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Jennifer A. Smith

Researcher at University of Michigan

Publications -  977
Citations -  94283

Jennifer A. Smith is an academic researcher from University of Michigan. The author has contributed to research in topics: Large Hadron Collider & Standard Model. The author has an hindex of 131, co-authored 862 publications receiving 83025 citations. Previous affiliations of Jennifer A. Smith include National Institutes of Health & Imperial College London.

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Set-Based Tests for the Gene-Environment Interaction in Longitudinal Studies.

TL;DR: A generalized score type test for set-based inference for the gene–environment interaction with longitudinally measured quantitative traits is proposed that is robust to misspecification of within subject correlation structure and has enhanced power compared to existing alternatives.
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Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Margaret A. Taub, +146 more
- 01 Jan 2022 - 
TL;DR: This article reported the first sequencing-based association study for TL across ancestrally-diverse individuals (European, African, Asian and Hispanic/Latino) from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program.

Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Paul S. de Vries, +265 more
TL;DR: A person's lipid profile is influenced by genetic variants and alcohol consumption, but the contribution of interactions between these exposures has not been studied, so gene-alcohol interactions are incorporated into a multiancestry genome-wide association study of levels of high-density lipoprotein cholesterol, low-density cholesterol, and triglycerides.
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Search for the standard model Higgs boson in the H → ZZ → ℓ+ℓ - τ +τ - decay channel in pp collisions at √s = 7 TeV

S. Chatrchyan, +2320 more
TL;DR: In this paper, a search for the standard model Higgs boson in the decay mode H to ZZ to tau plus lepton pairs, where the leptons are either electrons or muons, in proton-proton collisions at sqrt(s)=7 TeV, corresponding to an integrated luminosity of 4.7 inverse femtobarn collected with the CMS detector at the LHC.
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The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region

TL;DR: The results suggest that the effect of risk variants in the Chr9p21 region on susceptibility to CAD is likely to be mediated through both cis and trans mechanisms.