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J. LeFaive · SciRah

Researcher profile · Semantic Scholar

J. LeFaive

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J. LeFaive — researcher profile on SciRah

h-index: 15
Works: 32
Citations: 4,133

Most-cited papers

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D. Taliun, Daniel N. Harris, M. D. Kessler, Jedidiah Carlson +185 more
2019Nature2,049 citations Open access
Semantic Scholar
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Wei Zhou, J. Nielsen, Lars G. Fritsche, Rounak Dey +15 more
2017Nature Genetics1,284 citations Open access
Semantic Scholar
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts
Wei Zhou, Zhangchen Zhao, J. Nielsen, Lars G. Fritsche +10 more
2019Nature Genetics204 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
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
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
J. Nielsen, O. Rom, I. Surakka, Sarah E. Graham +103 more
2020Nature Communications53 citations Open access
Semantic Scholar
Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease
S. Sakaue, Saisriram Gurajala, Michelle Curtis, Yang Luo +15 more
2023Nature Protocols39 citations Open access
Semantic Scholar
Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels.
K. Yu, Sayantani Das, J. LeFaive, Alan M. Kwong +6 more
2022American Journal of Human Genetics38 citations Open access
Semantic Scholar
Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb
Lars G. Fritsche, Lauren J. Beesley, P. VandeHaar, Robert B Peng +14 more
2018bioRxiv31 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
FixItFelix: improving genomic analysis by fixing reference errors
S. Behera, J. LeFaive, P. Orchard, M. Mahmoud +8 more
2023Genome Biology27 citations Open access
Semantic Scholar
Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.
Sarah C. Hanks, L. Forer, Sebastian Schönherr, J. LeFaive +16 more
2022American Journal of Human Genetics26 citations Open access
Semantic Scholar
Insights from a Large-Scale Whole Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension
T. Kelly, Xiao Sun, Karen Y. He, Michael R. Brown +101 more
2022HYPERTENSION25 citations Open access
Semantic Scholar
Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries
Alan M. Kwong, T. Blackwell, J. LeFaive, M. de Andrade +42 more
2020bioRxiv20 citations Open access
Semantic Scholar
The phenotype-genotype reference map: Improving biobank data science through replication
L. Bastarache, Sarah Delozier, A. Pandit, Jing He +9 more
2022bioRxiv17 citations Open access
Semantic Scholar
Sparse allele vectors and the savvy software suite
J. LeFaive, A. Smith, H. Kang, G. Abecasis
2021Bioinform.13 citations Open access
Semantic Scholar
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers
L. Forer, D. Taliun, J. LeFaive, Albert V. Smith +6 more
2024Nucleic Acids Research12 citations Open access
Semantic Scholar
Telomere length is not a main factor for the development of islet autoimmunity and type 1 diabetes in the TEDDY study
C. Törn, Xiang Liu, S. Onengut-Gumuscu, Kevin Counts +237 more
2021Scientific Reports12 citations Open access
Semantic Scholar
Genome-wide association study of cardiac troponin I in the general population
M. R. Moksnes, H. Røsjø, A. Richmond, M. Lyngbakken +26 more
2021Human Molecular Genetics11 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
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
S. Zekavat, S. Ruotsalainen, R. Handsaker, M. Alver +339 more
2018Nature Communications7 citations Open access
Semantic Scholar
False discovery rates for genome-wide association tests in biobanks with thousands of phenotypes
Aubrey C. Annis, A. Pandit, J. LeFaive, S. G. Gagliano Taliun +6 more
20216 citations Open access
Semantic Scholar
A statistical genetics guide to identifying HLA alleles driving complex disease
S. Sakaue, Saisriram Gurajala, Michelle Curtis, Yang Luo +14 more
2022bioRxiv4 citations Open access
Semantic Scholar
Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease
J. Nielsen, O. Rom, I. Surakka, Sarah E. Graham +98 more
2019bioRxiv4 citations Open access
Semantic Scholar
Fixing reference errors efficiently improves sequencing results
S. Behera, J. LeFaive, P. Orchard, M. Mahmoud +8 more
2022bioRxiv3 citations Open access
Semantic Scholar
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Run-Jia Li, S. G. Gagliano Taliun, Kevin Liao, M. Flickinger +44 more
2024medRxiv2 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
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
B. Cade, Jiwon Lee, T. Sofer, He-Ming Wang +390 more
2021Genome Medicine2 citations Open access
Semantic Scholar
MethylModes: computationally efficient detection of multimodal distributions in DNA methylation data
T. Luo, J. LeFaive, J. Dou, K. Bakulski +2 more
2026Bioinform.0 citations
Semantic Scholar
Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Run-Jia Li, S. G. Gagliano Taliun, Kevin Liao, M. Flickinger +45 more
2025HGG advances0 citations Open access
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
Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population
M. R. Moksnes, H. Røsjø, A. Richmond, M. Lyngbakken +23 more
2020medRxiv0 citations Open access
Semantic Scholar

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