Juliane Winkelmann

Also affiliated with Centre for Biomedical Network Research on Rare Diseases, Munich Cluster for Systems Neurology, Institute of Human Genetics, Medizinische Zentrum für Gesundheit, Technical University of Munich

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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

2in 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 2 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 →

Papers

Driven by 4 papers. Top paper: “Can we predict sleep health based on brain features? A large-scale machine learning study using UK Biobank”.

Can we predict sleep health based on brain features? A large-scale machine learning study using UK Biobank

10.1101/2024.10.13.618080

N/A

0.165DataRank · unranked

2 citations

Hanwen Bi, Vera Komeyer, Jan Kasper, Sabrina A. Primus, Felix Hoffstaedter +8 more

Clinical, neuroimaging and molecular spectrum of TECPR2 -associated hereditary sensory and autonomic neuropathy with intellectual disability

medRxiv(2020)10.1101/2020.10.10.20202622

N/A

0DataRank · unranked

0 citations

Barbara Brechmann, Gali Heimer, Ines Brösse, Susanna Schubert, Lauren O’Grady +45 more

Clinical, neuroimaging, and molecular spectrum of TECPR2 ‐associated hereditary sensory and autonomic neuropathy with intellectual disability

Human Mutation(2021)10.1002/humu.24206

N/A

0DataRank · unranked

31 citations

Barbara Brechmann, Gali Heimer, Ines Brösse, Susanna Schubert, Lauren O’Grady +45 more

Systematic assessment of rare and de novo structural variants in 57 patient-parent trios using optical genome mapping

10.64898/2026.01.16.26344264

N/A

0DataRank · unranked

0 citations

Sandra Vorimo, Theresa Brunet, Aïcha Boughalem, Maureen Jacob, Ronald van Beek +24 more