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Author Details

Jennifer Wessel
2004
55
27
PMIDPaper TitleJournal TitlePublished Year
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
31651603Barriers to Weight Management Among Overweight and Obese Firefighters.2020
31118516Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.Nature2019
31564435Impact 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 Genet2019
30468781Maternal lipid profile differs by gestational diabetes physiologic subtype.Metabolism: Clinical and Experimental2019
30806820The Continuing Evolution of Precision Health in Type 2 Diabetes: Achievements and Challenges.Current Diabetes Reports2019
31160809Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2019
29273807Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
30421827Excess mortality among Indiana firefighters, 1985-2013.American Journal of Industrial Medicine2018
29549330Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
29549329Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
29326538Type 2 Diabetes Genetic Risk Scores Are Associated With Increased Type 2 Diabetes Risk Among African Americans by Cardiometabolic Status.Clin Med Insights Endocrinol Diabetes2018
29632382Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nat Genet2018
28146470Rare and low-frequency coding variants alter human adult height.Nature2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
28934312Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya.PLoS One2017
28784624Methodological Standards for Meta-Analyses and Qualitative Systematic Reviews of Cardiac Prevention and Treatment Studies: A Scientific Statement From the American Heart Association.Circulation2017
29083408Exome-wide association study of plasma lipids in &gt;300,000 individuals.Nat Genet2017
27920155<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.J Am Soc Nephrol2017
26822414A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans.BMC Endocr Disord2016
27252175A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease.Sci Transl Med2016
26884607Do Genes Determine Our Health? Implications for Designing Lifestyle Interventions and Drug Trials.Circulation: Cardiovascular Genetics2016
26789839Factors Motivating Individuals to Consider Genetic Testing for Type 2 Diabetes Risk Prediction.PLoS One2016
26385028Genetic 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 J2015
25631608Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.Nat Commun2015
24648440Genetic Testing and Type 2 Diabetes Risk Awareness.Diabetes Educator2014
21606948Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes.Pharmacogenomics J2012
22832964Genome-wide meta-analyses of smoking behaviors in African Americans.Transl Psychiatry2012
21493754Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits.J Pharmacol Exp Ther2011
22506313Environmental and genetic contributions to indicators of oral malodor in twins.Twin Res Hum Genet2011
20571875Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension.Cell Mol Neurobiol2010
21217814Presymptomatic risk assessment for chronic non-communicable diseases.PLoS One2010
20736995Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence.Neuropsychopharmacology2010
19959688Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample.Cancer Epidemiol Biomarkers Prev2009
19671882Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.J Pharmacol Exp Ther2009
20031608CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response.Circ Cardiovasc Genet2009
18163383Evidence for a heritable unidimensional symptom factor underlying obsessionality.Am J Med Genet B Neuropsychiatr Genet2008
19120120Adrenergic polymorphism and the human stress response.Ann N Y Acad Sci2008
18328234Inheritance of occlusal topography: a twin study.Eur Arch Paediatr Dent2008
18358322DNA sequence-based phenotypic association analysis.Adv Genet2008
18179393Heritability of oral microbial species in caries-active and caries-free twins.Twin Res Hum Genet2007
17698732Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo.Circulation2007
17211240C-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 Hypertens2007
17549743Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes.Genet Epidemiol2007
17584765An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension.Hum Mol Genet2007
17496725Single nucleotide polymorphism discovery and haplotype analysis of Ca2+-dependent K+ channel beta-1 subunit.Pharmacogenet Genomics2007
17353515Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism.Hypertension2007
17493783Accommodating pathway information in expression quantitative trait locus analysis.Genomics2007
17290446Heritability and clinical features of multigenerational families with obsessive-compulsive disorder and hoarding.Am J Med Genet B Neuropsychiatr Genet2007
17717598Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.J Clin Invest2007
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