Randi E. Zinberg

2.0k total citations
24 papers, 467 citations indexed

About

Randi E. Zinberg is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Randi E. Zinberg has authored 24 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Randi E. Zinberg's work include BRCA gene mutations in cancer (14 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (6 papers). Randi E. Zinberg is often cited by papers focused on BRCA gene mutations in cancer (14 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (6 papers). Randi E. Zinberg collaborates with scholars based in United States, United Kingdom and Germany. Randi E. Zinberg's co-authors include Saskia C. Sanderson, George A. Díaz, Michael D. Linderman, Andrew Kasarskis, Eric E. Schadt, Sabrina A. Suckiel, Melissa Wasserstein, Micol Zweig, Margaret M. McGovern and Kadija Ferryman and has published in prestigious journals such as Fertility and Sterility, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Randi E. Zinberg

23 papers receiving 453 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Randi E. Zinberg United States 13 311 196 80 76 54 24 467
Carol A. Christianson United States 12 328 1.1× 122 0.6× 47 0.6× 72 0.9× 36 0.7× 20 446
Sabrina A. Suckiel United States 13 323 1.0× 142 0.7× 48 0.6× 92 1.2× 32 0.6× 23 467
Karen Powell United States 15 374 1.2× 150 0.8× 64 0.8× 48 0.6× 46 0.9× 22 565
Anne‐Marie Laberge Canada 15 230 0.7× 148 0.8× 215 2.7× 85 1.1× 52 1.0× 55 604
Mark Kroese United Kingdom 14 241 0.8× 109 0.6× 203 2.5× 94 1.2× 32 0.6× 28 633
Beth Anderson United States 11 185 0.6× 140 0.7× 57 0.7× 26 0.3× 36 0.7× 17 414
Myra I. Roche United States 18 654 2.1× 252 1.3× 208 2.6× 94 1.2× 63 1.2× 41 890
Rachel Horton United Kingdom 10 186 0.6× 104 0.5× 57 0.7× 90 1.2× 38 0.7× 31 440
Dale Halsey Lea United States 14 349 1.1× 114 0.6× 107 1.3× 114 1.5× 64 1.2× 46 546
Suzanne M. O’Neill United States 15 344 1.1× 170 0.9× 83 1.0× 28 0.4× 18 0.3× 23 650

Countries citing papers authored by Randi E. Zinberg

Since Specialization
Citations

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

Fields of papers citing papers by Randi E. Zinberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Randi E. Zinberg. 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 Randi E. Zinberg. The network helps show where Randi E. Zinberg may publish in the future.

Co-authorship network of co-authors of Randi E. Zinberg

This figure shows the co-authorship network connecting the top 25 collaborators of Randi E. Zinberg. A scholar is included among the top collaborators of Randi E. Zinberg 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 Randi E. Zinberg. Randi E. Zinberg 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.
Biesecker, Barbara B., Sara Ackerman, Kyle B. Brothers, et al.. (2025). Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results. Genetics in Medicine. 27(4). 101363–101363.
2.
Zinberg, Randi E., et al.. (2023). Patient and Provider Experiences and Views on the Use of Telehealth in Genetics Clinics in Response to the COVID-19 Pandemic. Telemedicine Journal and e-Health. 30(1). 118–125. 2 indexed citations
3.
Bergner, Amanda L., et al.. (2021). The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm. Journal of Genetic Counseling. 30(4). 1057–1068. 5 indexed citations
4.
Sanderson, Saskia C., Michael D. Linderman, Sabrina A. Suckiel, et al.. (2017). Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project. European Journal of Human Genetics. 25(3). 280–292. 49 indexed citations
5.
Linderman, Michael D., Ali Bashir, George A. Díaz, et al.. (2015). Preparing the next generation of genomicists: a laboratory-style course in medical genomics. BMC Medical Genomics. 8(1). 47–47. 14 indexed citations
6.
Sanderson, Saskia C., Michael D. Linderman, Sabrina A. Suckiel, et al.. (2015). Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project. European Journal of Human Genetics. 24(1). 14–20. 90 indexed citations
7.
Sanderson, Saskia C., Michael D. Linderman, Randi E. Zinberg, et al.. (2015). How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study. Genetics in Medicine. 17(11). 866–874. 21 indexed citations
8.
Horowitz, Carol R., Noura S. Abul‐Husn, Michelle A. Ramos, et al.. (2015). Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry. Contemporary Clinical Trials. 47. 101–108. 33 indexed citations
9.
Sanderson, Saskia C., Michael A. Diefenbach, Randi E. Zinberg, et al.. (2013). Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study. Journal of Community Genetics. 4(4). 469–482. 58 indexed citations
10.
Sanderson, Saskia C., Samantha A. Streicher, Ethylin Wang Jabs, et al.. (2012). Genetic and Lifestyle Causal Beliefs about Obesity and Associated Diseases among Ethnically Diverse Patients: A Structured Interview Study. Public Health Genomics. 16(3). 83–93. 18 indexed citations
11.
Zinberg, Randi E., et al.. (2011). Genetic screening practices at oocyte donation programs. Fertility and Sterility. 96(3). S218–S218. 1 indexed citations
12.
McGovern, Margaret M., et al.. (2006). Use of Standardized Patients in, Undergraduate Medical Genetics Education. Teaching and Learning in Medicine. 18(3). 203–207. 19 indexed citations
13.
Zinberg, Randi E. & Kathleen Leask Capitulo. (2006). Genetic Testing:Is There a Right Not to Know?. MCN The American Journal of Maternal/Child Nursing. 31(3). 144–144. 4 indexed citations
14.
Brown, Karen L., et al.. (2005). Referral and Experience with Genetic Testing Among Women with Early Onset Breast Cancer. Genetic Testing. 9(4). 301–305. 28 indexed citations
15.
Zinberg, Randi E., et al.. (2003). Attitudes and psychosocial adjustment of unaffected siblings of patients with phenylketonuria. American Journal of Medical Genetics Part A. 126A(2). 156–160. 4 indexed citations
16.
McGovern, Margaret M., et al.. (2003). Interaction of genetic counselors with molecular genetic testing laboratories: Implications for non‐geneticist health care providers. American Journal of Medical Genetics Part A. 119A(3). 297–301. 12 indexed citations
17.
Zinberg, Randi E., Ruth Kornreich, Lisa Edelmann, & Robert J. Desnick. (2001). PRENATAL GENETIC SCREENING IN THE ASHKENAZI JEWISH POPULATION. Clinics in Perinatology. 28(2). 367–382. 10 indexed citations
18.
Rhodes, Rosamond, Judith P. Willner, Kurt Hirschhorn, et al.. (1998). Issues in Medical Ethics. DigitalGeorgetown (Georgetown University Library). 4 indexed citations
19.
Ashton‐Prolla, Patrícia, Arvind Babu, Richard L. Neu, et al.. (1997). Prenatal diagnosis of a familial interchromosomal insertion of Y chromosome heterochromatin. American Journal of Medical Genetics. 73(4). 470–473. 2 indexed citations
20.
Lynch, Lauren, et al.. (1994). Confined placental mosaicism in CVS and pregnancy outcome. Prenatal Diagnosis. 14(7). 589–593. 26 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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