Jeanette Erdmann

Also affiliated with Universität Hamburg, University Medical Center Hamburg-Eppendorf, Technical University of Applied Sciences Lübeck, German Centre for Cardiovascular Research, University of Lübeck

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

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 5%percentile

0.417Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x

Top 44%

0.417DataRank

Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Papers

Driven by 14 papers — median percentile 56. Top paper: “A genomic mutational constraint map using variation in 76,156 human genomes”.

A genomic mutational constraint map using variation in 76,156 human genomes

Nature(2023)10.1038/s41586-023-06045-0

N/A

9.6DataRank · unranked

1369 citations

Laurent C. Francioli, Julia K. Goodrich, Ryan L. Collins, Masahiro Kanai, Qingbo S. Wang +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

Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood

European Journal of Epidemiology(2020)10.1007/s10654-020-00638-z

N/A

0.670DataRank · unranked

12 citations

Tao Huang, Tiange Wang, Zhendong Mei, Zhonghan Sun, Tao Zhang +95 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

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

UNC Libraries(2020)10.17615/n5vd-xm37

N/A

0.477DataRank · unranked

23 citations

Björn O. Eriksen, Ivana Išgum, Annette Peters, Christopher D. O’Donnell, Christa Meisinger +67 more

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x

Top 44%

0.417DataRank

Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Female gene networks are expressed in myofibroblast-like smooth muscle cells in vulnerable atherosclerotic plaques

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.02.08.527690

N/A

0DataRank · unranked

5 citations

Santosh Karnewar, Michele F. Buono, Eloi Mili, Robin Hartman, Daniek Kapteijn +19 more

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

UNC Libraries(2024)10.17615/wkay-d758

N/A

0DataRank · unranked

0 citations

Stefan Weiß, Jeanette Erdmann, Kristian Hveem, Florian Kronenberg, Wen‐Jane Lee +95 more

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

UNC Libraries(2020)10.17615/pc2a-ev84

N/A

0DataRank · unranked

0 citations

Jeanette Erdmann, Paul L. Auer, Robert Roberts, John Danesh, Deborah Farlow +27 more

Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia

UNC Libraries(2020)10.17615/fj0q-na09

N/A

0DataRank · unranked

5 citations

C. Kooperberg, T. A. Barnes, L. Charnas, N. Martinelli, M. Orho-Melander +27 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.

Apollo (University of Cambridge)(2020)10.17863/cam.52580

N/A

0DataRank · unranked

0 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 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

Genome-wide meta-analysis of common variant differences between men and women

Faculty of Health; Institute of Health and Biomedical Innovation(2020)10.17615/psgr-b356

N/A

0DataRank · unranked

0 citations

Vincenza Colonna, Timothy M. Frayling, Stefania Bandinelli, Tōnu Esko, Jeanette Erdmann +27 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

PLoS Genetics(2020)10.1371/journal.pgen.1008629

N/A

0DataRank · unranked

169 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

Jeanette Erdmann

Indexed papers

Top data-sharing exemplar

Papers