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

Éric Vilain

Pontifical Gregorian University

ORCID: 0000-0002-5557-3709

Also affiliated with Children's Hospital of Orange County, Children's National, Oregon Health & Science University, University of California, Irvine, University of Utah, University of California System, UC Irvine Health

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
1.7Author DataRank

Indexed papers

3in 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 3 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.

A genome-wide spectrum of tandem repeat expansions in 338,963 humans

Cell(2024)10.1016/j.cell.2024.03.004
Top 18%
1.1DataRank
Top 18%39 citations

Wenbin Ye, Jason Sheng Li, Jingyi Jessica Li, Éric Vilain, Tamer Sallam +2 more

Papers

Driven by 32 papers — median percentile 52. Top paper: “A genome-wide spectrum of tandem repeat expansions in 338,963 humans”.

A genome-wide spectrum of tandem repeat expansions in 338,963 humans

Cell(2024)10.1016/j.cell.2024.03.004
Top 18%
1.1DataRank
Top 18%39 citations

Wenbin Ye, Jason Sheng Li, Jingyi Jessica Li, Éric Vilain, Tamer Sallam +2 more

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207
N/A
0.691DataRank · unranked
99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

nanotatoR: a tool for enhanced annotation of genomic structural variants

BMC Genomics(2021)10.1186/s12864-020-07182-w
N/A
0.505DataRank · unranked
11 citations

Hayk Barseghyan, Emmanuèle C. Délot, Éric Vilain, Surajit Bhattacharya

Genome-wide neonatal epigenetic changes associated with maternal exposure to the COVID-19 pandemic

BMC Medical Genomics(2023)10.1186/s12920-023-01707-4
N/A
0.434DataRank · unranked
17 citations

Surajit Bhattacharya, Nickie Andescavage, Miguel Almalvez, Diedtra Henderson, Éric Vilain +3 more

Long reads capture simultaneous enhancer–promoter methylation status for cell-type deconvolution

Bioinformatics(2021)10.1093/bioinformatics/btab306
N/A
0.406DataRank · unranked
14 citations

Yotam Abramson, Hila Sharim, Zohar Manber, Surajit Bhattacharya, Yiwen Chen +6 more

Pediatric SARS-CoV-2 long term outcomes study (PECOS): cross sectional analysis at baseline

Pediatric Research(2024)10.1038/s41390-024-03777-1
Top 48%
0.374DataRank
Top 48%7 citations

Lauren Arrigoni, Alexandra B. Yonts, Kevin Rubenstein, James E. Bost, Max T. Wolff +45 more

Motor control and cognition deficits associated with protein carbamoylation in food (cassava) cyanogenic poisoning: Neurodegeneration and genomic perspectives

Food and Chemical Toxicology(2020)10.1016/j.fct.2020.111917
N/A
0.373DataRank · unranked
11 citations

E.R. Ali, Matthew S. Bramble, Jason E. Gosschalk, Morris Kim, D.L. Yandju +9 more

Benchmarking long-read genome sequence alignment tools for human genomics applications

PeerJ(2023)10.7717/peerj.16515
N/A
0.360DataRank · unranked
10 citations

Emmanuèle C. Délot, Éric Vilain, Jonathan LoTempio

Genome sequencing reveals the impact of pseudoexons in rare genetic disease

Genetics in Medicine(2025)10.1016/j.gim.2025.101574
N/A
0.269DataRank · unranked
5 citations

Megan Hawley, Light Auriga, Ivan De Dios, Arthur Ko, Sofia Marmolejos +20 more

Identification of differential hypothalamic DNA methylation and gene expression associated with sexual partner preferences in rams

PLoS ONE(2022)10.1371/journal.pone.0263319
N/A
0.269DataRank · unranked
5 citations

Rebecka Amodei, Éric Vilain, Charles E. Roselli, Surajit Bhattacharya

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001
N/A
0.241DataRank · unranked
4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

Glutathione peroxidase 3 is a potential biomarker for konzo

Nature Communications(2024)10.1038/s41467-024-52136-5
N/A
0.208DataRank · unranked
3 citations

Victor Fourcassié, Neerja Vashist, Florence Roux‐Dalvai, Yun Zhou, Guy Makila Mabe Bumoko +16 more

Building a growing genomic repository for maternal and fetal health through the PING Consortium

Pediatric Research(2025)10.1038/s41390-024-03793-1
Top 70%
0.165DataRank
Top 70%2 citations

Shriya Singh, Blain Fasil, Allison R. Horvath, Sarah B. Mulkey, Carlos Curé +34 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

medRxiv(2024)10.1101/2024.12.22.24319370
N/A
0.104DataRank · unranked
1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +30 more

Newborn Screening Protocols and Positive Predictive Value for Congenital Adrenal Hyperplasia Vary across the United States

International Journal of Neonatal Screening(2020)10.3390/ijns6020037
N/A
0DataRank · unranked
34 citations

Reeti Chawla, Ming Chen, Alicia Diaz-Thomas, Courtney Finlayson, Meilan M. Rutter +7 more

Optical genome mapping identifies a novel pediatric embryonal tumor with a ZNF532::NUTM1 fusion

The Journal of Pathology(2023)10.1002/path.6085
N/A
0DataRank · unranked
8 citations

Augustine Eze, Surajit Bhattacharya, Ethan Putnam, M. Isabel Almira-Suarez, Christopher Rossi +13 more

Reprograming skin fibroblasts into Sertoli cells: a patient-specific tool to understand effects of genetic variants on gonadal development

Biology of Sex Differences(2024)10.1186/s13293-024-00599-y
N/A
0DataRank · unranked
6 citations

Emmanuèle C. Délot, Alejandra P. Reyes, Janelle Ryan, Surajit Bhattacharya, Vincent R. Harley +2 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438
N/A
0DataRank · unranked
10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Genome sequencing reveals the impact of pseudoexons in rare genetic disease

medRxiv(2024)10.1101/2024.12.21.24318325
N/A
0DataRank · unranked
3 citations

Megan Hawley, Light Auriga, Ivan De Dios, Arthur Ko, Sofia Marmolejos +20 more

Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.002
N/A
0DataRank · unranked
42 citations

Sarah L. Stenton, Seth Berger, Paolo Canigiula, Brandy McNulty, Ivo Violich +18 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100441
N/A
0DataRank · unranked
1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +31 more

The gut microbiome in konzo

Nature Communications(2021)10.1038/s41467-021-25694-1
N/A
0DataRank · unranked
25 citations

Neerja Vashist, Arthur Ko, Sambhawa Priya, Céleste Musasa, Alban Mathieu +17 more

Identification of de novo variants from parent-proband duos via long-read sequencing

medRxiv(2025)10.1101/2025.02.24.25322424
N/A
0DataRank · unranked
0 citations

Emmanuèle C. Délot, Georgia Pitsava, Christine Lambert, Cairbre Fanslow, Primo Baybayan +12 more

Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1665
N/A
0DataRank · unranked
18 citations

Hayk Barseghyan, Surajit Bhattacharya, Yulong Fu, Nicole L. Hoppman, Cherisse A. Marcou +8 more

Facial analysis technology for the detection of Down syndrome in the Democratic Republic of the Congo

European Journal of Medical Genetics(2021)10.1016/j.ejmg.2021.104267
N/A
0DataRank · unranked
17 citations

Matthew S. Bramble, Kizito Mosema Be Amoti, D’Andre Spencer, Cécile Dakande, Manya Bakatumana Hans +12 more

nanotatoR : A tool for enhanced annotation of genomic structural variants

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.18.254680
N/A
0DataRank · unranked
0 citations

Hayk Barseghyan, Emmanuèle C. Délot, Éric Vilain, Surajit Bhattacharya

Long Reads Capture Simultaneous Enhancer-Promoter Methylation Status for Cell-type Deconvolution

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.28.428654
N/A
0DataRank · unranked
5 citations

Yotam Abramson, Hila Sharim, Zohar Manber, Surajit Bhattacharya, Yi-Wen Chen +6 more

DNA methylation patterns associated with cyanogenic cassava exposure and konzo in Sub-Saharan Africa

medRxiv(2021)10.1101/2021.07.28.21261215
N/A
0DataRank · unranked
0 citations

Surajit Bhattacharya, Matthew S. Bramble, Daniel Okitundu-Luwa, Dieudonné Mumba Ngoyi, Désiré Tshala-Katumbay +2 more

DNA methylation patterns associated with konzo in Sub-Saharan Africa

Clinical Epigenetics(2022)10.1186/s13148-022-01372-x
N/A
0DataRank · unranked
5 citations

Surajit Bhattacharya, Matthew S. Bramble, Daniel Okitundu-Luwa, Dieudonné Mumba Ngoyi, Désiré Tshala-Katumbay +2 more

Optical Genome Mapping Identifies a Novel Pediatric Embryonal Tumor Subtype with a ZNF532-NUTM1 Fusion

medRxiv(2022)10.1101/2022.05.20.22275344
N/A
0DataRank · unranked
0 citations

Augustine Eze, Surajit Bhattacharya, Ethan Putnam, M. Isabel Almira-Suarez, Christopher Rossi +10 more

Optical Genome Mapping Identifies a Novel Pediatric Embryonal Tumor Subtype with a ZNF532-NUTM1 Fusion

Research Square(2022)10.21203/rs.3.rs-1879445/v1
N/A
0DataRank · unranked
0 citations

Augustine Eze, Surajit Bhattacharya, Ethan Putnam, M. Isabel Almira-Suarez, Christopher Rossi +13 more

Using a chat-based informed consent tool in large-scale genomic research

Journal of the American Medical Informatics Association(2023)10.1093/jamia/ocad181
N/A
0DataRank · unranked
20 citations

Jonathan LoTempio, Erica D. Smith, E. Hallie Andrew, Glòria Mas Martín, Amanda Kahn-Kirby +8 more