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

Juliana M. Ferraz Sallum

Institute of Human Genetics

ORCID: 0000-0002-7206-4447

Also affiliated with Associação Paulista de Medicina, Universidade Federal de São Paulo

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 4%percentile
0.653Author 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.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom

medRxiv(2024)10.1101/2024.03.24.24304809
Top 45%
0.405DataRank
Top 45%9 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga +32 more

Papers

Driven by 9 papers — median percentile 47. Top paper: “Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome”.

Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome

Ophthalmic Genetics(2021)10.1080/13816810.2021.1946704
N/A
0.533DataRank · unranked
34 citations

Cristy A. Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena Schiff, Byron L. Lam +16 more

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom

medRxiv(2024)10.1101/2024.03.24.24304809
Top 45%
0.405DataRank
Top 45%9 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga +32 more

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4
N/A
0.370DataRank · unranked
8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations

medRxiv(2025)10.1101/2025.07.03.25330767
Top 60%
0.248DataRank
Top 60%4 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Mital Shah, Gunjan Naik +32 more

Expanding the phenotypic and genotypic spectrum of patients with HGSNAT -related retinopathy

Ophthalmic Genetics(2023)10.1080/13816810.2023.2245035
N/A
0DataRank · unranked
6 citations

Molly Marra, Austin D. Igelman, Cristy A. Ku, Amanda Burr, Katherine Andersen +6 more

Ophthalmic genetics in South America

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2020)10.1002/ajmg.c.31832
N/A
0DataRank · unranked
8 citations

René Moya, Patricio G. Schlottmann, Robert B. Hufnagel, Claudia Arberas, Federico Fernández +6 more

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene

Nature Machine Intelligence(2025)10.1038/s42256-025-01040-8
N/A
0DataRank · unranked
23 citations

William Woof, Siying Lin, Biraja Ghoshal, Bernardo Mendes, Yoga Advaith Veturi +42 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169
N/A
0DataRank · unranked
15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

npj Genomic Medicine(2025)10.1038/s41525-025-00489-1
N/A
0DataRank · unranked
0 citations

Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung +44 more