Peter M. Visscher

Also affiliated with University of Oxford

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

10.9Author DataRank

Indexed papers

8in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 8 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

Papers

Driven by 52 papers — median percentile 60. Top paper: “Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel”.

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

Resource profile and user guide of the Polygenic Index Repository

Nature Human Behaviour(2021)10.1038/s41562-021-01119-3

Top 7%

3.0DataRank

Top 7%184 citations

Casper A.P. Burik, Grant Goldman, Nancy Wang, Hariharan Jayashankar, Michael Bennett +60 more

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0

N/A

2.8DataRank · unranked

151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 more

The Genetic Architecture of Gene Expression in Peripheral Blood

The American Journal of Human Genetics(2017)10.1016/j.ajhg.2017.01.026

N/A

2.7DataRank · unranked

84 citations

Alexander Holloway, Allan McRae, Jian Yang, Kerrin Small, Jing Zhao +11 more

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

Common Genetic Variants Explain the Majority of the Correlation Between Height and Intelligence: The Generation Scotland Study

Behavior Genetics(2014)10.1007/s10519-014-9644-z

N/A

1.8DataRank · unranked

52 citations

Riccardo E. Marioni, G. David Batty, Caroline Hayward, Shona M. Kerr, Archie Campbell +4 more

Biological insights from 108 schizophrenia-associated genetic loci

Nature(2014)10.1038/nature13595

N/A

1.3DataRank · unranked

8042 citations

Stephan Ripke, Aiden Corvin, Jesse R. Dixon, Kai-How Farh, Peter Holmans +284 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Nature Communications(2023)10.1038/s41467-023-36862-w

N/A

1.1DataRank · unranked

56 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +81 more

Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature(2008)10.1038/nature07239

N/A

1.1DataRank · unranked

1503 citations

Michael C O'Donovan, Catherine H. Wilson, Manfred Kayser, Pentti J. Tienari, Aiden Corvin +72 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725

N/A

1.1DataRank · unranked

1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 more

A unified framework for association and prediction from vertex‐wise grey‐matter structure

Human Brain Mapping(2020)10.1002/hbm.25109

Top 28%

0.705DataRank

Top 28%26 citations

Lachlan T. Strike, Futao Zhang, Yan Holtz, Zhili Zheng, Kathryn E. Kemper +7 more

Resource Profile and User Guide of the Polygenic Index Repository

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.08.443158

Top 52%

0.336DataRank

Top 52%5 citations

Casper A.P. Burik, Grant Goldman, Nancy Wang, Hariharan Jayashankar, Michael Bennett +37 more

The Australian Parkinson’s Genetics Study (APGS) - pilot (N = 1,532)

medRxiv(2021)10.1101/2021.04.02.21254825

Top 78%

0.104DataRank

Top 78%1 citations

George D. Mellick, Jacob Gratten, Richard Parker, Aoibhe Mulcahy, Philip Mosley +14 more

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

UCL Discovery (University College London)(2020)10.17615/snbr-qh40

N/A

0DataRank · unranked

0 citations

Kung‐Yee Liang, Per Hoffman, Stefan Herms, Gary Donohoe, Luba Kalaydjieva +94 more

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

UNC Libraries(2020)10.17615/3mxa-f008

N/A

0DataRank · unranked

0 citations

Naomi R. Wray, Peter M. Visscher, Stephan Ripke, Teresa R DeCandia, Matthew C. Keller +4 more

Across-cohort QC analyses of GWAS summary statistics from complex traits

UNC Libraries(2020)10.17615/mfev-3g68

N/A

0DataRank · unranked

0 citations

Jian Yang, Matthew R. Robinson, Sang Lee, Peter M. Visscher, Guo‐Bo Chen +12 more

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

Genome biology(2021)10.1186/s13059-021-02275-5

N/A

0DataRank · unranked

108 citations

Marta F. Nabais, the Alzheimer’s Disease Neuroimaging Initiative, Simon M. Laws, Tian Lin, Costanza L. Vallerga +67 more

Creating and Validating a DNA Methylation-Based Proxy for Interleukin-6

The Journals of Gerontology Series A(2021)10.1093/gerona/glab046

N/A

0DataRank · unranked

55 citations

Danni A. Gadd, Robert F. Hillary, Daniel L. McCartney, Archie Campbell, Rosie M. Walker +9 more

Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals

Nature Communications(2021)10.1038/s41467-021-21283-4

N/A

0DataRank · unranked

47 citations

Loïc Yengo, Zhili Zheng, Abdel Abdellaoui, Matthew C. Keller, Michael E. Goddard +4 more

Genomic partitioning of inbreeding depression in humans

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.005

N/A

0DataRank · unranked

20 citations

Jian Yang, Matthew C. Keller, Michael E. Goddard, Naomi R. Wray, Peter M. Visscher +1 more

A parsimonious model for mass-univariate vertex-wise analysis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.22.427735

N/A

0DataRank · unranked

2 citations

Futao Zhang, Kathryn E. Kemper, Julia Sidorenko, Naomi R. Wray, Peter M. Visscher +3 more

Genetic and Phenotypic Stability of Measures of Neuroticism Over 22 Years

UNC Libraries(2021)10.17615/51py-pr74

N/A

0DataRank · unranked

0 citations

Patrick F. Sullivan, Nicholas G. Martin, Peter M. Visscher, Naomi R. Wray, Andrew J. Birley

Epigenetic scores for the circulating proteome as tools for disease prediction

eLife(2022)10.7554/elife.71802

N/A

0DataRank · unranked

139 citations

Robert F. Hillary, Daniel L. McCartney, Shaza B. Zaghlool, Anna J. Stevenson, Yipeng Cheng +23 more

Assortative mating biases marker-based heritability estimators

Nature Communications(2022)10.1038/s41467-022-28294-9

N/A

0DataRank · unranked

95 citations

Sean O’Rourke, Teresa de Candia, Michael E. Goddard, Peter M. Visscher, Loïc Yengo +3 more

Discovery of genomic loci of the human cerebral cortex using genetically informed brain atlases

Science(2022)10.1126/science.abe8457

N/A

0DataRank · unranked

74 citations

Dennis van der Meer, Weixiu Dong, Hao Wang, Yan Wu, Jingjing Zou +13 more

Local CpG density affects the trajectory and variance of age-associated DNA methylation changes

Genome biology(2022)10.1186/s13059-022-02787-8

N/A

0DataRank · unranked

37 citations

Lyndsay Kerr, Qian Zhang, Rosie M. Walker, Sarah E. Harris, David M. Howard +12 more

15 years of GWAS discovery: Realizing the promise

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2022.12.011

N/A

0DataRank · unranked

572 citations

Loïc Yengo, Karin J. H. Verweij, Peter M. Visscher, Abdel Abdellaoui

Polygenic gene editing: the next frontier in genomic medicine?

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7513326

Top 100%

0DataRank

Top 100%0 citations

Christopher Gyngell, Loïc Yengo, Julian Savulescu, Peter M. Visscher

Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries

Nature Genetics(2024)10.1038/s41588-024-01704-y

N/A

0DataRank · unranked

171 citations

Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loïc Yengo +21 more

The importance of family-based sampling for biobanks

Nature(2024)10.1038/s41586-024-07721-5

N/A

0DataRank · unranked

24 citations

Gibran Hemani, Jenae M. Neiderhiser, Hilary C. Martin, Melinda Mills, Peter M. Visscher +4 more

Genetic influence on within-person longitudinal change in anthropometric traits in the UK Biobank

Nature Communications(2024)10.1038/s41467-024-47802-7

N/A

0DataRank · unranked

21 citations

Julia Sidorenko, Huanwei Wang, Ben J. Hayes, Naomi R. Wray, Loïc Yengo +4 more

Genetic architecture reconciles linkage and association studies of complex traits

Nature Genetics(2024)10.1038/s41588-024-01940-2

N/A

0DataRank · unranked

14 citations

Baptiste Couvy‐Duchesne, Kathryn E. Kemper, Gunn-Helen Moen, Laxmi Bhatta, Bjørn Olav Åsvold +23 more

Multi-ancestry polygenic risk scores for venous thromboembolism

Human Molecular Genetics(2024)10.1093/hmg/ddae097

N/A

0DataRank · unranked

6 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +42 more

Genetic evidence of assortative mating in humans

Carolina Digital Repository (University of North Carolina at Chapel Hill)(2024)10.17615/p1jd-v269

N/A

0DataRank · unranked

1 citations

Harold Snieder, Genetic Investigations of Anthropometric Traits consortium, M. McGue, Mariaelisa Graff, Jian Yang +17 more

Family-GWAS reveals effects of environment and mating on genetic associations

medRxiv(2024)10.1101/2024.10.01.24314703

N/A

0DataRank · unranked

39 citations

Hariharan Jayashankar, Junming Guan, Seyed Moeen Nehzati, Mahdi Mir, Michael Bennett +60 more

Grey‐Matter Structure Markers of Alzheimer's Disease, Alzheimer's Conversion, Functioning and Cognition: A Meta‐Analysis Across 11 Cohorts

Human Brain Mapping(2025)10.1002/hbm.70089

N/A

0DataRank · unranked

15 citations

Vincent Frouin, Vincent Bouteloup, Nikitas Koussis, Julia Sidorenko, Jiyang Jiang +17 more

Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids

Translational Psychiatry(2025)10.1038/s41398-025-03418-z

N/A

0DataRank · unranked

0 citations

Michael R. Brown, Solomon K. Musani, Karen Schwander, Thomas W. Winkler, Mario Sims +93 more

Local CpG density affects the trajectory of age-associated epigenetic changes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.08.451539

N/A

0DataRank · unranked

0 citations

Qian Zhang, Rosie M. Walker, Sarah E. Harris, David M. Howard, Emma L. Hawkins +11 more

Title Page / Table of Contents

Human Heredity(2015)10.1159/000448082

N/A

0DataRank · unranked

0 citations

Paul J. Newcombe, John P. A. Ioannidis, Emmanuelle Génin, Françoise Clerget‐Darpoux, Claire Dandine‐Roulland +10 more

Author and Subject Index

Human Heredity(2015)10.1159/000443902

N/A

0DataRank · unranked

0 citations

Paul J. Newcombe, John P. A. Ioannidis, Emmanuelle Génin, Françoise Clerget‐Darpoux, Claire Dandine‐Roulland +10 more

Contents Vol. 80, No. 4, 2015

Human Heredity(2015)10.1159/000447763

N/A

0DataRank · unranked

0 citations

Paul J. Newcombe, John P. A. Ioannidis, Emmanuelle C. Genin, Françoise Clerget‐Darpoux, Claire Dandine‐Roulland +9 more

Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

Nature Communications(2020)10.1038/s41467-020-15421-7

N/A

0DataRank · unranked

457 citations

Tian Lin, Zhen Qiao, Angli Xue, Yan Holtz, Zhihong Zhu +16 more

Risk prediction of late-onset Alzheimer’s disease implies an oligogenic architecture

Nature Communications(2020)10.1038/s41467-020-18534-1

N/A

0DataRank · unranked

286 citations

Julia Sidorenko, Baptiste Couvy‐Duchesne, Riccardo E. Marioni, Margaret J. Wright, Alison Goate +76 more

Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults

Genome Medicine(2020)10.1186/s13073-020-00754-1

N/A

0DataRank · unranked

70 citations

Daniel Trejo Baños, Athanasios Kousathanas, Daniel L. McCartney, Sarah E. Harris, Anna J. Stevenson +14 more

Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individuals

Aging(2020)10.18632/aging.103408

N/A

0DataRank · unranked

45 citations

Riccardo E. Marioni, Cavin Ward‐Caviness, Rahul Gondalia, Weihua Guan, Brian Chen +44 more

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Brain Communications(2020)10.1093/braincomms/fcaa064

N/A

0DataRank · unranked

56 citations

Steven Boeynaems, Mathias De Decker, Joke J.F.A. van Vugt, Lindy Kool, H. Stephan Goedee +81 more

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

UNC Libraries(2020)10.17615/9kkt-zw63

N/A

0DataRank · unranked

2 citations

Weihua Guan, Caroline S. Fox, Erica L. Kleinbrink, Åsa K. Hedman, Yao Chen +44 more

Integrative omics approach to identify the molecular architecture of inflammatory protein levels in healthy older adults

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.17.952135

N/A

0DataRank · unranked

2 citations

Daniel Trejo Baños, Athanasios Kousathanas, Daniel L. McCartney, Sarah E. Harris, Anna J. Stevenson +14 more

Variation in VKORC1 is associated with vascular dementia

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.31.231126

N/A

0DataRank · unranked

0 citations

Daniel L. McCartney, Daniel I. Chasman, Peter M. Visscher, Graciela Muñiz‐Terrera, Simon R. Cox +3 more

GWAS of epigenetic aging rates in blood reveals a critical role for TERT

UNC Libraries(2020)10.17615/p8eg-8t23

N/A

0DataRank · unranked

0 citations

Jordana T. Bell, İdil Yet, Morgan E. Levine, Nicholas J. Wareham, Themistocles L. Assimes +34 more

Population genetic differentiation of height and body mass index across Europe

UNC Libraries(2020)10.17615/1g42-fx24

N/A

0DataRank · unranked

0 citations

Peter M. Visscher

Peter M. Visscher

Indexed papers

Top data-sharing exemplar

Papers