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

Fostering Data Sharing

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Authors
Sabine M. Hölter

Sabine M. Hölter

Center for Environmental Health

ORCID: 0000-0003-4878-5241

Also affiliated with Helmholtz Munich

NeuroscienceBiochemistry, 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 3%percentile

1.4Author DataRank

Indexed papers

2in 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 2 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 →

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 14 papers — median percentile 61. Top paper: “A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes”.

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

Lifetime study in mice after acute low-dose ionizing radiation: a multifactorial study with special focus on cataract risk

Radiation and Environmental Biophysics(2018)10.1007/s00411-017-0728-z

N/A

0.557DataRank · unranked

40 citations

Frauke Neff, Savneet Kaur Bains, Scott Bright, Deborah Lord, Peter Reitmeir +29 more

Posterior subcapsular cataracts are a late effect after acute exposure to 0.5 Gy ionizing radiation in mice

International Journal of Radiation Biology(2021)10.1080/09553002.2021.1876951

N/A

0.518DataRank · unranked

8 citations

Alexander Cecil, Cornelia Prehn, Gabriele Möller, Andreas Ohlmann, Gerhild Wildner +14 more

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

BMC Biology(2023)10.1186/s12915-022-01475-0

N/A

0.477DataRank · unranked

23 citations

Louise Lanoue, Dave Clary, Kendall Higgins, Lynette Bower, Ann M. Flenniken +95 more

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Kidney International(2023)10.1016/j.kint.2023.11.032

N/A

0.345DataRank · unranked

9 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Nurit Assia Batzir +55 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

IMPC impact on preclinical mouse models

Mammalian Genome(2025)10.1007/s00335-025-10104-4

Top 61%

0.241DataRank

Top 61%4 citations

Pilar Cacheiro, Damian Smedley, K. C. Kent Lloyd, Sabine M. Hölter

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

medRxiv(2023)10.1101/2023.03.21.23287206

N/A

0.110DataRank · unranked

1 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Seha Saygılı +47 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