Shawn E. McCandless - Concepedia

Author

Shawn E. McCandless

Also Known As

McCandless, Shawn E., S McCandless, S. E. McCandless, S. McCandless, SHAWN E. McCANDLESS, Shawn E McCandless, Shawn E Mccandless, Shawn E. McCandless, Shawn E. Mccandless, Shawn McCandless

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

University of Colorado Denver Children's Hospital Colorado Children's National University of Toronto University of Florida

About

Shawn E. McCandless is an author at University of Colorado Denver specializing in medicine, pediatrics, and clinical nutrition.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	363
2	Education	1	1	191
3	Health Sciences	1	1	16
4	Public Health	1	1	13
5	Child Development	1	1	191

Shawn E. McCandless

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Health Supervision for Children With Prader-Willi Syndrome Shawn E. McCandless PEDIATRICS CounselingGenetic EpidemiologyDiagnosisClinical FeaturesEducation	2010	191
Effects of <scp>MetAP2</scp> inhibition on hyperphagia and body weight in Prader–Willi syndrome: A randomized, double‐blind, placebo‐controlled trial Shawn E. McCandless, Jack A. Yanovski, Jennifer Miller, Diabetes Obesity and Metabolism	2017	103
Automated syndrome diagnosis by three-dimensional facial imaging Benedikt Hallgrímsson, J. David Aponte, David C. Katz, Genetics in Medicine	2020	101
Molecular Mechanism of Angelman Syndrome in Two Large Families Involves an Imprinting Mutation Tohru Ohta, Karin Buiting, Hannaleena Kokkonen, The American Journal of Human Genetics Developmental BiologyMendelian DisorderImprinting MutationAngelman SyndromeGenetics	1999	88
Evaluation of 3‐methylcrotonyl‐CoA carboxylase deficiency detected by tandem mass spectrometry newborn screening Dwight D. Koeberl, David S. Millington, Wendy E. Smith, Journal of Inherited Metabolic Disease	2003	87
The Global Prader–Willi Syndrome Registry: Development, Launch, and Early Demographics Jessica Bohonowych, Jennifer Miller, Shawn E. McCandless, Genes	2019	85
Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders Roland Posset, Andrea Gropman, Sandesh C.S. Nagamani, Annals of Neurology	2019	67
Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire Sarah C. Grünert, Terry G. J. Derks, Katarina Adrian, Genetics in Medicine	2022	61
Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap S. Harvey Mudd, Nancy Braverman, Martin G. Pomper, Molecular Genetics and Metabolism Diagnostic TrapInherited Metabolic DiseaseClinical NutritionPediatricsPediatric Endocrinology	2003	55
Genu recurvatum: auditory biofeedback treatment for adult patients with stroke or head injuries. Raymond E. Hogue, Shawn E. McCandless PubMed	1983	45

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