Kevin M. Flanigan - Concepedia

Author

Kevin M. Flanigan

Also Known As

Dr. Kevin Flanigan, Emma Ciafaloni, K Flanigan, K M Flanigan, K. Flanigan, K. M. Flanigan, K.M. Flanigan, Keene, Bruce P., Kevin Flanigan, Kevin M Flanigan

347

Publications

15.7K

Citations

H-Index

179

Concepts

All Affiliations

Nationwide Children's Hospital University of Utah The Ohio State University Washington University in St. Louis Children's Hospital of Philadelphia

About

Kevin M. Flanigan is an author at Nationwide Children's Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	55	5.5K
2	Health Sciences	8	8	478
3	Education	2	2	205
4	Engineering	2	2	907
5	Management	1	1	12

Kevin M. Flanigan

139

Publications

14.2K

Citations

H-Index

Page 1

	Year	Citations
Evidence‐based path to newborn screening for duchenne muscular dystrophy Jerry R. Mendell, Chris Shilling, Nancy D. Leslie, Annals of Neurology	2012	790
Eteplirsen for the treatment of Duchenne muscular dystrophy Jerry R. Mendell, Louise R. Rodino‐Klapac, Zarife Sahenk, Annals of Neurology	2013	770
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations Catherine L. Bladen, David Salgado, Soledad Monges, Human Mutation Dmd MutationsTrial PlanningEngineeringMendelian DisorderGenetic Disorder	2015	717
Distinctive patterns of microRNA expression in primary muscular disorders Iris Eisenberg, Alal Eran, Ichizo Nishino, Proceedings of the National Academy of Sciences	2007	500
A phase I/IItrial of MYO‐029 in adult subjects with muscular dystrophy Kathryn R. Wagner, James L. Fleckenstein, Anthony A. Amato, Annals of Neurology	2008	457
Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial Craig M. McDonald, Craig Campbell, Ricardo Erazo Torricelli, The Lancet Rare DiseasesUrologyClinical TrialsDegenerative DiseaseRehabilitation	2017	446
Ataluren treatment of patients with nonsense mutation dystrophinopathy K. Bushby, Richard S. Finkel, Brenda Wong, Muscle & Nerve	2014	416
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Human Mutation	2009	308
Spinocerebellar Ataxia Type 31 Is Associated with “Inserted” Penta-Nucleotide Repeats Containing (TGGAA)n Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceNeurological DisorderNeuroanatomyGenetics	2009	291
Gentamicin‐induced readthrough of stop codons in duchenne muscular dystrophy Vinod Malik, Louise R. Rodino‐Klapac, Laurence Viollet, Annals of Neurology	2010	271

Page 1