| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 31651603 | Barriers to Weight Management Among Overweight and Obese Firefighters. | | 2020 |
| 31118516 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. | Nature | 2019 |
| 31564435 | Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. | Am J Hum Genet | 2019 |
| 30468781 | Maternal lipid profile differs by gestational diabetes physiologic subtype. | Metabolism: Clinical and Experimental | 2019 |
| 30806820 | The Continuing Evolution of Precision Health in Type 2 Diabetes: Achievements and Challenges. | Current Diabetes Reports | 2019 |
| 31160809 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2019 |
| 29273807 | Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 30421827 | Excess mortality among Indiana firefighters, 1985-2013. | American Journal of Industrial Medicine | 2018 |
| 29549330 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29549329 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29326538 | Type 2 Diabetes Genetic Risk Scores Are Associated With Increased Type 2 Diabetes Risk Among African Americans by Cardiometabolic Status. | Clin Med Insights Endocrinol Diabetes | 2018 |
| 29632382 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. | Nat Genet | 2018 |
| 28146470 | Rare and low-frequency coding variants alter human adult height. | Nature | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 28934312 | Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya. | PLoS One | 2017 |
| 28784624 | Methodological Standards for Meta-Analyses and Qualitative Systematic Reviews of Cardiac Prevention and Treatment Studies: A Scientific Statement From the American Heart Association. | Circulation | 2017 |
| 29083408 | Exome-wide association study of plasma lipids in >300,000 individuals. | Nat Genet | 2017 |
| 27920155 | <i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. | J Am Soc Nephrol | 2017 |
| 26822414 | A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans. | BMC Endocr Disord | 2016 |
| 27252175 | A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease. | Sci Transl Med | 2016 |
| 26884607 | Do Genes Determine Our Health? Implications for Designing Lifestyle Interventions and Drug Trials. | Circulation: Cardiovascular Genetics | 2016 |
| 26789839 | Factors Motivating Individuals to Consider Genetic Testing for Type 2 Diabetes Risk Prediction. | PLoS One | 2016 |
| 26385028 | Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL). | Am Heart J | 2015 |
| 25631608 | Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. | Nat Commun | 2015 |
| 24648440 | Genetic Testing and Type 2 Diabetes Risk Awareness. | Diabetes Educator | 2014 |
| 21606948 | Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes. | Pharmacogenomics J | 2012 |
| 22832964 | Genome-wide meta-analyses of smoking behaviors in African Americans. | Transl Psychiatry | 2012 |
| 21493754 | Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits. | J Pharmacol Exp Ther | 2011 |
| 22506313 | Environmental and genetic contributions to indicators of oral malodor in twins. | Twin Res Hum Genet | 2011 |
| 20571875 | Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension. | Cell Mol Neurobiol | 2010 |
| 21217814 | Presymptomatic risk assessment for chronic non-communicable diseases. | PLoS One | 2010 |
| 20736995 | Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence. | Neuropsychopharmacology | 2010 |
| 19959688 | Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample. | Cancer Epidemiol Biomarkers Prev | 2009 |
| 19671882 | Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs. | J Pharmacol Exp Ther | 2009 |
| 20031608 | CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response. | Circ Cardiovasc Genet | 2009 |
| 18163383 | Evidence for a heritable unidimensional symptom factor underlying obsessionality. | Am J Med Genet B Neuropsychiatr Genet | 2008 |
| 19120120 | Adrenergic polymorphism and the human stress response. | Ann N Y Acad Sci | 2008 |
| 18328234 | Inheritance of occlusal topography: a twin study. | Eur Arch Paediatr Dent | 2008 |
| 18358322 | DNA sequence-based phenotypic association analysis. | Adv Genet | 2008 |
| 18179393 | Heritability of oral microbial species in caries-active and caries-free twins. | Twin Res Hum Genet | 2007 |
| 17698732 | Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo. | Circulation | 2007 |
| 17211240 | C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway loci. | J Hypertens | 2007 |
| 17549743 | Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes. | Genet Epidemiol | 2007 |
| 17584765 | An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension. | Hum Mol Genet | 2007 |
| 17496725 | Single nucleotide polymorphism discovery and haplotype analysis of Ca2+-dependent K+ channel beta-1 subunit. | Pharmacogenet Genomics | 2007 |
| 17353515 | Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism. | Hypertension | 2007 |
| 17493783 | Accommodating pathway information in expression quantitative trait locus analysis. | Genomics | 2007 |
| 17290446 | Heritability and clinical features of multigenerational families with obsessive-compulsive disorder and hoarding. | Am J Med Genet B Neuropsychiatr Genet | 2007 |
| 17717598 | Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk. | J Clin Invest | 2007 |