Carrie Koval

530 total citations
5 papers, 199 citations indexed

About

Carrie Koval is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Carrie Koval has authored 5 papers receiving a total of 199 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Carrie Koval's work include BRCA gene mutations in cancer (3 papers), Genetic factors in colorectal cancer (2 papers) and Genomics and Rare Diseases (2 papers). Carrie Koval is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Genetic factors in colorectal cancer (2 papers) and Genomics and Rare Diseases (2 papers). Carrie Koval collaborates with scholars based in United States and United Kingdom. Carrie Koval's co-authors include Wendy K. Chung, Julia Wynn, Donna Russo, Elana Levinson, Heidi Lumish, Colleen F. Stevens, Darryl C. De Vivo, Michele Caggana, Denise M. Kay and Sally Dunaway Young and has published in prestigious journals such as Cancer Research, Genetics in Medicine and Journal of Genetic Counseling.

In The Last Decade

Carrie Koval

5 papers receiving 195 citations

Peers

Carrie Koval

GENET

MB

GENET

SURGE

PPCH

Marcela M. França Brazil

Janet Marcadier Canada

Tomi L. Toler United States

Maria Elfving Sweden

Grace E. VanNoy United States

Carolyn Chuang United States

A O'Rourke United Kingdom

Kevin D. Josephson United States

Matthew Osmond Canada

Julie Kaplan United States

Marcela M. França Brazil

Carrie Koval

173 ×1.6

GENET

163 ×1.9

MB

45 ×0.5

GENET

53 ×1.0

SURGE

14 ×0.4

PPCH

Citations per year, relative to Carrie Koval Carrie Koval (= 1×) peers Marcela M. França

Countries citing papers authored by Carrie Koval

Since Specialization

Citations

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

Fields of papers citing papers by Carrie Koval

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carrie Koval

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

All Works

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5 of 5 papers shown

1.

Trivedi, Meghna S., Wendy K. Chung, Roshni Rao, et al.. (2020). Abstract P6-08-11: Association between genetic testing for hereditary breast cancer and contralateral prophylactic mastectomy among young women diagnosed with early-stage breast cancer. Cancer Research. 80(4_Supplement). P6–8. 1 indexed citations

2.

Koval, Carrie, et al.. (2020). A qualitative study of Latinx parents' experiences of clinical exome sequencing. Journal of Genetic Counseling. 29(4). 574–586. 15 indexed citations

3.

Pendrick, Danielle, Jennifer A. Oberg, Susan J. Hsiao, et al.. (2019). Identification of a secondary RET mutation in a pediatric patient with relapsed acute myeloid leukemia leads to the diagnosis and treatment of asymptomatic metastatic medullary thyroid cancer in a parent: a case for sequencing the germline. Molecular Case Studies. 5(2). a003889–a003889. 2 indexed citations

4.

Kay, Denise M., Colleen F. Stevens, Carrie Koval, et al.. (2017). Pilot study of population-based newborn screening for spinal muscular atrophy in New York state. Genetics in Medicine. 20(6). 608–613. 94 indexed citations

5.

Lumish, Heidi, Carrie Koval, Donna Russo, et al.. (2017). Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients. Journal of Genetic Counseling. 26(5). 1116–1129. 87 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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