Pamela Arn

2.9k citations

36 papers · 1.8k indexed · h-index 20

Impact in

Rheumatology top 1%
- Glycogen Storage Diseases and Myoclonus
- Folate and B Vitamins Research
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in

Developmental Biology 2
Clinical Biochemistry 6
- Metabolism and Genetic Disorders 6

Co-authors: Deeksha Bali Priya S. Kishnani David A. Weinstein Anne Boney Wendy K. Chung Stephanie Austin J. E. Wraith Michael S. Watson
Journals: Genetics in Medicine (4 papers)The Journal of Pediatrics (2 papers)Journal of Pediatric Surgery (2 papers)Journal of Medical Genetics (2 papers)Health Affairs (1 paper)
Partner nations: United States United Kingdom Canada

In The Last Decade

Pamela Arn

34 papers receiving 1.8k citations

Peers

Countries citing papers authored by Pamela Arn

Since Specialization

Citations

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

Fields of papers citing papers by Pamela Arn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Pamela Arn, 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 Pamela Arn Line = papers co-authored together Pamela Arn links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Preferences for implementing pharmacogenomics in pediatric primary care: a discrete choice experiment Pediatric Research ·Benjamin Q. Duong, Nathan D. Seligson, M Ledwidge, Julija Gjorgjieva, Pamela Arn, Farrukh Munir, Vicky L. Funanage, Ramzi G. Salloum, Kathryn Blake	2025	0
2	TANGO2 Mutation: A Genetic Cause of Multifocal Combined Dystonia Movement Disorders Clinical Practice ·R. Füllner, Matthew R. Burns, Shannon Chiu, Aparna Wagle Shukla, С.В. Рекеда, سلمان كلش, Pamela Arn, Irene A. Malaty	2021	4
3	Phenotypic variability in deficiency of the α subunit of succinate‐CoA ligase JIMD Reports ·Didem Demirbas, David J. Harris, Pamela Arn, Xiaoping Huang, Susan E. Waisbren, Irina Anselm, Jordan Lerner‐Ellis, Lee‐Jun Wong, Harvey L. Levy, Gerard T. Berry	2019	7
4	Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Priya S. Kishnani, Jennifer Goldstein, Stephanie Austin, Pamela Arn, Bert Bachrach, Deeksha Bali, Wendy K. Chung, Areeg El‐Gharbawy, Laurie M. Brown, Stephen G. Kahler, Surekha Pendyal, Stimmlage -Das Minetti Quartett Im Gespräch, Olha Lehka-Paul, David A. Weinstein, Michael S. Watson	2019	86
5	The natural history of MPS I: global perspectives from the MPS I Registry Genetics in Medicine ·Michael Beck, Pamela Arn, Roberto Giugliani, Joseph Muenzer, Torayuki Okuyama, J. Michael Taylor, Shari Fallet	2014	118
6	Recessive Mutations in PCBD1 Cause a New Type of Early-Onset Diabetes Diabetes ·Deimantė Šimaitė, 肖小华, Maolian Gong, Franz Rüschendorf, Shiqi Jia, Pamela Arn, Walter Ojakäär, Carolyn Ellaway, Peter Kühnen, Georg F. Hoffmann, Nenad Blau, Francesca M. Spagnoli, Norbert Hübner, Klemens Raile	2014	39
7	Glycogen Storage Disease Type III diagnosis and management guidelines Genetics in Medicine ·Priya S. Kishnani, Stephanie Austin, Pamela Arn, Deeksha Bali, Anne Boney, Laura E. Case, Wendy K. Chung, Dev M. Desai, Areeg El‐Gharbawy, Ronald G. Haller, Gerrit Smit, Alastair D. Smith, Lisa D. Hobson‐Webb, Stephanie Burns Wechsler, David A. Weinstein, Michael S. Watson	2010	197
8	Education format and resource preferences among registrants of a pediatric-focused CME website Medical Teacher ·Michael Kin-Kong Li, Osama El-Saied Shalaby, Pamela Arn	2009	13
9	Characterization of Surgical Procedures in Patients with Mucopolysaccharidosis Type I: Findings from the MPS I Registry The Journal of Pediatrics ·Pamela Arn, J. E. Wraith, Lisa H. Underhill	2009	41
10	The MPS I registry: Design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I Molecular Genetics and Metabolism ·Gregory M. Pastores, Pamela Arn, Michael Beck, Joe T.R. Clarke, Nathalie Guffon, Paige Kaplan, Joseph Muenzer, Denise Norato, Elsa Shapiro, Janet A. Thomas, David Viskochil, J. E. Wraith	2007	158
11	Newborn Screening: Current Status Health Affairs ·Pamela Arn	2007	34
12	Galactosemia Current Treatment Options in Neurology ·Pamela Arn	2003	2
13	Hyperphenylalaninemia with High Levels of 7-Biopterin is Associated with Mutations in the PCBD Gene Encoding the Bifunctional Protein Pterin-4a-Carbinolamine Dehydratase and Transcriptional Coactivator (DCoH) The American Journal of Human Genetics ·Beat Thöny, Steven J. Semaan, L. Kierat, M. Blaskovics, Pamela Arn, Patrick Ferreira, Igor Rebrin, June E. Ayling, Nenad Blau	1998	40
14	Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature American Journal of Medical Genetics ·Pamela Arn, Xiang Zhu, Kiyonori Izumi, Joleen L. Zackowski, C. B. Mankinen, Laurel L. Estabrooks	1995	16
15	SRVX, a sex reversing locus in Xp21.2?p22.11 Human Genetics ·Pamela Arn, Harold Chen, A. Wawrzyniec, C. B. Mankinen, Gwendolyn Wachtel, Shibo Li, Serpil Guran, Amina Kimangano Kivaria	1994	49
16	Mild mandibulofacial dysostosis in a child with a deletion of 3p American Journal of Medical Genetics ·Pamela Arn, C. B. Mankinen, Ethylin Wang Jabs	1993	20
17	Analysis of DNA restriction fragments greater than 5.7 Mb in size from the centromeric region of human chromosomes Mammalian Genome ·Pamela Arn, Xiang Li, Cynthia L. Smith, Jonathan Andrés, David C. Schwartz, Ethylin Wang Jabs	1991	1
18	Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus New England Journal of Medicine ·Pamela Arn, Elizabeth R. Hauser, George H. Thomas, Gail E. Herman, David Hess, Saul W. Brusilow	1990	140
19	Outcome of pectus excavatum in patients with Marfan syndrome and in the general population The Journal of Pediatrics ·Pamela Arn, L.R. Scherer, Julia A. Haller, Michelle A. Langill	1989	41
20	Surgical management of children and young adults with marfan syndrome and pectus excavatum Journal of Pediatric Surgery ·L.R. Scherer, Pamela Arn, X.-H. Wang, Reed E. Pyeritz, Julia A. Haller	1988	49

About Pamela Arn

Pamela Arn is a scholar working on Developmental Biology, Clinical Biochemistry, Rheumatology, Pediatrics, Perinatology and Child Health and Genetics, having authored 36 papers that have together received 1.8k indexed citations. Recurring topics across this work include Glycogen Storage Diseases and Myoclonus (8 papers), Lysosomal Storage Disorders Research (7 papers), Metabolism and Genetic Disorders (6 papers), Neonatal Health and Biochemistry (4 papers), Biochemical and Molecular Research (4 papers), Carbohydrate Chemistry and Synthesis (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Rheumatology (809 citations), Clinical Biochemistry (294 citations), Physiology (661 citations), Genetics (592 citations) and Pharmacy (67 citations). Pamela Arn has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Deeksha Bali, Priya S. Kishnani, David A. Weinstein, Anne Boney, Wendy K. Chung, Stephanie Austin, J. E. Wraith, Michael S. Watson, Stephanie Burns Wechsler and Michael Beck. Their work appears in journals such as Genetics in Medicine, The Journal of Pediatrics, Journal of Pediatric Surgery, Journal of Medical Genetics and Health Affairs.

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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