Kāri Stefánsson

Also affiliated with University of Iceland

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 2%percentile

3.7Author DataRank

Indexed papers

6in 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 6 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.

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

Papers

Driven by 68 papers — median percentile 58. Top paper: “Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants”.

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature Genetics(2022)10.1038/s41588-022-01233-6

N/A

7.7DataRank · unranked

721 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri +92 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Nature Genetics(2023)10.1038/s41588-022-01285-8

N/A

6.1DataRank · unranked

775 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen +81 more

GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

Nature Communications(2020)10.1038/s41467-020-17718-z

N/A

4.0DataRank · unranked

141 citations

Ben Brumpton, Ömer Kabil, Jūlı́us Guðmundsson, Guðmar Þorleifsson, Joshua S. Weinstock +51 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

Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

Nature Medicine(2023)10.1038/s41591-023-02352-1

N/A

3.6DataRank · unranked

313 citations

Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko +38 more

Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

European Heart Journal(2023)10.1093/eurheartj/ehad142

N/A

2.9DataRank · unranked

113 citations

Christian Dina, Aeron Small, Christian M. Shaffer, Rebecca T. Levinson, Anna Helgadóttir +52 more

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

Nature Genetics(2022)10.1038/s41588-022-01115-x

N/A

2.1DataRank · unranked

123 citations

Younghun Han, Yafang Li, Jun Xia, Erping Long, Jiyeon Choi +80 more

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

Nature Genetics(2023)10.1038/s41588-023-01510-y

N/A

1.6DataRank · unranked

100 citations

Derek Klarin, Michael G. Levin, Joshua M. Spin, Yae Hyun Rhee, Alicia Deng +92 more

Identification of 22 susceptibility loci associated with testicular germ cell tumors

Nature Communications(2021)10.1038/s41467-021-24334-y

N/A

1.5DataRank · unranked

73 citations

Louise C. Pyle, Kevin T. Nead, Rona Wilf, Mingyao Li, Nandita Mitra +52 more

Largest GWAS (N=1,126,563) of Alzheimer’s Disease Implicates Microglia and Immune Cells

medRxiv(2020)10.1101/2020.11.20.20235275

N/A

1.5DataRank · unranked

43 citations

Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Arvid Rongve +52 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

medRxiv(2022)10.1101/2022.02.14.22270780

N/A

1.5DataRank · unranked

63 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Leila Farajzadeh +42 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

Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma

Nature Communications(2024)10.1038/s41467-023-44380-y

N/A

1.0DataRank · unranked

64 citations

Wenjun Yan, John M. Rouhana, Aboozar Monovarfeshani, Xinyi Jiang, Puja A. Mehta +65 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

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

Nature Genetics(2023)10.1038/s41588-023-01323-z

N/A

0.853DataRank · unranked

293 citations

Sally Mortlock, Marzieh Ghiasi, Peter Möller, Lilja Stefánsdóttir, Geneviève Galarneau +95 more

The Norwegian Mother, Father, and Child cohort study (MoBa) genotyping data resource: MoBaPsychGen pipeline v.1

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.23.496289

Top 25%

0.821DataRank

Top 25%103 citations

Alexey Shadrin, Oleksandr Frei, Zillur Rahman, Aihua Lin, Lavinia Athanasiu +22 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

Variable number tandem repeats mediate the expression of proximal genes

Nature Communications(2021)10.1038/s41467-021-22206-z

N/A

0.702DataRank · unranked

107 citations

Jonghun Park, Yuan-Chun Ding, Sharona Shleizer-Burko, Susan L. Neuhausen, Bjarni V. Halldórsson +4 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

Variable Number Tandem Repeats mediate the expression of proximal genes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.25.114082

N/A

0.685DataRank · unranked

14 citations

Jonghun Park, Yuan-Chun Ding, Sharona Shleizer-Burko, Susan L. Neuhausen, Bjarni V. Halldórsson +4 more

Genome-Wide Association Study of Peripheral Artery Disease

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.119.002862

N/A

0.670DataRank · unranked

86 citations

Alexander Stiby, Moustafa Abdalla, Erin Austin, Stela McLachlan, Efthymia Vlachopoulou +50 more

Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights

European Urology(2023)10.1016/j.eururo.2023.04.020

N/A

0.650DataRank · unranked

75 citations

Lambertus A. Kiemeney, Parichoy Pal Choudhury, Roger L. Milne, Evangelina López de Maturana, Yuanqing Ye +95 more

Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities

medRxiv(2022)10.1101/2022.08.24.22279149

N/A

0.648DataRank · unranked

12 citations

Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko +38 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

medRxiv(2021)10.1101/2021.05.24.21257377

N/A

0.637DataRank · unranked

69 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Elle M. Weeks +87 more

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Nature Genetics(2023)10.1038/s41588-023-01538-0

N/A

0.606DataRank · unranked

56 citations

Mona Ameri Chalmer, Lilja Stefánsdóttir, Ástrós Skúladóttir, Guðmundur Einarsson, Margrét B. Andrésdóttir +88 more

Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma

Nature Communications(2020)10.1038/s41467-020-14594-5

N/A

0.578DataRank · unranked

46 citations

Yuan Lin, Roxana Daneshjou, Andrey Ziyatdinov, Guðmar Þorleifsson, Adam J. Rubin +17 more

Genetic Associations and Architecture of Asthma-COPD Overlap

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

N/A

0.574DataRank · unranked

45 citations

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

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy

Nature Genetics(2025)10.1038/s41588-025-02159-5

N/A

0.571DataRank · unranked

44 citations

Koenraad De Wispelaere, Jonathan Lees, Marta Codina‐Solà, Brynjar Ö. Jensson, Emma Hales +47 more

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.002

N/A

0.568DataRank · unranked

43 citations

Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong +95 more

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Nature Communications(2020)10.1038/s41467-020-17315-0

N/A

0.546DataRank · unranked

37 citations

Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu +45 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

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

Molecular Psychiatry(2022)10.1038/s41380-022-01775-5

N/A

0.510DataRank · unranked

29 citations

Jeggan Tiego, Ditte Demontis, G. Bragi Walters, Hreinn Stefánsson, Kāri Stefánsson +4 more

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Human Reproduction(2023)10.1093/humrep/dead247

N/A

0.505DataRank · unranked

28 citations

Scott D. Gordon, David L Duffy, Nikki Hubers, Sally Mortlock, Jeffrey J. Beck +52 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

Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32951

Top 41%

0.456DataRank

Top 41%11 citations

Emma Sprooten, Peter Mulders, Janna N. Vrijsen, Janita Bralten, Ditte Demontis +8 more

Polygenic risk scores associate with blood pressure traits across the lifespan

European Journal of Preventive Cardiology(2023)10.1093/eurjpc/zwad365

N/A

0.449DataRank · unranked

19 citations

Emma Ingeström, Michail Spitieris, Vinicius Tragante, Kaitlin H Wade, Laurent F. Thomas +8 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

0.447DataRank · unranked

15 citations

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

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature Communications(2022)10.1038/s41467-022-35354-7

N/A

0.442DataRank · unranked

18 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA Working Groups on CNVs

PsyArXiv (OSF Preprints)(2021)10.31234/osf.io/57erc

Top 43%

0.437DataRank

Top 43%12 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Julio E. Villalón‐Reina, Ingrid Agartz +95 more

Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci

European Heart Journal(2022)10.1093/eurheartj/ehac322

N/A

0.434DataRank · unranked

17 citations

Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W. Skov, Dan M. Roden +22 more

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders

Biological Psychiatry(2024)10.1016/j.biopsych.2024.07.025

Top 44%

0.421DataRank

Top 44%13 citations

Matthew Halvorsen, Jakob Grove, Bergrún Ásbjörnsdóttir, Pétur Lúðvígsson, Ólafur Thorarensen +93 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

Recommendations for defining treatment outcomes in major psychiatric disorders using real-world data

The Lancet Psychiatry(2025)10.1016/s2215-0366(25)00061-6

N/A

0.406DataRank · unranked

14 citations

Sophie E. Smart, Guðmundur Einarsson, Anders Kämpe, Lina Jönsson, Maris Alver +25 more

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00752-9

N/A

0.385DataRank · unranked

12 citations

Vinicius Tragante, Garðar Sveinbjörnsson, Hannes Helgason, Árni Sturluson, Anna Bjornsdottir +18 more

Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study

Journal of the American Heart Association(2024)10.1161/jaha.123.034612

N/A

0.345DataRank · unranked

9 citations

Emma M. L. Ingeström, Michail Spitieris, Vinicius Tragante, Laurent F. Thomas, Ingelin Steinsland +7 more

Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

Nature Communications(2025)10.1038/s41467-024-55761-2

N/A

0.329DataRank · unranked

6 citations

Brandon E. M. Lim, Lena R Kaisinger, Valgerður Steinthórsdóttir, Luke N Sharp, Kashyap A. Patel +17 more

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

medRxiv(2024)10.1101/2024.07.13.24310361

N/A

0.312DataRank · unranked

7 citations

Tuuli Jürgenson, Guðmundur Einarsson, Brittany L. Mitchell, Arvid Harder, Luis M. García‐Marín +18 more

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

medRxiv(2021)10.1101/2021.12.16.21267871

N/A

0.292DataRank · unranked

6 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

Research Square(2024)10.21203/rs.3.rs-5418279/v1

N/A

0.277DataRank · unranked

4 citations

Tuuli Jürgenson, Guðmundur Einarsson, Brittany L. Mitchell, Arvid Harder, Luis M. García‐Marín +21 more

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

N/A

0.241DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

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

medRxiv(2020)10.1101/2020.11.26.20236760

N/A

0.165DataRank · unranked

2 citations

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

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

medRxiv(2025)10.1101/2025.05.06.25326635

N/A

0.165DataRank · unranked

2 citations

Eirny Tholl Thorolfsdottir, Ilana M. Nodelman, Sara Tholl Halldorsdottir, Stefania Benónísdóttir, Malak Alghamdi +64 more

Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases

medRxiv(2025)10.1101/2025.05.15.25327513

Top 70%

0.165DataRank

Top 70%2 citations

Maizy S. Brasher, Jack Pattee, Wei Zhou, Sinéad B. Chapman, Yon Ho Jee +79 more

Multi-polygenic scores in psychiatry: from disorder-specific to transdiagnostic perspectives

medRxiv(2022)10.1101/2022.05.30.22275563

N/A

0.118DataRank · unranked

1 citations

Emma Sprooten, Peter Mulders, Janna N. Vrijsen, Janita Bralten, Ditte Demontis +8 more

The genetic architecture of fibromyalgia across 2.5 million individuals

medRxiv(2025)10.1101/2025.09.18.25335914

N/A

0.104DataRank · unranked

1 citations

Gyða Björnsdóttir, Keon Arbabi, Lea Urpa, Hele Haapaniemi, Gudmar Thorleifsson +46 more

Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32967

N/A

0.104DataRank · unranked

1 citations

G. Bragi Walters, Hreinn Stefánsson, Kāri Stefánsson, Franziska Degenhardt, Markus M. Nöthen +7 more

Pregnancy-Associated Bleeding and Genetics: Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage

medRxiv(2023)10.1101/2023.08.10.23293932

N/A

0.104DataRank · unranked

1 citations

Valgerður Steinthórsdóttir, Lilja Stefánsdóttir, Palle Duun Rohde, Xiaoping Wu, Frank Geller +37 more

Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

medRxiv(2024)10.1101/2024.04.03.24305248

N/A

0.104DataRank · unranked

1 citations

Brandon E. M. Lim, Lena R Kaisinger, Valgerður Steinthórsdóttir, Luke N Sharp, Kashyap A. Patel +17 more

Disentangling the shared genetics of ADHD, cannabis use disorder and cannabis use and prediction of cannabis use disorder in ADHD

medRxiv(2024)10.1101/2024.02.22.24303124

N/A

0.104DataRank · unranked

1 citations

Jinjie Duan, Daniel Levey, G. Bragi Walters, Emma C. Johnson, Thorgeir E. Thorgeirsson +12 more

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.31.494251

N/A

0.104DataRank · unranked

1 citations

Jeggan Tiego, Ditte Demontis, G. Bragi Walters, Hreinn Stefánsson, Kāri Stefánsson +4 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

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

UCL Discovery (University College London)(2020)10.17615/snbr-qh40

N/A

0DataRank · unranked

0 citations

Kung‐Yee Liang, Per Hoffman, Stefan Herms, Gary Donohoe, Luba Kalaydjieva +94 more

PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.016

N/A

0DataRank · unranked

10 citations

Cory Rosenfelt, Virginie Vignard, Jonas Johannes Papendorf, Sophie Möller, Martin Wendlandt +42 more

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

UNC Libraries(2020)10.17615/p2f9-t736

N/A

0DataRank · unranked

0 citations

Jeff K. Trimmer, Pål R. Njølstad, Allan Linneberg, Kāri Stefánsson, David R. Cox +16 more

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

UNC Libraries(2020)10.17615/k3vg-tb84

N/A

0DataRank · unranked

0 citations

Stacy Steinberg, Johannes H. Smit, Tim B. Bigdeli, Kāri Stefánsson, Stefan Kloiber +71 more

Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

UNC Libraries(2020)10.17615/3aw7-xt71

N/A

0DataRank · unranked

0 citations

Daníel F. Guðbjartsson, Ranil DeSilva, Kāri Stefánsson, Gérard Waeber, Yuri Milaneschi +27 more

Data from Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

(2023)10.1158/0008-5472.c.6512925.v1

N/A

0DataRank · unranked

0 citations

Simon Stacey, Garðar Sveinbjörnsson, Guðmar Þorleifsson, Kristján Norland, Bárður Sigurgeirsson +34 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

Kāri Stefánsson

Indexed papers

Top data-sharing exemplar

Papers