Shawn E. McCandless

2.5k total citations
34 papers, 1.2k citations indexed

About

Shawn E. McCandless is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shawn E. McCandless has authored 34 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Clinical Biochemistry, 12 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shawn E. McCandless's work include Metabolism and Genetic Disorders (20 papers), Neonatal Health and Biochemistry (8 papers) and Mitochondrial Function and Pathology (7 papers). Shawn E. McCandless is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Neonatal Health and Biochemistry (8 papers) and Mitochondrial Function and Pathology (7 papers). Shawn E. McCandless collaborates with scholars based in United States, United Kingdom and Switzerland. Shawn E. McCandless's co-authors include Joseph Muenzer, Suzanne B. Cassidy, Dianne M. Frazier, Müge Güçsavaş‐Çalıkoğlu, Thomas Schuetz, Alan Kimura, Dwight D. Koeberl, Shu Chaing, David S. Millington and Nathaniel H. Robin and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and European Journal of Biochemistry.

In The Last Decade

Shawn E. McCandless

34 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shawn E. McCandless United States 17 604 495 372 299 277 34 1.2k
Elisabetta Pasquini Italy 23 698 1.2× 589 1.2× 232 0.6× 346 1.2× 158 0.6× 59 1.4k
Dimitar Gavrilov United States 15 437 0.7× 403 0.8× 345 0.9× 200 0.7× 121 0.4× 35 901
Anupam Chakrapani United Kingdom 19 628 1.0× 546 1.1× 466 1.3× 132 0.4× 108 0.4× 57 1.2k
Carolina Fischinger Moura de Souza Brazil 19 362 0.6× 507 1.0× 427 1.1× 103 0.3× 183 0.7× 110 1.2k
Jim McGill Australia 15 376 0.6× 306 0.6× 243 0.7× 155 0.5× 182 0.7× 34 829
Ali Dursun Türkiye 17 438 0.7× 434 0.9× 215 0.6× 110 0.4× 145 0.5× 97 995
Anupam Chakrapani United Kingdom 19 1.2k 2.0× 646 1.3× 449 1.2× 389 1.3× 155 0.6× 47 1.6k
Shauna Kearney United Kingdom 10 766 1.3× 460 0.9× 573 1.5× 193 0.6× 101 0.4× 20 1.1k
Ayşegül Tokatlı Türkiye 17 575 1.0× 610 1.2× 249 0.7× 157 0.5× 116 0.4× 101 1.3k
Jean Rey France 20 692 1.1× 585 1.2× 237 0.6× 114 0.4× 172 0.6× 45 1.1k

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

20 of 20 papers shown
1.
Posset, Roland, Sven F. Garbade, Nikolas Boy, et al.. (2019). Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—A successful strategy for clinical research of rare diseases. Journal of Inherited Metabolic Disease. 42(1). 93–106. 25 indexed citations
2.
Berry, Susan A., Jerry Vockley, Alexander A. Vinks, et al.. (2018). Pharmacokinetics of glycerol phenylbutyrate in pediatric patients 2 months to 2 years of age with urea cycle disorders. Molecular Genetics and Metabolism. 125(3). 251–257. 8 indexed citations
3.
Li, Hong, Heather M. Byers, Miriam B. Vos, et al.. (2018). Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas. Molecular Genetics and Metabolism. 123(4). 428–432. 29 indexed citations
4.
Berry, Susan A., Nicola Longo, George A. Díaz, et al.. (2017). Safety and efficacy of glycerol phenylbutyrate for management of urea cycle disorders in patients aged 2 months to 2 years. Molecular Genetics and Metabolism. 122(3). 46–53. 14 indexed citations
5.
DeBrosse, Suzanne D., et al.. (2017). Inborn Errors of Metabolism with Acidosis. Pediatric Clinics of North America. 65(2). 209–230. 14 indexed citations
6.
Greene, Carol L., Erin T. Strovel, Elaine Spector, et al.. (2016). The M405V allele of the glutaryl-CoA dehydrogenase gene is an important marker for glutaric aciduria type I (GA-I) low excretors. Molecular Genetics and Metabolism. 119(1-2). 50–56. 11 indexed citations
7.
Mokhtarani, Masoud, George A. Díaz, Uta Lichter‐Konecki, et al.. (2015). Urinary phenylacetylglutamine (U-PAGN) concentration as biomarker for adherence in patients with urea cycle disorders (UCD) treated with glycerol phenylbutyrate. SHILAP Revista de lepidopterología. 5. 12–14. 3 indexed citations
8.
Tim‐Aroon, Thipwimol, et al.. (2015). Stopping Parenteral Nutrition for 3 Hours Reduces False Positives in Newborn Screening. The Journal of Pediatrics. 167(2). 312–316. 5 indexed citations
9.
Berry, Susan A., Uta Lichter‐Konecki, George A. Díaz, et al.. (2014). Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes. Molecular Genetics and Metabolism. 112(1). 17–24. 27 indexed citations
10.
Deeb, Kristin K., Jirair K. Bedoyan, Raymond Wang, et al.. (2014). Somatic mosaicism for a novel PDHA1 mutation in a male with severe pyruvate dehydrogenase complex deficiency. Molecular Genetics and Metabolism Reports. 1. 362–367. 4 indexed citations
11.
Smith, Wendy E., George A. Díaz, Uta Lichter‐Konecki, et al.. (2013). Ammonia Control in Children Ages 2 Months through 5 Years with Urea Cycle Disorders: Comparison of Sodium Phenylbutyrate and Glycerol Phenylbutyrate. The Journal of Pediatrics. 162(6). 1228–1234.e1. 33 indexed citations
12.
Tarini, Beth A., Laura Konczal, Aaron J. Goldenberg, Edward B. Goldman, & Shawn E. McCandless. (2013). The Perils of SNP Microarray Testing: Uncovering Unexpected Consanguinity. Pediatric Neurology. 49(1). 50–53. 5 indexed citations
13.
Stacpoole, Peter W., Ton J. deGrauw, Annette S. Feigenbaum, et al.. (2012). Design and implementation of the first randomized controlled trial of coenzyme Q10 in children with primary mitochondrial diseases. Mitochondrion. 12(6). 623–629. 21 indexed citations
14.
McCandless, Shawn E., et al.. (2012). Sequencing from dried blood spots in infants with “false positive” newborn screen for MCAD deficiency. Molecular Genetics and Metabolism. 108(1). 51–55. 20 indexed citations
15.
Izumi, Kosuke, Isamu Hokuto, Shinya Yamaguchi, et al.. (2010). Diaphragm dysfunction with congenital cytomegalovirus infection. Journal of Perinatology. 30(10). 691–694. 5 indexed citations
16.
McCandless, Shawn E., et al.. (2004). The Burden of Genetic Disease on Inpatient Care in a Children’s Hospital. The American Journal of Human Genetics. 74(1). 121–127. 144 indexed citations
17.
18.
McCandless, Shawn E., Jennifer A. Scott, & Nathaniel H. Robin. (1998). Deletion 22q11. Archives of Pediatrics and Adolescent Medicine. 152(5). 481–4. 8 indexed citations
19.
McCandless, Shawn E. & Nathaniel H. Robin. (1998). Severe oculocerebrocutaneous (Delleman) syndrome: Overlap with Goldenhar anomaly. American Journal of Medical Genetics. 78(3). 282–285. 16 indexed citations
20.
Robin, Nathaniel H., et al.. (1997). Disorganization in mice and humans and its relation to sporadic birth defects. American Journal of Medical Genetics. 73(4). 425–436. 33 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.

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