Daníel F. Guðbjartsson

Also affiliated with University of Iceland, Mahindra and Mahindra Limited (India)

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

8.6Author DataRank

Indexed papers

3in 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 3 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.

Parental influence on human germline de novo mutations in 1,548 trios from Iceland

Nature(2017)10.1038/nature24018

Top 3%

6.4DataRank

Top 3%657 citations

Patrick Sulem, Birte Kehr, Snaedis Kristmundsdottir, Florian Zink, Eirikur Hjartarson +36 more

Papers

Driven by 38 papers — median percentile 85. Top paper: “The power of genetic diversity in genome-wide association studies of lipids”.

The power of genetic diversity in genome-wide association studies of lipids

Nature(2021)10.1038/s41586-021-04064-3

N/A

9.9DataRank · unranked

1069 citations

Shoa L. Clarke, Kuan-Han H. Wu, Stavroula Kanoni, Greg J. M. Zajac, Shweta Ramdas +95 more

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

Parental influence on human germline de novo mutations in 1,548 trios from Iceland

Nature(2017)10.1038/nature24018

Top 3%

6.4DataRank

Top 3%657 citations

Patrick Sulem, Birte Kehr, Snaedis Kristmundsdottir, Florian Zink, Eirikur Hjartarson +36 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

A large-scale genome-wide association study meta-analysis of cannabis use disorder

The Lancet Psychiatry(2020)10.1016/s2215-0366(20)30339-4

N/A

5.5DataRank · unranked

384 citations

Ditte Demontis, Thorgeir E. Thorgeirsson, Raymond K. Walters, Renato Polimanti, Alexander S. Hatoum +91 more

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

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 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

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

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 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

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

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

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 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

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

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Genome biology(2022)10.1186/s13059-022-02837-1

N/A

0.626DataRank · unranked

64 citations

Sarah E. Graham, Yuxuan Wang, Ida Surakka, Shweta Ramdas, Xiang Zhu +95 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

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Kidney International(2022)10.1016/j.kint.2022.05.021

N/A

0.601DataRank · unranked

54 citations

Humaira Rasheed, Alexander Teumer, Laurent F. Thomas, Sarah E. Graham, Garðar Sveinbjörnsson +94 more

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Communications Biology(2022)10.1038/s42003-022-03448-z

N/A

0.553DataRank · unranked

39 citations

Humaira Rasheed, Alexander Teumer, Mathias Gorski, Bryce Rowan, Kira J. Stanzick +94 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

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

Author Correction: The power of genetic diversity in genome-wide association studies of lipids

Nature(2023)10.1038/s41586-023-06194-2

N/A

0.416DataRank · unranked

15 citations

Shoa L. Clarke, Kuan-Han H. Wu, Stavroula Kanoni, Greg J. M. Zajac, Shweta Ramdas +95 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

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

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

The genetic architecture of fibromyalgia across 2.5 million individuals

medRxiv(2025)10.1101/2025.09.18.25335914

N/A

0DataRank · unranked

1 citations

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

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.06.012

N/A

0DataRank · unranked

64 citations

Jonathan Judd, Sarah E. Graham, Stavroula Kanoni, Yuxuan Wang, Ida Surakka +95 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

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

Human Reproduction(2023)10.1093/humrep/dead247

N/A

0DataRank · unranked

27 citations

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

0DataRank · unranked

1 citations

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

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

0DataRank · unranked

37 citations

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

Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage

Nature Genetics(2024)10.1038/s41588-024-01839-y

N/A

0DataRank · unranked

10 citations

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

0DataRank · unranked

8 citations

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

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 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

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more

Daníel F. Guðbjartsson

Indexed papers

Top data-sharing exemplar

Papers