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List of works by Jennifer Wessel

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Rare and low-frequency coding variants alter human adult height

scientific article (publication date: February 2017)
Exome-wide association study of plasma lipids in >300,000 individuals

scientific article published on 30 October 2017
Generalized genomic distance-based regression methodology for multilocus association analysis

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

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

scientific article published on 22 December 2017
Genome-wide meta-analyses of smoking behaviors in African Americans

scientific article
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

scientific article published on 9 April 2018
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 pathw

scientific article published in February 2007
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk

scientific article
Rho kinase polymorphism influences blood pressure and systemic vascular resistance in human twins: role of heredity

scientific article published on 3 April 2006
Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins

scientific article published on 14 September 2004
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo

scientific article published on 13 August 2007
Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence

scientific article
A comprehensive literature review of haplotyping software and methods for use with unrelated individuals

scientific article
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

scientific article published on June 2016
Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism.

scientific article published on 12 March 2007
Heritability and clinical features of multigenerational families with obsessive-compulsive disorder and hoarding

scientific article published in March 2007
Heritability of oral microbial species in caries-active and caries-free twins

scientific article
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
Replication of the association between the thrombospondin-4 A387P polymorphism and myocardial infarction

scientific article published in May 2004
CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response

scientific article published on 03 June 2009
Methodological Standards for Meta-Analyses and Qualitative Systematic Reviews of Cardiac Prevention and Treatment Studies: A Scientific Statement From the American Heart Association

scientific article published on 07 August 2017
DNA sequence-based phenotypic association analysis

scientific article published in January 2008
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

scientific article published on 24 March 2017
Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits

scientific article
Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes.

scientific article
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension

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

article
Accommodating pathway information in expression quantitative trait locus analysis

scientific article published on 9 May 2007
Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample

scientific article
Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension

scientific article
Evidence for a heritable unidimensional symptom factor underlying obsessionality

scientific article published in September 2008
Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs

scientific article published on 11 August 2009
Presymptomatic risk assessment for chronic non-communicable diseases

scientific article (publication date: 31 December 2010)
Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes

scientific article published in November 2007
Adrenergic polymorphism and the human stress response

scientific article published on December 2008
Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)

scientific article
Type 2 Diabetes Genetic Risk Scores Are Associated With Increased Type 2 Diabetes Risk Among African Americans by Cardiometabolic Status

scientific article published on 3 January 2018
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 16 March 2018
Single nucleotide polymorphism discovery and haplotype analysis of Ca2+-dependent K+ channel beta-1 subunit

scientific article published on April 2007
A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans

scientific article published on 28 January 2016
Maternal lipid profile differs by gestational diabetes physiologic subtype

article
Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya

scientific article published on 21 September 2017
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

scientific article published on 26 September 2019
Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article
Factors Motivating Individuals to Consider Genetic Testing for Type 2 Diabetes Risk Prediction

scientific article published on 20 January 2016
Genetic Testing for Type 2 Diabetes in High-Risk Children: the Case for Primordial Prevention

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

scientific article
Genetic Testing and Type 2 Diabetes Risk Awareness

scientific article published on March 19, 2014
The Continuing Evolution of Precision Health in Type 2 Diabetes: Achievements and Challenges

scientific article published on 26 February 2019

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