Year |
Title |
Altmetric |
2022
|
Inflammation biomarkers and incident coronary heart disease: the Reasons for Geographic And Racial Differences in Stroke Study.
American Heart Journal.
253:39-47.
2022
|
|
2021
|
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Molecular Psychiatry.
26:2111-2125.
2021
|
|
2021
|
Association of Sickle Cell Trait With Incidence of Coronary Heart Disease Among African American Individuals.
JAMA Network Open.
4:e2030435.
2021
|
|
2021
|
Epigenome-wide association study identifies DNA methylation sites associated with target organ damage in older African Americans.
Epigenetics.
16:862-875.
2021
|
|
2021
|
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
EBioMedicine.
63.
2021
|
|
2020
|
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.
Nature Communications.
11.
2020
|
|
2020
|
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (Nature Communications, (2018), 9, 1, (2606), 10.1038/s41467-018-04668-w).
Nature Communications.
11.
2020
|
|
2020
|
Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A.
American Journal of Clinical Nutrition.
112:1200-1211.
2020
|
|
2020
|
Genetic-based hypertension subtype identification using informative SNPs.
Genes.
11:1-13.
2020
|
|
2020
|
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature.
586:763-768.
2020
|
|
2020
|
Genome-Wide association meta-Analysis of individuals of european ancestry identifies suggestive loci for sodium intake, potassium intake, and their ratio measured from 24-Hour or half-Day urine samples
2020
|
|
2020
|
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
Nature Genetics.
52:969-983.
2020
|
|
2020
|
Transitions to family caregiving: enrolling incident caregivers and matched non-caregiving controls from a population-based study.
Aging Clinical and Experimental Research.
32:1829-1838.
2020
|
|
2020
|
A lipidome-wide association study of the lipoprotein insulin resistance index.
Lipids in Health and Disease.
19:153.
2020
|
|
2020
|
Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans.
Journal of Thrombosis and Haemostasis.
18:1335-1347.
2020
|
|
2020
|
Gout is associated with an increased risk for incident heart failure among older adults: The REasons for Geographic and Racial Differences in Stroke (REGARDS) cohort study.
Arthritis Research and Therapy.
22.
2020
|
|
2020
|
APOL1 Nephropathy Risk Alleles and Mortality in African American Adults: A Cohort Study.
American Journal of Kidney Diseases.
75:54-60.
2020
|
|
2020
|
Cardiovascular Health and Transition from Controlled Blood Pressure to Apparent Treatment Resistant Hypertension: The Jackson Heart Study and the REGARDS Study.
Hypertension.
1953-1961.
2020
|
|
2020
|
Severity of Hypertension Mediates the Association of Hyperuricemia With Stroke in the REGARDS Case Cohort Study.
Hypertension.
75:246-256.
2020
|
|
2020
|
Soluble cd14, ischemic stroke, and coronary heart disease risk in a prospective study: The regards cohort.
Journal of the American Heart Association.
9.
2020
|
|
2019
|
Apol1 nephropathy risk alleles and risk of sepsis in blacks.
Clinical Journal of the American Society of Nephrology.
14:1733-1740.
2019
|
|
2019
|
Gain of function in somatic TP53 mutations is associated with immune-rich breast tumors and changes in tumor-associated macrophages.
Molecular Genetics and Genomic Medicine.
7.
2019
|
|
2019
|
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group.
American Journal of Hypertension.
32:1146-1153.
2019
|
|
2019
|
Does the association of diabetes with stroke risk differ by age, race, and sex? Results from the reasons for geographic and racial differences in stroke (REGARDS) study.
Diabetes reviews (Alexandria, Va.).
42:1966-1972.
2019
|
|
2019
|
Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans.
Molecular Genetics and Genomic Medicine.
7.
2019
|
|
2019
|
Gene Variants at Loci Related to Blood Pressure Account for Variation in Response to Antihypertensive Drugs Between Black and White Individuals..
Hypertension.
74:614-622.
2019
|
|
2019
|
Integrating hypertension phenotype and genotype with hybrid non-negative matrix factorization..
Bioinformatics.
35:2885.
2019
|
|
2019
|
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.
Human Molecular Genetics.
28:2615-2633.
2019
|
|
2019
|
Association of sickle cell trait with atrial fibrillation: The REGARDS cohort.
Journal of Electrocardiology.
55:1-5.
2019
|
|
2019
|
Sickle cell trait and risk of cognitive impairment in African-Americans: The REGARDS cohort.
EClinicalMedicine.
11:27-33.
2019
|
|
2019
|
Integrating hypertension phenotype and genotype with hybrid non-negative matrix factorization.
Bioinformatics.
35:1395-1403.
2019
|
|
2019
|
Distracted Driving and Risk of Crash or Near-Crash Involvement among Older Drivers Using Naturalistic Driving Data with a Case-Crossover Study Design
2019
|
|
2019
|
Systematic Error Removal Using Random Forest for Normalizing Large-Scale Untargeted Lipidomics Data.
Analytical Chemistry.
91:3590-3596.
2019
|
|
2019
|
Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study.
Neurology.
92:E944-E950.
2019
|
|
2019
|
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
Human Genetics.
138:199-210.
2019
|
|
2019
|
Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry
2019
|
|
2019
|
A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study.
BMC Medical Genomics.
12.
2019
|
|
2019
|
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.
American Journal of Human Genetics.
104:112-138.
2019
|
|
2019
|
APOL1 kidney risk variants and cardiovascular disease: An individual participant data meta-analysis.
Journal of the American Society of Nephrology.
30:2027-2036.
2019
|
|
2019
|
An exome-wide sequencing study of the GOLDN cohort reveals novel associations of coding variants and fasting plasma lipids.
Frontiers in Genetics.
10.
2019
|
|
2019
|
Clinical correlates and heritability of cardiac mechanics: The HyperGEN study.
International Journal of Cardiology.
274:208-213.
2019
|
|
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.
PLoS Genetics.
15.
2019
|
|
2018
|
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Nature Communications.
9.
2018
|
|
2018
|
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Nature Communications.
9.
2018
|
|
2018
|
Erratum to: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (Nature Communications, (2018), 9, 1, (2606), 10.1038/s41467-018-04668-w).
Nature Communications.
9.
2018
|
|
2018
|
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
Nature Communications.
9.
2018
|
|
2018
|
Association of sickle cell trait with ischemic stroke among African americans a meta-analysis.
JAMA Neurology.
75:802-807.
2018
|
|
2018
|
West African ancestry and nocturnal blood pressure in African Americans: The Jackson Heart Study.
American Journal of Hypertension.
31:706-714.
2018
|
|
2018
|
Metabolic and inflammatory biomarkers are associated with epigenetic aging acceleration estimates in the GOLDN study.
Clinical Epigenetics.
10.
2018
|
|
2018
|
Epigenome-wide association study of metabolic syndrome in African-American adults.
Clinical Epigenetics.
10.
2018
|
|
2018
|
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Nature Genetics.
50:524-537.
2018
|
|
2018
|
Publisher correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes(Nature Genetics, (2018) 50, 4, (524-537), 10.1038/s41588-018-0058-3).
Nature Genetics.
51:1192-1193.
2018
|
|
2018
|
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
American Journal of Human Genetics.
102:375-400.
2018
|
|
2018
|
General cognitive impairment as a risk factor for motor vehicle collision involvement: A prospective population-based study.
Geriatrics.
3.
2018
|
|
2018
|
PCSK9 variants, low-density lipoprotein cholesterol, and neurocognitive impairment reasons for geographic and racial differences in stroke study (REGARDS).
Circulation.
137:1260-1269.
2018
|
|
2018
|
The association of nocturnal hypertension and nondipping blood pressure with treatment-resistant hypertension: The Jackson Heart Study.
Journal of the CardioMetabolic Syndrome.
20:438-446.
2018
|
|
2018
|
Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.
International Journal of Obesity.
42:384-390.
2018
|
|
2018
|
A DNA methylation biomarker of alcohol consumption.
Molecular Psychiatry.
23:422-433.
2018
|
|
2018
|
APOL1, CDKN2A/CDKN2B, and HDAC9 polymorphisms and small vessel ischemic stroke.
Acta Neurologica Scandinavica.
137:133-141.
2018
|
|
2018
|
An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort.
Journal of Lipid Research.
59:722-729.
2018
|
|
2017
|
DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.
American Journal of Human Genetics.
101:888-902.
2017
|
|
2017
|
Advancing stroke genomic research in the age of Trans-Omics big data science: Emerging priorities and opportunities.
Journal of the Neurological Sciences.
382:18-28.
2017
|
|
2017
|
Chronic kidney disease and incident apparent treatment-resistant hypertension among blacks: Data from the Jackson Heart Study.
Journal of the CardioMetabolic Syndrome.
19:1117-1124.
2017
|
|
2017
|
Influence of Kidney Transplant Status on Warfarin Dose, Anticoagulation Control, and Risk of Hemorrhage
2017
|
|
2017
|
An epigenome-wide association study of inflammatory response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network.
Pharmacogenomics.
18:1333-1341.
2017
|
|
2017
|
Interleukin–6 (IL-6) rs1800796 and cyclin dependent kinase inhibitor (CDKN2A/CDKN2B) rs2383207 are associated with ischemic stroke in indigenous West African Men.
Journal of the Neurological Sciences.
379:229-235.
2017
|
|
2017
|
Association of Estimated Sodium Intake With Adverse Cardiac Structure and Function: From the HyperGEN Study..
Journal of the American College of Cardiology.
70:715-724.
2017
|
|
2017
|
PCSK9 Loss-of-Function Variants, Low-Density Lipoprotein Cholesterol, and Risk of Coronary Heart Disease and Stroke: Data from 9 Studies of Blacks and Whites.
Circulation: Cardiovascular Genetics.
10.
2017
|
|
2017
|
Influence of common and rare genetic variation on warfarin dose among African-Americans and European-Americans using the exome array.
Pharmacogenomics.
18:1059-1073.
2017
|
|
2017
|
Sickle cell trait and the risk of ESRD in blacks.
Journal of the American Society of Nephrology.
28:2180-2187.
2017
|
|
2017
|
Genetics of Blood Pressure: New Insights Into a Complex Trait.
American Journal of Kidney Diseases.
69:723-725.
2017
|
|
2017
|
Genome- and CD4+ T-cell methylome-wide association study of circulating trimethylamine-N-oxide in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN)
2017
|
|
2017
|
Phenomapping for the Identification of Hypertensive Patients with the Myocardial Substrate for Heart Failure with Preserved Ejection Fraction.
Journal of Cardiovascular Translational Research.
10:275-284.
2017
|
|
2017
|
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci.
Human Genetics.
136:771-800.
2017
|
|
2017
|
Visual sensory and visual-cognitive function and rate of crash and near-crash involvement among older drivers using naturalistic driving data
2017
|
|
2017
|
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Journal of Clinical Investigation.
127:1798-1812.
2017
|
|
2017
|
Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events among African Americans in 2 Large Cohort Studies.
Circulation: Cardiovascular Genetics.
10.
2017
|
|
2017
|
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.
PLoS Genetics.
13.
2017
|
|
2017
|
National patterns in intensity and frequency of outpatient care for apparent treatment-resistant hypertension.
American Heart Journal.
186:29-39.
2017
|
|
2017
|
CPT1A methylation is associated with plasma adiponectin
2017
|
|
2017
|
Epigenetic Patterns in Blood Associated with Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results from Genome-Wide Association Studies.
Circulation: Cardiovascular Genetics.
10.
2017
|
|
2017
|
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations.
International Journal of Obesity.
41:324-331.
2017
|
|
2017
|
Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach.
PLoS Medicine.
14.
2017
|
|
2017
|
D-dimer in african americans whole genome sequence analysis and relationship to cardiovascular disease risk in the Jackson Heart Study
2017
|
|
2017
|
Local ancestry and clinical cardiovascular events among African Americans from the atherosclerosis risk in communities study.
Journal of the American Heart Association.
6.
2017
|
|
2017
|
Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studies.
2017
|
|
2016
|
Hemostasis biomarkers and risk of sepsis: the REGARDS cohort.
Journal of Thrombosis and Haemostasis.
14:2169-2176.
2016
|
|
2016
|
Epigenetic Signatures of Cigarette Smoking.
Circulation: Cardiovascular Genetics.
9:436-447.
2016
|
|
2016
|
Epigenetics of Lipid Phenotypes.
Current Cardiovascular Risk Reports.
10.
2016
|
|
2016
|
Heritable DNA methylation in CD4+ Cells among complex families displays genetic and non-genetic effects.
PLoS One.
11.
2016
|
|
2016
|
The effects of genes implicated in cardiovascular disease on blood pressure response to treatment among treatment-naive hypertensive African Americans in the GenHAT study.
Journal of Human Hypertension.
30:549-554.
2016
|
|
2016
|
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
American Journal of Human Genetics.
99:8-21.
2016
|
|
2016
|
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.
American Journal of Human Genetics.
99:56-75.
2016
|
|
2016
|
Admixture mapping of serum vitamin D and parathyroid hormone concentrations in the African American-Diabetes Heart Study.
Bone.
87:71-77.
2016
|
|
2016
|
Association of Central Adiposity with Adverse Cardiac Mechanics; Findings from the Hypertension Genetic Epidemiology Network Study.
Circulation: Cardiovascular Imaging.
9.
2016
|
|
2016
|
APOL1 nephropathy risk variants are associated with altered high-density lipoprotein profiles in African Americans.
Nephrology Dialysis Transplantation.
31:602-608.
2016
|
|
2016
|
Archeological Echocardiography: Digitization and Speckle Tracking Analysis of Archival Echocardiograms in the HyperGEN Study
2016
|
|
2016
|
Driving with pets and motor vehicle collision involvement among older drivers: A prospective population-based study.
Accident Analysis and Prevention.
88:169-174.
2016
|
|
2016
|
Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: A meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.
American Journal of Clinical Nutrition.
103:567-578.
2016
|
|
2016
|
The effects of omega-3 polyunsaturated fatty acids and genetic variants on methylation levels of the interleukin-6 gene promoter.
Molecular Nutrition and Food Research.
60:410-419.
2016
|
|
2016
|
A genome-wide study of lipid response to fenofibrate in Caucasians: A combined analysis of the GOLDN and ACCORD studies.
Pharmacogenetics and Genomics.
26:324-333.
2016
|
|
2016
|
Association of DNA methylation at CPT1A locus with metabolic syndrome in the genetics of lipid lowering drugs and diet network (GOLDN) study.
PLoS One.
11.
2016
|
|
2016
|
Epigenome-wide association study of triglyceride postprandial responses to a high-fat dietary challenge.
Journal of Lipid Research.
57:2200-2207.
2016
|
|
2015
|
Drug-gene interactions of antihypertensive medications and risk of incident cardiovascular disease: A pharmacogenomics study from the CHARGE consortium.
PLoS One.
10.
2015
|
|
2015
|
A family-specific linkage analysis of blood lipid response to fenofibrate in the Genetics of Lipid Lowering Drug and Diet Network.
Pharmacogenetics and Genomics.
25:511-514.
2015
|
|
2015
|
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci.
Human Molecular Genetics.
24:4464-4479.
2015
|
|
2015
|
Apparent treatment-resistant hypertension among individuals with history of stroke or transient ischemic attack.
American Journal of Medicine.
128:707-714.e2.
2015
|
|
2015
|
Epigenome-wide study identifies novel methylation loci associated with body mass index and waist circumference.
Obesity.
23:1493-1501.
2015
|
|
2015
|
Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individuals.
Journal of Human Genetics.
60:63-67.
2015
|
|
2015
|
Genetic loci associated with circulating phospholipid trans fatty acids: A meta-analysis of genome-wide association studies from the CHARGE consortium.
American Journal of Clinical Nutrition.
101:398-406.
2015
|
|
2015
|
Genetic variants modify the effect of age on APOE methylation in the genetics of lipid lowering drugs and diet network study.
Aging Cell.
14:49-59.
2015
|
|
2015
|
Lipid changes due to fenofibrate treatment are not associated with changes in DNA methylation patterns in the GOLDN study.
Frontiers in Genetics.
6.
2015
|
|
2015
|
PCSK9 variation and association with blood pressure in African Americans: Preliminary findings from the HyperGEN and REGARDS studies.
Frontiers in Genetics.
6.
2015
|
|
2014
|
Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study.
Pharmacogenetics and Genomics.
24:556-563.
2014
|
|
2014
|
Diastolic wall strain: A simple marker of abnormal cardiac mechanics.
Cardiovascular Ultrasound.
12.
2014
|
|
2014
|
Multi-ethnic fine-mapping of 14 central adiposity loci..
Human Molecular Genetics.
23:4738-4744.
2014
|
|
2014
|
Epigenome-wide association study of fasting blood lipids in the genetics of lipid-lowering drugs and diet network study.
Circulation.
130:565-572.
2014
|
|
2014
|
Genomics of post-prandial lipidomic phenotypes in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study.
PLoS One.
9.
2014
|
|
2014
|
Determination of prevalence, risk factors, and comorbidities in a large, population-based cohort.
Hypertension.
63:451-458.
2014
|
|
2014
|
CPT1A: The future of heart disease detection and personalized medicine?.
Clinical Lipidology.
9:9-12.
2014
|
|
2014
|
Epigenome-wide association study of fasting measures of glucose, insulin, and homa-ir in the genetics of lipid lowering drugs and diet network study.
Diabetes.
63:801-807.
2014
|
|
2014
|
HIV, inflammation, and calcium in atherosclerosis
2014
|
|
2014
|
Apparent treatment-resistant hypertension and risk for stroke, coronary heart disease, and all-cause mortality.
Journal of the American Society of Hypertension.
8:405-413.
2014
|
|
2014
|
Association of comorbidity burden with abnormal cardiac mechanics: Findings from the HyperGEN study.
Journal of the American Heart Association.
3.
2014
|
|
2014
|
Association of low-grade albuminuria with adverse cardiac mechanics: Findings from the hypertension genetic epidemiology network (hypergen) study.
Circulation.
129:42-50.
2014
|
|
2014
|
Healthy lifestyle factors and risk of cardiovascular events and mortality in treatment-resistant hypertension: The Reasons for Geographic and Racial Differences in Stroke study.
Hypertension.
64:465-471.
2014
|
|
2014
|
Incident ESRD and treatment-resistant hypertension: The reasons for geographic and racial differences in stroke (REGARDS) study.
American Journal of Kidney Diseases.
63:781-788.
2014
|
|
2014
|
RYR3 gene variants in subclinical atherosclerosis among HIV-infected women in the Women's Interagency HIV Study (WIHS).
Atherosclerosis.
233:666-672.
2014
|
|
2014
|
Response to should more significance be granted to medication response to antihypertensives in patients with resistant hypertension?.
Hypertension.
63.
2014
|
|
2014
|
The effects of angiotensinogen gene polymorphisms on cardiovascular disease outcomes during antihypertensive treatment in the GenHAT study..
Frontiers in Pharmacology.
5:210.
2014
|
|
2013
|
Genetic and adverse health outcome associations with treatment resistant hypertension in GenHAT.
International Journal of Hypertension.
2013.
2013
|
|
2013
|
Fine mapping and identification of BMI loci in African Americans.
American Journal of Human Genetics.
93:661-671.
2013
|
|
2013
|
Prevalence of apparent treatment-resistant hypertension among individuals with CKD.
Clinical Journal of the American Society of Nephrology.
8:1583-1590.
2013
|
|
2013
|
Genome-Wide Association of Body Fat Distribution in African Ancestry Populations Suggests New Loci.
PLoS Genetics.
9.
2013
|
|
2013
|
RYR3 gene polymorphisms and cardiovascular disease outcomes in the context of antihypertensive treatment
2013
|
|
2013
|
A431: Epigenetics of Fasting Insulin and Glucose Concentrations.
Diabetes.
62:A431-A431.
2013
|
|
2013
|
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
Nature Genetics.
45:690-696.
2013
|
|
2013
|
Pharmacogenomics of high-density lipoprotein-cholesterol-raising therapies.
Expert Review of Cardiovascular Therapy.
11:355-364.
2013
|
|
2013
|
A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study.
PLoS Genetics.
9.
2013
|
|
2013
|
Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network
2013
|
|
2013
|
SNPs located at CpG sites modulate genome-epigenome interaction.
Epigenetics.
8:802-806.
2013
|
|
2012
|
Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy.
Frontiers in Genetics.
3.
2012
|
|
2012
|
Variants Identified in a GWAS Meta-Analysis for Blood Lipids Are Associated with the Lipid Response to Fenofibrate.
PLoS One.
7.
2012
|
|
2012
|
Prevalence and Correlates of Low Medication Adherence in Apparent Treatment-Resistant Hypertension.
Journal of the CardioMetabolic Syndrome.
14:694-700.
2012
|
|
2012
|
Rare PPARA variants and extreme response to fenofibrate in the Genetics of Lipid-Lowering Drugs and Diet Network Study.
Pharmacogenetics and Genomics.
22:367-372.
2012
|
|
2011
|
A data-driven method for identifying rare variants with heterogeneous trait effects.
Genetic Epidemiology.
35:679-685.
2011
|
|
2011
|
Genome-wide detection of allele specific copy number variation associated with insulin resistance in african americans from the hyperGEN study.
PLoS One.
6.
2011
|
|
2011
|
Response to letter regarding article, "Apolipoprotein E polymorphisms and postprandial triglyceridemia before and after fenofibrate treatment in the GOLDN study".
Circulation: Cardiovascular Genetics.
4.
2011
|
|
2011
|
Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.
Pharmacogenetics and Genomics.
21:798-807.
2011
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2010
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Apolipoprotein e polymorphisms and postprandial triglyceridemia before and after fenofibrate treatment in the genetics of lipid lowering and diet network (GOLDN) study.
Circulation: Cardiovascular Genetics.
3:462-467.
2010
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2010
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A genome-wide association study of carotid atherosclerosis in HIV-infected men.
AIDS.
24:583-592.
2010
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2010
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Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT Study.
Journal of Hypertension.
28:2076-2083.
2010
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2008
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Barriers to genetic testing among persons at risk for alpha-1 antitrypsin deficiency.
Genetic Testing and Molecular Biomarkers.
12:501-505.
2008
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2008
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A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH genetic initiative.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
147:784-792.
2008
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2007
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Does genetic testing result in behavioral health change? Changes in smoking behavior following testing for alpha-1 antitrypsin deficiency.
Annals of Behavioral Medicine.
33:22-28.
2007
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2005
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Association studies of transforming growth factor-β1 and Alzheimer's disease.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.
139 B:38-41.
2005
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2005
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Delay in diagnosis of alpha1-antitrypsin deficiency: a continuing problem..
Chest.
128:1989-1994.
2005
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2004
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Genetic testing for alpha1-antitrypsin deficiency..
Genetics in Medicine.
6:204-210.
2004
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2001
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Drosophila E2f2 promotes the conversion from genomic DNA replication to gene amplification in ovarian follicle cells
2001
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