) (72)
- A major locus influencing plasma high-density lipoprotein cholesterol levels in the San Antonio Family Heart Study. Segregation and linkage analyses. (1995) (71)
- Evidence of genetic heterogeneity in the long QT syndrome. (1993) (71)
- Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees (2014) (70)
- Influence of age, sex and genetic factors on the human brain (2014) (69)
- Exploring Positional Candidate Genes: Linkage Conditional on Measured Genotype (2004) (69)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (68)
- Genetic and environmental influences on thyroid hormone variation in Mexican Americans. (2004) (68)
- Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees (1997) (68)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
- Common genetic influences on depression, alcohol, and substance use disorders in Mexican‐American families (2011) (67)
- Genetic association of preeclampsia to the inflammatory response gene SEPS1. (2008) (67)
- Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat (2015) (66)
- Diverse biological activities of the vascular non-inflammatory molecules - the Vanin pantetheinases. (2012) (66)
- Effects of genotype‐by‐sex interaction on quantitative trait linkage analysis (1997) (65)
- Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22. (2006) (65)
- Shared Genetic Factors Influence Head Motion During MRI and Body Mass Index (2016) (65)
- Genetic and environmental correlations among hormone levels and measures of body fat accumulation and topography. (1996) (65)
- Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study) (2009) (64)
- Methylation of SOCS3 is inversely associated with metabolic syndrome in an epigenome-wide association study of obesity (2016) (64)
- A Multimodal Assessment of the Genetic Control over Working Memory (2010) (64)
- Genetic analysis of apolipoprotein A-I in two dietary environments. (1990) (63)
- Identification of two novel quantitative trait loci for pre-eclampsia susceptibility on chromosomes 5q and 13q using a variance components-based linkage approach. (2007) (63)
- Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging (2013) (62)
- Gamete-competition models. (2000) (62)
- Benchmarking Relatedness Inference Methods with Genome-Wide Data from Thousands of Relatives (2017) (61)
- Prosaposin is a regulator of progranulin levels and oligomerization (2016) (61)
- Intercellular adhesion molecule-1 concentration is genetically correlated with insulin resistance, obesity, and HDL concentration in Mexican Americans. (2004) (60)
- Long-Term Changes in Adiposity and Glycemic Control Are Associated With Past Adenovirus Infection (2013) (60)
- Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022) (60)
- Quantitative trait linkage mapping in anthropology. (1999) (59)
- A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
- A kernel of truth: statistical advances in polygenic variance component models for complex human pedigrees. (2013) (59)
- Quantitative trait locus determining dietary macronutrient intakes is located on human chromosome 2p22. (2004) (58)
- Association between variants in the genes for adiponectin and its receptors with insulin resistance syndrome (IRS)-related phenotypes in Mexican Americans (2006) (58)
- Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemia (1998) (57)
- Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism. (2001) (57)
- Localization of multiple quantitative trait loci influencing susceptibility to infection with Ascaris lumbricoides. (2008) (57)
- Quantitative genetic analysis of skin reflectance: a multivariate approach. (1992) (56)
- The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification (2005) (55)
- Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study. (2010) (55)
- Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs (2014) (55)
- Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families (2016) (55)
- Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
- Genetic Analysis of Cortical Thickness and Fractional Anisotropy of Water Diffusion in the Brain (2011) (54)
- Genetic component to susceptibility to Trichuris trichiura: Evidence from two Asian populations (2002) (54)
- Genetic Variation at the FTO Locus Influences RBL2 Gene Expression (2009) (54)
- A Quantitative Trait Locus on Chromosome 16q Influences Variation in Plasma HDL-C Levels in Mexican Americans (2003) (54)
- Heritability of plasma amyloid β in typical late‐onset Alzheimer’s disease pedigrees (2001) (54)
- Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits (2017) (53)
- The Pro12Ala variant of peroxisome proliferator-activated receptor-gamma2 (PPAR-gamma2) is associated with measures of obesity in Mexican Americans. (2000) (53)
- Leptin's sexual dimorphism results from genotype by sex interactions mediated by testosterone. (2002) (53)
- Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree. (2005) (52)
- Population structure analysis using polygenic traits: estimation of migration matrices. (1990) (52)
- Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a northern european family population (2013) (52)
- Genetic determinants of variation in gallbladder disease in the Mexican‐American population (1999) (52)
- Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19 (2016) (51)
- Power of variance component linkage analysis to detect epistasis (1997) (51)
- The Positive Association of Obesity Variants with Adulthood Adiposity Strengthens over an 80-Year Period: A Gene-by-Birth Year Interaction (2013) (51)
- Genetic determinants of mitochondrial content. (2007) (51)
- Human Plasma Lipidome Is Pleiotropically Associated With Cardiovascular Risk Factors and Death (2014) (51)
- Genetic Effects on DNA Methylation and Its Potential Relevance for Obesity in Mexican Americans (2013) (50)
- Analysis of Genetic Variability and Whole Genome Linkage of Whole-Brain, Subcortical, and Ependymal Hyperintense White Matter Volume (2009) (49)
- Linkage of serum insulin concentrations to chromosome 3p in Mexican Americans. (2000) (48)
- Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate. (2016) (48)
- Major Quantitative Trait Locus for Resting Heart Rate Maps to a Region on Chromosome 4 (2004) (48)
- Quantitative Trait Nucleotide Analysis Using Bayesian Model Selection (2010) (47)
- Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. (2020) (47)
- Additive host genetic factors influence fecal egg excretion rates during Schistosoma mansoni infection in a rural area in Brazil. (2002) (47)
- Evidence for a Major Gene for Type II Diabetes and Linkage Analyses With Selected Candidate Genes in Mexican-Americans (1996) (47)
- MACROD2 gene associated with autistic-like traits in a general population sample (2014) (46)
- Waist Circumference Independently Associates with the Risk of Insulin Resistance and Type 2 Diabetes in Mexican American Families (2013) (46)
- Endothelial nitric oxide synthase (eNOS) gene polymorphisms and their association with type 2 diabetes-related traits in Mexican Americans (2008) (45)
- Quantitative Trait Nucleotide Analysis Using Bayesian Model Selection (2005) (45)
- Heritability estimates on resting state fMRI data using the ENIGMA analysis pipeline (2017) (45)
- Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits (2015) (45)
- Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia. (2009) (44)
- Whole Brain and Regional Hyperintense White Matter Volume and Blood Pressure: Overlap of Genetic Loci Produced by Bivariate, Whole-Genome Linkage Analyses (2010) (44)
- An X Chromosome Association Scan of the Norfolk Island Genetic Isolate Provides Evidence for a Novel Migraine Susceptibility Locus at Xq12 (2012) (44)
- Quantitative genetic analysis of susceptibility to hookworm infection in a population from rural Zimbabwe. (1997) (43)
- A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes (2017) (43)
- A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
- Shared Genetic Factors Influence Amygdala Volumes and Risk for Alcoholism (2015) (43)
- Human QTL linkage mapping (2009) (42)
- The Ser(326)Cys Polymorphism of 8-Oxoguanine Glycosylase 1 (OGG1) Is Associated with Type 2 Diabetes in Mexican Americans (2010) (42)
- Evidence for at least two major loci influencing human fatness. (1998) (42)
- Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis (2016) (42)
- Statin action favors normalization of the plasma lipidome in the atherogenic mixed dyslipidemia of MetS: potential relevance to statin-associated dysglycemia[S] (2015) (42)
- Protein C Levels Are Regulated by a Quantitative Trait Locus on Chromosome 16: Results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project (2004) (42)
- Linkage analysis without defined pedigrees (2011) (42)
- Principal Component for Metabolic Syndrome Risk Maps to Chromosome 4p in Mexican Americans: The San Antonio Family Heart Study (2004) (41)
- Multivariate quantitative genetic simulations in anthropology with an example from the South Pacific. (1993) (41)
- Assessment of gene‐by‐sex interaction effect on bone mineral density (2012) (41)
- A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q: Results From the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project (2003) (40)
- Obesity and obesogenic growth are both highly heritable and modified by diet in a nonhuman primate model, the African green monkey (Chlorocebus aethiops sabaeus) (2017) (40)
- Genetic epidemiology of seropositivity for Trypanosoma cruzi infection in rural Goias, Brazil. (1997) (40)
- Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2018) (40)
- Transcriptomic Identification of ADH1B as a Novel Candidate Gene for Obesity and Insulin Resistance in Human Adipose Tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES) (2015) (40)
- Pleiotropy and genotype by diet interaction in a baboon model for atherosclerosis: a multivariate quantitative genetic analysis of HDL subfractions in two dietary environments. (1999) (40)
- Phenotypical Characterisation of the Isolated Norfolk Island Population Focusing on Epidemiological Indicators of Cardiovascular Disease (2006) (40)
- Quantitative trait locus detection using combined linkage/disequilibrium analysis (1999) (39)
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- Hepatic Gene Networks in Morbidly Obese Patients With Nonalcoholic Fatty Liver Disease (2010) (38)
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- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
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- INSIG1 influences obesity-related hypertriglyceridemia in humans (2010) (36)
- Evidence for a Major Gene Affecting Postchallenge Insulin Levels in Mexican-Americans (1995) (36)
- A Genome Search for Genetic Determinants That Influence Plasma Fibrinogen Levels (2005) (36)
- Blood Pressure and Cerebral White Matter Share Common Genetic Factors in Mexican Americans (2011) (36)
- The F7 Gene and Clotting Factor VII Levels: Dissection of a Human Quantitative Trait Locus (2006) (36)
- Rediscovering the value of families for psychiatric genetics research (2018) (36)
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- Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives (2019) (36)
- Two quantitative trait loci influence whipworm (Trichuris trichiura) infection in a Nepalese population. (2008) (36)
- Genetic variation in BEACON influences quantitative variation in metabolic syndrome-related phenotypes. (2004) (36)
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- Genotype by Diabetes Interaction Effects on the Detection of Linkage of Glomerular Filtration Rate to a Region on Chromosome 2q in Mexican Americans (2007) (35)
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- Genetic determinants of obesity-related lipid traits Published, JLR Papers in Press, February 1, 2004. DOI 10.1194/jlr.M300474-JLR200 (2004) (35)
- Fishing for Pleiotropic QTLs in a Polygenic Sea (2005) (35)
- Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility (2014) (35)
- Phenotypic, genetic, and genome-wide structure in the metabolic syndrome (2003) (34)
- Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease. (2013) (34)
- A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility (2012) (34)
- Genes influencing variation in serum osteocalcin concentrations are linked to markers on chromosomes 16q and 20q. (2000) (34)
- Transcriptomics in type 2 diabetes: Bridging the gap between genotype and phenotype (2015) (34)
- Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease (2011) (34)
- Corrigendum to “Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group” [NeuroImage 81 (2013) 455–469] (2014) (33)
- GAW12: Simulated Genome Scan, Sequence, and Family Data for a Common Disease (2001) (33)
- Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits. (2013) (33)
- PLASMA DIHYDROCERAMIDE SPECIES ASSOCIATE WITH WAIST CIRCUMFERENCE IN MEXICAN AMERICAN FAMILIES (2013) (33)
- The Effect of Pedigree Complexity on Quantitative Trait Linkage Analysis (2001) (33)
- Quantitative genetics of serum sex hormone-binding globulin levels in participants in the San Antonio Family Heart Study. (1997) (33)
- A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies. (2006) (32)
- Seroprevalence of 13 common pathogens in a rapidly growing U.S. minority population: Mexican Americans from San Antonio, TX (2011) (32)
- The Arg59Trp variant in ANGPTL8 (betatrophin) is associated with total and HDL-cholesterol in American Indians and Mexican Americans and differentially affects cleavage of ANGPTL3. (2016) (32)
- Genome-wide significant loci for addiction and anxiety (2016) (32)
- The reliability and heritability of cortical folds and their genetic correlations across hemispheres (2019) (32)
- P2 Promoter Variants of the Hepatocyte Nuclear Factor 4α Gene Are Associated With Type 2 Diabetes in Mexican Americans (2007) (32)
- Genetics of variation in HOMA-IR and cardiovascular risk factors in Mexican-Americans (2008) (32)
- The lipidome in major depressive disorder: Shared genetic influence for ether-phosphatidylcholines, a plasma-based phenotype related to inflammation, and disease risk (2017) (31)
- Evidence for bivariate linkage of obesity and HDL-C levels in the Framingham Heart Study (2003) (31)
- Quantitative genetics of sexual dimorphism in body fat measurements (1993) (31)
- A variant in the LRRFIP1 gene is associated with adiposity and inflammation (2012) (31)
- Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans (2013) (31)
- Pleiotropic effects of genes for insulin resistance on adiposity in baboons. (2004) (31)
- Population sequencing data reveal a compendium of mutational processes in human germline (2020) (31)
- The selective neutrality of dermatoglyphic variation (1988) (30)
- STOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trøndelag Health Study (2010) (30)
- Influence of Processing Pipeline on Cortical Thickness Measurement (2019) (30)
- Metabolic Syndrome is linked to Chromosome 7q21 and associated with genetic variants in CD36 and GNAT3 in Mexican Americans (2012) (30)
- Genetic Factors Influence Serological Measures of Common Infections (2011) (30)
- Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels (2008) (29)
- Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes (2020) (29)
- An epigenetic map of age-associated autosomal loci in northern European families at high risk for the metabolic syndrome (2015) (29)
- GAW10: Simulated family data for a common oligogenic disease with quantitative risk factors (1997) (29)
- Genetic and Molecular Functional Characterization of Variants within TNFSF13B, a Positional Candidate Preeclampsia Susceptibility Gene on 13q (2010) (29)
- Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island (2010) (29)
- Exploiting pleiotropy to map genes for oligogenic phenotypes using extended pedigree data (1997) (29)
- Collection of Pedigree Data for Genetic Analysis in Isolate Populations (2006) (28)
- The Gly(972)Arg Variant of Human IRS1 Gene Is Associated With Variation in Glomerular Filtration Rate Likely Through Impaired Insulin Receptor Signaling (2012) (28)
- Pleiotropic QTL on chromosome 19q13 for triglycerides and adiposity: the HERITAGE Family Study. (2006) (28)
- Induced Pluripotent Stem Cells in Disease Modeling and Gene Identification. (2018) (28)
- A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration (2020) (28)
- Rapid, Phase-free Detection of Long Identical by Descent Segments Enables Effective Relationship Classification. (2020) (28)
- Heritability of Hemostasis Phenotypes and Their Correlation with Type 2 Diabetes Status in Mexican Americans (2005) (28)
- Discovering Schizophrenia Endophenotypes in Randomly Ascertained Pedigrees (2015) (28)
- Metabolites as novel biomarkers for childhood obesity‐related traits in Mexican–American children (2015) (28)
- Genotype×age interaction in human transcriptional ageing (2012) (28)
- Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. (2019) (27)
- Bivariate linkage between acylation-stimulating protein and BMI and high-density lipoproteins. (2004) (27)
- Genetic determinants of cutaneous malignant melanoma in Sinclair swine. (1996) (27)
- Shared and unique genetic effects among seven HDL phenotypes. (1997) (27)
- Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels. (2010) (27)
- A gene expression signature for insulin resistance. (2011) (27)
- Sulcal Depth-Position Profile Is a Genetically Mediated Neuroscientific Trait: Description and Characterization in the Central Sulcus (2013) (27)
- A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study. (2007) (27)
- Linkage disequilibrium analysis in the genetically isolated Norfolk Island population (2008) (27)
- Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees (2017) (27)
- Genetic variation in PARL influences mitochondrial content (2010) (27)
- Functional analysis of the genetic variability in the F7 gene promoter. (2007) (27)
- Genetic epidemiology of cardiometabolic risk factors and their clustering patterns in Mexican American children and adolescents: the SAFARI Study (2013) (27)
- Inferring identical by descent sharing of sample ancestors promotes high resolution relative detection (2018) (26)
- Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q (2003) (26)
- Genome-wide scans reveal quantitative trait Loci on 8p and 13q related to insulin action and glucose metabolism: the San Antonio Family Heart Study. (2004) (26)
- Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
- Evidence for a Gene on Chromosome 13 Influencing Postural Systolic Blood Pressure Change and Body Mass Index (2004) (26)
- Common genetic variants and gene expression associated with white matter microstructure in the human brain (2014) (26)
- The genetic basis of the comorbidity between cannabis use and major depression (2017) (26)
- TRAK2, a novel regulator of ABCA1 expression, cholesterol efflux and HDL biogenesis (2017) (26)
- An empirical test of the significance of an observed quantitative trait locus effect that preserves additive genetic variation (1999) (26)
- Statistical Genetic Approaches to Human Adaptability (2009) (26)
- Bivariate Linkage Analysis of the Insulin Resistance Syndrome Phenotypes on Chromosome 7q (2005) (25)
- A neural signature of metabolic syndrome (2019) (25)
- The Processing-Speed Impairment in Psychosis Is More Than Just Accelerated Aging (2017) (25)
- Quantitative genetics of relative organ weight variation in captive baboons. (1993) (25)
- Pedigree analysis of HDL cholesterol concentration in baboons on two diets. (1988) (25)
- Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome (1998) (25)
- Heritability of age at first birth in captive olive baboons (1995) (25)
- Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
- Strategy and model building in the fourth dimension: a null model for genotype × age interaction as a Gaussian stationary stochastic process (2003) (25)
- Heritability of Volume, Surface Area and Thickness for Anatomically Defined Cortical Brain Regions Estimated in a Large Extended Pedigree (2009) (25)
- A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation (2013) (25)
- A DNA polymorphism for LCAT is associated with altered LCAT activity and high density lipoprotein size distributions in baboons. (1992) (24)
- Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data (2009) (24)
- Genetics of leptin expression in baboons (2003) (24)
- Genetic risk for earlier menarche also influences peripubertal body mass index. (2013) (24)
- Linkage exclusion analysis of the chromosome 11 region containing UCP2 and UCP3 with obesity-related phenotypes in Mexican Americans (2000) (24)
- Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Mutations in brief no. 153. Online. (1998) (24)
- Multivariate genetic analysis of apo AI concentration and HDL subfractions: Evidence for major locus pleiotropy (1993) (24)
- Identification of Pleiotropic Genetic Effects on Obesity and Brain Anatomy (2013) (24)
- The Genetics of Obesity in Mexican Americans: The Evidence from Genome Scanning Efforts in the San Antonio Family Heart Study (2003) (24)
- Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos (2012) (23)
- Genetic influences on bone loss in the San Antonio Family Osteoporosis study (2008) (23)
- Genetic determinants of normal variation in coagulation factor (F) IX levels: genome‐wide scan and examination of the FIX structural gene (2006) (23)
- Genotype by smoking interaction for leptin levels in the San Antonio family heart study (2002) (23)
- Principal Component and Linkage Analysis of Cardiovascular Risk Traits in the Norfolk Isolate (2009) (23)
- Genome-Wide Linkage Scan for Genes Influencing Plasma Triglyceride Levels in the Veterans Administration Genetic Epidemiology Study (2009) (23)
- Genetic Architecture of Carotid Artery Intima-Media Thickness in Mexican Americans (2013) (23)
- A Locus on Chromosome 2 Influences Levels of Tissue Factor Pathway Inhibitor: Results From the GAIT study (2005) (23)
- Genetic variants in the renin-angiotensin system genes are associated with cardiovascular-renal-related risk factors in Mexican Americans (2008) (23)
- Electrocardiographic characteristics in a population with high rates of seropositivity for Trypanosoma cruzi infection. (2007) (23)
- Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm (2013) (23)
- Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes (2019) (23)
- Quantitative genetics of dehydroepiandrosterone sulfate and its relation to possible cardiovascular disease risk factors in Mexican Americans. (1996) (23)
- Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms (2016) (23)
- Linkage mapping of CVD risk traits in the isolated Norfolk Island population (2008) (23)
- Heritable changes in regional cortical thickness with age (2014) (23)
- A quantitative trait locus influencing type 2 diabetes susceptibility maps to a region on 5q in an extended French family. (2002) (22)
- Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island. (2012) (22)
- Genetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass (2012) (22)
- Genetic Influences on Type 2 Diabetes and Metabolic Syndrome Related Quantitative Traits in Mauritius (2009) (22)
- Attitudes towards helminthic infection in the Jirel population of eastern Nepal. (1998) (22)
- Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model (2010) (22)
- Genotype × adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase A2, a marker of inflammation and oxidative stress (2007) (22)
- Genetic influence on cognitive development between childhood and adulthood (2018) (22)
- Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease (2020) (22)
- Recurrent major depression and right hippocampal volume: A bivariate linkage and association study (2016) (22)
- Genetic epidemiology of Trypanosoma cruzi infection and Chagas' disease. (2003) (22)
- Genotype by Sex and Genotype by Age Interactions with Sedentary Behavior: The Portuguese Healthy Family Study (2014) (21)
- Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020) (21)
- ADAM28 is elevated in humans with the metabolic syndrome and is a novel sheddase of human tumour necrosis factor‐α (2012) (21)
- Multivariate genetic analysis of nevus measurements and melanoma. (1992) (21)
- Host genetics and population structure effects on parasitic disease (2012) (21)
- Genetic Regulation of Plasma Levels of Vitamin K-dependent Proteins Involved in Hemostasis (2001) (21)
- 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans (2021) (20)
- Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study (2015) (20)
- Analysis of SLC16A11 Variants in 12,811 American Indians: Genotype-Obesity Interaction for Type 2 Diabetes and an Association With RNASEK Expression (2015) (20)
- Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q. (2005) (20)
- Genomic Searches for Genes That Influence Atherosclerosis and Its Risk Factors (2000) (20)
- Epigenetic Age Acceleration Assessed with Human White-Matter Images (2017) (20)
- Shared genetic variance between obesity and white matter integrity in Mexican Americans (2015) (20)
- Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study[S] (2020) (20)
- A White Matter Connection of Schizophrenia and Alzheimer’s Disease (2020) (20)
- The 27-bp repeat polymorphism in intron 4 (27 bp-VNTR) of endothelial nitric oxide synthase (eNOS) gene is associated with albumin to creatinine ratio in Mexican Americans (2009) (20)
- Power of Variance Component Linkage Analysis—II. Discrete Traits (2004) (20)
- Association of Genetic Variation Within UBL5 with Phenotypes of Metabolic Syndrome (2006) (19)
- Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families (2003) (19)
- Gene-by-age effects on BMI from Birth to Adulthood: The Fels Longitudinal Study (2013) (19)
- Utility of Lymphoblastoid Cell Lines for Induced Pluripotent Stem Cell Generation (2016) (19)
- Oligogenic model selection using the bayesian information criterion: Linkage analysis of the P300 Cz event‐related brain potential (1999) (19)
- Disentangling the genetic overlap between cholesterol and suicide risk (2018) (19)
- Estimating the additive genetic effect of the X chromosome (2005) (19)
- Skin color variation in eastern Nepal. (1991) (19)
- Obesity and diabetes gene discovery approaches. (2003) (18)
- Genetic analysis of sexual dimorphism in serum apo AI and HDL‐C concentrations in baboons (1992) (18)
- Lipidomics in the Study of Hypertension in Metabolic Syndrome (2017) (18)
- Genetic diversity fuels gene discovery for tobacco and alcohol use (2022) (18)
- The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells (2011) (18)
- Transcriptomics of cortical gray matter thickness decline during normal aging (2013) (18)
- Genotype by sex interaction in measures of lipids, lipoproteins, and apolipoproteins (1993) (18)
- Genome sequencing unveils a regulatory landscape of platelet reactivity (2019) (18)
- Exome array analysis suggests an increased variant burden in families with schizophrenia (2017) (18)
- Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression. (2016) (18)
- Waist circumference is genetically correlated with incident Type 2 diabetes in Mexican‐American families (2014) (18)
- Genotype-by-smoking interaction for leptin levels in the Metabolic Risk Complications of Obesity Genes project (2003) (17)
- Differences in the Heritability of Growth and Growth Velocity During Infancy and Associations With FTO Variants (2011) (17)
- Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential (2022) (17)
- Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk. (2016) (17)
- Triiodothyronine exerts a major pleiotropic effect on reverse cholesterol transport phenotypes. (1996) (17)
- Impact of family structure and common environment on heritability estimation for neuroimaging genetics studies using Sequential Oligogenic Linkage Analysis Routines (2014) (17)
- Replication of Linkage to Quantitative Trait Loci: Variation in Location and Magnitude of the Lod Score (2001) (17)
- Imaging local genetic influences on cortical folding (2020) (17)
- Genetic analysis of personality traits and alcoholism using a mixed discrete continuous trait variance component model (1999) (17)
- Genetic epidemiology of fecal egg excretion during Schistosoma mansoni infection in an endemic area in Minas Gerais, Brazil. (2001) (17)
- The Genes Influencing Adiponectin Levels Also Influence Risk Factors for Metabolic Syndrome and Type 2 Diabetes (2007) (17)
- Genome-wide scan of resistin mRNA expression in omental adipose tissue of baboons (2005) (17)
- A Genome‐Wide Linkage Scan for Quantitative Trait Loci Influencing the Craniofacial Complex in Humans (Homo sapiens sapiens) (2011) (17)
- Sex-Specific Regulation of Mitochondrial DNA Levels: Genome-Wide Linkage Analysis to Identify Quantitative Trait Loci (2012) (16)
- Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetes (2000) (16)
- An EM algorithm for obtaining maximum likelihood estimates in the multi-phenotype variance components linkage model. (2000) (16)
- Human F7 sequence is split into three deep clades that are related to FVII plasma levels (2006) (16)
- Thromboplastin-thrombomodulin-mediated Time and Serum Folate Levels Are Genetically Correlated with the Risk of Thromboembolic Disease: Results from the GAIT Project (2002) (16)
- The F7 Gene and Clotting Factor VII Levels: Dissection of a Human Quantitative Trait Locus (2005) (16)
- Identification and Functional Characterization of G 6 PC 2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G 6 PC 2-ABCB 11 Locus (2015) (16)
- Pleiotropic QTL on Chromosome 12q23–q24 Influences Triglyceride and High-Density Lipoprotein Cholesterol Levels: The HERITAGE Family Study (2006) (16)
- Genetics of serum carotenoid concentrations and their correlation with obesity-related traits in Mexican American children. (2017) (16)
- Type I error rates in association versus joint linkage/association tests in related individuals (2007) (16)
- Variability in Associations of Phosphatidylcholine Molecular Species with Metabolic Syndrome in Mexican–American Families (2013) (16)
- Association of Genetic Variation in ENPP1 With Obesity‐related Phenotypes (2008) (16)
- Human Cortical Thickness Organized into Genetically-determined Communities across Spatial Resolutions (2019) (16)
- Fasting Insulin and Obesity-Related Phenotypes Are Linked to Chromosome 2p (2006) (15)
- A quantitative trait locus on chromosome 22 for serum leptin levels adjusted for serum testosterone. (2002) (15)
- Increased waist circumference is independently associated with hypothyroidism in Mexican Americans: replicative evidence from two large, population-based studies (2014) (15)
- Genome-Wide Analyses of Working-Memory Ability: A Review (2014) (15)
- Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes (2019) (15)
- Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed (2022) (15)
- Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity (2018) (15)
- A quantitative trait locus influencing estrogen levels maps to a region homologous to human chromosome 20. (2001) (15)
- Genetic control of apolipoprotein A-I distribution among HDL subclasses. (1995) (15)
- The Influence of Siblings On Wild Infant Chimpanzee Social Interaction (1997) (15)
- Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention (2022) (14)
- Genome-wide genetic investigation of serological measures of common infections (2015) (14)
- Evidence for genetic correlation between human cerebral white matter microstructure and inflammation (2019) (14)
- Serum phosphatidylinositol as a biomarker for bipolar disorder liability (2017) (14)
- Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22. (2014) (14)
- P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans (2012) (14)
- Genetic epidemiology of Chagas disease. (2011) (14)
- Contemporary model-free methods for linkage analysis. (2008) (14)
- Genetic Influences on Plasma Cytokine Variation in a Parasitized Population (2004) (14)
- Novel Associations of Nonstructural Loci with Paraoxonase Activity (2012) (13)
- Quantitative Traits and Population Structure: Introduction (1990) (13)
- Quantitative Trait Locus on Chromosome 1q Influences Bone Loss in Young Mexican American Adults (2009) (13)
- Familial analysis of bipolar affective disorder using logistic models (1989) (13)
- Genome-Wide Linkage Screen for Systolic Blood Pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and Confirmation of a Major Susceptibility Locus on Chromosome 6q14.1 (2011) (13)
- Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity. (2014) (13)
- Do Candidate Genes Affect the Brain’s White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans (2017) (13)
- A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies (2021) (13)
- Detecting Genotype × Age Interaction (2001) (13)
- Genetic Variants Influencing Joint Damage in Mexican Americans and European Americans With Rheumatoid Arthritis (2015) (13)
- Cortical bone health shows significant linkage to chromosomes 2p, 3p, and 17q in 10-year-old children. (2011) (13)
- Genome-wide scans for microalbuminuria in Mexican Americans: The San Antonio Family Heart Study (2007) (13)
- Plasma lipidome is independently associated with variability in metabolic syndrome in Mexican American families (2014) (13)
- UniMóvil: A Mobile Health Clinic Providing Primary Care to the Colonias of the Rio Grande Valley, South Texas (2019) (13)
- Quantitative genetic analysis of glucose transporter 4 mRNA levels in baboon adipose. (2004) (13)
- Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia (2018) (13)
- GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans (2016) (13)
- Pleiotropic locus for emotion recognition and amygdala volume identified using univariate and bivariate linkage. (2015) (13)
- The characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndrome. (2010) (12)
- Transcriptomic Profiling of Fibropapillomatosis in Green Sea Turtles (Chelonia mydas) From South Texas (2020) (12)
- Sex-specific genetic effects in physical activity: results from a quantitative genetic analysis (2015) (12)
- Common polygenic variation contributes to risk of migraine in the Norfolk Island population (2015) (12)
- Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican Americans. (2007) (12)
- Genomic kinship construction to enhance genetic analyses in the human connectome project data (2018) (12)
- Proximate determinants of fertility in the Kathmandu valley, Nepal: an anthropological case study (1986) (12)
- Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program (2020) (12)
- A QTL for Genotype by Sex Interaction for Anthropometric Measurements in Alaskan Eskimos (GOCADAN Study) on Chromosome 19q12–13 (2011) (12)
- QTL-based association analyses reveal novel genes influencing pleiotropy of Metabolic Syndrome (MetS) (2013) (12)
- Effects of genotype×sex interaction on linkage analysis of visual event‐related evoked potentials (1999) (12)
- Fast Genome‐Wide QTL Association Mapping on Pedigree and Population Data (2014) (12)
- Potential effects of ethnicity in genetic and environmental sources of variability in the stature, mass, and body mass index of children. (1999) (12)
- Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate (2011) (12)
- Genetic determination of biological age in the mennonites of the midwestern United States (2002) (12)
- Genetic analysis of chest dimensions in a high altitude Tibetan population from upper Chumik, Nepal (1993) (12)
- Genetic correlations between lipoprotein phenotypes and indicators of sex hormone levels in Mexican Americans. (1996) (11)
- Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. (2021) (11)
- Genome‐wide significant linkage of schizophrenia‐related neuroanatomical trait to 12q24 (2015) (11)
- Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p (2005) (11)
- Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines (2012) (11)
- Genetics of variation in adiponectin in pedigreed baboons: evidence for pleiotropic effects on adipocyte volume and serum adiponectin (2008) (11)
- Power to Localize the Major Gene for Disease Liability Is Increased After Accounting for the Effects of Related Quantitative Phenotypes (2001) (11)
- Cognitive impairment from early to middle adulthood in patients with affective and nonaffective psychotic disorders (2019) (11)
- A retrospective examination of mean relative telomere length in the Tasmanian Familial Hematological Malignancies Study (2014) (11)
- Epidemiologic investigation of tuberculosis in a Mexican population from Chihuahua State, Mexico: a pilot study. (2013) (11)
- A genetic association study of carotid intima-media thickness (CIMT) and plaque in Mexican Americans and European Americans with rheumatoid arthritis. (2017) (11)
- Effects of a major gene for apolipoprotein A-I concentration are thyroid hormone dependent in Mexican Americans. (1996) (11)
- Linkage Analysis of Quantitative Traits in Randomly Ascertained Pedigrees: Comparison of Penetrance‐Based and Variance Component Analysis (2001) (11)
- A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels (2008) (11)
- A Locus on Chromosome 13 Influences Levels of TAFI Antigen in Healthy Mexican Americans (2006) (10)
- Sex‐specific QTL effects on variation in paraoxonase 1 (PON1) activity in Mexican Americans (2007) (10)
- Genome-wide scan identifies a quantitative trait locus at 4p15.3 for serum urate (2010) (10)
- Genetic regulation of plasma levels of vitamin K-dependent proteins involved in hematostatis: results from the GAIT Project. Genetic Analysis of Idiopathic Thrombophilia. (2001) (10)
- Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1 (2013) (10)
- Gene Expression Differences Between Offspring of Long-Lived Individuals and Controls in Candidate Longevity Regions: Evidence for PAPSS2 as a Longevity Gene. (2016) (10)
- Cross-species replication of a resistin mRNA QTL, but not QTLs for circulating levels of resistin, in human and baboon (2008) (10)
- Evaluation of Polymorphisms in Paraoxonase 2 (PON2) Gene and Their Association with Cardiovascular-Renal Disease Risk in Mexican Americans (2009) (10)
- Longitudinal familial analysis of blood pressure involving parametric (co)variance functions (2003) (10)
- Genotype x adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase A2, a marker of inflammation and oxidative stress. (2007) (10)
- Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study (2017) (10)
- Localization of a major susceptibility locus influencing preterm birth. (2013) (10)
- Utilizing extended pedigree information for discovery and confirmation of copy number variable regions among Mexican Americans (2012) (10)
- Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate (2015) (10)
- Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p (2005) (10)
- Acanthosis nigricans as a composite marker of cardiometabolic risk and its complex association with obesity and insulin resistance in Mexican American children (2020) (9)
- Heritability of Brachydactyly Type A3 in Children, Adolescents, and Young Adults from an Endogamous Population in Eastern Nepal (2007) (9)
- Multiple QTLs Influence Variation in Paraoxonase 1 Activity in Mexican Americans (2006) (9)
- Genetic correlation between plasma levels of C4BP isoforms containing β chains and susceptibility to thrombosis (2004) (9)
- Why endophenotype development requires families (2011) (9)
- ADAM19: A Novel Target for Metabolic Syndrome in Humans and Mice (2017) (9)
- Evaluation of qualitative methods for phenotyping brachymesophalangia‐V from radiographs of children (2012) (9)
- Erratum: Hemoglobin concentration of high-altitude tibetans and Bolivian aymara (American Journal of Physical Anthropology (1998) 106 (385-400)) (1998) (9)
- Association of Neuropeptide Y Receptor Y5 Polymorphisms with Dyslipidemia in Mexican Americans (2007) (9)
- Identification of a large deletion and three novel mutations in exon 13 of the factor V gene in a Spanish family with normal factor V coagulant and anticoagulant properties (2002) (9)
- Soluble Forms of Intercellular and Vascular Cell Adhesion Molecules Independently Predict Progression to Type 2 Diabetes in Mexican American Families (2016) (9)
- Presentation, Heritability, and Genome-Wide Linkage Analysis the Midchildhood Growth Spurt in Healthy Children from the Fels Longitudinal Study (2008) (9)
- On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis (2003) (9)
- Introduction to genetic analysis workshop 17 summaries (2011) (9)
- Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
- Linkage disequilibrium across two different single-nucleotide polymorphism genome scans (2005) (9)
- Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes (2014) (9)
- ‘Mutiny on the Bounty’: the genetic history of Norfolk Island reveals extreme gender-biased admixture (2015) (9)
- A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American family (2006) (9)
- Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes (2021) (9)
- Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease (2022) (9)
- Gene by Smoking Interaction: Evidence for Effects on Low-Density Lipoprotein Size and Plasma Triglyceride and High-Density Lipoprotein Cholesterol Levels (2004) (9)
- Asymptotic power of likelihood‐ratio tests for detecting quantitative trait loci using the COGA data (1999) (9)
- Genetics of adult body mass and maintenance of adult body mass in captive baboons (Papio hamadryas subspecies) (1997) (9)
- Genetical genomics of Th1 and Th2 immune response in a baboon model of atherosclerosis risk factors. (2011) (8)
- Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS) (2018) (8)
- A Quantitative Trait Locus Influencing Activin-to-Estrogen Ratio in Pedigreed Baboons Maps to a Region Homologous to Human Chromosome 19 (2001) (8)
- Genome-wide linkage scan for loci influencing plasma triglyceride levels (2018) (8)
- Genome-wide discovery of maternal effect variants (2009) (8)
- Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program (2019) (8)
- Occurrence of soil-transmitted helminths in women at the Himalayan region of Nepal. (2006) (8)
- Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes (2020) (8)
- Evidence for genetic susceptibility to developing early childhood diarrhea among shantytown children living in northeastern Brazil. (2011) (8)
- Joint Linkage and Association Analysis of the Hepatic Lipase Promoter Polymorphism and Lipoprotein Size Phenotypes (2001) (8)
- Combined cis-regulator elements as important mechanism affecting FXII plasma levels. (2010) (8)
- Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate (2016) (8)
- Family-based analyses reveal novel genetic overlap between cytokine interleukin-8 and risk for suicide attempt (2019) (8)
- Evaluating a CLL susceptibility variant in ITGB2 in families with multiple subtypes of hematological malignancies. (2017) (8)
- Corrigendum to " Diverse biological activities of the vascular non-inflammatory molecules - The Vanin pantetheinases" [Biochem. Biophys. Res. Commun. 417 (2012) 653-658] (2012) (8)
- The Gly ( 972 ) Arg Variant of Human Insulin Receptor Substrate 1 Gene Is Associated With Variation in Glomerular Filtration Rate Likely Through Impaired Insulin Receptor Signaling (2012) (8)
- A comparison of univariate, bivariate, and trivariate whole-genome linkage screens of genetically correlated electrophysiological endophenotypes (2005) (8)
- Genotype by Energy Expenditure Interaction with Metabolic Syndrome Traits: The Portuguese Healthy Family Study (2013) (8)
- Integrating genomic analysis with the genetic basis of gene expression: preliminary evidence of the identification of causal genes for cardiovascular and metabolic traits related to nutrition in Mexicans. (2012) (7)
- Genomewide linkage analysis of soluble transferrin receptor plasma levels (2005) (7)
- Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2016) (7)
- Genetic analysis of serum alanine transaminase activity in normal and hepatitis C virus-infected chimpanzees: an application of research-oriented genetic management. (1996) (7)
- Hemoglobin Concentration of High-Altitude Tibetans (1998) (7)
- Genetic correlation of the plasma lipidome with type 2 diabetes, prediabetes and insulin resistance in Mexican American families (2017) (7)
- Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway[S] (2019) (7)
- Genetic Analysis of Quantitative Traits in Highly Ascertained Samples: Total Serum IgE in Families with Asthma (2001) (7)
- Mapping of Susceptibility Genes for Obesity, Type 2 Diabetes, and the Metabolic Syndrome in Human Populations (2015) (7)
- Apolipoprotein B and a second major gene locus contribute to phenotypic variation of spontaneous hypercholesterolemia in pigs. (1994) (7)
- Assessing the effects of candidate genes on quantitative traits in primate populations (1992) (7)
- Genetic architecture of the F7 gene in a Spanish population: implication for mapping complex diseases and for functional assays (2006) (7)
- An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels (2018) (7)
- Statistical genetic approaches to human adaptability. (1993) (7)
- APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups (2021) (7)
- Evaluation of gremlin 1 (GREM1) as a candidate susceptibility gene for albuminuria-related traits in Mexican Americans with type 2 diabetes mellitus. (2009) (7)
- Nonsyndromic brachydactyly type D and type E mapped to 7p15 in healthy children and adults from the jirel ethnic group in eastern nepal (2013) (7)
- Whole genome sequence analysis of blood lipid levels in >66,000 individuals (2021) (7)
- Effects of copy number variable regions on local gene expression in white blood cells of Mexican Americans (2015) (7)
- Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices (2021) (7)
- A quantitative trait locus influences coordinated variation in measures of ApoB-containing lipoproteins. (2004) (6)
- Associations of cannabis use disorder with cognition, brain structure, and brain function in African Americans (2020) (6)
- Highly efficient induced pluripotent stem cell reprogramming of cryopreserved lymphoblastoid cell lines (2020) (6)
- Human Host Susceptibility to Intestinal Worm Infections (2002) (6)
- Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma. (2019) (6)
- ELA and fertility in American Standardbred horses. (2009) (6)
- Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies (2018) (6)
- Pedigree-based random effect tests to screen gene pathways (2014) (6)
- Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family‐Based Linkage and Association in the IRAS Family Study (2017) (6)
- Quantitative Trait Locus on Chromosome 12q14.1 Influences Variation in Plasma Plasminogen Levels in the San Antonio Family Heart Study (2007) (6)
- Genetic polymorphisms in the renin-angiotensin system (RAS) genes and their association analysis with type 2 diabetes and related traits in Mexican Americans. (2008) (6)
- Linkage of Type 2 Diabetes on Chromosome 9p24 in Mexican Americans: Additional Evidence from the Veterans Administration Genetic Epidemiology Study (VAGES) (2013) (6)
- A variance component-based gene burden test (2014) (6)
- Anthropological Genetics: Mapping Genes Influencing Human Quantitative Trait Variation (2006) (6)
- X chromosome effects and their interactions with mitochondrial effects (2005) (6)
- Evolution of the Simulated Data Problem (2001) (6)
- Role of miRNA-mRNA Interaction in Neural Stem Cell Differentiation of Induced Pluripotent Stem Cells (2020) (6)
- Does Accounting for Mitochondrial Genetic Variation Improve the Fit of Genetic Models? (2001) (6)
- Genetic-epidemiological methods in anthropological research. (1993) (6)
- Lack of Association between SLC30A8 Variants and Type 2 Diabetes in Mexican American Families (2016) (6)
- Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. (2021) (6)
- Genetic epidemiology of non-insulin-dependent diabetes mellitus (NIDDM) in north India: distribution of Gm and Km allotypes in 'Punjabis'. (1990) (6)
- Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries (2018) (6)
- Reliability of genomic predictions of complex human phenotypes (2018) (5)
- Simulation of a common oligogenic disease with quantitative risk factors. GAW9 problem 2: The answers (1995) (5)
- Update to Blangero's “Statistical Genetic Approaches to Human Adaptability” (1993): A Unified Theory of Genotype × Environment Interaction (2009) (5)
- Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure (2014) (5)
- Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed (2019) (5)
- Dissecting the functions of DISC1 (2011) (5)
- Deficits in visual working-memory capacity and general cognition in African Americans with psychosis (2017) (5)
- A human case of Hymenolepis diminuta infection in Nepal (2007) (5)
- Combining meta- and mega- analytic approaches for multi-site diffusion imaging based genetic studies: From the ENIGMA-DTI working group (2014) (5)
- Unifying Ideas for Non-Parametric Linkage Analysis (2011) (5)
- Gestational Age and the Cord Blood Lipidomic Profile in Late Preterm and Term Infants (2018) (5)
- A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers (2015) (5)
- Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology (2020) (5)
- Genome‐Wide Genetic and Transcriptomic Investigation of Variation in Antibody Response to Dietary Antigens (2014) (5)
- Clonal hematopoiesis is driven by aberrant activation of TCL1A (2021) (5)
- Plasma lipid profi ling in a large population-based cohort (2013) (5)
- Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program (2020) (5)
- Autosomal Genome-Wide Linkage Analysis to Identify Loci for Gallbladder Wall Thickness in Mexican Americans (2008) (5)
- Do rare variant genotypes predict common variant genotypes? (2011) (5)
- Disease Modeling and Disease Gene Discovery in Cardiomyopathies: A Molecular Study of Induced Pluripotent Stem Cell Generated Cardiomyocytes (2021) (5)
- The Quantitative‐MFG Test: A Linear Mixed Effect Model to Detect Maternal‐Offspring Gene Interactions (2016) (5)
- The Cys(311)Ser polymorphism of paraoxonase 2 (PON2) is associated with albumin-to-creatinine ratio (ACR) in Mexican Americans. (2007) (5)
- Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population. (2010) (4)
- Rare genetic variants explain missing heritability in smoking (2022) (4)
- Genome-wide linkage scan for quantitative trait loci underlying normal variation in heel bone ultrasound measures (2011) (4)
- Minimal Relationship between Local Gyrification and General Cognitive Ability in Humans. (2020) (4)
- Modeling methylation data as an additional genetic variance component (2018) (4)
- Fast and powerful genome wide association of dense genetic data with high dimensional imaging phenotypes (2018) (4)
- Power Estimates for Voxel-Based Genetic Association Studies Using Diffusion Imaging (2013) (4)
- Genetic Influence on the Human Brain (2015) (4)
- Smoothing of the bivariate LOD score for non-normal quantitative traits (2005) (4)
- A performance assessment of relatedness inference methods using genome-wide data from thousands of relatives (2017) (4)
- Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation (2021) (4)
- Genetic epidemiology of non-insulin-dependent diabetes mellitus in north India: preliminary analyses of some genetic markers in Punjabis. (1991) (4)
- Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program (2021) (4)
- Genotype by Energy Expenditure Interaction and Body Composition Traits: The Portuguese Healthy Family Study (2014) (4)
- Genetic determinants of iron metabolism plasma phenotypes and their relationship with risk of thrombosis. (2003) (4)
- Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies (2022) (4)
- A Quantitative Trait Locus on Chromosome 5p Influences D-Dimer Levels in the San Antonio Family Heart Study (2010) (4)
- Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
- Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships (2018) (4)
- Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. (2021) (4)
- Erratum: Quantitative trait locus determining dietary macronutrient intakes is located on human chromosome 2p22 (American Journal of Clinical Nutrition (2004) 80, (1410-1414)) (2006) (4)
- Axial quantitative ultrasound assessment of pediatric bone quality in eastern Nepal (2015) (4)
- Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease (2019) (4)
- Power of variance component linkage analysis to detect quantitative trait loci (1999) (4)
- A linkage analysis of cigarette and alcohol consumption in an unselected Mexican American population (2008) (4)
- Progressive Bidirectional Age-Related Changes in Default Mode Network Effective Connectivity across Six Decades (2016) (4)
- Genetics of Human Host Susceptibility to Ascariasis (2013) (3)
- Genotype phasing in pedigrees using whole-genome sequence data (2020) (3)
- Genetic and environmental (physical fitness and sedentary activity) interaction effects on cardiometabolic risk factors in Mexican American children and adolescents (2018) (3)
- New approaches for the discovery of lipid.related genes (2011) (3)
- Lipidomic profiling in the Strong Heart Study identified American Indians at risk of chronic kidney disease. (2022) (3)
- Serum carotenoids and Pediatric Metabolic Index predict insulin sensitivity in Mexican American children (2021) (3)
- Chronic neuropsychiatric sequelae of SARS‐CoV‐2: Protocol and methods from the Alzheimer's Association Global Consortium (2022) (3)
- Evaluation of Neurotrophic Tyrosine Receptor Kinase 2 (NTRK2) as a positional candidate gene for variation in estimated Glomerular Filtration Rate (eGFR) in Mexican American participants of San Antonio Family Heart Study (2015) (3)
- Correction: Waist Circumference Independently Associates with the Risk of Insulin Resistance and Type 2 Diabetes in Mexican American Families (2013) (3)
- Genetic Research on Ocular Health and Disease in a Population from Nepal (2018) (3)
- Distribution of lod Scores in Oligogenic Linkage Analysis (2001) (3)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (3)
- Ontogenetic changes in genetic regulation of fetal morphometrics in baboons (Papio hamadryas subspp.). (1997) (3)
- Segregation Analysis, Complex (2005) (3)
- Challenges for genetic analysis in the 21st century: localizing and characterizing genes for common complex diseases and their quantitative risk factors (2000) (3)
- T33 Serum Phosphatidylinositol As A Biomarker For Bipolar Disorder Liability (2017) (3)
- Surprising impacts of crossover interference and sex-specific genetic maps on identical by descent distributions (2019) (3)
- Glycated Serum Protein Genetics and Pleiotropy with Cardiometabolic Risk Factors (2019) (3)
- Chapter 2.1.3 Linkage strategies for mapping genes for complex traits in man (1999) (3)
- OS077. The chromosome 2q22 preeclampsia susceptibility locus reveals shared novel risk factors for CVD. (2012) (3)
- Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders (2014) (3)
- Erratum to: ‘Mutiny on the Bounty’: the genetic history of Norfolk Island reveals extreme gender-biased admixture (2015) (3)
- Genetic Overlap Profiles of Cognitive Ability in Psychotic and Affective Illnesses: A Multisite Study of Multiplex Pedigrees (2021) (3)
- Molecular Profiling of Human Induced Pluripotent Stem Cell‐Derived Hypothalamic Neurones Provides Developmental Insights into Genetic Loci for Body Weight Regulation (2017) (3)
- Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries (2020) (3)
- Human genome meeting 2016 (2016) (3)
- Quantitative HLA‐class‐II/factor VIII (FVIII) peptidomic variation in dendritic cells correlates with the immunogenic potential of therapeutic FVIII proteins in hemophilia A (2020) (3)
- Genetic variants in transient receptor potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans. (2011) (3)
- OS049. Exome sequencing identifies likely functional variantsinfluencing preeclampsia and CVD risk. (2012) (3)
- Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
- Further evidence supporting a potential role for ADH1B in obesity (2019) (3)
- Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program (2021) (3)
- Characterizing the Extent of Human Genetic Variation for Performance-Related Traits (2010) (3)
- Genetic dissection of thrombin-activatable fibrinolysis inhibitor (TAFI) (2003) (3)
- Transcriptomic epidemiology of smoking (2007) (2)
- Evaluation of Gremlin1 ( GREM1 ) as a candidate susceptibility gene for albuminuria-related traits in Mexican Americans with Type 2 Diabetes (2010) (2)
- Update to Blangero et al.'s “Quantitative Trait Nucleotide Analysis Using Bayesian Model Selection” (2005): From QTL Localization to Functional Variant Identification (2009) (2)
- Quantitative physical activity assessment of children and adolescents in a rural population from Eastern Nepal (2016) (2)
- The reliability and heritability of cortical folds and their genetic correlations across hemispheres (2020) (2)
- Variation in osteoarthritis biomarker serum comp levels in Mexican Americans is associated with SNPs in a region of chromosome 22q encompassing MICAL3, BCL2L13, and BID (2013) (2)
- Familial Studies: Genetic Inferences (2015) (2)
- Using the Schmahmann Syndrome Scale to Assess Cognitive Impairment in Young Adults with Metabolic Syndrome: a Hypothesis-Generating Report (2020) (2)
- Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India: Findings From the INDIGENIUS Consortium (2022) (2)
- Erratum: Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular psychiatry (2020) 25 3 (584-602)) : Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2020) (2)
- Independent test assessment using the extreme value distribution theory (2016) (2)
- Genetic signal maximization using environmental regression (2011) (2)
- Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium (2021) (2)
- The Utility of Bayesian Model Averaging for Detecting Known Oligogenic Effects (2001) (2)
- 1.P.281 Two major genes influence levels of unesterified cholesterol in an HDL subfraction, HDL2a (1997) (2)
- Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension (2022) (2)
- Finding potential cis-regulatory loci using allele-specific chromatin accessibility as weights in a kernel-based variance component test (2016) (2)
- Genetics of DTI-derived parameters of cerebral white matter. A track-based heritability and linkage study in extended pedigree. (2009) (2)
- Identifying the Lipidomic Effects of a Rare Loss-of-Function Deletion in ANGPTL3 (2021) (2)
- Genetic Variants in Toll-Like Receptor 4 Gene and Their Association Analysis with Estimated Glomerular Filtration Rate in Mexican American Families (2016) (2)
- Planar cell polarity pathway and development of the human visual cortex (2018) (2)
- microRNA and mRNA interactions in induced pluripotent stem cell reprogramming of lymphoblastoid cell lines. (2019) (2)
- Searching for Imaging Biomarkers of Psychotic Dysconnectivity. (2020) (2)
- OS046. Genome-wide association scans identify novel maternalsusceptibility loci for preeclampsia. (2012) (2)
- Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2016) (1)
- Synchronous In-Vivo Large-Scale Transcriptional Profiling in Human Peripheral Blood Mononuclear Cells, Myocytes and Adipocytes (2010) (1)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Genetic architecture of smoking: Evaluating rare variant contribution from deep whole-genome sequencing of up to 26,000 individuals (2021) (1)
- Genome-wide physical activity interactions in adiposity (2017) (1)
- Part 6: The P blood group system: Genetic adaptation to helminthic zoonoses. (1982) (1)
- Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs (2014) (1)
- Association of Urinary Phthalates with Self-Reported Eye Affliction/Retinopathy in Individuals with Diabetes: National Health and Nutrition Examination Survey, 2001–2010 (2015) (1)
- Linkage Mapping: Localizing the Genes That Shape Human Variation (2015) (1)
- Amplitude of Visual P3 Phenotypic Marker for a Event-Related Potential as a Predisposition to Alcoholism: Preliminary Results from the COGA Project (1998) (1)
- Heritability of neurocognitive correlates of schizophrenia (2000) (1)
- The Genetic contribution to solving the cocktail-party problem (2022) (1)
- A variance component method for integrated pathway analysis of gene expression data (2016) (1)
- Genetic epidemiology of parasitic diseases (2004) (1)
- Abstract 367: Identification of the VNN1 Gene as a Novel CVD Risk Factor (2007) (1)
- Genetic structure of three populations of rhesus macaques (Macaca mulatta): Implications for genetic management (1992) (1)
- On the Role of Hemostasis Variables in Cardiometabolic Outcomes (2021) (1)
- Association of HIV-1 Infection and Antiretroviral Therapy With Type 2 Diabetes in the Hispanic Population of the Rio Grande Valley, Texas, USA (2021) (1)
- IDENTIFICATION OF GENETIC RISK VARIANTS FOR MAJOR PSYCHIATRIC DISORDERS IN COSTA RICAN FAMILIES USING WGS (2021) (1)
- Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
- Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population (2022) (1)
- The Role of Class II Human Leukocyte Antigens (cII-HLAs) in Determining the Immunogenic Potential of Therapeutic Factor VIII Proteins in Hemophilia Patients: The "Gate Keeper" Hypothesis (2018) (1)
- The association between changes in leptin concentration in adults and concurrent changes in body composition: The Fels Longitudinal Study (1998) (1)
- Data on genetic associations of carotid atherosclerosis markers in Mexican American and European American rheumatoid arthritis subjects (2018) (1)
- Publisher Correction: Brain charts for the human lifespan (2022) (1)
- Erratum to: Multi-region hemispheric specialization differentiates human from nonhuman primate brain function (2013) (1)
- Efficient Generation of Functional Hepatocytes from Human Induced Pluripotent Stem Cells for Disease Modeling and Disease Gene Discovery. (2021) (1)
- Obesity and Diabetes Gene Discovery Approaches (2005) (1)
- A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation (2013) (1)
- Non-alcoholic Fatty Liver Disease and Depression: Evidence for Genotype × Environment Interaction in Mexican Americans (2022) (1)
- Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease (2021) (1)
- A QTL on chromosome 3q23 influences processing speed in humans (2018) (1)
- A SEQUENCE VARIATION SCAN OF THE COAGULATION FACTOR ( F ) VIII STRUCTURAL GENE AND ASSOCIATIONS WITH PLASMA FVIII ACTIVITY ( FVIII : C ) LEVELS (2007) (1)
- A major gene for IGF-I serum concentration interacts with diet in Mexican Americans (1994) (1)
- Evaluation of COMT as a maternal preeclampsia candidate susceptibility gene, assessed by genotyping of the Val158Met polymorphism and by transcriptional profiling of decidual tissue (2009) (1)
- Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits (2017) (1)
- Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative (2021) (1)
- Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2019) (1)
- Genetic correlation of the plasma lipidome with type 2 diabetes, prediabetes and insulin resistance in Mexican American families (2017) (1)
- Presenilin associated, rhomboid-like protein: a mitochondrial intramembrane protease associated with insulin resistance and type 2 diabetes (2004) (1)
- Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program (2022) (1)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Metabolic syndrome predictors of brain gray matter volume in an age-stratified community sample of 776 Mexican- American adults: Results from the genetics of brain structure image archive (2022) (1)
- P059 Analysis of HLAcII peptidomes presented by dendritic cells (DCs) from healthy donors and hemophilia-A (HA) patients with or without factor VIII (FVIII) inhibitors after ex vivo administration of different therapeutic FVIII proteins (tFVIIIs) (2018) (1)
- Pleiotropic genetic influences on event-related brain potentials and alcoholism (1998) (1)
- Genz and Mendell-Elston Estimation of the High-Dimensional Multivariate Normal Distribution (2021) (1)
- Using Step‐Wise Linear Regression to Detect “Functional” Sequence Variants: Application to Simulated Data (2001) (1)
- Comprehensive genetic analysis of the human lipidome identifies novel loci controlling lipid homeostasis with links to coronary artery disease (2021) (1)
- Comparing empirical kinship derived heritability for imaging genetics traits in the UK biobank and human connectome project (2021) (1)
- Gene by smoking interaction (2004) (1)
- Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging (2012) (1)
- Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing (2023) (1)
- Permethrin pesticide residues in food mediate progressive neuronal disorder (2015) (1)
- Genotype phasing in pedigrees using whole-genome sequence data (2020) (1)
- ADAM 19 : A Novel Target for Metabolic Syndrome in Humans and Mice (2017) (1)
- Genetic analysis of glaucoma endophenotypes in a large Nepalese extended pedigree: The Jiri Eye Study. (2017) (0)
- Track-based study of age and gender difference in maturation and senescence of cerebral white matter. (2009) (0)
- Norfolk Island Population Origin Analysis (2004) (0)
- Quantitative trait loci fine mapping by expression profiling. (2005) (0)
- Abstract 2071: Genome-wide Association Study Identifies Genes Linking Abdominal Fat, Inflammation and Other Cardiovascular Disease Risk Factors in the Quebec Family Study (2009) (0)
- Rare coding variants in RCN3 are associated with blood pressure (2022) (0)
- Contraceptive efficacy among women at increased genetic risk. (1988) (0)
- 886. Can the General Cognitive Deficit in Psychosis Explain Small Working-Memory Capacity? (2017) (0)
- Association Between Polygenic Risk Score for Schizophrenia and Neurocognitive Measures in the Western Australian Family Study of Schizophrenia (Wafss) (2017) (0)
- Genetics of Factor VIII Inhibitor Development in Hemophilia Patients: Novel Statistical Approaches in the PATH Study (2018) (0)
- M18 An Exploratory Study of The Genetic Relationships Between Plasma-Based Measures of Inflammation And Brain Anatomy (2017) (0)
- Complex Rare Variation and Its Role in Endophenotypic Variation in Schizophrenia (2013) (0)
- F145. Extremely Weak Relationship Between Gyrification and Intelligence (2019) (0)
- Characterizing the genetic architecture of ocular biometrics in a south Asian population: The Jiri Eye Study (2016) (0)
- The genetic determinants of recurrent somatic mutations in 43,693 blood genomes (2023) (0)
- Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis (2023) (0)
- SU52 UTILITY OF PERIPHERAL miRNA EXPRESSION PROFILES AS BIOMARKERS AND PATHOLOGICAL INDICATORS OF NEUROPSYCHIATRIC DISEASE (2019) (0)
- Genomic reconstruction of Neandertal brain structure and function (2014) (0)
- The Utility of Genomics for Studying Primate Biology (2015) (0)
- The Prevalence of Glaucoma in the Jirel Ethnic Group of Nepal (2022) (0)
- Contents Vol. 75, 2013 (2013) (0)
- GENETIC INFLUENCE ON NEUROANATOMIC DEVELOPMENT BETWEEN CHILDHOOD AND ADULTHOOD (2019) (0)
- F49. Genetic Basis of Changes in Neurocognition and Psychopathology Between Childhood and Adulthood (2018) (0)
- Genetics of Cardiovascular Disease in Minority Populations (2015) (0)
- Specific Correction of the Intron-22 Inverted Factor VIII Gene in Autologous Blood Outgrowth Endothelial Cells from Patients with Severe Hemophilia A (2020) (0)
- Accurate Phasing of Pedigree Genotypes Using Whole Genome Sequence Data (2017) (0)
- Contents Vol. 71, 2011 (2011) (0)
- Identification of TNFSF13B as a genetic risk factor for preeclampsia: replication of association in Australian and Norwegian populations (2009) (0)
- LOCALIZING GENETIC LOCI FOR AFFECTIVE AND PSYCHOTIC DISORDERS WITH ENDOPHENOTYPES (2017) (0)
- Pleiotropy and genotype by diet interaction: A multivariate genetic analysis of HDL-C subfractions (1994) (0)
- Abstracts 389–428 (2002) (0)
- Combining linkage, genome-wide association and large-scale transcriptional profiling and to identify genes related to total antioxidant status (2009) (0)
- A genome-wide linkage analysis of migraine in the descendents of the Bounty Mutineers implicates the 13q chromosomal region (2009) (0)
- Heritable changes in regional cortical thickness with age (2014) (0)
- Genome-wide association of maxdrinks implicates a novel risk locus for alcohol dependence: CYP7B1 (2012) (0)
- Use of gene expression signature technology to identify VVP-808, a novel insulin sensitiser with efficacy in vitro and in vivo (2008) (0)
- Genetic studies in Psammomys obesus (2002) (0)
- O4. Genome wide sequencing approaches to identify missing heritability of preeclampsia (2015) (0)
- Contribution of Inbred Singletons to Variance Component Estimation of Heritability and Linkage (2018) (0)
- Erratum to: Multi-region hemispheric specialization differentiates human from nonhuman primate brain function (2013) (0)
- OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits. (2013) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- Quantitative trait locus determining dietary macronutrient intakes is located on human chromosome 2p22 1–3 (2004) (0)
- Safdgs Data. Genotypic Data of Rs7493 and Rs12704795 (0)
- Tapping the Power of Plasma Lipidome to Improve Hypertriglyceridemic Waist as a Predictor of Future Type 2 Diabetes (2015) (0)
- Childhood bone strength shows genetic linkage to chromosomes 2, 4 and 12: Results from the Fels Longitudinal Study (2007) (0)
- Genome-wide association of human amygdala volume identifies a QTL at IRX2 (2009) (0)
- SU74THE POTENTIAL OF LOCAL GYRIFICATION INDEX AS A NEUROPHENOTYPE (2019) (0)
- Exploratory analysis of imaging and behavioral phenotypes with sparse canonical correlation analysis (CCA) (2014) (0)
- Contents Vol. 6, 2016 (2016) (0)
- Molecular mechanisms of a disease susceptibility variant of SIRT1: Genotoxic stress‐induced, CTCF‐dependent activation of SIRT1 gene expression (2010) (0)
- Common polygenic variation contributes to risk of migraine in the Norfolk Island population (2015) (0)
- Investigating genetic correlations between the central sulcus and perirolandic cortex (2010) (0)
- VKučinskas-2001-2016 (2016) (0)
- Subject Index Vol. 60, 2005 (2006) (0)
- Erratum: Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p (International Journal of Obesity (2005) 29 (413-419) DOI: 10.1038/sj.ijo.0802817) (2005) (0)
- Genetic epidemiology of ocular health and disease in eastern Nepal: The Jiri Eye Study (JES) (2015) (0)
- Novel BMD loci identified by whole genome sequencing and CRISPR editing in zebrafish: The NHLBI Trans-Omics for Precision Medicine (TOPMED) study (2021) (0)
- Heritability of Central Corneal Thickness, Vertical Cup to Disc Ratio and Intraocular Pressure in an Isolated Greek Population (2009) (0)
- Lack of Association between SLC 30 A 8 Variants and Type 2 Diabetes in Mexican American Families (2016) (0)
- 1639-P: Effect of Educational Status on Fasting Glucose and HbA1c Concentrations Independent of Income and Population Differences in Indian Populations (2019) (0)
- Abnormal Morphology of an Adult Rocky Mountain Wood Tick, Dermacentor andersoni (2007) (0)
- Subject Index Vol. 46, 1996 (1996) (0)
- M9.2 Dissecting the allelic architecture of ERAP2: a novel preeclampsia susceptibility gene (2010) (0)
- Genetic correlations between circulating miRNAs and lipid profiles reveal novel biomarkers of CVD risk (2016) (0)
- Rare coding variants in RCN3 are associated with blood pressure (2022) (0)
- Genetic analysis of transcriptional profiles for the identification of genes influencing obesity (2006) (0)
- An EM algorithm for obtaining maximum likelihood estimates in the multi‐phenotype variance components linkage model (2000) (0)
- 64. The Processing-Speed Impairment in Psychosis is More than Just Accelerated Aging (2017) (0)
- 802. Cholesterol Efflux Mediates the Relationship between Suicide Risk and Unesterified Cholesterol (2017) (0)
- Cocaine Abuse Dependence Major depressive episode Current Lifetime Marijuana Abuse Dependence Mania Cunent Lifetime Obsessivekompulsive Opioid Abuse Dependence Panic disorder Sedative Abuse Dependence Somatization disorder Stimulant Abuse Deoendence (1998) (0)
- Association of the Thr377Met MYOC Mutation With IOP and Vertical Cup-to-Disc Ratios in a Small, Isolated Greek Population (2009) (0)
- Cocktail-party listening and cognitive abilities show strong pleiotropy (2023) (0)
- Bivariate Linkage Analysis for Albuminuria and Mean Arterial Pressure in Mexican Americans (2002) (0)
- Glaucoma demographics in Mexican American families: The San Antonio Family Eye Study (SAFES) (2017) (0)
- Influence of age, sex and genetic factors on the human brain (2013) (0)
- No Evidence of Cis-Acting SNPs In Immune Response Genes Previously Associated with Factor VIII Inhibitors: The San Antonio Family Heart Study (2010) (0)
- Fast and powerful genome wide association of dense genetic data with high dimensional imaging phenotypes (2018) (0)
- The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. (2023) (0)
- Linkage disequilibrium in an isolated population from Norfolk Island. (2006) (0)
- Response to Comment on: Lin et al. Long-Term Changes in Adiposity and Glycemic Control Are Associated With Past Adenovirus Infection. Diabetes Care 2013;36:701–707 (2013) (0)
- The Dendritic Cell HLA-Class-II/Therapeutic Factor VIII (FVIII) Peptidome Is Influenced in Unanticipated Ways By the B-Domain of FVIII and the FVIII Chaperon Protein, Von Willebrand Factor: The Outrigger and Glycosylation-Umbrella (GUMB) Hypotheses (2019) (0)
- OS070. Shared genetic risk factors for preeclampsia and cardiovascular disease. (2012) (0)
- Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts (2016) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (0)
- Genetic legacy of the mutiny on the Bounty: Use of the Norfolk Island population for CVD and migraine gene mapping (2009) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- Genetic epidemiology of cardiometabolic risk factors and their clustering patterns in Mexican American children and adolescents: the SAFARI Study (2013) (0)
- Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
- The Prevalence of Glaucoma among the Jirel Ethnic Group in Nepal: the Jiri Eye Study (2018) (0)
- T55 The Genetic Basis Of The Comorbidity Between Cannabis Use And Major Depression (2017) (0)
- Heritability of gyral surface area and gyral gray matter thickness (2009) (0)
- Human genome meeting 2016 (2016) (0)
- Genetic basis for the increased expression of vacuolar H+ translocating ATPase genes upon imatinib treatment in human lymphoblastoid cells (2013) (0)
- F8 and HLA-II Haplotypes in the Hispanic Population: Implications for Inhibitor Risk Development in Hispanic Hemophilia A Patients (2012) (0)
- Genetics of Latin American Diversity (GLAD) Project: insights into population genetics and association studies in recently admixed groups in the Americas (2023) (0)
- 1337-P: Prediction of Insulin Sensitivity Using Serum Carotenoid Concentrations and Pediatric Metabolic Index in Mexican-American Children (2019) (0)
- Genetic regulation of cognitive ability from early childhood to adolescence (2000) (0)
- M9.4 Endoplasmatic reticulum stress in decidual tissue from pregnancies complicated by preeclampsia (2010) (0)
- A quantitative trait locus for vascular cellular adhesion molecule-1 levels on chromosome 19 (2000) (0)
- Reliable heritability clustering - finding distinct genetic factors that influence cortical thickness (2010) (0)
- Evaluation of Neurotrophic Tyrosine Receptor Kinase 2 (NTRK2) as a positional candidate gene for variation in estimated Glomerular Filtration Rate (eGFR) in Mexican American participants of San Antonio Family Heart Study (2015) (0)
- Genetic Determinants of Metabolic Biomarkers and their Associations with Cardiometabolic Traits in Hispanic/Latino Adolescents (2021) (0)
- Migraine Linkage Mapping using the Norfolk Island Genetic Isolate. (2006) (0)
- Cell Survival in Corneal Endothelial Dystrophies Characterizing the Neural Signature of Metabolic Syndrome (2019) (0)
- A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration (2020) (0)
- DIRECT ESTIMATION OF GENETIC LIABILITY FOR MENTAL ILLNESS USING ENDOPHENOTYPES (2017) (0)
- The G505A Nonsynonymous Single-Nucleotide Polymorphism (SNP) in TAFI, the Gene Encoding Thrombin-Activatable Fibrinolysis Inhibitor (TAFI) Is Pleiotropically Associated with TAFI Antigen Levels and Coronary Heart Disease (CHD) in Mexican Americans of South Texas (2021) (0)
- Fast and Powerful Genome Wide Association Analysis of Dense Genetic Data with High Dimensional Imaging Phenotypes (2017) (0)
- From Anthropological Genetics to Discovery of Genes for Complex Diseases in Human Populations: The Transdisciplinary Impact of Professor Michael H. Crawford (2015) (0)
- Using the Schmahmann Syndrome Scale to Assess Cognitive Impairment in Young Adults with Metabolic Syndrome: a Hypothesis-Generating Report (2020) (0)
- Response to Comment on: Jowett et al. (2010) Genetic Variation at the FTO Locus Influences RBL2 Gene Expression. Diabetes;59:726–732 (2010) (0)
- Genetic analysis localizes a novel locus on chromosome 4q for the glaucoma endophenotype, cup-to-disc ratio: The Jiri Eye Study (2019) (0)
- T12 The Lipidome In Major Depressive Disorder: Shared Genetic Influence For Ether-Phosphatidylcholines, A Plasma-Based Phenotype Related To Inflammation, And Disease Risk (2017) (0)
- Association of ApoCIII common variants with risk of coronary artery disease: A Mendelian randomization study (2021) (0)
- 2093-P: Acanthosis Nigricans as a Composite Marker of Cardiometabolic Risk and Its Complex Association with Obesity and Insulin Resistance in Mexican-American Children (2019) (0)
- Analysis of LOXL1 SNPs and Glaucoma Endophenotypes: Central Corneal Thickness, Intraocular Pressure and Vertical Cup to Disc Ratio in an isolated Greek Population (2009) (0)
- Genotype by Diabetes Duration Interaction Effects on Gene Expression (2008) (0)
- Genetic study in psammomys obesus (2002) (0)
- A Q t L for Genotype by s ex Interaction for Anthropometric Measurements in Alaskan Eskimos (GOCADAN s tudy) on Chromosome (2011) (0)
- TRPV2 is a novel gut mechanosensor associated with obesity. (2006) (0)
- Disentangling the Effects of HLA DRB1*15:01 and DQB1*06:02 to Establish the True HLA Risk Allele for Inhibitor Development in the Treatment of Hemophilia A (2020) (0)
- Edinburgh Research Explorer Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex (2017) (0)
- Genome wide association and pathway analysis of segment-specific carotid intima-media thickness phenotypes: The San Antonio Family Heart Study (2011) (0)
- SU51 MIR-34A IN NEUROPSYCHIATRIC RESEARCH AND FUNCTIONAL ANALYSIS TO DEFINE ITS REGULATORY EFFECTS (2019) (0)
- Plasticity of the Human Plasma Lipidome is Genetically Influenced and Associated with Type 2 Diabetes in Mexican American Families (2015) (0)
- Large-Scale Transcriptional Profiling and Genome-Wide Association of Intelligence in the Genetics of Brain Structure and Function Study (2008) (0)
- Multivariate Quantitative Genetic Analysis of HDL Subfractions in Two Dietary Pleiotropy and Genotype by Diet Interaction in a Baboon Model for Atherosclerosis : A (1999) (0)
- 372. Healthy Developmental and Genetic Brain Modules Influence Maturation Abnormalities in Schizophrenia (2017) (0)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2018) (0)
- On study design in neuroimaging heritability analyses (2014) (0)
- gene and associations with plasma FVIII activity levels A sequence variation scan of the coagulation factor VIII (FVIII) structural (2009) (0)
- Serum carotenoids and Pediatric Metabolic Index predict insulin sensitivity in Mexican American children (2021) (0)
- Proteomic analysis of liver in rats chronically exposed to fluoride and AIN-93 M-hypercaloric diet (2013) (0)
- Effect of F7 Gene Promoter Polymorphisms on Factor VII Antigenic Levels. (2004) (0)
- 3069 Characterizing the Neural Signature of Metabolic Syndrome (2019) (0)
- Multiple Quantitative Trait Loci for Anti-EBNA-1 IgG Titres are Associated with Risk of Multiple Sclerosis (2015) (0)
- Acknowledgement to the Reviewers, Vol. 46, 1996 (1996) (0)
- Whole genome sequence association analysis of Brain MRI measures (2022) (0)
- P196 Quantizinghla-class-II (HLACII) peptidomic parameters as immunologically-relevantendophenotypes toimproveimmunogenicity risk prediction for protein therapeutics (“Biologics”) using factor(F) VIII inhibitor development in hemophilia a (HA) as a model (2017) (0)
- Genetic variation in PSARL is associated with plasma insulin concentration (2005) (0)
- O55. The Genetic Factors Influencing Externalizing Psychopathology Overlap With Those Influencing Neurocognition and Show Developmental Variation (2019) (0)
- Characterisation of migraine prevalence, heritability and symptom phenotypes in the Norfolk Island population (2009) (0)
- Dietary Environments (2006) (0)
- 45. The Effect of Sex and BMI on the Genetic Overlap Between Plasma-Based Interleukins (-6 and -8) and Suicide Attempt (2019) (0)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
- SA80INTERLEUKIN-8 (BUT NOT INTERLEUKIN-6) SHARES GENETIC OVERLAP WITH RISK FOR SUICIDE ATTEMPTS IN WOMEN (BUT NOT IN MEN) (2019) (0)
- The application of a population based ascertainment correction for the variance components analysis of quantitative traits in a single extended pedigree (2005) (0)
- Heritability of Ocular Traits in Hispanics: Findings from the Maracaibo Aging Study (2018) (0)
- Identification of a characteristic and predictive genes of insulin sensitivity and insulin resistance in 3T3-L1 adipocytes. (2006) (0)
- Contents, Vol. 46, 1996 (1993) (0)
- Abstract 2382: Genome-Wide Linkage Scan to Identify Loci for Albuminuria in the San Antonio Family Heart Study (2006) (0)
- AGT203, a new Type 2 diabetes target. (2003) (0)
- The relationship between adult height and ocular biometry in a Nepalese population: The Jiri Eye Study (2018) (0)
- A Nonsynonymous-Single-Nucleotide Polymorphism (ns-SNP) in TFPI, the Gene Encoding Tissue Factor Pathway Inhibitor (TFPI), is Pleiotropically Associated with Increased Plasma TFPI Levels and a Decreased Risk of Type 2 Diabetes (T2D) in Mexican Americans of South Texas (2022) (0)
- A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility (2012) (0)
- Structural variation across 138,134 samples in the TOPMed consortium (2023) (0)
- Endophenotype Ranking Facilitates Identification of Novel QTLs for Recurrent Major Depression (2011) (0)
- Title The Quantitative-MFG Test : A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions Permalink (2015) (0)
- T178. The Utility of Connectivity Phenotypes as Successful Biomarkers for Psychosis Diagnoses (2019) (0)
- 106. Genome-Wide Significant Locus on Chromosome 5 Influences Psychosis Risk and General Intellectual Ability (2018) (0)
- Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines (2012) (0)
- On the Role of F8 Sequence Mismatch and Class-II Human Leukocyte Antigen Binding in the Development of Neutralizing Antibodies ("Inhibitors") Directed Against Therapeutic Factor VIII Proteins (tFVIIIs): Evidence from the PATH Study (2019) (0)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (0)
- Genome-wide physical activity interactions in adiposity A meta-analysis of 200,452 adults Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2020) (0)
- BrainVISA Plug-In for Measurements of Sulcal Span (2009) (0)
- 20to a region homologous to human chromosome A quantitative trait locus influencing estrogen levels (2015) (0)
- Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium (2021) (0)
- Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families (2016) (0)
- APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups (2021) (0)
- Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a northern european family population (2013) (0)
- Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS) (2018) (0)
- Large scale transcriptional profiling for the identification of genes influencing total antioxidant status in relation to atherosclerosis and cardiovascular disease risk (2007) (0)
- 1717-P: Burden of Type 2 Diabetes and Its Genetic Determinants in Indian Populations: Findings from the INDIGENIUS Consortium (2019) (0)
- Co-alteration Network Architecture of Major Depressive Disorder: A Multi-modal Neuroimaging Assessment of Large-scale Disease Effects (2022) (0)
- The HMG-CoA reductase inhibitors, or statins, act to stabilize vulnerable lipid-rich atherosclerotic plaques and to reduce cardiovascular morbidity and mortality as a con- sequence of their marked lowering of circulating levels of atherogenic apoB-containing lipoproteins, and notably of LDL-choleste (2016) (0)
- Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits (2015) (0)
- The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations (2022) (0)
- Common SNPs within or near Three Immune Response Genes Implicated in the Risk of FVIII Immunogenicity in Hemophilia A Do Not Influence Steady-State Levels of Their Encoded mRNAs (2012) (0)
- Quantitative trait locus mapping methods for complex phenotypes: The state of the science (1998) (0)
- Variant-specific inflation factors for assessing population stratification at the phenotypic variance level (2021) (0)
- A large-Scale Deep-Coverage Whole Genome Sequencing to Identify Less Common and Rare Variants Associated with BMD and Fractures: The NHLBI Trans-Omics for Precision Medicine (TOPMED) Study (2019) (0)
- N-Linked Glycans on Therapeutic Factor VIII (FVIII) Proteins Attenuate Immunogenicity Potential: Evidence from Independent HLA-Class-II/FVIII (HLAcII/FVIII) Peptidomes (2020) (0)
- Influence of the Human Lipidome on Epicardial Fat Volume in Mexican American Individuals (2022) (0)
- An epigenetic map of age-associated autosomal loci in northern European families at high risk for the metabolic syndrome (2015) (0)
- Investigating migraine in the descendents of the Bounty Mutineers (2009) (0)
- P413. Gene × Sex Interactions on Cognitive Development (2022) (0)
- Genetics of Serum Carotenoid Levels and Obesity Related Traits in Mexican American Children (2013) (0)
- Genomic Studies of Human Populations: Resequencing Approaches to the Identification of Human Quantitative Loci (2015) (0)
- Oral Sessions (2010) (0)
- Trauma in Affective and Nonaffective Psychosis: Associations and Dissociations With Cognitive Functioning in Childhood and Adulthood (2020) (0)
- Contents Vol. 60, 2005 (2006) (0)
- Use of the Norfolk Island Genetic Isolate to Identify Genetic Risk Factors for CVD. (2005) (0)
- WHITE MATTER HYPERINTENSITIES IN LATIN AMERICANS: FINDINGS FROM THE MARACAIBO AGING STUDY (2018) (0)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (0)
- Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (0)
- The Path to Open Angle Glaucoma Gene Discovery: Using the Endophenotypes, Intraocular Pressure, Central Corneal Thickness and Cup-To-Disc Ratio to Identify POAG-Related Loci (2010) (0)
- Abstract 168: TMEM8A 1080A>G Polymorphism in a 3’UTR MicroRNA Target Site Influences Aerobic Capacity in Health Individuals: the HUNT Study (2013) (0)
- Disentangling The Shared Genetic Etiology Between Serum Cholesterol And Suicide Risk: A Potential Moderating Role For Cholesterol Efflux (2017) (0)
- Genetic Control Over the Default Mode Network (2010) (0)
- Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. (2023) (0)
- Endophenotypes (2021) (0)
- GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans (2016) (0)
- South American Indians, A case study in evolution. By Francisco M. Salzano and Sidia M. Callegari‐Jacques. New York: Oxford University Press. 1988. xii + 259 pp., figures, tables, appendix, index. $75.00 (cloth) (1989) (0)
- Front & Back Matter (2013) (0)
- A quantitative trait locus on chromosome 11 is the major genetic determinant of homocysteine plasma levels. Results from the GAIT Project (2003) (0)
- Plasma β‐Amyloid as a Surrogate Genetic Marker in Late‐Onset Alzheimer's Disease (2002) (0)
- Heritability and linkage analysis of hyperintense (FLAIR) white matter lesion volumes in normal aging. (2009) (0)
- The Factor II (FII) Expression Quantitative Trait Locus (eQTL) Prothrombin G20210A Is Pleiotropically Associated with Plasma Fibrinogen Levels and Has a Profound Effect on Obesity in Mexican Americans of South Texas (2021) (0)
- Conceptualizing Major Depression (2016) (0)
- Genome-Wide Combined Linkage/Association Scan Localizes Two QTLs Influencing Human Caudate Volume (2010) (0)
- Interrogating Heritability and Common Variants in Extended Pedigrees with Age-Related Macular Degeneration (2015) (0)
- Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study (2017) (0)
- Evidence for HDL-associated Variation in T-cell Receptor Gene Expression (2012) (0)
- Using normal variation in neuroanatomic traits to identify genes and pathways influencing disease: a joint linkage and association analysis of brain lesions (2011) (0)
- Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate (2015) (0)
- Confirmation of a New Statistical Method for Comprehensively Dissecting QTLs Using In Vitro Transcription, the Model Factor VII Gene and a Novel Modification of the G-Free Cassette. (2004) (0)
- Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function (2023) (0)
- The Nonsynonymous-Single-Nucleotide Polymorphism (ns-SNP) 353 R>q in the Coagulation Factor VII (FVII) Gene, F7, is Associated with Decreased Plasma FVII Levels and a Decreased Risk of Coronary Heart Disease (CHD) in Mexican Americans of South Texas (2022) (0)
- Contributors and Participants (1982) (0)
- Genomewide Linkage Scan for Genes Influencing Plasma Triglyceride Levels in the Veterans Administration Genetic Epidemiology Study (VAGES) (2008) (0)
- GWAS of self-reported osteoarthritis in Mexican Americans from the San Antonio Family Study (2013) (0)
- Structural variation across 138,134 samples in the TOPMed consortium (2023) (0)
- Genetic and age-related variance of resting-state functional connectomes (2014) (0)
- M16 Epigenetic Age Acceleration Assessed In White-Matter Integrity: Towards A Biomarker of Successfully Brain Aging (2017) (0)
- find-tfbs: a tool to identify functional non-coding variants associated with complex human traits using open chromatin maps and phased whole-genome sequences (2020) (0)
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Other Resources About John Blangero
What Schools Are Affiliated With John Blangero?
John Blangero is affiliated with the following schools:
- Wright State University
- University of Western Australia
- Youngstown State University
- University of Texas at Austin
- Medical College of Wisconsin
- University of Oxford
- University of Texas Health Science Center at San Antonio
- Trinity University
- University of Texas Rio Grande Valley
- University of Texas Health Science Center at Houston
- Case Western Reserve University
