Po-Ru Loh

Po-Ru Loh

Harvard University

H-index: 57

North America-United States

About Po-Ru Loh

Po-Ru Loh, With an exceptional h-index of 57 and a recent h-index of 51 (since 2020), a distinguished researcher at Harvard University, specializes in the field of Statistical Genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Author Correction: Clonal haematopoiesis and risk of chronic liver disease

Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection

Hidden protein-altering variants influence diverse human phenotypes

Identifying genetic variants that influence the abundance of cell states in single-cell data

Clonal haematopoiesis and risk of chronic liver disease

A pan-tissue survey of mosaic chromosomal alterations in 948 individuals

The lingering effects of Neanderthal introgression on human complex traits

Po-Ru Loh Information

University

Position

Brigham and Women's Hospital / Harvard Medical School

Citations(all)

31500

Citations(since 2020)

25948

Cited By

14888

hIndex(all)

57

hIndex(since 2020)

51

i10Index(all)

86

i10Index(since 2020)

80

Email

University Profile Page

Harvard University

Google Scholar

View Google Scholar Profile

Po-Ru Loh Skills & Research Interests

Statistical Genetics

Top articles of Po-Ru Loh

Title

Journal

Author(s)

Publication Date

Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Nature Genetics

Margaux LA Hujoel

Robert E Handsaker

Maxwell A Sherman

Nolan Kamitaki

Alison R Barton

...

2024/3/28

Author Correction: Clonal haematopoiesis and risk of chronic liver disease

Nature

Waihay J Wong

Connor Emdin

Alexander G Bick

Seyedeh M Zekavat

Abhishek Niroula

...

2023/7/20

Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection

Research Square

Martin Jinye Zhang

Arun Durvasula

Colby Chiang

Evan M Koch

Benjamin J Strober

...

2023/12/4

Hidden protein-altering variants influence diverse human phenotypes

bioRxiv

Margaux LA Hujoel

Robert E Handsaker

Maxwell A Sherman

Nolan Kamitaki

Alison R Barton

...

2023/6/9

Identifying genetic variants that influence the abundance of cell states in single-cell data

bioRxiv

Laurie Rumker

Saori Sakaue

Yakir Reshef

Joyce B Kang

Seyhan Yazar

...

2023/11/15

Clonal haematopoiesis and risk of chronic liver disease

Nature

Waihay J Wong

Connor Emdin

Alexander G Bick

Seyedeh M Zekavat

Abhishek Niroula

...

2023/4/27

A pan-tissue survey of mosaic chromosomal alterations in 948 individuals

Nature Genetics

Teng Gao

Maria Eleni Kastriti

Viktor Ljungström

Andreas Heinzel

Arthur S Tischler

...

2023/11

The lingering effects of Neanderthal introgression on human complex traits

Elife

Xinzhu Wei

Christopher R Robles

Ali Pazokitoroudi

Andrea Ganna

Alexander Gusev

...

2023/3/20

Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer

Cell

Ronen E Mukamel

Robert E Handsaker

Maxwell A Sherman

Alison R Barton

Margaux LA Hujoel

...

2023/8/17

Haplotype-aware analysis of somatic copy number variations from single-cell transcriptomes

Nature Biotechnology

Teng Gao

Ruslan Soldatov

Hirak Sarkar

Adam Kurkiewicz

Evan Biederstedt

...

2023/3

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Cell Genomics

Eduardo A Maury

Maxwell A Sherman

Giulio Genovese

Thomas G Gilgenast

Tushar Kamath

...

2023/8/9

Uncovering complex trait heritability hidden in the repeatome

Cell Genomics

Po-Ru Loh

2023/12/13

Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection

medRxiv

Aoxing Liu

Giulio Genovese

Yajie Zhao

Matti Pirinen

Maryam M Zekavat

...

2023/1/31

Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions

Scientific Reports

Giulio Genovese

Curtis J Mello

Po-Ru Loh

Robert E Handsaker

Seva Kashin

...

2022/7/14

Genome-wide mapping of somatic mutation rates uncovers drivers of cancer

Nature Biotechnology

Maxwell A Sherman

Adam U Yaari

Oliver Priebe

Felix Dietlein

Po-Ru Loh

...

2022/11

Incorporating family history of disease improves polygenic risk scores in diverse populations

Cell genomics

Margaux LA Hujoel

Po-Ru Loh

Benjamin M Neale

Alkes L Price

2022/7/13

A saturated map of common genetic variants associated with human height

Nature

Loïc Yengo

Sailaja Vedantam

Eirini Marouli

Julia Sidorenko

Eric Bartell

...

2022/10/27

A spectrum of recessiveness among Mendelian disease variants in UK Biobank

The American Journal of Human Genetics

Alison R Barton

Margaux LA Hujoel

Ronen E Mukamel

Maxwell A Sherman

Po-Ru Loh

2022/7/7

Genome-wide Mutation Rate Modeling Identifies Novel Driver Mutations

cancer

MA Sherman

AU Yaari

O Priebe

F Dietlein

PR Loh

...

2022/6/20

Influences of rare copy-number variation on human complex traits

Cell

Margaux LA Hujoel

Maxwell A Sherman

Alison R Barton

Ronen E Mukamel

Vijay G Sankaran

...

2022/10/27

See List of Professors in Po-Ru Loh University(Harvard University)