Harold Snieder

ORCID: 0000-0003-1949-2298

Also affiliated with University of Groningen

Biochemistry, Genetics and Molecular BiologyMedicine

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

8.2Author DataRank

Indexed papers

4in 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 4 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.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 54 papers — median percentile 85. Top paper: “A structural variation reference for medical and population genetics”.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

The genetic architecture of sporadic and multiple consecutive miscarriage

Nature Communications(2020)10.1038/s41467-020-19742-5

N/A

2.6DataRank · unranked

122 citations

Ana Gonçalves Soares, Teresa Ferreira, Jodie N. Painter, Jenny C. Censin, Samantha Laber +50 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

Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation

Mutation Research/Reviews in Mutation Research(2022)10.1016/j.mrrev.2022.108415

N/A

1.5DataRank · unranked

73 citations

Karen Huen, Paul Yousefi, Leanne K. Küpers, Juan R. González, Matthew Suderman +80 more

Genetic and environmental influences on blood pressure and body mass index in Han Chinese: a twin study

Hypertension Research(2011)10.1038/hr.2010.194

N/A

1.5DataRank · unranked

43 citations

Harold Snieder, Liming Li, Weihua Cao, Siyan Zhan, Jun Lv +5 more

Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure

Hypertension(2020)10.1161/hypertensionaha.120.14973

N/A

1.4DataRank · unranked

87 citations

Miina Ollikainen, Maheswary Muniandy, Tao Zhang, Jenny van Dongen, Guang Hao +47 more

Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms

Journal of the American Academy of Child & Adolescent Psychiatry(2022)10.1016/j.jaac.2021.11.035

Top 15%

1.4DataRank

Top 15%67 citations

Anke R. Hammerschlag, Hill F. Ip, Andrea G. Allegrini, Beben Benyamin, Richard Border +89 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Proceedings of the National Academy of Sciences(2017)10.1073/pnas.1705859115

N/A

1.2DataRank · unranked

36 citations

Alisa Manning, Marcio Almeida, Matthew Zawistowski, Katharina Domschke, Tanya M. Teslovich +82 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

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Molecular Psychiatry(2022)10.1038/s41380-022-01793-3

N/A

1.1DataRank · unranked

66 citations

Emil Uffelmann, Benjamin Williams, Lucía Colodro‐Conde, Éloi Gagnon, Travis T. Mallard +95 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

Genetic and environmental influences on stability and change in baseline levels of C-reactive protein: A longitudinal twin study

Atherosclerosis(2017)10.1016/j.atherosclerosis.2017.08.008

N/A

1.0DataRank · unranked

29 citations

Ahmad Vaez, Yalda Jamshidi, Ilja M. Nolte, Zoha Kamali, Timothy D. Spector +3 more

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

Molecular Psychiatry(2020)10.1038/s41380-020-0719-3

N/A

0.810DataRank · unranked

25 citations

Yun Ju Sung, Raymond Noordam, Thomas W. Winkler, Mary F. Feitosa, Karen Schwander +95 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

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

0.775DataRank · unranked

174 citations

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

Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes

Nature Communications(2021)10.1038/s41467-021-22338-2

N/A

0.731DataRank · unranked

130 citations

Marijana Vujković, Joshua Elliott, Evangelos Evangelou, Dipender Gill, Mohsen Ghanbari +95 more

DNA methylation and body mass index from birth to adolescence: meta-analyses of epigenome-wide association studies

Genome Medicine(2020)10.1186/s13073-020-00810-w

N/A

0.692DataRank · unranked

100 citations

Leanne K. Küpers, Gemma C. Sharp, Lucas A. Salas, Samantha Lent, Dereje D. Jima +80 more

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

medRxiv(2024)10.1101/2024.10.01.24314703

N/A

0.553DataRank · unranked

39 citations

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

Detecting SNPs and estimating allele frequencies in clonal bacterial populations by sequencing pooled DNA

Bioinformatics(2009)10.1093/bioinformatics/btp344

N/A

0.553DataRank · unranked

39 citations

E. Shyong Tai, Alexandra P. Lewis, Satheesh Nair, Gordon Dougan, John Wain +3 more

Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101430

N/A

0.510DataRank · unranked

29 citations

Arjun Bhattacharya, Wei Zhou, Dan Zhou, Ying Wang, Kristi Läll +31 more

Missing Heritability of Complex Traits and Diseases

Encyclopedia of Life Sciences(2019)10.1002/9780470015902.a0028223

N/A

0.451DataRank · unranked

12 citations

Felix Christian Tropf, Harold Snieder, Ilja Maria Nolte

Genetic architecture reconciles linkage and association studies of complex traits

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

N/A

0.406DataRank · unranked

14 citations

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

Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.004

N/A

0.396DataRank · unranked

13 citations

Josan Gandawijaya, Rosemary A. Bamford, Emily-Rose Martin, Andrew R. Wood, Peter J. van der Most +28 more

Multi-ancestry polygenic risk scores for venous thromboembolism

Human Molecular Genetics(2024)10.1093/hmg/ddae097

N/A

0.292DataRank · unranked

6 citations

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

Fast‐food environments and BMI changes in the Dutch adult general population: the Lifelines cohort

Obesity(2023)10.1002/oby.23781

N/A

0.269DataRank · unranked

5 citations

Sander K. R. van Zon, Tian Xie, Harold Snieder, Ute Bültmann, Nynke Smidt +1 more

Prenatal Smoking Exposures and Epigenome-Wide Methylation in Newborn Blood

Environmental Health Perspectives(2025)10.1021/ehp.6c00142

N/A

0.208DataRank · unranked

3 citations

Marta Cosín‐Tomás, Yunsung Lee, Giulietta S. Monasso, Zongli Xu, Shaobo Li +51 more

Epigenetic timing effects on child developmental outcomes: A longitudinal meta-regression of findings from the Pregnancy And Childhood Epigenetics Consortium

medRxiv(2024)10.1101/2024.02.29.24303506

N/A

0.165DataRank · unranked

2 citations

Sara Sammallahti, Marta Cosín‐Tomás, Sarah E. Reese, Matthew Suderman, Silvia Alemany +60 more

Genome-wide analyses of quantitative generalised anxiety symptom severity

medRxiv(2025)10.1101/2025.07.10.25331321

N/A

0.165DataRank · unranked

2 citations

Brittany L. Mitchell, Elham Assary, Danyang Li, Geneviève Morneau‐Vaillancourt, Alan E Murphy +51 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

0.116DataRank · unranked

1 citations

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

A Large-Scale Genome-Wide Gene-Sleep Interaction Study in 732,564 Participants Identifies Lipid Loci Explaining Sleep-Associated Lipid Disturbances

medRxiv(2024)10.1101/2024.09.02.24312466

Top 78%

0.104DataRank

Top 78%1 citations

Wenyi Wang, Pavithra Nagarajan, Heming Wang, Michael R. Brown, Amy R. Bentley +95 more

Rest-activity circadian rhythm and impaired glucose tolerance in adults: an analysis of NHANES 2011–2014

BMJ Open Diabetes Research & Care(2022)10.1136/bmjdrc-2021-002632

N/A

0DataRank · unranked

34 citations

Shaoyong Su, W. Vaughn McCall, Carlos M. Isales, Harold Snieder, Xiaoling Wang +1 more

Exploratory analysis and error modeling of a sequencing technology

bioRxiv (Cold Spring Harbor Laboratory)(2016)10.1101/043042

N/A

0DataRank · unranked

0 citations

Kerrin S. Small, E. Shyong Tai, Alexandra P. Lewis, Nava Whiteford, Tom Skelly +10 more

Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approach

Scientific Reports(2020)10.1038/s41598-020-68567-1

N/A

0DataRank · unranked

91 citations

Anastasia Emmanouilidou, Eugenia Mazzaferro, Silvia Vicenzi, Ida Höijer, Tiffany Klingström +10 more

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

UNC Libraries(2020)10.17615/jcdv-pt45

N/A

0DataRank · unranked

0 citations

Wei Zhao, Cathryn M. Lewis, Thomas G. Schulze, Philip L. De Jager, Markus M. Nöthen +95 more

Multi-ancestry polygenic risk scores for venous thromboembolism

medRxiv(2024)10.1101/2024.01.09.24300914

N/A

0DataRank · unranked

2 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +31 more

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.19.104455

N/A

0DataRank · unranked

8 citations

Felix R. Day, Nicola Barban, Felix C. Tropf, David M. Brazel, Ahmad Vaez +8 more

Positive and negative affect, related mental health traits, and cognitive performance: shared genetic architecture and potential causality

medRxiv(2024)10.1101/2024.11.01.24316562

N/A

0DataRank · unranked

2 citations

Naoise Mac Giollabhui, Peter J. van der Most, Ensor Rafael Palacios, Harold Snieder, Michel G. Nivard +4 more

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

Digital Commons@Becker (Washington University School of Medicine)(2024)10.17615/r2s5-pn26

N/A

0DataRank · unranked

0 citations

J.M. Norris, Evangelos Evangelou, C.E. Lewis, André G. Uitterlinden, M.Y. Tsai +95 more

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

Digital Commons@Becker (Washington University School of Medicine)(2024)10.17615/2bde-jk53

N/A

0DataRank · unranked

0 citations

A. Mahajan, Esteban J. Parra, Jeffrey Damman, Cecilia M. Lindgren, Johan Ärnlöv +67 more

Impact of psychosocial stress in early life on pace of aging in young adulthood

Clinical Epigenetics(2025)10.1186/s13148-025-02002-y

N/A

0DataRank · unranked

3 citations

Tené T. Lewis, Daniel W. Belsky, Yutao Liu, Kai Zhang, Harold Snieder +2 more

A Genome-Wide Methylation Study of Severe Vitamin D Deficiency in African American Adolescents

UNC Libraries(2020)10.17615/704m-wz58

N/A

0DataRank · unranked

3 citations

Bernard Gutin, Gregory A. Harshfield, Harold Snieder, Yanbin Dong, Haidong Zhu +3 more

Cell type-specific methylome-wide association studies of childhood ADHD symptoms

European Neuropsychopharmacology(2025)10.1016/j.euroneuro.2025.09.010

N/A

0DataRank · unranked

1 citations

Marieke Klein, Doretta Caramaschi, Shaunna L. Clark, Marta Cosín‐Tomás, Nastassja Koen +30 more

Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants

Atherosclerosis(2025)10.1016/j.atherosclerosis.2025.120603

N/A

0DataRank · unranked

1 citations

Wenyi Wang, Pavithra Nagarajan, Heming Wang, Michael R. Brown, Amy R. Bentley +95 more

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/5y99-4w88

N/A

0DataRank · unranked

5 citations

Terho Lehtimäki, P. Eline Slagboom, Albert V. Smith, Dennis O. Mook‐Kanamori, Paul Elliott +93 more

Cell type-specific methylome-wide association studies of childhood ADHD symptoms

medRxiv(2025)10.1101/2025.04.16.25325956

N/A

0DataRank · unranked

1 citations

Marieke Klein, Doretta Caramaschi, Shaunna L. Clark, Marta Cosín‐Tomás, Nastassja Koen +30 more

A Large-Scale Genome-wide Association Study of Blood Pressure Accounting for Gene-Depressive Symptomatology Interactions in 564,680 Individuals from Diverse Populations

Research Square(2025)10.21203/rs.3.rs-6025759/v1

N/A

0DataRank · unranked

0 citations

Clint L. Miller, Amy R. Bentley, Michael R. Brown, Pavithra Nagarajan, Raymond Noordam +95 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

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

UNC Libraries(2020)10.17615/2bje-6g29

N/A

0DataRank · unranked

0 citations

Deborah J. Thompson, Hannes Helgason, Timothy M. Frayling, Hilary K. Finucane, Patrick Sulem +211 more

Genomic analysis of diet composition finds novel loci and associations with health and lifestyle

Molecular Psychiatry(2020)10.1038/s41380-020-0697-5

N/A

0DataRank · unranked

154 citations

Ronald de Vlaming, Peter N. Bowers, Casper A.P. Burik, Richard Karlsson Linnér, Chan Wook Lee +39 more

Harold Snieder

Indexed papers

Top data-sharing exemplar

Papers