Willem H. Ouwehand

Also affiliated with NHS Blood and Transplant, University College London Hospitals NHS Foundation Trust, University of Dundee, University of Cambridge, Royal London Hospital, Cambridge University Hospitals NHS Foundation Trust, Ninewells Hospital, Bridge University, Cambridge University Health Partners, University College London

MedicineBiochemistry, Genetics and Molecular BiologyImmunology and Microbiology

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 100%percentile

0Author DataRank

Indexed papers

1in 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 1 indexed paper 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 →

Papers

Driven by 19 papers. Top paper: “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations”.

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

Cell(2020)10.1016/j.cell.2020.06.045

N/A

8.3DataRank · unranked

739 citations

Laura M. Raffield, Abdou Mousas, Saori Sakaue, Jennifer E. Huffman, Arden Moscati +95 more

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults

The Lancet(2017)10.1016/s0140-6736(17)32129-3

N/A

1.3DataRank · unranked

7558 citations

Ziad A Abdeen, Zargar Abdul Hamid, Niveen M Abu-Rmeileh, Benjamin Acosta-Cazares, Cecilia Acuin +1262 more

ACE inhibition and cardiometabolic risk factors, lung ACE2 and TMPRSS2 gene expression, and plasma ACE2 levels: a Mendelian randomization study

Royal Society Open Science(2020)10.1098/rsos.200958

N/A

1.2DataRank · unranked

19 citations

Marios Arvanitis, Paul Carter, Ana I. Hernández Cordero, Brian Jo, Ville Karhunen +28 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

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

Cell(2016)10.1016/j.cell.2016.10.042

N/A

1.1DataRank · unranked

1405 citations

Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice L. Mann +78 more

Bayesian refinement of association signals for 14 loci in 3 common diseases

Nature Genetics(2012)10.1038/ng.2435

N/A

0.947DataRank · unranked

552 citations

Jake Byrnes, Damjan Vukcevic, Kimmo Palin, Zhan Su, Joanna M. M. Howson +35 more

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Molecular Psychiatry(2021)10.1038/s41380-020-01006-9

N/A

0.686DataRank · unranked

22 citations

Fernando S. Goes, Adam E. Locke, Duncan S. Palmer, Weiqing Wang, Sarah Cohen‐Woods +71 more

Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing

iScience(2023)10.1016/j.isci.2023.108214

N/A

0.364DataRank · unranked

9 citations

Belén de la Morena-Barrio, Esther Navarro-Manzano, Jonathan Stevens, Willem H. Ouwehand, Nicholas S. Gleadall +3 more

Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function

Haematologica(2020)10.3324/haematol.2019.235895

N/A

0DataRank · unranked

10 citations

Melissa A. Hayman, Suthesh Sivapalaratnam, Marilena Crescente, Harriet E. Allan, Matthew L. Edin +20 more

Genetic Analyses of Blood Cell Structure for Biological and Pharmacological Inference

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.30.927483

N/A

0DataRank · unranked

9 citations

Dragana Vuckovic, Tao Jiang, Kousik Kundu, Roman Kreuzhuber, Erik L. Bao +28 more

G protein–coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1

Blood Advances(2021)10.1182/bloodadvances.2021005453

N/A

0DataRank · unranked

28 citations

Xuefei Zhao, Nicholas Gleadall, Harriet McKinney, Carly Kempster, Joana Batista +19 more

Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry

Transfusion(2020)10.1111/trf.15839

N/A

0DataRank · unranked

16 citations

Nicholas Gleadall, Judith Aeschlimann, Sunitha Vege, Alba Sanchis‐Juan, Jonathan Stephens +11 more

Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity

Nature(2022)10.1038/s41586-022-04474-x

N/A

0DataRank · unranked

1172 citations

Adam Abdullahi, Isabella A.T.M. Ferreira, Niluka Goonawardane, Akatsuki Saito, Izumi Kimura +95 more

Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas

Haematologica(2020)10.3324/haematol.2019.238147

N/A

0DataRank · unranked

22 citations

Osagie Izuogu, Natasha Andressa Nogueira Jorge, Denis Seyres, Mariona Bustamante, Frances Burden +22 more

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Nature Genetics(2024)10.1038/s41588-024-01763-1

N/A

0DataRank · unranked

55 citations

Chen Zhao, Steven Bell, Maria Didriksen, Muhammad Sulaman Nawaz, Nathalie Schandra +65 more

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

UNC Libraries(2024)10.17615/gad3-dw62

N/A

0DataRank · unranked

0 citations

R.S. Kahn, Gonçalo R. Abecasis, Neil Risch, Andrew McQuillin, Aiden Corvin +71 more

A coagulation defect arising from heterozygous premature termination of tissue factor

Journal of Clinical Investigation(2020)10.1172/jci133780

N/A

0DataRank · unranked

23 citations

Emale El-Darzi, Mary H.C. Florido, Max Friesen, Glenn Merrill‐Skoloff, Marisa A Brake +11 more