Judith Benkendorf

2.4k total citations · 1 hit paper
31 papers, 1.8k citations indexed

About

Judith Benkendorf is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Judith Benkendorf has authored 31 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 8 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Judith Benkendorf's work include BRCA gene mutations in cancer (17 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (5 papers). Judith Benkendorf is often cited by papers focused on BRCA gene mutations in cancer (17 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (5 papers). Judith Benkendorf collaborates with scholars based in United States. Judith Benkendorf's co-authors include Caryn Lerman, Jon Kerner, Michael S. Watson, Andres Gomez‐Caminero, Anthony R. Gregg, Robert G. Best, Susan Klugman, Brian G. Skotko, Kristin G. Monaghan and Komal Bajaj and has published in prestigious journals such as JNCI Journal of the National Cancer Institute, Cancer and Preventive Medicine.

In The Last Decade

Judith Benkendorf

30 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics

2016 472 citations Anthony R. Gregg, Brian G. Skotko et al. Genetics in Medicine profile →

Peers

Judith Benkendorf

GENET

PPCH

PHEOH

GHP

Robert G. Resta United States

Ainsley J. Newson Australia

Celine Lewis United Kingdom

Christine Patch United Kingdom

Megan Allyse United States

Kyle B. Brothers United States

Wybo Dondorp Netherlands

Benjamin E. Berkman United States

Alison Metcalfe United Kingdom

Regina H. Kenen United States

Robert G. Resta United States

Judith Benkendorf

954 ×0.9

GENET

1.3k ×1.8

PPCH

234 ×0.6

PHEOH

271 ×1.1

128 ×0.6

GHP

Citations per year, relative to Judith Benkendorf Judith Benkendorf (= 1×) peers Robert G. Resta

Countries citing papers authored by Judith Benkendorf

Since Specialization

Citations

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

Fields of papers citing papers by Judith Benkendorf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Benkendorf

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

All Works

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20 of 20 papers shown

South, Sarah T., Caroline Astbury, Michael T. Bashford, et al.. (2020). Risk categorization for oversight of laboratory-developed tests for inherited conditions: an updated position statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 22(6). 983–985.

Gregg, Anthony R., Brian G. Skotko, Judith Benkendorf, et al.. (2017). Noninvasive Prenatal Screening for Fetal Aneuploidy, 2016 Update: A Position Statement of the American College of Medical Genetics and Genomics. Obstetrical & Gynecological Survey. 72(1). 6–8. 11 indexed citations

Gregg, Anthony R., Brian G. Skotko, Judith Benkendorf, et al.. (2016). Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics. Genetics in Medicine. 18(10). 1056–1065. 472 indexed citations breakdown →

Scheuner, Maren T., Judith Benkendorf, Bruce Bowdish, et al.. (2014). Reporting genomic secondary findings: ACMG members weigh in. Genetics in Medicine. 17(1). 27–35. 39 indexed citations

Monaghan, Kristin G., Judith Benkendorf, Athena M. Cherry, et al.. (2013). Risk categorization for oversight of laboratory-developed tests for inherited conditions. Genetics in Medicine. 15(4). 314–315. 11 indexed citations

Benkendorf, Judith, et al.. (2010). Newborn screening residual dried blood spot use for newborn screening quality improvement. Genetics in Medicine. 12(12 Suppl). S269–S272. 7 indexed citations

Cooksey, Judith A., Gaetano Forte, Patricia A. Flanagan, Judith Benkendorf, & Miriam G. Blitzer. (2006). The medical genetics workforce: An analysis of clinical geneticist subgroups. Genetics in Medicine. 8(10). 603–614. 42 indexed citations

Cooksey, Judith A., Gaetano Forte, Judith Benkendorf, & Miriam G. Blitzer. (2005). The state of the medical geneticist workforce: Findings of the 2003 survey of American Board of Medical Genetics certified geneticists. Genetics in Medicine. 7(6). 439–443. 79 indexed citations

Benkendorf, Judith, et al.. (2002). A Conversation About the Indirect Road to Nondirective Genetic Counseling: A Defining Moment Through Research. Journal of Genetic Counseling. 11(4). 329–332. 3 indexed citations

10.

Benkendorf, Judith, et al.. (2001). Does indirect speech promote nondirective genetic counseling? Results of a sociolinguistic investigation. American Journal of Medical Genetics. 106(3). 199–207. 56 indexed citations

11.

Schwartz, Marc D., et al.. (2001). Consent to the use of stored DNA for genetics research: A survey of attitudes in the Jewish population. American Journal of Medical Genetics. 98(4). 336–342. 54 indexed citations

12.

Schwartz, Marc D., et al.. (2001). Impact of educational print materials on knowledge, attitudes, and interest in BRCA1/BRCA2. Cancer. 92(4). 932–940. 84 indexed citations

13.

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

14.

Lerman, Caryn, Chanita Hughes, Judith Benkendorf, et al.. (1999). Racial differences in testing motivation and psychological distress following pretest education for BRCA1 gene testing.. PubMed. 8(4 Pt 2). 361–7. 127 indexed citations

15.

Stefanek, Michael, Cheryl Enger, Judith Benkendorf, Susan Flamm Honig, & Caryn Lerman. (1999). Bilateral Prophylactic Mastectomy Decision Making: A Vignette Study. Preventive Medicine. 29(3). 216–221. 31 indexed citations

16.

Gomez‐Caminero, Andres, Judith Benkendorf, Jon Kerner, et al.. (1997). Ethnic differences in knowledge and attitudes about BRCA1 testing in women at increased risk. Patient Education and Counseling. 32(1-2). 51–62. 170 indexed citations

17.

Lerman, Caryn, Jon Kerner, Andres Gomez‐Caminero, et al.. (1997). Controlled Trial of Pretest Education Approaches to Enhance Informed Decision-Making for BRCA1 Gene Testing. JNCI Journal of the National Cancer Institute. 89(2). 148–157. 300 indexed citations

18.

Benkendorf, Judith, et al.. (1997). Patients' attitudes about autonomy and confidentiality in genetic testing for breast-ovarian cancer susceptibility. American Journal of Medical Genetics. 73(3). 296–303. 83 indexed citations

19.

Eglinton, Gary S., et al.. (1995). Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.. PubMed. 40(7). 537–9. 2 indexed citations

20.

Heimler, Audrey, et al.. (1992). American Board of Medical Genetics restructuring: make an informed decision.. PubMed. 51(5). v–vii. 3 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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