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

Neveen A. Soliman

Cairo University

ORCID: 0000-0002-8942-1973

Also affiliated with Egypt Center for Research and Regenerative Medicine, Egyptian Information Telecommunications Electronics and Software Alliance

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 3%percentile
1.3Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease

Kidney International Reports(2021)10.1016/j.ekir.2021.08.033
Top 16%
1.3DataRank
Top 16%38 citations

Jennifer Arroyo, Ronak Jagdeep Shah, Kalina J. Reese, Brenna N. Walton, Laura M. Reynolds +16 more

Papers

Driven by 9 papers — median percentile 84. Top paper: “Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease”.

Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease

Kidney International Reports(2021)10.1016/j.ekir.2021.08.033
Top 16%
1.3DataRank
Top 16%38 citations

Jennifer Arroyo, Ronak Jagdeep Shah, Kalina J. Reese, Brenna N. Walton, Laura M. Reynolds +16 more

Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.03.045
N/A
0.672DataRank · unranked
87 citations

Janet Chou, Laura Faletti, Veronika Haunerdinger, Lennart Opitz, Pascal Joset +55 more

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome

Journal of the American Society of Nephrology(2021)10.1681/asn.2020040490
N/A
0.505DataRank · unranked
28 citations

Slim Mzoughi, Ronen Schneider, Susanne J. Kühl, Denny Schanze, Verena Klämbt +38 more

Epigenomic and phenotypic characterization of DEGCAGS syndrome

European Journal of Human Genetics(2024)10.1038/s41431-024-01702-y
N/A
0DataRank · unranked
6 citations

Denisa Weis, Ingvild Aukrust, Tzung‐Chien Hsieh, Marie Horackova, Julie Paulsen +37 more

Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome

Genes & Diseases(2024)10.1016/j.gendis.2024.101280
N/A
0DataRank · unranked
3 citations

Shirlee Shril, Friedhelm Hildebrandt, Konstantin Deutsch, Kirollos Yousef, Camille Nicolas Frank +38 more

DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.008
N/A
0DataRank · unranked
34 citations

Konstantin Deutsch, Gregory J. Hoeprich, Jonathan Marquez, Tobias Hermle, Daniela A. Braun +28 more

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families

Genetics in Medicine(2025)10.1016/j.gim.2025.101432
N/A
0DataRank · unranked
5 citations

Caroline M. Kolvenbach, Chunyan Wang, Nils D. Mertens, Steve Seltzsam, Bshara Mansour +49 more

Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice

Science Advances(2021)10.1126/sciadv.abe1386
N/A
0DataRank · unranked
32 citations

Friedhelm Hildebrandt, Thomas Forbes, Verena Klämbt, Ronen Schneider, Konstantin Deutsch +34 more

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract

European Urology Open Science(2022)10.1016/j.euros.2022.08.004
N/A
0DataRank · unranked
12 citations

Tze Yin Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum +31 more