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

Maria Szczepańska

Medical University of Silesia

ORCID: 0000-0002-6772-1983
MedicineBiochemistry, 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 5 papers. Top paper: “X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems”.

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems

Journal of Medical Genetics(2022)10.1136/jmg-2022-108738
N/A
0DataRank · unranked
7 citations

Tim Felger, Luca Schierbaum, Isabelle Thiffault, Tomi Pastinen, Maria Szczepańska +18 more

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Journal of the American Society of Nephrology(2023)10.1681/asn.0000000000000132
N/A
0DataRank · unranked
15 citations

Tze Yin Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Monica Bodria +77 more

Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International Forum

Kidney International(2024)10.1016/j.kint.2024.09.012
N/A
0DataRank · unranked
21 citations

Gianluigi Ardissino, Vicky Brocklebank, Romy N. Bouwmeester, Arvind Bagga, Rob ter Heine +79 more

Genome-wide studies define new genetic mechanisms of IgA vasculitis

medRxiv(2024)10.1101/2024.10.10.24315041
N/A
0DataRank · unranked
5 citations

Li Zhu, Sara Monteiro-Martins, Aaron T. Griffin, Lukas Vlahos, Masashi Fujita +88 more

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

Kidney International(2025)10.1016/j.kint.2025.02.026
N/A
0DataRank · unranked
7 citations

Steffen Fieuws, Jonas Hofstetter, David Pitcher, Lotte Vanmeerbeek, Stefanie Haeberle +95 more