Hermine M. Pashayan

1.0k total citations
41 papers, 706 citations indexed

About

Hermine M. Pashayan is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Hermine M. Pashayan has authored 41 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Cancer Research. Recurrent topics in Hermine M. Pashayan's work include Cleft Lip and Palate Research (13 papers), Craniofacial Disorders and Treatments (9 papers) and Cancer-related molecular mechanisms research (6 papers). Hermine M. Pashayan is often cited by papers focused on Cleft Lip and Palate Research (13 papers), Craniofacial Disorders and Treatments (9 papers) and Cancer-related molecular mechanisms research (6 papers). Hermine M. Pashayan collaborates with scholars based in United States and Canada. Hermine M. Pashayan's co-authors include F. Clarke Fraser, Michael B. Lewis, Samuel Shapiro, Allen A. Mitchell, Carol Louik, Lynn Rosenberg, Louis Bartoshesky, Samuel Pruzansky, F. Clarke Fraser and J. Reichman and has published in prestigious journals such as New England Journal of Medicine, The Lancet and PEDIATRICS.

In The Last Decade

Hermine M. Pashayan

40 papers receiving 626 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hermine M. Pashayan United States 16 375 182 180 126 94 41 706
Philip M. Marden United States 8 323 0.9× 196 1.1× 214 1.2× 142 1.1× 84 0.9× 12 710
Richard C. Juberg United States 16 335 0.9× 198 1.1× 157 0.9× 108 0.9× 60 0.6× 45 617
Opitz Jm United States 14 317 0.8× 159 0.9× 227 1.3× 131 1.0× 31 0.3× 34 594
Philip D. Pallister United States 12 313 0.8× 167 0.9× 302 1.7× 157 1.2× 27 0.3× 19 655
Harold N. Bass United States 16 273 0.7× 195 1.1× 112 0.6× 64 0.5× 29 0.3× 34 552
E Tunçbilek Türkiye 15 195 0.5× 151 0.8× 175 1.0× 198 1.6× 54 0.6× 52 814
M. L. Martínez‐Frías Spain 16 215 0.6× 148 0.8× 121 0.7× 244 1.9× 35 0.4× 31 549
Roelof J. Odink Netherlands 21 317 0.8× 268 1.5× 334 1.9× 94 0.7× 67 0.7× 40 1.0k
Elisabeth G. Kaveggia United States 9 236 0.6× 169 0.9× 153 0.8× 114 0.9× 15 0.2× 18 455
Marilyn C. Higginbottom United States 14 231 0.6× 351 1.9× 151 0.8× 661 5.2× 58 0.6× 20 1.2k

Countries citing papers authored by Hermine M. Pashayan

Since Specialization
Citations

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

Fields of papers citing papers by Hermine M. Pashayan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hermine M. Pashayan. 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 Hermine M. Pashayan. The network helps show where Hermine M. Pashayan may publish in the future.

Co-authorship network of co-authors of Hermine M. Pashayan

This figure shows the co-authorship network connecting the top 25 collaborators of Hermine M. Pashayan. A scholar is included among the top collaborators of Hermine M. Pashayan 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 Hermine M. Pashayan. Hermine M. Pashayan 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.
Feingold, Murray & Hermine M. Pashayan. (1983). Genetics and birth defects in clinical practice. Little, Brown eBooks. 1 indexed citations
2.
Bartoshesky, Louis, et al.. (1982). Severe Cardiac and Ophthalmologic Malformations in an Infant Exposed to Diphenylhydantoin in Utero. PEDIATRICS. 69(2). 202–203. 18 indexed citations
3.
Bartoshesky, Louis, Michael B. Lewis, & Hermine M. Pashayan. (1978). Developmental abnormalities associated with long arm deletion of chromosome No. 6. Clinical Genetics. 13(1). 68–71. 30 indexed citations
4.
Pashayan, Hermine M., et al.. (1977). Bilateral absence of the kidneys and ureters. Three cases reported in one family.. Journal of Medical Genetics. 14(3). 205–209. 27 indexed citations
5.
GOLDEN, WILLIAM E. & Hermine M. Pashayan. (1976). The effect of parental education on the eventual mental development of noninstitutionalized children with down syndrome. The Journal of Pediatrics. 89(4). 603–605. 11 indexed citations
6.
Pashayan, Hermine M.. (1976). Basic Genetic Concepts for the Orthopedic Surgeon. Orthopedic Clinics of North America. 7(2). 265–280.
7.
Harris, John & Hermine M. Pashayan. (1976). Teratogenesis. Orthopedic Clinics of North America. 7(2). 281–289. 1 indexed citations
8.
Pashayan, Hermine M.. (1975). The Basic Concepts of Medical Genetics. Journal of Speech and Hearing Disorders. 40(2). 147–163. 1 indexed citations
9.
Pruzansky, Samuel, Hermine M. Pashayan, Sven Kreiborg, & Marissa A. Miller. (1975). Roentgencephalometric studies of the premature craniofacial synostoses: report of a family with the Saethre-Chotzen syndrome.. PubMed. 11(2). 226–37. 2 indexed citations
10.
Baum, Jules, et al.. (1975). A family with oculodentodigital dysplasia.. PubMed. 12. 323–9. 14 indexed citations
11.
Capek, Vlastimil, et al.. (1974). The neck in the XO and XX-XO mosaic Truner's syndrome.. PubMed. 5(1). 77–80. 2 indexed citations
12.
Pashayan, Hermine M., et al.. (1974). P--popliteal pterygium syndrome.. PubMed. 10(5). 252–6. 2 indexed citations
13.
Pashayan, Hermine M.. (1973). A Family With Blepharo-Naso-Facial Malformations. Archives of Pediatrics and Adolescent Medicine. 125(3). 389–389. 16 indexed citations
14.
Pashayan, Hermine M., Louis Dallaire, & Patricia MacLeod. (1973). Bilateral aniridia, multiple webs and severe mental retardation in a 47, XXY/48, XXXY mosaic. Clinical Genetics. 4(2). 125–129. 13 indexed citations
15.
Pashayan, Hermine M., et al.. (1971). BILATERAL APLASIA OF THE TIBIA, POLYDACTYLY AND ABSENT THUMB IN FATHER AND DAUGHTER. Journal of Bone and Joint Surgery - British Volume. 53-B(3). 495–499. 32 indexed citations
16.
Pashayan, Hermine M. & Fraser Fc. (1971). Facial features associated with predisposition to cleft lip.. PubMed. 7(7). 58–63. 3 indexed citations
17.
Pashayan, Hermine M., F. Clarke Fraser, & R. B. Goldbloom. (1971). A family showing hereditary nephropathy.. PubMed. 23(6). 555–67. 7 indexed citations
18.
Pashayan, Hermine M., E Lévy, & F. Clarke Fraser. (1970). Can the de Lange syndrome always be diagnosed at birth?. PubMed. 46(6). 940–2. 9 indexed citations
19.
Pashayan, Hermine M., E Lévy, & F. Clarke Fraser. (1970). Can the de Lange Syndrome Always Be Diagnosed at Birth?. PEDIATRICS. 46(6). 940–942. 10 indexed citations
20.
Pashayan, Hermine M., et al.. (1969). Variability of the de Lange syndrome: Report of 3 cases and genetic analysis of 54 families. The Journal of Pediatrics. 75(5). 853–858. 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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