Bryce A. Seifert

Also affiliated with National Institute of Allergy and Infectious Diseases, Office of Extramural Research

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 100%percentile

0Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12

Top 100%

0DataRank

Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 more

Papers

Driven by 14 papers — median percentile 0. Top paper: “The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1”.

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

New England Journal of Medicine(2024)10.1056/nejmoa2312665

N/A

1.4DataRank · unranked

82 citations

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

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

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 Risk Factors for Early-Onset Merkel Cell Carcinoma

JAMA Dermatology(2024)10.1001/jamadermatol.2023.5362

N/A

0.406DataRank · unranked

14 citations

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

Further Personalizing Medicine in Immune Disorders: Genomic Findings and Hematopoietic Cell Transplantation Survival

Transplantation(2025)10.1097/tp.0000000000005504

N/A

0.104DataRank · unranked

1 citations

Sarah A. Bannon, Jia Yan, Rajarshi Ghosh, Ekaterina Damskey, Breanna Beers +41 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

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

Human Mutation(2020)10.1002/humu.24152

N/A

0DataRank · unranked

166 citations

Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L. Mai, Kelvin C. de Andrade +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

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

medRxiv(2020)10.1101/2020.02.26.20024679

N/A

0DataRank · unranked

10 citations

Stephanie B. Crowley, Myra I. Roche, Ann Katherine M. Foreman, Julianne O’Daniel, Bryce A. Seifert +22 more

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

medRxiv(2020)10.1101/2020.04.25.20078931

N/A

0DataRank · unranked

5 citations

Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L. Mai, Kelvin C. de Andrade +18 more

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12

Top 100%

0DataRank

Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 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

Myotonic dystrophy type 1 testing, 2024 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2024)10.1016/j.gim.2024.101145

N/A

0DataRank · unranked

12 citations

Honey V. Reddi, Benjamin E. Kang, Lora Jh Bean, Amy Shealy, Nancy C. Rose +1 more

Bryce A. Seifert

Indexed papers

Top data-sharing exemplar

Papers