Cathy A. Stevens

3.5k total citations
52 papers, 1.3k citations indexed

About

Cathy A. Stevens is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Cathy A. Stevens has authored 52 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 22 papers in Surgery and 20 papers in Molecular Biology. Recurrent topics in Cathy A. Stevens's work include Congenital limb and hand anomalies (12 papers), Orthopedic Surgery and Rehabilitation (9 papers) and Genomic variations and chromosomal abnormalities (8 papers). Cathy A. Stevens is often cited by papers focused on Congenital limb and hand anomalies (12 papers), Orthopedic Surgery and Rehabilitation (9 papers) and Genomic variations and chromosomal abnormalities (8 papers). Cathy A. Stevens collaborates with scholars based in United States, Netherlands and Germany. Cathy A. Stevens's co-authors include John C. Carey, William B. Dobyns, Cynthia A. Moore, Ann O. Shigeoka, Jack H. Rubinstein, Raoul C. M. Hennekam, Nancy Lanphear, Susan Wiley, J. J. P. van de Kamp and Larry A. Sargent and has published in prestigious journals such as Brain, The Journal of Clinical Endocrinology & Metabolism and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Cathy A. Stevens

50 papers receiving 1.2k citations

Peers

Cathy A. Stevens

GENET

SURGE

PPCH

Margherita Lerone Italy

Donatella Milani Italy

M A Patton United Kingdom

Carol L. Clericuzio United States

Susan Holder United Kingdom

Muriel Holder‐Espinasse France

Georg C. Schwabe Germany

Jean‐Pierre Fryns Belgium

Yoshio Makita Japan

Christèle Dubourg France

Margherita Lerone Italy

Cathy A. Stevens

827 ×1.6

GENET

1.1k ×2.4

1.3k ×3.7

SURGE

113 ×0.4

181 ×1.2

PPCH

Citations per year, relative to Cathy A. Stevens Cathy A. Stevens (= 1×) peers Margherita Lerone

Countries citing papers authored by Cathy A. Stevens

Since Specialization

Citations

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

Fields of papers citing papers by Cathy A. Stevens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cathy A. Stevens. 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 Cathy A. Stevens. The network helps show where Cathy A. Stevens may publish in the future.

Co-authorship network of co-authors of Cathy A. Stevens

This figure shows the co-authorship network connecting the top 25 collaborators of Cathy A. Stevens. A scholar is included among the top collaborators of Cathy A. Stevens 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 Cathy A. Stevens. Cathy A. Stevens 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

Ng, Bobby G., Hunter R. Underhill, Lars Palm, et al.. (2018). DPAGT1 Deficiency with Encephalopathy (DPAGT1-CDG): Clinical and Genetic Description of 11 New Patients. JIMD Reports. 44. 85–92. 15 indexed citations

Stevens, Cathy A.. (2015). Intestinal malrotation in Rubinstein–Taybi syndrome. American Journal of Medical Genetics Part A. 167(10). 2399–2401.

Stevens, Cathy A., Pei‐Wen Chiang, & Ludwine Messiaen. (2012). Café‐au‐lait macules and intertriginous freckling in piebaldism: Clinical overlap with neurofibromatosis type 1 and Legius syndrome. American Journal of Medical Genetics Part A. 158A(5). 1195–1199. 20 indexed citations

Stevens, Cathy A.. (2010). Steinfeld syndrome: Further delineation. American Journal of Medical Genetics Part A. 152A(7). 1789–1792. 4 indexed citations

Stevens, Cathy A. & Ralph S. Lachman. (2010). New lethal skeletal dysplasia with Dandy–Walker malformation, congenital heart defects, abnormal thumbs, hypoplastic genitalia, and distinctive facies. American Journal of Medical Genetics Part A. 152A(8). 1915–1918. 2 indexed citations

Stevens, Cathy A., et al.. (2009). Familial odontoid hypoplasia. American Journal of Medical Genetics Part A. 149A(6). 1290–1292. 10 indexed citations

Stevens, Cathy A. & Wesley K. Galen. (2008). The hair collar sign. American Journal of Medical Genetics Part A. 146A(4). 484–487. 9 indexed citations

Antic, Nick A., Beth A. Malow, R. Doug McEvoy, et al.. (2006). PHOX2B Mutation–confirmed Congenital Central Hypoventilation Syndrome. American Journal of Respiratory and Critical Care Medicine. 174(8). 923–927. 97 indexed citations

Stevens, Cathy A., et al.. (2005). Significance of bifid epiglottis. American Journal of Medical Genetics Part A. 134A(4). 447–449. 23 indexed citations

10.

Stevens, Cathy A., et al.. (2005). Growth in the Rubinstein-Taybi syndrome. American Journal of Medical Genetics. 37(S6). 51–55. 16 indexed citations

11.

Stevens, Cathy A., et al.. (2005). Rubinstein-Taybi syndrome: A natural history study. American Journal of Medical Genetics. 37(S6). 30–37. 44 indexed citations

12.

Stevens, Cathy A. & William B. Dobyns. (2003). Septo‐optic dysplasia and amniotic bands: Further evidence for a vascular pathogenesis. American Journal of Medical Genetics Part A. 125A(1). 12–16. 56 indexed citations

13.

Nakano, Aoi, Leena Pulkkinen, Dédée F. Murrell, et al.. (2001). Epidermolysis Bullosa with Congenital Pyloric Atresia: Novel Mutations in the β4 Integrin Gene (ITGB4) and Genotype/Phenotype Correlations. Pediatric Research. 49(5). 618–626. 75 indexed citations

14.

Huang, Bing, Bonnie Anne Salbert, J.A. Brown, et al.. (1994). Mental retardation and Ullrich‐Turner syndrome in cases with 45,X/46,X,+ mar: Additional support for the loss of the X‐inactivation center hypothesis. American Journal of Medical Genetics. 52(2). 136–145. 19 indexed citations

15.

Stevens, Cathy A., et al.. (1994). Pulmonary hyperplasia in the Fraser cryptophthalmos syndrome. American Journal of Medical Genetics. 52(4). 427–431. 13 indexed citations

16.

Stevens, Cathy A.. (1993). Malformations and deformations in abdominal pregnancy. American Journal of Medical Genetics. 47(8). 1189–1195. 47 indexed citations

17.

Qumsiyeh, Mazin Β. & Cathy A. Stevens. (1993). Two sibs with different phenotypes due to adjacent‐1 segregation of a subtle translocation t(4;5)(p16.3;p15.3) mat. American Journal of Medical Genetics. 47(3). 387–391. 2 indexed citations

18.

Salbert, Bonnie Anne, Cathy A. Stevens, & J. Edward Spence. (1991). Tracheomalacia in Hallermann–Streiff Syndrome. American Journal of Medical Genetics. 41(4). 521–523. 7 indexed citations

19.

Stevens, Cathy A., et al.. (1988). Development of human palmar and digital flexion creases. The Journal of Pediatrics. 113(1). 128–132. 14 indexed citations

20.

Stevens, Cathy A., et al.. (1988). Report of two cases of distal deletion of the long arm of chromosome 6. American Journal of Medical Genetics. 29(4). 807–814. 30 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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