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Kevin M. Flanigan

nationwide children's hospital and abigail wexner research institute

68H-index
365Paper Count
1.6WCitation Count
Published Papers 105
Publication Date
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Plasma EV Proteomics Identifies ECM Remodeling and Inflammatory Proteins LUM and C7 as Candidate Biomarkers in FSHD
errAnnals of Clinical and Translational Neurology
IF3.9
err2026-05-20
err0
errOAAI
errMustafa Bilal Bayazit; Chiranth K. Nagaraj; Jackson S. Newell; Kim Truc Nguyen; Xilal Y. Rima; Jacob Doon-Ralls; Eduardo Reátegui; Jeffrey M. Statland; Rabi Tawil; Kevin M. Flanigan; Scott Q. Harper; Nizar Y. Saad
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Unraveling the spatial landscape of dystrophinopathies: a transcriptomic approach to Becker and Duchenne muscular dystrophies
errThe Journal of Pathology
IF0
err2026-05-01
err0
errOAAI
errLaura GM Heezen; Qirong Mao; Stefan Nicolau; Claudio Novella Rausell; Julia van der Weerd; Jan Kueckelhaus; Rasya Gokul Nath; Jordi Diaz- Manera; Hermien E Kan; Erik H Niks; Maaike van Putten; Annemieke Aartsma-Rus; Kevin M Flanigan; Ahmed Mahfouz; Pietro Spitali
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Gene x environment interaction analysis confirms genetic modifier effects on steroid efficacy via TGF-β pathway in Duchenne muscular dystrophy
errEuropean Journal of Human Genetics
IF4.6
err2026-04-20
err0
errOAAI
errVeronica J. Vieland; Sang-Cheol Seok; Megan A. Waldrop; Leigh M. Gabel; Diane M. Dunn; Kevin M. Flanigan; Robert B. Weiss
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Predicting subtypes of glycogen storage disease type IV: Challenges of hepatic subtypes and genotype-phenotype correlation
errMolecular Genetics and Metabolism
IF3.5
err2025-11-24
err0
PREAI
errAnne Taylor; Desale Yacob; Bonita Fung; Shamlal Mangray; Daniel R. Boué; Kevin M. Flanigan; Rebecca L. Koch; Priya S. Kishnani; Deeksha Bali; Alexander Weymann; Mari Mori
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Re-evaluating acceptable risk of death from gene therapy: A threshold study among individuals with Duchenne muscular dystrophy and their caregivers in the US and UK
errEUROPEAN JOURNAL OF MEDICAL GENETICS
IF1.7
err2025-10-01
err0
errOAAI
errPeay, Holly; Fischer, Ryan; McNiff, Megan; Heslop, Emma; Pierce, Anna; Denger, Brian; Camino, Eric; Johnson, Alexandra; Cope, Heidi; Hill, Christine; Beaverson, Katherine L.; Ganot, Annie; Phillips, Dawn; Woollacott, Ione O. C.; Bateman-House, Alison; Flanigan, Kevin M.; Goemans, Nathalie; Servais, Laurent; Guglieri, Michela; Mansfield, Carol
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Consensus recommendations and considerations for the delivery and monitoring of gene therapy in patients with Duchenne muscular dystrophy
errNeuromuscular Disorders
IF2.8
err2025-08-23
err0
PREAI
errJodi M. Wolff; Nora Capocci; Evrim Atas; Diana X. Bharucha-Goebel; John F. Brandsema; Russell J. Butterfield; Christina B. Chadwick; Manuela Corti; Thomas O. Crawford; Linda Cripe; John W. Day; Tina Duong; Mai K. ElMallah; Kevin M. Flanigan; Lindsey A. George; Natalie L. Goedeker; Erica Goude; Sharon Hesterlee; Brian Lin; Natalie K. Katz; Susan E. Matesanz; Craig McDonald; Elizabeth M. McNally; Claudia Mercado-Rodriguez; Deipanjan Nandi; Julie A. Parsons; Crystal Proud; Leigh Ramos-Platt; Angela Lek; Stephanie M. Salabarria; Eric Camino; Rachel Schrader; Erin Shea; Richard Shell; Perry B. Shieh; Jonathan H. Soslow; Jane B. Taylor; Aravindhan Veerapandiyan; Chet Villa; Michele L. Yang; Craig M. Zaidman; Carmen Leon-Astudillo; Barry J. Byrne
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Like father, like son: RNA-sequencing from a 30-year-old muscle biopsy identifies a novel splice variant in ACTA1 as the cause of an attenuated nemaline myopathy phenotype
errNeuromuscular Disorders
IF2.8
err2025-06-04
err0
errOAAI
errAlayne P. Meyer; Sana Yousfi; Stefan Nicolau; Afrooz Rashnonejad; Jingting Zhu; Zarife Sahenk; Emma Frair; Hui Lin; Swetha Ramadesikan; Daniel Koboldt; Kevin M. Flanigan
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Treatment with UX111 gene therapy rapidly reduced heparansulfate (HS) exposure in cerebrospinalfluid (CSF) and improvedlong-term cognitive function in children withmucopolysaccharidosis type IIIA (MPS IIIA)
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2025-02-01
err0
PREAI
errLau, Heather A.; Patra, Kaushik; Wolf, Melissa; Smith, Nicholas J. C.; Couce, Maria L.; Rajan, Deepa; Truxal, Kristen; Castro Lopez, Maria Jose De; Fuller, Maria; Monteagudo-Vilavedra, Eines; Dunia Dougherty-De Miguel, Lucia; Riera, Mireia Del Toro; Flanigan, Kevin M.
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Gross motor delays in infants and young boys with Duchenne muscular dystrophy
errJOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
err2024-12-08
err0
errOAAI
errLowes, Linda P.; Reash, Natalie F.; Iammarino, Megan A.; Connolly, Anne M.; Pietruszewski, Lindsay; Smith, Melissa A.; Peng, Jing; Steiner, Christopher L.; Tsao, Chang-Yong; Waldrop, Megan A.; Flanigan, Kevin M.; Chagat, Shannon; Meyer, Alayne P.; Mendell, Jerry R.; Alfano, Lindsay N.
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Evaluation of safety and early efficacy of AAV gene therapy in mouse models of vanishing white matter disease
errMOLECULAR THERAPY
IF12
err2024-06-01
err1
PREAI
errHerstine, Jessica A.; Chang, Pi -Kai; Chornyy, Sergiy; Stevenson, Tamara J.; Sunshine, Alex C.; Nokhrina, Ksenia; Rediger, Jessica; Wentz, Julia; Vetter, Tatyana A.; Scholl, Erika; Holaway, Caleb; Pyne, Nettie K.; Bratasz, Anna; Yeoh, Stewart; Flanigan, Kevin M.; Bonkowsky, Joshua L.; Bradbury, Allison M.
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Increase in Full-Length Dystrophin by Exon Skipping in Duchenne Muscular Dystrophy Patients with Single Exon Duplications: An Open-label Study
errJOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
err2024-03-08
err4
errOAAI
errNicolau, Stefan; Malhotra, Jyoti; Kaler, Maryann; Coxen, Pamela Magistrado; Iammarino, Megan A.; Reash, Natalie F.; Frair, Emma C.; Wijeratne, Saranga; Kelly, Benjamin J.; White, Peter; Lowes, Linda P.; Waldrop, Megan A.; Flanigan, Kevin M.
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Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies - Developing Potential Treatments for the Entire Spectrum of Disease
errJOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
err2024-02-13
err2
errOAAI
errMcDonald, Craig; Camino, Eric; Escandon, Rafael; Finkel, Richard S.; Fischer, Ryan; Flanigan, Kevin; Furlong, Pat; Juhasz, Rose; Martin, Ann S.; Villa, Chet; Sweeney, H. Lee
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A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2023-03-20
err7
errOAAI
errFlanigan, Kevin M.; Waldrop, Megan A.; Martin, Paul T.; Alles, Roxane; Dunn, Diane M.; Alfano, Lindsay N.; Simmons, Tabatha R.; Moore-Clingenpeel, Melissa; Burian, John; Seok, Sang-Cheol; Weiss, Robert B.; Vieland, Veronica J.
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Interim results of Transpher A, a multicenter, single-dose clinical trial of UX111 gene therapy for Sanfilippo syndrome type A (mucopolysaccharidosis IIIA)
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2023-02-01
err3
PREAI
errFlanigan, Kevin M.; Smith, Nicholas; Luz Couce, Maria; Rajan, Deepa; Truxal, Kristen; McBride, Kim L.; de Castro Lopez, Maria Jose; Fuller, Maria; Taylor, John; Del Campo, Ana B.; Grachev, Igor; Lau, Heather
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Systemic PPMO-mediated dystrophin expression in the Dup2 mouse model of Duchenne muscular dystrophy
errMOLECULAR THERAPY-NUCLEIC ACIDS
IF0
err2022-12-01
err8
errOAAI
errGushchina, Liubov V.; Vetter, Tatyana A.; Frair, Emma C.; Bradley, Adrienne J.; Grounds, Kelly M.; Lay, Jacob W.; Huang, Nianyuan; Suhaiba, Aisha; Schnell, Frederick J.; Hanson, Gunnar; Simmons, Tabatha R.; Wein, Nicolas; Flanigan, Kevin M.
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Letter by Duan et al Regarding Article, Therapeutic Exon Skipping Through a CRISPR-Guided Cytidine Deaminase Rescues Dystrophic Cardiomyopathy In Vivo
errCIRCULATION
IF38.6
err2022-05-03
err0
errOAAI
errDuan, Dongsheng; Flanigan, Kevin M.; Aartsma-Rus, Annemieke
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Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy
errHUMAN MUTATION
IF3.7
err2022-03-07
err27
errOAAI
errWaldrop, Megan A.; Moore, Steven A.; Mathews, Katherine D.; Darbro, Benjamin W.; Medne, Livja; Finkel, Richard; Connolly, Anne M.; Crawford, Thomas O.; Drachman, Daniel; Wein, Nicolas; Habib, Ali A.; Krzesniak-Swinarska, Monika A.; Zaidman, Craig M.; Collins, James J.; Jokela, Manu; Udd, Bjarne; Day, John W.; Ortiz-Guerrero, Gloria; Statland, Jeff; Butterfield, Russell J.; Dunn, Diane M.; Weiss, Robert B.; Flanigan, Kevin M.
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Phenotypic Spectrum of Dystrophinopathy Due to Duchenne Muscular Dystrophy Exon 2 Duplications
errNEUROLOGY
IF8.5
err2022-02-15
err6
errOAAI
errZambon, Alberto A.; Waldrop, Megan A.; Alles, Roxane; Weiss, Robert B.; Conroy, Sara; Moore-Clingenpeel, Melissa; Previtali, Stefano; Flanigan, Kevin M.
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Interim results of Transpher A, a multicentre, single-dose, phase 1/2 clinical trial of ABO-102 investigational gene therapy for Sanfilippo syndrome type A (mucopolysaccharidosis IIIA)
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2022-02-01
err0
PREAI
errFlanigan, Kevin M.; Smith, Nicholas J. N.; Couce, Maria L.; Escolar, Maria; Truxal, Kristen V.; McBride, Kim L.; de Castro, Maria J.; Fuller, Maria; Paneda, A.; Ruiz, J.; del Campo, A. B.; Grachev, I.
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Automated immunofluorescence analysis for sensitive and precise dystrophin quantification in muscle biopsies
errNEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
IF3.4
err2021-12-28
err9
errOAAI
errVetter, Tatyana A.; Nicolau, Stefan; Bradley, Adrienne J.; Frair, Emma C.; Flanigan, Kevin M.
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Research Directions

No research directions
Co-authors
Cooperation Journals
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Richard K. Wilson
H-index: 189 · Papers: 682
M
Mathias Uhlén
H-index: 131 · Papers: 1.1K
I
Isaac S. Kohane
H-index: 119 · Papers: 921
J
Justin C. McArthur
H-index: 115 · Papers: 461
J
J. Philip Miller
H-index: 115 · Papers: 1.1K
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