Carolyn Trunca

414 total citations
14 papers, 301 citations indexed

About

Carolyn Trunca is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Carolyn Trunca has authored 14 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Carolyn Trunca's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Carolyn Trunca is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Carolyn Trunca collaborates with scholars based in United States and United Kingdom. Carolyn Trunca's co-authors include Eeva Therman, John M. Opitz, Celia I. Kaye, Evelyn M. Kuhn, Gloria E. Sarto, Burton Rochelson, Z. Rosenwaks, Kasper Hansen, Cynthia Kaplan and Athena M. Cherry and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Life Sciences and Journal of Medical Genetics.

In The Last Decade

Carolyn Trunca

14 papers receiving 291 citations

Peers

Carolyn Trunca
Drew Duckett United Kingdom
Constance J. Sandlin United States
Paula R. Martens United States
D A Couzin United Kingdom
Drew Duckett United Kingdom
Carolyn Trunca
Citations per year, relative to Carolyn Trunca Carolyn Trunca (= 1×) peers Drew Duckett

Countries citing papers authored by Carolyn Trunca

Since Specialization
Citations

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

Fields of papers citing papers by Carolyn Trunca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carolyn Trunca

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

All Works

14 of 14 papers shown
1.
Trunca, Carolyn, Nancy R. Mendell, & Samantha L.P. Schilit. (2022). Reproductive Risk Estimation Calculator for Balanced Translocation Carriers. Current Protocols. 2(12). e633–e633. 1 indexed citations
2.
Meck, Jeanne, Ludmila Matyakhina, Ayala Aviram, et al.. (2015). Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings. American Journal of Obstetrics and Gynecology. 213(2). 214.e1–214.e5. 41 indexed citations
3.
Migeon, Barbara R., et al.. (2007). X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X. European Journal of Human Genetics. 16(2). 153–162. 18 indexed citations
4.
Mao, Rong, Elizabeth Berry‐Kravis, Ann Garber, et al.. (1998). Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases. American Journal of Medical Genetics. 80(5). 473–480. 30 indexed citations
5.
Rochelson, Burton, et al.. (1990). A quantitative analysis of placental vasculature in the third‐trimester fetus with autosomal trisomy. International Journal of Gynecology & Obstetrics. 33(1). 84–84. 34 indexed citations
6.
Rochelson, Burton, Cynthia Kaplan, Carolyn Trunca, et al.. (1989). Doppler Velocimetry in the Fetus with Abnormal Karyotype. Echocardiography. 6(3). 271–275. 1 indexed citations
7.
Heneghan, Margery A., et al.. (1987). Femoral cylinder index in the diagnosis of the Ullrich-Turner syndrome.. PubMed. 23(1). 401–10. 1 indexed citations
8.
Therman, Eeva, Carolyn Trunca, Evelyn M. Kuhn, & Gloria E. Sarto. (1986). Dicentric chromosomes and the inactivation of the centromere. Human Genetics. 72(3). 191–195. 56 indexed citations
9.
Rochelson, Burton, et al.. (1986). The use of a rapid in situ technique for third-trimester diagnosis of trisomy 18. American Journal of Obstetrics and Gynecology. 155(4). 835–836. 6 indexed citations
10.
Kaplan, Cynthia, Bernard Lane, Frederick W. Miller, D.A. Baker, & Carolyn Trunca. (1985). Renal Pathology of Prenatally Diagnosed Nephrosis. Pediatric Pathology. 3(2-4). 271–281. 2 indexed citations
11.
Angulo, Moris, et al.. (1984). Endocrine abnormalities in a patient with partial trisomy 4q.. Journal of Medical Genetics. 21(4). 303–307. 16 indexed citations
12.
Trunca, Carolyn, Eeva Therman, & Z. Rosenwaks. (1984). The phenotypic effects of small, distal Xq deletions. Human Genetics. 68(1). 87–89. 23 indexed citations
13.
Trunca, Carolyn, John M. Opitz, & Celia I. Kaye. (1977). Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 → 14qter). American Journal of Medical Genetics. 1(2). 217–228. 61 indexed citations
14.
Koella, Werner P., et al.. (1965). Serotonin: Effect on recruiting responses of the cat. Life Sciences. 4(2). 173–181. 11 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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