Claire N. Singletary

1000 total citations
22 papers, 700 citations indexed

About

Claire N. Singletary is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Claire N. Singletary has authored 22 papers receiving a total of 700 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 11 papers in Genetics and 7 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Claire N. Singletary's work include Prenatal Screening and Diagnostics (10 papers), BRCA gene mutations in cancer (8 papers) and Fetal and Pediatric Neurological Disorders (7 papers). Claire N. Singletary is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), BRCA gene mutations in cancer (8 papers) and Fetal and Pediatric Neurological Disorders (7 papers). Claire N. Singletary collaborates with scholars based in United States and Canada. Claire N. Singletary's co-authors include Jennifer K. Litton, Banu Arun, Susan K. Peterson, Denise Nebgen, Michelle Jackson, Jacqueline Mersch, Minjeong Park, Jennifer Czerwinski, Lara Friel and Sarah Noblin and has published in prestigious journals such as Journal of Clinical Oncology, Cancer and American Journal of Obstetrics and Gynecology.

In The Last Decade

Claire N. Singletary

22 papers receiving 686 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claire N. Singletary United States 12 320 218 189 163 122 22 700
Carolyn Durham United States 10 679 2.1× 174 0.8× 124 0.7× 133 0.8× 96 0.8× 15 867
Beatty G. Watts United States 9 345 1.1× 89 0.4× 70 0.4× 211 1.3× 36 0.3× 10 622
Flavia M. Facio United States 13 650 2.0× 260 1.2× 149 0.8× 48 0.3× 166 1.4× 25 1.0k
Rachel Nusbaum United States 17 785 2.5× 239 1.1× 155 0.8× 176 1.1× 175 1.4× 28 1.0k
B. Schlehe Germany 11 212 0.7× 78 0.4× 263 1.4× 231 1.4× 315 2.6× 23 826
Shelley R. McCormick United States 9 361 1.1× 125 0.6× 91 0.5× 125 0.8× 70 0.6× 16 518
Michael Gattas Australia 15 552 1.7× 174 0.8× 147 0.8× 178 1.1× 101 0.8× 21 848
Kyriaki Michailidou Cyprus 15 140 0.4× 71 0.3× 202 1.1× 70 0.4× 71 0.6× 57 601
Eileen Dimond United States 14 342 1.1× 87 0.4× 205 1.1× 226 1.4× 86 0.7× 38 861
Nancy Feldman United States 11 249 0.8× 45 0.2× 114 0.6× 174 1.1× 75 0.6× 24 563

Countries citing papers authored by Claire N. Singletary

Since Specialization
Citations

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

Fields of papers citing papers by Claire N. Singletary

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Claire N. Singletary. 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 Claire N. Singletary. The network helps show where Claire N. Singletary may publish in the future.

Co-authorship network of co-authors of Claire N. Singletary

This figure shows the co-authorship network connecting the top 25 collaborators of Claire N. Singletary. A scholar is included among the top collaborators of Claire N. Singletary 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 Claire N. Singletary. Claire N. Singletary 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.
Hashmi, S. Shahrukh, et al.. (2024). Status of abortion curriculum in genetic counseling: Survey of graduate programs and recent graduates in the United States. Journal of Genetic Counseling. 34(1). e1875–e1875. 2 indexed citations
2.
Veach, Patricia McCarthy, et al.. (2021). Influence of genetic counselor medical history on specialty and psychosocial practice in North America. Journal of Genetic Counseling. 31(3). 663–676. 3 indexed citations
3.
Northrup, Hope, et al.. (2021). Hypoglycemia in mitochondrial disorders. Mitochondrion. 58. 179–183. 7 indexed citations
4.
Stein, Quinn, et al.. (2021). Genesurance counseling: Current training practices of genetic counseling graduate programs in the United States. Journal of Genetic Counseling. 30(6). 1757–1766. 1 indexed citations
5.
6.
Stevens, Blair, et al.. (2019). It takes two: uptake of carrier screening among male reproductive partners. Prenatal Diagnosis. 40(3). 311–316. 19 indexed citations
7.
Hashmi, S. Shahrukh, et al.. (2019). Current genetic counseling practice in the United States following positive non‐invasive prenatal testing for sex chromosome abnormalities. Journal of Genetic Counseling. 28(4). 802–811. 12 indexed citations
8.
Singletary, Claire N., et al.. (2018). Prenatal chromosomal microarray uptake with invasive prenatal diagnosis: How many patients take the leap?. Prenatal Diagnosis. 38(10). 748–754. 6 indexed citations
9.
Czerwinski, Jennifer, et al.. (2018). Attitudes Toward and Uptake of Prenatal Genetic Screening and Testing in Twin Pregnancies. Journal of Genetic Counseling. 27(5). 1238–1247. 8 indexed citations
10.
Hoskovec, Jennifer, et al.. (2017). Relieving the Bottleneck: An Investigation of Barriers to Expansion of Supervision Networks at Genetic Counseling Training Programs. Journal of Genetic Counseling. 27(1). 241–251. 12 indexed citations
11.
Hashmi, S. Shahrukh, et al.. (2016). Patient Perception of Negative Noninvasive Prenatal Testing Results. American Journal of Perinatology Reports. 6(4). e391–e406. 16 indexed citations
12.
Streff, Haley, Jessica Profato, Yuanqing Ye, et al.. (2016). Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers. The Oncologist. 21(7). 869–874. 37 indexed citations
13.
Baty, Bonnie Jeanne, Angela Trepanier, Robin L. Bennett, et al.. (2016). Developing a Model of Advanced Training to Promote Career Advancement for Certified Genetic Counselors: An Investigation of Expanded Skills, Advanced Training Paths, and Professional Opportunities. Journal of Genetic Counseling. 25(4). 625–634. 11 indexed citations
14.
Mitri, Zahi, Michelle Jackson, Juhee Song, et al.. (2015). BRCAPRO 6.0 Model Validation in Male Patients Presenting for BRCA Testing. The Oncologist. 20(6). 593–597. 11 indexed citations
15.
Mitri, Zahi, Michelle Jackson, Sharon H. Giordano, et al.. (2014). BRCAPRO 6.0 model validation in male patients presenting for BRCA testing.. Journal of Clinical Oncology. 32(15_suppl). 1559–1559. 1 indexed citations
16.
Mersch, Jacqueline, Michelle Jackson, Minjeong Park, et al.. (2014). Cancers associated with BRCA1 and BRCA2 mutations other than breast and ovarian. Cancer. 121(2). 269–275. 356 indexed citations
17.
Nuccio, Regina, S. Shahrukh Hashmi, Joan Mastrobattista, et al.. (2014). Influence of Anchoring on Miscarriage Risk Perception Associated with Amniocentesis. Journal of Genetic Counseling. 24(2). 278–284. 5 indexed citations
18.
Czerwinski, Jennifer, Claire N. Singletary, & Lara Friel. (2013). The Impact of Noninvasive Prenatal Testing on the Practice of Maternal–Fetal Medicine. American Journal of Perinatology. 31(9). 759–764. 26 indexed citations
19.
Friel, Lara, Jennifer Czerwinski, & Claire N. Singletary. (2012). 555: The impact of non-invasive prenatal testing on the practice of maternal fetal medicine. American Journal of Obstetrics and Gynecology. 208(1). S238–S238. 15 indexed citations
20.
Wilson, Karen L., Jan Czerwiński, Jennifer Hoskovec, et al.. (2012). NSGC Practice Guideline: Prenatal Screening and Diagnostic Testing Options for Chromosome Aneuploidy. Journal of Genetic Counseling. 22(1). 4–15. 91 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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Rankless by CCL
2026