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Authors whose works are in public domain in at least one jurisdiction

List of works by Jennifer Wessel

1-50 of 59 results

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