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2519. Urban vs Rural HIV-infected Persons Have Differential Gene Expression for Estrogen Signaling, Inflammation, and Cytokine Production Pathways

A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS).

artículo científico publicado en 2015

A Ground Truth Based Comparative Study on Detecting Epistatic SNPs

artículo científico publicado en 2009

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A comparison of risk factors for calcified atherosclerotic plaque in the coronary, carotid, and abdominal aortic arteries: the diabetes heart study

artículo científico publicado en 2007

A comparison of type 2 diabetes risk allele load between African Americans and European Americans.

artículo científico publicado en 2014

A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap

artículo científico publicado en 2011

A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus

artículo científico publicado en 2012

A functional polymorphism in the lymphotoxin-alpha gene is associated with carotid artery wall thickness: the Diabetes Heart Study

artículo científico publicado en 2006

A genome scan for ESRD in black families enriched for nondiabetic nephropathy

scientific article published on 01 October 2004

A genome scan for all-cause end-stage renal disease in African Americans

artículo científico publicado en 2005

A genome scan for diabetic nephropathy in African Americans

artículo científico publicado en 2004

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.

artículo científico publicado en 2005

A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).

artículo científico publicado en 2009

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A genome-wide association study for diabetic nephropathy genes in African Americans

artículo científico publicado en 2010

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

artículo científico publicado en 2007

A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study

artículo científico publicado en 2017

A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage

scientific article published on 01 September 2004

A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q.

artículo científico publicado en 2004

A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma

artículo científico publicado el 25 de octubre de 2003

A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2013

A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity

scientific article published on 01 January 2006

A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans

artículo científico publicado en 2007

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

artículo científico publicado en 2013

A molecular biomarker for prediction of clinical outcome in children with ASD, constipation, and intestinal inflammation

artículo científico publicado en 2019

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy

artículo científico publicado en 2017

A pilot study assessing the impact of rs174537 on circulating PUFAs and the inflammatory response in TBI patients

artículo científico publicado en 2020

A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus

scholarly article by Zubin Patel published in April 2018

A polymorphism within IL21R confers risk for systemic lupus erythematosus

scientific article published on August 2009

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

artículo científico publicado en 2004

ABIN1 dysfunction as a genetic basis for lupus nephritis

artículo científico publicado en 2013

APOL1 Genotype and Kidney Transplantation Outcomes From Deceased African American Donors

artículo científico publicado en 2015

APOL1 Kidney Risk Variants and Cardiovascular Disease: An Individual Participant Data Meta-Analysis

scientific article published on 05 August 2019

APOL1 Kidney-Risk Variants Induce Mitochondrial Fission

artículo científico publicado en 2020

APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO): Design and Rationale

scientific article published on 13 December 2019

APOL1 Renal-Risk Variants Induce Mitochondrial Dysfunction

artículo científico publicado en 2016

APOL1 associations with nephropathy, atherosclerosis, and all-cause mortality in African Americans with type 2 diabetes

artículo científico publicado en 2014

APOL1 renal-risk genotypes associate with longer hemodialysis survival in prevalent nondiabetic African American patients with end-stage renal disease

artículo científico publicado en 2016

APOL1 renal-risk variants associate with reduced cerebral white matter lesion volume and increased gray matter volume

artículo científico publicado en 2016

Adiponectin as a novel determinant of bone mineral density and visceral fat.

artículo científico publicado en 2003

Adipose Tissue Transferrin and Insulin Resistance

artículo científico publicado en 2018

Adipose tissue depot volume relationships with spinal trabecular bone mineral density in African Americans with diabetes

artículo científico publicado en 2018

Adiposity is inversely associated with hippocampal volume in African Americans and European Americans with diabetes

artículo científico publicado en 2016

Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus

artículo científico publicado en 2012

Admixture mapping of serum vitamin D and parathyroid hormone concentrations in the African American-Diabetes Heart Study

artículo científico publicado en 2016

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

artículo científico publicado en 2012

Age-stratified QTL genome scan analyses for anthropometric measures

artículo científico publicado en 2003

Age-stratified heritability estimation in the Framingham Heart Study families

artículo científico publicado en 2003

Aggressiveness of care following intracerebral hemorrhage in women and men.

artículo científico publicado en 2017

Albuminuria associates with calcified atherosclerotic plaque in African Americans with diabetes

artículo científico publicado en 2013

Alcohol use and risk of intracerebral hemorrhage

artículo científico publicado en 2017

Allele-specific methylation in the FADS genomic region in DNA from human saliva, CD4+ cells, and total leukocytes

artículo científico publicado en 2018

An Islet-Targeted Genome-Wide Association Scan Identifies Novel Genes Implicated in Cytokine-Mediated Islet Stress in Type 2 Diabetes

artículo científico publicado en 2015

An algorithm for learning maximum entropy probability models of disease risk that efficiently searches and sparingly encodes multilocus genomic interactions

artículo científico publicado en 2009

An exploration of sex-specific linkage disequilibrium on chromosome X in Caucasians from the COGA study

artículo científico publicado en 2005

Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study

artículo científico publicado en 2009

Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort

artículo científico publicado en 2010

Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries

artículo científico publicado en 2020

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study

artículo científico publicado en 2017

Analysis of a cardiovascular disease genetic risk score in the Diabetes Heart Study

artículo científico publicado en 2015

Analysis of advanced glycation end products in the DHS Mind Study

artículo científico publicado en 2015

Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus

artículo científico publicado en 2011

Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans

artículo científico publicado en 2010

Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans

artículo científico publicado en 2014

Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.

artículo científico publicado en 2014

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

artículo científico publicado en 2022

Apolipoprotein E, statins, and risk of intracerebral hemorrhage

artículo científico publicado en 2013

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

artículo científico publicado en 2013

Apolipoprotein L1 gene variants associate with prevalent kidney but not prevalent cardiovascular disease in the Systolic Blood Pressure Intervention Trial

artículo científico publicado en 2014

Apolipoprotein L1 gene variants in deceased organ donors are associated with renal allograft failure

artículo científico publicado en 2015

Apolipoprotein L1 nephropathy risk variants associate with HDL subfraction concentration in African Americans

artículo científico publicado el 19 de septiembre de 2011

Assessing the accuracy of neuromuscular ultrasound for inclusion body myositis

scientific article published on 17 February 2019

Assessment of the interaction of age and sex on 90-day outcome after intracerebral hemorrhage

artículo científico publicado en 2017

Association Between Inflammatory Biomarker C-Reactive Protein and Radiotherapy-Induced Early Adverse Skin Reactions in a Multiracial/Ethnic Breast Cancer Population

artículo científico publicado en 2018

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study

artículo científico publicado en 2017

Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies

artículo científico publicado en 2008

Association analysis of genes in the renin-angiotensin system with subclinical cardiovascular disease in families with Type 2 diabetes mellitus: The Diabetes Heart Study

article

Association analysis of the ephrin-B2 gene in African-Americans with end-stage renal disease

artículo científico publicado en 2008

Association analysis of the plasminogen activator inhibitor-1 4G/5G polymorphism in Hispanics and African Americans: the IRAS family study

artículo científico publicado en 2004

Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study

artículo científico publicado en 2012

Association methods in human genetics

artículo científico publicado en 2007

Association of 25-hydroxyvitamin D with blood pressure in predominantly 25-hydroxyvitamin D deficient Hispanic and African Americans

artículo científico publicado en 2009

Association of APOL1 variants with mild kidney disease in the first-degree relatives of African American patients with non-diabetic end-stage renal disease

artículo científico publicado en 2012

Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity: A Meta-analysis

artículo científico publicado en 2019

Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study

artículo científico publicado en 2008

Association of Natural Killer Cell Ligand Polymorphism HLA-C Asn80Lys With the Development of Anti-SSA/Ro-Associated Congenital Heart Block.

artículo científico publicado en 2017

Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study

artículo científico publicado el 13 de enero de 2011

Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups

artículo científico publicado en 2011

Association of SLCO1B1 *14 Allele with Poor Response to Methotrexate in Juvenile Idiopathic Arthritis Patients

scientific article published on 15 March 2019

Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study

artículo científico publicado en 2013

Association of SSTR2 polymorphisms and glucose homeostasis phenotypes: the Insulin Resistance Atherosclerosis Family Study

artículo científico publicado en 2009

Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans

artículo científico publicado en 2007

Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

artículo científico publicado en 2011

Association of adiponectin gene polymorphisms with type 2 diabetes in an African American population enriched for nephropathy

scientific article published on 03 December 2008

Association of adipose tissue deposition and beta-2 adrenergic receptor variants: the IRAS family study

artículo científico publicado en 2005

Association of an IL-1A 3'UTR polymorphism with end-stage renal disease and IL-1 alpha expression

artículo científico publicado en 2003

Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes

artículo científico publicado en 2008

Association of genes of lipid metabolism with measures of subclinical cardiovascular disease in the Diabetes Heart Study.

artículo científico publicado en 2005

Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility

artículo científico publicado en 2011

Association of plasma vitamin D levels with adiposity in Hispanic and African Americans

scientific article published on 23 June 2009

Association of polymorphisms in cyclooxygenase (COX)-2 with coronary and carotid calcium in the Diabetes Heart Study

artículo científico publicado en 2008

Association of polymorphisms in the klotho gene with severity of non-diabetic ESRD in African Americans

artículo científico publicado en 2010

Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study

artículo científico publicado en 2005

Association of protein tyrosine phosphatase 1B gene polymorphisms with measures of glucose homeostasis in Hispanic Americans: the insulin resistance atherosclerosis study (IRAS) family study

artículo científico publicado en 2004

Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes

artículo científico publicado en 2004

Association of protein tyrosine phosphatase-N1 polymorphisms with coronary calcified plaque in the Diabetes Heart Study.

artículo científico publicado en 2006

Association of the IL2RA/CD25 gene with juvenile idiopathic arthritis

artículo científico publicado en 2009

Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans

artículo científico publicado en 2008

Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy

artículo científico publicado en 2008

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

artículo científico publicado en 2007

Association of the mu-opioid receptor gene with type 2 diabetes mellitus in an African American population

artículo científico publicado en 2005

Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population

artículo científico publicado en 2007

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

artículo científico publicado en 2010

Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus

artículo científico publicado en 2012

Association of α2-Heremans-Schmid Glycoprotein Polymorphisms with Subclinical Atherosclerosis

artículo científico publicado en 2006

Author response: Ischemic Lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage

artículo científico publicado en 2017

Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension

artículo científico publicado en 2002

Bladder Capacity is a Biomarker for a Bladder Centric versus Systemic Manifestation in Interstitial Cystitis/Bladder Pain Syndrome

artículo científico publicado en 2017

Bladder Hydrodistention Does Not Result in a Significant Change in Bladder Capacity for Interstitial Cystitis/Bladder Pain Syndrome Patients

scientific article published on 09 July 2019

Bone Mineral Density and Progression of Subclinical Atherosclerosis in African-Americans With Type 2 Diabetes

artículo científico publicado en 2016

Bone morphogenetic protein 7 (BMP7) gene polymorphisms are associated with inverse relationships between vascular calcification and BMD: the Diabetes Heart Study

artículo científico publicado en 2009

Bootstrap aggregating of alternating decision trees to detect sets of SNPs that associate with disease

artículo científico publicado en 2012

Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis.

artículo científico publicado en 2018

Brief report: enrichment of associations in genes with fibrosis, apoptosis, and innate immunity functions with cardiac manifestations of neonatal lupus

artículo científico publicado en 2012

Bulk and Single-Cell Profiling of Breast Tumors Identifies TREM-1 as a Dominant Immune Suppressive Marker Associated With Poor Outcomes

artículo científico publicado en 2021

Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage

artículo científico publicado en 2012

Calcified atherosclerotic plaque and bone mineral density in type 2 diabetes: the diabetes heart study

artículo científico publicado en 2007

Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Cardioembolic Stroke Risk and Recovery After Anticoagulation-Related Intracerebral Hemorrhage

artículo científico publicado en 2018

Characterization of European ancestry nonalcoholic fatty liver disease-associated variants in individuals of African and Hispanic descent

artículo científico publicado en 2013

Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes

artículo científico publicado en 2013

Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy

artículo científico publicado en 2010

Clinician judgment vs formal scales for predicting intracerebral hemorrhage outcomes

artículo científico publicado en 2015

Coding variants in nephrin (NPHS1) and susceptibility to nephropathy in African Americans

artículo científico publicado en 2014

Coincident Linkage of Type 2 Diabetes, Metabolic Syndrome, and Measures of Cardiovascular Disease in a Genome Scan of the Diabetes Heart Study

scientific article published on 01 July 2006

Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants

artículo científico publicado el 13 de noviembre de 2010

Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms

artículo científico publicado en 2020

Combining Imaging and Genetics to Predict Recurrence of Anticoagulation-Associated Intracerebral Hemorrhage

artículo científico publicado en 2020

Common Variants in the Periostin Gene Influence Development of Atherosclerosis in Young Persons

artículo científico publicado el 7 de abril de 2011

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

artículo científico publicado en 2015

Comparative analyses of single-nucleotide polymorphisms in the TNF promoter region provide further validation for the vervet monkey model of obesity

artículo científico publicado en 2009

Comparative analysis of methods for detecting interacting loci

artículo científico publicado el 5 de julio de 2011

Comparison of Genetic and Self-Identified Ancestry in Modeling Intracerebral Hemorrhage Risk

scientific article published on 06 July 2018

Complement factor H gene associations with end-stage kidney disease in African Americans.

artículo científico publicado en 2014

Complement genes contribute sex-biased vulnerability in diverse disorders

scientific article published on 11 May 2020

Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing

artículo científico publicado en 2009

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

artículo científico publicado en 2008

Correlates of coronary artery calcified plaque in blacks and whites with type 2 diabetes

artículo científico publicado en 2011

Deceased donor multidrug resistance protein 1 and caveolin 1 gene variants may influence allograft survival in kidney transplantation

artículo científico publicado en 2015

Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production

artículo científico publicado en 2016

Dense Genotyping of Immune-Related Regions Identifies Loci for Rheumatoid Arthritis Risk and Damage in African Americans

artículo científico publicado en 2017

Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.

artículo científico publicado en 2013

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

artículo científico publicado en 2010

Differences in arachidonic acid levels and fatty acid desaturase (FADS) gene variants in African Americans and European Americans with diabetes or the metabolic syndrome

artículo científico publicado en 2011

Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans

artículo científico publicado en 2011

Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production

artículo científico publicado en 2011

Early-life environmental exposures interact with genetic susceptibility variants in pediatric patients with eosinophilic esophagitis

artículo científico publicado en 2017

Effect of a Single Apolipoprotein L1 Gene Nephropathy Variant on the Risk of Advanced Lupus Nephritis in Brazilians

scientific article published on 15 November 2019

Effects of Intensive Systolic Blood Pressure Control on All-Cause Hospitalizations

artículo científico publicado en 2020

Effects of weight-based ultrafiltration rate limits on intradialytic hypotension in hemodialysis

artículo científico publicado en 2017

Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels

artículo científico publicado en 2014

End-stage renal disease in African Americans with lupus nephritis is associated with APOL1

scientific article published on February 2014

Epigenetic methylation in Eosinophilic Esophagitis: Molecular aging and novel biomarkers for treatment response

artículo científico publicado en 2020

Erratum: Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing

article

Erratum: Genetic associations of LYN with systemic lupus erythematosus

article

Estimating the Contributions of Rare and Common Genetic Variations and Clinical Measures to a Model Trait: Adiponectin

artículo científico publicado el 2 de octubre de 2012

Ethnic differences in the relationship between albuminuria and calcified atherosclerotic plaque: the African American-diabetes heart study

artículo científico publicado en 2009

Ethnic differences in the relationship between pericardial adipose tissue and coronary artery calcified plaque: African-American-diabetes heart study

artículo científico publicado en 2010

European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus

artículo científico publicado en 2009

Evaluation of C1q genomic region in minority racial groups of lupus

artículo científico publicado en 2009

Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study

artículo científico publicado en 2009

Evaluation of TRAF6 in a large multiancestral lupus cohort

artículo científico publicado en 2012

Evaluation of candidate nephropathy susceptibility genes in a genome-wide association study of African American diabetic kidney disease

artículo científico publicado en 2014

Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort

artículo científico publicado en 2011

Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosus

artículo científico publicado en 2012

Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).

artículo científico publicado en 2018

Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease

artículo científico publicado en 2008

Exploring differences in adiposity in two U.S. Hispanic populations of Mexican origin using social, behavioral, physiologic and genetic markers: the IRAS Family Study

artículo científico publicado en 2012

Exploring pleiotropy using principal components

artículo científico publicado en 2003

Exposure of the Bone Marrow Microenvironment to Simulated Solar and Galactic Cosmic Radiation Induces Biological Bystander Effects on Human Hematopoiesis.

artículo científico publicado en 2018

FGF23 Concentration and APOL1 Genotype Are Novel Predictors of Mortality in African Americans With Type 2 Diabetes.

artículo científico publicado en 2017

Factors Considered by Clinicians when Prognosticating Intracerebral Hemorrhage Outcomes

artículo científico publicado en 2017

Familial aggregation and linkage analysis of autoantibody traits in pedigrees multiplex for systemic lupus erythematosus

article

Familial aggregation of coronary artery calcium in families with type 2 diabetes

artículo científico publicado en 2001

Familial autoimmunity in the Childhood Arthritis and Rheumatology Research Alliance registry.

artículo científico publicado en 2016

FcalphaRI (CD89) alleles determine the proinflammatory potential of serum IgA.

artículo científico publicado en 2007

Features associated with, and the impact of, hemolytic anemia in patients with systemic lupus erythematosus: LX, results from a multiethnic cohort

artículo científico publicado en 2008

Fine mapping chromosome 16q12 in a collection of 231 systemic lupus erythematosus sibpair and multiplex families.

artículo científico publicado en 2005

Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups

artículo científico publicado en 2012

Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21

artículo científico publicado en 2011

Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12.

artículo científico publicado en 2006

Fine-mapping the MHC locus in juvenile idiopathic arthritis (JIA) reveals genetic heterogeneity corresponding to distinct adult inflammatory arthritic diseases

artículo científico publicado en 2016

Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2.

artículo científico publicado en 2000

Further evidence supporting a potential role for ADH1B in obesity

artículo científico

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

artículo científico publicado en 2018

GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region

scientific journal article

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020

Gene-gene interactions in APOL1-associated nephropathy

artículo científico publicado en 2013

Genetic Architecture of Primary Open Angle Glaucoma in Individuals of African Descent: The African Descent & Glaucoma Evaluation Study (ADAGES) III

article

Genetic Association Mapping Based on Discordant Sib Pairs: The Discordant-Alleles Test

artículo científico publicado el 1 de abril de 1998

Genetic Regulation of enoyl-CoA hydratase Domain-Containing 3 in Adipose Tissue Determines Insulin Sensitivity in African Americans and Europeans

artículo científico publicado en 2019

Genetic Risk Assessment of Type 2 Diabetes–Associated Polymorphisms in African Americans

artículo científico publicado el 1 de febrero de 2012

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

artículo científico publicado en 2014

Genetic Variation in the Peroxisome Proliferator Activated Receptor-Gamma Gene Is Associated with Histologically Advanced NAFLD

artículo científico publicado el 9 de diciembre de 2011

Genetic admixture: a tool to identify diabetic nephropathy genes in African Americans.

artículo científico publicado en 2008

Genetic analyses of interferon pathway-related genes reveal multiple new loci associated with systemic lupus erythematosus

artículo científico publicado en 2011

Genetic analysis of HNF4A polymorphisms in Caucasian-American type 2 diabetes

artículo científico publicado en 2005

Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study.

artículo científico publicado en 2005

Genetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans

artículo científico publicado en 2013

Genetic analysis of advanced glycation end products in the DHS MIND study.

artículo científico publicado en 2016

Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping

artículo científico publicado en 2009

Genetic analysis of haptoglobin polymorphisms with cardiovascular disease and type 2 diabetes in the Diabetes Heart Study

artículo científico publicado en 2013

Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.

artículo científico publicado en 2014

Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study

artículo científico publicado en 2008

Genetic ancestry, serum interferon-α activity, and autoantibodies in systemic lupus erythematosus

artículo científico publicado en 2012

Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans

artículo científico publicado en 2008

Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications

article

Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos

artículo científico publicado en 2017

Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy

artículo científico publicado en 2011

Genetic association of CD247 (CD3ζ) with SLE in a large-scale multiethnic study.

artículo científico publicado en 2015

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

artículo científico publicado en 2004

Genetic associations of LYN with systemic lupus erythematosus

artículo científico publicado en 2009

Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus

artículo científico publicado en 2015

Genetic epidemiology in kidney disease

artículo científico publicado en 2017

Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods

artículo científico publicado en 2003

Genetic epidemiology of subclinical cardiovascular disease in the diabetes heart study

artículo científico publicado en 2008

Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis

artículo científico publicado en 2010

Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans

scholarly article by Ken B Hanscombe published in November 2018

Genetic influences on susceptibility to rheumatoid arthritis in African-Americans

scientific article published on 01 March 2019

Genetic linkage and association of Fc? receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus

article

Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus

artículo científico publicado en 2001

Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study

artículo científico publicado en 2006

Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study

artículo científico publicado en 2006

Genetic mapping of vascular calcified plaque loci on chromosome 16p in European Americans from the diabetes heart study.

artículo científico publicado en 2011

Genetic regulation of adipose tissue transcript expression is involved in modulating serum triglyceride and HDL-cholesterol

artículo científico

Genetic risk score associations with cardiovascular disease and mortality in the Diabetes Heart Study

artículo científico publicado en 2014

Genetic susceptibility contributes to renal and cardiovascular complications of type 2 diabetes mellitus

artículo científico publicado en 2006

Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies

scientific article published on May 2009

Genetic variants in CETP increase risk of intracerebral hemorrhage

artículo científico publicado en 2016

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variants in selenoprotein P plasma 1 gene (SEPP1) are associated with fasting insulin and first phase insulin response in Hispanics

artículo científico publicado en 2014

Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke

artículo científico publicado en 2017

Genetic variation at 16q24.2 is associated with small vessel stroke

artículo científico publicado en 2016

Genetic variation in the CRP promoter: association with systemic lupus erythematosus

artículo científico publicado en 2008

Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage

scientific article published on 11 April 2020

Genetics of autoimmune diseases: insights from population genetics

artículo científico publicado en 2015

Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA)

scientific article published on 01 May 2004

Genome screen in familial intracranial aneurysm

Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci

artículo científico publicado en 2017

Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium

scientific article published on 20 June 2019

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

artículo científico publicado en 2020

Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture

artículo científico publicado en 2015

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

artículo científico publicado en 2015

Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study

artículo científico publicado en 2016

Genome-Wide Linkage of Plasma Adiponectin Reveals a Major Locus on Chromosome 3q Distinct From the Adiponectin Structural Gene: The IRAS Family Study

article

Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans

artículo científico publicado en 2017

Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13

scientific journal article

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

artículo científico publicado en 2019

Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes

artículo científico publicado en 2011

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

artículo científico publicado en 2008

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

artículo científico publicado en 2018

Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study

artículo científico publicado en 2009

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

Genome-wide association study of cerebral small vessel disease reveals established and novel loci

artículo científico publicado en 2019

Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes

artículo científico publicado en 2017

Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk

artículo científico publicado en 2012

Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study

artículo científico publicado en 2010

Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study

artículo científico publicado en 2019

Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk

artículo científico publicado en 2014

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

scientific journal article

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

artículo científico publicado en 2016

Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans

artículo científico publicado en 2016

Genome-wide linkage scan in Gullah-speaking African American families with type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).

artículo científico publicado en 2008

Genome-wide linkage scans for renal function and albuminuria in Type 2 diabetes mellitus: the Diabetes Heart Study

artículo científico publicado en 2008

Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study

artículo científico publicado en 2011

Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma

artículo científico publicado en 2001

Genome‐Wide Association of BMI in African Americans

artículo científico publicado el 23 de junio de 2011

Genomic Insights into the Ancestry and Demographic History of South America

artículo científico publicado en 2015

Genomics in Rheumatic Diseases: Hope for the Future

artículo científico publicado en 2017

HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis

artículo científico publicado en 2015

Heritability and expression of C-reactive protein in type 2 diabetes in the Diabetes Heart Study

artículo científico publicado en 2006

Heritability and genetic association analysis of cognition in the Diabetes Heart Study

artículo científico publicado en 2014

Heritability and genetic association analysis of neuroimaging measures in the Diabetes Heart Study

artículo científico publicado en 2014

Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus

artículo científico publicado en 2004

Heritability of body composition measured by DXA in the diabetes heart study.

artículo científico publicado en 2005

Heritability of carotid artery intima-medial thickness in type 2 diabetes

artículo científico publicado en 2002

Heritability of spinal trabecular volumetric bone mineral density measured by QCT in the Diabetes Heart Study

artículo científico publicado en 2004

Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1.

artículo científico publicado en 2008

Hierarchicell: an R-package for estimating power for tests of differential expression with single-cell data

artículo científico publicado en 2021

High-density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups

artículo científico publicado en 2009

Hormone replacement therapy is associated with increased C-reactive protein in women with Type 2 diabetes in the Diabetes Heart Study.

artículo científico publicado en 2006

Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study

artículo científico publicado en 2010

Hypertension and intracerebral hemorrhage recurrence among white, black, and Hispanic individuals

article

IL-6 trans-signaling increases expression of airways disease genes in airway smooth muscle

artículo científico publicado en 2015

IL6 receptor358Ala variant and trans-signaling are disease modifiers in amyotrophic lateral sclerosis

artículo científico publicado en 2019

INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study

artículo científico publicado en 2009

Identification and Validation of Hematoma Volume Cutoffs in Spontaneous, Supratentorial Deep Intracerebral Hemorrhage

scientific article published on 26 June 2019

Identification of ATPAF1 as a novel candidate gene for asthma in children

artículo científico publicado en 2011

Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease

artículo científico publicado en 2009

Identification of IRAK1 as a risk gene with critical role in the pathogenesis of systemic lupus erythematosus

scholarly article

Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study

artículo científico publicado en 2012

Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans

artículo científico publicado en 2015

Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study

artículo científico publicado en 2010

Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus

artículo científico publicado en 2010

Identification of new SLE-associated genes with a two-step Bayesian study design.

artículo científico publicado en 2009

Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study

artículo científico publicado en 2011

Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study

artículo científico publicado en 2004

Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder

artículo científico publicado el 9 de junio de 2012

Impact of HDL genetic risk scores on coronary artery calcified plaque and mortality in individuals with type 2 diabetes from the Diabetes Heart Study.

artículo científico publicado en 2013

Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations

artículo científico publicado en 2012

Impact of rs174537 on Critically Ill Patients with Acute Lung Injury: A Secondary Analysis of the OMEGA Randomized Clinical Trial

artículo científico publicado en 2020

Implication of European-derived adiposity loci in African Americans

artículo científico publicado el 12 de julio de 2011

Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium

artículo científico publicado en 2016

In vitro and in vivo assessment of direct effects of simulated solar and galactic cosmic radiation on human hematopoietic stem/progenitor cells

artículo científico publicado en 2016

Incontinence and gait disturbance after intraventricular extension of intracerebral hemorrhage

artículo científico publicado en 2016

Infection after intracerebral hemorrhage: risk factors and association with outcomes in the ethnic/racial variations of intracerebral hemorrhage study

artículo científico publicado en 2014

Informed conditioning on clinical covariates increases power in case-control association studies

artículo científico publicado en 2012

Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans

artículo científico publicado en 2014

Insulin sensitivity, insulin secretion, and abdominal fat: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study

artículo científico publicado en 2003

Integrative Analysis of Glucometabolic Traits, Adipose Tissue DNA Methylation and Gene Expression Identifies Epigenetic Regulatory Mechanisms of Insulin Resistance and Obesity in African Americans

scientific article published on 14 September 2020

Integrative Approaches to Understanding the Pathogenic Role of Genetic Variation in Rheumatic Diseases

artículo científico publicado en 2017

Integrative Genetics Analysis of Juvenile Idiopathic Arthritis Identifies Novel Loci

Integrative analysis of DNA methylation in discordant twins unveils distinct architectures of systemic sclerosis subsets

artículo científico publicado en 2019

Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage

artículo científico publicado en 2004

Interferon regulatory factor-5 is genetically associated with systemic lupus erythematosus in African Americans

article

Intrinsic DNA topology as a prioritization metric in genomic fine-mapping studies

artículo científico publicado en 2020

Investigation of rheumatoid arthritis susceptibility loci in juvenile idiopathic arthritis confirms high degree of overlap

artículo científico publicado en 2012

Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations

scientific article published on 01 March 2007

Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report

artículo científico publicado en 2010

Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage

artículo científico publicado en 2017

JC Viruria Is Associated With Reduced Risk of Diabetic Kidney Disease

JC polyoma viruria associates with protection from chronic kidney disease independently from apolipoprotein L1 genotype in African Americans

artículo científico publicado en 2018

JC polyoma virus interacts with APOL1 in African Americans with nondiabetic nephropathy

artículo científico publicado el 15 de mayo de 2013

Juvenile idiopathic arthritis and HLA class I and class II interactions and age-at-onset effects

artículo científico publicado en 2010

Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD

artículo científico publicado en 2014

Latent autoimmunity across disease-specific boundaries in at-risk first-degree relatives of SLE and RA patients

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

artículo científico publicado el 3 de julio de 2012

Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study

artículo científico publicado en 2004

Loci contributing to adult height and body mass index in African American families ascertained for type 2 diabetes

artículo científico publicado en 2005

Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression

artículo científico publicado en 2015

Lupus nephritis susceptibility loci in women with systemic lupus erythematosus

artículo científico publicado en 2014

Lupus risk variants in the PXK locus alter B-cell receptor internalization

artículo científico publicado en 2014

Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase

artículo científico publicado en 2011

MHC associations with clinical and autoantibody manifestations in European SLE.

artículo científico publicado en 2014

Mapping Genes for NIDDM: Design of the Finland—United States Investigation of NIDDM Genetics (FUSION) Study

artículo científico publicado el 1 de junio de 1998

Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity

artículo científico publicado en 2016

Measurement of Trabecular Bone Mineral Density in the Thoracic Spine Using Cardiac Gated Quantitative Computed Tomography

artículo científico publicado en 2004

Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans

artículo científico publicado en 2015

Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage

artículo científico publicado en 2014

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

artículo científico publicado en 2014

Meta-analysis of genome-wide linkage scans for renal function traits

artículo científico publicado en 2011

Metabolomics Identifies Distinctive Metabolite Signatures for Measures of Glucose Homeostasis: The Insulin Resistance Atherosclerosis Family Study (IRAS-FS).

artículo científico publicado en 2018

MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus

artículo científico publicado en 2013

MicroRNA-3148 modulates differential gene expression of the SLE-associated TLR7 variant.

artículo científico publicado en 2012

Minority Patients are Less Likely to Undergo Withdrawal of Care After Spontaneous Intracerebral Hemorrhage

artículo científico publicado en 2018

Mo-P2:196 A genome scan for subclinical cardiovascular disease in the diabetes heart study

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

artículo científico publicado el 5 de agosto de 2010

Monocyte Count and 30-Day Case Fatality in Intracerebral Hemorrhage.

artículo científico publicado en 2015

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

artículo científico publicado en 2019

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2018

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

artículo científico publicado en 2016

Multilocus and interaction-based genome scan for alcoholism risk factors in Caucasian Americans: the COGA study

artículo científico publicado en 2005

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

artículo científico publicado en 2022

Mutational Landscapes of Smoking-Related Cancers in Caucasians and African Americans: Precision Oncology Perspectives at Wake Forest Baptist Comprehensive Cancer Center

artículo científico publicado en 2017

Nephropathy Progression in African Americans With a Family History of ESKD: Implications for Clinical Trials in APOL1-Associated Nephropathy

artículo científico publicado en 2019

Nephropathy in siblings of African Americans with overt type 2 diabetic nephropathy

artículo científico publicado en 2002

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

artículo científico publicado en 2009

Nonparametric linkage regression. II: Identification of influential pedigrees in tests for linkage

scientific article published on 01 January 2001

Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.

artículo científico publicado en 2016

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

Novel genetic associations with interferon in systemic lupus erythematosus identified by replication and fine-mapping of trait-stratified genome-wide screen

artículo científico publicado en 2019

Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster

scientific article published on 01 August 2003

Ordered subset analysis in genetic linkage mapping of complex traits

artículo científico publicado en 2004

P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study

artículo científico publicado en 2005

PReS-FINAL-2135: Analysis of the HLA region in a large cohort of juvenile idiopathic arthritis cases identifies independent effects at HLA-DRB1.

artículo científico publicado en 2013

PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes

artículo científico publicado en 2013

Pericardial and Visceral Adipose Tissues Measured Volumetrically With Computed Tomography Are Highly Associated in Type 2 Diabetic Families

artículo científico publicado en 2005

Peroxisome proliferator-activated receptor gamma 2 and acyl-CoA synthetase 5 polymorphisms influence diet response

artículo científico publicado en 2007

Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus

artículo científico publicado en 2011

Plasma Dickkopf1 (DKK1) concentrations negatively associate with atherosclerotic calcified plaque in African-Americans with type 2 diabetes

artículo científico publicado en 2012

Plasma FGF23 and Calcified Atherosclerotic Plaque in African Americans with Type 2 Diabetes Mellitus

artículo científico publicado en 2015

Plasma apoM and S1P levels are inversely associated with mortality in African Americans with type 2 diabetes mellitus

artículo científico publicado en 2019

Platelet glycoprotein Ib alpha chain as a putative therapeutic target for juvenile idiopathic arthritis: a Mendelian randomization study

artículo científico publicado en 2020

Pleiotropy and heterogeneity in the expression of atherogenic lipoproteins: the IRAS Family Study

artículo científico publicado en 2003

Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans

artículo científico publicado en 2011

Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study.

artículo científico publicado en 2012

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

scientific article published on 28 January 2009

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study

artículo científico publicado en 2009

Polymorphisms near SOCS3 are associated with obesity and glucose homeostasis traits in Hispanic Americans from the Insulin Resistance Atherosclerosis Family Study

artículo científico publicado en 2008

Power for genetic association studies with random allele frequencies and genotype distributions

artículo científico publicado en 2004

Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA.

artículo científico publicado en 2014

Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression

artículo científico publicado en 2013

Preferential transmission of genetic risk variants of candidate loci at 6p21 from asymptomatic grandparents to mothers of children with neonatal lupus.

artículo científico publicado en 2012

Prevalence of nephropathy in black patients with type 2 diabetes mellitus

artículo científico publicado en 2002

Progress towards understanding the genetic pathogenesis of systemic lupus erythematosus

artículo científico publicado en 2005

Prophylactic Antiepileptic Drug Use and Outcome in the Ethnic/Racial Variations of Intracerebral Hemorrhage Study

artículo científico publicado en 2015

Protective association between JC polyoma viruria and kidney disease

artículo científico publicado en 2019

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2019

Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis

artículo científico publicado en 2012

Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study

artículo científico publicado en 2008

Quantitative trait loci for abdominal fat and BMI in Hispanic-Americans and African-Americans: the IRAS Family study.

artículo científico publicado en 2005

RGS6 Variants Are Associated With Dietary Fat Intake in Hispanics: The IRAS Family Study

artículo científico publicado el 13 de enero de 2011

Race-Specific Relationships Between Coronary and Carotid Artery Calcification and Carotid Intimal Medial Thickness

artículo científico publicado en 2004

Race/ethnicity influences outcomes in young adults with supratentorial intracerebral hemorrhage

artículo científico publicado en 2020

Racial differences in intervention rates in individuals with ALS: A case-control study

scientific article published on 27 March 2019

Racial-ethnic disparities in acute blood pressure after intracerebral hemorrhage

artículo científico publicado en 2016

Racial/ethnic variation of APOE alleles for lobar intracerebral hemorrhage

artículo científico publicado en 2018

Rare Coding Variation and Risk of Intracerebral Hemorrhage

artículo científico publicado en 2015

Rare and low-frequency coding variants alter human adult height

artículo científico publicado en 2017

Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression

artículo científico publicado en 2015

Regional adipose tissue associations with calcified atherosclerotic plaque: African American-diabetes heart study

artículo científico publicado en 2010

Relationship between albuminuria and cardiovascular disease in Type 2 diabetes

artículo científico publicado en 2005

Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study

artículo científico publicado en 2009

Relationships between calcified atherosclerotic plaque and bone mineral density in African Americans with type 2 diabetes

artículo científico publicado en 2011

Relationships between measures of adiposity with subclinical atherosclerosis in patients with type 2 diabetes

artículo científico publicado en 2016

Relationships between serum MCP-1 and subclinical kidney disease: African American-Diabetes Heart Study

artículo científico publicado en 2012

Relationships between serum adiponectin and bone density, adiposity and calcified atherosclerotic plaque in the African American-Diabetes Heart Study

artículo científico publicado en 2013

Relevance of the ACTN4 Gene in African-Americans with Non-Diabetic End-Stage Renal Disease

artículo científico publicado el 4 de septiembre de 2012

Renal artery calcified plaque associations with subclinical renal and cardiovascular disease.

artículo científico publicado en 2004

Replication of the BANK1 genetic association with systemic lupus erythematosus in a European-derived population

scientific article published on 02 April 2009

Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant

artículo científico publicado en 2010

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

artículo científico publicado en 2010

Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes

artículo científico publicado en 2011

Risk factors for intracerebral hemorrhage differ according to hemorrhage location

artículo científico publicado en 2012

Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis

artículo científico publicado en 2011

Salivary dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus

scientific article published on 31 October 2019

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

artículo científico publicado en 2013

Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2016

Sex differences in human adipose tissue gene expression and genetic regulation involve adipogenesis

scientific article published on 23 September 2020

Shared genetic background between SARS-CoV-2 infection and large artery stroke

artículo científico publicado en 2022

Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans

artículo científico publicado en 2011

Single-cell expression quantitative trait loci (eQTL) analysis of SLE-risk loci in lupus patient monocytes

artículo científico publicado en 2021

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.

artículo científico publicado en 2005

Single‐Nucleotide Polymorphisms in the TNF Gene Are Associated With Obesity‐Related Phenotypes in Vervet Monkeys

artículo científico publicado el 17 de febrero de 2011

Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE

artículo científico publicado en 2007

Subphenotype mapping in systemic lupus erythematosus identifies multiple novel loci associated with circulating interferon alpha

artículo científico publicado en 2014

Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls

scientific article published on 15 July 2019

Systemic inflammatory response syndrome, infection, and outcome in intracerebral hemorrhage

artículo científico publicado en 2017

Systemic juvenile idiopathic arthritis is associated with HLA-DRB1 in Europeans and Americans of European descent

artículo científico publicado en 2012

T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study

artículo científico publicado en 2005

TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad.

artículo científico publicado en 2018

Testing gene‐environment interactions in family‐based association studies using trait‐based ascertained samples

artículo científico publicado el 6 de agosto de 2013

The APOL1 Gene and Allograft Survival after Kidney Transplantation

artículo científico publicado el 12 de abril de 2011

The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data

artículo científico publicado en 2018

The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) study protocol

artículo científico publicado en 2013

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

artículo científico publicado en 2000

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.

artículo científico publicado en 2000

The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share

artículo científico publicado en 2014

The Role of Copy Number Variation in African Americans with Type 2 Diabetes-Associated End Stage Renal Disease

artículo científico publicado en 2013

The Subtype Specificity of Genetic Loci Associated with Stroke in 16,664 cases and 32,792 controls

The TMAO-Producing Enzyme Flavin-Containing Monooxygenase 3 Regulates Obesity and the Beiging of White Adipose Tissue

artículo científico publicado en 2017

The TMAO-Producing Enzyme Flavin-Containing Monooxygenase 3 Regulates Obesity and the Beiging of White Adipose Tissue.

artículo científico publicado en 2017

The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sample

artículo científico publicado en 1999

The acetyl-coenzyme A carboxylase beta (ACACB) gene is associated with nephropathy in Chinese patients with type 2 diabetes.

artículo científico publicado en 2010

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

scientific article published on 05 August 2010

The association between innate immunity gene (IRAK1) and C-reactive protein in the Diabetes Heart Study

artículo científico publicado en 2007

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).

artículo científico publicado en 2009

The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans

artículo científico publicado en 2011

The impact of ethnicity and sex on subclinical cardiovascular disease: the Diabetes Heart Study

artículo científico publicado en 2005

The impact of pedigree structure on heritability estimates for pulse pressure in three studies

scientific article published on 08 September 2005

The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans

artículo científico publicado en 2009

The new era of APOL1-associated glomerulosclerosis

artículo científico publicado el 2 de febrero de 2012

The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans

artículo científico publicado en 2010

The nuclear structural protein NuMA is a negative regulator of 53BP1 in DNA double-strand break repair

artículo científico publicado en 2019

The nuclear structural protein NuMA is a negative regulator of 53BP1 in DNA double-strand break repair

artículo científico publicado en 2019

The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease

artículo científico publicado en 2014

The relationship between C-reactive protein and subclinical cardiovascular disease in the Diabetes Heart Study (DHS).

artículo científico publicado en 2005

The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm

artículo científico publicado en 2010

The role of genetic variation near interferon-kappa in systemic lupus erythematosus

artículo científico publicado en 2010

The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1

artículo científico publicado en 2010

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

artículo científico publicado en 2018

Tissue-Specific and Genetic Regulation of Insulin Sensitivity-Associated Transcripts in African Americans.

artículo científico publicado en 2016

Trans-Ethnic Mapping of Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks

scholarly article by Manuel Martínez-Bueno published in August 2018

Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4.

artículo científico publicado en 2013

Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.

artículo científico publicado en 2018

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

artículo científico publicado en 2016

Transancestral mapping and genetic load in systemic lupus erythematosus

artículo científico

Transcriptional Regulatory Mechanisms in Adipose and Muscle Tissue Associated with Composite Glucometabolic Phenotypes

artículo científico publicado en 2018

Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study

artículo científico publicado en 2012

Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription

artículo científico publicado en 2014

Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect

article

Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs

artículo científico publicado en 1999

Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster

artículo científico publicado en 2017

Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans

artículo científico publicado en 2012

Untreated Hypertension: A Powerful Risk Factor for Lobar and Nonlobar Intracerebral Hemorrhage in Whites, Blacks, and Hispanics

artículo científico

Use of Statins and Outcomes in Intracerebral Hemorrhage Patients

artículo científico publicado en 2017

Usefulness of biventricular volume as a predictor of mortality in patients with diabetes mellitus (from the Diabetes Heart Study).

artículo científico publicado en 2013

Variability in the Use of Platelet Transfusion in Patients with Intracerebral Hemorrhage: Observations from the Ethnic/Racial Variations of Intracerebral Hemorrhage Study

artículo científico publicado en 2017

Variability of Serum Soluble Intercellular Adhesion Molecule-1 Measurements Attributable to a Common Polymorphism

artículo científico publicado en 2004

Variable association of reactive intermediate genes with systemic lupus erythematosus in populations with different African ancestry

artículo científico publicado en 2013

Variant in the 3' region of the IkappaBalpha gene associated with insulin resistance in Hispanic Americans: The IRAS Family Study

artículo científico publicado en 2009

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

artículo científico publicado en 2016

Variants in adiponectin signaling pathway genes show little association with subclinical CVD in the diabetes heart study.

artículo científico publicado en 2013

Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans

artículo científico publicado en 2009

Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS)

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

artículo científico publicado en 2007

Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC.

artículo científico publicado en 2009

Variation in the ICAM1-ICAM4-ICAM5 locus is associated with systemic lupus erythematosus susceptibility in multiple ancestries

artículo científico publicado en 2012

Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus.

scientific article published on 26 July 2002

Vitamin d, adiposity, and calcified atherosclerotic plaque in african-americans

artículo científico publicado en 2010

We-W45:5 Human lipoxygenase gene variation in subclinical atherosclerosis: The diabetes heart study

article

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004

artículo