Shawn E. McCandless

1.6k total citations
33 papers, 632 citations indexed

About

Shawn E. McCandless is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Shawn E. McCandless has authored 33 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Pediatrics, Perinatology and Child Health and 14 papers in Clinical Biochemistry. Recurrent topics in Shawn E. McCandless's work include Metabolism and Genetic Disorders (14 papers), Genetic Syndromes and Imprinting (10 papers) and Neonatal Health and Biochemistry (7 papers). Shawn E. McCandless is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Genetic Syndromes and Imprinting (10 papers) and Neonatal Health and Biochemistry (7 papers). Shawn E. McCandless collaborates with scholars based in United States, Canada and Germany. Shawn E. McCandless's co-authors include Theresa V. Strong, Jessica Bohonowych, Jennifer Miller, Hannaleena Kokkonen, Tohru Ohta, Bernhard Horsthemke, Shauna Heeger, Suzanne B. Cassidy, Karin Buiting and Daniel J. Driscoll and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Shawn E. McCandless

33 papers receiving 618 citations

Peers

Countries citing papers authored by Shawn E. McCandless

Since Specialization

Citations

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

Fields of papers citing papers by Shawn E. McCandless

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shawn E. McCandless. 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 Shawn E. McCandless. The network helps show where Shawn E. McCandless may publish in the future.

Co-authorship network of co-authors of Shawn E. McCandless

This figure shows the co-authorship network connecting the top 25 collaborators of Shawn E. McCandless. A scholar is included among the top collaborators of Shawn E. McCandless 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 Shawn E. McCandless. Shawn E. McCandless is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis 2024 ·Mitochondrion ·Johan L.K. Van Hove, Marisa W. Friederich, Daniella H. Hock, David A. Stroud, Nikeisha J. Caruana, Uwe Christians, Björn Schniedewind, Cole R. Michel, Richard Reisdorph, (unknown), Charles Brenner, (unknown), Jessica C. Lee, Kathryn C. Chatfield, Austin Larson, Peter R. Baker, Shawn E. McCandless, (unknown)	3
2	Behavioral changes in patients with Prader-Willi syndrome receiving diazoxide choline extended-release tablets compared to the PATH for PWS natural history study 2024 ·Journal of Neurodevelopmental Disorders ·Theresa V. Strong, Jennifer Miller, Shawn E. McCandless, Evelien Gevers, Jack A. Yanovski, (unknown), Jessica Bohonowych, Shaila Ballal, (unknown), (unknown), (unknown), Anish Bhatnagar	3
3	Thrombosis Risk History and D-dimer Levels in Asymptomatic Individuals with Prader–Willi Syndrome 2022 ·Journal of Clinical Medicine ·(unknown), Jennifer Miller, Shawn E. McCandless, Jaret Malloy, Jessica Bohonowych, Caroline Vrana, Theresa V. Strong	2
4	REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseases 2021 ·Molecular Genetics and Metabolism ·(unknown), Peter R. Baker, Janet A. Thomas, Heather E. Skillman, Laurie Bernstein, Sommer Gaughan, (unknown), Curtis R. Coughlin, Shawn E. McCandless, Austin Larson, (unknown), (unknown), Erica Wymore, (unknown), Michael Woontner, Johan L.K. Van Hove	6
5	A novel cause of emergent hyperammonemia: Cryptococcal fungemia and meningitis 2021 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), (unknown), (unknown), Shawn E. McCandless, Laura Konczal	5
6	Long-term preservation of intellectual functioning in sapropterin-treated infants and young children with phenylketonuria: A seven-year analysis 2021 ·Molecular Genetics and Metabolism ·Susan E. Waisbren, Barbara K. Burton, Annette Feigenbaum, Laura Konczal, (unknown), Shawn E. McCandless, Richard Rowell, Amarilis Sanchez‐Valle, (unknown), Nicola Longo	11
7	Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry 2021 ·BMC Ophthalmology ·Jessica Bohonowych, Caroline Vrana, Jennifer L. Miller, Shawn E. McCandless, Theresa V. Strong	8
8	Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders 2020 ·Molecular Genetics and Metabolism ·Nicola Longo, George A. Díaz, Uta Lichter‐Konecki, Andreas Schulze, Michal Inbar‐Feigenberg, Robert L. Conway, (unknown), Shawn E. McCandless, Roberto T. Zori, Bryan E. Hainline, Nicholas Ah Mew, (unknown), Thomas Vescio, (unknown), Marty H. Porter, Susan A. Berry	10
9	Developing interactions with industry in rare diseases: lessons learned and continuing challenges 2019 ·Genetics in Medicine ·Susan A. Berry, Curtis R. Coughlin, Shawn E. McCandless, Robert McCarter, Jennifer Seminara, (unknown), Cynthia LeMons	20
10	Long-term safety and efficacy of glycerol phenylbutyrate for the management of urea cycle disorder patients 2019 ·Molecular Genetics and Metabolism ·George A. Díaz, Andreas Schulze, Nicola Longo, William J. Rhead, Annette Feigenbaum, Derek A. Wong, J. Lawrence Merritt, William Berquist, Renata C. Gallagher, Dennis Bartholomew, Shawn E. McCandless, Wendy E. Smith, Cary O. Harding, Roberto Zori, Uta Lichter‐Konecki, Jerry Vockley, (unknown), Thomas Vescio, Robert J. Holt, Susan A. Berry	10
11	Life-threatening presentations of propionic acidemia due to the Amish PCCB founder variant 2019 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), (unknown), M. Zacharias, Shawn E. McCandless, Anthony Wynshaw‐Boris, Laura Konczal, Jirair K. Bedoyan	6
12	The Global Prader–Willi Syndrome Registry: Development, Launch, and Early Demographics 2019 ·Genes ·Jessica Bohonowych, Jennifer Miller, Shawn E. McCandless, Theresa V. Strong	41
13	Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders 2019 ·Annals of Neurology ·Roland Posset, Andrea Gropman, Sandesh C.S. Nagamani, Lindsay C. Burrage, Jirair K. Bedoyan, Derek A. Wong, Susan A. Berry, Matthias R. Baumgartner, Marc Yudkoff, Matthias Zielonka, Georg F. Hoffmann, Peter Burgard, Andreas Schulze, Shawn E. McCandless, Ángeles García‐Cazorla, Jennifer Seminara, Sven F. Garbade, Stefan Kölker	37
14	Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—a successful strategy for clinical research of rare diseases 2018 ·Journal of Inherited Metabolic Disease ·Roland Posset, Sven F. Garbade, Nikolas Boy, Alberto Burlina, Carlo Dionisi‐Vici, Dries Dobbelaere, Ángeles García‐Cazorla, Pascale de Lonlay, Elisa Leão Teles, Roshni Vara, Nicholas Ah Mew, Mark L. Batshaw, Matthias R. Baumgartner, Shawn E. McCandless, Jennifer Seminara, Marshall Summar, Georg F. Hoffmann, Stefan Kölker, Peter Burgard	3
15	Risk for ingestion of toxic substances in children with Prader–Willi syndrome 2012 ·American Journal of Medical Genetics Part A ·Shawn E. McCandless, Karen Powell, (unknown)	2
16	Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies 2010 ·American Journal of Medical Genetics Part A ·Hussam Al‐Kateb, (unknown), Julie M. Gastier‐Foster, Linda Jo Bone Jeng, Shawn E. McCandless, Christine A. Curtis	10
17	Health Supervision for Children With Prader-Willi Syndrome 2010 ·PEDIATRICS ·Shawn E. McCandless	114
18	Metachromatic leukodystrophy in the Navajo: Fallout of the American-Indian wars of the Nineteenth Century 2001 ·American Journal of Medical Genetics ·Steve Holve, Diana Hu, Shawn E. McCandless	11
19	Case Studies 1999 ·Journal of Developmental & Behavioral Pediatrics ·Carolyn E. Ievers‐Landis, Ronald T. Brown, Shawn E. McCandless, (unknown)	7
20	Molecular Mechanism of Angelman Syndrome in Two Large Families Involves an Imprinting Mutation 1999 ·The American Journal of Human Genetics ·Tohru Ohta, Karin Buiting, Hannaleena Kokkonen, Shawn E. McCandless, Shauna Heeger, (unknown), Daniel J. Driscoll, Suzanne B. Cassidy, Bernhard Horsthemke, Robert D. Nicholls	69

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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