Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

Caitlin P. McHugh · SciRah

Researcher profile · Semantic Scholar

Caitlin P. McHugh

Share profile

Caitlin P. McHugh — researcher profile on SciRah

h-index: 22
Works: 52
Citations: 2,854

Most-cited papers

Quality control and quality assurance in genotypic data for genome-wide association studies
C. Laurie, K. Doheny, D. Mirel, E. Pugh +21 more
2010Genetic Epidemiology487 citations Open access
Semantic Scholar
Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.
Matthew P. Conomos, C. Laurie, A. Stilp, S. Gogarten +33 more
2016American Journal of Human Genetics314 citations Open access
Semantic Scholar
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
M. H. Kowalski, Huijun Qian, Zi-Yi Hou, Jonathan D. Rosen +74 more
2019bioRxiv244 citations Open access
Semantic Scholar
GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies
S. Gogarten, T. Bhangale, Matthew P. Conomos, C. Laurie +12 more
2012Bioinform.205 citations Open access
Semantic Scholar
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
C. Amos, Li-E Wang, Jeffrey E. Lee, J. Gershenwald +30 more
2011Human Molecular Genetics203 citations Open access
Semantic Scholar
Clonal hematopoiesis and risk of chronic liver disease
Wai-Hay J. Wong, C. Emdin, A. Bick, S. Zekavat +435 more
2023Nature174 citations Open access
Semantic Scholar
Identification of HKDC1 and BACE2 as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies
M. Hayes, M. Urbanek, M. Hivert, Loren L. Armstrong +20 more
2013Diabetes138 citations Open access
Semantic Scholar
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren’s Syndrome According to Ancestry
K. Taylor, Q. Wong, D. Levine, Caitlin P. McHugh +16 more
2017Arthritis & Rheumatology117 citations Open access
Semantic Scholar
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
K. Desch, A. B. Ozel, D. Siemieniak, Yossi Kalish +18 more
2012Proceedings of the National Academy of Sciences of the United States of America101 citations Open access
Semantic Scholar
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program
Alyna T. Khan, S. Gogarten, Caitlin P. McHugh, A. Stilp +12 more
2022Cell Genomics91 citations Open access
Semantic Scholar
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
U. Schick, D. Jain, C. Hodonsky, J. Morrison +34 more
2016American Journal of Human Genetics78 citations Open access
Semantic Scholar
Detectable clonal mosaicism from birth to old age and its relationship to cancer
Cathy C. Laurie, C. Laurie, Kenneth M. Rice, K. Doheny +69 more
2012Nature Genetics76 citations Open access
Semantic Scholar
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
M. Taub, Matthew P. Conomos, Rebecca Keener, K. Iyer +144 more
2022Cell Genomics67 citations Open access
Semantic Scholar
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma
S. Verma, H. V. Gudiseva, V. Chavali, R. Salowe +54 more
2024Cell55 citations Open access
Semantic Scholar
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole-genome sequencing studies
Xi-Hao Li, Corbin Quick, Hufeng Zhou, Sheila M. Gaynor +420 more
2022Nature Genetics55 citations Open access
Semantic Scholar
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
C. Hodonsky, D. Jain, U. Schick, J. Morrison +23 more
2017PLoS Genetics49 citations Open access
Semantic Scholar
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
M. Urbanek, M. Hayes, Loren L. Armstrong, J. Morrison +17 more
2013Human Molecular Genetics44 citations Open access
Semantic Scholar
The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans
B. S. Cole, H. V. Gudiseva, Maxwell Pistilli, R. Salowe +6 more
2021Investigative Ophthalmology and Visual Science32 citations Open access
Semantic Scholar
Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program
Yao Hu, A. Stilp, Caitlin P. McHugh, D. Jain +71 more
2020medRxiv32 citations Open access
Semantic Scholar
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Yao Hu, A. Stilp, Caitlin P. McHugh, Shu-Quan Rao +75 more
2021American Journal of Human Genetics31 citations Open access
Semantic Scholar
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
S. Choi, S. Jurgens, Ling Xiao, M. Hill +496 more
2025Nature Genetics29 citations Open access
Semantic Scholar
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
A. Mikhaylova, Caitlin P. McHugh, L. Polfus, L. Raffield +89 more
2021American Journal of Human Genetics26 citations Open access
Semantic Scholar
Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing
T. Austin, Caitlin P. McHugh, J. Brody, J. Bis +34 more
2022European Journal of Epidemiology22 citations Open access
Semantic Scholar
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies. Diabetes 2013;62:3282–3291
M. Hayes, M. Urbanek, M. Hivert, Loren L. Armstrong +20 more
2013Diabetes20 citations Open access
Semantic Scholar
The pursuit of approaches to federate data to accelerate Alzheimer’s disease and related dementia research: GAAIN, DPUK, and ADDI
A. Toga, M. Phatak, I. Pappas, S. Thompson +5 more
2023Frontiers in Neuroinformatics18 citations Open access
Semantic Scholar
Multi-ethnic genome-wide and HLA association study of total serum IgE
M. Daya, Corey Cox, N. Acevedo, M. Boorgula +43 more
2021Journal of Allergy and Clinical Immunology17 citations Open access
Semantic Scholar
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
M. Wheeler, A. Stilp, Shu-Quan Rao, B. Halldórsson +55 more
2022Nature Communications15 citations Open access
Semantic Scholar
Detecting Heterogeneity in Population Structure Across the Genome in Admixed Populations
Caitlin P. McHugh, L. Brown, T. Thornton
2015Genetics15 citations Open access
Semantic Scholar
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
P. D. de Vries, Matthew P. Conomos, Kuldeep Singh, Christopher J. Nicholson +113 more
2023Nature Cardiovascular Research14 citations Open access
Semantic Scholar
Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative.
Amarise Little, Yao Hu, Quan Sun, D. Jain +63 more
2021Human Molecular Genetics13 citations Open access
Semantic Scholar
Genome wide-association study identifies novel loci in the Primary Open-Angle African American Glaucoma Genetics (POAAGG) study
H. V. Gudiseva, S. Verma, V. Chavali, R. Salowe +27 more
2020bioRxiv12 citations Open access
Semantic Scholar
Evaluating the harmonisation potential of diverse cohort datasets
S. Bauermeister, M. Phatak, K. Sparks, Lana Sargent +10 more
2023European Journal of Epidemiology11 citations Open access
Semantic Scholar
1.0 USING FAMILY DATA AS A STANDARD TO EVALUATE COPY NUMBER VARIATION CALLING STRATEGIES FOR GENETIC ASSOCIATION STUDIES
Xiaojing Zheng, John R. Shaffer, Caitlin P. McHugh, Cathy C. Laurie +5 more
2012Genetic Epidemiology11 citations Open access
Semantic Scholar
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xi-Hao Li, Han Chen, M. Selvaraj, Eric Van Buren +438 more
2025Nature Computational Science8 citations Open access
Semantic Scholar
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: experiences from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program
Alyna T. Khan, S. Gogarten, Caitlin P. McHugh, A. Stilp +12 more
20218 citations
Semantic Scholar
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Xin-Ruo Zhang, J. Brody, M. Graff, H. Highland +122 more
2025Nature Communications5 citations Open access
Semantic Scholar
Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program
M. Wheeler, A. Stilp, Shu-Quan Rao, B. Halldórsson +55 more
2021medRxiv5 citations Open access
Semantic Scholar
Guidelines on the use and reporting of race, ethnicity, and ancestry in the NHLBI Trans-Omics for Precision Medicine (TOPMed) program
Alyna T. Khan, Caitlin P. McHugh, Matthew P. Conomos, S. Gogarten +1 more
20205 citations
Semantic Scholar
Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed
M. Taub, Matthew P. Conomos, Rebecca Keener, K. Iyer +144 more
2019bioRxiv5 citations Open access
Semantic Scholar
The chromosome 3 q 25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study
M. Urbanek, M. Hayes, Loren L. Armstrong, J. Morrison +17 more
20135 citations
Semantic Scholar
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE
Xin-Ruo Zhang, J. Brody, M. Graff, H. Highland +118 more
2023medRxiv4 citations Open access
Semantic Scholar
Author Correction: Clonal haematopoiesis and risk of chronic liver disease
Wai-Hay J. Wong, C. Emdin, A. Bick, S. Zekavat +435 more
2023Nature2 citations Open access
Semantic Scholar
Statistical Methods for the Analysis of Autosomal and X Chromosome Genetic Data in Samples with Unknown Structure
Caitlin P. McHugh
20161 citations
Semantic Scholar
with measures of adiposity in newborns in a multi-ethnic genome-wide association study
M. Urbanek, M. Hayes, Loren L. Armstrong, J. Morrison +17 more
20131 citations
Semantic Scholar
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed.
Peter Orchard, T. Blackwell, L. Kachuri, Peter J. Castaldi +281 more
2026Science0 citations Open access
Semantic Scholar
Closing the gap in Alzheimer’s disease research through the Sex | Gender in Neurodegeneration Consortium
Caitlin P. McHugh, Rachel F. Buckley, M. Clement, T. Hohman +4 more
2026Nature Aging0 citations
Semantic Scholar
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
A. Bick, J. Weinstock, Satish K. Nandakumar, Charles P. Fulco +411 more
2021Nature0 citations Open access
Semantic Scholar
find-tfbs: a tool to identify functional non-coding variants associated with complex human traits using open chromatin maps and phased whole-genome sequences
Sébastian Méric de Bellefon, F. Thibord, P. Auer, J. Blangero +12 more
2020bioRxiv0 citations Open access
Semantic Scholar
Combining SNP P-Values in Gene Sets: the cpvSNP Package
Caitlin P. McHugh, J. Hackney, Jessica, L. Larson
20160 citations
Semantic Scholar
When the shear modulus approaches zero: Fluids don’t bend and Scholte leaves the room
R. Odom, Donna Sylvester, Caitlin P. McHugh
20060 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Matthew P. Conomos×24
Invite
Matthew P. Conomos — researcher profile on SciRah
D. Jain×19
Invite
D. Jain — researcher profile on SciRah
C. Laurie×18
Invite
C. Laurie — researcher profile on SciRah
A. Stilp×17
Invite
A. Stilp — researcher profile on SciRah

×17

Invite

M. Fornage — researcher profile on SciRah

Invite

R. Mathias — researcher profile on SciRah

Invite

L. Yanek — researcher profile on SciRah

Invite

C. Laurie — researcher profile on SciRah

S. Gogarten×16

Invite

S. Gogarten — researcher profile on SciRah

Invite

R. Loos — researcher profile on SciRah

Invite

J. Brody — researcher profile on SciRah

Invite

A. Reiner — researcher profile on SciRah