Samuli Ripatti

Also affiliated with University of Helsinki, Helsinki Institute of Physics, Institute for Molecular Medicine Finland

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

6.9Author DataRank

Indexed papers

5in 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 5 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 56 papers — median percentile 21. Top paper: “Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression”.

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature Genetics(2021)10.1038/s41588-021-00913-z

N/A

11.2DataRank · unranked

2226 citations

Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng +89 more

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

Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

Nature(2020)10.1038/s41586-020-2786-7

N/A

4.1DataRank · unranked

151 citations

Satish K. Nandakumar, Xiaotian Liao, Alexander G. Bick, Juha Karjalainen, Marcin Tabaka +79 more

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

Nature Communications(2022)10.1038/s41467-022-29143-5

N/A

3.9DataRank · unranked

196 citations

Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke +33 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Genome-wide association study identifies 48 common genetic variants associated with handedness

Nature Human Behaviour(2020)10.1038/s41562-020-00956-y

N/A

3.7DataRank · unranked

157 citations

Joyce Y. Tung, Nicholas Eriksson, Eva Albrecht, Fazil Alıev, Ole A. Andreassen +95 more

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

Genome Research(2010)10.1101/gr.106534.110

N/A

2.6DataRank · unranked

61 citations

Kati Kristiansson, Verneri Anttila, Michael Inouye, Chris Barnes, Loukas Moutsianas +6 more

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Nature Genetics(2024)10.1038/s41588-024-01714-w

N/A

2.4DataRank · unranked

193 citations

Zoha Kamali, Tian Xie, Ahmad Vaez, Ariel Williams, Slavina B. Goleva +95 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

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nature Communications(2021)10.1038/s41467-021-22339-1

N/A

1.1DataRank · unranked

51 citations

Akhil Pampana, Sarah E. Graham, Sanni Ruotsalainen, James A. Perry, Paul S. de Vries +95 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

Genomic prediction of alcohol-related morbidity and mortality

Translational Psychiatry(2020)10.1038/s41398-019-0676-2

N/A

1.1DataRank · unranked

30 citations

Nina Mars, Teemu Palviainen, Jukka Koskela, Joel Rämö, Pietari Ripatti +10 more

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Nature Genetics(2014)10.1038/ng.2897

N/A

1.0DataRank · unranked

1086 citations

Anubha Mahajan, Min Jin Go, Weihua Zhang, Jennifer E Below, Kyle J Gaulton +327 more

The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

EBioMedicine(2023)10.1016/j.ebiom.2023.104630

N/A

1.0DataRank · unranked

28 citations

Fahrisa I. Maisha, Satu Strausz, Vilma Lammi, Brian E. Cade, Anniina Tervi +88 more

Genetics of 35 blood and urine biomarkers in the UK Biobank

Nature Genetics(2021)10.1038/s41588-020-00757-z

N/A

1.0DataRank · unranked

806 citations

Yosuke Tanigawa, David Amar, Nina Mars, Christian Benner, Matthew Aguirre +19 more

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Nature Genetics(2022)10.1038/s41588-021-00990-0

N/A

0.900DataRank · unranked

402 citations

Bendik Slagsvold Winsvold, Sanni Ruotsalainen, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman +68 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

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

The American Journal of Human Genetics(2018)10.1016/j.ajhg.2018.05.002

N/A

0.713DataRank · unranked

115 citations

F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse +45 more

Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

Stroke(2023)10.1161/strokeaha.123.043052

N/A

0.706DataRank · unranked

27 citations

Anni Kauko, Sarah E. Tom, Hannele Laivuori, Teemu Niiranen, Natalie A. Bello +86 more

Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank

Nature Genetics(2021)10.1038/s41588-021-00956-2

N/A

0.693DataRank · unranked

14 citations

Yosuke Tanigawa, David Amar, Nina Mars, Christian Benner, Matthew Aguirre +19 more

Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

Nature Communications(2023)10.1038/s41467-023-35974-7

N/A

0.680DataRank · unranked

22 citations

Jaakko Tyrmi, Nilüfer Rahmioğlu, Krina T. Zondervan, Christian M. Becker, FinnGen +95 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes

medRxiv(2025)10.1101/2025.01.31.25321397

N/A

0.395DataRank · unranked

11 citations

Helena L. Davies, Sang Hyuck Lee, Jessica Dennis, Christopher Hübel, Jessica Johnson +95 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Narcolepsy as a potential risk factor for Schizophrenia

Translational Psychiatry(2025)10.1038/s41398-025-03259-w

N/A

0.248DataRank · unranked

3 citations

Anniina Tervi, Samuel E. Jones, FinnGen, Aarno Palotie, Mark Daly +95 more

Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts

EClinicalMedicine(2024)10.1016/j.eclinm.2024.102956

N/A

0.214DataRank · unranked

3 citations

Lindsay Wilson, Daniel F. Levey, Livia Parodi, Ewout W. Steyerberg, Sylvia Richardson +95 more

Genome-wide association study of 1,391 plasma metabolites in 6,136 Finnish men identifies 303 novel signals and provides biological insights into human diseases

medRxiv(2021)10.1101/2021.10.19.21265094

N/A

0.208DataRank · unranked

3 citations

Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke +32 more

Genetic and functional analysis of Raynaud’s syndrome implicates loci in vasculature and immunity

Cell Genomics(2024)10.1016/j.xgen.2024.100630

N/A

0DataRank · unranked

5 citations

Markus Ramste, Erik Abner, Paul Cheng, Jacqueline M. Lane, Matthew Maher +24 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 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

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

Työväentutkimus Vuosikirja(2020)10.1161/circgen.119.002725

N/A

0DataRank · unranked

104 citations

Pietari Ripatti, Joel Rämö, Nina Mars, Yu Fu, Jake Lin +15 more

Polygenic risk, susceptibility genes, and breast cancer over the life course

medRxiv(2020)10.1101/2020.04.17.20069229

N/A

0DataRank · unranked

11 citations

Elisabeth Widén, Sini Kerminen, Tuomo J Meretoja, Matti Pirinen, Priit Palta +7 more

Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

medRxiv(2020)10.1101/2020.11.15.20227868

N/A

0DataRank · unranked

4 citations

Tuomo Kiiskinen, Juha Karjalainen, Kristi Krebs, Mitja Kurki, Aki S. Havulinna +17 more

Genetic associations and architecture of asthma-chronic obstructive pulmonary disease overlap

medRxiv(2020)10.1101/2020.11.26.20236760

N/A

0DataRank · unranked

2 citations

Anna L. Guyatt, Nick Shrine, Richard Packer, Thorunn A. Olafsdottir, Jiangyuan Liu +49 more

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

UNC Libraries(2020)10.17615/y892-y714

N/A

0DataRank · unranked

0 citations

Wen‐Chi Hsueh, Eric Orwoll, Serkalem Demissie, Liisa Byberg, Arjun Verma +95 more

The Genetic Structure of the Swedish Population

UNC Libraries(2020)10.17615/fvdj-e024

Top 100%

0DataRank

Top 100%0 citations

Jianjun Liu, Per Hall, Pamela Sklar, Samuli Ripatti, Henrik Grönberg +18 more

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

UNC Libraries(2020)10.17615/kf29-bk98

Top 100%

0DataRank

Top 100%0 citations

Karl Gertow, Veikko Salomaa, John D. Eicher, Anders Hamsten, Inga Prokopenko +94 more

Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

Nature Medicine(2021)10.1038/s41591-021-01549-6

N/A

0DataRank · unranked

445 citations

Adebowale Adeyemo, Mary K. Balaconis, Deanna R. Darnes, Segun Fatumo, Palmira Granados Moreno +22 more

Leveraging global multi-ancestry meta-analysis in the study of Idiopathic Pulmonary Fibrosis genetics

medRxiv(2021)10.1101/2021.12.29.21268310

N/A

0DataRank · unranked

14 citations

Paavo Häppölä, Wei Zhou, Arto Lehistö, Mari Ainola, Eva Sutinen +17 more

Genome-wide risk prediction of common diseases across ancestries in one million people

Cell Genomics(2022)10.1016/j.xgen.2022.100118

N/A

0DataRank · unranked

93 citations

Sini Kerminen, Yen‐Chen Anne Feng, Masahiro Kanai, Kristi Läll, Laurent F. Thomas +15 more

Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.007

N/A

0DataRank · unranked

62 citations

Debraj Bose, Annie Kwon, Sarah C. Hanks, Anne Jackson, Heather M. Stringham +24 more

Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics

Cell Genomics(2022)10.1016/j.xgen.2022.100181

N/A

0DataRank · unranked

56 citations

Paavo Häppölä, Wei Zhou, Arto Lehistö, Mari Ainola, Eva Sutinen +22 more

Genetic Associations and Architecture of Asthma-COPD Overlap

CHEST Journal(2022)10.1016/j.chest.2021.12.674

N/A

0DataRank · unranked

45 citations

Anna L. Guyatt, Nick Shrine, Richard Packer, Thorunn A. Olafsdottir, Jiangyuan Liu +49 more

Immune system-wide Mendelian randomization and triangulation analyses support autoimmunity as a modifiable component in dementia-causing diseases

Nature Aging(2022)10.1038/s43587-022-00293-x

N/A

0DataRank · unranked

42 citations

Nina Mars, Pyry N. Sipilä, Archana Singh‐Manoux, Heiko Runz, FinnGen +7 more

Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health

medRxiv(2023)10.1101/2023.06.26.23291721

N/A

0DataRank · unranked

8 citations

Jack Li, Debraj Bose, Jeffrey Okamoto, Annie Kwon, Anne Jackson +14 more

Limited overlap between genetic effects on disease susceptibility and disease survival

medRxiv(2023)10.1101/2023.10.10.23296544

N/A

0DataRank · unranked

5 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +19 more

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

medRxiv(2023)10.1101/2023.09.24.23295485

N/A

0DataRank · unranked

0 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +56 more

Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.04.020

N/A

0DataRank · unranked

17 citations

Mari Vehviläinen, Shuang Luo, Jarmo Ritari, Juha Karjalainen, Javier Gracia‐Tabuenca +14 more

Nightmares share genetic risk factors with sleep and psychiatric traits

Translational Psychiatry(2024)10.1038/s41398-023-02637-6

N/A

0DataRank · unranked

18 citations

Nicholas A. Sinnott-Armstrong, Katri Kantojärvi, Martin Broberg, Teemu Palviainen, Samuel E. Jones +13 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks

medRxiv(2024)10.1101/2024.09.11.24313458

N/A

0DataRank · unranked

1 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery

Nature Medicine(2025)10.1038/s41591-025-03645-3

N/A

0DataRank · unranked

36 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

Limited overlap between genetic effects on disease susceptibility and disease survival

Nature Genetics(2025)10.1038/s41588-025-02342-8

N/A

0DataRank · unranked

16 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +20 more

Samuli Ripatti

Indexed papers

Top data-sharing exemplar

Papers