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

Ana C. Onuchic-Whitford

Brigham and Women's Hospital

ORCID: 0000-0003-0362-0400

Also affiliated with Boston Children's Hospital, Harvard University

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 6%percentile
0.266Author 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.

Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.01.494352
Top 58%
0.266DataRank
Top 58%3 citations

Michelle T. McNulty, Christopher J. Benway, Pei Wen, Anya Greenberg, Ana C. Onuchic-Whitford +8 more

Papers

Driven by 12 papers — median percentile 42. Top paper: “De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis”.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008
N/A
1.2DataRank · unranked
27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 more

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

Science Advances(2021)10.1126/sciadv.abe1386
N/A
0.524DataRank · unranked
32 citations

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

Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans

Nephrology Dialysis Transplantation(2020)10.1093/ndt/gfaa215
N/A
0.292DataRank · unranked
6 citations

Max Werth, Ana C. Onuchic-Whitford, Maike Getwan, Thomas M. Kitzler, Friedhelm Hildebrandt +15 more

Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.01.494352
Top 58%
0.266DataRank
Top 58%3 citations

Michelle T. McNulty, Christopher J. Benway, Pei Wen, Anya Greenberg, Ana C. Onuchic-Whitford +8 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
0.208DataRank · unranked
3 citations

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

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis

Kidney International(2025)10.1016/j.kint.2025.12.013
N/A
0DataRank · unranked
0 citations

Kristen M. Gibson, Juntao Ke, Zachary T. Sentell, Juliana E Arcila Galvis, Satoshi Koyama +23 more

Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome

Kidney International Reports(2020)10.1016/j.ekir.2020.10.040
N/A
0DataRank · unranked
11 citations

Ronen Schneider, Peter F. M. van der Ven, Marvin Aßent, Keerthika Lohanadan, Verena Klämbt +24 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

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

Journal of the American Society of Nephrology(2022)10.1681/asn.2022010050
N/A
0DataRank · unranked
8 citations

Friedhelm Hildebrandt, Chunyan Wang, Thomas Naert, Karin Richter, Theresa Nauth +28 more

Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs

Nature Communications(2023)10.1038/s41467-023-37691-7
N/A
0DataRank · unranked
28 citations

Michelle T. McNulty, Christopher J. Benway, Pei Wen, Anya Greenberg, Ana C. Onuchic-Whitford +11 more

Advanced CKD of Uncertain Etiology Among Children in Guatemala: Genetic and Clinical Characteristics

Kidney Medicine(2024)10.1016/j.xkme.2024.100910
N/A
0DataRank · unranked
0 citations

Ana Morales, Shirlee Shril, Elizabeth Benoit, Dalia Pantel, Angie Aguilar‐González +5 more