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

Juliane Winkelmann

Technical University of Munich

ORCID: 0000-0002-3074-599X

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 4%percentile
0.614Author 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 →

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.

Reassessment of candidate gene studies for idiopathic restless legs syndrome in a large genome-wide association study dataset of European ancestry

SLEEP(2022)10.1093/sleep/zsac098
Top 32%
0.614DataRank
Top 32%10 citations

Chen Zhao, Aaro V. Salminen, Konrad Oexle, Juliane Winkelmann, Barbara Schormair

Papers

Driven by 15 papers — median percentile 68. Top paper: “Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients”.

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207
N/A
0.691DataRank · unranked
99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

Reassessment of candidate gene studies for idiopathic restless legs syndrome in a large genome-wide association study dataset of European ancestry

SLEEP(2022)10.1093/sleep/zsac098
Top 32%
0.614DataRank
Top 32%10 citations

Chen Zhao, Aaro V. Salminen, Konrad Oexle, Juliane Winkelmann, Barbara Schormair

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Nature Genetics(2024)10.1038/s41588-024-01763-1
N/A
0.609DataRank · unranked
57 citations

Chen Zhao, Steven Bell, Maria Didriksen, Muhammad Sulaman Nawaz, Nathalie Schandra +65 more

POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.014
N/A
0.457DataRank · unranked
20 citations

Kristin E.N. Watt, Satoru Ide, Kristina Baltrunaite, Chad Brunswick, Katherine Inskeep +40 more

Beyond volume: Unraveling the genetics of human brain geometry

Science Advances(2025)10.1126/sciadv.adr1644
N/A
0.241DataRank · unranked
4 citations

Felix Hoffstaedter, Federico Raimondo, Simon B. Eickhoff, Juliane Winkelmann, Konrad Oexle +2 more

Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulation

Human Molecular Genetics(2021)10.1093/hmg/ddab355
N/A
0DataRank · unranked
9 citations

Ana Nikolić, Chen Zhao, Nazanin Mirza‐Schreiber, Wojciech Krężel, Konrad Oexle +2 more

Intronic elements associated with insomnia and restless legs syndrome exhibit cell type-specific epigenetic features contributing to MEIS1 regulation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.03.458823
N/A
0DataRank · unranked
0 citations

Ana Nikolić, Chen Zhao, Nazanin Mirza‐Schreiber, Wojciech Krężel, Konrad Oexle +2 more

The genetic etiology of periodic limb movement in sleep

SLEEP(2022)10.1093/sleep/zsac121
N/A
0DataRank · unranked
21 citations

Logan Schneider, David Amar, Andreas Brink-Kjær, Katie L.J. Cederberg, Zoltán Kutalik +17 more

A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic Paraplegia

Movement Disorders(2021)10.1002/mds.28821
N/A
0DataRank · unranked
22 citations

Michael Zech, Robert B. Hufnagel, Jesse Slone, Xinjian Wang, Shelli M. Homan +13 more

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Nature Genetics(2021)10.1038/s41588-021-00886-z
N/A
0DataRank · unranked
108 citations

Blake A. Creighton, Keith A. Breau, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +70 more

Dietary and supplemental intake of vitamins C and E is associated with altered DNA methylation in an epigenome-wide association study meta-analysis

Epigenetics(2023)10.1080/15592294.2023.2211361
N/A
0DataRank · unranked
13 citations

Roby Joehanes, Jiantao Ma, Gha Young Lee, Ricardo Costeira, Pei-Chien Tsai +29 more

Pathogenic SPTBN1 variants cause a novel autosomal dominant neurodevelopmental syndrome

medRxiv(2020)10.1101/2020.08.31.20184481
N/A
0DataRank · unranked
3 citations

Keith A. Breau, Blake A. Creighton, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +63 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

A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice

SLEEP(2024)10.1093/sleep/zsae015
N/A
0DataRank · unranked
4 citations

Daniel D. Lam, Aaro V. Salminen, Benedikt Wefers, Lore Becker, Lillian Garrett +7 more

Candidate variants in TUB are associated with familial tremor

PLoS Genetics(2020)10.1371/journal.pgen.1009010
N/A
0DataRank · unranked
4 citations

Fereshteh Jahanbani, Charles W. Abbott, Hayan Lee, Amin Zia, Shannon Rego +13 more