| Year |
Title |
Altmetric |
| 2022
|
Determinants of metabolic syndrome and its prognostic implications among stroke patients in Africa: Findings from the Stroke Investigative Research and Educational Network (SIREN) study.
Journal of the Neurological Sciences.
441.
2022
|
|
| 2022
|
Habitual Intake of Marine-Derived n-3 PUFAs is Inversely Associated with a Cardiometabolic Inflammatory Profile in Yup'ik Alaska Native People
2022
|
|
| 2022
|
Mendelian randomization in the multivariate general linear model framework.
Genetic Epidemiology.
46:17-31.
2022
|
|
| 2022
|
Risk Factor Characterization of Ischemic Stroke Subtypes Among West Africans..
Stroke.
53:134-144.
2022
|
|
| 2021
|
Genetic Contributors of Incident Stroke in 10,700 African Americans With Hypertension: A Meta-Analysis From the Genetics of Hypertension Associated Treatments and Reasons for Geographic and Racial Differences in Stroke Studies.
Frontiers in Genetics.
12.
2021
|
|
| 2021
|
Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci
2021
|
|
| 2021
|
Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease.
Journal of Cachexia, Sarcopenia and Muscle.
12:1803-1817.
2021
|
|
| 2021
|
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome Biology.
22.
2021
|
|
| 2021
|
Genomic alterations associated with mutational signatures, DNA damage repair and chromatin remodeling pathways in cervical carcinoma.
npj Genomic Medicine.
6.
2021
|
|
| 2021
|
A 6-CpG validated methylation risk score model for metabolic syndrome: The HyperGEN and GOLDN studies.
PLoS One.
16.
2021
|
|
| 2021
|
Genomics of postprandial lipidomics in the genetics of lipid-lowering drugs and diet network study.
Nutrients.
13.
2021
|
|
| 2021
|
Predicting the Probability of Chlamydia Reinfection in African American Women Using Immunologic and Genetic Determinants in a Bayesian Model.
Sexually Transmitted Diseases.
48:813-818.
2021
|
|
| 2021
|
A Novel Afrocentric Stroke Risk Assessment Score: Models from the Siren Study.
Journal of Stroke and Cerebrovascular Diseases.
30.
2021
|
|
| 2021
|
Influence of age on links between major modifiable risk factors and stroke occurrence in West Africa.
Journal of the Neurological Sciences.
428.
2021
|
|
| 2021
|
Genomic characterization and therapeutic targeting of hpv undetected cervical carcinomas.
Cancers.
13.
2021
|
|
| 2021
|
A novel Mendelian randomization method with binary risk factor and outcome.
Genetic Epidemiology.
45:549-560.
2021
|
|
| 2021
|
Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries
2021
|
|
| 2021
|
The copy number variation and stroke (CaNVAS) risk and outcome study.
PLoS One.
16.
2021
|
|
| 2021
|
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (Nature, (2020), 586, 7831, (763-768), 10.1038/s41586-020-2819-2).
Nature.
591:E27.
2021
|
|
| 2021
|
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population.
Frontiers in Genetics.
12.
2021
|
|
| 2021
|
Epigenome-wide association study identifies DNA methylation sites associated with target organ damage in older African Americans.
Epigenetics.
16:862-875.
2021
|
|
| 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
|
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature.
586:763-768.
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
|
A lipidome-wide association study of the lipoprotein insulin resistance index.
Lipids in Health and Disease.
19:153.
2020
|
|
| 2020
|
Genetic Admixture and Survival in Diverse Populations with Pulmonary Arterial Hypertension.
American Journal of Respiratory and Critical Care Medicine.
201:1407-1415.
2020
|
|
| 2020
|
Heme metabolism genes Downregulated in COPD Cachexia.
Respiratory Research.
21.
2020
|
|
| 2020
|
Salivary AMY1 Copy Number Variation Modifies Age-Related Type 2 Diabetes Risk
2020
|
|
| 2020
|
Unraveling the risk factors for spontaneous intracerebral hemorrhage among West Africans.
Neurology.
94:e998-e1012.
2020
|
|
| 2020
|
Erratum: Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection (BMC Infectious Diseases (2019) 19 (1046) DOI: 10.1186/s12879-019-4681-0).
BMC Infectious Diseases.
20.
2020
|
|
| 2020
|
The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders.
PLoS Genetics.
16.
2020
|
|
| 2019
|
Genetic risk of Spontaneous intracerebral hemorrhage: Systematic review and future directions.
Journal of the Neurological Sciences.
407.
2019
|
|
| 2019
|
Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection.
BMC Infectious Diseases.
19.
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
|
Echocardiographic Abnormalities and Determinants of 1-Month Outcome of Stroke Among West Africans in the SIREN Study.
Journal of the American Heart Association.
8.
2019
|
|
| 2019
|
Differential Impact of Risk Factors on Stroke Occurrence Among Men Versus Women in West Africa: The SIREN Study.
Stroke.
50:820-827.
2019
|
|
| 2019
|
Genetic influences on susceptibility to rheumatoid arthritis in African-Americans.
Human Molecular Genetics.
28:858-874.
2019
|
|
| 2019
|
Identification of gene variants associated with melanocyte stem cell differentiation in mice predisposed for hair graying
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
|
A Systematic Scoping Review of Surgically Manipulated Adipose Tissue and the Regulation of Energetics and Body Fat in Animals.
Obesity.
27:1404-1417.
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
|
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
|
Disentangling associations between DNA methylation and blood lipids: A Mendelian randomization approach.
BMC Proceedings.
12.
2018
|
|
| 2018
|
Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population.
Diabetologia.
61:2005-2015.
2018
|
|
| 2018
|
An introduction to Mendelian randomization with applications in neurology.
Multiple Sclerosis and Related Disorders.
24:72-78.
2018
|
|
| 2018
|
Single molecule mtDNA fiber FISH for analyzing numtogenesis.
Analytical Biochemistry.
552:45-49.
2018
|
|
| 2018
|
Biobanking in a Challenging African Environment: Unique Experience from the SIREN Project..
Biopreservation and Biobanking.
16:217-232.
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
|
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
|
|
| 2018
|
Knowledge, attitudes and practices related to stroke in Ghana and Nigeria: A SIREN call to action..
PLoS One.
13:e0206548.
2018
|
|
| 2017
|
Numtogenesis as a mechanism for development of cancer.
Seminars in Cancer Biology.
47:101-109.
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
|
Post-Deepwater Horizon Oil Spill Exposure Patterns among Children in Mobile County, Alabama.
Journal of Occupational and Environmental Medicine.
59:993-999.
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
|
Exploring Overlaps Between the Genomic and Environmental Determinants of LVH and Stroke: A Multicenter Study in West Africa.
Global Heart.
12:107-113.e5.
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
|
Prevalence and Prognostic Features of ECG Abnormalities in Acute Stroke: Findings From the SIREN Study Among Africans.
Global Heart.
12:99-105.
2017
|
|
| 2017
|
Stroke in Indigenous Africans, African Americans, and European Americans: Interplay of Racial and Geographic Factors.
Stroke.
48:1169-1175.
2017
|
|
| 2017
|
Migration of mitochondrial DNA in the nuclear genome of colorectal adenocarcinoma
2017
|
|
| 2017
|
Biomarkers associated with bronchopulmonary dysplasia/mortality in premature infants.
Pediatric Research.
81:519-525.
2017
|
|
| 2017
|
CPT1A methylation is associated with plasma adiponectin
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
|
Polymorphisms in stearoyl coa desaturase and sterol regulatory element binding protein interact with N-3 polyunsaturated fatty acid intake to modify associations with anthropometric variables and metabolic phenotypes in Yup’ik people.
Molecular Nutrition and Food Research.
60:2642-2653.
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
|
Linkage and association analysis of circulating vitamin D and parathyroid hormone identifies novel loci in Alaska native Yup’ik people
2016
|
|
| 2016
|
Training in metabolomics research. II. Processing and statistical analysis of metabolomics data, metabolite identification, pathway analysis, applications of metabolomics and its future.
Journal of Mass Spectrometry.
51:535-548.
2016
|
|
| 2016
|
Training in metabolomics research. II. Processing and statistical analysis of metabolomics data, metabolite identification, pathway analysis, applications of metabolomics and its future.
Journal of Mass Spectrometry.
51:535-548.
2016
|
|
| 2016
|
Neurogenomics in Africa: Perspectives, progress, possibilities and priorities.
Journal of the Neurological Sciences.
366:213-223.
2016
|
|
| 2016
|
Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples
2016
|
|
| 2016
|
Training in metabolomics research. I. Designing the experiment, collecting and extracting samples and generating metabolomics data.
Journal of Mass Spectrometry.
461-475.
2016
|
|
| 2016
|
Training in metabolomics research. I. Designing the experiment, collecting and extracting samples and generating metabolomics data.
Journal of Mass Spectrometry.
51:ii-iii.
2016
|
|
| 2016
|
EM adaptive LASSO-a multilocus modeling strategy for detecting SNPs associated with zero-inflated count phenotypes.
Frontiers in Genetics.
7.
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
|
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
|
Estimation of cell-type composition including T and B cell subtypes for whole blood methylation microarray data.
Frontiers in Genetics.
7.
2016
|
|
| 2016
|
Genetics, diet, and season are associated with serum 25-hydroxycholecalciferol concentration in a Yup'ik study population from southwestern Alaska
2016
|
|
| 2016
|
Multilingual validation of the questionnaire for verifying stroke-free status in West Africa.
Stroke.
47:167-172.
2016
|
|
| 2015
|
Endothelin-1 pathway polymorphisms and outcomes in pulmonary arterial hypertension.
American Journal of Respiratory and Critical Care Medicine.
192:1345-1354.
2015
|
|
| 2015
|
Mitochondrial DNA polymerase POLG1 disease mutations and germline variants promote tumorigenic properties.
PLoS One.
10.
2015
|
|
| 2015
|
Phenotyping Stroke in Sub-Saharan Africa: Stroke Investigative Research and Education Network (SIREN) Phenomics Protocol.
Neuroepidemiology.
45:73-82.
2015
|
|
| 2015
|
Genome-wide association study of triglyceride response to a high-fat meal among participants of the NHLBI Genetics of Lipid Lowering Drugs and Diet Network (GOLDN)
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
|
A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model
2015
|
|
| 2015
|
Epigenome-wide study identifies novel methylation loci associated with body mass index and waist circumference.
Obesity.
23:1493-1501.
2015
|
|
| 2015
|
Variation in genes controlling warfarin disposition and response in American Indian and Alaska Native people: CYP2C9, VKORC1, CYP4F2, CYP4F11, GGCX.
Pharmacogenetics and Genomics.
25:343-353.
2015
|
|
| 2015
|
Linkage and association analysis of obesity traits reveals novel loci and interactions with dietary n-3 fatty acids in an Alaska Native (Yup'ik) population
2015
|
|
| 2015
|
Stroke genomics in people of African ancestry: Charting new paths
2015
|
|
| 2015
|
The burden of stroke in Africa: A glance at the present and a glimpse into the future
2015
|
|
| 2015
|
Associating multivariate quantitative phenotypes with genetic variants in family samples with a novel kernel machine regression method
2015
|
|
| 2015
|
Integrated genomic and BMI analysis for type 2 diabetes risk assessment.
Frontiers in Genetics.
5.
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
|
Longevity and plasticity of CFTR provide an argument for noncanonical SNP organization in hominid DNA.
PLoS One.
9.
2014
|
|
| 2014
|
Genetic risk scores associated with baseline lipoprotein subfraction concentrations do not associate with their responses to fenofibrate.
Biology.
3:536-550.
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
|
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
|
DNA methylation patterns are associated with n-3 fatty acid intake in Yup'ik people
2014
|
|
| 2014
|
Genetic association analysis of 30 genes related to obesity in a European American population.
International Journal of Obesity.
38:724-729.
2014
|
|
| 2014
|
Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.
Genetic Epidemiology.
38:447-456.
2014
|
|
| 2014
|
Methylation at CPT1A locus is associated with lipoprotein subfraction profi les.
Journal of Lipid Research.
55:1324-1330.
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
|
Editorial: Ethnic-specific genetic analyses in rheumatoid arthritis: Incremental gains but valuable contributions to the big picture.
Arthritis and Rheumatism.
65:3014-3016.
2013
|
|
| 2013
|
Evidence for novel genetic loci associated with metabolic traits in Yup'ik people.
American Journal of Human Biology.
25:673-680.
2013
|
|
| 2013
|
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.
Genetic Epidemiology.
37:560-570.
2013
|
|
| 2013
|
Obesity polymorphisms identified in genome-wide association studies interact with n-3 polyunsaturated fatty acid intake and modify the genetic association with adiposity phenotypes in Yup'ik people
2013
|
|
| 2013
|
Risk-stratified imputation in survival analysis.
Clinical Trials.
10:530-539.
2013
|
|
| 2013
|
The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: The GOLDN study
2013
|
|
| 2013
|
A431: Epigenetics of Fasting Insulin and Glucose Concentrations.
Diabetes.
62:A431-A431.
2013
|
|
| 2013
|
Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity.
Human Genetics.
132:405-413.
2013
|
|
| 2013
|
Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network
2013
|
|
| 2013
|
The association between LRP-1 variants and chylomicron uptake after a high fat meal
2013
|
|
| 2012
|
Copy number variations associated with obesity-related traits in African Americans: A joint analysis between GENOA and HyperGEN.
Obesity.
20:2431-2437.
2012
|
|
| 2012
|
The utility of mitochondrial and Y chromosome phylogenetic data to improve correction for population stratification.
Frontiers in Genetics.
3.
2012
|
|
| 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
|
Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs.
Genetic Epidemiology.
36:572-582.
2012
|
|
| 2012
|
Genotype Imputation for African Americans Using Data From HapMap Phase II Versus 1000 Genomes Projects.
Genetic Epidemiology.
36:508-516.
2012
|
|
| 2012
|
Similarity-Based Multimarker Association Tests for Continuous Traits.
Annals of Human Genetics.
76:246-260.
2012
|
|
| 2012
|
The impact of errors in copy number variation detection algorithms on association results.
PLoS One.
7.
2012
|
|
| 2012
|
Association between family risk of stroke and myocardial infarction with prevalent risk factors and coexisting diseases.
Stroke.
43:974-979.
2012
|
|
| 2012
|
Age-related somatic structural changes in the nuclear genome of human blood cells.
American Journal of Human Genetics.
90:217-228.
2012
|
|
| 2012
|
Preliminary evidence for an association between LRP-1 genotype and body mass index in humans.
PLoS One.
7.
2012
|
|
| 2012
|
Response to the Letter 'Efficiency loss due to varying cluster sizes in cluster randomized trials and how to compensate for it: Comment on You et al. (2011)' by van Breukelen and Candel.
Clinical Trials.
9:126-127.
2012
|
|
| 2012
|
A simple distribution-free algorithm for generating simulated high-dimensional correlated data with an autoregressive structure
2012
|
|
| 2012
|
Genetic polymorphisms in carnitine palmitoyltransferase 1A gene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos.
Journal of Lipid Research.
53:175-184.
2012
|
|
| 2012
|
Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.
Pharmacogenetics and Genomics.
22:750-757.
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 clustering analysis of lipoprotein diameters in the metabolic syndrome.
Lipids in Health and Disease.
10.
2011
|
|
| 2011
|
Association of allelic variation in genes mediating aspects of energy homeostasis with weight gain during administration of antipsychotic drugs (CATIE study).
Frontiers in Genetics.
2.
2011
|
|
| 2011
|
Characterization of autosomal copy-number variation in African Americans: The HyperGEN Study.
European Journal of Human Genetics.
19:1271-1275.
2011
|
|
| 2011
|
Dietary carbohydrate modifies the inverse association between saturated fat intake and cholesterol on very low-density lipoproteins.
Lipid Insights.
4:7-15.
2011
|
|
| 2011
|
Grand challenges in statistical genetics/genomics methodology.
Frontiers in Genetics.
2.
2011
|
|
| 2011
|
Imputation of incident events in longitudinal cohort studies.
American Journal of Epidemiology.
174:718-726.
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
|
Lipoprotein Lipase S447X variant associated with VLDL, LDL and HDL diameter clustering in the MetS.
Lipids in Health and Disease.
10.
2011
|
|
| 2011
|
Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families.
Circulation Research.
108:279-283.
2011
|
|
| 2011
|
Relative efficiency and sample size for cluster randomized trials with variable cluster sizes.
Clinical Trials.
8:27-36.
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
|
Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: The HyperGEN study.
BMC Medical Genomics.
4.
2011
|
|
| 2011
|
A Method to Assess Linkage Disequilibrium between CNVs and SNPs Inside Copy Number Variable Regions..
Frontiers in Genetics.
2:17.
2011
|
|
| 2011
|
Accurate and flexible power calculations on the spot: Applications to genomic research.
Statistics and its Interface.
4:353-358.
2011
|
|
| 2011
|
Association of a common LAMA5 variant with anthropometric and metabolic traits in an Italian cohort of healthy elderly subjects.
Experimental Gerontology.
46:60-64.
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
|
|
| 2010
|
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
|
|
| 2010
|
Mixed linear model approach adapted for genome-wide association studies.
Nature Genetics.
42:355-360.
2010
|
|
| 2010
|
Within-Cluster Resampling for Analysis of Family Data: Ready for Prime-Time?.
Statistics and its Interface.
3:169-176.
2010
|
|
| 2010
|
Association test of multiallelic gene copy numbers in family trios.
Genetic Epidemiology.
34:2-6.
2010
|
|
| 2010
|
Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT Study.
Journal of Hypertension.
28:2076-2083.
2010
|
|
| 2009
|
The FCRL3 -169CT promoter single-nucleotide polymorphism, which is associated with systemic lupus erythematosus in a Japanese population, predicts expression of receptor protein on CD19+ B cells.
Arthritis and Rheumatism.
60:3510-3512.
2009
|
|
| 2009
|
A new estimate of family disease history providing improved prediction of disease risks.
Statistics in Medicine.
28:1269-1283.
2009
|
|
| 2009
|
Database mining for selection of SNP markers useful in admixture mapping.
BioData Mining.
2.
2009
|
|
| 2009
|
Multiple imputation to correct for measurement error in admixture estimates in genetic structured association testing
2009
|
|
| 2009
|
The use of plasmodes as a supplement to simulations: A simple example evaluating individual admixture estimation methodologies.
Computational Statistics and Data Analysis.
53:1755-1766.
2009
|
|
| 2009
|
An african ancestry-specific allele of CTLA4 confers protection against rheumatoid arthritis in african americans.
PLoS Genetics.
5.
2009
|
|
| 2009
|
Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations
2009
|
|
| 2009
|
Retraction: an African ancestry-specific allele of CTLA4 confers protection against rheumatoid arthritis in African Americans..
PLoS Genetics.
5.
2009
|
|
| 2008
|
Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles.
American Journal of Human Genetics.
82:763-771.
2008
|
|
| 2008
|
Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principles
2008
|
|
| 2008
|
Statistical issues in the analysis of DNA Copy Number Variations..
International Journal of Computational Biology and Drug Design.
1:368-395.
2008
|
|
| 2007
|
Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes.
Genetic Epidemiology.
31:789-796.
2007
|
|
| 2007
|
Effects of chronic stress and interleukin-10 gene polymorphisms on antibody response to tetanus vaccine in family caregivers of patients with Alzheimer's disease.
Psychosomatic Medicine.
69:551-559.
2007
|
|
| 2007
|
Problems with genome-wide association studies [2].
Science.
316:1840-1841.
2007
|
|
| 2007
|
Detection of gene x gene interactions in genome-wide association studies of human population data
2007
|
|
| 2006
|
Regional admixture mapping and structured association testing: Conceptual unification and an extensible general linear model.
PLoS Genetics.
2:1254-1264.
2006
|
|
| 2006
|
Racial or ethnic differences in allele frequencies of sinqle-nucleotide polymorphisms in the methylenetetrahydrofolate reductase gene and their influence on response to methotrexate in rheumatoid arthritis.
Annals of the Rheumatic Diseases.
65:1213-1218.
2006
|
|
| 2006
|
Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model..
PLoS Genetics.
2.
2006
|
|
| 2006
|
Association of K121Q polymorphism in ENPP1 (PC-1) with BMI in Caucasian and African-American adults.
International Journal of Obesity.
30:233-237.
2006
|
|
| 2005
|
COGA phenotypes and linkages on chromosome 2.
BMC Genomic Data.
6.
2005
|
|
| 2005
|
A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26.
Annals of Neurology.
58:449-458.
2005
|
|
| 2005
|
Is GAD2 on chromosome 10p12 a potential candidate gene for morbid obesity?.
Nutrition Reviews.
63:315-319.
2005
|
|
| 2005
|
New joint covariance- and marginal-based tests for association and linkage for quantitative traits for random and non-random sampling.
Genetic Epidemiology.
28:48-57.
2005
|
|
| 2004
|
The influence of genetic variation in the HLA-DRB1 and LTA-TNF regions on the response to treatment of early rheumatoid arthritis with methotrexate or etanercept.
Arthritis and Rheumatism.
50:2750-2756.
2004
|
|
| 2004
|
Genome scans for human nutritional traits: what have we learned?.
Nutrition.
20:9-13.
2004
|
|
| 2003
|
Do allelic variants of SLC6A14 predispose to obesity?.
Journal of Clinical Investigation.
112:1633-1636.
2003
|
|
| 2003
|
Early rheumatoid arthritis in African-Americans: The CLEAR registry.
Clinical and Experimental Rheumatology.
21.
2003
|
|
| 2003
|
X-linked extension of the revised Haseman-Elston algorithm for linkage analysis in sib pairs
2003
|
|
| 2003
|
Heritability analysis of cytokines as intermediate phenotypes of tuberculosis.
Journal of Infectious Diseases.
187:1679-1685.
2003
|
|
| 2003
|
Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism.
American Journal of Human Genetics.
72:879-890.
2003
|
|
| 2003
|
A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans..
American Journal of Hypertension.
16:151-153.
2003
|
|
| 2003
|
Early rheumatoid arthritis in African-Americans: the CLEAR Registry..
Clinical and Experimental Rheumatology.
21:S138-S145.
2003
|
|
| 2003
|
Familial correlations and heritability of maxillary midline diastema.
American Journal of Orthodontics and Dentofacial Orthopedics.
123:35-39.
2003
|
|
| 2003
|
Structural equation model-based genome scan for the metabolic syndrome..
BMC Genomic Data.
4 Suppl 1.
2003
|
|
| 2002
|
Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations..
American Journal of Human Genetics.
70:1172-1182.
2002
|
|
| 1998
|
Restrictions on components of variance for epistatic models.
Theoretical Population Biology.
54:161-174.
1998
|
|
| 1997
|
Linkage of multilocus components of variance to polymorphic markers..
Annals of Human Genetics.
61:253-261.
1997
|
|
| 1996
|
DNA sequences of Alu elements indicate a recent replacement of the human autosomal genetic complement
1996
|
|
| |
Integration of Multi-Layer Omic Data for Prediction of Disease Risk
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