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

Miriam Schmidts

Radboud University Nijmegen

ORCID: 0000-0002-1714-6749

Also affiliated with University of Freiburg, University Medical Center Freiburg, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences

Biochemistry, Genetics and Molecular BiologyMedicine

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 7%percentile
0.165Author 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.

Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive

Journal of Clinical Investigation(2025)10.1172/jci189830
Top 70%
0.165DataRank
Top 70%2 citations

Khaing Phyu Aung, Vivian W. Y. Liao, Nathan L. Absalom, Han Chow Chua, Xuetao Gan +46 more

Papers

Driven by 13 papers — median percentile 30. Top paper: “Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine”.

Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine

Nature Genetics(2023)10.1038/s41588-023-01409-8
N/A
1.7DataRank · unranked
88 citations

Nora Scherer, Franziska Grundner-Culemann, Sara Monteiro-Martins, Stefan Haug, Inga Steinbrenner +28 more

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201
N/A
0.831DataRank · unranked
253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 more

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Kidney International(2023)10.1016/j.kint.2023.11.032
N/A
0.345DataRank · unranked
9 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Nurit Assia Batzir +55 more

Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive

Journal of Clinical Investigation(2025)10.1172/jci189830
Top 70%
0.165DataRank
Top 70%2 citations

Khaing Phyu Aung, Vivian W. Y. Liao, Nathan L. Absalom, Han Chow Chua, Xuetao Gan +46 more

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

medRxiv(2023)10.1101/2023.03.21.23287206
N/A
0.110DataRank · unranked
1 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Seha Saygılı +47 more

Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

UNC Libraries(2021)10.17615/tf25-rz86
N/A
0DataRank · unranked
18 citations

Johnny L. Carson, Niki T. Loges, Thomas W. Ferkol, Margaret Rosenfeld, Maimoona A. Zariwala +16 more

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

Human Mutation(2020)10.1002/humu.24127
N/A
0DataRank · unranked
21 citations

Lokuliyange D. S. Senaratne, Elisabeth Ott, Asbjørn Holmgren, Dulika Sumathipala, Selma Mujezinović Larsen +25 more

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

PLoS Genetics(2023)10.1371/journal.pgen.1010796
N/A
0DataRank · unranked
26 citations

Oscar A. Cabrera, Julia Hoefele, Dinu Antony, Kaman Wu, Michael W. Stuck +21 more

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Brain(2023)10.1093/brain/awad380
N/A
0DataRank · unranked
19 citations

Abolfazl Rad, Sheng‐Jia Lin, Aida M. Bertoli‐Avella, Wouter W. Kallemeijn, Annie Godwin +84 more

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Brain(2020)10.1093/brain/awaa085
N/A
0DataRank · unranked
32 citations

Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tüysüz +40 more

Mutations in CCDC 39 and CCDC 40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms

UNC Libraries(2020)10.17615/bke0-4f52
N/A
0DataRank · unranked
25 citations

Jane S. Lucas, Amelia Shoemark, Mitra Forouhan, Martine Jaspers, Margaret W. Leigh +27 more

DYX1C1 is required for axonemal dynein assembly and ciliary motility

UNC Libraries(2020)10.17615/z79a-w507
N/A
0DataRank · unranked
0 citations

Cecilia Lo, Hannah M. Mitchison, Michael R. Knowles, Maimoona A. Zariwala, Ronald Roepman +6 more

Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects

UNC Libraries(2020)10.17615/3853-0b14
N/A
0DataRank · unranked
0 citations

Niki T. Loges, Margaret W. Leigh, Angelina Heer, Hanswalter Zentgraf, Richard Reinhardt +12 more