Amy Harper

795 citations

19 papers · 281 indexed · h-index 8

Impact in

Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neuroscience and Neuropharmacology Research
Neurology

Papers in

Cellular and Molecular Neuroscience 6
- Hereditary Neurological Disorders 4
- Genetic Neurodegenerative Diseases 4
Neurology 2
- Neurological diseases and metabolism 2

Co-authors: Eric P. Hoffman Elena Pegoraro Erynn S. Gordon Anne Rutkowski Susana Quijano‐Roy Mohamad A. Mikati Dmitry Tchapyjnikov Susan Sparks
Journals: Neuromuscular Disorders (3 papers)Journal of Personalized Medicine (1 paper)Journal of Neuromuscular Diseases (1 paper)Seizure (1 paper)PEDIATRICS (1 paper)
Partner nations: United States United Kingdom Canada

In The Last Decade

Amy Harper

18 papers receiving 278 citations

Peers

Countries citing papers authored by Amy Harper

Since Specialization

Citations

This map shows the geographic impact of Amy Harper's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Amy Harper with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy Harper more than expected).

Fields of papers citing papers by Amy Harper

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amy Harper. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Amy Harper. The network helps show where Amy Harper may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Amy Harper, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Amy Harper Line = papers co-authored together Amy Harper links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	407P RGX-202, an investigational gene therapy for the treatment of Duchenne muscular dystrophy: interim clinical data Neuromuscular Disorders ·Kcap Architects, Aravindhan Veerapandiyan, Vamshi K. Rao, Carolina Tesi Rocha, Amy Harper, Svenja Fischer, D Wolna, H.V. Kehiaian, Gerold Meyer von Knonau, Clare Wilson, Nidal Boulos, Michelle Gilmor, Lin Yang, 正和永木, Muthia Novita Ramadhani, M. Kossov	2024	0
2	Findings from the Longitudinal CINRG Becker Natural History Study Journal of Neuromuscular Diseases ·Paula R. Clemens, Heather Gordish‐Dressman, Gabriela Niizawa, Ksenija Gorni, Michela Guglieri, Anne M. Connolly, Matthew Wicklund, Tulio E. Bertorini, Jean K. Mah, Mathula Thangarajh, Edward C. Smith, Nancy L. Kuntz, Craig M. McDonald, Erik Henricson, C. García‐Bermúdez, Barry J. Byrne, Georgios Manousakis, Amy Harper, Susan T. Iannaccone, Utkarsh J. Dang	2023	2
3	Effect of a NICU to Home Physical Therapy Intervention on White Matter Trajectories, Motor Skills, and Problem-Solving Skills of Infants Born Very Preterm: A Case Series Journal of Personalized Medicine ·Christiana Butera, M.A. Bundin, Claire E. Kelly, Thijs Dhollander, Deanne K. Thompson, Jessica L. Wisnowski, P.J. Clifford, Barbara Sargent, Natasha Leporé, محمد عزیز رضایی, J. Dabbagh Yarishah, Mary S. Shall, 貢岩本, Richard D. Stevenson, LI Huiju, Amy Harper, Karen D. Hendricks‐Muñoz, Stacey C. Dusing	2022	4
4	Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review Ophthalmic Genetics ·Ananda de Arruda e Silva Ricardo, Rakesh K. Jain, Ann Jewell, Minuri Rajapakse, Amy Harper, Claude Labrecque, Paola Luciolli	2022	2
5	TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function Annals of Clinical and Translational Neurology ·Arens Taga, 장승택, Benedikt Goretzki, Thomas Q. Gallagher, Ann M. Ritter, Amy Harper, Thomas O. Crawford, Ute A. Hellmich, Charlotte J. Sumner, Brett A. McCray	2022	15
6	P.14 Analysis of the longitudinal CINRG Becker natural history study dataset Neuromuscular Disorders ·SoSren S. Sorensen, Heather Gordish‐Dressman, Gabriela Niizawa, Ksenija Gorni, Kim Jeffrey, Ron Canepa, Karn Hollyras, T. E. Bertoríni, Danqing Wang, Mathula Thangarajh, Edward C. Smith, 脩治米井, Ruijie Xiao, Erik Henricson, A. Mozi, Bryan Byrne, Georgios Manousakis, Amy Harper, ST Iannaccone, Utkarsh J. Dang	2022	1
7	Aggressive vertebral hemangioma masquerading as neurological disease in a pediatric patient SHILAP Revista de lepidopterología ·E Neri, Priti Balchandani, Gary Tye, Amy Harper, Hope Richard, India Sisler, Ana Guadalupe Cornejo Morales, Shun IKEUCHI, Dennis J. Rivet, Sanny Hahury	2021	4
8	P.337Dystrophin restoration by exon 53 skipping in patients with Duchenne muscular dystrophy after viltolarsen treatment: phase 2 study update Neuromuscular Disorders ·Paula R. Clemens, Vamshi K. Rao, Anne M. Connolly, Craig M. Zaidman, Amy Harper, Jean K. Mah, Beta Hermansyah, Toshinari Yamashita, Eric P. Hoffman	2019	1
9	A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American Frontiers in Neurology ·Sean C. Dougherty, Amy Harper, Claude Labrecque, Priti Balchandani, 조미라	2018	7
10	Anti-HMGCR myopathy may resemble limb-girdle muscular dystrophy Neurology Neuroimmunology & Neuroinflammation ·Payam Mohassel, Océane Landon‐Cardinal, A. Reghan Foley, Sandra Donkervoort, Katherine Pak, Colleen E. Wahl, Robert T. Shebert, Amy Harper, José María Souvirón, Matthew N. Meriggioli, Camilo Toro, Daniel B. Drachman, Yves Allenbach, Olivier Benvéniste, Anthony Béhin, B. Eymard, Pascal Laforêt, Tanya Stojkovic, Andrew L. Mammen, Carsten G. Bönnemann	2018	81
11	Autosomal recessive MFN2‐related Charcot‐Marie‐Tooth disease with diaphragmatic weakness: Case report and literature review American Journal of Medical Genetics Part A ·Christopher Tan, Adikari Chamara, Szabó Anikó, M. Jody Westbrook, JAIME BERNAL, Keith Nykamp, Anne Deucher, Amy Harper, Laurie Demmer	2016	14
12	KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction Annals of Neurology ·Jessica Duis, Shannon L. Dean, Carolyn Applegate, Amy Harper, Rui Xiao, Weimin He, Aminova Dilnoza Khikmatilla qizi, Lisa R. Sun, Clemens Griesel, Thomas O. Crawford, Ada Hamosh, Carl E. Stafstrom	2016	39
13	Response to immunotherapy in a patient with Landau‐Kleffner syndrome and GRIN2A mutation Epileptic Disorders ·Nina Fainberg, Amy Harper, Dmitry Tchapyjnikov, Mohamad A. Mikati	2016	21
14	Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2‐p12) deletion Muscle & Nerve ·Nivedita U. Jerath, John Kamholz, Tiffany Grider, Amy Harper, Andrea Swenson, Michael E. Shy	2015	6
15	Congenital Muscular Dystrophy Overview Susan Sparks, Susana Quijano‐Roy, Amy Harper, Anne Rutkowski, Erynn S. Gordon, Eric P. Hoffman, Elena Pegoraro	2012	38
16	Congenital Muscular Dystrophy Overview – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY KarÃn Lesnik-Oberstein, Susana Quijano‐Roy, Amy Harper, Anne Rutkowski, Erynn S. Gordon, УРБАНАВИЧЮС Г.П., Elena Pegoraro	2012	4
17	Successful ECT treatment for medically refractory nonconvulsive status epilepticus in pediatric patient Seizure ·Hae Won Shin, Cormac A. O’Donovan, Jane Boggs, Tim Lüeddecke, Amy Harper, William L. Bell, W. Vaughn McCall, Peter B. Rosenquist	2011	35
18	A limping child BMJ ·Daniel C. Perry, Amy Harper, Colin Bruce	2011	1
19	La Crosse Virus Encephalitis Preceding Neurosarcoidosis Diagnosed by Brain Biopsy PEDIATRICS ·Daisuke Kobayashi, Kelly Rouster‐Stevens, Amy Harper	2011	6

About Amy Harper

Amy Harper is a scholar working on Cellular and Molecular Neuroscience, Neurology, Virology, Sensory Systems and Genetics, having authored 19 papers that have together received 281 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (7 papers), Hereditary Neurological Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers), Cardiomyopathy and Myosin Studies (3 papers), Neurological diseases and metabolism (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), RNA Research and Splicing (2 papers) and Neonatal and fetal brain pathology (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (99 citations), Neurology (57 citations), Neurology (29 citations), Genetics (36 citations) and Psychiatry and Mental health (48 citations). Amy Harper has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Eric P. Hoffman, Elena Pegoraro, Erynn S. Gordon, Anne Rutkowski, Susana Quijano‐Roy, Mohamad A. Mikati, Dmitry Tchapyjnikov, Susan Sparks, Thomas O. Crawford and Nina Fainberg. Their work appears in journals such as Neuromuscular Disorders, Journal of Personalized Medicine, Journal of Neuromuscular Diseases, Seizure and PEDIATRICS.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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