Stephen S Rich
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Computer Science
Stephen S Rich's Degrees
- PhD Computer Science Stanford University
- Masters Computer Science University of California, Berkeley
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(Suggest an Edit or Addition)Stephen S Rich'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
- Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
- Robust relationship inference in genome-wide association studies (2010) (1852)
- Familial clustering of diabetic kidney disease. Evidence for genetic susceptibility to diabetic nephropathy. (1989) (1004)
- Gut Microbiomes of Malawian Twin Pairs Discordant for Kwashiorkor (2013) (967)
- Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes (2010) (952)
- Genome-wide association study and meta-analysis finds over 40 loci affect risk of type 1 diabetes (2009) (818)
- Loss-of-function mutations in APOC3, triglycerides, and coronary disease. (2014) (799)
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) (785)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
- Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (2011) (711)
- A genome-wide search for asthma susceptibility loci in ethnically diverse populations (1997) (692)
- The health status of adults on the autism spectrum (2015) (679)
- Early-onset stroke and vasculopathy associated with mutations in ADA2. (2014) (618)
- Functional aspects of meningeal lymphatics in aging and Alzheimer’s disease (2018) (612)
- High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis (2012) (595)
- Mendelian randomization of blood lipids for coronary heart disease (2014) (580)
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (578)
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) (563)
- Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens (2013) (554)
- Pervasive Sharing of Genetic Effects in Autoimmune Disease (2011) (537)
- Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (2015) (520)
- Genetics of congenital heart disease: the glass half empty. (2013) (497)
- Exome-wide association study of plasma lipids in >300,000 individuals (2017) (428)
- Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction (2014) (426)
- Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function (2011) (401)
- A structural variation reference for medical and population genetics (2020) (394)
- A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families. (1998) (375)
- Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus. (1988) (372)
- Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium (2011) (353)
- Risk of recurrent seizures after two unprovoked seizures. (1998) (352)
- Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1). (1999) (348)
- Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis (2013) (339)
- Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis (2013) (337)
- Multiancestry association study identifies new asthma risk loci that colocalize with immune cell enhancer marks (2017) (337)
- Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project (2011) (325)
- The landscape of recombination in African Americans (2011) (312)
- Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis (2017) (308)
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification (2015) (308)
- Mapping Genes in Diabetes: Genetic Epidemiological Perspective (1990) (301)
- Genetics of Type 1 Diabetes: What's Next? (2010) (297)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
- Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. (2014) (292)
- Inactivating mutations in NPC1L1 and protection from coronary heart disease. (2014) (289)
- Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. (2012) (282)
- Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials (2011) (281)
- Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism (2015) (276)
- Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis (2017) (275)
- Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes (2009) (271)
- A gene responsible for cavernous malformations of the brain maps to chromosome 7q. (1995) (269)
- Genetics of type 1A diabetes. (2009) (264)
- Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families. (2005) (257)
- Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans. (2008) (254)
- Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium (2013) (250)
- Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels (2018) (246)
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) (242)
- Genome screening in human systemic lupus erythematosus: results from a second Minnesota cohort and combined analyses of 187 sib-pair families. (2000) (241)
- Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. (2012) (238)
- Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic Nephropathy (1997) (228)
- Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations (2020) (225)
- Microbiota alteration is associated with the development of stress-induced despair behavior (2017) (224)
- Recovery of trait heritability from whole genome sequence data (2019) (223)
- Functional IL6R 358Ala Allele Impairs Classical IL-6 Receptor Signaling and Influences Risk of Diverse Inflammatory Diseases (2013) (220)
- Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus. (2002) (216)
- Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke (2009) (213)
- Cellular basis of diabetic nephropathy: 1. Study design and renal structural-functional relationships in patients with long-standing type 1 diabetes. (2002) (211)
- ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy (2013) (208)
- A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release (2007) (207)
- Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes (2014) (205)
- Negligible impact of rare autoimmune-locus coding-region variants on missing heritability (2013) (203)
- Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk (2015) (199)
- Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis. (2014) (198)
- The Type 1 Diabetes Genetics Consortium (2006) (197)
- Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. (2014) (197)
- Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. (2012) (187)
- Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest. (1998) (187)
- Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions (2020) (186)
- Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis. (2014) (186)
- Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility (2015) (185)
- Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes (2020) (184)
- A genome scan for diabetic nephropathy in African Americans. (2004) (183)
- Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease. (2020) (181)
- Laws restricting health insurers' use of genetic information: impact on genetic discrimination. (2000) (179)
- New Susceptibility Locus for NIDDM Is Localized to Human Chromosome 20q (1997) (170)
- Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function (2012) (167)
- Mutations at the BLK locus linked to maturity onset diabetes of the young and β-cell dysfunction (2009) (167)
- Genome scan of human systemic lupus erythematosus by regression modeling: evidence of linkage and epistasis at 4p16-15.2. (2000) (167)
- Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans. (2014) (163)
- Familial aggregation of coronary artery calcium in families with type 2 diabetes. (2001) (162)
- Heritability of Carotid Artery Intima-Medial Thickness in Type 2 Diabetes (2002) (161)
- Accuracy of proband reported family history: The NHLBI Family Heart Study (FHS) (1999) (161)
- Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods. (2003) (161)
- Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction (2019) (160)
- Promoter (4G/5G) Plasminogen Activator Inhibitor-1 Genotype and Plasminogen Activator Inhibitor-1 Levels in Blacks, Hispanics, and Non-Hispanic Whites: The Insulin Resistance Atherosclerosis Study (2003) (158)
- Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases (2015) (156)
- Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. (2003) (156)
- Circulating and Dietary Omega‐3 and Omega‐6 Polyunsaturated Fatty Acids and Incidence of CVD in the Multi‐Ethnic Study of Atherosclerosis (2013) (155)
- Familial Clustering of Insulin Sensitivity (1992) (154)
- Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (153)
- The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (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)
- Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: systematic review and meta-analysis of 14,015 stroke cases and pooled analysis of primary biomarker data from up to 60,883 individuals. (2013) (151)
- Asthma and incident cardiovascular disease: the Atherosclerosis Risk in Communities Study (2005) (150)
- Autoimmune diseases — connecting risk alleles with molecular traits of the immune system (2016) (149)
- Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus. (2002) (148)
- Genome-Wide Scans for Diabetic Nephropathy and Albuminuria in Multiethnic Populations (2007) (148)
- Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction (2014) (147)
- Genome-Wide Association Study of Plasma N6 Polyunsaturated Fatty Acids Within the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (2014) (147)
- Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. (2002) (146)
- Pericardial and Visceral Adipose Tissues Measured Volumetrically With Computed Tomography Are Highly Associated in Type 2 Diabetic Families (2005) (145)
- Directional dominance on stature and cognition in diverse human populations (2015) (144)
- Candidate Gene Association Resource (CARe): Design, Methods, and Proof of Concept (2010) (143)
- Genome-wide association analysis identifies six new loci associated with forced vital capacity (2014) (141)
- Development and Standardization of an Improved Type 1 Diabetes Genetic Risk Score for Use in Newborn Screening and Incident Diagnosis (2019) (135)
- Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus. (2004) (134)
- Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project. (2012) (134)
- Genetic analysis of mammographic breast density in adult women: evidence of a gene effect. (1997) (134)
- The Insulin Resistance Atherosclerosis Study Family Study (2004) (133)
- Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes. (2004) (130)
- HLA class I sequence-based typing. (1993) (130)
- A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans. (2007) (126)
- Phosphodiesterase 4D and 5‐lipoxygenase activating protein in ischemic stroke (2005) (125)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2017) (124)
- Complex segregation analysis of febrile convulsions. (1987) (123)
- Association analyses of East Asian individuals and trans‐ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels (2017) (119)
- Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies (2016) (118)
- Variants of the Transcription Factor 7-Like 2 (TCF7L2) Gene Are Associated With Type 2 Diabetes in an African-American Population Enriched for Nephropathy (2007) (118)
- Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic Nephropathy (2009) (116)
- Links Between Insulin Resistance, Adenosine A2B Receptors, and Inflammatory Markers in Mice and Humans (2011) (116)
- A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes. (2006) (115)
- Biomarkers of Dairy Fatty Acids and Risk of Cardiovascular Disease in the Multi‐Ethnic Study of Atherosclerosis (2013) (115)
- Precision medicine in diabetes: a Consensus Report from the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD) (2020) (113)
- Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin. (2003) (113)
- A Human Type 1 Diabetes Susceptibility Locus Maps to Chromosome 21q22.3 (2008) (113)
- Genetic polymorphisms of the IL-1α and IL-1β genes in African-American LJP patients and an African-American control population (2000) (112)
- Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms (2017) (110)
- Risk of diabetes in siblings of index cases with Type 2 diabetes: implications for genetic studies (2002) (107)
- Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD) (2020) (107)
- Evidence for major genes influencing pulmonary function in the NHLBI Family Heart Study (2000) (107)
- Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy (2020) (107)
- A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes (2018) (105)
- Early Progression of Diabetic Nephropathy Correlates With Methylglyoxal-Derived Advanced Glycation End Products (2013) (104)
- Variants in Intron 13 of the ELMO1 Gene are Associated with Diabetic Nephropathy in African Americans (2009) (104)
- Chromosomal organization of the human major histocompatibility complex class I gene family [published erratum appears in J Exp Med 1989 Apr 1;169(4):1517] (1989) (104)
- Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. (2003) (103)
- Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2. (2000) (103)
- Meningeal lymphatics affect microglia responses and anti-Aβ immunotherapy (2021) (103)
- Urinary albumin excretion in families with type 2 diabetes is heritable and genetically correlated to blood pressure. (2000) (102)
- Validation study of self-reported measures of fat distribution. (1996) (102)
- Studies of kidney and muscle biopsy specimens from identical twins discordant for type I diabetes mellitus. (1985) (100)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (98)
- Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants. (2015) (98)
- Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes (2018) (98)
- Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. (2019) (98)
- Role of Type 1 Diabetes–Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study (2014) (94)
- DNA Methylation of the Aryl Hydrocarbon Receptor Repressor Associations With Cigarette Smoking and Subclinical Atherosclerosis (2015) (94)
- Genome-Wide Scan for Linkage to Type 1 Diabetes in 2,496 Multiplex Families From the Type 1 Diabetes Genetics Consortium (2009) (94)
- 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)
- Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
- Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies (2019) (92)
- The Siblings With Ischemic Stroke Study (SWISS) Protocol (2002) (91)
- HLA-DRB1*07:01 is associated with a higher risk of asparaginase allergies. (2014) (90)
- The impact of ethnicity and sex on subclinical cardiovascular disease: the Diabetes Heart Study (2005) (90)
- Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p. (1991) (89)
- A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage. (2004) (88)
- Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
- Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. (2014) (88)
- Genome-Wide Association Study Identifies Novel Loci Associated With Concentrations of Four Plasma Phospholipid Fatty Acids in the De Novo Lipogenesis Pathway: Results From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium (2013) (88)
- Genetic factors in the electrocardiogram and heart rate of twins reared apart and together. (1989) (87)
- Patients' fear of genetic discrimination by health insurers: the impact of legal protections (2000) (87)
- Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry (2015) (87)
- Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study. (2004) (86)
- Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect. (2002) (86)
- Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. (1995) (86)
- Is diabetic nephropathy inherited? Studies of glomerular structure in type 1 diabetic sibling pairs. (1999) (85)
- Mapping and characterization of structural variation in 17,795 human genomes (2020) (84)
- Population Structure of Hispanics in the United States: The Multi-Ethnic Study of Atherosclerosis (2012) (84)
- HLA class II "typing": direct sequencing of DRB, DQB, and DQA genes. (1992) (84)
- Genome‐wide linkage analyses of total serum IgE using variance components analysis in asthmatic families (2001) (82)
- Cellular basis of diabetic nephropathy: II. The transforming growth factor-beta system and diabetic nephropathy lesions in type 1 diabetes. (2002) (82)
- Aldose reductase gene polymorphisms and susceptibility to diabetic nephropathy in Type 1 diabetes mellitus (2000) (82)
- The Genetic Landscape of Renal Complications in Type 1 Diabetes. (2017) (82)
- Chronic and recurrent otitis media: a genome scan for susceptibility loci. (2004) (82)
- Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. (2016) (81)
- Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results. (2014) (81)
- An open resource of structural variation for medical and population genetics (2019) (80)
- Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology (2017) (79)
- A Genome-Wide Scan for Urinary Albumin Excretion in Hypertensive Families (2003) (79)
- Fine-mapping, trans-ancestral, and genomic analyses identify causal variants, cells, genes, and drug targets for type 1 diabetes (2020) (79)
- Linkage heterogeneity of end-stage renal disease on human chromosome 10. (2002) (78)
- Genetic susceptibility to ischemic stroke (2011) (78)
- Relationship between albuminuria and cardiovascular disease in Type 2 diabetes. (2005) (78)
- Sex differences in the late first trimester human placenta transcriptome (2018) (78)
- A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q. (2004) (77)
- Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium (2014) (77)
- Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
- A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma (2003) (77)
- A Genome-Wide Linkage Scan for Genes Controlling Variation in Renal Function Estimated by Serum Cystatin C Levels in Extended Families With Type 2 Diabetes (2006) (77)
- Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project. (2016) (77)
- Familial clustering of breast and prostate cancers and risk of postmenopausal breast cancer. (1994) (77)
- Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset. (2014) (76)
- Human airway branch variation and chronic obstructive pulmonary disease (2018) (75)
- Genome Scan for Quantitative Trait Loci Linked to High-Density Lipoprotein Cholesterol: The NHLBI Family Heart Study (2001) (74)
- Familial clustering for features of the metabolic syndrome: the National Heart, Lung, and Blood Institute (NHLBI) Family Heart Study. (2006) (74)
- Genetic linkage analysis of growth factor loci and end-stage renal disease in African Americans. (1997) (74)
- Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: A prospective study in children (2018) (73)
- Sex differences in stroke severity, symptoms, and deficits after first-ever ischemic stroke. (2007) (73)
- Association of autoimmune thyroid disease with microsatellite markers for the thyrotropin receptor gene and CTLA-4 in Japanese patients. (2000) (73)
- Coincident Linkage of Type 2 Diabetes, Metabolic Syndrome, and Measures of Cardiovascular Disease in a Genome Scan of the Diabetes Heart Study (2006) (73)
- Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. (2019) (73)
- Familial Hypercholesterolemia: The Lipids or the Genes? (2011) (73)
- Diet, Genetics, and Disease: A Focus on the Middle East and North Africa Region (2012) (71)
- Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function (2018) (71)
- Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. (2011) (71)
- Segregation analysis of urinary albumin excretion in families with type 2 diabetes. (2000) (70)
- Association of Stein‐Leventhal syndrome with the incidence of postmenopausal breast carcinoma in a large prospective study of women in Iowa (1997) (70)
- Genetics of diabetes and its complications. (2006) (69)
- Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study. (2006) (69)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (68)
- Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. (2013) (68)
- Insulin-dependent diabetes--associated HLA-D region encoded determinants. (1985) (68)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
- Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans. (2016) (68)
- Associations of autozygosity with a broad range of human phenotypes (2019) (68)
- Co-occurrence of Type 1 Diabetes and Celiac Disease Autoimmunity (2017) (67)
- Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans. (2015) (67)
- Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study. (2004) (67)
- Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs (2016) (66)
- Genetic analysis of nitric oxide and endothelin in end-stage renal disease. (2000) (66)
- Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. (2015) (65)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
- Association of the estrogen receptor-alpha gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study. (2007) (64)
- Evidence of Gene-Gene Interaction and Age-at-Diagnosis Effects in Type 1 Diabetes (2012) (64)
- The Ischemic Stroke Genetics Study (ISGS) Protocol (2003) (63)
- Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis (2014) (63)
- Plasma 25-Hydroxyvitamin D Concentration and Risk of Islet Autoimmunity (2017) (63)
- Calcified atherosclerotic plaque and bone mineral density in type 2 diabetes: the diabetes heart study. (2008) (62)
- Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations (2018) (62)
- Genetic variation at 16q24.2 is associated with small vessel stroke (2017) (61)
- Genome-Wide Scan for Estimated Glomerular Filtration Rate in Multi-Ethnic Diabetic Populations (2008) (61)
- Interobserver agreement in the trial of org 10172 in acute stroke treatment classification of stroke based on retrospective medical record review. (2006) (61)
- Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study (2008) (61)
- Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. (2019) (61)
- An ImmunoChip study of multiple sclerosis risk in African Americans. (2015) (60)
- Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022) (60)
- Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes (2013) (60)
- Lung cancer detection and prevention: evidence for an interaction between smoking and genetic predisposition. (1992) (60)
- A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases (2016) (59)
- Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease (2018) (59)
- Segregation analysis of serum uric acid in the NHLBI Family Heart Study (2000) (58)
- Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans (2015) (58)
- Identification of human plasma kallikrein gene polymorphisms and evaluation of their role in end-stage renal disease. (1998) (58)
- A generalized family-based association test for dichotomous traits. (2009) (57)
- Pangenomics enables genotyping of known structural variants in 5202 diverse genomes (2021) (57)
- Overview of the Type I Diabetes Genetics Consortium (2009) (57)
- Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23. (2004) (57)
- Familial cerebral cavernous angioma: A gene localized to a 15‐cm interval on chromosome 7q (1996) (56)
- Quantitative trait loci for abdominal fat and BMI in Hispanic-Americans and African-Americans: the IRAS Family Study (2005) (56)
- Design and Implementation of the International Genetics and Translational Research in Transplantation Network (2015) (56)
- Genomic structure of the human plasma prekallikrein gene, identification of allelic variants, and analysis in end-stage renal disease. (2000) (56)
- Association of autoimmune thyroid disease with a microsatellite marker for the thyrotropin receptor gene and CTLA-4 in a Japanese population. (1997) (56)
- Linkage analysis between loci in the renin-angiotensin axis and end-stage renal disease in African Americans. (1996) (56)
- Age-stratified heritability estimation in the Framingham Heart Study families (2003) (56)
- Saturated fat intake modulates the association between an obesity genetic risk score and body mass index in two US populations. (2014) (56)
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- Erratum: Cellular basis of diabetic nephropathy. 1. Study design and renal structural-functional relationships in patients with long-standing type 1 diabetes (Diabetes (2002) 51 (506-513) (2002) (38)
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- Insulin Sensitivity and Insulin Clearance are Heritable and Have Strong Genetic Correlation in Mexican Americans (2013) (37)
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- Association of the Distal Region of the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 Gene With Type 2 Diabetes in an African-American Population Enriched for Nephropathy (2008) (36)
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- An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes. (2011) (33)
- Genetic susceptibility contributes to renal and cardiovascular complications of type 2 diabetes mellitus. (2006) (33)
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- Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity (2013) (32)
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- Evaluation of markers on human chromosome 10, including the homologue of the rodent Rf-1 gene, for linkage to ESRD in black patients. (1999) (31)
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- Evidence for asthma susceptibility genes on chromosome 11 in an African-American population (2003) (31)
- Genetic analysis of the GLUT10 glucose transporter (SLC2A10) polymorphisms in Caucasian American type 2 diabetes (2005) (30)
- Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study (2010) (30)
- Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced Nephropathy (2018) (30)
- A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021) (30)
- Gene Expression Differences in Skin Fibroblasts in Identical Twins Discordant for Type 1 Diabetes (2012) (30)
- Evaluation of 15 Functional Candidate Genes for Association with Chronic Otitis Media with Effusion and/or Recurrent Otitis Media (COME/ROM) (2011) (29)
- Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis (2018) (29)
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- Genetic initiation of hypertensive and diabetic nephropathy. (1998) (27)
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- Comprehensive evaluation of the estrogen receptor α gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population (2008) (27)
- APOE genotype modifies the association between plasma omega-3 fatty acids and plasma lipids in the Multi-Ethnic Study of Atherosclerosis (MESA). (2013) (27)
- GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient (2015) (27)
- Detection of diabetic nephropathy from advanced glycation endproducts (AGEs) differs in plasma and urine, and is dependent on the method of preparation (2014) (26)
- Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
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- Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis (2017) (25)
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- APOL1 nephropathy risk variants are associated with altered high-density lipoprotein profiles in African Americans. (2016) (24)
- Diabetes: Still a geneticist's nightmare (2016) (24)
- No Evidence for Linkage Between Diabetes and the Kidd Marker (1982) (24)
- Associations between Genetic Variants in the ACE, AGT, AGTR1 and AGTR2 Genes and Renal Function in the Multi-Ethnic Study of Atherosclerosis (2010) (24)
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- Environmental factors can confound identification of a major gene effect: Results from a segregation analysis of a simulated population of lung cancer families (1998) (24)
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- Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans (2019) (24)
- Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans (2019) (24)
- Association of Integrin α2 Gene Variants with Ischemic Stroke (2008) (23)
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- Genotyping common, large structural variations in 5,202 genomes using pangenomes, the Giraffe mapper, and the vg toolkit (2020) (22)
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- Gene‐centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans (2015) (21)
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- Family-Based Association Analysis Confirms the Role of the Chromosome 9q21.32 Locus in the Susceptibility of Diabetic Nephropathy (2013) (21)
- Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes (2014) (21)
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- Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction (2018) (20)
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- Association of Triglyceride-Related Genetic Variants With Mitral Annular Calcification. (2017) (20)
- Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes (2015) (20)
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- A Review of Genetics, Arterial Stiffness, and Blood Pressure in African Americans (2012) (20)
- Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations. (2017) (20)
- AtheroSpectrum Reveals Novel Macrophage Foam Cell Gene Signatures Associated With Atherosclerotic Cardiovascular Disease Risk (2021) (19)
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- Association of the μ-opioid receptor gene with type 2 diabetes mellitus in an African American population (2006) (19)
- Genome‐wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans (2018) (19)
- Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke (2017) (19)
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- Genome-Wide Interaction with Selected Type 2 Diabetes Loci Reveals Novel Loci for Type 2 Diabetes in African Americans (2017) (12)
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- Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016)) (2016) (8)
- Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes (2020) (8)
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- INSULIN DEPENDENT DIABETIC FAMILIES: SEX RATIO AND HLA HAPLOTYPE SEGREGATION (1981) (8)
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- Fine-mapping identifies causal variants for RA and T1D in DNASE1L3, SIRPG, MEG3, TNFAIP3 and CD28/CTLA4 loci (2017) (8)
- Joint analysis reveals shared autoimmune disease associations and identifies common mechanisms (2021) (7)
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- Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes (2021) (7)
- Autoantibodies Directed Toward a Novel IA-2 Variant Protein Enhance Prediction of Type 1 Diabetes (2019) (7)
- Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function (2018) (7)
- A Genetic Risk Score Associated with Chronic Obstructive Pulmonary Disease Susceptibility and Lung Structure on Computed Tomography (2019) (7)
- Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study (2017) (7)
- Positional Cloning Works!: Identification of Genes That Cause IDDM (1995) (7)
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- An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels (2018) (7)
- Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices (2021) (7)
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- Monogenic and Polygenic Contributions to QTc Prolongation in the Population (2021) (7)
- Detection of novel sequence heterogeneity and haplotypic diversity of HLA class II genes (2004) (7)
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- Serology, restriction fragment length polymorphism, and sequence analysis of a unique HLA class II antigen, DR5x6. (1991) (7)
- Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425)) (2012) (6)
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- Cellular basis of diabetic nephropathy: IV. Antioxidant enzyme mRNA expression levels in skin fibroblasts of type 1 diabetic sibling pairs. (2006) (6)
- Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma. (2019) (6)
- Multi-ancestry genome-wide association study improves resolution of genes, pathways and pleiotropy for lung function and chronic obstructive pulmonary disease (2022) (6)
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- 5‐Lipoxygenase Gene Variants Are Not Associated With Atherosclerosis or Incident Coronary Heart Disease in the Multi‐Ethnic Study of Atherosclerosis Cohort (2016) (6)
- Children’s erythrocyte fatty acids are associated with the risk of islet autoimmunity (2021) (6)
- Low-density lipoprotein levels and not mutation status predict intima-media thickness in familial hypercholesterolemia. (2014) (6)
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- Interpreting Clinical Trials With Omega-3 Supplements in the Context of Ancestry and FADS Genetic Variation (2022) (6)
- The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia (2012) (6)
- The genetic basis of glucose homeostasis. (2005) (6)
- Acculturation and Plasma Fatty Acid Concentrations in Hispanic and Chinese-American Adults: The Multi-Ethnic Study of Atherosclerosis (2016) (6)
- Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease (2022) (6)
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- 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)
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- Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes (2020) (5)
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- Effect sizes of causal variants for gene expression and complex traits differ between populations (2021) (5)
- Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium (2020) (5)
- Diabetes Care: “Taking It to the Limit One More Time” (2016) (5)
- Multiethnic meta-analysis identifies new loci for pulmonary function (2017) (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)
- Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. (2022) (5)
- Status of Diabetes Care: New Challenges, New Concepts, New Measures—Focusing on the Future! (2015) (5)
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- Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed (2019) (5)
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- No association of 9p21 with arterial elasticity and retinal microvascular findings. (2013) (5)
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- Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease (2022) (5)
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- Genetic Heterogeneity ofInsulin-Dependent (TypeI)Diabetes Mellitus: Evidence fromaStudyofExtended Haplotypes (1984) (4)
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- Heterogeneous long‐term trajectories of glycaemic control in type 1 diabetes (2021) (4)
- Epidemiology of IDDM: Is It Needed? (1989) (4)
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- Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants. (2023) (4)
- Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease (2019) (4)
- Cystic mucinous tumors of the urachus: carcinoma in situ or adenoma of unknown malignant potential? (2012) (4)
- Novel Genetic Determinants of Diabetic Kidney Disease (2016) (4)
- Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy (2020) (4)
- Multiset correlation and factor analysis enables exploration of multi-omic data (2022) (4)
- Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. (2021) (4)
- Rare genetic variants explain missing heritability in smoking (2022) (4)
- Genetic Basis of Kidney Disease (2012) (4)
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- Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations (2021) (4)
- Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program (2021) (4)
- Rare Genetic Variants Associated With Myocardial Fibrosis: Multi-Ethnic Study of Atherosclerosis (2022) (4)
- Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis. (2018) (4)
- Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis. (1988) (4)
- Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (HSD17B14) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes (2021) (4)
- Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis (2022) (4)
- Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies (2022) (4)
- Design and user experience testing of a polygenic score report: a qualitative study of prospective users (2021) (4)
- Building Momentum: Taking on the Real “Issues” of Diabetes Care! (2015) (3)
- Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure (2020) (3)
- Gene Variants In ICAM-1 And Lung Function Among European- And African-Americans In Seven Population-Based Cohorts. The Candidate-Gene Association Resource (CARe) (2012) (3)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (3)
- Author Correction: A structural variation reference for medical and population genetics (2021) (3)
- Confirmation of Genetic Associations at ELMO 1 in the GoKinD Collection Support its Role as a Susceptibility Gene in Diabetic Nephropathy Short running title : ELMO 1 and susceptibility of nephropathy (2009) (3)
- Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea. (2022) (3)
- The Promise and Practice of Genetics on Diabetes Care: The Fog Rises to Reveal a Field of Genetic Complexity in HNF1B (2017) (3)
- Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study (2021) (3)
- Improving the Prediction of Type 1 Diabetes Across Ancestries (2022) (3)
- Epigenome-wide association study of mitochondrial genome copy number. (2021) (3)
- Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies (2019) (3)
- Big Topics for Diabetes Care in 2018: Clinical Guidelines, Costs of Diabetes, and Information Technology (2018) (3)
- Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
- Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations (2021) (3)
- A framework for integrated clinical risk assessment using population sequencing data (2021) (3)
- Genetic relationships between type I and type II diabetes mellitus. (1988) (3)
- Validity of the Family-Based Association Test for Copy Number Variant Data in the Case of Non-Linear Intensity-Genotype Relationship (2012) (3)
- Genetic Contribution to Risk for Diabetic Kidney Disease. (2018) (3)
- Fatty Acid Desaturase Gene‐Induced Omega‐3 Deficiency in Amerindian‐Ancestry Hispanic Populations (2020) (3)
- Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes (2021) (3)
- Late Breaking Abstract - Associations between a COPD genetic risk score and lung structure on computed tomography (CT): SPIROMICS (2018) (3)
- Differences in Metabolomic Profiles Between Black and White Women and Risk of Coronary Heart Disease: an Observational Study of Women From Four US Cohorts (2022) (3)
- Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program (2021) (3)
- Summary of the Type 1 Diabetes Genetics Consortium Autoantibody Workshop (2015) (3)
- Large Meta-Analysis Provides Evidence for an Association of Serum Vitamin D with Pulmonary Function (2017) (2)
- DRw52-group haplotypes are frequent acceptors of DRw15-Dw2 DQ genes in DQA1-DRB1 recombination (2004) (2)
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- Regulation of Gene Expression in Autoimmune Disease Loci and the Genetic Basis of Proliferation in CD 4 + Effector Memory T Cells (2014) (2)
- Amerind ancestry predicts the impact of FADS genetic variation on omega-3 PUFA deficiency, cardiometabolic and inflammatory risk in Hispanic populations (2021) (2)
- Cardiovascular Disease : The Multi-Ethnic Study of Atherosclerosis Variants With Subclinical Atherosclerosis and Incident SCARB 1 Association of (2012) (2)
- Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis (2022) (2)
- Capillary basement membranes and diabetes mellitus. (1985) (2)
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- Telomere length is not a main factor for the development of islet autoimmunity and type 1 diabetes in the TEDDY study (2021) (2)
- Sugar-sweetened Beverage Consumption May Modify Associations between Genetic Variants in the CHREBP Locus and HDL-C and TG Concentrations. (2021) (2)
- Defining the Relative Role of Insulin Clearance in Early Dysglycemia in Relation to Insulin Sensitivity and Insulin Secretion: The Microbiome and Insulin Longitudinal Evaluation Study (MILES) (2021) (2)
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- Dynamic changes in immune gene co-expression networks predict development of type 1 diabetes (2021) (2)
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- HLA and susceptibility to type I diabetes. Hypothesis. (1982) (1)
- Identifying variants that contribute to linkage for dichotomous and quantitative traits in extended pedigrees (2011) (1)
- THE R21C MUTATION IN TROPONIN I HAS A FOUNDER EFFECT IN SOUTH LEBANON AND CAUSES MALIGNANT HYPERTROPHIC CARDIOMYOPATHY (2015) (1)
- Nontargeted and Targeted Metabolomic Profiling Reveals Novel Metabolite Biomarkers of Incident Diabetes in African Americans (2022) (1)
- Genetics of forced vital capacity: genome-wide association study meta-analysis and follow-up identifies six new loci (2014) (1)
- University of Groningen Genome-wide association studies identify CHRNA 5 / 3 and HTR 4 in the development of airflow obstruction (2017) (1)
- Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program (2022) (1)
- Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease (2022) (1)
- Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile (2019) (1)
- Genetic evidence favouring cytotoxic T cell forbidden clones as the cause of insulin-dependent diabetes mellitus. (1988) (1)
- Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program (2022) (1)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- Genetic architecture of smoking: Evaluating rare variant contribution from deep whole-genome sequencing of up to 26,000 individuals (2021) (1)
- A Novel Role for CSRP 1 in a Lebanese Family with Congenital Cardiac Defects (2017) (1)
- The KAG motif of HLA-DRB1 (β71, β74, β86) predicts seroconversion and development of type 1 diabetes (2021) (1)
- Sequencing Project levels, and factor VIII levels in African Americans: the NHLBI Exome ) coding variants, VWF VWF Common and rare von Willebrand factor ( (2013) (1)
- Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study (2021) (1)
- Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program (2022) (1)
- Trans-ethnic genome-wide association study of kidney function provides novel insight into effector genes and causal effects on kidney-specific disease aetiologies (2018) (1)
- Genomic Medicine and Ethnic Differences in Cardiovascular Disease Risk (2016) (1)
- Correlations between complex human phenotypes vary by genetic background, gender, and environment (2022) (1)
- Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes (2022) (1)
- Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus (1991) (1)
- Su1746 Rare Variants of TNFSF15 Are Significantly Associated With Crohn's Disease in Non-Jewish Caucasian Independent of the Known Common Susceptibility SNPs (2013) (1)
- BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion (2021) (1)
- Associations of hiatus hernia with CT-based interstitial lung changes: the MESA Lung Study (2022) (1)
- Diabetes Care: “Lagniappe” and “Seeing Is Believing”! (2016) (1)
- Predicting diabetes risk in diverse populations: what next? (2021) (1)
- Abstract 15044: Risk of Myocardial Infarction in Carriers of Familial Hypercholesterolemia Mutations is Modified by Common Variant Genetic Background or Adherence to a Healthy Lifestyle (2019) (1)
- Disentangling the direct and indirect effects of childhood adiposity on type 1 diabetes and immune-associated diseases: a multivariable Mendelian randomization study (2021) (1)
- Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer’s disease (2022) (1)
- Genetic and environmental correlations between complex phenotypes differ by race/ethnicity and sex (2021) (1)
- Common airway variants and chronic obstructive pulmonary disease (2015) (1)
- Discovery and Refinement Supplementary (2015) (1)
- Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function (2021) (1)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing (2023) (1)
- CHROMOSOMAL ORGANIZATION OF THE HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I GENE FAMILY By BEVERLY H . KOLLER, DANIEL E . GERAGHTY, ROBERT DEMARS,* (2003) (1)
- Special Issue: Fine mapping of the MHC Region for Type 1 diabetes genes. (2009) (1)
- APOM and High-Density Lipoprotein are associated with Lung Function and Percent Emphysema (2014) (1)
- Lower Oxygen Saturation During Sleep Is Associated with Reduced Expressions of CD1D and RAB20 That Is Potentially Reversed by CPAP Therapy (2019) (1)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
- Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals (2023) (1)
- Cesarean Delivery and Insulin Sensitivity in the Older Adult: The Microbiome and Insulin Longitudinal Evaluation Study (2021) (1)
- Genome-wide association and large scale follow-up identifies 16 novel loci for lung function (2011) (1)
- SUBCLINICAL ATHEROSCLEROSIS AND CORONARY ARTERY CALCIUM SCORES IN PATIENTS WITH COARCTATION OF THE AORTA (2018) (1)
- Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
- Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
- Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative (2021) (1)
- A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples (2014) (1)
- Functional Evaluation of RNLS, a Gene Harboring Risk Variants for Type 1 Diabetes in European and African Ancestry Subjects (2018) (1)
- Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function (2018) (1)
- HLA-DRB1*07:01 Is Associated With Asparaginase Allergies In Children With Acute Lymphoblastic Leukemia (2013) (1)
- Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes (2022) (0)
- Blood monocyte transcriptome and epigenome analyses reveal loci associated with human atherosclerosis (2017) (0)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
- Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis (2023) (0)
- Abstract 3507: Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing (2023) (0)
- Abstract 4411: Associations Between Genetic Variations in NOS1AP and QT Interval Duration in Four Racial/Ethnic Groups in the Multi-Ethnic Study of Atherosclerosis (MESA) (2008) (0)
- Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans (2019) (0)
- Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data (2019) (0)
- The impact of Mendelian sleep and circadian genetic variants in a population setting (2022) (0)
- Germline genetic variants are associated with development of insulin-dependent diabetes in cancer patients treated with immune checkpoint inhibitors (2023) (0)
- Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans (2019) (0)
- A Genome-wide Association Study of Dysanapsis Among Adults and Children (2023) (0)
- Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function (2023) (0)
- A structural variation reference for medical and population genetics (2020) (0)
- Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci (2020) (0)
- Uncovering Cross-Cohort Molecular Features with Multi-Omics Integration Analysis (2022) (0)
- Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohorts (2023) (0)
- Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy (2020) (0)
- Structural variation across 138,134 samples in the TOPMed consortium (2023) (0)
- Genetic association analysis of type 1 diabetes in > 60,000 ancestrally diverse subjects: refinement of existing association signals and discovery of novel type 1 diabetes risk loci (2019) (0)
- POLYGENIC RISK SCORES AND INCIDENT ATHEROSCLEROTIC CARDIOVASCULAR DISEASE AMONG INDIVIDUALS WITH A CAC SCORE OF ZERO: THE MULTI-ETHNIC STUDY OF ATHEROSCLEROSIS: MESA (2022) (0)
- Systemic Biomarkers of Lung Function and FEV 1 Decline Across Multiple Cohorts (2020) (0)
- Power was computed using TDT Power Calculator [15] varying SNP minor allele frequency (MAF) and genetic relative risk (GRR). (2014) (0)
- Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants (2023) (0)
- Rare coding variants in RCN3 are associated with blood pressure (2022) (0)
- Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium (2021) (0)
- Genetics of Latin American Diversity (GLAD) Project: insights into population genetics and association studies in recently admixed groups in the Americas (2023) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (0)
- Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
- Abstract 66: Clonal Hematopoiesis of Indeterminate Potential and Incident Type 2 Diabetes Risk (2023) (0)
- Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels (2018) (0)
- Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
- Race/ethnic, social, environmental, and genetic correlates to lung function decline: the Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study (2022) (0)
- Shifts in isoform usage underlie transcriptional differences in regulatory T cells in type 1 diabetes (2022) (0)
- Race/ethnic, Ancestral, Social, and Environmental Correlates of Lung Function Decline: The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study (2023) (0)
- The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations (2022) (0)
- Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci (2021) (0)
- Associations between ambient air pollutants and clonal hematopoiesis of indeterminate potential (CHIP) (2021) (0)
- Polymorphisms of Candidate Genes in a Vascular Endothelial Cell Pathway and Lung Function. The MESA-Lung Study. (2009) (0)
- Short title: Musunuru et al; Design of NHLBI CARe (2017) (0)
- Systemic Biomarkers of Lung Function and FEV1 Decline Across Multiple Cohorts (2020) (0)
- Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease (2018) (0)
- Abstract 11049: Rare Genetic Variants in Individuals with Low ASCVD Risk and Hard Chd or High Coronary Artery Disease: Multi-Ethnic Study of Atherosclerosis (2021) (0)
- Mo-P2:196 A genome scan for subclinical cardiovascular disease in the diabetes heart study (2006) (0)
- Variant-specific inflation factors for assessing population stratification at the phenotypic variance level (2021) (0)
- Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study (2018) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2020) (0)
- Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes (2018) (0)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
- Precision Diagnostics: Using Islet Autoantibodies to Characterize Heterogeneity in Type 1 Diabetes (2023) (0)
- The functional impact of rare variation across the regulatory cascade (2022) (0)
- Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (0)
- Association of a Multiancestry Genome-Wide Blood Pressure Polygenic Risk Score With Adverse Cardiovascular Events (2022) (0)
- Reducing Bias in Academic Publishing: The Diabetes Care Approach. (2023) (0)
- An integrated multi-omics analysis of sleep-disordered breathing traits across multiple blood cell types (2022) (0)
- Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data. (2020) (0)
- Introduction: Linkage Analysis of Full‐Genome Screens (2001) (0)
- Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA) (2017) (0)
- Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis (2022) (0)
- Abstract MP065: Genetic Loci Associated With Plasma Phospholipid Fatty Acids in the De Novo Lipogenesis Pathway: A Meta-analysis of Genome-wide Association Studies From the Charge Consortium (2012) (0)
- Interactions Between Candidate Cardiovascular Disease Genes, Traffic Proximity, And Left Ventricular Mass: The Multi-Ethnic Study Of Atherosclerosis (MESA) (2010) (0)
- Abstract P135: Dietary Sources Of Linoleic Acid (LA) Differ By Race/ethnicity In Adults Participating In The National Health And Nutrition Examination Survey (NHANES) Between 2015-2016 (2021) (0)
- The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. (2023) (0)
- 1125-P: Do Non-HLA Genes Contribute to Age of Type 1 Diabetes Onset in Monozygotic Twins? (2021) (0)
- 50th European Mathematical Genetics Meeting (EMGM) 2022 (2022) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- Setting the stage (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)
- Whole genome sequence analysis of pulmonary function and COPD in 19,996 multiethnic participants. (2020) (0)
- Infertility and treatments utilized have minimal effects on first trimester placenta DNA methylation and gene expression. (2022) (0)
- Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (0)
- Reply (1990) (0)
- Genetic modification of inflammation and clonal hematopoiesis-associated coronary artery disease (2022) (0)
- Leveraging type 1 diabetes human genetic and genomic data in the T1D Knowledge Portal (2023) (0)
- Proband race/ethnicity affects pedigree completion rate in a genetic study of ischemic stroke. (2008) (0)
- Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes (2021) (0)
- The genetic determinants of recurrent somatic mutations in 43,693 blood genomes (2023) (0)
- Rare coding variants in RCN3 are associated with blood pressure (2022) (0)
- Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations (2019) (0)
- Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations (2018) (0)
- Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing (2022) (0)
- Rare loss of function variants in candidate genes and risk of colorectal cancer (2018) (0)
- 1535-P: An Insulin Resistance Genetic Risk Score (IR_GRS) Is Associated with Mortality in Type 1 Diabetes (T1D) (2019) (0)
- We-W45:5 Human lipoxygenase gene variation in subclinical atherosclerosis: The diabetes heart study (2006) (0)
- Regulation of Gene Expression in Autoimmune Disease Loci and the Genetic Basis of Proliferation in CD4[superscript +] Effector Memory T Cells (2014) (0)
- Genome-wide Search for Ischemic Stroke Genes: The Siblings with Ischemic Stroke Study (SWISS) (2011) (0)
- Identification of Genes That Cause IDDM (1995) (0)
- DNA Variants in NOS3 Are Associated with Improved Small Artery Elasticity and Decreased Systolic Blood Pressure in Asymptomatic Individuals (2011) (0)
- Perspectives in Diabetes Positional Cloning Works ! (2006) (0)
- Erratum and Announcement (2002) (0)
- Abstract 53: Transcriptomics and Methylomics of Atherosclerosis in Circulating Monocytes - the Multi-Ethnic Study of Atherosclerosis (2015) (0)
- 112-OR: Integrative Analysis of Chromatin Accessibility and Genetic Risk in T1D Patients and Controls (2020) (0)
- 1269-P: The Type 1 Diabetes Knowledge Portal: An Open-Access Resource for Insights into the Genetic and Genomic Basis of Type 1 Diabetes (2022) (0)
- Dear Ol' Mom (1983) (0)
- Ongoing Promises and Public Expectations of the HGP (0)
- Multiple class I and DP sequence mismatches in most serologically- and Dw-identical unrelated donor/recipient marrow pairs (1992) (0)
- Mo-W2:6 The relationship between calcified atherosclerotic plaque and bone mineral density: The diabetes heart study (2006) (0)
- Transcriptional survey of peripheral blood links lower oxygen saturation during sleep with reduced expressions of CD1D and RAB20 that is reversed by CPAP therapy (2019) (0)
- Mechanisms of Disease Genetics of Type 1 A Diabetes (2009) (0)
- 243-OR: Integrating Genetic Risk Score and Islet Autoantibody Characteristics in the Predictive Model for Type 1 Diabetes in the TrialNet Study (2021) (0)
- Running title: Stitziel et al., Exome Sequencing in Monogenic Dyslipidemias (2015) (0)
- Indirect Evidence that Favors a Genetic Basis of DN (2006) (0)
- Genome-wide association analysis identifies six new loci associated with forced vital capacity | NOVA. The University of Newcastle's Digital Repository (2014) (0)
- Precision Medicine in Type 1 Diabetes (2023) (0)
- Association analysis of HLA-DRB3, DRB4, DRB5 alleles and type 1 diabetes using next-generation sequencing with the titanium GSFLX system (type 1 diabetes consortium) (2010) (0)
- Abstract 16514: Interpretation of Whole Genome Sequences for Risk of Early-Onset Myocardial Infarction (2017) (0)
- Human Na 1 / H 1 Exchanger Genes Identification of Polymorphisms by Radiation Hybrid Mapping and Analysis of Linkage in End-Stage Renal Disease (2000) (0)
- Precision medicine in diabetes: a consensus report from the ADA and EASD (2020) (0)
- Correction: A Functionally Significant Polymorphism in ID3 Is Associated with Human Coronary Pathology (2014) (0)
- Abstract 47: Genetically Elevated Low-Density Lipoprotein Cholesterol is Associated with Aortic Valve Calcification and Incident Aortic Stenosis (2014) (0)
- Genome search for pollen reactivity loci: Genome screen for susceptibility loci contributing to pollen sensitivity in US populations (2003) (0)
- Genome screen for susceptibility loci contributing to mite sensitivity in US populations (2002) (0)
- 0291 Sleep Disordered Breathing Associated with Epigenetic Age Acceleration: Evidence from the Multi-Ethnic Study of Atherosclerosis (2019) (0)
- Genome-Wide Association Study (GWAS) Of Lung Function Among African-Americans In 5 National Heart, Lung, And Blood Institute (NHLBI) Cohorts. The Candidate-Gene Association Resource (CARE) (2011) (0)
- 107-OR: Novel Genetic Risk Factors Influence Islet Autoimmunity Progression (2020) (0)
- Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations (2018) (0)
- COMMON GENETIC VARIANTS AND LEFT VENTRICULAR STRUCTURE IN THE MULTI-ETHNIC STUDY OF ATHEROSCLEROSIS (2016) (0)
- Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies (2018) (0)
- Linkage Analysisewoen Locn theenin-Angiofen3n 1 Axis and End-Stage Renal Disease in African Americans (1996) (0)
- Abstract 545: Differential mRNA Expression is Influenced by Apolipoprotein A-I in Order to Promote Foam Cell Regression (2016) (0)
- The 3p21.31 genetic locus promotes progression to type 1 diabetes through the CCR2/CCL2 pathway (2021) (0)
- OR24-07 Fetal Sex Impacts First Trimester Maternal-Fetal Communication in Humans (2020) (0)
- Abstract 21316: Mitochondrial DNA Copy Number and Ventricular Remodeling: Multi-Ethnic Study of Atherosclerosis (2017) (0)
- OR15-6 Epigenetic Differences in First Trimester Pregnancies Conceived with Infertility (2019) (0)
- Past Successes of Genetic Findings Familial Hypercholesterolemia and Low-Density Lipoprotein Cholesterol Lowering (2015) (0)
- Glucose Homeostasis and the Metabolic Syndrome (2012) (0)
- A Comprehensive Type 1 Diabetes Genetic Risk Score Is Associated with Type 2 Diabetes in the Framingham Heart Study (2018) (0)
- Etiologic Stroke Subtypes in the NINDS Stroke Genetics Network Study (S32.001) (2013) (0)
- Results of NOTCH3 Sequencing in Siblings with Ischemic Stroke Study Probands (2011) (0)
- BRCA 1 Susceptibility Markers and Postmenopausal Breast Cancer : The Iowa Women ’ s Health Study 1 (2000) (0)
- Erratum: Causal effects of body mass index on cardiometabolic traits and events: A mendelian randomization analysis (American Journal of Human Genetics (2014) 94 (198-208)) (2014) (0)
- Abstract P361: The First Genome-Wide Association Study (GWAS) of GlycA, an NMR-Derived Marker of Inflammation, Reveals Associations With a Variant in the Intron of TXNL4B Across Two Cohorts (2015) (0)
- A Genome-Wide Association Study of > 250,000 Subjects Identifies Novel Risk Loci for COPD (2018) (0)
- Genome-wide linkage scan for type 1 diabetes: the type 1 diabetes genetics consortium (2008) (0)
- Apical-Basilar Ratio In Percent Emphysema Predicts Incident Cardiovascular Events. The MESA Lung Study (2010) (0)
- 388 Identifying Genetically Homogeneous Crohn's Disease Subgroups Through Serological Profiling (2015) (0)
- No Association Between NIDD and Kidd (1982) (0)
- Summary of estimated genetic additive effects of rs4238001 allele T on LDL-C (mg/dL), LDL particle number (nmol/L) and LDL particle size (log nm) under a basic regression model (Model 1). (2015) (0)
- Abstract P256: Association of Genetic Variants on the Metabochip With Urine Albumin-Creatinine Ratio in African Americans: The Population Architecture using Genomics and Epidemiology (PAGE) Study (2014) (0)
- 210-OR: A Combined Method Improves Risk Prediction for Childhood Type 1 Diabetes in the TEDDY Study (2019) (0)
- Characteristics of MESA participants across three ethnic groups. (2015) (0)
- Abstract 202: The R21C Mutation in Troponin I Has a Founder Effect in South Lebanon and Causes Malignant Hypertrophic Cardiomyopathy (2019) (0)
- Protocol for genetic testing in Huntington disease (1991) (0)
- Genetic and Clinical Factors Underlying a Self-Reported Family History of Heart Disease. (2023) (0)
- Original A genome scan for all-cause end-stage renal disease in African Americans (2005) (0)
- Genome-Wide Scan for Estimated GFR in Multi-Ethnic Diabetic Populations: The Family Investigation of Nephropathy and Diabetes of Nephropathy (2007) (0)
- Iconography : Frequency of Guideline-Based Statin Therapy in Adults With Congenital Heart Disease (2017) (0)
- P329GATA5: a key player in congenital heart diseases (2014) (0)
- ehp Air Pollution and Percent Emphysema Identified by Computed Tomography in the Multi-Ethnic Study of Atherosclerosis (2014) (0)
- Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (2021) (0)
- Differences in n‐3 and n‐6 PUFA biosynthesis in African and European Americans (806.16) (2014) (0)
- A Genome-Wide Association Study To Assess Loci Associated With Lung Function Among Hispanic-Americans And Asian-Americans: The Mesa Lung Share Study (2011) (0)
- allergies *07:01 is associated with a higher risk of asparaginase HLA-DRB1 (2014) (0)
- TCT-558 Unique Features of Coronary Artery Disease in Women Based on Coronary Angiography Data of More Than 50,000 Patients (2022) (0)
- ATHEROSCLEROTIC CARDIOVASCULAR DISEASE RISK IN ADULTS WITH CONGENITAL HEART DISEASE (2016) (0)
- Yellow plaques on the hands of a 10-year-old girl. (2017) (0)
- Polygenic score informed by genome-wide association studies of multiple ancestries and related traits improves risk prediction for coronary artery disease (2023) (0)
- TCT-579 Expedited Radial Hemostatic Compression Device Removal Protocol and Subsequent Clinical Outcomes (2022) (0)
- A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy? (2015) (0)
- Carotid Disease: Genetics of carotid atherosclerosis (2006) (0)
- 1697-P: Functional Impact of Type 1 Diabetes Risk Variants Identified in African- and European-Ancestry Populations (2019) (0)
- Genetic Thoracic Aortic Diseases (2018) (0)
- Structural variation across 138,134 samples in the TOPMed consortium (2023) (0)
- Abstract P263: Biomarkers of Dairy Fatty Acids and Incidence of Cardiovascular Disease in the Multi-Ethnic Study of Atherosclerosis (MESA) (2013) (0)
- Polygenic Risk Scores in Chronic Obstructive Pulmonary Disease and Related Phenotypes (2020) (0)
- 1691-P: A Variant in the Melanocortin-4 Receptor (MC4R) Locus Is Associated with Glycemic Control and Insulin Resistance (IR) in Type 1 Diabetes (T1D) (2019) (0)
- PEDIATRIC CARDIOMYOPATHY MUTATIONS IN A HIGHLY CONSANGUINEOUS POPULATION (2016) (0)
- Connecting the Lines betweenHypogonadism and Atherosclerosis (2014) (0)
- Assessing the Robustness and Internal Consistency of the Pooled Cohort Equations (2022) (0)
- P569A novel role for NFATC1 in patients with both congenital heart disease and glaucoma (2014) (0)
- Stable Ischemic Heart Disease (2020) (0)
- Abstract 17030: Stress-Related Neurobiological Activity Contributes to the Link Between Cardiovascular Polygenic Risk Score and Myocardial Infarction (2020) (0)
- CYP2C19 Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine? (2022) (0)
- Regulation of Gene Expression in Autoimmune Disease Loci and the Genetic Basis of Proliferation in CD 4 [ superscript + ] Effector Memory T Cells (2014) (0)
- Supplementary material : Frequency of Guideline-Based Statin Therapy in Adults With Congenital Heart Disease (2017) (0)
- A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy? (2015) (0)
- Coarctation of the Aorta (2018) (0)
- 1254-P: Genetic Prediction of C-Peptide Trajectory before Type 1 Diabetes Diagnosis in TrialNet (2022) (0)
- Does Mechanical Circulatory Support–Assisted Percutaneous Coronary Intervention Improve Left Ventricular Function? (2022) (0)
- Genetic Epidemiology: Preface (2001) (0)
- Genome-wide association study of longitudinal urinary albumin excretion in patients with type 1 diabetes (2022) (0)
- A CombinedSegregation andLinkageAnalysis ofInsulin-dependent Diabetes Mellitus (1987) (0)
- Type 1 Diabetes Prevention: a systematic review of studies testing disease-modifying therapies and features linked to treatment response (2023) (0)
- Abstract P187: Blood Pressure Control in Adults with Autistic Spectrum Disorders in a Large Integrated Medical Care Program is Better Than in a Demographically Matched Comparison Group (2016) (0)
- Abstract 18346: Common Genetic Variants and Subclinical Atherosclerosis in the Multi-Ethnic Study of Atherosclerosis (2013) (0)
- Childhood body size directly increases type 1 diabetes risk based on a lifecourse randomization approach. (2022) (0)
- Epigenome-Wide Associations Study of Sleep Disordered Breathing Traits in the Multi-Ethnic Study of Atherosclerosis (2019) (0)
- SNPS IN NOS3 ARE ASSOCIATED WITH A CARDIOVASCULAR DISEASE SCORE IN ASYMPTOMATIC INDIVIDUALS (2011) (0)
- Subject Index Vol. 71, Suppl. 1, 2009 (2009) (0)
- Single Nucleotide Polymorphisms In The Apolipoprotein M Gene Are Associated With Percent Emphysema, HDL And HDL Subfractions Among European- And African-Americans: The MESA Lung And SNP Health Association Resource (SHARe) Studies (2012) (0)
- The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk (2022) (0)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (0)
- Endophenotype Effect Sizes Provide Evidence Supporting Variant Pathogenicity in Monogenic Disease Susceptibility Genes (2021) (0)
- General Cardiology: Hypertension, Prevention and Lipids16. HypertensionDNA VARIANTS IN NOS3 ARE ASSOCIATED WITH IMPROVED SMALL ARTERY ELASTICITY AND DECREASED SYSTOLIC BLOOD PRESSURE IN ASYMPTOMATIC INDIVIDUALS (2011) (0)
- Development and validation of a metabolite index for obstructive sleep apnea across race/ethnicities (2022) (0)
- HLA and susceptibility to type I diabetes (2008) (0)
- DETERMINANTS OF INCIDENT STROKE AMONG THOSE WITH ABSENT CORONARY ARTERY CALCIFICATION: RESULTS FROM THE MULTI-ETHNIC STUDY OF ATHEROSCLEROSIS (2023) (0)
- Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations Coeliac (2018) (0)
- Proteomic Fingerprinting: A novel privacy concern (2022) (0)
- Serum IgA and Gd-IgA1 Levels Associate With Chronic Lung Disease Phenotypes. The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study (2023) (0)
- Abstract P548: Epigenome-Wide Association Meta-Analysis of Obesity in African Americans (2023) (0)
- MUC5B, telomere length and longitudinal quantitative interstitial lung changes: the MESA Lung Study. (2022) (0)
- Author Correction: A structural variation reference for medical and population genetics (2021) (0)
- Sex differences in the late first trimester human placenta transcriptome (2018) (0)
- Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks (2017) (0)
- Multivariate adaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations (2023) (0)
- Abstract 14629: Rare Variants for Electrocardiographic Traits Identify Arrhythmia Susceptibility Genes (2020) (0)
- Su1750 Transethnic Fine-Mapping of the IL12B Locus Identifies Two Independent Signals Associated With IBD Susceptibility and Disease Behaviors (2013) (0)
- Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis (2023) (0)
- RARE GENETIC VARIANTS ASSOCIATED WITH MYOCARDIAL FIBROSIS; MULTI-ETHNIC STUDY OF ATHEROSCLEROSIS (MESA) (2021) (0)
- Abstract 16656: DNA Methylation and mRNA Sequencing of Monocytes From a Large Cohort Identifies Associations Between an Epigenetic Biomarker of Smoking, AHRR Expression, and Atherosclerosis (2014) (0)
- Whole genome sequence association analysis of Brain MRI measures (2022) (0)
- 1276-P: Transancestral Genomic Analysis Links Dysregulation of Valine Metabolism to the Development of Heart Failure in Type 2 Diabetes (2022) (0)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2018) (0)
- Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity (2012) (0)
- Associations between adherence to the dietary approaches to stop hypertension (DASH) diet and six glucose homeostasis traits in the Microbiome and Insulin Longitudinal Evaluation Study (MILES). (2022) (0)
- Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience. (2022) (0)
- Genome-wide discovery for diabetes-dependent triglycerides-associated loci (2022) (0)
- Interaction Between Dietary Iron Intake and Genetically Determined Iron Overload: Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in the TEDDY Study. (2023) (0)
- Analysis of family- and population-based samples in cohort genome-wide association studies (2011) (0)
- Mapping and characterization of structural variation in 17,795 human genomes (2020) (0)
- Publisher Correction: Functional aspects of meningeal lymphatics in ageing and Alzheimer’s disease (2018) (0)
- Detection of diabetic nephropathy from advanced glycation endproducts (AGEs) differs in plasma and urine, and is dependent on the method of preparation (2013) (0)
- Abstract MP67: Fatty Acid Desaturase Gene-induced Omega-3 Deficiency In Amerindian-Ancestry Hispanic Populations (2020) (0)
- Airway Tree Caliber and Subclinical Interstitial Lung Disease in Community-dwelling Adults: The Multi-ethnic Study of Atherosclerosis (MESA) (2023) (0)
- Genome-Wide Association Studies and fine-mapping of genomic loci for n-3 and n-6 Polyunsaturated Fatty Acids in Hispanic American and African American Cohorts (2023) (0)
- risk variants are associated with altered high-density lipoprotein pro fi les in African Americans (2016) (0)
- GENETICALLY ELEVATED LOW-DENSITY LIPOPROTEIN CHOLESTEROL IS ASSOCIATED WITH AORTIC VALVE CALCIFICATION AND INCIDENT AORTIC STENOSIS: A MENDELIAN RANDOMIZATION STUDY (2014) (0)
- Proteomics of COPD-Related Phenotypes in the General Population. The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study (2023) (0)
- Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
- An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling (2023) (0)
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What Schools Are Affiliated With Stephen S Rich?
Stephen S Rich is affiliated with the following schools:
