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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 Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

artículo científico publicado en 2017

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 Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

artículo científico publicado en 2017

A Novel Hierarchical Level Set with AR-boost for White Matter Lesion Segmentation in Diabetes

A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families

artículo científico publicado en 1998

A common variant in the CLDN7/ELP5 locus predicts adiponectin change with lifestyle intervention and improved fitness in obese individuals with diabetes

artículo científico publicado en 2015

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

artículo científico publicado en 2004

A high-resolution 6.0-megabase transcript map of the type 2 diabetes susceptibility region on human chromosome 20

artículo científico publicado en 2001

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

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 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 noncoding variant near PPP1R3B promotes liver glycogen storage and MetS, but protects against myocardial infarction

artículo científico publicado en 2020

A physical map of the 20q12-q13.1 region associated with type 2 diabetes

scientific article published on 01 December 1999

A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes

artículo científico publicado en 2010

APOE Genotypes Associate With Cognitive Performance but Not Cerebral Structure: Diabetes Heart Study MIND.

artículo científico publicado en 2016

APOL1 Genotype and Kidney Transplantation Outcomes From Deceased African American Donors

artículo científico publicado en 2015

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

scientific article published on 13 December 2019

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 Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study

artículo científico publicado en 2017

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

artículo científico publicado en 2003

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

Albuminuria associates with calcified atherosclerotic plaque in African Americans with diabetes

artículo científico publicado en 2013

An ACACB variant implicated in diabetic nephropathy associates with body mass index and gene expression in obese subjects

artículo científico publicado en 2013

An Exome-wide Association Study for Type 2 Diabetes–Attributed End-Stage Kidney Disease in African Americans.

artículo científico publicado en 2018

An integrated physical and genetic map of the PLS locus interval on chromosome 11q14

artículo científico publicado en 2000

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 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 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

Analysis of the HNF4 alpha gene in Caucasian type II diabetic nephropathic patients

artículo científico publicado en 2000

Analysis of the relationships between type 2 diabetes status, glycemic control, and neuroimaging measures in the Diabetes Heart Study Mind.

artículo científico publicado en 2015

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 nephropathy risk variants associate with HDL subfraction concentration in African Americans

artículo científico publicado el 19 de septiembre de 2011

Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.

artículo científico publicado en 2016

Association Analysis of the Reticulon 1 Gene in End-Stage Kidney Disease.

artículo científico publicado en 2015

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 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 Genetic Variants with Primary Open-Angle Glaucoma among Individuals with African Ancestry

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 PNPLA3 SNP rs738409 with liver density in African Americans with type 2 diabetes mellitus

artículo científico publicado en 2011

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 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 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study.

artículo científico publicado en 2015

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 an insulin gene promoter insertion polymorphism with type 2 diabetes and diabetic nephropathy in African Americans

artículo científico publicado en 2004

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 kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans

artículo científico publicado en 2016

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 FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study

artículo científico publicado en 2006

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 the tissue kallikrein gene promoter with ESRD and hypertension

artículo científico publicado en 2002

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

artículo científico publicado en 2010

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

artículo científico publicado en 2006

Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patients

scientific article published on 09 April 2003

Associations between NOS1AP Single Nucleotide Polymorphisms (SNPs) and QT Interval Duration in Four Racial/Ethnic Groups in the Multi‐Ethnic Study of Atherosclerosis (MESA)

artículo científico publicado el 1 de enero de 2013

Associations between anxiety and depression symptoms and cognitive testing and neuroimaging in type 2 diabetes.

artículo científico publicado en 2015

Associations between electrocardiographic interval durations and coronary artery calcium scores: the Diabetes Heart Study

artículo científico publicado en 2008

Associations of Early Kidney Disease With Brain Magnetic Resonance Imaging and Cognitive Function in African Americans With Type 2 Diabetes Mellitus.

artículo científico publicado en 2017

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Associations of adiponectin with body fat distribution and insulin sensitivity in nondiabetic Hispanics and African-Americans

artículo científico publicado en 2007

Associations of coronary artery calcified plaque density with mortality in type 2 diabetes: the Diabetes Heart Study.

artículo científico publicado en 2018

Automated white matter total lesion volume segmentation in diabetes.

artículo científico publicado en 2013

Blood pressure indices and cardiovascular disease mortality in persons with or without diabetes mellitus.

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Bone Mineral Density of the Radius Predicts All-Cause Mortality in Patients With Type 2 Diabetes: Diabetes Heart Study

artículo científico publicado en 2017

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

C-reactive protein concentration predicts mortality in type 2 diabetes: the Diabetes Heart Study

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

Cerebral structural changes in diabetic kidney disease: African American-Diabetes Heart Study MIND.

artículo científico publicado en 2014

Cerebral structure and cognitive performance in African Americans and European Americans with type 2 diabetes

artículo científico publicado en 2018

Cerebral white matter hyperintensity in African Americans and European Americans with type 2 diabetes

artículo científico publicado en 2012

Characterization of radiation/fusion hybrids containing parts of human chromosome 10 and their use in mapping chromosome 10-specific probes

artículo científico publicado el 1 de mayo de 1992

Chromogranin A polymorphisms are associated with hypertensive renal disease.

artículo científico publicado en 2008

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

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

artículo científico publicado en 2021

Chronic and recurrent otitis media: a genome scan for susceptibility loci

artículo científico publicado en 2004

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

Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

artículo científico publicado en 2011

Comparative genomic analysis of the HNF-4alpha transcription factor gene

artículo científico publicado en 2004

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

artículo científico publicado en 2014

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

Contributors to mortality in high-risk diabetic patients in the Diabetes Heart Study

artículo científico publicado en 2014

Coronary calcium score and prediction of all-cause mortality in diabetes: the diabetes heart study

artículo científico publicado en 2011

Coronary calcium score predicts cardiovascular mortality in diabetes: diabetes heart study

artículo científico publicado en 2012

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

artículo científico publicado en 2011

Cross-sectional analysis of calcium intake for associations with vascular calcification and mortality in individuals with type 2 diabetes from the Diabetes Heart Study

artículo científico publicado en 2014

D20S16 is a complex interspersed repeated sequence: genetic and physical analysis of the locus

artículo científico publicado en 1995

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10.

artículo científico publicado en 1994

Diabetes: Unravelling the enigma of T2DM and cardiovascular disease

artículo científico publicado en 2013

Diabetic Microvascular Disease: An Endocrine Society Scientific Statement

artículo científico publicado en 2017

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 expression of facilitative glucose transporters in normal and tumour kidney tissues

scientific article published on 01 May 2007

Differential expression of glucose transporters in normal and pathologic thyroid tissue

artículo científico publicado en 2004

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

artículo científico publicado en 2017

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

artículo científico publicado en 2020

Effects of Type 2 Diabetes on Brain Structure and Cognitive Function: African American-Diabetes Heart Study MIND.

artículo científico publicado en 2015

Electrochemical Skin Conductance in Diabetic Kidney Disease

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Epigenetic profiles of pre-diabetes transitioning to type 2 diabetes and nephropathy

artículo científico publicado en 2015

Erratum. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes 2019;68:441-456

scientific article published on 27 April 2020

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

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

Ethnic variation in the correlation between random serum glucose concentration and glycated haemoglobin

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 a SNP map of 6q24-27 confirms diabetic nephropathy loci and identifies novel associations in type 2 diabetes patients with nephropathy from an African-American population

artículo científico publicado en 2008

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 genetic association and expression reduction of TRPC1 in the development of diabetic nephropathy

artículo científico publicado en 2008

Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients

scientific article published on 01 July 2003

Evaluation of markers on human chromosome 10, including the homologue of the rodent Rf-1 gene, for linkage to ESRD in black patients

scientific article published on 01 February 1999

Evidence for a novel type 1 diabetes susceptibility locus on chromosome 8

artículo científico publicado en 2002

Examination of Rare Variants in HNF4 α in European Americans with Type 2 Diabetes

artículo científico publicado en 2011

Exome Chip Analysis Identifies Low-Frequency a on Brain Magnetic Imaging

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

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

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

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

artículo científico publicado en 2017

Factor V Leiden, Hormone Replacement Therapy, and Risk of Venous Thromboembolic Events in Women With Coronary Disease

scientific article published on 01 June 2002

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

artículo científico publicado en 2001

Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA).

artículo científico publicado en 2012

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

artículo científico publicado en 2018

Functional ENTPD1 polymorphisms in African Americans with diabetes and end-stage renal disease

artículo científico publicado en 2008

Functional characterization of the promoter of the human glucose transporter 10 gene

artículo científico publicado en 2005

Further definition of 20q deletion in myeloid leukemia using fluorescence in situ hybridization

scientific article published on 01 October 1994

GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS.

artículo científico publicado en 2016

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

artículo científico publicado en 2018

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

Generalization of Rare Variant Association Tests for Longitudinal Family Studies

artículo científico publicado en 2016

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

article

Genetic Initiation of Hypertensive and Diabetic Nephropathy

artículo científico publicado el 1 de febrero de 1998

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 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 nitric oxide and endothelin in end-stage renal disease

artículo científico publicado en 2000

Genetic analysis of the GLUT10 glucose transporter (SLC2A10) polymorphisms in Caucasian American type 2 diabetes

artículo científico publicado en 2005

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

artículo científico publicado en 2008

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

artículo científico publicado en 2011

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 in diabetic nephropathy

artículo científico publicado en 2007

Genetic linkage analysis of growth factor loci and end-stage renal disease in African Americans

artículo científico publicado en 1997

Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21

artículo científico publicado el 1 de diciembre de 1997

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 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

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 Interaction with Insulin Secretion Loci Reveals Novel Loci for Type 2 Diabetes in African Americans

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

artículo científico publicado en 2011

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 coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes

artículo científico publicado en 2017

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

artículo científico publicado en 2011

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

artículo científico publicado en 2010

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

artículo científico publicado en 2014

Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.

artículo científico publicado en 2018

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

artículo científico publicado en 2016

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

artículo científico publicado en 2008

Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group

artículo científico publicado en 2009

Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2007

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

artículo científico publicado en 2007

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Genome‐Wide Association of BMI in African Americans

artículo científico publicado el 23 de junio de 2011

Genomic structure of the human plasma prekallikrein gene, identification of allelic variants, and analysis in end-stage renal disease.

artículo científico publicado en 2000

Glomerular filtration rate and albuminuria predict mortality independently from coronary artery calcified plaque in the Diabetes Heart Study

artículo científico publicado en 2013

Glucose transporters in the thyroid

artículo científico publicado en 2005

HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

scientific article published on 28 October 2019

Heart rate is an independent predictor of all-cause mortality in individuals with type 2 diabetes: The diabetes heart study

artículo científico publicado en 2018

Heart rate-corrected QT interval is an independent predictor of all-cause and cardiovascular mortality in individuals with type 2 diabetes: the Diabetes Heart Study

artículo científico publicado en 2014

Hepatic steatosis and subclinical cardiovascular disease in a cohort enriched for type 2 diabetes: the Diabetes Heart Study

artículo científico publicado en 2008

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

Heritability of the severity of diabetic retinopathy: the FIND-Eye study

artículo científico publicado en 2008

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

artículo científico publicado en 2008

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 Na+/H+ exchanger genes : identification of polymorphisms by radiation hybrid mapping and analysis of linkage in end-stage renal disease

artículo científico publicado en 2000

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

artículo científico publicado en 2010

ICAM1 and VCAM1 polymorphisms, coronary artery calcium, and circulating levels of soluble ICAM-1: the multi-ethnic study of atherosclerosis (MESA).

artículo científico publicado en 2008

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

artículo científico publicado en 2009

Id3 is a novel atheroprotective factor containing a functionally significant single-nucleotide polymorphism associated with intima-media thickness in humans

artículo científico publicado en 2010

Identification and characterization of PRKCBP1, a candidate RACK-like protein

artículo científico publicado en 2000

Identification of Human Plasma Kallikrein Gene Polymorphisms and Evaluation of Their Role in End-Stage Renal Disease

artículo científico publicado el 1 de abril de 1998

Identification of a CA/TG Repeat Polymorphism Proximal to the Human DLX3 Gene

artículo científico publicado el 1 de septiembre de 1998

Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease

artículo científico publicado en 2005

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

artículo científico publicado en 2004

Identification of type 2 diabetes loci in 433,540 East Asian individuals

artículo científico publicado en 2020

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

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 situ localization of the genetic locus encoding the lysosomal acid lipase/cholesteryl esterase (LIPA) deficient in Wolman disease to chromosome 10q23.2-q23.3.

artículo científico publicado en 1993

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

artículo científico publicado en 2012

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

artículo científico publicado en 2020

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

artículo científico publicado en 2014

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

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

scientific article published on 15 May 2013

Kidney disease and cognitive function: African American-diabetes heart study MIND

artículo científico publicado en 2014

Kidney volume associations with subclinical renal and cardiovascular disease: the Diabetes Heart Study

artículo científico publicado en 2007

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

artículo científico publicado en 2014

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Linkage analysis between loci in the renin-angiotensin axis and end-stage renal disease in African Americans

artículo científico publicado en 1996

Linkage heterogeneity of end-stage renal disease on human chromosome 10

scientific article published on 01 September 2002

Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy

artículo científico publicado en 1997

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

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

artículo científico publicado en 2017

Low plasma levels of FGF-2 and PDGF-BB are associated with cardiovascular events in type II diabetes mellitus (diabetes heart study).

artículo científico publicado en 2007

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

MODY: a model for the study of the molecular genetics of NIDDM.

artículo científico publicado en 1992

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

artículo científico publicado en 2008

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

Maturity onset diabetes of the young (MODY).

artículo científico publicado en 1996

Maturity-onset diabetes of the young

artículo científico publicado en 1994

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

Metabolomic profile associated with insulin resistance and conversion to diabetes in the Insulin Resistance Atherosclerosis Study

artículo científico publicado en 2014

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

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

Montreal Cognitive Assessment and Modified Mini Mental State Examination in African Americans

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

Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.

artículo científico publicado en 2016

Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control

scientific article published on 28 November 2018

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

artículo científico publicado en 2016

Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease

artículo científico publicado en 2005

Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome

artículo científico publicado en 1999

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

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

artículo científico publicado en 2018

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

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

artículo científico publicado en 2005

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

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

artículo científico publicado en 2005

Physical localization of chromosome 20 markers using somatic cell hybrid cell lines and fluorescence in situ hybridization

artículo científico publicado el 1 de octubre de 1992

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

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 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

Potential donor-recipient MYH9 genotype interactions in posttransplant nephrotic syndrome after pediatric kidney transplantation

artículo científico publicado en 2009

Predicting Mortality in African Americans With Type 2 Diabetes Mellitus: Soluble Urokinase Plasminogen Activator Receptor, Coronary Artery Calcium, and High-Sensitivity C-Reactive Protein.

artículo científico publicado en 2018

Prediction of mortality using a multi-bed vascular calcification score in the Diabetes Heart Study.

artículo científico publicado en 2014

Predictors of all-cause and cardiovascular disease mortality in type 2 diabetes: Diabetes Heart Study

artículo científico publicado en 2015

Prevalence and determinants of electrocardiographic abnormalities in African Americans with type 2 diabetes

artículo científico publicado en 2014

Prevalence of nephropathy in black patients with type 2 diabetes mellitus

artículo científico publicado en 2002

Progression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosis.

artículo científico publicado en 2010

Protein Kinase C-β Gene Variants and Type 2 Diabetes–Associated Kidney Failure: What Can We Learn From Gene Association Studies in Diabetic Nephropathy?

artículo científico publicado el 13 de diciembre de 2010

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

Psoas and Paraspinous Muscle Measurements on Computed Tomography Predict Mortality in European Americans with Type 2 Diabetes Mellitus

scientific article published on 01 January 2019

Psoas and paraspinous muscle index as a predictor of mortality in African American men with type 2 diabetes mellitus

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

QRS duration is associated with all-cause mortality in type 2 diabetes: The diabetes heart study

artículo científico publicado en 2019

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

Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes

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

Region-based association tests for sequencing data on survival traits

artículo científico publicado en 2017

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 Cognitive Performance, Neuroimaging and Vascular Disease: The DHS-MIND Study.

artículo científico publicado en 2015

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

artículo científico publicado en 2011

Relationships between cerebral structure and cognitive function in African Americans with type 2 diabetes

scientific article published on 29 May 2018

Relationships between electrochemical skin conductance and kidney disease in Type 2 diabetes

artículo científico publicado en 2013

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

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 factors: Race, renal disease and albuminuria

artículo científico publicado en 2011

Role of a proline insertion in the insulin promoter factor 1 (IPF1) gene in African Americans with type 2 diabetes

artículo científico publicado en 2006

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

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

Severe prekallikrein deficiency associated with homozygosity for an Arg94Stop nonsense mutation

artículo científico publicado en 2004

Shroom3 contributes to the maintenance of the glomerular filtration barrier integrity

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Sleep duration and five-year abdominal fat accumulation in a minority cohort: the IRAS family study.

artículo científico publicado en 2010

Structural and functional assessment of the brain in European Americans with mild-to-moderate kidney disease: Diabetes Heart Study-MIND.

artículo científico publicado en 2015

Subclinical Atherosclerosis Is Inversely Associated With Gray Matter Volume in African Americans With Type 2 Diabetes.

artículo científico publicado en 2015

Sublocalization of the Papillon-Lefevre syndrome locus on 11q14-q21

artículo científico publicado en 1998

Symptoms Suggestive of Gastroparesis in a Community-Based Cohort of European Americans and African Americans with Type 2 Diabetes Mellitus

scientific article published on 09 December 2019

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

artículo científico publicado en 2005

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 Challenging Search for Diabetic Nephropathy Genes

artículo científico publicado el 1 de agosto de 2012

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

artículo científico publicado en 2013

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 type 2 diabetes

artículo científico publicado en 2016

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 influence of subclinical cardiovascular disease and related risk factors on cognition in type 2 diabetes mellitus: The DHS-Mind study

artículo científico publicado en 2013

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

artículo científico publicado en 2010

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

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

artículo científico publicado en 2016

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

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

Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource

artículo científico publicado en 2012

Trends in racial disparities in care

artículo científico publicado en 2005

Type 2 diabetes is not independently associated with spinal trabecular volumetric bone mineral density measured by QCT in the Diabetes Heart Study.

artículo científico publicado en 2006

Urinary F2-isoprostanes and metabolic markers of fat oxidation

artículo científico publicado en 2015

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

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

artículo científico publicado en 2004

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 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

Vitamin D Associations With Renal, Bone, and Cardiovascular Phenotypes: African American-Diabetes Heart Study

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Volumetric bone mineral density of the spine predicts mortality in African-American men with type 2 diabetes

artículo científico publicado en 2018

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

article

β-cell failure in type 2 diabetes: postulated mechanisms and prospects for prevention and treatment

artículo científico publicado en 2014

β-cell failure in type 2 diabetes: postulated mechanisms and prospects for prevention and treatment

artículo científico publicado en 2014

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

artículo