Charles I. Scott

5.0k total citations
99 papers, 3.2k citations indexed

About

Charles I. Scott is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Charles I. Scott has authored 99 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Genetics, 37 papers in Molecular Biology and 19 papers in Surgery. Recurrent topics in Charles I. Scott's work include Connective tissue disorders research (29 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Genomic variations and chromosomal abnormalities (8 papers). Charles I. Scott is often cited by papers focused on Connective tissue disorders research (29 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Genomic variations and chromosomal abnormalities (8 papers). Charles I. Scott collaborates with scholars based in United States, Canada and United Kingdom. Charles I. Scott's co-authors include Judith G. Hall, Jacqueline T. Hecht, David L. Rimoin, William A. Horton, Alasdair G. W. Hunter, Victor A. McKusick, Linda K. Nicholson, David Sillence, Richard M. Pauli and John Rogers and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and American Journal of Clinical Nutrition.

In The Last Decade

Charles I. Scott

97 papers receiving 3.1k citations

Peers

Charles I. Scott

GENET

SURGE

RHEUM

PRM

Ahmad S. Teebi Canada

Patrick MacLeod Canada

Arthur S. Aylsworth United States

Peter Meinecke Germany

Alasdair G. W. Hunter Canada

Marcia Willing United States

John Tolmie United Kingdom

Bryan D. Hall United States

Roberta A Pagon United States

Dvorah Abeliovich Israel

Ahmad S. Teebi Canada

Charles I. Scott

1.3k ×0.8

GENET

1.3k ×1.1

522 ×0.9

SURGE

342 ×0.7

RHEUM

226 ×0.5

PRM

Citations per year, relative to Charles I. Scott Charles I. Scott (= 1×) peers Ahmad S. Teebi

Countries citing papers authored by Charles I. Scott

Since Specialization

Citations

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

Fields of papers citing papers by Charles I. Scott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charles I. Scott

This figure shows the co-authorship network connecting the top 25 collaborators of Charles I. Scott. A scholar is included among the top collaborators of Charles I. Scott 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 Charles I. Scott. Charles I. Scott 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

Bober, Michael B., Nadia Khan, Jennifer A. Kaplan, et al.. (2010). Majewski Osteodysplastic Primordial Dwarfism Type II (MOPD II): Expanding the vascular phenotype. American Journal of Medical Genetics Part A. 152A(4). 960–965. 63 indexed citations

Gripp, Karen W., Charles I. Scott, Linda K. Nicholson, et al.. (2008). Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts. American Journal of Medical Genetics Part A. 146A(4). 468–473. 7 indexed citations

Hoover‐Fong, Julie, John McGready, Kerry Schulze, H. Verdain Barnes, & Charles I. Scott. (2007). Weight for age charts for children with achondroplasia. American Journal of Medical Genetics Part A. 143A(19). 2227–2235. 45 indexed citations

Gripp, Karen W., Angela E. Lin, Deborah L. Stabley, et al.. (2005). HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation. American Journal of Medical Genetics Part A. 140A(1). 1–7. 133 indexed citations

Gripp, Karen W., Charles I. Scott, Linda K. Nicholson, et al.. (2002). Five additional Costello syndrome patients with rhabdomyosarcoma: Proposal for a tumor screening protocol. American Journal of Medical Genetics. 108(1). 80–87. 101 indexed citations

Assadi, Farahnak, et al.. (1999). Hypercalciuria and urolithiasis in a case of Costello syndrome. Pediatric Nephrology. 13(1). 57–59. 11 indexed citations

Givon, Uri, S. Jay Kumar, & Charles I. Scott. (1999). Involvement of the Humerus in Two Generations With Spondyloepiphyseal Dysplasia. Clinical Orthopaedics and Related Research. 366(366). 174–177. 6 indexed citations

Wallerstein, Robert S., Charles I. Scott, & Linda Nicholson. (1997). Extended survival in a new case of ter Haar syndrome: Further delineation of the syndrome. American Journal of Medical Genetics. 70(3). 267–272. 8 indexed citations

Gripp, Karen W., et al.. (1996). Extending the spectrum of distal arthrogryposis. American Journal of Medical Genetics. 65(4). 286–290. 4 indexed citations

10.

Finucane, Brenda, et al.. (1994). The Spasmodic Upper‐body Squeeze: a Chalacteristic Behavior in Smith‐Magenis Syndrome. Developmental Medicine & Child Neurology. 36(1). 78–83. 74 indexed citations

11.

Velinov, Milen, Susan A. Slaugenhaupt, Ivaylo Stoilov, et al.. (1994). The gene for achondroplasia maps to the telomeric region of chromosome 4p. Nature Genetics. 6(3). 314–317. 84 indexed citations

12.

Stevenson, Roger E., Melanie May, J. Fernando Arena, et al.. (1994). Aarskog‐Scott syndrome: Confirmation of linkage to the pericentromeric region of the X chromosome. American Journal of Medical Genetics. 52(3). 339–345. 12 indexed citations

13.

Langer, Leonard O., Barbara J. Wolfson, Charles I. Scott, et al.. (1993). Further delineation of spondylo‐meta‐epiphyseal dysplasia, short limb‐abnormal calcification type, with emphasis on diagnostic features. American Journal of Medical Genetics. 45(4). 488–500. 20 indexed citations

14.

Parrish, Julia, Michael J. Wagner, Jacqueline T. Hecht, Charles I. Scott, & Dan E. Wells. (1991). Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome. Genomics. 11(1). 54–61. 23 indexed citations

15.

Mandell, G. A., et al.. (1989). Identification of avascular necrosis in the dysplastic proximal femoral epiphysis. Skeletal Radiology. 18(4). 273–281. 12 indexed citations

16.

Mandell, G. A., et al.. (1989). Scintigraphic differentiation of congenital soft-tissue extremity enlargement with Tc-99m DTPA. Skeletal Radiology. 18(1). 33–41. 7 indexed citations

17.

Horton, William A., David L. Rimoin, Ralph S. Lachman, et al.. (1978). The phenotypic variability of diastrophic dysplasia. The Journal of Pediatrics. 93(4). 609–613. 51 indexed citations

18.

Daentl, Donna L., David W. Smith, Charles I. Scott, Bryan D. Hall, & Charles A. Gooding. (1975). Femoral hypoplasia — unusual facies syndrome. The Journal of Pediatrics. 86(1). 107–111. 69 indexed citations

19.

Scott, Charles I.. (1974). Progress in pediatric radiology. Vol. 4: Intrinsic diseases of bones. The American Journal of Human Genetics. 26(3). 418–419. 8 indexed citations

20.

Thurmon, Theodore F., et al.. (1971). Two kindreds with a sex-linked recessive form of spastic paraplegia.. PubMed. 7(1). 219–21. 29 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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