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L. Petty · SciRah

Researcher profile · Semantic Scholar

L. Petty

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L. Petty — researcher profile on SciRah

h-index: 21
Works: 55
Citations: 3,337

Most-cited papers

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
A. Mahajan, D. Taliun, Matthias Thurner, N. Robertson +111 more
2018Nature Genetics1,497 citations Open access
Semantic Scholar
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
A. Mahajan, C. Spracklen, Wei-Hua Zhang, M. Ng +345 more
2022Nature Genetics616 citations Open access
Semantic Scholar
Identification of type 2 diabetes loci in 433,540 East Asian individuals
C. Spracklen, M. Horikoshi, Y. J. Kim, Kuang Lin +108 more
2020Nature401 citations Open access
Semantic Scholar
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders
K. Ngo, Jessica E. Rexach, Ha-Ne Lee, L. Petty +22 more
2019Human Mutation80 citations Open access
Semantic Scholar
Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis
N. Dinçkan, R. Du, L. Petty, Z. Coban-Akdemir +14 more
2018Journal of dentistry research59 citations Open access
Semantic Scholar
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
M. Loh, Wei-Hua Zhang, H. Ng, Katharina T. Schmid +43 more
2022Communications Biology57 citations Open access
Semantic Scholar
Genetic discovery and risk characterization in type 2 diabetes across diverse populations
L. Polfus, B. Darst, H. Highland, Xin Sheng +50 more
2021HGG advances42 citations Open access
Semantic Scholar
Gut Microbiome Alterations Associated with Diabetes in Mexican Americans in South Texas
Suet-Ying Kwan, Caroline M. Sabotta, Aron Y. Joon, P. Wei +9 more
2022mSystems34 citations Open access
Semantic Scholar
Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier
Dillon G. Pruett, D. Shaw, Hung-Hsin Chen, L. Petty +4 more
2021Journal of Fluency Disorders32 citations Open access
Semantic Scholar
Population-based genetic effects for developmental stuttering
Hannah G. Polikowsky, D. Shaw, L. Petty, Hung-Hsin Chen +11 more
2021HGG advances29 citations Open access
Semantic Scholar
Genetically regulated expression in late-onset Alzheimer’s disease implicates risk genes within known and novel loci
Hung-Hsin Chen, L. Petty, Jin Sha, Yi Zhao +6 more
2021Translational Psychiatry28 citations Open access
Semantic Scholar
Host genetic effects in pneumonia
Hung-Hsin Chen, D. Shaw, L. Petty, M. Graff +14 more
2020American Journal of Human Genetics28 citations Open access
Semantic Scholar
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications
Ken Suzuki, K. Hatzikotoulas, L. Southam, H. Taylor +347 more
2023medRxiv27 citations Open access
Semantic Scholar
Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering
D. Shaw, Hannah P. Polikowsky, Dillon G. Pruett, Hung-Hsin Chen +6 more
2021American Journal of Human Genetics27 citations Open access
Semantic Scholar
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study
Yao Hu, M. Graff, J. Haessler, S. Buyske +49 more
2020PLoS Genetics26 citations Open access
Semantic Scholar
Importance of Genetic Studies of Cardiometabolic Disease in Diverse Populations
L. Fernández-Rhodes, Kristin L. Young, Adam G. Lilly, L. Raffield +10 more
2020Circulation Research26 citations Open access
Semantic Scholar
Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis
R. Du, N. Dinçkan, Xiao-Fei Song, Z. Coban-Akdemir +14 more
2018Human Genetics26 citations Open access
Semantic Scholar
Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.
He-Ming Wang, B. Cade, Han Chen, Kevin J. Gleason +19 more
2016Human Molecular Genetics25 citations Open access
Semantic Scholar
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Raúl Méndez-Giráldez, S. Gogarten, J. Below, Jie Yao +21 more
2017Scientific Reports24 citations Open access
Semantic Scholar
Prevalence of spinocerebellar ataxia 36 in a US population
Juliana M. Valera, T. Diaz, L. Petty, B. Quintáns +12 more
2017Neurology: Genetics22 citations Open access
Semantic Scholar
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
E. Parra, Andrew Mazurek, C. Gignoux, Alexandra Sockell +8 more
2017PLoS ONE21 citations Open access
Semantic Scholar
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas
E. Brown, J. Below, R. Fischer, H. T. Essigmann +7 more
2015PLoS ONE21 citations Open access
Semantic Scholar
Polygenic risk impacts PDGFRA mutation penetrance in nonsyndromic cleft lip and palate.
Yao Yu, Rolando Alvarado, L. Petty, Ryan J Bohlender +10 more
2022Human Molecular Genetics19 citations Open access
Semantic Scholar
A Genome-Wide Association Study Identifies Blood Disorder–Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos
Jee-Young Moon, T. Louie, D. Jain, T. Sofer +21 more
2019Diabetes Care18 citations Open access
Semantic Scholar
Identification of type 2 diabetes loci in 433,540 East Asian individuals
C. Spracklen, M. Horikoshi, Y. J. Kim, Kuang Lin +107 more
2019bioRxiv18 citations Open access
Semantic Scholar
Expanding the global prevalence of spinocerebellar ataxia type 42
K. Ngo, Mamdouh Aker, L. Petty, Jason A. Chen +11 more
2018Neurology: Genetics17 citations Open access
Semantic Scholar
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes
A. Huerta-Chagoya, Philip H. Schroeder, R. Mandla, A. Deutsch +60 more
2022Diabetologia16 citations Open access
Semantic Scholar
Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease
Caroline M. Sabotta, Suet-Ying Kwan, L. Petty, J. Below +5 more
2022Frontiers in Genetics12 citations Open access
Semantic Scholar
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
Brenton R. Swenson, T. Louie, Henry J. Lin, Raúl Méndez-Giráldez +26 more
2018bioRxiv12 citations Open access
Semantic Scholar
Genome-wide association study identifies novel risk loci for apical periodontitis.
L. Petty, R. Silva, L. C. de Souza, A. Vieira +3 more
2023Journal of Endodontics11 citations Open access
Semantic Scholar
Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL
A. Justice, K. Young, S. Gogarten, T. Sofer +29 more
2021medRxiv11 citations Open access
Semantic Scholar
Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.
Andy Castañeda, L. Petty, M. Scholz, R. Jansen +43 more
2021Human Molecular Genetics10 citations Open access
Semantic Scholar
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample
L. Petty, H. Highland, E. Gamazon, Hao Hu +21 more
2019Human Molecular Genetics10 citations Open access
Semantic Scholar
Multiomics reveal key inflammatory drivers of severe obesity: IL4R, LILRA5, and OSM
Hung-Hsin Chen, H. Highland, Elizabeth G. Frankel, Alyssa C. Scartozzi +35 more
2025Cell Genomics8 citations Open access
Semantic Scholar
GWAS and Beyond: Using Omics Approaches to Interpret SNP Associations
Hung-Hsin Chen, L. Petty, W. Bush, A. Naj +1 more
2019Current Genetic Medicine Reports6 citations Open access
Semantic Scholar
IMMerge: merging imputation data at scale
Wan-Ying Zhu, Hung-Hsin Chen, Alexander S. Petty, L. Petty +4 more
2022Bioinform.5 citations Open access
Semantic Scholar
Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes
Hung-Hsin Chen, L. Petty, K. North, J. McCormick +3 more
2022Human Molecular Genetics4 citations Open access
Semantic Scholar
[O1–03–01]: GENOME‐WIDE RARE VARIANT IMPUTATION AND TISSUE‐SPECIFIC TRANSCRIPTOMIC ANALYSIS IDENTIFY NOVEL RARE VARIANT CANDIDATE LOCI IN LATE‐ONSET ALZHEIMER's DISEASE: THE ALZHEIMER's DISEASE GENETICS CONSORTIUM
A. Naj, J. Below, Yi Zhao, Hung-Hsin Chen +15 more
20174 citations
Semantic Scholar
Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations
M. Anwar, Antoine R. Baldassari, Hannah G. Polikowsky, C. Sitlani +21 more
2022BMC Medical Genomics3 citations Open access
Semantic Scholar
Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations
M. Anwar, Antoine R. Baldassari, Hannah G. Polikowsky, C. Sitlani +21 more
2022BMC Medical Genomics3 citations Open access
Semantic Scholar
Optimizing Genetic Analyses of Serum Lipids in Longitudinal Data
Hung-Hsin Chen, L. Petty, E. Gamazon, Quinn S. Wells +1 more
2020Circulation Research2 citations Open access
Semantic Scholar
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries
A. Huerta-Chagoya, Joohyun Kim, R. Mandla, Ying-Chang Lu +32 more
2026The Lancet Diabetes and Endocrinology1 citations Open access
Semantic Scholar
COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstruction
Grahame F. Evans, James T. Baker, L. Petty, Alexander S. Petty +14 more
2025American Journal of Human Genetics1 citations Open access
Semantic Scholar
Tissue‐specific genetically regulated expression in late‐onset Alzheimer’s disease implicates risk genes within known and 30 novel loci
Hung-Hsin Chen, L. Petty, Bommi Lee, Jin Sha +5 more
2020Alzheimer's & Dementia1 citations Open access
Semantic Scholar
241-LB: Identification of Novel and Population-Specific Signals for Type 2 Diabetes in Large-Scale Study of Hispanic/Latino Individuals
L. Petty, J. Below
2019Diabetes1 citations
Semantic Scholar
Type 2 diabetes genetics in 125,000 admixed adults from Mexico City
J. M. Torres, J. Berumen, D. Aguilar-Ramírez, E. Trichia +33 more
2026medRxiv0 citations Open access
Semantic Scholar
74-OR: Improving Performance of Type 2 Diabetes Polygenic Scores in African and Hispanic Ancestries
Alicia Huerta, Joohyun Kim, R. Mandla, Ying-Chang Lu +17 more
2023Diabetes0 citations
Semantic Scholar
Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
M. Loh, Wei-Hua Zhang, H. Ng, Katharina T. Schmid +43 more
2022Communications Biology0 citations Open access
Semantic Scholar
Abstract 13286: Finding the Missing Heritability of Serum Lipids: Leveraging the Relatedness in a Large-scale Biobank
Hung-Hsin Chen, Ryan J Bohlender, L. Petty, Quinn S. Wells +2 more
2020Circulation0 citations
Semantic Scholar
A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders (2006)
K. Ngo, Jessica Rexach, Hane Lee, L. Petty +22 more
2020Neurology0 citations Open access
Semantic Scholar

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