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

Anne Gregor

University of Bern

ORCID: 0000-0001-9166-6593

Also affiliated with University Hospital of Bern, Center for Human Genetics, Institute of Human Genetics

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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster”.

Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster

Scientific Reports(2020)10.1038/s41598-020-58182-5
N/A
0DataRank · unranked
14 citations

Anne Gregor, Tatjana Sauerer, Anna Fliedner, Laila Distel, Christine Suchy +4 more

Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.019
N/A
0DataRank · unranked
25 citations

Philipp Kirchner, Antje Wiesener, Irma van de Beek, Quinten Waisfisz, Mieke M. van Haelst +43 more

Negative selection on human genes causing severe inborn errors depends on disease outcome and both the mode and mechanism of inheritance

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.07.938894
N/A
0DataRank · unranked
1 citations

Bertrand Boisson, Anne Gregor, Vivien Béziat, Stéphanie Boisson‐Dupuis, Jacinta Bustamante +11 more

Novel association of Dandy–Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63363
N/A
0DataRank · unranked
11 citations

Lucia Guidugli, Monia Hammer, Chelsea Barrows, Anne Gregor, Sangmoon Lee +9 more

Deregulated ion channels contribute to RHOBTB2-associated developmental and epileptic encephalopathy

Human Molecular Genetics(2025)10.1093/hmg/ddae183
N/A
0DataRank · unranked
5 citations

Anne Gregor, Niels R. Ntamati, Arif B. Ekici, Beate Winner, Thomas Nevian +2 more

Proteasomal activation ameliorates neuronal phenotypes linked to FBXO11-deficiency

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100425
N/A
0DataRank · unranked
0 citations

Laila Distel, A Ekici, Philipp Kirchner, Steffen Uebe, Mandy Krumbiegel +4 more