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, Shelley R. McCormick, Wendy McKinnon 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

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	The Genetic Testing Experience of Individuals with Parkinson's Disease 2022 ·Movement Disorders Clinical Practice ·(unknown), Weiyi Mu, Rachel Nusbaum, (unknown), (unknown)	2
2	Telehealth for genetic counseling: A systematic evidence review 2021 ·Journal of Genetic Counseling ·(unknown), Lola Cook, Kate Shane-Carson, (unknown), (unknown), Rachel Nusbaum, Susan Steelman, Jennifer Malinowski	46
3	Predictors of contralateral prophylactic mastectomy in genetically high risk newly diagnosed breast cancer patients 2020 ·Breast Cancer Research and Treatment ·(unknown), Beth N. Peshkin, Claudine Isaacs, Shawna C. Willey, Heiðdís Valdimarsdóttir, Rachel Nusbaum, Gillian W. Hooker, Suzanne C. O’Neill, Lina Jandorf, Scott P. Kelly, (unknown), Sarah A. Kelleher, Elizabeth Poggi, Marc D. Schwartz	9
4	Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions 2019 ·Journal of Genetic Counseling ·(unknown), Rachel Nusbaum, Constance Smith‐Hicks, Leila Jamal, (unknown), Sonal Mahida	14
5	Randomized trial of proactive rapid genetic counseling versus usual care for newly diagnosed breast cancer patients 2018 ·Breast Cancer Research and Treatment ·Marc D. Schwartz, Beth N. Peshkin, Claudine Isaacs, Shawna C. Willey, Heiðdís Valdimarsdóttir, Rachel Nusbaum, Gillian W. Hooker, Suzanne C. O’Neill, Lina Jandorf, Scott P. Kelly, (unknown), (unknown), Katia Khoury	14
6	Randomized Noninferiority Trial of Telephone vs In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer: A 12-Month Follow-Up 2017 ·JNCI Cancer Spectrum ·(unknown), (unknown), Beth N. Peshkin, Heiðdís Valdimarsdóttir, Rachel Nusbaum, Morgan Similuk, Tiffani A. DeMarco, Gillian W. Hooker, Kristi D. Graves, Claudine Isaacs, Marie Wood, Wendy McKinnon, Judy E. Garber, Shelley R. McCormick, (unknown), Anita Y. Kinney, Mark D. Schwartz	15
7	Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer 2016 ·Familial Cancer ·Aryana Jacobs, Marc D. Schwartz, Heiðdís Valdimarsdóttir, Rachel Nusbaum, Gillian W. Hooker, Tiffani A. DeMarco, (unknown), Wendy McKinnon, Shelley R. McCormick, (unknown), Andrea Forman, Alexandra Lebensohn, Emily Dalton, (unknown), Kristi D. Graves, Morgan Similuk, Scott P. Kelly, Beth N. Peshkin	25
8	Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing 2015 ·Genetics in Medicine ·Lisa R. Susswein, Megan L. Marshall, Rachel Nusbaum, Kristen J. Vogel Postula, Scott M. Weissman, (unknown), (unknown), (unknown), Jessica K. Booker, Mattia Cremona, Federica Gibellini, Patricia D. Murphy, Daniel Pineda‐Alvarez, Guido D. Pollevick, Zhixiong Xu, (unknown), Sherri J. Bale, Rachel T. Klein, Kathleen S. Hruska, Wendy K. Chung	199
9	Patient Perceptions of Telephone vs. In‐Person BRCA1/BRCA2 Genetic Counseling 2015 ·Journal of Genetic Counseling ·Beth N. Peshkin, Scott P. Kelly, Rachel Nusbaum, Morgan Similuk, Tiffani A. DeMarco, Gillian W. Hooker, Heiðdís Valdimarsdóttir, Andrea Forman, (unknown), (unknown), Shelley R. McCormick, Wendy McKinnon, Kristi D. Graves, Claudine Isaacs, Judy E. Garber, Marie Wood, Lina Jandorf, Marc D. Schwartz	46
10	Discussing race-related limitations of genomic testing for colon cancer risk: Implications for education and counseling 2014 ·Social Science & Medicine ·Morgan Butrick, (unknown), (unknown), Gillian W. Hooker, Rachel Nusbaum, Beth N. Peshkin, (unknown), (unknown), Marc D. Schwartz, Kristi D. Graves	7
11	Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling 2014 ·Genetics in Medicine ·Morgan Butrick, Scott P. Kelly, Beth N. Peshkin, George Luta, Rachel Nusbaum, Gillian W. Hooker, Kristi D. Graves, (unknown), Claudine Isaacs, Heiðdís Valdimarsdóttir, Lina Jandorf, Tiffani A. DeMarco, Marie Wood, Wendy McKinnon, Judy E. Garber, Shelley R. McCormick, Marc D. Schwartz	85
12	Behavioral and psychosocial responses to genomic testing for colorectal cancer risk 2013 ·Genomics ·Kristi D. Graves, (unknown), Rachel Nusbaum, (unknown), Gillian W. Hooker, Beth N. Peshkin, Morgan Butrick, William Tuong, (unknown), David Goerlitz, (unknown), Peter G. Shields, Marc D. Schwartz	31
13	Translational genomic research: protocol development and initial outcomes following SNP testing for colon cancer risk 2012 ·Translational Behavioral Medicine ·Rachel Nusbaum, (unknown), Gillian W. Hooker, Beth N. Peshkin, Morgan Butrick, (unknown), William Tuong, Susan Eggly, (unknown), David Goerlitz, Peter G. Shields, Marc D. Schwartz, Kristi D. Graves	25
14	Intentions for bilateral mastectomy among newly diagnosed breast cancer patients 2012 ·Journal of Surgical Oncology ·Lesley G. King, Suzanne C. O’Neill, (unknown), Beth N. Peshkin, Heiðdís Valdimarsdóttir, Shawna C. Willey, (unknown), Tiffani A. DeMarco, Rachel Nusbaum, Elizabeth Feldman, Lina Jandorf, Marc D. Schwartz	20
15	Prevalence and correlates of mothers and fathers attending pretest cancer genetic counseling together 2009 ·Patient Education and Counseling ·Tiffani A. DeMarco, Rachel Nusbaum, Beth N. Peshkin, Andrea Farkas Patenaude, Katherine A. Schneider, Judy E. Garber, Heiðdís Valdimarsdóttir, Kenneth P. Tercyak	7
16	Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial 2008 ·Genetic Testing ·Beth N. Peshkin, Tiffani A. DeMarco, Kristi D. Graves, Karen Brown, Rachel Nusbaum, (unknown), Andrea Forman, Heiðdís Valdimarsdóttir, Marc D. Schwartz	1
17	Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial 2008 ·Genetic Testing ·Beth N. Peshkin, Tiffani A. DeMarco, Kristi D. Graves, Karen Brown, Rachel Nusbaum, (unknown), Andrea Forman, Heiðdís Valdimarsdóttir, Marc D. Schwartz	41
18	A Qualitative Description of Receiving a Diagnosis of Clefting in the Prenatal or Postnatal Period 2008 ·Journal of Genetic Counseling ·Rachel Nusbaum, Robin E. Grubs, Joseph E. Losee, (unknown), Matthew D. Ford, Mary L. Marazita	74
19	Practical Aspects of Delivering Hereditary Cancer Risk Counseling 2007 ·Seminars in Oncology ·Tiffani A. DeMarco, Karen L. Smith, Rachel Nusbaum, Beth N. Peshkin, Marc D. Schwartz, Claudine Isaacs	23
20	Management Updates for Women with a BRCA1 or BRCA2 Mutation 2007 ·Molecular Diagnosis & Therapy ·Rachel Nusbaum, Claudine Isaacs	25

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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