Carl D. D. Langefeld
#139,086
Most Influential Person Now
Carl D. D. Langefeld's AcademicInfluence.com Rankings
Carl D. D. Langefeldbiology Degrees
Biology
#9737
World Rank
#12978
Historical Rank
Genetics
#1000
World Rank
#1098
Historical Rank

Download Badge
Biology
Carl D. D. Langefeld's Degrees
- PhD Genetics Stanford University
- Bachelors Biology University of California, Berkeley
Similar Degrees You Can Earn
Why Is Carl D. D. Langefeld Influential?
(Suggest an Edit or Addition)Carl D. D. Langefeld's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genetic 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)
This paper list is powered by the following services:
What Schools Are Affiliated With Carl D. D. Langefeld?
Carl D. D. Langefeld is affiliated with the following schools: