Reedik Mägi

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

14.4Author DataRank

Indexed papers

11in 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 11 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.

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

The Lancet Respiratory Medicine(2015)10.1016/s2213-2600(15)00283-0

Top 2%

7.7DataRank

Top 2%438 citations

Nick Shrine, Suzanne Miller, Victoria E. Jackson, Ioanna Ntalla, María Soler Artigas +39 more

Papers

Driven by 70 papers — median percentile 77. 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

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

The Lancet Respiratory Medicine(2015)10.1016/s2213-2600(15)00283-0

Top 2%

7.7DataRank

Top 2%438 citations

Nick Shrine, Suzanne Miller, Victoria E. Jackson, Ioanna Ntalla, María Soler Artigas +39 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

Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study

The Lancet Public Health(2022)10.1016/s2468-2667(22)00042-1

N/A

4.6DataRank · unranked

169 citations

Anikó Lovik, Anna Bára Unnarsdóttir, Daniel L. McCartney, Helga Ask, Kadri Kõiv +44 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

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

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

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

N/A

2.3DataRank · unranked

93 citations

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

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y

Top 15%

1.4DataRank

Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 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

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Nature Genetics(2010)10.1038/ng.520

N/A

1.2DataRank · unranked

2239 citations

Josée Dupuis, Claudia Langenberg, Inga Prokopenko, Richa Saxena, Nicole Soranzo +257 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

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

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 trans-ancestral genomic architecture of glycemic traits

Nature Genetics(2021)10.1038/s41588-021-00852-9

N/A

1.0DataRank · unranked

907 citations

Cassandra N. Spracklen, Gaëlle Marenne, Arushi Varshney, Laura J. Corbin, Jian’an Luan +95 more

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature Genetics(2012)10.1038/ng.2274

N/A

1.0DataRank · unranked

897 citations

Marie-France Hivert, Robert A Scott, Jonna L Grimsby, Nabila Bouatia-Naji, Han Chen +211 more

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Nature Genetics(2012)10.1038/ng.2385

N/A

1.0DataRank · unranked

862 citations

Vasiliki Lagou, Ryan P Welch, Eleanor Wheeler, May E Montasser, Jian'an Luan +209 more

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

medRxiv(2023)10.1101/2023.10.04.23296543

N/A

0.872DataRank · unranked

31 citations

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

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes

Human Molecular Genetics(2022)10.1093/hmg/ddac050

N/A

0.730DataRank · unranked

129 citations

Gunn-Helen Moen, Maria Carolina Borges, Teresa Ferreira, James P. Cook, Catherine Allard +68 more

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Cell Genomics(2023)10.1016/j.xgen.2022.100241

N/A

0.710DataRank · unranked

113 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +83 more

Genetic effects on the timing of parturition and links to fetal birth weight

Nature Genetics(2023)10.1038/s41588-023-01343-9

N/A

0.695DataRank · unranked

102 citations

Christopher Flatley, Valgerður Steinthórsdóttir, Marc Vaudel, Julius Juodakis, Jing Chen +80 more

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Diabetologia(2023)10.1007/s00125-023-05922-7

N/A

0.676DataRank · unranked

16 citations

Laura Brenner, Varinderpal Kaur, Katherine Figueroa, Philip Schroeder, Alicia Huerta‐Chagoya +95 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

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

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

N/A

0.663DataRank · unranked

82 citations

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

Characterising the genetic architecture of changes in adiposity during adulthood using electronic health records

Nature Communications(2024)10.1038/s41467-024-49998-0

Top 30%

0.656DataRank

Top 30%19 citations

Habib Ganjgahi, Duncan S. Palmer, Kayesha Coley, Gregorio V. Linchangco, Qin Hui +19 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

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

0.538DataRank · unranked

35 citations

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

Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

Nature Communications(2024)10.1038/s41467-024-50295-z

N/A

0.489DataRank · unranked

25 citations

Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie +4 more

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

Molecular Psychiatry(2021)10.1038/s41380-021-01087-0

N/A

0.483DataRank · unranked

24 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02156-8

N/A

0.464DataRank · unranked

21 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +57 more

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development

JHEP Reports(2025)10.1016/j.jhepr.2025.101485

N/A

0.410DataRank · unranked

11 citations

Helene Gellert‐Kristensen, Colm J. O’Rourke, Anne-Sofie Seidelin, Gudmar Thorleifsson, Garðar Sveinbjörnsson +43 more

Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection

medRxiv(2023)10.1101/2023.01.28.23285140

N/A

0.312DataRank · unranked

7 citations

Giulio Genovese, Yajie Zhao, Matti Pirinen, Maryam M. Zekavat, Katherine A. Kentistou +39 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

0.241DataRank · unranked

4 citations

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

Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity

WOS(2020)10.17615/5vbx-b108

N/A

0.241DataRank · unranked

4 citations

Inês Barroso, Andrea Benazzo, Denis Rybin, Felicity Payne, Niels Grarup +27 more

Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

medRxiv(2023)10.1101/2023.11.27.23297542

N/A

0.241DataRank · unranked

4 citations

Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie +3 more

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Oxford University Research Archive (ORA) (University of Oxford)(2020)10.17615/gc55-0r45

N/A

0.221DataRank · unranked

2 citations

Sonsoles Morcillo, Nicholas J. Wareham, Richard A. Jensen, Allan Linnenberg, Josée Dupuis +74 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.123505

N/A

0.208DataRank · unranked

3 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 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

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

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

Top 100%

0DataRank

Top 100%0 citations

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

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

UNC Libraries(2020)10.17615/qy4d-rv77

N/A

0DataRank · unranked

0 citations

Albert V. Smith, Stefan Gustafsson, Laura J. Rasmussen‐Torvik, J. Wouter Jukema, P. Johnson +27 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

N/A

0DataRank · unranked

33 citations

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

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

UNC Libraries(2020)10.17615/ebqa-yt43

N/A

0DataRank · unranked

0 citations

Elisabeth Widén, Nicole M. Warrington, Paul Elliott, Nabila Bouatia‐Naji, Philippe Froguel +27 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

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

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

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

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

Genome-wide association study identifies five risk loci for pernicious anemia and implicates the role of HLA-DR15 haplotype

medRxiv(2020)10.1101/2020.10.13.20211912

N/A

0DataRank · unranked

0 citations

Maarja Lepamets, Reedik Mägi, Triin Laisk

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

N/A

0DataRank · unranked

0 citations

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

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

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum

medRxiv(2024)10.1101/2024.03.19.24304530

N/A

0DataRank · unranked

15 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +46 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

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

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

GWAS meta-analysis identifies five susceptibility loci for endometrial cancer

EBioMedicine(2025)10.1016/j.ebiom.2025.105830

N/A

0DataRank · unranked

3 citations

Xue Min Wang, Triin Laisk, Ying Zheng, Nathan Ingold, Daffodil M. Canson +69 more

Genome-wide analysis of 64 male reproductive phenotypes reveals novel loci and shared biological pathways

medRxiv(2025)10.64898/2025.12.20.25342734

N/A

0DataRank · unranked

0 citations

Toomas Haller, Margus Punab, Triin Laisk, Reedik Mägi, Jéssica Figuerêdo

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

A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgz326

N/A

0DataRank · unranked

64 citations

Ky’Era V. Actkins, Jennifer A. Pacheco, Anna O. Basile, Robert J. Carroll, David R. Crosslin +66 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

Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics

Science Translational Medicine(2020)10.1126/scitranslmed.aay6570

N/A

0DataRank · unranked

117 citations

Kristi Krebs, Chia‐Yen Chen, Ruth Boxall, Jenny C. Censin, Teresa Ferreira +15 more

Global biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

medRxiv(2021)10.1101/2021.11.18.21266545

N/A

0DataRank · unranked

25 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +25 more

Advancing our understanding of genetic risk factors and potential personalized strategies in pelvic organ prolapse: largest GWAS to date reveals 19 novel associated loci

medRxiv(2021)10.1101/2021.07.08.21260068

N/A

0DataRank · unranked

0 citations

Kristi Läll, Maarja Lepamets, Henna‐Riikka Rossi, Riikka K. Arffman, Terhi Piltonen +3 more

Patterns of genetic connectedness between modern and medieval Estonian genomes reveal the origins of a major ancestry component of the Finnish population

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.07.012

N/A

0DataRank · unranked

26 citations

Lehti Saag, Ruoyun Hui, Simone Andrea Biagini, Vasili Pankratov, Eugenia D’Atanasio +16 more

Reedik Mägi

Indexed papers

Top data-sharing exemplar

Papers