Shawna Feely - Concepedia

Author

Shawna Feely

Also Known As

Carly E. Siskind, Feely, Shawna, S Feely, S M E Feely, S. Feely, S. M. E. Feely, S.M.E. Feely, Shawna Feely, Shawna M E Feely, Shawna M. E. Feely

Publications

Citations

H-Index

Concepts

All Affiliations

University of Iowa Wayne State University University College London University of Miami Stanford University

About

Shawna Feely is an author at University of Iowa specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	820
2	Health Sciences	2	2	44
3	Social Sciences	2	2	84
4	Natural Sciences	1	1	33
5	Biochemistry	1	1	33

Shawna Feely

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Charcot‐marie‐tooth disease subtypes and genetic testing strategies A. Saporta, Stephanie L. Sottile, Lindsey J. Miller, Annals of Neurology	2011	520
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis Vera Fridman, Brian N. Bundy, Mary M. Reilly, Journal of Neurology Neurosurgery & Psychiatry	2014	336
<i>MFN2</i> mutations cause severe phenotypes in most patients with CMT2A Shawna Feely, Matilde Laurá, Carly E. Siskind, Neurology	2011	214
Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy Marina Kennerson, Garth A. Nicholson, Stephen G. Kaler, The American Journal of Human Genetics Missense MutationsGenetic DisorderMedicineGeneticsMolecular Biology	2010	186
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes Andrea Cortese, Yi Zhu, Adriana Rebelo, Nature Genetics Biallelic MutationsSomatic VariantGenetic DisorderGeneticsDiabetes	2020	170
A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease Michael Gonzalez, Shawna Feely, Fiorella Speziani, Brain	2014	138
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia Martina Minnerop, Delia Kurzwelly, Holger Wagner, Brain	2017	118
Genotype–phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the <i>MPZ</i> gene Oranee Sanmaneechai, Shawna Feely, Steven S. Scherer, Brain	2015	106
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study Menelaos Pipis, Shawna Feely, James M. Polke, Brain	2020	87
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2 Petra Laššuthová, Adriana Rebelo, Gianina Ravenscroft, The American Journal of Human Genetics Genome InstabilityMolecular PhysiologyGenetic DisorderGeneticsMolecular Biology	2018	76

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