Stephanie DeArmey

932 total citations
19 papers, 573 citations indexed

About

Stephanie DeArmey is a scholar working on Physiology, Rheumatology and Psychiatry and Mental health. According to data from OpenAlex, Stephanie DeArmey has authored 19 papers receiving a total of 573 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Physiology, 13 papers in Rheumatology and 7 papers in Psychiatry and Mental health. Recurrent topics in Stephanie DeArmey's work include Lysosomal Storage Disorders Research (18 papers), Glycogen Storage Diseases and Myoclonus (12 papers) and Child Nutrition and Feeding Issues (7 papers). Stephanie DeArmey is often cited by papers focused on Lysosomal Storage Disorders Research (18 papers), Glycogen Storage Diseases and Myoclonus (12 papers) and Child Nutrition and Feeding Issues (7 papers). Stephanie DeArmey collaborates with scholars based in United States, Canada and France. Stephanie DeArmey's co-authors include Priya S. Kishnani, Laura E. Case, Sean N. Prater, Suhrad G. Banugaria, Sarah P. Young, Harrison N. Jones, Raymond Wang, Joanne Mackey, Deeksha Bali and Eleanor G. Botha and has published in prestigious journals such as PLoS ONE, Molecular Therapy and Clinical Neurophysiology.

In The Last Decade

Stephanie DeArmey

19 papers receiving 562 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Stephanie DeArmey United States	14	467	319	128	117	117	19	573
Nesrin Karabul Germany	15	466 1.0×	230 0.7×	130 1.0×	132 1.1×	89 0.8×	24	580
Johanna M. P. van den Hout Netherlands	12	634 1.4×	420 1.3×	150 1.2×	145 1.2×	140 1.2×	31	729
Carine I. van Capelle Netherlands	14	490 1.0×	408 1.3×	93 0.7×	123 1.1×	169 1.4×	18	600
Joanne Mackey United States	12	580 1.2×	439 1.4×	186 1.5×	152 1.3×	91 0.8×	16	781
Léon P. F. Winkel Netherlands	10	753 1.6×	610 1.9×	130 1.0×	196 1.7×	199 1.7×	11	878
Norberto Guelbert Argentina	16	514 1.1×	232 0.7×	216 1.7×	68 0.6×	68 0.6×	39	651
Miriam Rigoldi Italy	16	286 0.6×	228 0.7×	114 0.9×	88 0.8×	42 0.4×	29	544
N. Strigl‐Pill Germany	6	361 0.8×	309 1.0×	66 0.5×	92 0.8×	103 0.9×	7	456
K. Eger Germany	9	226 0.5×	206 0.6×	61 0.5×	62 0.5×	53 0.5×	19	464
J.H.J. Wokke Netherlands	7	303 0.6×	240 0.8×	49 0.4×	79 0.7×	68 0.6×	15	530

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

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

Smith, Edward C., Sam Hopkins, Laura E. Case, et al.. (2023). Phase I study of liver depot gene therapy in late-onset Pompe disease. Molecular Therapy. 31(7). 1994–2004. 24 indexed citations

Gospe, Sidney M., Cecilia Santiago-Turla, Stephanie DeArmey, et al.. (2019). Ectopic Ocular Surface Calcification in Patients With Hypophosphatasia Treated With Asfotase Alfa. Cornea. 38(7). 896–900. 9 indexed citations

DeArmey, Stephanie, et al.. (2018). Corticobasal syndrome in a man with Gaucher disease type 1: Expansion of the understanding of the neurological spectrum. Molecular Genetics and Metabolism Reports. 17. 69–72. 7 indexed citations

Mori, Mari, Gloria Haskell, Zoheb B. Kazi, et al.. (2017). Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease. Molecular Genetics and Metabolism. 122(4). 189–197. 19 indexed citations

Desai, Ankit K., et al.. (2017). Enzyme replacement therapy with alglucosidase alfa in Pompe disease: Clinical experience with rate escalation. Molecular Genetics and Metabolism. 123(2). 92–96. 13 indexed citations

Kansagra, Sujay, Stephanie Austin, Stephanie DeArmey, et al.. (2015). Longitudinal polysomnographic findings in infantile Pompe disease. American Journal of Medical Genetics Part A. 167(4). 858–861. 9 indexed citations

Case, Laura E., Carl Bjartmar, Claire Morgan, et al.. (2014). Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease. Neuromuscular Disorders. 25(4). 321–332. 44 indexed citations

Prakalapakorn, S. Grace, Alan D. Proia, Tammy L. Yanovitch, et al.. (2014). Ocular and Histologic Findings in a Series of Children With Infantile Pompe Disease Treated With Enzyme Replacement Therapy. Journal of Pediatric Ophthalmology & Strabismus. 51(6). 355–362. 21 indexed citations

Kansagra, Sujay, Stephanie Austin, Stephanie DeArmey, Priya S. Kishnani, & Richard M. Kravitz. (2013). Polysomnographic findings in infantile Pompe disease. American Journal of Medical Genetics Part A. 161(12). 3196–3200. 19 indexed citations

10.

Banugaria, Suhrad G., Sean N. Prater, Trusha Patel, et al.. (2013). 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. PLoS ONE. 8(6). e67052–e67052. 87 indexed citations

11.

DeArmey, Stephanie, et al.. (2012). Low anal sphincter tone in infantile-onset Pompe Disease: An emerging clinical issue in enzyme replacement therapy patients requiring special attention. Molecular Genetics and Metabolism. 108(2). 142–144. 5 indexed citations

12.

Prater, Sean N., Suhrad G. Banugaria, Stephanie DeArmey, et al.. (2012). The emerging phenotype of long-term survivors with infantile Pompe disease. Genetics in Medicine. 14(9). 800–810. 143 indexed citations

13.

El‐Gharbawy, Areeg, et al.. (2011). An individually, modified approach to desensitize infants and young children with Pompe disease, and significant reactions to alglucosidase alfa infusions. Molecular Genetics and Metabolism. 104(1-2). 118–122. 26 indexed citations

14.

Hobson‐Webb, Lisa D., Stephanie DeArmey, & Priya S. Kishnani. (2011). The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings. Clinical Neurophysiology. 122(11). 2312–2317. 36 indexed citations

15.

Prater, Sean N., Suhrad G. Banugaria, Joanne Mackey, et al.. (2011). The clinical phenotype of Long-term infantile Pompe disease survivors. Molecular Genetics and Metabolism. 102(2). S36–S37. 1 indexed citations

16.

Barker, Piers, Sara K. Pasquali, Stephen Darty, et al.. (2010). Use of cardiac magnetic resonance imaging to evaluate cardiac structure, function and fibrosis in children with infantile Pompe disease on enzyme replacement therapy. Molecular Genetics and Metabolism. 101(4). 332–337. 24 indexed citations

17.

Case, Laura E., Dwight D. Koeberl, Sarah P. Young, et al.. (2008). Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study. Molecular Genetics and Metabolism. 95(4). 233–235. 26 indexed citations

18.

Ross, Allison Kinder, Jennifer S. Li, Stephanie DeArmey, et al.. (2007). Cardiac arrhythmias following anesthesia induction in infantile‐onset Pompe disease: a case series. Pediatric Anesthesia. 17(8). 738–748. 36 indexed citations

19.

Case, Laura E., Donald P. Frush, Stephanie DeArmey, et al.. (2007). Fractures in children with Pompe disease: a potentiallong-term complication. Pediatric Radiology. 37(5). 437–445. 24 indexed citations

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.

Explore authors with similar magnitude of impact