Christian Fuchsberger

Also affiliated with Institute for Biomedicine

Medicine

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

25.9Author DataRank

Indexed papers

7in 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 7 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 global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 46 papers — median percentile 49. Top paper: “Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion”.

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Nature Genetics(2013)10.1038/ng.2507

N/A

11.0DataRank · unranked

295 citations

Anne U Jackson, Marie P Fogarty, Martin L Buchkovich, Alena Stančáková, Heather M Stringham +24 more

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +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

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

Nature Communications(2022)10.1038/s41467-022-29143-5

N/A

3.9DataRank · unranked

196 citations

Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke +33 more

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

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

N/A

1.6DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Proceedings of the National Academy of Sciences(2017)10.1073/pnas.1705859115

N/A

1.2DataRank · unranked

36 citations

Alisa Manning, Marcio Almeida, Matthew Zawistowski, Katharina Domschke, Tanya M. Teslovich +82 more

Reference-based phasing using the Haplotype Reference Consortium panel

Nature Genetics(2016)10.1038/ng.3679

N/A

1.1DataRank · unranked

1987 citations

Chris O’Sullivan, Pier Francesco Palamara, Christian Fuchsberger, Yakir A Reshef, Hilary K. Finucane +9 more

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Nature Genetics(2012)10.1038/ng.2354

N/A

1.1DataRank · unranked

1873 citations

Christian Fuchsberger, Matthew Stephens, Jonathan Marchini, Gonçalo R. Abecasis, Bryan Howie

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

A saturated map of common genetic variants associated with human height

Nature(2022)10.1038/s41586-022-05275-y

N/A

1.0DataRank · unranked

911 citations

Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue +95 more

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Nature Medicine(2025)10.1038/s41591-025-03827-z

N/A

0.665DataRank · unranked

34 citations

Kaitlin H Wade, Qin Hui, Joshua Arias, Xianyong Yin, Malene R. Christiansen +95 more

Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations

Genetic Epidemiology(2020)10.1002/gepi.22326

N/A

0.665DataRank · unranked

83 citations

Pramod Anugu, Solomon K. Musani, Scott T. Weiss, Esteban G. Burchard, Marquitta J. White +6 more

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Nature Communications(2024)10.1038/s41467-024-44701-9

N/A

0.648DataRank · unranked

74 citations

Inga Steinbrenner, Yong Li, Melissa Bujnis, Tatsuhiko Naito, Eirini Marouli +95 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

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Nature Communications(2022)10.1038/s41467-022-32821-z

N/A

0.596DataRank · unranked

52 citations

Najim Lahrouchi, Aaron Isaacs, ThuyVy Duong, Luisa Foco, Farah Ahmed +95 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

Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank

Nature Communications(2023)10.1038/s41467-023-36864-8

N/A

0.483DataRank · unranked

24 citations

Eva König, Maria‐Alexandra Katsara, Holger Kirsten, Saeed Khomeijani Farahani, Alexander Teumer +8 more

Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences

PLoS Genetics(2020)10.1371/journal.pgen.1009019

N/A

0.470DataRank · unranked

22 citations

Apoorva K. Iyengar, Swarooparani Vadlamudi, Chelsea K. Raulerson, Anne Jackson, Sarah M. Brotman +20 more

MagicalRsq: Machine-learning-based genotype imputation quality calibration

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.009

N/A

0.449DataRank · unranked

19 citations

Yingxi Yang, Jonathan D. Rosen, Min-Zhi Jiang, Jiawen Chen, Weifang Liu +14 more

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

Nature Communications(2023)10.1038/s41467-023-36997-w

N/A

0.434DataRank · unranked

17 citations

Jeffrey Haessler, Jan Walter Benjamins, L. Repetto, Jie Yao, Aaron Isaacs +89 more

Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

Blood(2024)10.1182/blood.2023022596

N/A

0.416DataRank · unranked

15 citations

Jayna Nicholas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

Arteriosclerosis Thrombosis and Vascular Biology(2023)10.1161/atvbaha.122.318213

N/A

0.312DataRank · unranked

7 citations

Gerard Temprano‐Sagrera, Lori A. Holle, Allison Bebo, Jennifer A. Brody, Ngoc‐Quynh Le +36 more

Genome-wide association meta-analysis of human olfactory identification discovers sex-specific and sex-differential genetic variants

Nature Communications(2025)10.1038/s41467-025-61330-y

N/A

0.269DataRank · unranked

5 citations

David Emmert, Katrin Horn, Janne Pott, Johannes Frasnelli, Mohammed Aslam Imtiaz +18 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

MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.04.001

N/A

0.241DataRank · unranked

4 citations

Yingxi Yang, Jonathan D. Rosen, Jiawen Chen, Xihao Li, Wyliena Guan +22 more

Rare-variant association studies: When are aggregation tests more powerful than single-variant tests?

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.07.002

N/A

0.208DataRank · unranked

3 citations

Christian Fuchsberger, Michael Boehnke, Debraj Bose

Genome-wide association study of 1,391 plasma metabolites in 6,136 Finnish men identifies 303 novel signals and provides biological insights into human diseases

medRxiv(2021)10.1101/2021.10.19.21265094

N/A

0.208DataRank · unranked

3 citations

Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke +32 more

Antithrombin, protein C and protein S: Genome and transcriptome wide association studies identify 7 novel loci regulating plasma levels

medRxiv(2022)10.1101/2022.11.01.22281689

N/A

0.183DataRank · unranked

2 citations

Gerard Temprano‐Sagrera, Lori A. Holle, Allison Bebo, Jennifer A. Brody, Ngoc‐Quynh Le +35 more

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

RePEc: Research Papers in Economics(2021)10.17615/ctnf-k559

N/A

0.104DataRank · unranked

1 citations

Nancy J. Cox, T D-GENES, M. Laakso, C. Pihoker, L. Groop +95 more

Genome-Wide Association Study Meta-Analysis Uncovers Novel Genetic Variants Associated with Olfactory Dysfunction

View(2024)10.1101/2024.08.09.24311665

N/A

0.104DataRank · unranked

1 citations

Konstantinos Melas, Adrienne Tin, Valentina Talevi, Honglei Chen, Myriam Fornage +13 more

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

medRxiv(2023)10.1101/2023.06.07.23291095

N/A

0.104DataRank · unranked

1 citations

Jayna Nicolas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease

Nature Protocols(2023)10.1038/s41596-023-00853-4

N/A

0DataRank · unranked

44 citations

Saisriram Gurajala, Michelle Curtis, Yang Luo, Wanson Choi, Kazuyoshi Ishigaki +14 more

A Common Functional Regulatory Variant at a Type 2 Diabetes Locus Upregulates ARAP1 Expression in the Pancreatic Beta Cell

UNC Libraries(2020)10.17615/gfrr-b738

N/A

0DataRank · unranked

0 citations

Christian Fuchsberger, Johanna Kuusisto, Markku Laakso, Michael Boehnke, Michael L. Stitzel +5 more

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol

UNC Libraries(2020)10.17615/b3ee-r077

N/A

0DataRank · unranked

0 citations

Karen L. Mohlke, Mete Civelek, Ying Wu, Marie P. Fogarty, Amanda F. Marvelle +17 more

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

UNC Libraries(2021)10.17615/shbq-nv48

N/A

0DataRank · unranked

0 citations

Douglas M. Ruderfer, Goo Jun, Ji Zhang, Yun Li, Leslie A. Lange +27 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

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

UNC Libraries(2020)10.17615/63sx-0c91

N/A

0DataRank · unranked

0 citations

Mark J. Daly, Johanna Kuusisto, Francis S. Collins, Markku Laakso, Kimberly F. Doheny +24 more

Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.007

N/A

0DataRank · unranked

62 citations

Debraj Bose, Annie Kwon, Sarah C. Hanks, Anne Jackson, Heather M. Stringham +24 more

Imputation-powered whole-exome analysis identifies rare coding variants and genes associated with kidney function and disease in the UK Biobank

Research Square(2022)10.21203/rs.3.rs-1936427/v1

N/A

0DataRank · unranked

0 citations

Eva König, Maria‐Alexandra Katsara, Holger Kirsten, Saeed Khomeijani Farahani, Alexander Teumer +8 more

Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits

UNC Libraries(2020)10.17615/455d-6a15

Top 100%

0DataRank

Top 100%0 citations

Anne Jackson, Mete Civelek, Charles Tilford, Karen L. Mohlke, Calvin Q. Pan +21 more

Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number

Scientific Reports(2024)10.1038/s41598-024-52373-0

N/A

0DataRank · unranked

13 citations

Michele Filosi, Hansi Weißensteiner, Federica Fazzini, Mathias Gorski, Cristian Pattaro +14 more

Taxonize-gb: A tool for filtering GenBank non-redundant databases based on taxonomy

View(2024)10.1101/2024.03.22.586347

N/A

0DataRank · unranked

1 citations

Michele Filosi, Frank Maixner, Christian Fuchsberger, Mohamed S. Sarhan

Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunction

BMC Genomic Data(2025)10.1186/s12863-025-01360-z

Top 100%

0DataRank

Top 100%0 citations

Konstantinos Melas, Adrienne Tin, Valentina Talevi, Honglei Chen, Myriam Fornage +13 more

MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

UNC Libraries(2025)10.17615/4609-8b83

N/A

0DataRank · unranked

0 citations

Byron C. Jaeger, Michael J. Bamshad, Alex P. Reiner, Yun Li, Jerome I. Rotter +22 more

Christian Fuchsberger

Indexed papers

Top data-sharing exemplar

Papers