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

Brenda Finucane

Autism & Developmental Medicine Institute

ORCID: 0000-0003-4841-669X
Biochemistry, Genetics and Molecular BiologyNeuroscience

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

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation”.

Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation

Current Opinion in Genetics & Development(2021)10.1016/j.gde.2020.12.016
N/A
0DataRank · unranked
52 citations

David H. Ledbetter, Jacob Vorstman, Brenda Finucane

Frequency of truncating FLCN variants and Birt-Hogg-Dubé–associated phenotypes in a health care system population

Genetics in Medicine(2022)10.1016/j.gim.2022.05.006
N/A
0DataRank · unranked
33 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome

Genetics in Medicine(2022)10.1016/j.gim.2022.09.011
N/A
0DataRank · unranked
10 citations

Brenda Finucane, Andrés Moreno-De-Luca, Lauren K. Walsh, Christa Lese Martin, David H. Ledbetter +1 more

Frequency of FLCN Loss of Function Variants and Birt-Hogg-Dubé-Associated Phenotypes in a Healthcare System Population

medRxiv(2022)10.1101/2022.01.31.22269926
N/A
0DataRank · unranked
0 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Response to van Riel et al

Genetics in Medicine(2022)10.1016/j.gim.2022.10.008
N/A
0DataRank · unranked
0 citations

Matthew T. Oetjens, Scott M. Myers, Brenda Finucane, Juliann M. Savatt

Gathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research

Genes(2023)10.3390/genes14010169
N/A
0DataRank · unranked
5 citations

T. Blaine Crowley, Brenda Finucane, Emily McClellan, Sarah Donoghue, Sixto García‐Miñáur +10 more

A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

Nature Communications(2024)10.1038/s41467-024-53211-7
N/A
0DataRank · unranked
15 citations

Brenda Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin +3 more

X and Y gene dosage effects are primary contributors to human sexual dimorphism: The case of height

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2503039122
N/A
0DataRank · unranked
4 citations

Brenda Finucane, Scott M. Myers, Christa L. Martin, David H. Ledbetter, Huntington F. Willard +2 more