Scott E. Hickey

2.0k total citations
40 papers, 671 citations indexed

About

Scott E. Hickey is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Scott E. Hickey has authored 40 papers receiving a total of 671 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 19 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Scott E. Hickey's work include Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (9 papers) and Congenital heart defects research (7 papers). Scott E. Hickey is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (9 papers) and Congenital heart defects research (7 papers). Scott E. Hickey collaborates with scholars based in United States, Italy and Canada. Scott E. Hickey's co-authors include Cynthia J. Curry, Helga V. Toriello, R G Powell, Marcus Eng Hock Ong, Joseph P. Ornato, Dean C. Williams, Mary Ann Peberdy, Harinder Dhindsa, Al M. Best and D. P. Edwards and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JAMA and SHILAP Revista de lepidopterología.

In The Last Decade

Scott E. Hickey

38 papers receiving 654 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Scott E. Hickey United States 13 253 175 157 108 86 40 671
William T. Smith United States 16 44 0.2× 147 0.8× 49 0.3× 111 1.0× 33 0.4× 39 755
Anthony Lander United Kingdom 16 93 0.4× 154 0.9× 69 0.4× 441 4.1× 97 1.1× 64 808
Nozomu Sasaki Japan 18 251 1.0× 204 1.2× 23 0.1× 245 2.3× 103 1.2× 79 1.1k
Erminia Romeo Italy 17 281 1.1× 91 0.5× 43 0.3× 493 4.6× 22 0.3× 32 830
Giora Treister Israel 23 45 0.2× 122 0.7× 98 0.6× 308 2.9× 56 0.7× 78 1.6k
Henry M. Taylor United States 12 32 0.1× 68 0.4× 46 0.3× 52 0.5× 80 0.9× 33 468
Eva Valverde Spain 12 68 0.3× 76 0.4× 61 0.4× 81 0.8× 273 3.2× 34 578
Amrit Bhangoo United States 19 241 1.0× 391 2.2× 66 0.4× 95 0.9× 62 0.7× 39 838
George T. Roberts Saudi Arabia 13 45 0.2× 138 0.8× 30 0.2× 42 0.4× 57 0.7× 37 863
A Dohnalová Czechia 13 39 0.2× 109 0.6× 16 0.1× 54 0.5× 47 0.5× 64 549

Countries citing papers authored by Scott E. Hickey

Since Specialization
Citations

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

Fields of papers citing papers by Scott E. Hickey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Scott E. Hickey

This figure shows the co-authorship network connecting the top 25 collaborators of Scott E. Hickey. A scholar is included among the top collaborators of Scott E. Hickey 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 Scott E. Hickey. Scott E. Hickey 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.
Ames, Elizabeth G., et al.. (2024). Multicenter appraisal of comorbid TANGO2 deficiency disorder in patients with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 194(10). e63778–e63778. 1 indexed citations
2.
Mustillo, Peter, Kathleen E. Sullivan, Iván K. Chinn, et al.. (2023). Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development. Journal of Clinical Immunology. 43(2). 247–270. 22 indexed citations
3.
Koboldt, Daniel C., Scott E. Hickey, Adam P. Ostendorf, et al.. (2022). De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy. Molecular Case Studies. 8(4). a006172–a006172. 6 indexed citations
4.
Ramadesikan, Swetha, Scott E. Hickey, Emily de los Reyes, et al.. (2022). Biallelic SEPSECS variants in two siblings with pontocerebellar hypoplasia type 2D underscore the relevance of splice-disrupting synonymous variants in disease.. Molecular Case Studies. 8(2). mcs.a006165–mcs.a006165. 1 indexed citations
5.
Hickey, Scott E., Katherine E. Miller, Kathleen M. Schieffer, et al.. (2021). Maternal mosaicism for a missense variant in the SMS gene that causes Snyder–Robinson syndrome. Molecular Case Studies. 7(6). a006122–a006122. 1 indexed citations
6.
Barrie, Elizabeth S., Catherine E. Cottrell, Julie M. Gastier‐Foster, et al.. (2019). Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 gene. European Journal of Medical Genetics. 63(3). 103735–103735. 11 indexed citations
7.
Mosher, Theresa Mihalic, Daniel C. Koboldt, Benjamin Kelly, et al.. (2019). Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasia. European Journal of Human Genetics. 27(10). 1569–1577. 13 indexed citations
8.
Repnikova, Elena, Dmitry Lyalin, Kimberly S. McDonald, et al.. (2019). CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. European Journal of Medical Genetics. 63(1). 103636–103636. 5 indexed citations
9.
Hickey, Scott E., Daniel C. Koboldt, Theresa Mihalic Mosher, et al.. (2019). Novel in-frame FLNB deletion causes Larsen syndrome in a three-generation pedigree. Molecular Case Studies. 5(6). a004176–a004176. 1 indexed citations
10.
11.
Koboldt, Daniel C., Theresa Mihalic Mosher, Benjamin Kelly, et al.. (2018). A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge–Ropers syndrome. Molecular Case Studies. 4(3). a002410–a002410. 29 indexed citations
12.
Hashimoto, Sayaka, et al.. (2017). Partial tetrasomy 11q resulting from an intrachromosomal triplication of a 22 Mb region of chromosome 11. American Journal of Medical Genetics Part A. 173(4). 1056–1060. 2 indexed citations
13.
Pillalamarri, Vamsee, Tammy Kammin, Joan Atkin, et al.. (2016). Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis. Human Molecular Genetics. 25(7). 1255–1270. 27 indexed citations
14.
Astbury, Caroline, et al.. (2016). 17p13.3 microduplication including CRK leads to overgrowth and elevated growth factors: A case report. European Journal of Medical Genetics. 59(10). 512–516. 8 indexed citations
15.
Thrush, Devon Lamb, Scott E. Hickey, Sayaka Hashimoto, et al.. (2014). Atypical breakpoint in a t(6;17) translocation case of acampomelic campomelic dysplasia. European Journal of Medical Genetics. 57(7). 315–318. 6 indexed citations
16.
Mori, Mari, John R. Mytinger, Lisa Martin, Dennis Bartholomew, & Scott E. Hickey. (2014). m.8993T>G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening. JIMD Reports. 17. 47–51. 13 indexed citations
17.
Hickey, Scott E., Cynthia J. Curry, & Helga V. Toriello. (2013). ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing. Genetics in Medicine. 15(2). 153–156. 110 indexed citations
18.
Hickey, Scott E., Theresa Mihalic Mosher, Ruthann Pfau, et al.. (2013). Duplication of the Xq27.3–q28 region, including the FMR1 gene, in an X‐linked hypogonadism, gynecomastia, intellectual disability, short stature, and obesity syndrome. American Journal of Medical Genetics Part A. 161(9). 2294–2299. 17 indexed citations
19.
Ong, Marcus Eng Hock, Joseph P. Ornato, D. P. Edwards, et al.. (2006). Use of an Automated, Load-Distributing Band Chest Compression Device for Out-of-Hospital Cardiac Arrest Resuscitation. JAMA. 295(22). 2629–37. 157 indexed citations
20.
Stutts, John T., Scott E. Hickey, & Morton L. Kasdan. (2003). Malingering by Proxy: A Form of Pediatric Condition Falsification. Journal of Developmental & Behavioral Pediatrics. 24(4). 276–278. 11 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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