Jonas B. Nielsen

Also affiliated with Copenhagen University Hospital, Aalborg Zoo, University of Gothenburg, Aalborg University

MedicineBiochemistry, 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

5.3Author 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.

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

PLoS Genetics(2020)10.1371/journal.pgen.1008725

Top 13%

1.6DataRank

Top 13%57 citations

Judith M. Vonk, Hansjörg Baurecht, Ingo Marenholz, Chao Tian, Joshua Hoffman +36 more

Papers

Driven by 35 papers — median percentile 81. Top paper: “A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease”.

A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

Nature Genetics(2021)10.1038/s41588-021-00921-z

N/A

8.0DataRank · unranked

1105 citations

Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Dominic Holland +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

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 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

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

PLoS Genetics(2020)10.1371/journal.pgen.1008725

Top 13%

1.6DataRank

Top 13%57 citations

Judith M. Vonk, Hansjörg Baurecht, Ingo Marenholz, Chao Tian, Joshua Hoffman +36 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

The HUNT study: A population-based cohort for genetic research

Cell Genomics(2022)10.1016/j.xgen.2022.100193

Top 14%

1.5DataRank

Top 14%108 citations

Sarah E. Graham, Ida Surakka, Anne Heidi Skogholt, Mari Løset, Lars G. Fritsche +25 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

Mitochondrial genome-wide association study of migraine – the HUNT Study

Cephalalgia(2020)10.1177/0333102420906835

Top 19%

1.1DataRank

Top 19%28 citations

John‐Anker Zwart, Anne Heidi Skogholt, Maiken E. Gabrielsen, Laurent F. Thomas, Lars G. Fritsche +13 more

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

Hypertension(2022)10.1161/hypertensionaha.122.19324

Top 24%

0.842DataRank

Top 24%29 citations

Xiao Sun, Karen He, Michael R. Brown, Sarah A. Gagliano Taliun, Jacklyn N. Hellwege +95 more

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Nature Genetics(2022)10.1038/s41588-022-01078-z

N/A

0.793DataRank · unranked

197 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +86 more

Divergent role of Mitochondrial Amidoxime Reducing Component 1 (MARC1) in human and mouse

PLoS Genetics(2024)10.1371/journal.pgen.1011179

N/A

0.679DataRank · unranked

15 citations

Lisa M. Shihanian, Ivory J. Mintah, Parnian Bigdelou, Yuliya Livson, Heather M. Brown +14 more

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Human Molecular Genetics(2013)10.1093/hmg/ddt588

N/A

0.650DataRank · unranked

75 citations

A. D. Johnson, B. M. Snively, Jarmo Virtamo, P. L. Auer, Jonas B. Nielsen +34 more

Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

Stroke(2023)10.1161/strokeaha.122.040715

N/A

0.520DataRank · unranked

31 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik Slagsvold Winsvold, John‐Anker Zwart +95 more

A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

medRxiv(2021)10.1101/2020.12.26.20248491

N/A

0.425DataRank · unranked

16 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +85 more

Agendas, Alternatives, and Public Policies

Journal of Policy Analysis and Management(1985)10.2307/3323801

N/A

0.425DataRank · unranked

16 citations

John W. Kingdon, James L. Perry, Jonas B. Nielsen

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

COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study

Osteoarthritis and Cartilage Open(2023)10.1016/j.ocarto.2023.100424

N/A

0DataRank · unranked

8 citations

Sigrid Børte, Lene Bjerke Laborie, Hege Kristiansen, Annette Schäfer, Amy E. Martinsen +25 more

Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

EBioMedicine(2024)10.1016/j.ebiom.2024.105233

N/A

0DataRank · unranked

14 citations

Chelsea A. Isom, Yangzi Liu, David-Alexandre Trégouët, Sara Lindström, Lu Wang +52 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

0DataRank · unranked

141 citations

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

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

0DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +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

0DataRank · unranked

37 citations

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

Assessment of a causal relationship between body mass index and atopic dermatitis

Journal of Allergy and Clinical Immunology(2020)10.1016/j.jaci.2020.04.050

N/A

0DataRank · unranked

26 citations

Sarah Watkins, Ben Brumpton, Mari Løset, Jessica Tyrrell, Ellen Heilmann Modalsli +10 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

0DataRank · unranked

43 citations

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

Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population

medRxiv(2020)10.1101/2020.09.04.20187401

N/A

0DataRank · unranked

0 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +22 more

Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools

Brain(2021)10.1093/brain/awab267

N/A

0DataRank · unranked

66 citations

Guy Hindley, Bendik Slagsvold Winsvold, Kevin S. O’Connell, Oleksandr Frei, Alexey Shadrin +35 more

Genome-wide association study of cardiac troponin I in the general population

Human Molecular Genetics(2021)10.1093/hmg/ddab124

N/A

0DataRank · unranked

20 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +25 more

Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2

iScience(2021)10.1016/j.isci.2021.103196

N/A

0DataRank · unranked

17 citations

Brooke N. Wolford, Haocheng Lu, Wenying Liang, Jinjian Sun, Wei Zhou +20 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

0DataRank · unranked

69 citations

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

Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT

medRxiv(2021)10.1101/2021.09.20.21262960

N/A

0DataRank · unranked

3 citations

Ailin Falkmo Hansen, Sarah E. Graham, Sarah A. Gagliano Taliun, Kuan-Han Wu, Wei Zhou +14 more

Utility of family history in disease prediction in the era of polygenic scores

medRxiv(2021)10.1101/2021.06.25.21259158

N/A

0DataRank · unranked

1 citations

Ida Surakka, Sarah E. Graham, Jonas B. Nielsen, Wei Zhou, Maiken E. Gabrielsen +11 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Germline Mutations in CIDEB and Protection against Liver Disease

New England Journal of Medicine(2022)10.1056/nejmoa2117872

N/A

0DataRank · unranked

125 citations

Mary E. Haas, Jonas B. Nielsen, Olukayode Sosina, Minhee Kim, Parsa Akbari +42 more

Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

Journal of Clinical Investigation(2022)10.1172/jci158788

N/A

0DataRank · unranked

74 citations

Daniel J. Tyrrell, Alexi Vasbinder, Changli Wei, Feriel Presswalla, Hui Wang +37 more

Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT

Communications Biology(2022)10.1038/s42003-022-03529-z

N/A

0DataRank · unranked

39 citations

Sarah E. Graham, Kuan-Han H. Wu, Ailin Falkmo Hansen, Sarah A. Gagliano Taliun, Wei Zhou +14 more

Jonas B. Nielsen

Indexed papers

Top data-sharing exemplar

Papers