A citation-based method for searching scientific literature

Catalina Villegas, Susanne B Haga. J Pers Med 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
114
54

Genetics workforce: distribution of genetics services and challenges to health care in California.
Monica Penon-Portmann, Jiyoo Chang, Mira Cheng, Joseph T Shieh. Genet Med 2020
14
36

Analysis of Advantages, Limitations, and Barriers of Genetic Counseling Service Delivery Models.
Stephanie A Cohen, Rachelle C Huziak, Shanna Gustafson, Robin E Grubs. J Genet Couns 2016
33
27

Current conditions in medical genetics practice.
Deborah R Maiese, Alisha Keehn, Megan Lyon, David Flannery, Michael Watson. Genet Med 2019
41
27

Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?
Kathryn A Phillips, Patricia A Deverka, Gillian W Hooker, Michael P Douglas. Health Aff (Millwood) 2018
67
27

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
27

Differences in BRCA counseling and testing practices based on ordering provider type.
Deborah Cragun, Lucia Camperlengo, Emily Robinson, Meghan Caldwell, Jongphil Kim, Catherine Phelan, Alvaro N Monteiro, Susan T Vadaparampil, Thomas A Sellers, Tuya Pal. Genet Med 2015
27
18

Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
Katrina Armstrong, Ellyn Micco, Amy Carney, Jill Stopfer, Mary Putt. JAMA 2005
281
18

Decision Making About Genetic Testing Among Women With a Personal and Family History of Breast Cancer.
Danika Scott, Sue Friedman, Melinda L Telli, Allison W Kurian. JCO Oncol Pract 2020
6
33

Confronting genetic testing disparities: knowledge is power.
Michael Hall, Olufunmilayo I Olopade. JAMA 2005
63
18

Provider Discussions of Genetic Tests With U.S. Women at Risk for a BRCA Mutation.
Leland E Hull, Jennifer S Haas, Steven R Simon. Am J Prev Med 2018
12
18


Prevalence and healthcare actions of women in a large health system with a family history meeting the 2005 USPSTF recommendation for BRCA genetic counseling referral.
Cecelia A Bellcross, Steven Leadbetter, Sharon Hensley Alford, Lucy A Peipins. Cancer Epidemiol Biomarkers Prev 2013
41
18

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
Douglas K Owens, Karina W Davidson, Alex H Krist, Michael J Barry, Michael Cabana, Aaron B Caughey, Chyke A Doubeni, John W Epling, Martha Kubik, C Seth Landefeld,[...]. JAMA 2019
107
18

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
63
18

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
18

Genetic counselor workflow study: The times are they a-changin'?
Courtney A Attard, Erin P Carmany, Angela M Trepanier. J Genet Couns 2019
14
18


A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling.
Barbara A Athens, Samantha L Caldwell, Kendall L Umstead, Philip D Connors, Ethan Brenna, Barbara B Biesecker. J Genet Couns 2017
36
18

Genetic counseling, 2030: An on-demand service tailored to the needs of a price conscious, genetically literate, and busy world.
Misha D Rashkin, Johnathan Bowes, Keith Dunaway, Jasmine Dhaliwal, Erick Loomis, Stephen Riffle, Nicole L Washington, Chris Ziegler, James Lu, Elissa Levin. J Genet Couns 2019
5
40

DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.
Patricia Birch, S Adam, N Bansback, R R Coe, J Hicklin, A Lehman, K C Li, J M Friedman. J Genet Couns 2016
20
18


Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
48
18

Clinical application of whole-exome sequencing across clinical indications.
Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan,[...]. Genet Med 2016
433
18

Disparities in genetic testing: thinking outside the BRCA box.
Michael J Hall, Olufunmilayo I Olopade. J Clin Oncol 2006
116
18

Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.
Anne Marie McCarthy, Mirar Bristol, Susan M Domchek, Peter W Groeneveld, Younji Kim, U Nkiru Motanya, Judy A Shea, Katrina Armstrong. J Clin Oncol 2016
73
18

Use of an educational computer program before genetic counseling for breast cancer susceptibility: effects on duration and content of counseling sessions.
Michael J Green, Susan K Peterson, Maria Wagner Baker, Lois C Friedman, Gregory R Harper, Wendy S Rubinstein, June A Peters, David T Mauger. Genet Med 2005
73
18

Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Yvonne Bombard, Marc Clausen, Salma Shickh, Chloe Mighton, Selina Casalino, Theresa H M Kim, Sarah M Muir, Lindsay Carlsson, Nancy Baxter, Adena Scheer,[...]. Genet Med 2020
7
28

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.
Yvonne Bombard, Marc Clausen, Chloe Mighton, Lindsay Carlsson, Selina Casalino, Emily Glogowski, Kasmintan Schrader, Michael Evans, Adena Scheer, Nancy Baxter,[...]. Eur J Hum Genet 2018
18
18

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.
Salma Shickh, Marc Clausen, Chloe Mighton, Selina Casalino, Esha Joshi, Emily Glogowski, Kasmintan A Schrader, Adena Scheer, Christine Elser, Seema Panchal,[...]. BMJ Open 2018
15
18

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
58
18

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
148
18

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
61
18

Predictors of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers.
K Metcalfe, S Gershman, H T Lynch, P Ghadirian, N Tung, C Kim-Sing, O I Olopade, S Domchek, J McLennan, A Eisen,[...]. Br J Cancer 2011
116
9

Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry.
Tehillah S Menes, Mary Beth Terry, David Goldgar, Irene L Andrulis, Julia A Knight, Esther M John, Yuyan Liao, Melissa Southey, Alexander Miron, Wendy Chung,[...]. Breast Cancer Res Treat 2015
14
9

Risk-reducing strategies for women carrying BRCA1/2 mutations with a focus on prophylactic surgery.
Mohamed Salhab, Selina Bismohun, Kefah Mokbel. BMC Womens Health 2010
41
9

Cancer genetic risk assessment and referral patterns in primary care.
Hetal S Vig, Joanne Armstrong, Brian L Egleston, Carla Mazar, Michele Toscano, Angela R Bradbury, Mary B Daly, Neal J Meropol. Genet Test Mol Biomarkers 2009
41
9

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
9

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
152
9

Impact of Payer Constraints on Access to Genetic Testing.
Pat Whitworth, Peter Beitsch, Christopher Arnell, Hannah C Cox, Krystal Brown, John Kidd, Johnathan M Lancaster. J Oncol Pract 2017
23
9

Health and Racial Disparity in Breast Cancer.
Clement G Yedjou, Jennifer N Sims, Lucio Miele, Felicite Noubissi, Leroy Lowe, Duber D Fonseca, Richard A Alo, Marinelle Payton, Paul B Tchounwou. Adv Exp Med Biol 2019
27
9

Mutations in context: implications of BRCA testing in diverse populations.
Gabriela E S Felix, Yonglan Zheng, Olufunmilayo I Olopade. Fam Cancer 2018
11
9

Genetic Counseling Referral Rates in Long-Term Survivors of Triple-Negative Breast Cancer.
Carlos H Barcenas, Maryam N Shafaee, Arup K Sinha, Akshara Raghavendra, Babita Saigal, Rashmi K Murthy, Ashley H Woodson, Banu Arun. J Natl Compr Canc Netw 2018
8
12

Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast Cancer.
Allison W Kurian, Yun Li, Ann S Hamilton, Kevin C Ward, Sarah T Hawley, Monica Morrow, M Chandler McLeod, Reshma Jagsi, Steven J Katz. J Clin Oncol 2017
129
9

Population-based study of the risk of second primary contralateral breast cancer associated with carrying a mutation in BRCA1 or BRCA2.
Kathleen E Malone, Colin B Begg, Robert W Haile, Ake Borg, Patrick Concannon, Lina Tellhed, Shanyan Xue, Sharon Teraoka, Leslie Bernstein, Marinela Capanu,[...]. J Clin Oncol 2010
112
9

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
82
9

Clinical genetics issues encountered by family physicians.
Louise S Acheson, Kurt C Stange, Stephen Zyzanski. Genet Med 2005
42
9

Olaparib for Metastatic Breast Cancer in Patients with a Germline BRCA Mutation.
Mark Robson, Seock-Ah Im, Elżbieta Senkus, Binghe Xu, Susan M Domchek, Norikazu Masuda, Suzette Delaloge, Wei Li, Nadine Tung, Anne Armstrong,[...]. N Engl J Med 2017
9

Risk-reducing mastectomy for the prevention of primary breast cancer.
Nora E Carbine, Liz Lostumbo, Judi Wallace, Henry Ko. Cochrane Database Syst Rev 2018
81
9

Gaps in Receipt of Clinically Indicated Genetic Counseling After Diagnosis of Breast Cancer.
Steven J Katz, Kevin C Ward, Ann S Hamilton, M Chandler Mcleod, Lauren P Wallner, Monica Morrow, Reshma Jagsi, Sarah T Hawley, Allison W Kurian. J Clin Oncol 2018
36
9


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.