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

Lillian Garrett

Helmholtz Zentrum München

ORCID: 0000-0003-4880-7076
Biochemistry, Genetics and Molecular BiologyNeuroscience

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: “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

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

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

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

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
0DataRank · unranked
68 citations

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

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

BMC Biology(2023)10.1186/s12915-022-01475-0
N/A
0DataRank · unranked
23 citations

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