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Po‐Ru Loh

Broad Institute ·
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Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Genetic Mapping and Diversity in Plants and Animals, Genetic and phenotypic traits in livestock, and Bioinformatics and Genomic Networks.
h-index
63
citations
52,976
works
193
NIH funding
primary concept
Biology
email

Recent publications

Human and bacterial genetic variation shape oral microbiomes and health
Nature 2026cited by 6position: lastdoi
Insights into DNA repeat expansions among 900,000 biobank participants
Nature 2026cited by 4position: lastdoi
The DNA virome varies with human genes and environments
Nature 2026cited by 1position: lastdoi
The Somatic Mosaicism across Human Tissues Network
Nature 2025cited by 39position: middledoi
Protein-altering variants at copy number-variable regions influence diverse human phenotypes
Nature Genetics 2024cited by 35position: lastdoi
Clonal haematopoiesis and risk of chronic liver disease
Nature 2023cited by 198position: middledoi
Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer
Cell 2023cited by 47position: lastdoi
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Cell Genomics 2023cited by 43position: middledoi
The lingering effects of Neanderthal introgression on human complex traits
eLife 2023cited by 41position: middledoi
Author Correction: Clonal haematopoiesis and risk of chronic liver disease
Nature 2023cited by 2position: middledoi
Genome-wide mapping of somatic mutation rates uncovers drivers of cancer
Nature Biotechnology 2022cited by 82position: middledoi
Influences of rare copy-number variation on human complex traits
Cell 2022cited by 61position: lastdoi
A spectrum of recessiveness among Mendelian disease variants in UK Biobank
The American Journal of Human Genetics 2022cited by 60position: lastdoi
Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific <i>NRXN1</i> disruptions
medRxiv 2022cited by 4position: middledoi
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
Nature Genetics 2021cited by 357position: lastdoi
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
Nature Medicine 2021cited by 188position: middledoi
Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets
Nature Communications 2021cited by 153position: middledoi
Large mosaic copy number variations confer autism risk
Nature Neuroscience 2021cited by 61position: lastdoi
A model and test for coordinated polygenic epistasis in complex traits
Proceedings of the National Academy of Sciences 2021cited by 33position: middledoi
Fast, sensitive and accurate integration of single-cell data with Harmony
Nature Methods 2019cited by 10,240position: middledoi
Genetic predisposition to mosaic Y chromosome loss in blood
Nature 2019cited by 336position: middledoi
Genes with High Network Connectivity Are Enriched for Disease Heritability
The American Journal of Human Genetics 2019cited by 70position: middledoi
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
Nature Genetics 2018cited by 1,205position: middledoi
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
The American Journal of Human Genetics 2018cited by 1,069position: middledoi
Mixed-model association for biobank-scale datasets
Nature Genetics 2018cited by 910position: firstdoi
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations
Nature 2018cited by 428position: firstdoi
A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases
Nature Genetics 2018cited by 249position: middledoi
Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits
Nature Genetics 2018cited by 234position: middledoi
Estimating cross‐population genetic correlations of causal effect sizes
Genetic Epidemiology 2018cited by 99position: middledoi
Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk
Nature Genetics 2018cited by 75position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Alkes L. Price · Harvard University17 papers (2015–2019)Hilary K. Finucane · Broad Institute13 papers (2015–2019)Bonnie Berger · Broad Institute13 papers (2012–2022)Mark Lipson · Massachusetts Institute of Technology9 papers (2012–2015)Alexander Gusev · Harvard University9 papers (2015–2023)Ronen E. Mukamel · Broad Institute8 papers (2021–2026)David Reich · Harvard University8 papers (2012–2023)Maxwell A. Sherman · Profectus Biosciences (United States)8 papers (2021–2024)Steven A. McCarroll · Broad Institute7 papers (2018–2026)Benjamin M. Neale · Broad Institute7 papers (2015–2018)Yakir Reshef · Harvard University7 papers (2015–2018)Steven Gazal · University of Southern California7 papers (2017–2019)Brendan Bulik‐Sullivan · Broad Institute6 papers (2015–2017)Pier Francesco Palamara · Columbia University6 papers (2016–2026)Alison R. Barton · Broad Institute6 papers (2021–2024)Nick Patterson · Broad Institute6 papers (2012–2015)Margaux L.A. Hujoel · Broad Institute6 papers (2022–2026)Robert E. Handsaker · Broad Institute5 papers (2018–2026)Priya Moorjani · University of California, Berkeley4 papers (2013–2014) · 4 papers (2017–2018)
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