🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Lore Becker

Helmholtz Munich

ORCID: 0000-0002-6890-4984
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 3%percentile
1.2Author 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes

Mammalian Genome(2020)10.1007/s00335-020-09827-3
Top 17%
1.2DataRank
Top 17%33 citations

Heike Kollmus, Helmut Fuchs, Christoph Lengger, Hamed Haselimashhadi, Molly A. Bogue +36 more

Papers

Driven by 12 papers — median percentile 83. Top paper: “Inhibition of LTβR signalling activates WNT-induced regeneration in lung”.

Inhibition of LTβR signalling activates WNT-induced regeneration in lung

Nature(2020)10.1038/s41586-020-2882-8
N/A
4.1DataRank · unranked
178 citations

Gerrit John-Schuster, Danijela Heide, Dominik Pfister, Mareike Lehmann, Yan Hu +47 more

A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes

Mammalian Genome(2020)10.1007/s00335-020-09827-3
Top 17%
1.2DataRank
Top 17%33 citations

Heike Kollmus, Helmut Fuchs, Christoph Lengger, Hamed Haselimashhadi, Molly A. Bogue +36 more

Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

Nature Cardiovascular Research(2022)10.1038/s44161-022-00018-8
N/A
0.635DataRank · unranked
68 citations

Gregor Miller, Tudor I. Oprea, Chih‐Wei Hsu, Gisela Fobo, Goar Frishman +95 more

Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice

Nature Communications(2022)10.1038/s41467-022-34515-y
N/A
0.568DataRank · unranked
43 citations

Helmut Fuchs, Enzo Scifo, Dan Liu, Ahmad Aziz, Juan Antonio Aguilar‐Pimentel +44 more

Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density

PLoS Genetics(2020)10.1371/journal.pgen.1009190
N/A
0.515DataRank · unranked
30 citations

Christine Schütt, Jan Rozman, Maria del Mar Muñiz Moreno, Stefan Brandmaier, Michelle Simon +59 more

Publisher Correction: Inhibition of LTβR signalling activates WNT-induced regeneration in lung

Nature(2020)10.1038/s41586-020-03087-6
N/A
0.312DataRank · unranked
7 citations

Gerrit John-Schuster, Danijela Heide, Dominik Pfister, Mareike Lehmann, Yan Hu +47 more

Deep Phenotyping and Lifetime Trajectories Reveal Limited Effects of Longevity Regulators on the Aging Process in C57BL/6J Mice

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.25.485824
N/A
0.292DataRank · unranked
6 citations

Helmut Fuchs, Enzo Scifo, Dan Liu, Ahmad Aziz, Juan Antonio Aguilar-Pimentel +44 more

Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain

Neuroscience Applied(2024)10.1016/j.nsa.2024.104075
N/A
0.292DataRank · unranked
6 citations

Dietrich Trümbach, Donghyung Lee, Silvia Mandillo, Rodney C. Samaco, Ann M. Flenniken +87 more

X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes

Nature Communications(2024)10.1038/s41467-024-54673-5
N/A
0.272DataRank · unranked
5 citations

Sarah Hoelzl, Zachary D. Smith, Chiara Gerhardinger, Marion O. C. Gonner, Juan Antonio Aguilar‐Pimentel +21 more

Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism

iScience(2025)10.1016/j.isci.2025.113617
N/A
0DataRank · unranked
0 citations

Louise Gerard, Wilfred D. Vieira, Marie Fourrez, Florence Rodriguez Gaudray, Birgit Rathkolb +17 more

A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice

SLEEP(2024)10.1093/sleep/zsae015
N/A
0DataRank · unranked
4 citations

Daniel D. Lam, Aaro V. Salminen, Benedikt Wefers, Lore Becker, Lillian Garrett +7 more

Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.013
N/A
0DataRank · unranked
43 citations

Tianyu Guo, Chen Wang, Lillian Garrett, Angad Jolly, Moez Dawood +63 more