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

Morag A. Lewis

King's College London

ORCID: 0000-0002-1846-8600
NeuroscienceBiochemistry, Genetics and Molecular Biology

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 9 papers. Top paper: “Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank”.

Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank

BMC Biology(2022)10.1186/s12915-022-01349-5
N/A
0DataRank · unranked
22 citations

Bradley A. Schulte, Judy R. Dubno, Karen P. Steel, Morag A. Lewis

Investigating the Characteristics of Genes and Variants Associated with Self-Reported Hearing Difficulty in Older Adults in the UK Biobank

medRxiv(2022)10.1101/2022.01.28.22269991
N/A
0DataRank · unranked
0 citations

Bradley A. Schulte, Judy R. Dubno, Karen P. Steel, Morag A. Lewis

Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss

PLoS Genetics(2023)10.1371/journal.pgen.1011058
N/A
0DataRank · unranked
9 citations

Jennifer Schulte, Lois J. Matthews, Kenneth I. Vaden, Claire J. Steves, Frances M. K. Williams +4 more

Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.26.564008
N/A
0DataRank · unranked
5 citations

Wan Du, Arun Prabhu Rameshbabu, Ariel Miura Armstrong, Stewart Silver, Yehree Kim +7 more

Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss

medRxiv(2023)10.1101/2023.04.27.23289040
N/A
0DataRank · unranked
3 citations

Jennifer Schulte, Lois J. Matthews, Kenneth I. Vaden, Claire J. Steves, Frances M. K. Williams +4 more

Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation

Science Translational Medicine(2024)10.1126/scitranslmed.adn0689
N/A
0DataRank · unranked
24 citations

Wan Du, Arun Prabhu Rameshbabu, Ariel Miura Armstrong, Stewart Silver, Yehree Kim +7 more

Large-scale audiometric phenotyping identifies distinct genes and pathways involved in hearing loss subtypes

Communications Biology(2025)10.1038/s42003-025-08778-2
N/A
0DataRank · unranked
4 citations

Kenneth I. Vaden, Morag A. Lewis, Darren Leitao, Karen P. Steel, Judy R. Dubno +2 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

The importance of accurate phenotyping in large-scale analyses of common disorders such as hearing loss

European Journal of Human Genetics(2025)10.1038/s41431-025-01957-z
N/A
0DataRank · unranked
0 citations

Bradley A. Schulte, Judy R. Dubno, Karen P. Steel, Morag A. Lewis