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

Rajarshi Ghosh

National Institute of Allergy and Infectious Diseases

ORCID: 0000-0001-7368-8940
Biochemistry, Genetics and Molecular BiologyImmunology and Microbiology

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 5%percentile
0.469Author 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.

PhenoRerank: A re-ranking model for phenotypic concept recognition pre-trained on human phenotype ontology

Journal of Biomedical Informatics(2022)10.1016/j.jbi.2022.104059
Top 41%
0.469DataRank
Top 41%6 citations

Ling Luo, Po‐Ting Lai, Daniel Veltri, Andrew J. Oler, Sandhya Xirasagar +5 more

Papers

Driven by 18 papers — median percentile 59. Top paper: “Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations”.

Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.06.009
N/A
1.3DataRank · unranked
67 citations

Jia Yan, Rajarshi Ghosh, Andrew J. Oler, Luis M. Franco, Michael Setzer +95 more

PhenoRerank: A re-ranking model for phenotypic concept recognition pre-trained on human phenotype ontology

Journal of Biomedical Informatics(2022)10.1016/j.jbi.2022.104059
Top 41%
0.469DataRank
Top 41%6 citations

Ling Luo, Po‐Ting Lai, Daniel Veltri, Andrew J. Oler, Sandhya Xirasagar +5 more

Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity

Frontiers in Immunology(2023)10.3389/fimmu.2023.1172004
N/A
0.413DataRank · unranked
8 citations

Morgan N Similuk, Rajarshi Ghosh, Bryce A. Seifert, Leila Jamal, Michael Kamen +31 more

Genetic evaluation of pediatric pituitary adenomas and USP8-related genotype-phenotype correlations in Cushing’s disease

Pituitary(2025)10.1007/s11102-025-01557-6
N/A
0.165DataRank · unranked
2 citations

Sukhvir Kaur, Justin Lack, Morgan N Similuk, Mayank Tandon, Rajarshi Ghosh +8 more

The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome

Blood Advances(2022)10.1182/bloodadvances.2021005835
N/A
0DataRank · unranked
10 citations

Susan Price, Morgan N Similuk, Elaine Kulm, Jia Yan, Michael Setzer +6 more

Chromosomal Microarray Analysis Supplements Exome Sequencing to Diagnose Children with Suspected Inborn Errors of Immunity

Research Square(2022)10.21203/rs.3.rs-2211010/v1
N/A
0DataRank · unranked
1 citations

Morgan N Similuk, Rajarshi Ghosh, Bryce A. Seifert, Leila Jamal, Michael Kamen +30 more

The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1

New England Journal of Medicine(2024)10.1056/nejmoa2312665
N/A
0DataRank · unranked
79 citations

Grace Smith, Gregory Constantine, Monica M Schmitt, Elise M. N. Ferré, Julie C Alejo +61 more

A deep intronic splice–altering AIRE variant causes APECED syndrome through antisense oligonucleotide-targetable pseudoexon inclusion

Science Translational Medicine(2024)10.1126/scitranslmed.adk0845
N/A
0DataRank · unranked
12 citations

Amy P. Hsu, Andrew J. Oler, Dhaneshwar Kumar, Daniel Chauss, Jan Piet van Hamburg +44 more

Genetic Risk Factors for Early-Onset Merkel Cell Carcinoma

JAMA Dermatology(2024)10.1001/jamadermatol.2023.5362
N/A
0DataRank · unranked
14 citations

Devin Hunt, Jia Yan, Austin J. Jabbour, Paul Nghiem, Jaehyuk Choi +15 more

Case report: Deep sequencing and long-read genome sequencing refine prior genetic analyses in families with apparent gonadal mosaicism in PIK3CD-related activated PI3K delta syndrome

Frontiers in Immunology(2024)10.3389/fimmu.2024.1451212
N/A
0DataRank · unranked
2 citations

Jia Yan, Alex Paul, Mari Tokita, Yan Ding, Rajarshi Ghosh +17 more

The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA, DCLRE1C, IL2RG, IL7R, JAK3, RAG1, and RAG2

Genetics in Medicine(2025)10.1016/j.gim.2025.101613
N/A
0DataRank · unranked
5 citations

Michelle Zelnick, Shannon McNulty, Justyne E Ross, Namrata Khurana, Xueyang Pan +38 more

The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA , DCLRE1C , IL2RG , IL7R , JAK3 , RAG1 , and RAG2

medRxiv(2025)10.1101/2025.02.11.25322033
N/A
0DataRank · unranked
2 citations

Michelle Zelnick, Shannon McNulty, Justyne E Ross, Namrata Khurana, Xueyang Pan +19 more

Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2025)10.1002/ajmg.b.33036
N/A
0DataRank · unranked
0 citations

Morgan N Similuk, Alexandra Hehn, Rylee Duncan, Margaret Pekar, Eliza Gordon‐Lipkin +17 more

GARS‐related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61544
N/A
0DataRank · unranked
28 citations

Rajarshi Ghosh, Molly E. Kuo, William Hong, Jaehyung Lim, Saunder Bernes +14 more

Long‐Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia

Case Reports in Genetics(2025)10.1155/crig/5109434
N/A
0DataRank · unranked
0 citations

Morgan N Similuk, Laura M. Amendola, Katie L. Lewis, Magdalena Walkiewicz, Mari Tokita +3 more

PhenoTagger: a hybrid method for phenotype concept recognition using human phenotype ontology

Bioinformatics(2021)10.1093/bioinformatics/btab019
N/A
0DataRank · unranked
78 citations

Shankai Yan, Po‐Ting Lai, Daniel Veltri, Andrew J. Oler, Sandhya Xirasagar +5 more

SASH3variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation

Blood(2021)10.1182/blood.2020008629
N/A
0DataRank · unranked
56 citations

Jenna Bergerson, Tomoki Kawai, Hye Sun Kuehn, David H. McDermott, Irene Cortese +30 more

FOXI3 haploinsufficiency contributes to low T-cell receptor excision circles and T-cell lymphopenia

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.08.005
N/A
0DataRank · unranked
21 citations

Marita Bosticardo, Sunita Singh, Morgan N Similuk, Ottavia M. Delmonte, Francesca Pala +10 more