Item Type | Name |
Academic Article
|
Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension.
|
Academic Article
|
Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus.
|
Academic Article
|
Association of an IL-1A 3'UTR polymorphism with end-stage renal disease and IL-1 alpha expression.
|
Academic Article
|
Age-stratified heritability estimation in the Framingham Heart Study families.
|
Academic Article
|
Exploring pleiotropy using principal components.
|
Academic Article
|
A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q.
|
Academic Article
|
Power for genetic association studies with random allele frequencies and genotype distributions.
|
Academic Article
|
A promoter haplotype of the immunoreceptor tyrosine-based inhibitory motif-bearing FcgammaRIIb alters receptor expression and associates with autoimmunity. I. Regulatory FCGR2B polymorphisms and their association with systemic lupus erythematosus.
|
Academic Article
|
Ordered subset analysis in genetic linkage mapping of complex traits.
|
Academic Article
|
Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study.
|
Academic Article
|
Association analysis of the plasminogen activator inhibitor-1 4G/5G polymorphism in Hispanics and African Americans: the IRAS family study.
|
Academic Article
|
Variability of serum soluble intercellular adhesion molecule-1 measurements attributable to a common polymorphism.
|
Academic Article
|
Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes.
|
Academic Article
|
Association of protein tyrosine phosphatase 1B gene polymorphisms with measures of glucose homeostasis in Hispanic Americans: the insulin resistance atherosclerosis study (IRAS) family study.
|
Academic Article
|
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.
|
Academic Article
|
T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study.
|
Academic Article
|
Genetic analysis of HNF4A polymorphisms in Caucasian-American type 2 diabetes.
|
Academic Article
|
P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study.
|
Academic Article
|
Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect.
|
Academic Article
|
A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity.
|
Academic Article
|
Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study.
|
Academic Article
|
Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12.
|
Academic Article
|
Genetic susceptibility contributes to renal and cardiovascular complications of type 2 diabetes mellitus.
|
Academic Article
|
A functional polymorphism in the lymphotoxin-alpha gene is associated with carotid artery wall thickness: the Diabetes Heart Study.
|
Academic Article
|
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
|
Academic Article
|
A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans.
|
Academic Article
|
Peroxisome proliferator-activated receptor gamma 2 and acyl-CoA synthetase 5 polymorphisms influence diet response.
|
Academic Article
|
Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy.
|
Academic Article
|
Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population.
|
Academic Article
|
Comprehensive evaluation of the estrogen receptor alpha gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population.
|
Academic Article
|
Association methods in human genetics.
|
Academic Article
|
Association analysis of the ephrin-B2 gene in African-Americans with end-stage renal disease.
|
Academic Article
|
Association of polymorphisms in cyclooxygenase (COX)-2 with coronary and carotid calcium in the Diabetes Heart Study.
|
Academic Article
|
Polymorphisms near SOCS3 are associated with obesity and glucose homeostasis traits in Hispanic Americans from the Insulin Resistance Atherosclerosis Family Study.
|
Academic Article
|
Genome screen in familial intracranial aneurysm.
|
Academic Article
|
Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
|
Academic Article
|
Association of SSTR2 polymorphisms and glucose homeostasis phenotypes: the Insulin Resistance Atherosclerosis Family Study.
|
Academic Article
|
Identification of IRAK1 as a risk gene with critical role in the pathogenesis of systemic lupus erythematosus.
|
Academic Article
|
High-density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups.
|
Academic Article
|
Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies.
|
Academic Article
|
The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans.
|
Academic Article
|
Bone morphogenetic protein 7 (BMP7) gene polymorphisms are associated with inverse relationships between vascular calcification and BMD: the Diabetes Heart Study.
|
Academic Article
|
A polymorphism within IL21R confers risk for systemic lupus erythematosus.
|
Academic Article
|
European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus.
|
Academic Article
|
Variant in the 3' region of the IkappaBalpha gene associated with insulin resistance in Hispanic Americans: The IRAS Family Study.
|
Academic Article
|
Comparative analyses of single-nucleotide polymorphisms in the TNF promoter region provide further validation for the vervet monkey model of obesity.
|
Academic Article
|
Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report.
|
Academic Article
|
Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy.
|
Academic Article
|
Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.
|
Academic Article
|
Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study.
|
Academic Article
|
Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans.
|
Academic Article
|
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.
|
Academic Article
|
The role of genetic variation near interferon-kappa in systemic lupus erythematosus.
|
Academic Article
|
Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants.
|
Academic Article
|
Correlates of coronary artery calcified plaque in blacks and whites with type 2 diabetes.
|
Academic Article
|
RGS6 variants are associated with dietary fat intake in Hispanics: the IRAS Family Study.
|
Academic Article
|
Single-nucleotide polymorphisms in the TNF gene are associated with obesity-related phenotypes in vervet monkeys.
|
Academic Article
|
Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.
|
Academic Article
|
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.
|
Academic Article
|
Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21.
|
Academic Article
|
Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study.
|
Academic Article
|
Common variants in the periostin gene influence development of atherosclerosis in young persons.
|
Academic Article
|
The impact of FADS genetic variants on ?6 polyunsaturated fatty acid metabolism in African Americans.
|
Academic Article
|
Meta-analysis of genome-wide linkage scans for renal function traits.
|
Academic Article
|
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility.
|
Academic Article
|
Identification of ATPAF1 as a novel candidate gene for asthma in children.
|
Academic Article
|
Genome-wide association of BMI in African Americans.
|
Academic Article
|
Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans.
|
Academic Article
|
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
Academic Article
|
Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosus.
|
Academic Article
|
Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy.
|
Academic Article
|
Genetic variation in the peroxisome proliferator activated receptor-gamma gene is associated with histologically advanced NAFLD.
|
Academic Article
|
Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase.
|
Academic Article
|
Evaluation of TRAF6 in a large multiancestral lupus cohort.
|
Academic Article
|
Investigation of rheumatoid arthritis susceptibility loci in juvenile idiopathic arthritis confirms high degree of overlap.
|
Academic Article
|
The new era of APOL1-associated glomerulosclerosis.
|
Academic Article
|
Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.
|
Academic Article
|
Genetic ancestry, serum interferon-a activity, and autoantibodies in systemic lupus erythematosus.
|
Academic Article
|
Exploring differences in adiposity in two U.S. Hispanic populations of Mexican origin using social, behavioral, physiologic and genetic markers: the IRAS Family Study.
|
Academic Article
|
Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans.
|
Academic Article
|
Bootstrap aggregating of alternating decision trees to detect sets of SNPs that associate with disease.
|
Academic Article
|
Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations.
|
Academic Article
|
Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis.
|
Academic Article
|
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
|
Academic Article
|
Relevance of the ACTN4 gene in African-Americans with non-diabetic end-stage renal disease.
|
Academic Article
|
Estimating the contributions of rare and common genetic variations and clinical measures to a model trait: adiponectin.
|
Academic Article
|
Informed conditioning on clinical covariates increases power in case-control association studies.
|
Academic Article
|
Risk factors for intracerebral hemorrhage differ according to hemorrhage location.
|
Academic Article
|
Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study.
|
Academic Article
|
Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus.
|
Academic Article
|
MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus.
|
Academic Article
|
Heritability of carotid artery intima-medial thickness in type 2 diabetes.
|
Academic Article
|
Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus.
|
Academic Article
|
Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods.
|
Academic Article
|
Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster.
|
Academic Article
|
Pleiotropy and heterogeneity in the expression of atherogenic lipoproteins: the IRAS Family Study.
|
Academic Article
|
A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma.
|
Academic Article
|
Age-stratified QTL genome scan analyses for anthropometric measures.
|
Academic Article
|
Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study.
|
Academic Article
|
Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage.
|
Academic Article
|
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.
|
Academic Article
|
A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage.
|
Academic Article
|
A genome scan for diabetic nephropathy in African Americans.
|
Academic Article
|
A genome scan for ESRD in black families enriched for nondiabetic nephropathy.
|
Academic Article
|
A genome scan for all-cause end-stage renal disease in African Americans.
|
Academic Article
|
Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study.
|
Academic Article
|
Progress towards understanding the genetic pathogenesis of systemic lupus erythematosus.
|
Academic Article
|
Association of the mu-opioid receptor gene with type 2 diabetes mellitus in an African American population.
|
Academic Article
|
Multilocus and interaction-based genome scan for alcoholism risk factors in Caucasian Americans: the COGA study.
|
Academic Article
|
Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS).
|
Academic Article
|
Genome-wide linkage of plasma adiponectin reveals a major locus on chromosome 3q distinct from the adiponectin structural gene: the IRAS family study.
|
Academic Article
|
Coincident linkage of type 2 diabetes, metabolic syndrome, and measures of cardiovascular disease in a genome scan of the diabetes heart study.
|
Academic Article
|
Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations.
|
Academic Article
|
Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE.
|
Academic Article
|
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.
|
Academic Article
|
Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans.
|
Academic Article
|
Genetic variation in the CRP promoter: association with systemic lupus erythematosus.
|
Academic Article
|
Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy.
|
Academic Article
|
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
|
Academic Article
|
Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study.
|
Academic Article
|
Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study.
|
Academic Article
|
Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
|
Academic Article
|
Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study.
|
Academic Article
|
Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans.
|
Academic Article
|
Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes.
|
Academic Article
|
Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.
|
Academic Article
|
Genetic admixture: a tool to identify diabetic nephropathy genes in African Americans.
|
Academic Article
|
Genome-wide linkage scan in Gullah-speaking African American families with type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).
|
Academic Article
|
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.
|
Academic Article
|
INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study.
|
Academic Article
|
An algorithm for learning maximum entropy probability models of disease risk that efficiently searches and sparingly encodes multilocus genomic interactions.
|
Academic Article
|
Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.
|
Academic Article
|
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).
|
Academic Article
|
Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study.
|
Academic Article
|
Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
|
Academic Article
|
The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm.
|
Academic Article
|
Juvenile idiopathic arthritis and HLA class I and class II interactions and age-at-onset effects.
|
Academic Article
|
The acetyl-coenzyme A carboxylase beta (ACACB) gene is associated with nephropathy in Chinese patients with type 2 diabetes.
|
Academic Article
|
The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans.
|
Academic Article
|
Association of trypanolytic ApoL1 variants with kidney disease in African Americans.
|
Academic Article
|
Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.
|
Academic Article
|
The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1.
|
Academic Article
|
Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.
|
Academic Article
|
A genome-wide association study for diabetic nephropathy genes in African Americans.
|
Academic Article
|
Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study.
|
Academic Article
|
Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study.
|
Academic Article
|
Genetic mapping of vascular calcified plaque loci on chromosome 16p in European Americans from the diabetes heart study.
|
Academic Article
|
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.
|
Academic Article
|
Genetic analyses of interferon pathway-related genes reveal multiple new loci associated with systemic lupus erythematosus.
|
Academic Article
|
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups.
|
Academic Article
|
Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus.
|
Academic Article
|
Comparative analysis of methods for detecting interacting loci.
|
Academic Article
|
Differences in arachidonic acid levels and fatty acid desaturase (FADS) gene variants in African Americans and European Americans with diabetes or the metabolic syndrome.
|
Academic Article
|
Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study.
|
Academic Article
|
Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.
|
Academic Article
|
Preferential transmission of genetic risk variants of candidate loci at 6p21 from asymptomatic grandparents to mothers of children with neonatal lupus.
|
Academic Article
|
Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus.
|
Academic Article
|
A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap.
|
Academic Article
|
A genome-wide association search for type 2 diabetes genes in African Americans.
|
Academic Article
|
Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans.
|
Academic Article
|
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study.
|
Academic Article
|
Variation in the ICAM1-ICAM4-ICAM5 locus is associated with systemic lupus erythematosus susceptibility in multiple ancestries.
|
Academic Article
|
Association of APOL1 variants with mild kidney disease in the first-degree relatives of African American patients with non-diabetic end-stage renal disease.
|
Academic Article
|
Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus.
|
Academic Article
|
Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups.
|
Academic Article
|
Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage.
|
Academic Article
|
Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.
|
Academic Article
|
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans.
|
Academic Article
|
Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study.
|
Academic Article
|
Genetic analysis of haptoglobin polymorphisms with cardiovascular disease and type 2 diabetes in the Diabetes Heart Study.
|
Concept
|
Body Weights and Measures
|
Concept
|
Sequence Analysis, RNA
|
Concept
|
Radiotherapy
|
Concept
|
Tissue Embedding
|
Concept
|
Genetic Diseases, Inborn
|
Concept
|
Neurosurgical Procedures
|
Concept
|
Glucose Tolerance Test
|
Concept
|
Glucose Clamp Technique
|
Concept
|
Pain Measurement
|
Concept
|
Absorptiometry, Photon
|
Concept
|
Electrophoresis
|
Concept
|
Longitudinal Studies
|
Concept
|
Physical Therapy Modalities
|
Concept
|
Physical Chromosome Mapping
|
Concept
|
Epigenesis, Genetic
|
Concept
|
Respiration, Artificial
|
Concept
|
Reverse Transcriptase Polymerase Chain Reaction
|
Concept
|
Diffusion Magnetic Resonance Imaging
|
Concept
|
Models, Genetic
|
Concept
|
Tomography, Spiral Computed
|
Concept
|
Electrophoretic Mobility Shift Assay
|
Concept
|
Polymorphism, Genetic
|
Concept
|
Research Design
|
Concept
|
Genetic Testing
|
Concept
|
Antibodies, Antinuclear
|
Concept
|
Interviews as Topic
|
Concept
|
Physical Examination
|
Concept
|
Epidemiologic Studies
|
Concept
|
Demography
|
Concept
|
Family
|
Concept
|
Cohort Studies
|
Concept
|
Databases, Genetic
|
Concept
|
Skin Tests
|
Concept
|
Blotting, Western
|
Concept
|
Radiography
|
Concept
|
Guideline Adherence
|
Concept
|
Tissue and Organ Procurement
|
Concept
|
Renal Dialysis
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Behavioral Risk Factor Surveillance System
|
Concept
|
Genetics, Medical
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Genetic Loci
|
Concept
|
Biopsy
|
Concept
|
Family Characteristics
|
Concept
|
Leukocyte Count
|
Concept
|
Logistic Models
|
Concept
|
Preventive Health Services
|
Concept
|
Radioimmunoassay
|
Concept
|
Genetic Markers
|
Concept
|
Clinical Trials as Topic
|
Concept
|
Genetic Variation
|
Concept
|
Transcription, Genetic
|
Concept
|
Chromatography, High Pressure Liquid
|
Concept
|
Hormone Replacement Therapy
|
Concept
|
Mutagenesis, Insertional
|
Concept
|
Ultrafiltration
|
Concept
|
Multicenter Studies as Topic
|
Concept
|
Kidney Function Tests
|
Concept
|
Genetic Heterogeneity
|
Concept
|
Glomerular Filtration Rate
|
Concept
|
DNA Mutational Analysis
|
Concept
|
Biomedical Research
|
Concept
|
Donor Selection
|
Concept
|
Gene Expression Profiling
|
Concept
|
Enzyme-Linked Immunosorbent Assay
|
Concept
|
Resuscitation Orders
|
Concept
|
Anesthesia
|
Concept
|
Genetic Load
|
Concept
|
Prognosis
|
Concept
|
Sequence Analysis, DNA
|
Concept
|
Patient Selection
|
Concept
|
Kidney Transplantation
|
Concept
|
Imaging, Three-Dimensional
|
Concept
|
Post-Exposure Prophylaxis
|
Concept
|
Genetic Association Studies
|
Concept
|
Tracheostomy
|
Concept
|
Fasting
|
Concept
|
Radiography, Abdominal
|
Concept
|
Anthropometry
|
Concept
|
Epistasis, Genetic
|
Concept
|
Magnetic Resonance Imaging
|
Concept
|
Metabolic Clearance Rate
|
Concept
|
Fluorescent Antibody Technique
|
Concept
|
Genetics, Population
|
Concept
|
Selection, Genetic
|
Concept
|
Validation Studies as Topic
|
Concept
|
Case-Control Studies
|
Concept
|
Palliative Care
|
Concept
|
Prospective Studies
|
Concept
|
Cross-Sectional Studies
|
Concept
|
Chromosome Mapping
|
Concept
|
Randomized Controlled Trials as Topic
|
Concept
|
Withholding Treatment
|
Concept
|
Genome-Wide Association Study
|
Concept
|
Tomography, X-Ray Computed
|
Concept
|
Emergency Medical Services
|
Concept
|
Models, Theoretical
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
Concept
|
Polymerase Chain Reaction
|
Concept
|
Blood Pressure Determination
|
Concept
|
Neuropsychological Tests
|
Concept
|
Ultrasonography
|
Concept
|
Risk Assessment
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Recombination, Genetic
|
Concept
|
Follow-Up Studies
|
Concept
|
Autopsy
|
Concept
|
Gene Knockdown Techniques
|
Concept
|
Ventriculostomy
|
Concept
|
Cardiac-Gated Imaging Techniques
|
Concept
|
Electrocardiography
|
Concept
|
Mendelian Randomization Analysis
|
Concept
|
Platelet Transfusion
|
Academic Article
|
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
|
Academic Article
|
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.
|
Academic Article
|
Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study.
|
Academic Article
|
Impact of HDL genetic risk scores on coronary artery calcified plaque and mortality in individuals with type 2 diabetes from the Diabetes Heart Study.
|
Academic Article
|
Variable association of reactive intermediate genes with systemic lupus erythematosus in populations with different African ancestry.
|
Academic Article
|
Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4.
|
Academic Article
|
PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.
|
Academic Article
|
Characterization of European ancestry nonalcoholic fatty liver disease-associated variants in individuals of African and Hispanic descent.
|
Academic Article
|
Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression.
|
Academic Article
|
ABIN1 dysfunction as a genetic basis for lupus nephritis.
|
Academic Article
|
JC polyoma virus interacts with APOL1 in African Americans with nondiabetic nephropathy.
|
Academic Article
|
Genetic variants in selenoprotein P plasma 1 gene (SEPP1) are associated with fasting insulin and first phase insulin response in Hispanics.
|
Academic Article
|
Genetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans.
|
Academic Article
|
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.
|
Academic Article
|
Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk.
|
Academic Article
|
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.
|
Academic Article
|
Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans.
|
Academic Article
|
Testing gene-environment interactions in family-based association studies using trait-based ascertained samples.
|
Academic Article
|
Gene-gene interactions in APOL1-associated nephropathy.
|
Academic Article
|
A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND).
|
Academic Article
|
Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans.
|
Academic Article
|
End-stage renal disease in African Americans with lupus nephritis is associated with APOL1.
|
Academic Article
|
Evaluation of candidate nephropathy susceptibility genes in a genome-wide association study of African American diabetic kidney disease.
|
Academic Article
|
Genetic risk score associations with cardiovascular disease and mortality in the Diabetes Heart Study.
|
Academic Article
|
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
|
Academic Article
|
Heritability and genetic association analysis of cognition in theĀ Diabetes Heart Study.
|
Academic Article
|
Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.
|
Academic Article
|
Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.
|
Academic Article
|
Lupus nephritis susceptibility loci in women with systemic lupus erythematosus.
|
Academic Article
|
Coding variants in nephrin (NPHS1) and susceptibility to nephropathy in African Americans.
|
Academic Article
|
The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease.
|
Academic Article
|
Apolipoprotein L1 gene variants associate with prevalent kidney but not prevalent cardiovascular disease in the Systolic Blood Pressure Intervention Trial.
|
Academic Article
|
The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share.
|
Academic Article
|
A comparison of type 2 diabetes risk allele load between African Americans and European Americans.
|
Academic Article
|
Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels.
|
Academic Article
|
Heritability and genetic association analysis of neuroimaging measures in the Diabetes Heart Study.
|
Academic Article
|
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.
|
Academic Article
|
Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.
|
Academic Article
|
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.
|
Academic Article
|
Analysis of a cardiovascular disease genetic risk score in the Diabetes Heart Study.
|
Academic Article
|
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.
|
Academic Article
|
Rare Coding Variation and Risk of Intracerebral Hemorrhage.
|
Academic Article
|
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).
|
Academic Article
|
Deceased donor multidrug resistance protein 1 and caveolin 1 gene variants may influence allograft survival in kidney transplantation.
|
Academic Article
|
Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression.
|
Academic Article
|
Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
|
Academic Article
|
Genetics of autoimmune diseases: insights from population genetics.
|
Academic Article
|
Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus.
|
Academic Article
|
A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS).
|
Academic Article
|
Genomic Insights into the Ancestry and Demographic History of South America.
|
Academic Article
|
Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA.
|
Academic Article
|
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.
|
Academic Article
|
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.
|
Academic Article
|
Tissue-Specific and Genetic Regulation of Insulin Sensitivity-Associated Transcripts in African Americans.
|
Academic Article
|
Genetic analysis of advanced glycation end products in the DHS MIND study.
|
Academic Article
|
Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans.
|
Academic Article
|
Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).
|
Academic Article
|
Admixture mapping of serum vitamin D and parathyroid hormone concentrations in the African American-Diabetes Heart Study.
|
Academic Article
|
Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia.
|
Academic Article
|
Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium.
|
Academic Article
|
Trans-ethnic Meta-analysis and Functional Annotation Illuminates theĀ Genetic Architecture of Fasting Glucose and Insulin.
|
Academic Article
|
Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity.
|
Academic Article
|
Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production.
|
Academic Article
|
Genetic variants in CETP increase risk of intracerebral hemorrhage.
|
Academic Article
|
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
|
Academic Article
|
Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study.
|
Academic Article
|
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.
|
Academic Article
|
Genetic variation at 16q24.2 is associated with small vessel stroke.
|
Academic Article
|
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
|
Academic Article
|
Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans.
|
Academic Article
|
Rare and low-frequency coding variants alter human adult height.
|
Grant
|
Genetic Architecture of Obesity and Inflammation in Hispanic Americans
|
Grant
|
Genetics of Juvenile Idiopathic Arthritis and Subtypes
|
Grant
|
Exome Sequencing to Identify CVD Risk Variants in Hispanics & African Americans
|
Academic Article
|
Genetic epidemiology in kidney disease.
|
Academic Article
|
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
|
Academic Article
|
A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study.
|
Academic Article
|
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy.
|
Academic Article
|
Integrative Approaches to Understanding the Pathogenic Role of Genetic Variation in Rheumatic Diseases.
|
Academic Article
|
Aggressiveness of care following intracerebral hemorrhage in women and men.
|
Academic Article
|
Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci.
|
Academic Article
|
CYP2C19*2 and CYP2C19*17 variants and effect of tamoxifen on breast cancer recurrence: Analysis of the International Tamoxifen Pharmacogenomics Consortium dataset.
|
Academic Article
|
Genetic regulation of adipose tissue transcript expression is involved in modulating serum triglyceride and HDL-cholesterol.
|
Grant
|
Genetics and the Microbiome in Anti-Ro Preclinical and Established Autoimmunity
|
Academic Article
|
Transancestral mapping and genetic load in systemic lupus erythematosus.
|
Academic Article
|
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke.
|
Academic Article
|
Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos.
|
Academic Article
|
Early-life environmental exposures interact with genetic susceptibility variants in pediatric patients with eosinophilic esophagitis.
|
Academic Article
|
Association of Natural Killer Cell Ligand Polymorphism HLA-C Asn80Lys With the Development of Anti-SSA/Ro-Associated Congenital Heart Block.
|
Academic Article
|
Comparison of Genetic and Self-Identified Ancestry in Modeling Intracerebral Hemorrhage Risk.
|
Academic Article
|
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.
|
Academic Article
|
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations.
|
Academic Article
|
Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).
|
Academic Article
|
Racial/ethnic variation of APOE alleles for lobar intracerebral hemorrhage.
|
Academic Article
|
A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus.
|
Academic Article
|
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.
|
Academic Article
|
Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks.
|
Academic Article
|
Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans.
|
Academic Article
|
Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis.
|
Academic Article
|
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
Academic Article
|
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
|
Academic Article
|
Genetic Architecture of Primary Open-Angle Glaucoma in Individuals of African Descent: The African Descent and Glaucoma Evaluation Study III.
|
Academic Article
|
Genetic Regulation of Enoyl-CoA Hydratase Domain-Containing 3 in Adipose Tissue Determines Insulin Sensitivity in African Americans and Europeans.
|
Academic Article
|
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
Academic Article
|
Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.
|
Academic Article
|
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
|
Academic Article
|
APOL1 Kidney Risk Variants and Cardiovascular Disease: An Individual Participant Data Meta-Analysis.
|
Academic Article
|
Novel genetic associations with interferon in systemic lupus erythematosus identified by replication and fine-mapping of trait-stratified genome-wide screen.
|
Academic Article
|
Genetic influences on susceptibility to rheumatoid arthritis in African-Americans.
|
Academic Article
|
Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity: A Meta-analysis.
|
Academic Article
|
Latent autoimmunity across disease-specific boundaries in at-risk first-degree relatives of SLE and RA patients.
|
Academic Article
|
Subtype Specificity of Genetic Loci Associated With Stroke in 16?664 Cases and 32?792 Controls.
|
Academic Article
|
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
|
Academic Article
|
Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study.
|
Academic Article
|
Integrative analysis of DNA methylation in discordant twins unveils distinct architectures of systemic sclerosis subsets.
|
Grant
|
Integrated Omics Analysis of Pain: Omics Data Generation Center
|