Rachel Nusbaum

1.3k total citations
28 papers, 1.0k citations indexed

About

Rachel Nusbaum is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Sociology and Political Science. According to data from OpenAlex, Rachel Nusbaum has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 8 papers in Sociology and Political Science. Recurrent topics in Rachel Nusbaum's work include BRCA gene mutations in cancer (24 papers), Childhood Cancer Survivors' Quality of Life (8 papers) and Family Support in Illness (8 papers). Rachel Nusbaum is often cited by papers focused on BRCA gene mutations in cancer (24 papers), Childhood Cancer Survivors' Quality of Life (8 papers) and Family Support in Illness (8 papers). Rachel Nusbaum collaborates with scholars based in United States and Iceland. Rachel Nusbaum's co-authors include Beth N. Peshkin, Claudine Isaacs, Kristi D. Graves, Heiðdís Valdimarsdóttir, Marc D. Schwartz, Judy E. Garber, Tiffani A. DeMarco, Wendy McKinnon, Shelley R. McCormick and Marie Wood and has published in prestigious journals such as Journal of Clinical Oncology, Social Science & Medicine and Genomics.

In The Last Decade

Rachel Nusbaum

28 papers receiving 990 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Rachel Nusbaum 785 239 176 175 170 28 1.0k
Vickie L. Venne 536 0.7× 155 0.6× 196 1.1× 135 0.8× 138 0.8× 27 848
Andrea Forman 543 0.7× 161 0.7× 142 0.8× 150 0.9× 172 1.0× 28 732
Carolyn Durham 679 0.9× 174 0.7× 133 0.8× 96 0.5× 126 0.7× 15 867
Michael Gattas 552 0.7× 174 0.7× 178 1.0× 101 0.6× 71 0.4× 21 848
Angela Trepanier 550 0.7× 187 0.8× 77 0.4× 99 0.6× 114 0.7× 35 841
Agnes Masny 625 0.8× 188 0.8× 250 1.4× 80 0.5× 129 0.8× 17 930
Amanda Gammon 678 0.9× 137 0.6× 317 1.8× 251 1.4× 97 0.6× 34 1.1k
Charité Ricker 871 1.1× 95 0.4× 258 1.5× 262 1.5× 190 1.1× 60 1.1k
Brita Arver 562 0.7× 99 0.4× 298 1.7× 325 1.9× 106 0.6× 30 952
Conny A. van der Meer 550 0.7× 184 0.8× 140 0.8× 87 0.5× 73 0.4× 10 683

Countries citing papers authored by Rachel Nusbaum

Since Specialization
Citations

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

Fields of papers citing papers by Rachel Nusbaum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Nusbaum

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Nusbaum. A scholar is included among the top collaborators of Rachel Nusbaum 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 Rachel Nusbaum. Rachel Nusbaum 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.
Cook, Lola, et al.. (2021). Telehealth for genetic counseling: A systematic evidence review. Journal of Genetic Counseling. 30(5). 1361–1378. 46 indexed citations
2.
Peshkin, Beth N., Claudine Isaacs, Shawna C. Willey, et al.. (2020). Predictors of contralateral prophylactic mastectomy in genetically high risk newly diagnosed breast cancer patients. Breast Cancer Research and Treatment. 180(1). 177–185. 9 indexed citations
3.
Nusbaum, Rachel, et al.. (2019). Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions. Journal of Genetic Counseling. 28(2). 304–312. 14 indexed citations
4.
Schwartz, Marc D., Beth N. Peshkin, Claudine Isaacs, et al.. (2018). Randomized trial of proactive rapid genetic counseling versus usual care for newly diagnosed breast cancer patients. Breast Cancer Research and Treatment. 170(3). 517–524. 14 indexed citations
5.
Peshkin, Beth N., Heiðdís Valdimarsdóttir, Rachel Nusbaum, et al.. (2017). Randomized Noninferiority Trial of Telephone vs In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer: A 12-Month Follow-Up. JNCI Cancer Spectrum. 1(1). pkx002–pkx002. 15 indexed citations
6.
Jacobs, Aryana, Marc D. Schwartz, Heiðdís Valdimarsdóttir, et al.. (2016). Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer. Familial Cancer. 15(4). 529–539. 25 indexed citations
7.
Susswein, Lisa R., Megan L. Marshall, Rachel Nusbaum, et al.. (2015). Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. Genetics in Medicine. 18(8). 823–832. 199 indexed citations
8.
Peshkin, Beth N., Scott P. Kelly, Rachel Nusbaum, et al.. (2015). Patient Perceptions of Telephone vs. In‐Person BRCA1/BRCA2 Genetic Counseling. Journal of Genetic Counseling. 25(3). 472–482. 46 indexed citations
9.
Butrick, Morgan, Scott P. Kelly, Beth N. Peshkin, et al.. (2014). Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling. Genetics in Medicine. 17(6). 467–475. 85 indexed citations
10.
Butrick, Morgan, Gillian W. Hooker, Rachel Nusbaum, et al.. (2014). Discussing race-related limitations of genomic testing for colon cancer risk: Implications for education and counseling. Social Science & Medicine. 114. 26–37. 7 indexed citations
11.
Schwartz, Mark D., Heiðdís Valdimarsdóttir, Beth N. Peshkin, et al.. (2014). Randomized Noninferiority Trial of Telephone Versus In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer. Journal of Clinical Oncology. 32(7). 618–626. 201 indexed citations
12.
Graves, Kristi D., Rachel Nusbaum, Gillian W. Hooker, et al.. (2013). Behavioral and psychosocial responses to genomic testing for colorectal cancer risk. Genomics. 102(2). 123–130. 31 indexed citations
13.
King, Lesley G., Suzanne C. O’Neill, Beth N. Peshkin, et al.. (2012). Intentions for bilateral mastectomy among newly diagnosed breast cancer patients. Journal of Surgical Oncology. 107(7). 772–776. 20 indexed citations
14.
Nusbaum, Rachel, Gillian W. Hooker, Beth N. Peshkin, et al.. (2012). Translational genomic research: protocol development and initial outcomes following SNP testing for colon cancer risk. Translational Behavioral Medicine. 3(1). 17–29. 25 indexed citations
15.
DeMarco, Tiffani A., Rachel Nusbaum, Beth N. Peshkin, et al.. (2009). Prevalence and correlates of mothers and fathers attending pretest cancer genetic counseling together. Patient Education and Counseling. 78(1). 29–33. 7 indexed citations
16.
Peshkin, Beth N., Tiffani A. DeMarco, Kristi D. Graves, et al.. (2008). Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial. Genetic Testing. 0(0). 2685938514–2685938514. 1 indexed citations
17.
Peshkin, Beth N., Tiffani A. DeMarco, Kristi D. Graves, et al.. (2008). Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial. Genetic Testing. 12(1). 37–52. 41 indexed citations
18.
Nusbaum, Rachel, et al.. (2008). A Qualitative Description of Receiving a Diagnosis of Clefting in the Prenatal or Postnatal Period. Journal of Genetic Counseling. 17(4). 336–350. 74 indexed citations
19.
DeMarco, Tiffani A., Karen L. Smith, Rachel Nusbaum, et al.. (2007). Practical Aspects of Delivering Hereditary Cancer Risk Counseling. Seminars in Oncology. 34(5). 369–378. 23 indexed citations
20.
Nusbaum, Rachel & Claudine Isaacs. (2007). Management Updates for Women with a BRCA1 or BRCA2 Mutation. Molecular Diagnosis & Therapy. 11(3). 133–144. 25 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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