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

Angela M. Kaindl

German Center for Neurodegenerative Diseases

ORCID: 0000-0001-9454-206X

Also affiliated with Humboldt-Universität zu Berlin, German Center for Pediatric and Adolescent Rheumatology, Center for Children, German Centre for Cardiovascular Research, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Institute of Cell Biology and Neurobiology, Institute of Neurobiology, Charité - Universitätsmedizin Berlin

MedicineBiochemistry, 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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome”.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52
N/A
0DataRank · unranked
0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

Infratentorial MRI Findings in Rasmussen Encephalitis Suggest Primary Cerebellar Involvement

Neurology Neuroimmunology & Neuroinflammation(2021)10.1212/nxi.0000000000001058
N/A
0DataRank · unranked
11 citations

Bastian David, Selma Enders, Conrad C. Prillwitz, Tobias Bauer, Deniz A. Atalay +10 more

Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants

Neurology(2022)10.1212/wnl.0000000000200032
N/A
0DataRank · unranked
10 citations

Ning Chang, Kaoru Inoue, Angela Delaney, Ying Hu, Sandra Donkervoort +17 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