A citation-based method for searching scientific literature

Morgan Butrick, Scott Kelly, Beth N Peshkin, George Luta, Rachel Nusbaum, Gillian W Hooker, Kristi Graves, Lisa Feeley, Claudine Isaacs, Heiddis B Valdimarsdottir, Lina Jandorf, Tiffani DeMarco, Marie Wood, Wendy McKinnon, Judy Garber, Shelley R McCormick, Marc D Schwartz. Genet Med 2015
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity


Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review.
Juan R Canedo, Stephania T Miller, Hector F Myers, Maureen Sanderson. J Genet Couns 2019
16
18

Interest and beliefs about BRCA genetic counseling among at-risk Latinas in New York City.
Katarina M Sussner, Lina Jandorf, Hayley S Thompson, Heiddis B Valdimarsdottir. J Genet Couns 2010
29
10

Trends in utilization and costs of BRCA testing among women aged 18-64 years in the United States, 2003-2014.
Zhuo Chen, Katherine Kolor, Scott D Grosse, Juan L Rodriguez, Julie A Lynch, Ridgely Fisk Green, W David Dotson, M Scott Bowen, Muin J Khoury. Genet Med 2018
26
11

Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.
Jennifer L Caswell-Jin, Anjali D Zimmer, Will Stedden, Kerry E Kingham, Alicia Y Zhou, Allison W Kurian. J Natl Cancer Inst 2019
31
9

Telegenetics: a systematic review of telemedicine in genetics services.
Jennifer S Hilgart, Julie A Hayward, Bernadette Coles, Rachel Iredale. Genet Med 2012
76
5

A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.
Kurt D Christensen, Wendy R Uhlmann, J Scott Roberts, Erin Linnenbringer, Peter J Whitehouse, Charmaine D M Royal, Thomas O Obisesan, L Adrienne Cupples, Melissa B Butson, Grace-Ann Fasaye,[...]. Genet Med 2018
21
14

Service Delivery Model and Experiences in a Cancer Genetics Clinic for an Underserved Population.
Ashley H Woodson, Jessica L Profato, Minjeong Park, Sarah H Rizvi, Nisreen Elsayegh, Alyssa G Rieber, Banu K Arun. J Health Care Poor Underserved 2015
7
42

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018
40
7

Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population.
Cecelia A Bellcross, Amy A Lemke, Laura S Pape, Angela L Tess, Lorraine T Meisner. Genet Med 2009
65
5

A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings.
Huma Q Rana, Sarah R Cochrane, Elaine Hiller, Ruth N Akindele, Callie M Nibecker, Ludmila A Svoboda, Angel M Cronin, Judy E Garber, Christopher S Lathan. J Community Genet 2018
7
42

Predictors of BRCA1/2 genetic testing among Black women with breast cancer: a population-based study.
Tarsha Jones, Anne Marie McCarthy, Younji Kim, Katrina Armstrong. Cancer Med 2017
27
11



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
7


The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
Fred H Menko, Jacqueline A Ter Stege, Lizet E van der Kolk, Kiki N Jeanson, Winnie Schats, Daoud Ait Moha, Eveline M A Bleiker. Fam Cancer 2019
32
9

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
60

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
761
5

Assessment of the Effectiveness of Genetic Counseling by Telephone Compared to a Clinic Visit.
Karan K Sangha, Anita Dircks, Sylvie Langlois. J Genet Couns 2003
27
7


Report from the National Society of Genetic Counselors service delivery model task force: a proposal to define models, components, and modes of referral.
Stephanie A Cohen, Shanna L Gustafson, Monica L Marvin, Bronson D Riley, Wendy R Uhlmann, S Bonnie Liebers, Julie A Rousseau. J Genet Couns 2012
42
4

Results of a randomized study of telephone versus in-person breast cancer risk counseling.
Almut W Helmes, Julie O Culver, Deborah J Bowen. Patient Educ Couns 2006
51
3

Errors in delivery of cancer genetics services: implications for practice.
Karina L Brierley, Danielle Campfield, Whitney Ducaine, Lindsay Dohany, Talia Donenberg, Kristen Shannon, Robin C Schwartz, Ellen T Matloff. Conn Med 2010
64
3


BRCA in breast cancer: ESMO Clinical Practice Guidelines.
J Balmaña, O Díez, I T Rubio, F Cardoso. Ann Oncol 2011
112
3

A rapid genetic counselling and testing in newly diagnosed breast cancer is associated with high rate of risk-reducing mastectomy in BRCA1/2-positive Italian women.
L Cortesi, E Razzaboni, A Toss, E De Matteis, I Marchi, V Medici, G Tazzioli, A Andreotti, G De Santis, M Pignatti,[...]. Ann Oncol 2014
23
8

Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians.
L Wideroff, S T Vadaparampil, M H Greene, S Taplin, L Olson, A N Freedman. J Med Genet 2005
108
3


Family history-taking in community family practice: implications for genetic screening.
L S Acheson, G L Wiesner, S J Zyzanski, M A Goodwin, K C Stange. Genet Med 2000
174
3

Limited family structure and BRCA gene mutation status in single cases of breast cancer.
Jeffrey N Weitzel, Veronica I Lagos, Carey A Cullinane, Patricia J Gambol, Julie O Culver, Kathleen R Blazer, Melanie R Palomares, Katrina J Lowstuter, Deborah J MacDonald. JAMA 2007
130
3

Use of a web-based risk appraisal tool for assessing family history and lifestyle factors in primary care.
Heather J Baer, Louise I Schneider, Graham A Colditz, Hank Dart, Analisa Andry, Deborah H Williams, E John Orav, Jennifer S Haas, George Getty, Elizabeth Whittemore,[...]. J Gen Intern Med 2013
24
8

Development of a risk assessment tool for women with a family history of breast cancer.
Dejana Braithwaite, Stephen Sutton, James Mackay, Judith Stein, Jon Emery. Cancer Detect Prev 2005
24
8

Validation of My Family Health Portrait for six common heritable conditions.
Flavia M Facio, W Gregory Feero, Amy Linn, Neal Oden, Kandamurugu Manickam, Leslie G Biesecker. Genet Med 2010
54
3


Cancer risk assessment: quality and impact of the family history interview.
Harvey J Murff, Daniel Byrne, Sapna Syngal. Am J Prev Med 2004
78
3



Factors associated with psychological distress among women of African descent at high risk for BRCA mutations.
Yael R Cukier, Hayley S Thompson, Katarina Sussner, Andrea Forman, Lina Jandorf, Tiffany Edwards, Dana H Bovbjerg, Marc D Schwartz, Heiddis B Valdimarsdottir. J Genet Couns 2013
12
16

Effect of routine assessment of specific psychosocial problems on personalized communication, counselors’ awareness, and distress levels in cancer genetic counseling practice: a randomized controlled trial.
Willem Eijzenga, Neil K Aaronson, Daniela E E Hahn, Grace N Sidharta, Lizet E van der Kolk, Mary E Velthuizen, Margreet G E M Ausems, Eveline M A Bleiker. J Clin Oncol 2014
15
13

Evaluation of a clinical genetics service--a quality initiative.
Alison M Elliott, Bernard N Chodirker, Patricia Bocangel, Aizeddin A Mhanni. J Genet Couns 2014
3
66

Linking genetic counseling content to short-term outcomes in individuals at elevated breast cancer risk.
Kimberly M Kelly, Lee Ellington, Nancy Schoenberg, Parul Agarwal, Thomas Jackson, Stephanie Dickinson, Jame Abraham, Electra D Paskett, Howard Leventhal, Michael Andrykowski. J Genet Couns 2014
9
22

Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition.
Linda J Patrick-Miller, Brian L Egleston, Dominique Fetzer, Andrea Forman, Lisa Bealin, Christina Rybak, Candace Peterson, Melanie Corbman, Julio Albarracin, Evelyn Stevens,[...]. JMIR Res Protoc 2014
17
11

Ethnic, racial and cultural identity and perceived benefits and barriers related to genetic testing for breast cancer among at-risk women of African descent in New York City.
K M Sussner, T A Edwards, H S Thompson, L Jandorf, N O Kwate, A Forman, K Brown, N Kapil-Pair, D H Bovbjerg, M D Schwartz,[...]. Public Health Genomics 2011
26
7


Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers.
Allison W Kurian, Bronislava M Sigal, Sylvia K Plevritis. J Clin Oncol 2010
150
3

DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct.
Aisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Arjen R Mensenkamp, Marjolijn J Ligtenberg, Han G Brunner, Judith B Prins, Nicoline Hoogerbrugge. BMC Womens Health 2012
11
18


The contribution of BRCA1 and BRCA2 to ovarian cancer.
Susan J Ramus, Simon A Gayther. Mol Oncol 2009
105
3

Screening for founder mutations in BRCA1 and BRCA2 in unselected Jewish women.
Kelly A Metcalfe, Aletta Poll, Robert Royer, Marcia Llacuachaqui, Anna Tulman, Ping Sun, Steven A Narod. J Clin Oncol 2010
103
3

Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis.
Dejana Braithwaite, Jon Emery, Fiona Walter, A Toby Prevost, Stephen Sutton. Fam Cancer 2006
63
3


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.