Author details

Full Name

Lauren E Petty

Affiliation

ORCID

Career Start Year

2015

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37499862	Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis.	J Endod	2023
36413071	IMMerge: merging imputation data at scale.	Bioinformatics	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36718543	Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study.	Ann N Y Acad Sci	2023
37148359	The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.	Diabetologia	2023
35157052	Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.	Hum Mol Genet	2022
35393509	Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.	Commun Biol	2022
35513483	Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.	Commun Biol	2022
36088317	Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.	BMC Med Genomics	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35477306	Gut Microbiome Alterations Associated with Diabetes in Mexican Americans in South Texas.	mSystems	2022
36386790	Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease.	Frontiers in Genetics	2022
34633706	Gut microbiome features associated with liver fibrosis in Hispanics, a population at high risk for fatty liver disease.	Hepatology	2022
34788810	Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.	Hum Mol Genet	2022
35147171	Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate.	Hum Mol Genet	2022
34873149	Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci.	Transl Psychiatry	2021
34165540	Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.	Hum Mol Genet	2021
33894541	Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier.	J Fluency Disord	2021
33357513	Host genetic effects in pneumonia.	Am J Hum Genet	2021
33386679	Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta).	Mol Ecol Resour	2021
35047858	Population-based genetic effects for developmental stuttering.	HGG Adv	2021
34861174	Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering.	American Journal of Human Genetics	2021
34604815	Genetic discovery and risk characterization in type 2 diabetes across diverse populations.	HGG Adv	2021
32873181	Optimizing Genetic Analyses of Serum Lipids in Longitudinal Data.	Circ Res	2020
31692161	A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders.	Hum Mutat	2020
32226016	Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.	PLoS Genet	2020
32496918	Importance of Genetic Studies of Cardiometabolic Disease in Diverse Populations.	Circ Res	2020
31251759	GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.	PLoS One	2019
33312764	GWAS and Beyond: Using Omics Approaches to Interpret SNP Associations.	Curr Genet Med Rep	2019
30624610	Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.	Hum Mol Genet	2019
29629410	Expanding the global prevalence of spinocerebellar ataxia type 42.	Neurol Genet	2018
28813618	Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.	J Dent Res	2018
30297969	Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.	Nat Genet	2018
30046887	Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis.	Hum Genet	2018
28245265	Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.	PLoS One	2017
28761930	Prevalence of spinocerebellar ataxia 36 in a US population.	Neurol Genet	2017
29213071	GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.	Sci Rep	2017
27798093	Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.	Hum Mol Genet	2016
26569114	Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.	PLoS One	2015