Cheryl S. Reid

718 total citations
18 papers, 483 citations indexed

About

Cheryl S. Reid is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Cheryl S. Reid has authored 18 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Surgery. Recurrent topics in Cheryl S. Reid's work include Connective tissue disorders research (8 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Prenatal Screening and Diagnostics (3 papers). Cheryl S. Reid is often cited by papers focused on Connective tissue disorders research (8 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Prenatal Screening and Diagnostics (3 papers). Cheryl S. Reid collaborates with scholars based in United States and Canada. Cheryl S. Reid's co-authors include Reed E. Pyeritz, Ranajit Chakraborty, Jacqueline T. Hecht, William A. Horton, Ethylin Wang Jabs, Steven E. Kopits, Andrew Levitas, John A. Phillips, Orest Hurko and Bernard L. Maria and has published in prestigious journals such as Radiology, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Cheryl S. Reid

17 papers receiving 457 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cheryl S. Reid United States	11	321	152	101	89	49	18	483
Kathryn J. McKenzie United Kingdom	9	131 0.4×	58 0.4×	60 0.6×	214 2.4×	51 1.0×	12	556
Giorgio Filippi Italy	14	281 0.9×	54 0.4×	61 0.6×	304 3.4×	18 0.4×	27	581
Douglas L. Vander Woude United States	7	300 0.9×	178 1.2×	33 0.3×	227 2.6×	14 0.3×	8	558
J. Garcı́a Rodrı́guez Spain	9	163 0.5×	120 0.8×	96 1.0×	161 1.8×	11 0.2×	54	431
Constance K. Stein United States	10	346 1.1×	35 0.2×	95 0.9×	380 4.3×	16 0.3×	17	666
Francesco Benedicenti Italy	10	123 0.4×	66 0.4×	37 0.4×	165 1.9×	28 0.6×	21	417
Moira Blyth United Kingdom	12	162 0.5×	57 0.4×	75 0.7×	139 1.6×	21 0.4×	22	379
V. Kim Horton United States	7	241 0.8×	127 0.8×	77 0.8×	65 0.7×	18 0.4×	9	318
S. Samuel Yang United States	14	325 1.0×	137 0.9×	40 0.4×	192 2.2×	14 0.3×	24	560
Diana Carli Italy	14	272 0.8×	124 0.8×	36 0.4×	279 3.1×	29 0.6×	51	599

Countries citing papers authored by Cheryl S. Reid

Since Specialization

Citations

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

Fields of papers citing papers by Cheryl S. Reid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cheryl S. Reid. 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 Cheryl S. Reid. The network helps show where Cheryl S. Reid may publish in the future.

Co-authorship network of co-authors of Cheryl S. Reid

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

All Works

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18 of 18 papers shown

1.

Levitas, Andrew & Cheryl S. Reid. (2002). An angel with Down syndrome in a sixteenth century Flemish Nativity painting. American Journal of Medical Genetics Part A. 116A(4). 399–405. 29 indexed citations

2.

Schnur, Rhonda E., et al.. (1997). Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome. American Journal of Medical Genetics. 72(1). 24–29. 2 indexed citations

3.

Schnur, Rhonda E., et al.. (1997). Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome. American Journal of Medical Genetics. 72(1). 24–29. 13 indexed citations

4.

Hunter, Alasdair G. W., Cheryl S. Reid, Richard M. Pauli, & Charles I. Scott. (1996). Standard curves of chest circumference in achondroplasia and the relationship of chest circumference to respiratory problems. American Journal of Medical Genetics. 62(1). 91–97. 10 indexed citations

5.

Lazzarini, Alice, Edward S. Stenroos, Thomas Lehner, et al.. (1995). Short tandem repeat polymorphism linkage studies in a new family with X‐linked mental retardation (MRX20). American Journal of Medical Genetics. 57(4). 552–557. 12 indexed citations

6.

Lewanda, Amy Feldman, et al.. (1995). Two craniosynostotic patients with 11q deletions, and review of 48 cases. American Journal of Medical Genetics. 59(2). 193–198. 41 indexed citations

7.

Reid, Cheryl S.. (1995). Introductory Remarks. The Cleft Palate-Craniofacial Journal. 32(6). 520–520. 1 indexed citations

8.

Lewanda, Amy Feldman, et al.. (1994). Study of two patients with craniosynostosis and deletions of 11q: One with features of Saethre-Chotzen syndrome and the other with concomitant partial trisomy 4q. The American Journal of Human Genetics. 55. 1 indexed citations

9.

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

10.

Reid, Cheryl S., Lydia E. McMorrow, Donna M. McDonald‐McGinn, et al.. (1993). Saethre‐Chotzen syndrome with familial translocation at chromosome 7p22. American Journal of Medical Genetics. 47(5). 637–639. 35 indexed citations

11.

Hecht, Jacqueline T., William A. Horton, Cheryl S. Reid, Reed E. Pyeritz, & Ranajit Chakraborty. (1989). Growth of the foramen magnum in achondroplasia. American Journal of Medical Genetics. 32(4). 528–535. 99 indexed citations

12.

Greenbaum, Barbara H., Warren R. Heymann, Cheryl S. Reid, Susan F Travis, & Milton H. Donaldson. (1988). Chemotherapy‐associated eccrine hidradenitis: Neutrophilic eccrine hidradenitis reevaluated: The role of neutrophilic infiltration. Medical and Pediatric Oncology. 16(5). 351–355. 29 indexed citations

13.

Carson, Benjamin S., et al.. (1988). Surgical Management of Cervicomedullary Compression in Achondroplastic Patients. PubMed. 48. 207–214. 15 indexed citations

14.

Reid, Cheryl S., Reed E. Pyeritz, Steven E. Kopits, et al.. (1988). Cervicomedullary Cord Compression in Young Children with Achondroplasia: Value of Comprehensive Neurologic and Respiratory Evaluation. PubMed. 48. 199–206. 10 indexed citations

15.

Reid, Cheryl S., Reed E. Pyeritz, Steven E. Kopits, et al.. (1987). Cervicomedullary compression in young patients with achondroplasia: Value of comprehensive neurologic and respiratory evaluation. The Journal of Pediatrics. 110(4). 522–530. 108 indexed citations

16.

Rosenbaum, A. E., et al.. (1987). Pediatric patients with achondroplasia: CT evaluation of the craniocervical junction.. Radiology. 164(2). 515–519. 57 indexed citations

17.

Reid, Cheryl S., S. Metz, Robert G. Meny, et al.. (1984). RESPIRATORY PROBLEMS IN ACHONDROPLASIA. Pediatric Research. 18. 402A–402A. 1 indexed citations

18.

Reid, Cheryl S., Robert H. McPherson, Mária Bohdalová, et al.. (1984). CERVICAL CORD COMPRESSION IN ACHONDROPLASIA. Pediatric Research. 18. 382A–382A.

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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