Carl D. D. Langefeld
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Carl D. D. Langefeldbiology Degrees
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Biology
Carl D. D. Langefeld's Degrees
- PhD Genetics Stanford University
- Bachelors Biology University of California, Berkeley
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(Suggest an Edit or Addition)Carl D. D. Langefeld's Published Works
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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 Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
- A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans (2012) (1691)
- Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans (2010) (1659)
- Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci (2008) (1309)
- Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018) (735)
- Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. (2004) (689)
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (578)
- Rare and low-frequency coding variants alter human adult height (2016) (511)
- Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data (2006) (412)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Colonic neoplasia in asymptomatic persons with negative fecal occult blood tests: influence of age, gender, and family history. (1993) (354)
- Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis (2013) (337)
- Human polymorphism at microRNAs and microRNA target sites. (2013) (330)
- Insulin sensitivity, insulin secretion, and abdominal fat: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study. (2003) (317)
- Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study (2017) (302)
- Adiponectin as a novel determinant of bone mineral density and visceral fat. (2003) (299)
- Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies (2009) (286)
- The APOL1 Gene and Allograft Survival after Kidney Transplantation (2011) (282)
- Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus (2011) (267)
- Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans. (2008) (254)
- Transancestral mapping and genetic load in systemic lupus erythematosus (2017) (253)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (252)
- The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans. (2010) (251)
- Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma. (2001) (248)
- A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry (2013) (244)
- Identification of IRAK1 as a risk gene with critical role in the pathogenesis of systemic lupus erythematosus (2009) (236)
- Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort (2011) (231)
- Integrated Omics: Tools, Advances, and Future Approaches. (2019) (227)
- End‐Stage Renal Disease in African Americans With Lupus Nephritis Is Associated With APOL1 (2014) (226)
- Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. (2014) (217)
- Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus. (2002) (216)
- Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans (2012) (215)
- A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release (2007) (207)
- Differential Genetic Associations for Systemic Lupus Erythematosus Based on Anti–dsDNA Autoantibody Production (2011) (205)
- Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes (2014) (205)
- Association of Genetic Variants in Complement Factor H and Factor H-Related Genes with Systemic Lupus Erythematosus Susceptibility (2011) (193)
- Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans. (2009) (190)
- Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
- A genome scan for diabetic nephropathy in African Americans. (2004) (183)
- A Promoter Haplotype of the Immunoreceptor Tyrosine-Based Inhibitory Motif-Bearing FcγRIIb Alters Receptor Expression and Associates with Autoimmunity. I. Regulatory FCGR2B Polymorphisms and Their Association with Systemic Lupus Erythematosus12 (2004) (182)
- Genomic Insights into the Ancestry and Demographic History of South America (2015) (179)
- Ordered subset analysis in genetic linkage mapping of complex traits (2004) (178)
- Association of plasma vitamin D levels with adiposity in Hispanic and African Americans. (2009) (177)
- Single-nucleotide polymorphisms in the C-reactive protein (CRP) gene promoter that affect transcription factor binding, alter transcriptional activity, and associate with differences in baseline serum CRP level (2005) (176)
- The TMAO-Producing Enzyme Flavin-Containing Monooxygenase 3 Regulates Obesity and the Beiging of White Adipose Tissue. (2017) (167)
- A Comprehensive Analysis of Shared Loci between Systemic Lupus Erythematosus (SLE) and Sixteen Autoimmune Diseases Reveals Limited Genetic Overlap (2011) (165)
- Risk Alleles for Systemic Lupus Erythematosus in a Large Case-Control Collection and Associations with Clinical Subphenotypes (2011) (165)
- Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE (2007) (164)
- Familial aggregation of coronary artery calcium in families with type 2 diabetes. (2001) (162)
- Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods. (2003) (161)
- Heritability of Carotid Artery Intima-Medial Thickness in Type 2 Diabetes (2002) (161)
- Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study. (2012) (159)
- The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
- Differences in arachidonic acid levels and fatty acid desaturase (FADS) gene variants in African Americans and European Americans with diabetes or the metabolic syndrome (2011) (150)
- A genome-wide association study for diabetic nephropathy genes in African Americans. (2011) (150)
- Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus. (2002) (148)
- Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase (2011) (147)
- Apolipoprotein L1 Gene Variants in Deceased Organ Donors Are Associated With Renal Allograft Failure (2015) (146)
- Pericardial and Visceral Adipose Tissues Measured Volumetrically With Computed Tomography Are Highly Associated in Type 2 Diabetic Families (2005) (145)
- Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans. (2012) (143)
- Association Analysis in African Americans of European-Derived Type 2 Diabetes Single Nucleotide Polymorphisms From Whole-Genome Association Studies (2008) (142)
- Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) (2015) (135)
- APOL1 Genotype and Kidney Transplantation Outcomes From Deceased African American Donors (2016) (134)
- Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus. (2004) (134)
- The Insulin Resistance Atherosclerosis Study Family Study (2004) (133)
- Quantification of afferent vessels shows reduced brain vascular density in subjects with leukoaraiosis. (2004) (131)
- Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes. (2004) (130)
- Validation of Probabilistic Predictions (1993) (130)
- Characterization of european ancestry nonalcoholic fatty liver disease‐associated variants in individuals of african and hispanic descent (2013) (129)
- A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans. (2007) (126)
- HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis (2015) (125)
- Behavioral intervention to increase condom use among high-risk female adolescents. (1996) (124)
- Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease (2009) (124)
- The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans (2011) (122)
- Genome‐Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture (2015) (122)
- A polymorphism within IL21R confers risk for systemic lupus erythematosus. (2009) (121)
- Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study. (2011) (119)
- 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)
- Quantitative Trait Analysis of Type 2 Diabetes Susceptibility Loci Identified From Whole Genome Association Studies in the Insulin Resistance Atherosclerosis Family Study (2008) (118)
- Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications (2016) (118)
- The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1. (2010) (118)
- Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus (2011) (117)
- Heritability of body composition measured by DXA in the diabetes heart study. (2005) (116)
- Risk factors for intracerebral hemorrhage differ according to hemorrhage location (2012) (113)
- Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease (2015) (111)
- Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms (2017) (110)
- Genetics of autoimmune diseases: insights from population genetics (2015) (109)
- Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD. (2009) (109)
- Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk (2012) (109)
- Mast cell growth factor (c-kit ligand) enhances cytokine stimulation of proliferation of the human factor-dependent cell line, M07e. (1991) (108)
- Vitamin d, adiposity, and calcified atherosclerotic plaque in african-americans. (2010) (108)
- Lupus nephritis susceptibility loci in women with systemic lupus erythematosus. (2014) (106)
- Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis (2015) (106)
- Juvenile idiopathic arthritis and HLA class I and class II interactions and age-at-onset effects. (2010) (106)
- Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study (2009) (106)
- Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2. (2000) (103)
- Interferon regulatory factor-5 is genetically associated with systemic lupus erythematosus in African Americans (2008) (102)
- Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1 (2013) (101)
- A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. (2018) (100)
- Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation (2016) (100)
- MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus (2013) (99)
- Association of the IL2RA/CD25 Gene With Juvenile Idiopathic Arthritis (2009) (98)
- The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study Protocol (2013) (98)
- GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region (2014) (98)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (98)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (98)
- Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension (2002) (97)
- Mapping Genes for NIDDM: Design of the Finland—United States Investigation of NIDDM Genetics (FUSION) Study (1998) (95)
- Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups (2012) (95)
- APOL1 Renal-Risk Variants Induce Mitochondrial Dysfunction. (2017) (93)
- Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis. (2010) (90)
- The impact of ethnicity and sex on subclinical cardiovascular disease: the Diabetes Heart Study (2005) (90)
- Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study. (2010) (90)
- Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans. (2012) (89)
- Analysis of autosomal genes reveals gene–sex interactions and higher total genetic risk in men with systemic lupus erythematosus (2011) (89)
- Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study. (2011) (88)
- A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage. (2004) (88)
- High-density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups. (2009) (88)
- Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria (2019) (86)
- Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study. (2004) (86)
- Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. (2010) (84)
- Differential Effects of MYH9 and APOL1 Risk Variants on FRMD3 Association with Diabetic ESRD in African Americans (2011) (83)
- Review of the Diabetes Heart Study (DHS) family of studies: a comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications. (2010) (82)
- Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations. (2012) (81)
- Apolipoprotein L1 gene variants associate with prevalent kidney but not prevalent cardiovascular disease in the Systolic Blood Pressure Intervention Trial (2014) (81)
- Genetic associations of LYN with systemic lupus erythematosus (2009) (81)
- Informed Conditioning on Clinical Covariates Increases Power in Case-Control Association Studies (2012) (81)
- Polymorphisms in the Nonmuscle Myosin Heavy Chain 9 Gene (MYH9) Are Associated with Albuminuria in Hypertensive African Americans: The HyperGEN Study (2009) (78)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Relationship between albuminuria and cardiovascular disease in Type 2 diabetes. (2005) (78)
- Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
- A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q. (2004) (77)
- Association of protein tyrosine phosphatase 1B gene polymorphisms with measures of glucose homeostasis in Hispanic Americans: the insulin resistance atherosclerosis study (IRAS) family study. (2004) (77)
- A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma (2003) (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)
- Factors associated with condom use by sexually active male adolescents at risk for sexually transmitted disease. (1993) (76)
- Resequencing and Analysis of Variation in the TCF7L2 Gene in African Americans Suggests That SNP rs7903146 Is the Causal Diabetes Susceptibility Variant (2011) (75)
- Association of PNPLA3 with non‐alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study (2011) (75)
- The polymorphic exon 1 androgen receptor CAG repeat in men with a potential inherited predisposition to prostate cancer. (2000) (74)
- Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15 (2010) (74)
- Clinician judgment vs formal scales for predicting intracerebral hemorrhage outcomes (2016) (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)
- Genome‐Wide Association of BMI in African Americans (2012) (72)
- Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus. (2012) (72)
- Factors associated with condom use among sexually active female adolescents. (1992) (72)
- APOL1 associations with nephropathy, atherosclerosis, and all-cause mortality in African Americans with type 2 diabetes (2014) (72)
- Genetic variation in the CRP promoter: association with systemic lupus erythematosus. (2008) (72)
- Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans (2015) (71)
- Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study (2005) (71)
- ABIN1 dysfunction as a genetic basis for lupus nephritis. (2013) (70)
- Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage (2017) (70)
- The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans (2009) (70)
- Association of NOS1AP Genetic Variants With QT Interval Duration in Families From the Diabetes Heart Study (2007) (68)
- Association of APOL1 variants with mild kidney disease in first-degree relatives of African American patients with non-diabetic end stage renal disease (2012) (67)
- Enhanced stimulation of human bone marrow macrophage colony formation in vitro by recombinant human macrophage colony-stimulating factor in agarose medium and at low oxygen tension. (1990) (67)
- The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share. (2014) (67)
- Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study. (2004) (67)
- Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia (2016) (66)
- The triglyceride to high-density lipoprotein cholesterol (TG/HDL-C) ratio as a predictor of insulin resistance, β-cell function, and diabetes in Hispanics and African Americans. (2019) (66)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
- A practical solution to pseudoreplication bias in single-cell studies (2021) (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)
- Genetic Analysis of the Pathogenic Molecular Sub-phenotype Interferon Alpha Identifies Multiple Novel Loci Involved in Systemic Lupus Erythematosus (2014) (63)
- Transferability and Fine Mapping of Type 2 Diabetes Loci in African Americans (2013) (63)
- Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosus. (2012) (63)
- Implication of European-derived adiposity loci in African Americans (2012) (62)
- Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes. (2013) (62)
- Calcified atherosclerotic plaque and bone mineral density in type 2 diabetes: the diabetes heart study. (2008) (62)
- Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study (2008) (61)
- Genetic variation at 16q24.2 is associated with small vessel stroke (2017) (61)
- Familial aggregation and linkage analysis of autoantibody traits in pedigrees multiplex for systemic lupus erythematosus (2006) (61)
- Peroxisome Proliferator‐activated Receptor γ 2 and Acyl‐CoA Synthetase 5 Polymorphisms Influence Diet Response (2007) (61)
- Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13. (2012) (61)
- Early‐life environmental exposures interact with genetic susceptibility variants in pediatric patients with eosinophilic esophagitis (2018) (61)
- Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes (2013) (60)
- Association of 25-hydroxyvitamin D with blood pressure in predominantly 25-hydroxyvitamin D deficient Hispanic and African Americans. (2009) (60)
- Genome-wide association study of cerebral small vessel disease reveals established and novel loci. (2019) (60)
- Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription. (2014) (60)
- JC polyoma virus interacts with APOL1 in African Americans with non-diabetic nephropathy (2013) (59)
- Measurement of Trabecular Bone Mineral Density in the Thoracic Spine Using Cardiac Gated Quantitative Computed Tomography (2004) (59)
- Genome-wide association study of vitamin D concentrations in Hispanic Americans: The IRAS Family Study (2010) (59)
- Monocyte Count and 30-Day Case Fatality in Intracerebral Hemorrhage (2015) (59)
- Trans-Ancestral Studies Fine Map the SLE-Susceptibility Locus TNFSF4 (2013) (58)
- PTPN22 Association in Systemic Lupus Erythematosus (SLE) with Respect to Individual Ancestry and Clinical Sub-Phenotypes (2013) (58)
- Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans (2015) (58)
- Variation in the ICAM1–ICAM4–ICAM5 locus is associated with systemic lupus erythematosus susceptibility in multiple ancestries (2012) (57)
- An algorithm for learning maximum entropy probability models of disease risk that efficiently searches and sparingly encodes multilocus genomic interactions (2009) (57)
- Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis (2011) (57)
- The Role of Genetic Variation Near Interferon-Kappa in Systemic Lupus Erythematosus (2010) (56)
- Age-stratified heritability estimation in the Framingham Heart Study families (2003) (56)
- Quantitative trait loci for abdominal fat and BMI in Hispanic-Americans and African-Americans: the IRAS Family Study (2005) (56)
- A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus (2012) (54)
- Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21. (2011) (54)
- Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions. (2018) (54)
- A comparison of type 2 diabetes risk allele load between African Americans and European Americans (2014) (54)
- Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin. (2016) (54)
- Genetic Risk Assessment of Type 2 Diabetes–Associated Polymorphisms in African Americans (2012) (53)
- Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort (2011) (53)
- Genetic analyses of interferon pathway-related genes reveal multiple new loci associated with systemic lupus erythematosus. (2011) (53)
- Controlled prospective randomized comparison of high-frequency jet ventilation and conventional ventilation in neonates with respiratory failure and persistent pulmonary hypertension. (1997) (52)
- Evaluation of TRAF6 in a large multiancestral lupus cohort. (2012) (51)
- Identification of new SLE-associated genes with a two-step Bayesian study design (2009) (51)
- Association of adipose tissue deposition and beta-2 adrenergic receptor variants: the IRAS family study (2005) (51)
- Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study. (2017) (50)
- Untreated Hypertension: A Powerful Risk Factor for Lobar and Nonlobar Intracerebral Hemorrhage in Whites, Blacks, and Hispanics (2016) (50)
- Infection After Intracerebral Hemorrhage: Risk Factors and Association With Outcomes in the Ethnic/Racial Variations of Intracerebral Hemorrhage Study (2014) (50)
- Genome‐Wide Association Meta‐Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci (2017) (50)
- Author ' s response to reviews Title : Chromosome 7 p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy (2009) (50)
- Power for genetic association studies with random allele frequencies and genotype distributions. (2004) (50)
- A genome scan for ESRD in black families enriched for nondiabetic nephropathy. (2004) (50)
- Genome‐wide Association Study and Follow‐up Analysis of Adiposity Traits in Hispanic Americans: The IRAS Family Study (2009) (50)
- Race-Specific Relationships Between Coronary and Carotid Artery Calcification and Carotid Intimal Medial Thickness (2004) (50)
- Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans. (2008) (50)
- Evaluation of Candidate Nephropathy Susceptibility Genes in a Genome-Wide Association Study of African American Diabetic Kidney Disease (2014) (49)
- The Relationship Between Smoking and Replicated Sequence Variants on Chromosomes 8 and 9 With Familial Intracranial Aneurysm (2010) (49)
- Bone Morphogenetic Protein 7 (BMP7) Gene Polymorphisms Are Associated With Inverse Relationships Between Vascular Calcification and BMD: The Diabetes Heart Study (2009) (49)
- Genomewide Linkage Scan for Diabetic Renal Failure and Albuminuria: The FIND Study (2011) (49)
- Association of Adiponectin Gene Polymorphisms With Type 2 Diabetes in an African American Population Enriched for Nephropathy (2009) (49)
- Replication of the BANK1 genetic association with systemic lupus erythematosus in a European-derived population (2009) (49)
- Genetic analysis of haptoglobin polymorphisms with cardiovascular disease and type 2 diabetes in the diabetes heart study (2013) (49)
- A comparison of risk factors for calcified atherosclerotic plaque in the coronary, carotid, and abdominal aortic arteries: the diabetes heart study. (2007) (48)
- Admixture Mapping of Coronary Artery Calcified Plaque in African Americans With Type 2 Diabetes Mellitus (2013) (48)
- Genetic analysis of HNF4A polymorphisms in Caucasian-American type 2 diabetes. (2005) (48)
- A genome scan for all-cause end-stage renal disease in African Americans. (2005) (47)
- Burden of Risk Alleles for Hypertension Increases Risk of Intracerebral Hemorrhage (2012) (47)
- A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS) (2009) (47)
- Genetic Variation in the Peroxisome Proliferator Activated Receptor-Gamma Gene Is Associated with Histologically Advanced NAFLD (2012) (47)
- Sclerostin is positively associated with bone mineral density in men and women and negatively associated with carotid calcified atherosclerotic plaque in men from the African American-Diabetes Heart Study. (2014) (47)
- Association of alpha2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis. (2007) (46)
- Genetic variants in selenoprotein P plasma 1 gene (SEPP1) are associated with fasting insulin and first phase insulin response in Hispanics. (2014) (46)
- Comparative analysis of methods for detecting interacting loci (2011) (46)
- Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus (2001) (46)
- T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study. (2005) (46)
- The association between innate immunity gene (IRAK1) and C-reactive protein in the Diabetes Heart Study. (2007) (46)
- Genes Associated with SLE Are Targets of Recent Positive Selection (2014) (45)
- Genome‐wide linkage scans for renal function and albuminuria in Type 2 diabetes mellitus: the Diabetes Heart Study (2008) (45)
- Preferential Binding to Elk-1 by SLE-Associated IL10 Risk Allele Upregulates IL10 Expression (2013) (44)
- Evaluation of C1q genomic region in minority racial groups of lupus (2009) (44)
- Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study (2013) (44)
- APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO): Design and Rationale (2019) (43)
- Plasma Dickkopf1 (DKK1) concentrations negatively associate with atherosclerotic calcified plaque in African-Americans with type 2 diabetes. (2013) (43)
- Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster. (2003) (43)
- Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2 (2016) (43)
- Investigation of rheumatoid arthritis susceptibility loci in juvenile idiopathic arthritis confirms high degree of overlap (2012) (42)
- FcαRI (CD89) Alleles Determine the Proinflammatory Potential of Serum IgA1 (2007) (42)
- Human Lipoxygenase Pathway Gene Variation and Association with Markers of Subclinical Atherosclerosis in the Diabetes Heart Study (2010) (42)
- Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1. (2008) (42)
- Polymorphisms near SOCS3 are associated with obesity and glucose homeostasis traits in Hispanic Americans from the Insulin Resistance Atherosclerosis Family Study (2009) (42)
- Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes (2017) (42)
- Genetic influences on susceptibility to rheumatoid arthritis in African‐Americans (2018) (42)
- Brief Report: The Genetic Profile of Rheumatoid Factor–Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis (2018) (42)
- Apolipoprotein E, Statins, and Risk of Intracerebral Hemorrhage (2013) (42)
- The acetyl-coenzyme A carboxylase beta (ACACB) gene is associated with nephropathy in Chinese patients with type 2 diabetes. (2010) (42)
- Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study. (2006) (40)
- Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. (2011) (40)
- Apolipoprotein L1 nephropathy risk variants associate with HDL subfraction concentration in African Americans. (2011) (40)
- Heritability and Expression of C‐Reactive Protein in Type 2 Diabetes in the Diabetes Heart Study (2006) (40)
- Genome-Wide Linkage of Plasma Adiponectin Reveals a Major Locus on Chromosome 3q Distinct From the Adiponectin Structural Gene (2006) (40)
- Nephropathy in siblings of African Americans with overt type 2 diabetic nephropathy. (2002) (40)
- Analysis of common and coding variants with cardiovascular disease in the diabetes heart study (2014) (40)
- Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans. (2010) (39)
- Prophylactic Antiepileptic Drug Use and Outcome in the Ethnic/Racial Variations of Intracerebral Hemorrhage Study (2015) (39)
- Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS). (2006) (39)
- Association of polymorphisms in cyclooxygenase (COX)-2 with coronary and carotid calcium in the Diabetes Heart Study. (2009) (38)
- Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression. (2015) (38)
- Relationships between calcified atherosclerotic plaque and bone mineral density in African Americans with type 2 diabetes (2011) (38)
- Insulin Sensitivity and Insulin Clearance are Heritable and Have Strong Genetic Correlation in Mexican Americans (2013) (37)
- Gene-gene interactions in APOL1-associated nephropathy. (2014) (37)
- Bladder Capacity is a Biomarker for a Bladder Centric versus Systemic Manifestation in Interstitial Cystitis/Bladder Pain Syndrome (2017) (37)
- Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA (2010) (36)
- Genetic variants in CETP increase risk of intracerebral hemorrhage (2016) (36)
- Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population. (2007) (36)
- 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)
- Variability of serum soluble intercellular adhesion molecule-1 measurements attributable to a common polymorphism. (2004) (36)
- Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy. (2012) (35)
- A Genome-Wide Scan for Type 2 Diabetes in African-American Families Reveals Evidence for a Locus on Chromosome 6 q (2004) (35)
- Identification of ATPAF1 as a novel candidate gene for asthma in children. (2011) (35)
- Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans (2018) (35)
- Use of Statins and Outcomes in Intracerebral Hemorrhage Patients (2017) (34)
- Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity (2016) (34)
- Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans. (2011) (33)
- Genetic susceptibility contributes to renal and cardiovascular complications of type 2 diabetes mellitus. (2006) (33)
- Appraising gender role portrayals in TV commercials (1993) (32)
- The relationship between C-reactive protein and subclinical cardiovascular disease in the Diabetes Heart Study (DHS). (2005) (32)
- An Islet-Targeted Genome-Wide Association Scan Identifies Novel Genes Implicated in Cytokine-Mediated Islet Stress in Type 2 Diabetes. (2015) (31)
- Lupus risk variants in the PXK locus alter B-cell receptor internalization (2015) (31)
- Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage (2003) (31)
- FcalphaRI (CD89) alleles determine the proinflammatory potential of serum IgA. (2007) (31)
- In vitro and in vivo assessment of direct effects of simulated solar and galactic cosmic radiation on human hematopoietic stem/progenitor cells (2017) (30)
- Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder (2012) (30)
- Genome screen in familial intracranial aneurysm (2009) (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)
- Genetic Ancestry, Serum Interferon-α Activity, and Autoantibodies in Systemic Lupus Erythematosus (2012) (30)
- Association of genes of lipid metabolism with measures of subclinical cardiovascular disease in the Diabetes Heart Study (2005) (30)
- Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations (2018) (30)
- Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12. (2006) (30)
- European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus. (2009) (30)
- The nuclear structural protein NuMA is a negative regulator of 53BP1 in DNA double-strand break repair (2019) (29)
- Levels of free fatty acids (FFA) are associated with insulin resistance but do not explain the relationship between adiposity and insulin resistance in Hispanic Americans: the IRAS Family Study. (2012) (29)
- Plasma FGF23 and Calcified Atherosclerotic Plaque in African Americans with Type 2 Diabetes Mellitus (2015) (29)
- Heritability and genetic association analysis of cognition in the Diabetes Heart Study (2014) (29)
- Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
- Common variation in COL 4 A 1 / COL 4 A 2 is associated with sporadic cerebral small vessel disease (29)
- Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing (2009) (29)
- Investigation of the Estrogen Receptor-α Gene With Type 2 Diabetes and/or Nephropathy in African-American and European-American Populations (2007) (29)
- Features associated with, and the impact of, hemolytic anemia in patients with systemic lupus erythematosus: LX, results from a multiethnic cohort. (2008) (29)
- Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study. (2005) (29)
- Alcohol use and risk of intracerebral hemorrhage (2017) (28)
- Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity (2019) (28)
- Genetic Risk Score Associations With Cardiovascular Disease and Mortality in the Diabetes Heart Study (2014) (28)
- A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. (2019) (28)
- Association Between Inflammatory Biomarker C-Reactive Protein and Radiotherapy-Induced Early Adverse Skin Reactions in a Multiracial/Ethnic Breast Cancer Population. (2018) (28)
- The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease. (2014) (28)
- Age-Stratified QTL Genome Scan Analyses for Anthropometric Measures (2003) (28)
- INSIG2 SNPs Associated With Obesity and Glucose Homeostasis Traits in Hispanics: The IRAS Family Study (2009) (27)
- Genome-Wide Association Scan for Survival on Dialysis in African-Americans with Type 2 Diabetes (2011) (27)
- Genetic Architecture of Primary Open-Angle Glaucoma in Individuals of African Descent: The African Descent and Glaucoma Evaluation Study III. (2019) (27)
- Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease (2008) (27)
- Hypertension and intracerebral hemorrhage recurrence among white, black, and Hispanic individuals (2018) (27)
- Pleiotropy and Heterogeneity in the Expression of Atherogenic Lipoproteins: The IRAS Family Study (2003) (27)
- Relationships between serum adiponectin and bone density, adiposity and calcified atherosclerotic plaque in the African American-Diabetes Heart Study. (2013) (27)
- 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)
- Common Variants in the Periostin Gene Influence Development of Atherosclerosis in Young Persons (2011) (26)
- Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
- Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster (2017) (26)
- Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing (2009) (26)
- Heritability of Spinal Trabecular Volumetric Bone Mineral Density Measured by QCT in the Diabetes Heart Study (2004) (26)
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (26)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Renal artery calcified plaque associations with subclinical renal and cardiovascular disease. (2004) (25)
- FGF23 Concentration and APOL1 Genotype Are Novel Predictors of Mortality in African Americans With Type 2 Diabetes (2017) (25)
- A Genome-Wide Search for Linkage of Estimated Glomerular Filtration Rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND) (2013) (25)
- Mutational Landscapes of Smoking-Related Cancers in Caucasians and African Americans: Precision Oncology Perspectives at Wake Forest Baptist Comprehensive Cancer Center (2017) (24)
- Visual loss and performance in blind athletes. (1993) (24)
- Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage (2020) (24)
- Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans (2019) (24)
- Ethnic differences in the relationship between pericardial adipose tissue and coronary artery calcified plaque: African-American-diabetes heart study. (2010) (24)
- Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study. (2013) (23)
- Ethnic Differences in the Relationship Between Albuminuria and Calcified Atherosclerotic Plaque (2009) (23)
- APOL1 renal-risk genotypes associate with longer hemodialysis survival in prevalent nondiabetic African American patients with end-stage renal disease. (2016) (23)
- A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study. (2005) (23)
- Relationships between serum MCP-1 and subclinical kidney disease: African American-Diabetes Heart Study (2012) (23)
- APOL1 Kidney-Risk Variants Induce Mitochondrial Fission (2020) (23)
- Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms (2020) (23)
- Sex differences in human adipose tissue gene expression and genetic regulation involve adipogenesis (2020) (22)
- Association Analysis of the Plasminogen Activator Inhibitor-1 4G/5G Polymorphism in Hispanics and African Americans: The IRAS Family Study (2004) (22)
- Association methods in human genetics. (2007) (22)
- Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants. (2011) (22)
- Tissue-Specific and Genetic Regulation of Insulin Sensitivity-Associated Transcripts in African Americans. (2016) (22)
- Association of protein tyrosine phosphatase-N1 polymorphisms with coronary calcified plaque in the Diabetes Heart Study. (2006) (22)
- The Impact of Pedigree Structure on Heritability Estimates for Pulse Pressure in Three Studies (2005) (22)
- Assessment of the interaction of age and sex on 90-day outcome after intracerebral hemorrhage (2017) (22)
- Deceased donor multidrug resistance protein 1 and caveolin 1 gene variants may influence allograft survival in kidney transplantation (2015) (22)
- A plausibly causal functional lupus-associated risk variant in the STAT1–STAT4 locus (2018) (22)
- Integrative analysis of DNA methylation in discordant twins unveils distinct architectures of systemic sclerosis subsets (2019) (22)
- A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity. (2006) (21)
- Effects of weight‐based ultrafiltration rate limits on intradialytic hypotension in hemodialysis (2018) (21)
- The new era of APOL1-associated glomerulosclerosis. (2012) (21)
- Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican-Americans: The GUARDIAN Consortium. (2019) (21)
- The Non-Muscle Myosin Heavy Chain 9 Gene (MYH9) Is Not Associated with Lupus Nephritis in African Americans (2010) (21)
- APOL1 Kidney Risk Variants and Cardiovascular Disease: An Individual Participant Data Meta-Analysis. (2019) (21)
- Erratum: The TMAO-Producing Enzyme Flavin-Containing Monooxygenase 3 Regulates Obesity and the Beiging of White Adipose Tissue (Cell Reports (2017) 19(12) (2451–2461) (S2211124717307519) (10.1016/j.celrep.2017.05.077)) (2017) (21)
- Genetic association of CD247 (CD3ζ) with SLE in a large-scale multiethnic study (2015) (20)
- Racial/ethnic variation of APOE alleles for lobar intracerebral hemorrhage (2018) (20)
- A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy (2018) (20)
- A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS) (2015) (20)
- A ground truth based comparative study on detecting epistatic SNPs (2009) (20)
- JC polyoma viruria associates with protection from chronic kidney disease independently from apolipoprotein L1 genotype in African Americans (2018) (20)
- Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes. (2008) (20)
- Association of polymorphisms in the klotho gene with severity of non-diabetic ESRD in African Americans. (2010) (20)
- Bootstrap Aggregating of Alternating Decision Trees to Detect Sets of SNPs That Associate With Disease (2012) (19)
- Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report. (2010) (19)
- Latent autoimmunity across disease-specific boundaries in at-risk first-degree relatives of SLE and RA patients (2019) (19)
- Association of the μ-opioid receptor gene with type 2 diabetes mellitus in an African American population (2006) (19)
- Association analysis of genes in the renin‐angiotensin system with subclinical cardiovascular disease in families with Type 2 diabetes mellitus: The Diabetes Heart Study (2006) (19)
- Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans (2014) (19)
- RGS6 Variants Are Associated With Dietary Fat Intake in Hispanics: The IRAS Family Study (2011) (19)
- Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos (2017) (19)
- Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study (2006) (19)
- A genome-wide linkage scan in Gullah-speaking African American families with type 2 diabetes : The Sea Islands Genetic African American Registry ( Project SuGAR ) (2008) (19)
- Genome‐Wide Family‐Based Linkage Analysis of Exome Chip Variants and Cardiometabolic Risk (2014) (18)
- Correlates of coronary artery calcified plaque in blacks and whites with type 2 diabetes. (2011) (18)
- Nonparametric Linkage Regression I: Combined Caucasian CSGA and German Genome Scans for Asthma (2001) (18)
- Novel genetic associations with interferon in systemic lupus erythematosus identified by replication and fine-mapping of trait-stratified genome-wide screen. (2020) (18)
- Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke (2020) (17)
- Coding variants in nephrin (NPHS1) and susceptibility to nephropathy in African Americans. (2014) (17)
- Allele-specific methylation in the FADS genomic region in DNA from human saliva, CD4+ cells, and total leukocytes (2018) (17)
- Association of an IL-1A 3′UTR polymorphism with end-stage renal disease and IL-1α expression (2003) (17)
- Hormone replacement therapy is associated with increased C‐reactive protein in women with Type 2 diabetes in the Diabetes Heart Study (2006) (17)
- Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility (2016) (17)
- Metabolomics Identifies Distinctive Metabolite Signatures for Measures of Glucose Homeostasis: The Insulin Resistance Atherosclerosis Family Study (IRAS-FS) (2018) (17)
- Regional Adipose Tissue Associations With Calcified Atherosclerotic Plaque: African American–Diabetes Heart Study (2010) (17)
- Relationship between Genetic Variants in Myocardial Sodium and Potassium Channel Genes and QT Interval Duration in Diabetics: The Diabetes Heart Study (2009) (17)
- Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping (2009) (17)
- Genome-Wide Linkage Scan in Gullah-Speaking African American Families With Type 2 Diabetes (2009) (16)
- Meta-analysis of genome-wide linkage scans for renal function traits. (2012) (16)
- P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study. (2005) (16)
- Infection after Intracerebral Hemorrhage: Risk Factors and Association with Outcomes in the ERICH Study (2014) (16)
- Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study. (2010) (16)
- Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study (2019) (16)
- Progress towards understanding the genetic pathogenesis of systemic lupus erythematosus. (2005) (16)
- Plasma apoM and S1P levels are inversely associated with mortality in African Americans with type 2 diabetes mellitus (2019) (16)
- Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for Systemic Lupus Erythematosus within the MHC (2009) (15)
- Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy (2010) (15)
- Familial autoimmunity in the childhood arthritis and rheumatology research alliance registry (2016) (15)
- CD117/c-kit defines a prostate CSC-like subpopulation driving progression and TKI resistance (2021) (15)
- Systemic inflammatory response syndrome, infection, and outcome in intracerebral hemorrhage (2017) (15)
- Primary care physician productivity: the physician factor. (1995) (15)
- Dense Genotyping of Immune-Related Regions Identifies Loci for Rheumatoid Arthritis Risk and Damage in African Americans (2017) (15)
- Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study. (2012) (15)
- Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect (2006) (15)
- Racial differences in intervention rates in individuals with ALS (2019) (15)
- Risks of peritoneal membrane failure in children undergoing long-term peritoneal dialysis (1993) (15)
- Arg206Cys substitution in DNASE1L3 causes a defect in DNASE1L3 protein secretion that confers risk of systemic lupus erythematosus (2021) (14)
- Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA (2014) (14)
- Genetic Analysis of HNF 4 A Polymorphisms in Caucasian-American Type 2 Diabetes (2005) (14)
- Association of an IL-1A 3'UTR polymorphism with end-stage renal disease and IL-1 alpha expression. (2003) (14)
- Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries. (2020) (14)
- Complement factor H gene associations with end-stage kidney disease in African Americans. (2014) (14)
- APOL1 renal-risk variants associate with reduced cerebral white matter lesion volume and increased gray matter volume. (2016) (14)
- Association of SLCO1B1 *14 Allele with Poor Response to Methotrexate in Juvenile Idiopathic Arthritis Patients (2019) (14)
- Racial-ethnic disparities in acute blood pressure after intracerebral hemorrhage (2016) (14)
- Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity A Meta-analysis (2019) (14)
- Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production (2016) (14)
- Heritability and genetic association analysis of neuroimaging measures in the Diabetes Heart Study (2015) (14)
- Cardioembolic Stroke Risk and Recovery After Anticoagulation-Related Intracerebral Hemorrhage (2018) (14)
- Effect of a Single Apolipoprotein L1 Gene Nephropathy Variant on the Risk of Advanced Lupus Nephritis in Brazilians (2019) (13)
- Admission Hemoglobin Levels Are Associated With Functional Outcome in Spontaneous Intracerebral Hemorrhage (2021) (13)
- Prevalence of Nephropathy in Black Patients with Type 2 Diabetes mellitus (2002) (13)
- Identification and Validation of Hematoma Volume Cutoffs in Spontaneous, Supratentorial Deep Intracerebral Hemorrhage. (2019) (13)
- Combining Imaging and Genetics to Predict Recurrence of Anticoagulation-Associated Intracerebral Hemorrhage (2020) (13)
- Nonparametric Linkage Regression II: Identification of Influential Pedigrees in Tests for Linkage (2001) (13)
- Adipose Tissue Transferrin and Insulin Resistance (2018) (13)
- Bone Mineral Density and Progression of Subclinical Atherosclerosis in African-Americans With Type 2 Diabetes. (2016) (13)
- Ethnic and Racial Variation in Intracerebral Hemorrhage Risk Factors and Risk Factor Burden (2021) (13)
- Minority Patients are Less Likely to Undergo Withdrawal of Care After Spontaneous Intracerebral Hemorrhage (2018) (13)
- Adiposity is inversely associated with hippocampal volume in African Americans and European Americans with diabetes. (2016) (13)
- Aggressiveness of care following intracerebral hemorrhage in women and men (2017) (12)
- Genetic analysis of advanced glycation end products in the DHS MIND study. (2016) (12)
- Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke (2017) (12)
- Relationships between measures of adiposity with subclinical atherosclerosis in patients with type 2 diabetes (2016) (12)
- Genetic associations of LYN with systemic lupus erythematosus (2010) (12)
- Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (12)
- Care of Diabetic Pregnant Women by Primary-Care Physicians: Reported Strategies for Managing Pregestational and Gestational Diabetes (1992) (12)
- Brief report: enrichment of associations in genes with fibrosis, apoptosis, and innate immunity functions with cardiac manifestations of neonatal lupus. (2012) (12)
- Association of the mu-opioid receptor gene with type 2 diabetes mellitus in an African American population. (2006) (12)
- Impact of HDL genetic risk scores on coronary artery calcified plaque and mortality in individuals with type 2 diabetes from the Diabetes Heart Study (2013) (12)
- Genetic Mapping of Vascular Calcified Plaque Loci on Chromosome 16p in European Americans from the Diabetes Heart Study (2011) (12)
- Race/ethnicity influences outcomes in young adults with supratentorial intracerebral hemorrhage (2020) (12)
- Antifibrotic factor KLF4 is repressed by the miR-10/TFAP2A/TBX5 axis in dermal fibroblasts: insights from twins discordant for systemic sclerosis (2021) (12)
- IFRD1 polymorphisms in cystic fibrosis with potential link to altered neutrophil function (2009) (11)
- Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG 16 L 2 , FCHSD 2 , and P 2 RY 2 in Koreans (2016) (11)
- Factors Considered by Clinicians when Prognosticating Intracerebral Hemorrhage Outcomes (2017) (11)
- Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression (2015) (11)
- A molecular biomarker for prediction of clinical outcome in children with ASD, constipation, and intestinal inflammation (2019) (11)
- Analysis of a cardiovascular disease genetic risk score in the Diabetes Heart Study (2015) (11)
- Variability in the Use of Platelet Transfusion in Patients with Intracerebral Hemorrhage: Observations from the Ethnic/Racial Variations of Intracerebral Hemorrhage Study. (2017) (11)
- Variant in the 3′ Region of the IκBα Gene Associated With Insulin Resistance in Hispanic Americans: The IRAS Family Study (2010) (11)
- Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks (2018) (11)
- The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data. (2018) (11)
- Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. (2021) (10)
- Some techniques for the analysis of work sampling data. (1996) (10)
- Variable Association of Reactive Intermediate Genes with Systemic Lupus Erythematosus in Populations with Different African Ancestry (2013) (10)
- Contribution of Racial and Ethnic Differences in Cerebral Small Vessel Disease Subtype and Burden to Risk of Cerebral Hemorrhage Recurrence (2021) (10)
- Genetic Analysis of Adiponectin Variation and its Association with Type 2 Diabetes in African Americans (2013) (10)
- Chromosome 2 q 31 . 1 Associates with ESRD in Women with Type 1 Diabetes (2013) (10)
- Genome-wide study of subcutaneous and visceral adipose tissue reveals novel sex-specific adiposity loci in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (2017) (10)
- Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus. (2015) (10)
- Variants in adiponectin signaling pathway genes show little association with subclinical CVD in the diabetes heart study (2013) (10)
- Estimating the Contributions of Rare and Common Genetic Variations and Clinical Measures to a Model Trait: Adiponectin (2013) (10)
- Rare Coding Variation and Risk of Intracerebral Hemorrhage (2015) (9)
- Fine mapping chromosome 16q12 in a collection of 231 systemic lupus erythematosus sibpair and multiplex families (2005) (9)
- Exploring pleiotropy using principal components (2003) (9)
- The genetic architecture of lipoprotein subclasses in Gullah-speaking African American families enriched for type 2 diabetes: The Sea Islands Genetic African American Registry (Project SuGAR) (2010) (9)
- Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci (2020) (9)
- Brief Report: Association of Natural Killer Cell Ligand Polymorphism HLA–C Asn80Lys With the Development of Anti‐SSA/Ro–Associated Congenital Heart Block (2017) (9)
- Genetic Regulation of Enoyl-CoA Hydratase Domain-Containing 3 in Adipose Tissue Determines Insulin Sensitivity in African Americans and Europeans (2019) (9)
- FTY 720 combined with tacrolimus in de novo renal transplantation : 1-year , multicenter , open-label randomized study (9)
- Analysis of advanced glycation end products in the DHS Mind Study. (2016) (9)
- Salivary dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus. (2020) (9)
- Assessing the accuracy of neuromuscular ultrasound for inclusion body myositis (2019) (9)
- A functional polymorphism in the lymphotoxin-α gene is associated with carotid artery wall thickness: The Diabetes Heart Study (2006) (9)
- Exposure of the Bone Marrow Microenvironment to Simulated Solar and Galactic Cosmic Radiation Induces Biological Bystander Effects on Human Hematopoiesis. (2018) (9)
- Female Roles in television Advertising: Viewers' Use of Gender Role Cues in Appraising Stereotypic and Non-Stereotypic Role Portrayals (1991) (8)
- Association of the Estrogen Receptor-α Gene With the Metabolic Syndrome and Its Component Traits in African-American Families (2007) (8)
- Risk Factors Associated With Mortality and Neurologic Disability After Intracerebral Hemorrhage in a Racially and Ethnically Diverse Cohort (2022) (8)
- Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS) (2018) (8)
- Genetic regulation of adipose tissue transcript expression is involved in modulating serum triglyceride and HDL-cholesterol. (2017) (8)
- Patterns of referral and examination for retinopathy in pregnant women with diabetes by primary care physicians. (1995) (8)
- Genetic admixture: a tool to identify diabetic nephropathy genes in African Americans. (2008) (8)
- The treatment of patients with insulin-requiring diabetes mellitus by primary care physicians (1991) (8)
- Comparison of Genetic and Self-Identified Ancestry in Modeling Intracerebral Hemorrhage Risk (2018) (8)
- A genome wide association study of systemic lupus erythematosus (SLE) by SLEGEN, the International SLE Genetics Consortium. (2008) (8)
- JC Viruria Is Associated With Reduced Risk of Diabetic Kidney Disease. (2019) (8)
- Multilocus and interaction-based genome scan for alcoholism risk factors in Caucasian Americans: the COGA study (2005) (8)
- Primary care physician productivity (1995) (8)
- Adipose tissue depot volume relationships with spinal trabecular bone mineral density in African Americans with diabetes (2018) (7)
- The Subtype Specificity of Genetic Loci Associated with Stroke in 16,664 cases and 32,792 controls (2018) (7)
- The TMAO-Producing Enzyme Flavin-Containing Monooxygenase 3 Regulates Obesity and the Beiging of White Adipose Tissue. (2017) (7)
- Epigenetic methylation in Eosinophilic Esophagitis: Molecular ageing and novel biomarkers for treatment response (2020) (7)
- Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans. (2008) (7)
- TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad (2018) (7)
- Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease (2008) (7)
- Preferential transmission of genetic risk variants of candidate loci at 6p21 from asymptomatic grandparents to mothers of children with neonatal lupus. (2012) (7)
- Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels (2015) (7)
- Preventive foot-care practices among adults with diabetes in North Carolina, 1997 to 2001. (2004) (7)
- The Role of Copy Number Variation in African Americans with Type 2 Diabetes-Associated End Stage Renal Disease. (2013) (7)
- Bladder Hydrodistention Does Not Result In a Significant Change In Bladder Capacity For Interstitial Cystitis/Bladder Pain Syndrome Patients. (2019) (7)
- Hierarchicell: an R-package for estimating power for tests of differential expression with single-cell data (2021) (7)
- Protective association between JC polyoma viruria and kidney disease (2019) (7)
- Integrative Analysis of Glucometabolic Traits, Adipose Tissue DNA Methylation, and Gene Expression Identifies Epigenetic Regulatory Mechanisms of Insulin Resistance and Obesity in African Americans (2020) (7)
- Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD. (2015) (6)
- Comparative analyses of single-nucleotide polymorphisms in the TNF promoter region provide further validation for the vervet monkey model of obesity. (2009) (6)
- Untreated HypertensionClinical Perspective (2016) (6)
- Re-sequencing and Analysis of Variation in the TCF 7 L 2 Gene in African Americans Suggests the SNP rs 7903146 is the Causal Diabetes Susceptibility Variant Running Title : TCF 7 L 2 in African Americans (2010) (6)
- A polymorphism within interleukin-21 receptor (IL21R) confers risk for systemic lupus erythematosus and is associated with malar rash in lupus patients (49.17) (2009) (6)
- Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family‐Based Linkage and Association in the IRAS Family Study (2017) (6)
- Erratum: The nuclear structural protein NuMA is a negative regulator of 53BP1 in DNA double-strand break repair (Nucleic acids research (2019) 47 6 (2703-2715)) (2019) (6)
- Integrative Approaches to Understanding the Pathogenic Role of Genetic Variation in Rheumatic Diseases. (2017) (6)
- A genome‐wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (2017) (6)
- Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls. (2019) (5)
- Usefulness of biventricular volume as a predictor of mortality in patients with diabetes mellitus (from the Diabetes Heart Study). (2013) (5)
- Single-cell expression quantitative trait loci (eQTL) analysis of SLE-risk loci in lupus patient monocytes (2021) (5)
- A Comprehensively Examined Sample for Genetic and Epide- miological Studies of Type 2 Diabetes and its Complications (2011) (5)
- Rare Missense Functional Variants at COL4A1 and COL4A2 in Sporadic Intracerebral Hemorrhage (2021) (5)
- Sa.31. A Genome-wide Association Scan in Women with Systemic Lupus Erythematosus Identifies Risk Variants in ITGAM, PXK, KIAA1542 and Other Loci and Confirms Multiple Loci Contributing to Disease Susceptibility (2008) (5)
- Association Analysis of the Ephrin-B2 Gene in African-Americans with End-Stage Renal Disease (2008) (5)
- Transcriptional regulatory mechanisms in adipose and muscle tissue associate with composite gluco-metabolic phenotypes (2017) (5)
- Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium (2016) (5)
- Single‐Nucleotide Polymorphisms in the TNF Gene Are Associated With Obesity‐Related Phenotypes in Vervet Monkeys (2011) (5)
- Relevance of the ACTN4 Gene in African-Americans with Non-Diabetic End-Stage Renal Disease (2012) (5)
- The new era of APOL 1-associated glomerulosclerosis (2012) (5)
- Genome Wide Association Meta-Analysis Implicates HLA-DRB1, The BTNL2/HLA-DRA region, and a Novel Susceptibility Locus On Chromosome 1 In Systemic Juvenile Idiopathic Arthritis (2013) (5)
- Abstract W MP54: Risk Factors for Nosocomial Infections after Intracerebral Hemorrhage and Their Impact on Outcome: The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (2014) (5)
- Anesthetic Bladder Capacity is a Clinical Biomarker for Interstitial Cystitis/Bladder Pain Syndrome Subtypes. (2021) (5)
- The nuclear structural protein NuMA is a negative regulator of 53BP1 in DNA double-strand break repair (2019) (5)
- Exploring differences in adiposity in two U.S. Hispanic populations of Mexican origin using social, behavioral, physiologic and genetic markers: the IRAS Family Study. (2012) (4)
- Characteristics of engraftment after repeated autologous bone marrow transplantation. (1990) (4)
- Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND) (2016) (4)
- An exploration of sex-specific linkage disequilibrium on chromosome X in Caucasians from the COGA study (2005) (4)
- Obstructive Sleep Apnea as a Risk Factor for Intracerebral Hemorrhage (2021) (4)
- Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals (2022) (4)
- Multilocus Linkage Analysis of the German Asthma Data (2001) (4)
- Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study (2021) (4)
- Comparative Study of Prostate Cancer Biophysical and Migratory Characteristics via Iterative Mechanoelectrical Properties (iMEP) and Standard Migration Assays. (2020) (4)
- Admixture mapping of serum vitamin D and parathyroid hormone concentrations in the African American-Diabetes Heart Study. (2016) (4)
- Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations. (2018) (4)
- Association of SSTR2 Polymorphisms and Glucose Homeostasis Phenotypes (2009) (4)
- Incontinence and gait disturbance after intraventricular extension of intracerebral hemorrhage (2016) (4)
- Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations (2021) (4)
- miR-181a Mediates Inflammatory Gene Expression After Intracerebral Hemorrhage: An Integrated Analysis of miRNA-seq and mRNA-seq in a Swine ICH Model (2021) (4)
- Genetic Landscape of Gullah African Americans (2020) (4)
- Genome-wide Linkage and Association Analysis of Cardiometabolic Phenotypes in Hispanic Americans (2016) (4)
- Association of PPP2CA polymorphisms with SLE susceptibility in multiple ethnic groups (2011) (3)
- Platelet Glycoprotein Ib α‐Chain as a Putative Therapeutic Target for Juvenile Idiopathic Arthritis: A Mendelian Randomization Study (2020) (3)
- Cigarette smoking status has a modifying effect on the association between polymorphisms in KALRN and measures of cardiovascular risk in the diabetes heart study (2011) (3)
- Integrative analysis of DNA methylation in discordant twins unveils distinct architectures of systemic sclerosis subsets (2019) (3)
- Genetic epidemiology in kidney disease: Clinical Epidemiology in Nephrology (2017) (3)
- 464 - Genome-Wide Epigenetic Scan of Eosinophilic Esophagitis Patients with and without Treatment Response to Topical Steroids (2018) (3)
- Pseudoreplication bias in single-cell studies; a practical solution (2020) (3)
- Risk of intracerebral haemorrhage from hypertension is greatest at an early age (2021) (3)
- Transcriptome-wide Analyses of Adipose Tissue in Outbred Rats Reveal Genetic Regulatory Mechanisms Relevant for Human Obesity (2022) (3)
- Detection of complex interactions of multi-locus SNPS (2008) (3)
- Bulk and Single-Cell Profiling of Breast Tumors Identifies TREM-1 as a Dominant Immune Suppressive Marker Associated With Poor Outcomes (2021) (3)
- Mendelian randomization and pathway analysis demonstrate shared genetic associations between lupus and coronary artery disease (2022) (3)
- Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses (2019) (3)
- A single APOL1 nephropathy variant increases risk of advanced lupus nephritis in Brazilians (2019) (2)
- CHARACTERIZATION OF SNPS WITHIN THE MMP-1 PROMOTOR REGION IN WOMEN WITH AND WITHOUT POP (2011) (2)
- Genome-Wide Association Meta-Analysis of Eight Independent Systemic Juvenile Idiopathic Arthritis Collections Reveals Regional Association Spanning the Major Histocompatibility Complex Class II and III Gene Cluster (2012) (2)
- Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis (2022) (2)
- Effects of Intensive Systolic Blood Pressure Control on All-Cause Hospitalizations (2020) (2)
- A pilot study assessing the impact of rs174537 on circulating PUFAs and the inflammatory response in TBI patients. (2020) (2)
- Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
- A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage (2022) (2)
- Increasing the Use of Intensified Management of Diabetes: An Education Program for Physicians. (1991) (2)
- Mortality prediction and interval until death in near-term and term neonates with respiratory failure. (1993) (2)
- Pathogenesis and Treatment of Kidney Disease and Hypertension Heritability of GFR and Albuminuria in Caucasians With Type 2 Diabetes Mellitus (2004) (2)
- Nucleic Acid-Sensing and Interferon-Inducible Pathways Show Differential Methylation in MZ Twins Discordant for Lupus and Overexpression in Independent Lupus Samples: Implications for Pathogenic Mechanism and Drug Targeting (2021) (2)
- Metabolomic architecture of obesity implicates metabolonic lactone sulfate in cardiometabolic disease (2021) (2)
- Systemic juvenile idiopathic arthritis is associated with HLA-DRB1 in Europeans and Americans of European descent (2012) (2)
- Reply to: A balanced measure shows superior performance of pseudobulk methods in single-cell RNA-sequencing analysis (2022) (2)
- Intrinsic DNA topology as a prioritization metric in genomic fine-mapping studies (2019) (2)
- Impact of Resident Participation in a Multidisciplinary Diabetes Team (1993) (2)
- Identification of Influential Variants in Significant Aggregate Rare Variant Tests (2020) (2)
- A Pilot Study Assessing the Impact of rs174537 on Circulating Polyunsaturated Fatty Acids and the Inflammatory Response in Patients with Traumatic Brain Injury (2020) (1)
- Abstract 24: Race/Ethnic Differences in Microbleed Characteristics and Association of Microbleeds with Poor Outcomes in the ERICH Study (2015) (1)
- Abstract TP137: Ethnic/racial Variations Of Intracerebral Hemorrhage Genetics (erich-gene) Study Protocol (2022) (1)
- Author response: Ischemic Lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage (2017) (1)
- Abstract NS20: Discharge Disposition After Intracerebral Hemorrhage (2015) (1)
- Major Histocompatibility Complex Class II Gene Cluster Harbors Systemic Juvenile Idiopathic Arthritis Susceptibility Locus (2011) (1)
- Abstract W P235: Predictors of Platelet Transfusion in Patients with Intracerebral Hemorrhage (2014) (1)
- A120: Familial Autoimmunity in the CARRA Registry (2014) (1)
- Albuminuria Associates With Calcified Atherosclerotic Plaque in African Americans With Diabetes (2013) (1)
- Erratum: Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans (The American Journal of Human Genetics (2012) 91 (778-793)) (2015) (1)
- Abstract 49: Withdrawal of Care in the Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (2013) (1)
- Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes (2021) (1)
- PRIORITIZATION OF RESULTS FROM WHOLE EXOME SEQUENCING IN FAMILIAL INTRACRANIAL ANEURYSM (2012) (1)
- Erratum to: Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels (2015) (1)
- Abstract 3559: Differential Effect of High Cholesterol by Intracerebral Hemorrhage Location (2012) (1)
- GG-08 Transancestral mapping and genetic load in systemic lupus erythematosus (2016) (1)
- Gut dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus (2022) (1)
- Feitosa, M. F., & Levy, D. (2018). Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K (2018) (1)
- Testing gene‐environment interactions in family‐based association studies using trait‐based ascertained samples (2014) (1)
- Anti-Epileptic Drug Use and Outcome in the Ethnic and Racial Variations in Intracerebral Hemorrhage (ERICH) Study (S23.005) (2012) (1)
- Abstract T P330: Migraine and Risk of Intracerebral Hemorrhage in the Ethnic/racial Variations of Intracerebral Hemorrhage (ERICH) Study (2014) (1)
- Nephropathy Progression in African Americans With a Family History of ESKD: Implications for Clinical Trials in APOL1-Associated Nephropathy. (2019) (1)
- Racial Variation in Comfort Measures Only Status in Patients with Intracerebral Hemorrhage (S42.008) (2018) (1)
- 1640-P: Common and Ethnic-Specific Molecular Networks and Drivers of Insulin Resistance in African and European Ancestry Individuals (2020) (1)
- Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels (2014) (1)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
- Impact of rs174537 on Critically Ill Patients with Acute Lung Injury: A Secondary Analysis of the OMEGA Randomized Clinical Trial (2020) (1)
- Abstract TP359: Admission Systemic Inflammatory Response Syndrome and Outcome Following Intracerebral Hemorrhage in a Multicenter Study (2016) (1)
- Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis (2012) (1)
- Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis (2012) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- APOL1 Risk Variants Impair Multiple Mitochondrial Pathways in a Metabolomics Analysis. (2020) (1)
- Alzheimer’s disease related single nucleotide polymorphisms and correlation with intracerebral hemorrhage incidence (2022) (1)
- Abstract W P259: ICH &FUNC Scores in the Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (2014) (1)
- The Use of Linkage Data To Prioritize Results from Whole Exome Sequencing in Familial Intracranial Aneurysm (S53.001) (2012) (1)
- Abstract WP357: The Impact of Specific Neuroanatomical Location in Deep Supratentorial Intracerebral Hemorrhage (ICH): Findings From the Ethnic/Racial Variations of ICH Study (2016) (1)
- Abstract T MP65: Moderate Alcohol Use Protects from Intracerebral Hemorrhage: Findings from the Ethnic/racial Variations of Intracerebral Hemorrhage (ERICH) Study. (2014) (1)
- Integrative Genetics Analysis of Juvenile Idiopathic Arthritis Identifies Novel Loci (2020) (1)
- Relationship Between a Vitamin D Genetic Risk Score and Autoantibodies Among First-Degree Relatives of Probands With Rheumatoid Arthritis and Systemic Lupus Erythematosus (2022) (1)
- Abstract TP347: Obstructive Sleep Apnea Frequency in Intracerebral Hemorrhage (2020) (0)
- A Comparison of Optimality Measures for Estimating Untyped SNP Using the Allele Frequencies of Neighboring SNPs (2015) (0)
- Insulin Action/Molecular Metabolism (2016) (0)
- Contents Vol. 29, 2009 (2009) (0)
- Abstract 3726: Rate of Inappropriate Statin Use after Intracerebral Hemorrhage (2012) (0)
- Abstract WP410: Hemoglobin Levels and Poor Outcome in Intracerebral Hemorrhage: An Exploratory Analysis of Individual Patient Data Across Multiple Studies (2020) (0)
- Abstract MP40: Klotho -vS Heterozygosity is Associated With Lower Risk of Lobar Intracerebral Hemorrhage (2021) (0)
- Subject Index Vol. 29, 2009 (2009) (0)
- Abstract W MP71: Effect of Race/Ethnicity on Oral Anticoagulant-Associated Intracerebral Hemorrhage (2015) (0)
- Abstract TP10: Inflammatory And Neurodegenerative Gene Expression Changes Occur Long-term After ICH (2022) (0)
- Late Breast Toxicity Rates in a Prospective Evaluation of Radiation Therapy (RT) in a Multiracial/Ethnic Population of Breast Cancer (BC) Patients (2015) (0)
- Abstract 1927: Evaluating molecular determinants of elesclomol sensitivity in breast cancer cells: An implication for metastatic properties (2020) (0)
- A159: The Autoimmune Genetic Architecture of Childhood Onset Rheumatoid Arthritis (2014) (0)
- Obstructive Sleep Apnea: A Prevalent and Novel Risk Factor for Intracerebral Hemorrhage (2020) (0)
- Abstract W P255: Prior Use of Statins May Reduce Hematoma Growth in Intracerebral Hemorrhage Patients (2014) (0)
- 1401 A Genome Wide Association Scan of SLE genetic risk in a cohort of African-American persons (2022) (0)
- Mo-P2:196 A genome scan for subclinical cardiovascular disease in the diabetes heart study (2006) (0)
- Contents Vol. 28, 2008 (2008) (0)
- Erratum: Genetic associations of LYN with systemic lupus erythematosus (Genes and Immunity (2009) 10 (397-403) DOI: 10.1038/gene.2009.19) (2010) (0)
- Deep resequencing of the 1q22 locus in non-lobar intracerebral hemorrhage (2023) (0)
- Contents Vol. 33, 2011 (2011) (0)
- BD-01 E-genes identified via transancestral SNP mapping and gene expression analysis reveal novel targeted therapies for african-american and european-american SLE patients (2018) (0)
- Subphenotype mapping in systemic lupus erythematosus identifies multiple novel loci associated with circulating interferon alpha (2014) (0)
- CASE REPORT Is Collapsing C1q Nephropathy Another MYH9-Associated Kidney Disease? A Case Report (2010) (0)
- Gene-Based Analysis of Sarcoidosis Susceptibility in European-Descent Americans (2021) (0)
- Abstract T MP77: Intraventricular Hemorrhage and Long-term Incontinencea and Dysmobility After Intracerebral Hemorrhage (2015) (0)
- 140-OR: Machine Learning for Metabolite Estimation to Examine Contributors to Glucose Homeostasis and Adiposity: The GUARDIAN Consortium (2022) (0)
- GG-05 Predictive ability of SLE genetic risk factors varies across ethnicities (2018) (0)
- Abstract 3122: Delays in Warfarin Reversal following Intracerebral Hemorrhage: A Population-Based Study (2012) (0)
- A prospective evaluation of radiotherapy (RT) related skin reactions in a multi-racial/ethnic population of women with newly diagnosed breast cancer (BC). (2015) (0)
- CD117/c-kit defines a prostate CSC-like subpopulation driving progression and TKI resistance (2021) (0)
- Factors Considered by Physicians Versus Nurses When Prognosticating Acute Intracerebral Hemorrhage Outcomes (S46.003) (2016) (0)
- Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS) (2023) (0)
- Hierarchicell: an R-package for estimating power for tests of differential expression with single-cell data (2021) (0)
- Consultants for the American Journal of Nephrology 2008 (2008) (0)
- Analysis Of The MHC Region In a Large Cohort Of Juvenile Idiopathic Arthritis Cases Identifies Independent Effects At HLA-DRB1 (2013) (0)
- A cis-regulatory element regulates ERAP2 expression through autoimmune disease risk SNPs (2023) (0)
- Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease (2022) (0)
- Abstract 211: Do Women Receive Less Aggressive Care Following Intracerebral Hemorrhage? (2016) (0)
- 177-P: Association of HLA-DR-DQ haplotypes with juvenile idiopathic arthritis (JIA) (2008) (0)
- Supplementary Material for: Plasma FGF23 and Calcified Atherosclerotic Plaque in African Americans with Type 2 Diabetes Mellitus (2016) (0)
- Genome-Wide Search for Linkage of Estimated Glomerular Filtration Rate (eGFR) in the Family and Diabetes (2013) (0)
- Abstract W MP110: INR reversal of Oral Anticoagulant-Associated Intracerebral Hemorrhage (2015) (0)
- Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study (2019) (0)
- Race/Ethnicity Influences Outcomes in Young Adults with Intracerebral Hemorrhage (S10.007) (2018) (0)
- Front & Back Matter (2012) (0)
- Subject Index Vol. 28, 2008 (2008) (0)
- Asthma and lower airway disease Identification of ATPAF 1 as a novel candidate gene for asthma in children (2011) (0)
- 4277 Functional consequences of the juvenile idiopathic arthritis risk variant at 1q24.3 (2020) (0)
- Multi-Site Observational Study to Assess Biomarkers for Susceptibility or Resilience to Chronic Pain: The Acute to Chronic Pain Signatures (A2CPS) Study Protocol (2022) (0)
- TGFBR1*6A as a modifier of breast cancer risk and progression: advances and future prospects (2022) (0)
- Abstract 154: Genetic Variants in CETP That Increase HDL Levels also Increase Risk of Intracerebral Hemorrhage (2017) (0)
- Abstract P360: Meta-Analysis of up to 14,262 Individuals Identifies Loci Associated with Measures of Subcutaneous Fat Volume and Attenuation (2015) (0)
- Abstract WMP82: Diffusion Tensor Imaging Is Independently Associated With Mobility After Intracerebral Hemorrhage (2022) (0)
- Genetically-Regulated Mechanisms of Insulin Resistance in Adipose Tissue (2018) (0)
- Abstract 97: Ischemic Lesions in Intracerebral Hemorrhage Associated with Drop in Blood Pressure and Poor Outcomes in the ERICH Study (2015) (0)
- Abstract 17: Apolipoprotein E and Intracerebral Hemorrhage: A Trans-Ethnic Meta-Analysis (2019) (0)
- of the Diabetes Heart Study ( DHS ) Family of Studies : A Comprehensively Examined Sample for Genetic and Epidemiological Studies of Type 2 Diabetes and its Complications (2017) (0)
- GENETIC ADMIXTURE :A T OOL TO IDENTIFY DIABETIC NEPHROPATHY GENES IN (2008) (0)
- Abstract 211: Subjective Judgments of Physicians and Nurses Are More Accurate Than Formal Clinical Scales in Predicting Functional Outcome After Intracerebral Hemorrhage (2014) (0)
- Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans (2014) (0)
- Social Factors, Epigenomics and Lupus in African American Women (SELA) Study: protocol for an observational mechanistic study examining the interplay of multiple individual and social factors on lupus outcomes in a health disparity population (2022) (0)
- TGFBR1*6A as a modifier of breast cancer risk and progression: advances and future prospects (2022) (0)
- Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans (2019) (0)
- Giulio Genovese African Americans Association of Trypanolytic ApoL 1 Variants with Kidney Disease in (2014) (0)
- Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos (2017) (0)
- Initial antihypertensive agent effects on acute blood pressure after intracerebral haemorrhage (2022) (0)
- Original A genome scan for all-cause end-stage renal disease in African Americans (2005) (0)
- P20 The identification of novel genetic susceptibility loci for juvenile idiopathic arthritis by analysis across clinical subgroups (2020) (0)
- Asymmetric Independence Model for Detecting Interactions between Variables (2015) (0)
- Abstract 179: Racial-ethnic Blood Pressure Differences in Acute Intracerebral Hemorrhage. (2014) (0)
- An Evaluation of the MiDCoP Method for Imputing Allele Frequency in Genome Wide Association Studies (2015) (0)
- Oral abstracts 7: Molecular mechanisms of disease—osteoarthritisS1. Identification of novel osteoarthritis genes using zebrafish (2012) (0)
- Lupus Nephritis Susceptibility Markers in PDGRFA-GSX2, SLC5A11, ID4, and HAS2-SNTB1 Regions Identified From a Meta-Analysis of Genome Wide Association Studies of Women with Systemic Lupus Erythematosus (2011) (0)
- Abstract 53: Comparison of Genetic Ancestry versus Self-Identified Race and Ethnicity as Risk Factor for Intracerebral Hemorrhage (2018) (0)
- Factors Associated With Participation in Clinical Trials Among Patients With Lupus (2022) (0)
- Acknowledgement to the Reviewers (2015) (0)
- Determinants of Poor Outcome after Intracerebral Hemorrhage: Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (2019) (0)
- Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND) (2016) (0)
- Autosomal genomewide linkage scan for coronary artery calcification loci. (2001) (0)
- O35. THE AUTOIMMUNE GENETIC ARCHITECTURE OF CHILDHOOD-ONSET RHEUMATOID ARTHRITIS (2017) (0)
- Coincident idiopathic FSGS collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants (2011) (0)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (0)
- THE ROLE OF POLYUNSATURATED FATTY ACID METABOLISM ON PROSTATE CANCER AGGRESSIVENESS: AN ANALYSIS OF THE NORTH CAROLINA‐LOUISIANA PROSTATE CANCER PROJECT (PCAP): MP70‐18 (2018) (0)
- Subjective Judgments of Physicians and Nurses Are More Accurate Than Formal Clinical Scales in Predicting Functional Outcome After Intracerebral Hemorrhage (S45.006) (2014) (0)
- Multi-omic integration reveals cell-type-specific regulatory networks of insulin resistance in distinct ancestry populations. (2023) (0)
- 243-OR: Integrative Multiomics Analysis of Glucometabolic Traits, Adipose Tissue DNA Methylation, and Gene Expression Identifies Epigenetic Regulatory Mechanisms of Insulin Resistance and Obesity in African Americans (2020) (0)
- THE AUTOIMMUNE GENETIC ARCHITECTURE OF CHILDHOOD-ONSET RHEUMATOID ARTHRITIS (2017) (0)
- Abstract 75: Predictors of Poor Outcome After Intracerebral Hemorrhage: Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (2019) (0)
- Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS) (2018) (0)
- Abstract W P126: Accurate Outcome Predictions for Intracerebral Hemorrhage Patients Are More Likely Than Inaccurate Predictions to Be Influenced by Co-morbidities Not Included in Clinical Scales (2015) (0)
- OP0122 Fine Mapping of the CHR 22Q13.1 Juvenile Idiopathic Arthritis Risk Locus (2015) (0)
- Abstract WMP79: Elevated Cardiac Troponin Levels In Patients With Non-traumatic Intracerebral Hemorrhage (2022) (0)
- Gene-environment Interaction in Pediatric Eosinophilic Esophagitis: 422 (2016) (0)
- Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
- Clinical presentation and outcomes of young adults enrolled in the Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (P2.267) (2017) (0)
- Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia (2016) (0)
- Americans Association of Plasma Vitamin D Levels with Adiposity in Hispanic and African (2009) (0)
- Genomics in Rheumatic Diseases: Hope for the Future. (2017) (0)
- Abstract W MP111: The Impact of Fever on Presentation in Intracerebral Hemorrhage: The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) Study (2015) (0)
- Abstract WMP96: Racial Variation in Comfort Measures Only Status in Patients With Intracerebral Hemorrhage (2018) (0)
- 168 – Epigenetic Analysis Indicates Accelerated Molecular Ageing in Eosinophilic Esophagitis (2019) (0)
- Exploiting three-dimensional human hepatic constructs to investigate the impact of rs174537 on fatty acid metabolism (2022) (0)
- Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant (2022) (0)
- Genomics in Rheumatic Diseases (2017) (0)
- C8orf13/BLK association with systemic lupus erythematosus across different ethnicities (136.28) (2009) (0)
- 45-OR: Fine-Mapping of MHC Region Variants in Juvenile Idiopathic Arthritis (JIA) Reveals Evidence of Additional Predisposing Sites Telomeric to Class I (2010) (0)
- Genetic Variation in the Peroxisome Proliferator Activated Receptor-gamma Gene Is Associated with NAFLD and Its Histological Phenotypes: 358 (2007) (0)
- DNA methylation of the TPMT gene and azathioprine pharmacokinetics in children with very early onset inflammatory bowel disease. (2022) (0)
- COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection (2022) (0)
- Genome wide and candidate gene studies of African American type 2 diabetes (2009) (0)
- 252. Chromatin Marks Mapping to Juvenile Idiopathic Arthritis Associated Genomic Regions Identify CD4 and Regulatory T Cells as Critical Cell Types in JIA (2015) (0)
- Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing (2019) (0)
- Accurate outcome predictions for intracerebral hemorrhage patients are more likely than inaccurate predictions to be influenced by co-morbidities not included in clinical scales (I2-5D) (2015) (0)
- Acute to Chronic Pain Signatures Program (a2CPS): Implementation of Remote Training for a Multisite Observation Study During COVID-19 (2022) (0)
- Abstract 181: Meta-Analysis of Genome-Wide Association Studies Identifies Two New Susceptibility Loci for Intracerebral Hemorrhage (2014) (0)
- Contents Vol. 42, 2015 (2016) (0)
- Mo-W2:6 The relationship between calcified atherosclerotic plaque and bone mineral density: The diabetes heart study (2006) (0)
- Abstract WP360: Race and Ethnicity Are Associated with Intracerebral Hemorrhage Recurrence Risk (2017) (0)
- 220-P: Examination of HLA class II amino acid variation in juvenile idiopathic arthritis (JIA) implicates P4 with position 86 (2009) (0)
- Novel targeted therapies for African-American and European-American SLE patients identified from E-Genes elucidated by transancestral SNP mapping (2018) (0)
- Abstract T MP92: Variation of Blood Pressure Response of Antihypertensive Agents in Acute Intracerebral Hemorrhage (ICH) (2015) (0)
- OP0121 Analysis of the MHC Region in a Large Cohort of Juvenile Idiopathic Arthritis Cases Identifies Independent Effects at HLA-DRB1 for the Most Common Subtypes of JIA (2015) (0)
- Erratum to: Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels (2014) (0)
- A comparison of type 2 diabetes risk allele load between African Americans and European Americans (2014) (0)
- The modifying influence of HLA class II DQB1*06:02 on the Streptococcus and clinical phenotype correlation among anti-Ro+ mothers of children with neonatal lupus (2022) (0)
- Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity (2016) (0)
- Erratum and Announcement (2002) (0)
- THU0002 SOLVING THE COMPLEX MHC ASSOCIATIONS IN SLE IDENTIFIES SEX-RELATED GENE EFFECTS (2020) (0)
- Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis (2022) (0)
- Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII (2022) (0)
- Abstract 126: Importance of Untreated Hypertension for Intracerebral Hemorrhage (2016) (0)
- A molecular biomarker for prediction of clinical outcome in children with ASD, constipation, and intestinal inflammation (2019) (0)
- We-W45:5 Human lipoxygenase gene variation in subclinical atherosclerosis: The diabetes heart study (2006) (0)
- Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. (2023) (0)
- Abstract W MP93: The STICH II Prognostic Score Predicts Outcomes in the ERICH Study (2014) (0)
- 1703-P: Altered DNA-Methylation Modulates Adipose Tissue Gene Expression and Is Associated with Insulin Resistance in African Americans (2019) (0)
- Differential DNA Methylation in Lower Airways Epithelial Cells Associate with Lung Function and CT Scan-Based Lung Structure in SPIROMICS (2022) (0)
- ANALYSIS OF THE IMMUNOCHIP IN A LARGE COHORT OF OLIGO- AND POLYARTHRITIS JUVENILE IDIOPATHIC ARTHRITIS CASES CONFIRMS PREVIOUS AND IDENTIFIES NOVEL ASSOCIATIONS (2012) (0)
- Abstract T P340: Delays in Seeking Medical Attention in Intracerebral Hemorrhage (2014) (0)
- Diversity of risk alleles for SLE in African–American, European and Hispanic-American samples with those in Indian individuals (2014) (0)
- Abstract 20: Cross-Phenotype Meta-Analysis of Intracerebral Hemorrhageand Small Vessel Ischemic Stroke Identifies Two Novel Genetic Loci at 2q33 and 13q34 (2019) (0)
- Abstract WP372: Preeclampsia and Intracerebral Hemorrhage Risk in Later Life (2016) (0)
- Analysis of the Immunochip in a Large Cohort of Juvenile Idiopathic Arthritis Cases Identifies 17 Loci At Genome-Wide Significance (2012) (0)
- An Intronic CR2 Polymorphism Associated With Systemic Lupus Erythematosus Alters CTCF Binding and CR1 Expression (2013) (0)
- Erratum: Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing (Genes and Immunity (2009) vol. 10 (457-469) 10.1038/gene.2009.27) (2009) (0)
- Abstract WP292: Discharge Disposition After Intracerebral Hemorrhage and Functional Outcomes (2016) (0)
- Abstract TP209: Time Of Stroke Onset Is Not Associated With Risk Of Obstructive Sleep Apnea In Intracerebral Hemorrhage. (2013) (0)
- Allele-specific methylation in the FADS genomic region in DNA from human saliva, CD4+ cells, and total leukocytes (2018) (0)
- Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes (2017) (0)
- Genetic Architecture of Primary Open Angle Glaucoma in Individuals of African Descent: The African Descent & Glaucoma Evaluation Study (ADAGES) III (2018) (0)
- Abstract T MP68: Validating the Association of Peripheral Monocyte Count with 30-Day Case-Fatality in Intracerebral Hemorrhage (2015) (0)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (0)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (0)
- Molecular pathways identified from single nucleotide polymorphisms demonstrate mechanistic differences in systemic lupus erythematosus patients of Asian and European ancestry (2023) (0)
- Reduction of foot abnormalities in noninsulin-dependent diabetes (1993) (0)
- Kidney pathology alters cell-clustering in single cell RNA sequencing (2021) (0)
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What Schools Are Affiliated With Carl D. D. Langefeld?
Carl D. D. Langefeld is affiliated with the following schools:
