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

Hannah Klinkhammer

University of Bonn

ORCID: 0000-0003-3752-1275

Also affiliated with Zimmer Biomet (Netherlands)

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
1.5Author DataRank

Indexed papers

3in 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 3 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.

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

medRxiv(2023)10.1101/2023.06.06.23290887
Top 32%
0.614DataRank
Top 32%25 citations

Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Pilar Caro +95 more

Papers

Driven by 8 papers — median percentile 66. Top paper: “GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases”.

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

medRxiv(2023)10.1101/2023.06.06.23290887
Top 32%
0.614DataRank
Top 32%25 citations

Alexander Hustinx, Shahida Moosa, Hannah Klinkhammer, Elaine Marchi, Pilar Caro +95 more

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology

European Journal of Human Genetics(2023)10.1038/s41431-023-01445-2
Top 34%
0.579DataRank
Top 34%20 citations

Elia Marcos-Grañeda, Linnea A. Weiss, Christina A. Gurnett, Anne Marie Jelsig, Susanne H. Vineke +50 more

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

Research Square(2024)10.21203/rs.3.rs-4438861/v1
Top 59%
0.261DataRank
Top 59%4 citations

Hellen Lesmann, Alexander Hustinx, Shahida Moosa, Elaine Marchi, Maria del Pilar Caro Martin +95 more

Loss‐of‐Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder

Annals of Neurology(2024)10.1002/ana.27077
N/A
0DataRank · unranked
10 citations

Frédéric Ebstein, Tzung‐Chien Hsieh, Marialetizia Motta, Francesca Clementina Radio, Johanna C. Herkert +74 more

Expanding the Phenotypic spectrum of NAA10 -related neurodevelopmental syndrome and NAA15 -related neurodevelopmental syndrome

medRxiv(2022)10.1101/2022.08.22.22279061
N/A
0DataRank · unranked
7 citations

Marall Vedaie, Travis Besheim, Agnes Park, Elaine Marchi, Leah Gottlieb +19 more

Artificial intelligence-driven genotype–epigenotype–phenotype approaches to resolve challenges in syndrome diagnostics

EBioMedicine(2025)10.1016/j.ebiom.2025.105677
N/A
0DataRank · unranked
6 citations

Hannah Klinkhammer, Sanaa Choufani, Nikola Reko, Angela K Christman, Elise Pisan +36 more

Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome

European Journal of Human Genetics(2023)10.1038/s41431-023-01368-y
N/A
0DataRank · unranked
52 citations

Marall Vedaie, Travis Beisheim, Agnes Park, Elaine Marchi, Leah Gottlieb +19 more

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Nature Genetics(2024)10.1038/s41588-024-01836-1
N/A
0DataRank · unranked
49 citations

Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Tzung‐Chien Hsieh +95 more