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

Margaret A. Kenna

Boston Children's Hospital

ORCID: 0000-0003-0851-9272
NeuroscienceMedicine

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
0.581Author 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.

Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes

npj Genomic Medicine(2024)10.1038/s41525-024-00441-9
Top 48%
0.373DataRank
Top 48%11 citations

Nancy C. Andrews, Alan H. Beggs, Philip M. Boone, Catherine A. Brownstein, Maya Chopra +32 more

Papers

Driven by 12 papers — median percentile 43. Top paper: “Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes”.

Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes

npj Genomic Medicine(2024)10.1038/s41525-024-00441-9
Top 48%
0.373DataRank
Top 48%11 citations

Nancy C. Andrews, Alan H. Beggs, Philip M. Boone, Catherine A. Brownstein, Maya Chopra +32 more

Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients With Enlarged Vestibular Aqueduct or GJB2 Mutation

Otology & Neurotology(2023)10.1097/mao.0000000000003879
Top 65%
0.208DataRank
Top 65%3 citations

Charlotte Morse-Fortier, Amanda M. Griffin, David Faller, Michael S. Cohen, Margaret A. Kenna +3 more

Association of Blood Type With Postsurgical Mucosal Bleeding in Pediatric Patients Undergoing Tonsillectomy With or Without Adenoidectomy

JAMA Network Open(2020)10.1001/jamanetworkopen.2020.1804
N/A
0DataRank · unranked
9 citations

Peter W. Forbes, Jenna M. Dargie, Juliana Manganella, Greg R. Licameli, Margaret A. Kenna +2 more

Selective excision of the centromere chromatin complex from Saccharomyces cerevisiae

Research Explorer (The University of Manchester)(2020)10.17615/6pgq-7666
N/A
0DataRank · unranked
0 citations

Enrique Amaya, Kerry Bloom, Margaret A. Kenna

Neuroimaging in Kabuki syndrome and another KMT2D‐related disorder

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62450
N/A
0DataRank · unranked
14 citations

Margaret A. Kenna, Devon Barrett, Thomas E. Mullen, Olaf A. Bodamer, Pankaj B. Agrawal +3 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w
N/A
0DataRank · unranked
17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

medRxiv(2021)10.1101/2021.01.27.21250652
N/A
0DataRank · unranked
8 citations

Marina T. DiStefano, Andrea M. Oza, Madeline Y. Hughes, Emma H. Wilcox, Sarah E. Hemphill +18 more

PKHD1L1 , A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss

medRxiv(2023)10.1101/2023.10.08.23296081
N/A
0DataRank · unranked
3 citations

Pedro De‐la‐Torre, Mina Zamani, Hanjun Wang, Hina Khan, T. Morris +12 more

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

Science(2024)10.1126/science.adf5489
N/A
0DataRank · unranked
48 citations

Sabrina Méchaussier, Patricia L. Yeyati, Fraser McPhie, Jacob R. Anderson, Chen Jing Khoo +75 more

Genomic diversity of bacteriophages infecting Microbacterium spp

PLoS ONE(2020)10.1371/journal.pone.0234636
N/A
0DataRank · unranked
71 citations

Lawrence Abad, Richard M. Alvey, Kirk R. Anders, Haley G. Aull, Suparna Bhalla +50 more

ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time

Genetics in Medicine(2025)10.1016/j.gim.2025.101392
N/A
0DataRank · unranked
1 citations

Marina T. DiStefano, Andrea M. Oza, Pamela Ajuyah, Ryan Webb, Enyonam Edoh +76 more

Preclinical testing of AAV9-PHP.B for transgene expression in the non-human primate cochlea

Hearing Research(2020)10.1016/j.heares.2020.107930
N/A
0DataRank · unranked
63 citations

Killian S. Hanlon, Maya K. Devine, Kelly Tenneson, Frederick Émond, J. Lafond +4 more