Stephanie DeArmey

932 citations

19 papers · 573 indexed · h-index 14

Co-authors: Priya S. Kishnani Laura E. Case Suhrad G. Banugaria Sean N. Prater Sarah P. Young Chanika Phornphutkul Deeksha Bali Raymond Wang
Topics: Lysosomal Storage Disorders Research (18 papers)Glycogen Storage Diseases and Myoclonus (12 papers)Child Nutrition and Feeding Issues (7 papers)
Cited by: Rheumatology Physiology Psychiatry and Mental health
Journals: PLoS ONE Molecular Therapy Clinical Neurophysiology
Partner nations: United States Canada Australia

In The Last Decade

Stephanie DeArmey

19 papers receiving 562 citations

Peers

Countries citing papers authored by Stephanie DeArmey

Since Specialization

Citations

This map shows the geographic impact of Stephanie DeArmey'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 Stephanie DeArmey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie DeArmey more than expected).

Fields of papers citing papers by Stephanie DeArmey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie DeArmey. 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 Stephanie DeArmey. The network helps show where Stephanie DeArmey may publish in the future.

Co-authorship network of co-authors of Stephanie DeArmey

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie DeArmey. A scholar is included among the top collaborators of Stephanie DeArmey based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephanie DeArmey. Stephanie DeArmey is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Phase I study of liver depot gene therapy in late-onset Pompe disease 2023 ·Molecular Therapy ·Edward C. Smith,Sam Hopkins,Laura E. Case,Ming Xu,(unknown),Stephanie DeArmey,Sang-oh Han,(unknown),Jessica A. Chichester,Edward H. Bossen,Christoph P. Hornik,Jennifer L. Cohen,Deeksha Bali,Priya S. Kishnani,Dwight D. Koeberl	24
2	Ectopic Ocular Surface Calcification in Patients With Hypophosphatasia Treated With Asfotase Alfa 2019 ·Cornea ·Sidney M. Gospe,Cecilia Santiago-Turla,Stephanie DeArmey,Thomas J. Cummings,Priya S. Kishnani,M. Tariq Bhatti	9
3	Corticobasal syndrome in a man with Gaucher disease type 1: Expansion of the understanding of the neurological spectrum 2018 ·Molecular Genetics and Metabolism Reports ·(unknown),(unknown),Stephanie DeArmey,Roy N. Alcalay,Jeffrey W. Cooney,Priya S. Kishnani	7
4	Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease 2017 ·Molecular Genetics and Metabolism ·Mari Mori,Gloria Haskell,Zoheb B. Kazi,Xiaolin Zhu,Stephanie DeArmey,Jennifer Goldstein,Deeksha Bali,Catherine Rehder,Elizabeth T. Cirulli,Priya S. Kishnani	19
5	Enzyme replacement therapy with alglucosidase alfa in Pompe disease: Clinical experience with rate escalation 2017 ·Molecular Genetics and Metabolism ·Ankit K. Desai,(unknown),Heidi Cope,Zoheb B. Kazi,Stephanie DeArmey,Priya S. Kishnani	13
6	Longitudinal polysomnographic findings in infantile Pompe disease 2015 ·American Journal of Medical Genetics Part A ·Sujay Kansagra,Stephanie Austin,Stephanie DeArmey,Zoheb B. Kazi,Richard M. Kravitz,Priya S. Kishnani	9
7	Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease 2014 ·Neuromuscular Disorders ·Laura E. Case,Carl Bjartmar,Claire Morgan,Robin Casey,Joel Charrow,John Clancy,Majed Dasouki,Stephanie DeArmey,Khan Nedd,(unknown),Heidi Peters,Dawn Phillips,Zachary Spigelman,Cynthia J. Tifft,Priya S. Kishnani	44
8	Ocular and Histologic Findings in a Series of Children With Infantile Pompe Disease Treated With Enzyme Replacement Therapy 2014 ·Journal of Pediatric Ophthalmology & Strabismus ·S. Grace Prakalapakorn,Alan D. Proia,Tammy L. Yanovitch,Stephanie DeArmey,Nancy J. Mendelsohn,Kyrieckos A. Aleck,Priya S. Kishnani	21
9	Polysomnographic findings in infantile Pompe disease 2013 ·American Journal of Medical Genetics Part A ·Sujay Kansagra,Stephanie Austin,Stephanie DeArmey,Priya S. Kishnani,Richard M. Kravitz	19
10	Algorithm for the Early Diagnosis and Treatment of Patients with Cross Reactive Immunologic Material-Negative Classic Infantile Pompe Disease: A Step towards Improving the Efficacy of ERT 2013 ·PLoS ONE ·Suhrad G. Banugaria,Sean N. Prater,Trusha Patel,Stephanie DeArmey,(unknown),Kathryn L. Berrier,Deeksha Bali,Catherine Rehder,Julian Raiman,(unknown),François Labarthe,Joel Charrow,Paul Harmatz,Pranesh Chakraborty,Amy S. Rosenberg,Priya S. Kishnani	87
11	Low anal sphincter tone in infantile-onset Pompe Disease: An emerging clinical issue in enzyme replacement therapy patients requiring special attention 2012 ·Molecular Genetics and Metabolism ·(unknown),(unknown),Stephanie DeArmey,Priya S. Kishnani	5
12	The emerging phenotype of long-term survivors with infantile Pompe disease 2012 ·Genetics in Medicine ·Sean N. Prater,Suhrad G. Banugaria,Stephanie DeArmey,Eleanor G. Botha,(unknown),Laura E. Case,Harrison N. Jones,Chanika Phornphutkul,Raymond Wang,Sarah P. Young,Priya S. Kishnani	143
13	An individually, modified approach to desensitize infants and young children with Pompe disease, and significant reactions to alglucosidase alfa infusions 2011 ·Molecular Genetics and Metabolism ·Areeg El‐Gharbawy,Joanne Mackey,Stephanie DeArmey,(unknown),(unknown),(unknown),Robert L. Conway,Priya S. Kishnani	26
14	The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings 2011 ·Clinical Neurophysiology ·Lisa D. Hobson‐Webb,Stephanie DeArmey,Priya S. Kishnani	36
15	The clinical phenotype of Long-term infantile Pompe disease survivors 2011 ·Molecular Genetics and Metabolism ·Sean N. Prater,Suhrad G. Banugaria,Joanne Mackey,(unknown),Laura E. Case,Stephanie DeArmey,Priya S. Kishnani	1
16	Use of cardiac magnetic resonance imaging to evaluate cardiac structure, function and fibrosis in children with infantile Pompe disease on enzyme replacement therapy 2010 ·Molecular Genetics and Metabolism ·Piers Barker,Sara K. Pasquali,Stephen Darty,Richard J. Ing,Jennifer S. Li,Raymond J. Kim,Stephanie DeArmey,Priya S. Kishnani,Michael J. Campbell	24
17	Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study 2008 ·Molecular Genetics and Metabolism ·Laura E. Case,Dwight D. Koeberl,Sarah P. Young,Deeksha Bali,Stephanie DeArmey,Joanne Mackey,Priya S. Kishnani	26
18	Fractures in children with Pompe disease: a potentiallong-term complication 2007 ·Pediatric Radiology ·Laura E. Case,(unknown),Donald P. Frush,(unknown),Stephanie DeArmey,Joanne Mackey,Anne Boney,Claire Morgan,Deyanira Corzo,(unknown),Thomas J. Weber,Yuan-Tsong Chen,Priya S. Kishnani	24
19	Cardiac arrhythmias following anesthesia induction in infantile‐onset Pompe disease: a case series 2007 ·Pediatric Anesthesia ·(unknown),Allison Kinder Ross,Jennifer S. Li,Stephanie DeArmey,Joanne Mackey,MaryAlice Worden,Deyanira Corzo,Claire Morgan,Priya S. Kishnani	36

About Stephanie DeArmey

Stephanie DeArmey is a scholar working on Rheumatology, Physiology and Psychiatry and Mental health, having authored 19 papers that have together received 573 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (18 papers), Glycogen Storage Diseases and Myoclonus (12 papers) and Child Nutrition and Feeding Issues (7 papers). The work is most often cited by research in Rheumatology (319 citations), Physiology (467 citations) and Psychiatry and Mental health (117 citations). Stephanie DeArmey has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Priya S. Kishnani, Laura E. Case, Suhrad G. Banugaria, Sean N. Prater, Sarah P. Young, Chanika Phornphutkul, Deeksha Bali, Raymond Wang, Eleanor G. Botha and Harrison N. Jones. Their work appears in journals such as PLoS ONE, Molecular Therapy and Clinical Neurophysiology.

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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