A citation-based method for searching scientific literature

Rena J Pasick, Galen Joseph, Susan Stewart, Celia Kaplan, Robin Lee, Judith Luce, Sharon Davis, Titas Marquez, Tung Nguyen, Claudia Guerra. Am J Public Health 2016
Times Cited: 12







List of co-cited articles
36 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.
Anita Y Kinney, Laurie E Steffen, Barbara H Brumbach, Wendy Kohlmann, Ruofei Du, Ji-Hyun Lee, Amanda Gammon, Karin Butler, Saundra S Buys, Antoinette M Stroup,[...]. J Clin Oncol 2016
57
41

Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients.
Galen Joseph, Rena J Pasick, Dean Schillinger, Judith Luce, Claudia Guerra, Janice Ka Yan Cheng. J Genet Couns 2017
42
33

Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.
Marc D Schwartz, Heiddis B Valdimarsdottir, Beth N Peshkin, Jeanne Mandelblatt, Rachel Nusbaum, An-Tsun Huang, Yaojen Chang, Kristi Graves, Claudine Isaacs, Marie Wood,[...]. J Clin Oncol 2014
143
33

Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling.
Morgan Butrick, Scott Kelly, Beth N Peshkin, George Luta, Rachel Nusbaum, Gillian W Hooker, Kristi Graves, Lisa Feeley, Claudine Isaacs, Heiddis B Valdimarsdottir,[...]. Genet Med 2015
55
25

Will Precision Medicine Improve Population Health?
Muin J Khoury, Sandro Galea. JAMA 2016
102
25

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
223
25

Future health applications of genomics: priorities for communication, behavioral, and social sciences research.
Colleen M McBride, Deborah Bowen, Lawrence C Brody, Celeste M Condit, Robert T Croyle, Marta Gwinn, Muin J Khoury, Laura M Koehly, Bruce R Korf, Theresa M Marteau,[...]. Am J Prev Med 2010
100
25

Underutilization of BRCA1/2 testing to guide breast cancer treatment: black and Hispanic women particularly at risk.
Douglas E Levy, Stacey D Byfield, Catherine B Comstock, Judy E Garber, Sapna Syngal, William H Crown, Alexandra E Shields. Genet Med 2011
149
25

From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
48
25

The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017
60
25

Telephone genetic counseling for high-risk women undergoing BRCA1 and BRCA2 testing: rationale and development of a randomized controlled trial.
Beth N Peshkin, Tiffani A Demarco, Kristi D Graves, Karen Brown, Rachel H Nusbaum, Diana Moglia, Andrea Forman, Heiddis Valdimarsdottir, Marc D Schwartz. Genet Test 2008
42
16


Expert and Advocacy Group Consensus Findings on the Horizon of Public Health Genetic Testing.
Stephen M Modell, Karen Greendale, Toby Citrin, Sharon L R Kardia. Healthcare (Basel) 2016
13
16


How race becomes biology: embodiment of social inequality.
Clarence C Gravlee. Am J Phys Anthropol 2009
171
16

Using a Historical Lens to Envision the Next Generation of Genomic Translation Research.
Colleen M McBride, Leah R Abrams, Laura M Koehly. Public Health Genomics 2015
5
40

Validation of an Efficient Screening Tool to Identify Low-Income Women at High Risk for Hereditary Breast Cancer.
Susan L Stewart, Celia P Kaplan, Robin Lee, Galen Joseph, Leah Karliner, Jennifer Livaudais-Toman, Rena J Pasick. Public Health Genomics 2016
10
20

Genomic Disparities in Breast Cancer Among Latinas.
Filipa Lynce, Kristi D Graves, Lina Jandorf, Charite Ricker, Eida Castro, Laura Moreno, Bianca Augusto, Laura Fejerman, Susan T Vadaparampil. Cancer Control 2016
23
16

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
52
16

Educating underserved Latino communities about family health history using lay health advisors.
K A Kaphingst, C R Lachance, A Gepp, L Hoyt D'Anna, B Rios-Ellis. Public Health Genomics 2011
29
16

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
16

Awareness of cancer susceptibility genetic testing: the 2000, 2005, and 2010 National Health Interview Surveys.
Phuong L Mai, Susan Thomas Vadaparampil, Nancy Breen, Timothy S McNeel, Louise Wideroff, Barry I Graubard. Am J Prev Med 2014
67
16

Racial and ethnic disparities in awareness of genetic testing for cancer risk.
José A Pagán, Dejun Su, Lifeng Li, Katrina Armstrong, David A Asch. Am J Prev Med 2009
64
16

Genetic counseling gone awry: miscommunication between prenatal genetic service providers and Mexican-origin clients.
C H Browner, H Mabel Preloran, Maria Christina Casado, Harold N Bass, Ann P Walker. Soc Sci Med 2003
61
16

Family communication of BRCA1/2 results and family uptake of BRCA1/2 testing in a diverse population of BRCA1/2 carriers.
Julia Fehniger, Feng Lin, Mary S Beattie, Galen Joseph, Celia Kaplan. J Genet Couns 2013
42
16

Randomized trial of a web-based survivor intervention on melanoma prevention behaviors of first-degree relatives.
Deborah J Bowen, Jennifer Hay, Hendrika Meischke, Joni A Mayer, Julie Harris-Wai, Wylie Burke. Cancer Causes Control 2019
6
33

ACE gene haplotypes and social networks: Using a biocultural framework to investigate blood pressure variation in African Americans.
Kia C Fuller, Christopher McCarty, Cynthia Seaborn, Clarence C Gravlee, Connie J Mulligan. PLoS One 2018
4
50

Tracking the dissemination of a culturally targeted brochure to promote awareness of hereditary breast and ovarian cancer among Black women.
Courtney Lynam Scherr, Linda Bomboka, Alison Nelson, Tuya Pal, Susan Thomas Vadaparampil. Patient Educ Couns 2017
7
28

Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts.
Alanna Kulchak Rahm, Deborah Cragun, Jessica Ezzell Hunter, Mara M Epstein, Jan Lowery, Christine Y Lu, Pamala A Pawloski, Ravi N Sharaf, Su-Ying Liang, Andrea N Burnett-Hartman,[...]. BMC Health Serv Res 2018
14
16

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017
725
16


Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.
Beth Anderson, Jennifer McLosky, Elizabeth Wasilevich, Sarah Lyon-Callo, Debra Duquette, Glenn Copeland. J Cancer Epidemiol 2012
58
16


Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.
Deborah Cragun, Anne Weidner, Courtney Lewis, Devon Bonner, Jongphil Kim, Susan T Vadaparampil, Tuya Pal. Cancer 2017
76
16


Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
Megan C Roberts, W David Dotson, Christopher S DeVore, Erica M Bednar, Deborah J Bowen, Theodore G Ganiats, Ridgely Fisk Green, Georgia M Hurst, Alisdair R Philp, Charité N Ricker,[...]. Health Aff (Millwood) 2018
40
16

Li-Fraumeni syndrome--a molecular and clinical review.
J M Varley, D G Evans, J M Birch. Br J Cancer 1997
236
8

Inherited susceptibility to common cancers.
William D Foulkes. N Engl J Med 2008
305
8



Building a tool to identify risk for Lynch syndrome among individuals presenting for screening colonoscopy.
Deborah Rabinowitz-Abrams, Debra Morgan, James Morse, Susan Miesfeldt. J Genet Couns 2010
1
100


Development and validation of a simple questionnaire for the identification of hereditary breast cancer in primary care.
Patricia Ashton-Prolla, Juliana Giacomazzi, Aishameriane V Schmidt, Fernanda L Roth, Edenir I Palmero, Luciane Kalakun, Ernestina S Aguiar, Susana M Moreira, Erica Batassini, Vanessa Belo-Reyes,[...]. BMC Cancer 2009
38
8

Population prevalence of hereditary breast cancer phenotypes and implementation of a genetic cancer risk assessment program in southern Brazil.
Edenir I Palmero, Maira Caleffi, Lavínia Schüler-Faccini, Fernanda L Roth, Luciane Kalakun, Cristina Brinkmann Oliveira Netto, Giovana Skonieski, Juliana Giacomazzi, Bernadete Weber, Roberto Giugliani,[...]. Genet Mol Biol 2009
15
8


The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees' outcome.
Ulla Platten, Johanna Rantala, Annika Lindblom, Yvonne Brandberg, Gunilla Lindgren, Brita Arver. Fam Cancer 2012
28
8

Knowledge and perceptions of familial and genetic risks for breast cancer risk in adolescent girls.
Angela R Bradbury, Linda Patrick-Miller, Brian L Egleston, Lisa A Schwartz, Colleen B Sands, Rebecca Shorter, Cynthia W Moore, Lisa Tuchman, Paula Rauch, Shreya Malhotra,[...]. Breast Cancer Res Treat 2012
21
8

Consistency of self-reported first-degree family history of cancer in a population-based study.
Fernanda Lenara Roth, Suzi Alves Camey, Maira Caleffi, Lavínia Schuler-Faccini, Edenir Inêz Palmero, Carla Bochi, Susana Mayer Moreira, Luciane Kalakun, Roberto Giugliani, Patrícia Ashton-Prolla. Fam Cancer 2009
16
8


[Genetic counseling about cancer in Peru].
Javier E Manrique, Yasser Sullcahuamán-Allende, Abel Limache-García. Rev Peru Med Exp Salud Publica 2013
3
33


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.