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

Janine Altmüller

Helmholtz Association of German Research Centres

ORCID: 0000-0003-4372-1521

Also affiliated with University of Cologne, Max Delbrück Center, Berlin Institute of Health at Charité - Universitätsmedizin Berlin

Biochemistry, 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 5%percentile
0.570Author DataRank

Indexed papers

4in 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 4 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.

De Novo-Whole Genome Assembly of the Roborovski Dwarf Hamster ( Phodopus roborovskii ) Genome: An Animal Model for Severe/Critical COVID-19

Genome Biology and Evolution(2022)10.1093/gbe/evac100
Top 52%
0.328DataRank
Top 52%7 citations

Janine Altmüller, Claudia Quedenau, Tatiana Borodina, Geraldine Nouailles, Luiz Gustavo Teixeira Alves +5 more

Papers

Driven by 15 papers — median percentile 43. Top paper: “De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis”.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008
N/A
1.2DataRank · unranked
27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 more

Frequent and Focal FGFR1 Amplification Associates with Therapeutically Tractable FGFR1 Dependency in Squamous Cell Lung Cancer

Science Translational Medicine(2010)10.1126/scitranslmed.3001451
N/A
1.0DataRank · unranked
823 citations

Martin L. Sos, Danila Seidel, Charles M. Perou, Thomas Zander, Johannes M. Heuckmann +66 more

Swarm Learning for decentralized and confidential clinical machine learning

Nature(2021)10.1038/s41586-021-03583-3
N/A
1.0DataRank · unranked
821 citations

Hartmut Schultze, Krishnaprasad Lingadahalli Shastry, Sathyanarayanan Manamohan, Saikat Mukherjee, Vishesh Garg +183 more

cfNOMe — A single assay for comprehensive epigenetic analyses of cell-free DNA

Genome Medicine(2020)10.1186/s13073-020-00750-5
N/A
0.641DataRank · unranked
71 citations

Deborah Nörling, Domenica Borchert, Esther Leenen, Sandra Habbig, Michael S. Wiesener +8 more

Spatial and single-cell profiling of the metabolome, transcriptome and epigenome of the aging mouse liver

Nature Aging(2023)10.1038/s43587-023-00513-y
N/A
0.621DataRank · unranked
62 citations

Niklas Kleinenkuhnen, Swati Parekh, Tonantzi Sandoval, Christoph Ziegenhain, Farina Schneider +13 more

Do Not Trust the Pedigree: Reduced and Sex-Dependent Penetrance at a Novel Mutation Hotspot in ATL1 Blurs Autosomal Dominant Inheritance of Spastic Paraplegia

Human Mutation(2013)10.1002/humu.22309
N/A
0.489DataRank · unranked
25 citations

Rebecca Schüle, Hicham Fadel, Irene Valenzuela, Fiorella Speziani, Michael Gonzalez +11 more

NIK/MAP3K14 in hepatocytes orchestrates NASH to hepatocellular carcinoma progression via JAK2/STAT5 inhibition

Molecular Metabolism(2022)10.1016/j.molmet.2022.101626
N/A
0.396DataRank · unranked
13 citations

Alexander Jaïs, Paul Klemm, Lukas Steuernagel, P. Wienand, Morten Fog-Tonnesen +19 more

De Novo-Whole Genome Assembly of the Roborovski Dwarf Hamster ( Phodopus roborovskii ) Genome: An Animal Model for Severe/Critical COVID-19

Genome Biology and Evolution(2022)10.1093/gbe/evac100
Top 52%
0.328DataRank
Top 52%7 citations

Janine Altmüller, Claudia Quedenau, Tatiana Borodina, Geraldine Nouailles, Luiz Gustavo Teixeira Alves +5 more

De Novo Whole Genome Assembly of the Roborovski Dwarf Hamster ( Phodopus roborovskii ) Genome, an Animal Model for Severe/Critical COVID-19

bioRxiv (Cold Spring Harbor Laboratory)10.1101/2021.10.02.462569
Top 61%
0.241DataRank
Top 61%4 citations

Janine Altmüller, Claudia Quedenau, Tatiana Borodina, Geraldine Nouailles, Luiz Gustavo Teixeira Alves +5 more

RB1-Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation

Cancers(2022)10.3390/cancers14092166
N/A
0DataRank · unranked
11 citations

Julia Woestefeld, Hannah Döpper, Morgane Bozet, Alexandra Brenzel, Janine Altmüller +5 more

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita

Research Square(2022)10.21203/rs.3.rs-2121654/v1
N/A
0DataRank · unranked
0 citations

Elisabeth Schuler, Almundher Al‐Maawali, Ankur Chaurasia, Steffen Syrbe, Adila Al‐Kindi +10 more

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly

Human Genetics(2023)10.1007/s00439-023-02528-2
N/A
0DataRank · unranked
6 citations

Elisabeth Schuler, Almundher Al‐Maawali, Ankur Chaurasia, Steffen Syrbe, Adila Al‐Kindi +10 more

SEC24C deficiency causes trafficking and glycosylation abnormalities in an epileptic encephalopathy with cataracts and dyserythropoeisis

JCI Insight(2025)10.1172/jci.insight.173484
N/A
0DataRank · unranked
5 citations

Büşranur Çavdarlı, Taylor Nagai, Miroslav P. Milev, Alexander Wolff, Mahsa Mehranfar +20 more

Genome-wide association study of lung function decline in adults with and without asthma

UNC Libraries(2020)10.17615/710g-2y61
N/A
0DataRank · unranked
0 citations

Gerard H. Koppelman, Miriam F. Moffatt, Florian Kronenberg, Stefano Guerra, David P. Strachan +29 more

An Autochthonous Mouse Model of Myd88 - and BCL2 -Driven Diffuse Large B-cell Lymphoma Reveals Actionable Molecular Vulnerabilities

Blood Cancer Discovery(2020)10.1158/2643-3230.bcd-19-0059
N/A
0DataRank · unranked
38 citations

Tim Rehkämper, Pascal Nieper, Pauline Pfeiffer, Alessandra Holzem, Sebastian Klein +33 more