Megan A. Waldrop

Also affiliated with The Ohio State University Wexner Medical Center, The Ohio State University

MedicineBiochemistry, 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 6 papers. Top paper: “Parental Experiences with Newborn Screening and Gene Replacement Therapy for Spinal Muscular Atrophy”.

Parental Experiences with Newborn Screening and Gene Replacement Therapy for Spinal Muscular Atrophy

Journal of Neuromuscular Diseases(2023)10.3233/jnd-230082

N/A

0.345DataRank · unranked

9 citations

Anne M. Connolly, Kathryn Vannatta, N. Hacker, Andrea Hatfield, Abigail Decipeda +4 more

A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity

medRxiv(2021)10.1101/2021.11.03.21265887

N/A

0.104DataRank · unranked

1 citations

Megan A. Waldrop, Paul T. Martin, Roxane Alles, Diane M. Dunn, Lindsay N. Alfano +7 more

Candidate gene modifiers of dystrophinopathy identified by the uniform application of genome-wide datasets to novel GWAS-identified loci

medRxiv(2021)10.1101/2021.11.03.21265899

N/A

0DataRank · unranked

2 citations

Megan A. Waldrop, Paul T. Martin, Roxane Alles, Diane M. Dunn, Lindsay N. Alfano +7 more

A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity

European Journal of Human Genetics(2023)10.1038/s41431-023-01329-5

N/A

0DataRank · unranked

13 citations

Megan A. Waldrop, Paul T. Martin, Roxane Alles, Diane M. Dunn, Lindsay N. Alfano +7 more

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features

medRxiv(2024)10.1101/2024.09.23.24313872

N/A

0DataRank · unranked

3 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +33 more

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101399

N/A

0DataRank · unranked

5 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +32 more