Tōnu Esko

ORCID: 0000-0003-1982-6569

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

21.2Author DataRank

Indexed papers

15in 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 15 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 103 papers — median percentile 52. Top paper: “Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals”.

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Nature Metabolism(2020)10.1038/s42255-020-00287-2

N/A

10.0DataRank · unranked

782 citations

Stefan Gustafsson, Qin Wang, Daniel Hvidberg Hansen, Åsa K. Hedman, Andrew J. Schork +78 more

A genomic mutational constraint map using variation in 76,156 human genomes

Nature(2023)10.1038/s41586-023-06045-0

N/A

9.6DataRank · unranked

1369 citations

Laurent C. Francioli, Julia K. Goodrich, Ryan L. Collins, Masahiro Kanai, Qingbo S. Wang +95 more

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

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

Genetic diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 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

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Nature Genetics(2022)10.1038/s41588-022-01165-1

N/A

4.4DataRank · unranked

242 citations

Andrew Emmerich, Nicolas J. Pillon, Timothy M. Moore, Daiane Hemerich, Marilyn C. Cornelis +95 more

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Assessment of Osteoarthritis Candidate Genes in a Meta‐Analysis of Nine Genome‐Wide Association Studies

Arthritis & Rheumatology(2014)10.1002/art.38300

Top 6%

3.9DataRank

Top 6%131 citations

Manuel Calaza, Evangelos Evangelou, Ana M. Valdes, Nigel Arden, Francisco J. Blanco +54 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

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Nature Neuroscience(2016)10.1038/nn.4404

N/A

3.3DataRank · unranked

113 citations

Giulio Genovese, Daniel P. Howrigan, Andrea Byrnes, Mitja I Kurki, Seyedeh M. Zekavat +31 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

Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study

Annals of the Rheumatic Diseases(2011)10.1136/ard.2010.141473

N/A

2.9DataRank · unranked

121 citations

K S Elliott, N. Wrayner, G Zhai, C. Beazley, G. Thorleifsson +108 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

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

The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males

Annals of the Rheumatic Diseases(2013)10.1136/annrheumdis-2012-203182

N/A

2.3DataRank · unranked

60 citations

Ana M. Valdes, Martha C Castano-Betancourt, Sally Doherty, Tonu Esko, Thorvaldur Ingvarsson +21 more

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

Nature Communications(2020)10.1038/s41467-020-17002-0

N/A

2.1DataRank · unranked

76 citations

Pamela M. Rist, Iyas Daghlas, Franco Giulianini, Padhraig Gormley, Verneri Anttila +95 more

Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease

Gut(2021)10.1136/gutjnl-2020-323868

N/A

2.1DataRank · unranked

44 citations

David Ellinghaus, Simonas Juzėnas, François Cossais, Greta Burmeister, Gabriele Mayr +80 more

Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.008

N/A

1.7DataRank · unranked

56 citations

Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson +64 more

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.010

N/A

1.6DataRank · unranked

76 citations

Maxim B. Freidin, Linda Broer, Berthe C. Oosterloo, Shuyang Yao, Yitian Zhou +65 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

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

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

Nature Human Behaviour(2023)10.1038/s41562-023-01528-6

N/A

1.3DataRank · unranked

59 citations

Felix R. Day, Nicola Barban, Felix C. Tropf, David M. Brazel, Diana van Heemst +92 more

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 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

Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance

Journal of Medical Genetics(2014)10.1136/jmedgenet-2014-102478

N/A

1.1DataRank · unranked

25 citations

Sarah Metrustry, Nigel Arden, Anne C Bay-Jensen, Marian Beekman, Anton J. M. de Craen +28 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

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

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

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Cell(2020)10.1016/j.cell.2020.08.008

N/A

0.988DataRank · unranked

722 citations

Erik L. Bao, Parsa Akbari, Caleb A. Lareau, Abdou Mousas, Tao Jiang +95 more

Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/561472

N/A

0.977DataRank · unranked

17 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric Vallabh Minikel, Konrad J. Karczewski +35 more

Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium

Journal of Psychiatric Research(2021)10.1016/j.jpsychires.2021.02.027

N/A

0.893DataRank · unranked

16 citations

Tim B. Bigdeli, Stephan Ripke, Silviu‐Alin Bacanu, Pablo V. Gejman, Douglas F. Levinson +16 more

Effect of predicted protein-truncating genetic variants on the human transcriptome

Science(2015)10.1126/science.1261877

N/A

0.877DataRank · unranked

345 citations

Matti Pirinen, Donald F. Conrad, Monkol Lek, Emily K. Tsang, Konrad J. Karczewski +206 more

The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium

ESC Heart Failure(2021)10.1002/ehf2.13517

Top 24%

0.829DataRank

Top 24%22 citations

Sonia Shah, Honghuang Lin, Tomasz Czuba, Albert Henry, Daniel I. Swerdlow +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

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Nature Communications(2021)10.1038/s41467-020-19366-9

N/A

0.771DataRank · unranked

170 citations

Reedik Mägi, Jouke‐Jan Hottenga, Harald Grallert, John R. B. Perry, Nabila Bouatia‐Naji +95 more

Common Genetic Variation and Age of Onset of Anorexia Nervosa

Biological Psychiatry Global Open Science(2021)10.1016/j.bpsgos.2021.09.001

N/A

0.726DataRank · unranked

30 citations

Laura M. Thornton, Zeynep Yılmaz, Jessica H. Baker, Jonathan R. I. Coleman, Roger A.H. Adan +95 more

A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response

medRxiv(2020)10.1101/2020.07.16.20155606

Top 28%

0.708DataRank

Top 28%15 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Kenichi Yamamoto, Kotaro Ogawa +24 more

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0.665DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 more

GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets

Nature Communications(2025)10.1038/s41467-025-56719-8

N/A

0.631DataRank · unranked

66 citations

Philip E. Stuart, John Bowes, David Ellinghaus, Joanne Nititham, Jake Saklatvala +89 more

Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction

Nature Communications(2024)10.1038/s41467-024-53595-6

N/A

0.533DataRank · unranked

14 citations

Sudhanshu Shekhar, Daniel F. Levey, Péter Straub, Julia Kraft, Georgia Panagiotaropoulou +35 more

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

Nature Communications(2024)10.1038/s41467-024-49338-2

N/A

0.466DataRank · unranked

10 citations

Georgii Dolgalev, Sylvain Moser, Laura T. Jiménez-Barrón, Till F. M. Andlauer, Moritz von Scheidt +95 more

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x

Top 44%

0.417DataRank

Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

UEF eRepo (University of Eastern Finland)(2024)10.17615/k2gw-9005

N/A

0.360DataRank · unranked

10 citations

James R. Staley, M.E. Jørgensen, T. Tuomi, R. Rauramaa, Robin Young +95 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

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

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 more

An Updated Polygenic Index Repository: Expanded Phenotypes, New Cohorts, and Improved Causal Inference

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.14.653986

Top 60%

0.253DataRank

Top 60%4 citations

Anastasia Terskaya, Matthew D. Howell, Junming Guan, Harry Sands, Aaron Kleinman +45 more

Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00979-9

N/A

0.246DataRank · unranked

4 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

356 COMMON VARIANTS IN SKELETAL DYSPLASIA GENES ARE ASSOCIATED WITH OSTEOARTHRITIS

Osteoarthritis and Cartilage(2011)10.1016/s1063-4584(11)60383-x

N/A

0.210DataRank · unranked

3 citations

M. Irving, Katharina Domschke, Unnur Styrkarsdottir, Y. Zhu, Aravinda Chakravarti +34 more

83 ANALYSIS OF CANDIDATE OSTEOARTHRITIS GENES IN A META-ANALYSIS OF 8 GENOME-WIDE ASSOCIATION STUDIES

Osteoarthritis and Cartilage(2011)10.1016/s1063-4584(11)60110-6

N/A

0.210DataRank · unranked

3 citations

Members of the Rheumatoid Arthritis Challenge Consortium, N.K. Arden, Aravinda Chakravarti, Katharina Domschke, Juan J. Gomez‐Reino Carnota +39 more

Genome-wide meta-analysis of common variant differences between men and women

Faculty of Health; Institute of Health and Biomedical Innovation(2020)10.17615/psgr-b356

N/A

0DataRank · unranked

0 citations

Vincenza Colonna, Timothy M. Frayling, Stefania Bandinelli, Tōnu Esko, Jeanette Erdmann +27 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

Mediation Analysis Demonstrates That Trans-eQTLs Are Often Explained by Cis-Mediation: A Genome-Wide Analysis among 1,800 South Asians

UNC Libraries(2020)10.17615/5c5w-zd03

N/A

0DataRank · unranked

0 citations

Tōnu Esko, Muhammad G. Kibriya, Harm-Jan Westra, Shantanu Roy, Lude Franke +12 more

Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease

Cell Reports Medicine(2021)10.1016/j.xcrm.2021.100437

N/A

0DataRank · unranked

256 citations

Erik Abner, Connor A. Emdin, Émilie Gobeil, Nele Taba, Mary E. Haas +15 more

Electronic Health Record-Based Genome-Wide Meta-Analysis and Mendelian Randomization Identify Metabolic and Phenotypic Consequences of Non-Alcoholic Fatty Liver Disease

(2020)10.21203/rs.3.rs-97977/v1

N/A

0DataRank · unranked

1 citations

Erik Abner, Émilie Gobeil, Nele Taba, Alexis St-Amand, Nicolas Perrot +10 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

Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics

UNC Libraries(2020)10.17615/qhxy-td18

N/A

0DataRank · unranked

1 citations

Kari E. North, D. Y. Lin, Andrea Ganna, Felix R. Day, Eleanor Wheeler +23 more

Genome-wide association study identifies five risk loci for pernicious anemia

Nature Communications(2021)10.1038/s41467-021-24051-6

N/A

0DataRank · unranked

52 citations

Maarja Lepamets, Mariann Koel, Erik Abner, Andres Metspalu, Mari Nelis +4 more

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

WOS(2020)10.17615/dkeh-7r02

N/A

0DataRank · unranked

1 citations

Jian Yang, Guðmar Þorleifsson, Josine L. Min, Andrew R. Wood, Keri L. Monda +27 more

Common variants associated with plasma triglycerides and risk for coronary artery disease

UNC Libraries(2020)10.17615/3nfp-v503

N/A

0DataRank · unranked

4 citations

Hsing‐Yi Chang, Åsa Johansson, Pierre Fontanillas, Martin L. Buchkovich, Ross M. Fraser +27 more

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/9vzs-j703

N/A

0DataRank · unranked

4 citations

Lin, P, Antonio Terracciano, Dale R. Nyholt, Anu Realo, Scott D. Gordon +27 more

Polymorphic Inversions Underlie the Shared Genetic Susceptibility of Obesity-Related Diseases

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.017

N/A

0DataRank · unranked

26 citations

Carlos Ruiz-Arenas, Alejandro Cáceres, Ignasi Morán, Marcos López‐Sánchez, Lorena Alonso +8 more

Using genetic variation to disentangle the complex relationship between food intake and health outcomes.

DOAJ (DOAJ: Directory of Open Access Journals)(2021)10.17863/cam.85186

N/A

0DataRank · unranked

16 citations

Ciara McDonnell, Eryk J. Grzeszkowiak, Ninon Mounier, Fumiaki Imamura, Jordi Merino +16 more

Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

medRxiv(2021)10.1101/2021.04.01.21254789

N/A

0DataRank · unranked

9 citations

Jack Gisby, Artemis Papadaki, Marisa D. Muckian, Erin Macdonald-Dunlop, Jing Hua Zhao +64 more

Electronic Health Record-Based Genome-Wide Meta-Analysis and Mendelian Randomization Identify Metabolic and Phenotypic Consequences of Non-Alcoholic Fatty Liver Disease

Research Square(2021)10.21203/rs.3.rs-97977/v2

N/A

0DataRank · unranked

0 citations

Erik Abner, Connor A. Emdin, Émilie Gobeil, Nele Taba, Mary J. Haas +16 more

Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort study

European Heart Journal(2020)10.1093/eurheartj/ehaa571

N/A

0DataRank · unranked

30 citations

Kristi Läll, Oliver Dukes, Giovanni Veronesi, Hynek Pikhart, Anne Peasey +11 more

Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies

Addiction Biology(2020)10.1111/adb.12880

N/A

0DataRank · unranked

74 citations

Emma C. Johnson, Yi‐Ling Chou, Jonathan R. I. Coleman, Laura M. Thornton, Raymond K. Walters +95 more

Differences in local population history at the finest level: the case of the Estonian population

European Journal of Human Genetics(2020)10.1038/s41431-020-0699-4

N/A

0DataRank · unranked

83 citations

Francesco Montinaro, Alena Kushniarevich, Georgi Hudjashov, Flora Jay, Lauri Saag +16 more

Genetic and In Vitro Inhibition of PCSK9 and Calcific Aortic Valve Stenosis

JACC Basic to Translational Science(2020)10.1016/j.jacbts.2020.05.004

N/A

0DataRank · unranked

90 citations

Vincenza Valerio, Donato Moschetta, S. Matthijs Boekholdt, Christian Dina, Hao Yu Chen +24 more

Using genetic variation to disentangle the complex relationship between food intake and health outcomes

PLoS Genetics(2022)10.1371/journal.pgen.1010162

N/A

0DataRank · unranked

82 citations

Ciara McDonnell, Eryk J. Grzeszkowiak, Ninon Mounier, Fumiaki Imamura, Jordi Merino +16 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

Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse

Nature Communications(2022)10.1038/s41467-022-31188-5

N/A

0DataRank · unranked

35 citations

Kristi Läll, Maarja Lepamets, Andres Metspalu, Mari Nelis, Lili Milani +8 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.30.486451

N/A

0DataRank · unranked

3 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +7 more

The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

UNC Libraries(2020)10.17615/3we9-ae42

Top 100%

0DataRank

Top 100%0 citations

David S. DeLuca, Ayellet V. Segrè, Timothy J. Sullivan, Timothy R. Young, Ellen T. Gelfand +27 more

Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis

Gastroenterology(2023)10.1053/j.gastro.2023.01.028

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0DataRank · unranked

74 citations

Erik Abner, Hasanga D. Manikpurage, Natàlia Pujol‐Gualdo, Triin Laisk, Émilie Gobeil +8 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

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0 citations

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

HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases

Communications Biology(2023)10.1038/s42003-023-05496-5

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33 citations

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GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets

medRxiv(2023)10.1101/2023.10.04.23296543

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0DataRank · unranked

31 citations

Philip E. Stuart, John Bowes, David Ellinghaus, Joanne Nititham, Jake Saklatvala +81 more

HLA allele-calling using whole-exome sequencing identifies 129 novel associations in 11 autoimmune diseases: a multi-ancestry analysis in the UK Biobank

medRxiv(2023)10.1101/2023.01.15.23284570

N/A

0DataRank · unranked

1 citations

Yossi Farjoun, Tomoko Nakanishi, Tianyuan Lu, Erik Abner, Yiheng Chen +17 more

Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

Nature Genetics(2024)10.1038/s41588-023-01607-4

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0DataRank · unranked

82 citations

Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jacqueline I. Goldstein +23 more

Genetic drivers and cellular selection of female mosaic X chromosome loss

Nature(2024)10.1038/s41586-024-07533-7

N/A

0DataRank · unranked

45 citations

Giulio Genovese, Yajie Zhao, Matti Pirinen, Seyedeh M. Zekavat, Katherine A. Kentistou +95 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

High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6

medRxiv(2024)10.1101/2024.07.09.24310146

N/A

0DataRank · unranked

1 citations

Pekka Nieminen, Priyanka Kumari, Emma Juuri, Tiit Nikopensius, Kitt Paraiso +23 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

UNC Libraries(2024)10.17615/9849-hx54

N/A

0DataRank · unranked

0 citations

M. FORNAGE, J.I. Rotter, Michael R. Brown, L.-P. Lyytikäinen, B. Kühnel +95 more

Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction

UNC Libraries(2024)10.17615/14dq-dd86

N/A

0DataRank · unranked

0 citations

Ingileif Jónsdóttir, Ástrós Skúladóttir, Kāri Stefánsson, Hreinn Stefánsson, Rafael Meleka Hanna +35 more

An Updated Polygenic Index Repository: Expanded Phenotypes, New Cohorts, and Improved Causal Inference

Research Square(2025)10.21203/rs.3.rs-7828579/v1

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Robel Alemu, Anastasia Terskaya, Matthew Howell, Junming Guan, Harry Sands +45 more

FTO genotype is associated with phenotypic variability of body mass index

UNC Libraries(2020)10.17615/yvv7-bx40

N/A

0DataRank · unranked

0 citations

Ayşe Demirkan, David Hadley, Cameron D. Palmer, Sarah E. Medland, Ruth J. F. Loos +27 more

Mechanistic endotyping of the ROS/cGMP disease cluster in the Estonian Biobank

Mechanistic endotyping of the ROS/cGMP disease cluster in the Estonian Biobank10.58647/rexpo.23000033.v1

N/A

0DataRank · unranked

0 citations

Jaanika Kronberg, Alexandra Petraina, Mayra Pacheco Pachado, Mari Nelis, Lili Milani +5 more

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

Research at the University of Copenhagen (University of Copenhagen)(2020)10.17615/07fz-zt78

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0DataRank · unranked

0 citations

Stavroula Kanoni, Ghazaleh Fatemifar, Tiina Laatikainen, Cristina Menni, Yingchang Lu +95 more

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

UNC Libraries(2020)10.17615/vn1s-8a35

N/A

0DataRank · unranked

0 citations

Frank J.A. van Rooij, Raha Pazoki, Albert Hofman, Nathan Pankratz, Richard A. Gibbs +51 more

Quality control and conduct of genome-wide association meta-analyses

UNC Libraries(2020)10.17615/e53z-k780

N/A

0DataRank · unranked

0 citations

Damien C. Croteau‐Chonka, Reedik Mägi, Joshua C. Randall, Zoltán Kutalik, Mariaelisa Graff +15 more

GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk

UNC Libraries(2020)10.17615/rrsv-7t13

N/A

0DataRank · unranked

0 citations

Paul S. de Vries, Marco Colombo, Athina Spiliopoulou, Paul McKeigue, Peter Kraft +11 more

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

UNC Libraries(2020)10.17615/a384-d483

N/A

0DataRank · unranked

0 citations

Jerome I. Rotter, Alex P. Reiner, André G. Uitterlinden, Gonçalo R. Abecasis, Digna R. Velez Edwards +95 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

0DataRank · unranked

0 citations

Lisa R. Yanek, Kjell Nikus, Salman M. Tajuddin, Jussi Hernesniemi, Dawn Waterworth +95 more

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

UNC Libraries(2020)10.17615/7b47-zt44

N/A

0DataRank · unranked

0 citations

Niek Verweij, Daniel O. Stram, Folkert W. Asselbergs, John C. Chambers, Hirotsugu Ueshima +24 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

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Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 more

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

UNC Libraries(2020)10.17615/kf29-bk98

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