Chahira Kozma

2.1k total citations
38 papers, 1.4k citations indexed

About

Chahira Kozma is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Chahira Kozma has authored 38 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Chahira Kozma's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). Chahira Kozma is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). Chahira Kozma collaborates with scholars based in United States, Denmark and United Kingdom. Chahira Kozma's co-authors include Joan Weiss, E. Virginia Lapham, Jeanne Meck, Natalia V. Kuznetsova, Melissa A. Scott, Wayne A. Cabral, Dorothy Bulas, Kenneth N. Rosenbaum, Sergey Leikin and Cynthia J. Tifft and has published in prestigious journals such as Science, Nature Genetics and Human Genetics.

In The Last Decade

Chahira Kozma

37 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chahira Kozma United States 16 813 377 319 191 179 38 1.4k
Juan Clinton Llerena Brazil 23 601 0.7× 400 1.1× 346 1.1× 237 1.2× 219 1.2× 112 1.6k
Y. Gillerot Belgium 22 616 0.8× 740 2.0× 426 1.3× 112 0.6× 176 1.0× 74 1.8k
M O Rethoré France 21 754 0.9× 599 1.6× 395 1.2× 310 1.6× 200 1.1× 62 1.5k
Kathleen A. Leppig United States 23 681 0.8× 662 1.8× 209 0.7× 176 0.9× 95 0.5× 57 2.0k
Dianne Abuelo United States 23 768 0.9× 757 2.0× 298 0.9× 158 0.8× 93 0.5× 52 1.9k
Helen Kingston United Kingdom 24 645 0.8× 839 2.2× 161 0.5× 118 0.6× 202 1.1× 63 1.9k
Agnes Bankier Australia 27 990 1.2× 767 2.0× 357 1.1× 55 0.3× 128 0.7× 80 2.0k
Renata Laxová United States 19 623 0.8× 765 2.0× 289 0.9× 119 0.6× 119 0.7× 53 1.6k
Géraldine Viot France 21 647 0.8× 674 1.8× 280 0.9× 97 0.5× 94 0.5× 56 1.4k
Yoshikazu Kuroki Japan 26 1.4k 1.8× 835 2.2× 400 1.3× 89 0.5× 76 0.4× 106 2.2k

Countries citing papers authored by Chahira Kozma

Since Specialization
Citations

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

Fields of papers citing papers by Chahira Kozma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chahira Kozma. 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 Chahira Kozma. The network helps show where Chahira Kozma may publish in the future.

Co-authorship network of co-authors of Chahira Kozma

This figure shows the co-authorship network connecting the top 25 collaborators of Chahira Kozma. A scholar is included among the top collaborators of Chahira Kozma 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 Chahira Kozma. Chahira Kozma 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.
Kozma, Chahira, et al.. (2011). The ancient Egyptian dwarfs of the pyramids: The high official and the female worker. American Journal of Medical Genetics Part A. 155(8). 1817–1824. 12 indexed citations
2.
Kozma, Chahira & Jayashree Ramasethu. (2011). Methotrexate and misoprostol teratogenicity: Further expansion of the clinical manifestations. American Journal of Medical Genetics Part A. 155(7). 1723–1728. 17 indexed citations
3.
Kozma, Chahira. (2010). The ancient Egyptian dwarfs of the Walters Art Museum. American Journal of Medical Genetics Part A. 152A(10). 2556–2562. 7 indexed citations
4.
Kozma, Chahira. (2008). Skeletal dysplasia in ancient Egypt. American Journal of Medical Genetics Part A. 146A(23). 3104–3112. 26 indexed citations
5.
Mitchell, Jean M., Darrell J. Gaskin, & Chahira Kozma. (2008). Health Supervision Visits among SSI-Eligible Children in the D.C. Medicaid Program: A Comparison of Enrollees in Fee-for-Service and Partially Capitated Managed Care. INQUIRY The Journal of Health Care Organization Provision and Financing. 45(2). 198–214. 5 indexed citations
6.
Cabral, Wayne A., Weizhong Chang, Aileen M. Barnes, et al.. (2007). Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta. Nature Genetics. 39(3). 359–365. 317 indexed citations
7.
Kozma, Chahira, et al.. (2003). Survey of Nursing and Medical Profile Prior to Deinstitutionalization of a Population with Profound Mental Retardation. Clinical Nursing Research. 12(1). 8–22. 14 indexed citations
8.
Kozma, Chahira, Anne Slavotinek, & Jeanne Meck. (2003). Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent‐1 segregants. American Journal of Medical Genetics Part A. 124A(2). 118–128. 22 indexed citations
9.
Kozma, Chahira. (2001). Valproic acid embryopathy: Report of two siblings with further expansion of the phenotypic abnormalities and a review of the literature. American Journal of Medical Genetics. 98(2). 168–175. 95 indexed citations
10.
Kozma, Chahira, Bassem R. Haddad, & Jeanne Meck. (2000). Trisomy 7p resulting from 7p15;9p24 translocation: Report of a new case and review of associated medical complications. American Journal of Medical Genetics. 91(4). 286–290. 25 indexed citations
11.
Lapham, E. Virginia, Chahira Kozma, Joan Weiss, Judith Benkendorf, & Mary Ann Wilson. (2000). The gap between practice and genetics education of health professionals: HuGEM survey results. Genetics in Medicine. 2(4). 226–231. 58 indexed citations
12.
Kozma, Chahira, et al.. (1997). Whom would you trust with your genetic information?. PubMed. 61(4). A24–A24. 2 indexed citations
13.
Kozma, Chahira, et al.. (1996). PRENATAL DETECTION OFDE NOVO INVERSION OF CHROMOSOME (2) (p13q11.2) AND POSTNATAL FOLLOW-UP. Prenatal Diagnosis. 16(4). 366–370. 3 indexed citations
14.
Kozma, Chahira, et al.. (1996). The microcephaly-lymphoedema syndrome: report of an additional family. Clinical Dysmorphology. 5(1). 49–54. 13 indexed citations
15.
Kozma, Chahira. (1996). Autosomal dominant inheritance of Brachmann-de Lange syndrome. American Journal of Medical Genetics. 66(4). 445–448. 12 indexed citations
16.
Roa, Benjamin B., Frank Greenberg, Preethi H. Gunaratne, et al.. (1996). Duplication of thePMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1A neuropathy. Human Genetics. 97(5). 642–649. 10 indexed citations
17.
Roa, B. B., Frank Greenberg, Preethi H. Gunaratne, et al.. (1996). Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy.. PubMed. 97(5). 642–9. 50 indexed citations
18.
Meck, Jeanne, et al.. (1994). Prenatal diagnosis of trisomy 12 mosaicism: Physical and developmental follow‐up. Prenatal Diagnosis. 14(9). 878–883. 12 indexed citations
19.
Kozma, Chahira, et al.. (1991). De novo duplication of 17p [dup(17)(p12→p11.2)]: Report of an additional case with confirmation of the cytogenetic, phenotypic, and developmental aspects. American Journal of Medical Genetics. 41(4). 446–450. 26 indexed citations
20.
Kozma, Chahira, et al.. (1990). Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye. Ophthalmic Paediatrics and Genetics. 11(1). 23–30. 10 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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