A citation-based method for searching scientific literature


List of co-cited articles
1 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
61
100

Long-term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance.
Marc D Schwartz, Claudine Isaacs, Kristi D Graves, Elizabeth Poggi, Beth N Peshkin, Christy Gell, Clinton Finch, Scott Kelly, Kathryn L Taylor, Lauren Perley. Cancer 2012
90
50

Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
50

Impact of family history on choosing risk-reducing surgery among BRCA mutation carriers.
Krishna Singh, Jenny Lester, Beth Karlan, Catherine Bresee, Tali Geva, Ora Gordon. Am J Obstet Gynecol 2013
36
50

Motivation-based intervention to promote colonoscopy screening: an integration of a fear management model and motivational interviewing.
Watcharaporn Pengchit, Scott T Walters, Rebecca G Simmons, Wendy Kohlmann, Randall W Burt, Marc D Schwartz, Anita Y Kinney. J Health Psychol 2011
20
50

Telehealth personalized cancer risk communication to motivate colonoscopy in relatives of patients with colorectal cancer: the family CARE Randomized controlled trial.
Anita Y Kinney, Watcharaporn Boonyasiriwat, Scott T Walters, Lisa M Pappas, Antoinette M Stroup, Marc D Schwartz, Sandra L Edwards, Amy Rogers, Wendy K Kohlmann, Kenneth M Boucher,[...]. J Clin Oncol 2014
41
50

Assessment of clinical practices among cancer genetic counselors.
Deborah Wham, Thuy Vu, Gayun Chan-Smutko, Christine Kobelka, Diana Urbauer, Brandie Heald. Fam Cancer 2010
41
50

Inherited Mutations in Women With Ovarian Carcinoma.
Barbara M Norquist, Maria I Harrell, Mark F Brady, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Sarah S Bernards, Silvia Casadei, Qian Yi, Robert A Burger,[...]. JAMA Oncol 2016
335
50


Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Jason L Hornick, Chinedu I Ukaegbu, Lauren K Brais, Philip G McNamara, Robert J Mayer,[...]. J Clin Oncol 2017
165
50

Physician interpretation of variants of uncertain significance.
Sarah K Macklin, Jessica L Jackson, Paldeep S Atwal, Stephanie L Hines. Fam Cancer 2019
25
50

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
37
50

Exploring barriers to payer utilization of genetic counselors.
Nan Doyle, Allison Cirino, Amber Trivedi, Maureen Flynn. J Genet Couns 2015
7
50

Genetic counselor opinions of, and experiences with telephone communication of BRCA1/2 test results.
A R Bradbury, L Patrick-Miller, D Fetzer, B Egleston, S A Cummings, A Forman, L Bealin, C Peterson, M Corbman, J O'Connell,[...]. Clin Genet 2011
31
50

Video Education on Hereditary Breast and Ovarian Cancer (HBOC) for Physicians: an Interventional Study.
Bhuma Krishnamachari, Mahin Rehman, Jason E Cohn, Vivian Chan, Neil Modi, Ofri Leitner, Kelly Tangney, April O'Connor, William Blazey, Sharon Koehler,[...]. J Cancer Educ 2018
4
50

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
46
50

Disseminating universal genetic testing to a diverse, indigent patient population at a county hospital gynecologic oncology clinic.
Erica M Bednar, Charlotte C Sun, Bethsaida Camacho, John Terrell, Alyssa G Rieber, Lois M Ramondetta, Ralph S Freedman, Karen H Lu. Gynecol Oncol 2019
3
50

Cancer Genomics: Diversity and Disparity Across Ethnicity and Geography.
Daniel S W Tan, Tony S K Mok, Timothy R Rebbeck. J Clin Oncol 2016
88
50

Expanding the criteria for BRCA mutation testing in breast cancer survivors.
Janice S Kwon, Angelica M Gutierrez-Barrera, Diana Young, Charlotte C Sun, Molly S Daniels, Karen H Lu, Banu Arun. J Clin Oncol 2010
99
50

Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
Jeanna M McCuaig, Susan Randall Armel, Melanie Care, Alexandra Volenik, Raymond H Kim, Kelly A Metcalfe. Cancers (Basel) 2018
29
50

Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force.
Stephanie A Cohen, Monica L Marvin, Bronson D Riley, Hetal S Vig, Julie A Rousseau, Shanna L Gustafson. J Genet Couns 2013
74
50

Telemedicine uptake among Genetics Professionals in Europe: room for expansion.
Ellen Otten, Erwin Birnie, Anneke M Lucassen, Adelita V Ranchor, Irene M Van Langen. Eur J Hum Genet 2016
23
50

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
61
50

Development of a culturally tailored genetic counseling booklet about hereditary breast and ovarian cancer for Black women.
Jennifer Permuth-Wey, Susan Vadaparampil, Alnecia Rumphs, Anita Yeomans Kinney, Tuya Pal. Am J Med Genet A 2010
16
50

Low Referral Rate for Genetic Testing in Racially and Ethnically Diverse Patients Despite Universal Colorectal Cancer Screening.
Charles Muller, Sang Mee Lee, William Barge, Shazia M Siddique, Shivali Berera, Gina Wideroff, Rashmi Tondon, Jeremy Chang, Meaghan Peterson, Jessica Stoll,[...]. Clin Gastroenterol Hepatol 2018
28
50

Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
Chunling Hu, Steven N Hart, Eric C Polley, Rohan Gnanaolivu, Hermela Shimelis, Kun Y Lee, Jenna Lilyquist, Jie Na, Raymond Moore, Samuel O Antwi,[...]. JAMA 2018
159
50

Closing the gap in a generation: health equity through action on the social determinants of health.
Michael Marmot, Sharon Friel, Ruth Bell, Tanja A J Houweling, Sebastian Taylor. Lancet 2008
50

Telegenetics: a systematic review of telemedicine in genetics services.
Jennifer S Hilgart, Julie A Hayward, Bernadette Coles, Rachel Iredale. Genet Med 2012
85
50

Self administered screening for hereditary cancers in conjunction with mammography and ultrasound.
Charles H McDonnell, David J Seidenwurm, Diana E McDonnell, Kristie A Bobolis. Fam Cancer 2013
7
50

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
22
50

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
8
50

A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.
Saundra S Buys, John F Sandbach, Amanda Gammon, Gayle Patel, John Kidd, Krystal L Brown, Lavania Sharma, Jennifer Saam, Johnathan Lancaster, Mary B Daly. Cancer 2017
168
50

Possible barriers for genetic counselors returning actionable genetic research results across state lines.
Megan C Roberts, Elisabeth M Wood, Jill Bennett Gaieski, Angela R Bradbury. Genet Med 2017
7
50

Achieving cultural appropriateness in health promotion programs: targeted and tailored approaches.
Matthew W Kreuter, Susan N Lukwago, R D Dawn C Bucholtz, Eddie M Clark, Vetta Sanders-Thompson. Health Educ Behav 2003
547
50


Missed opportunities: Genetic counseling and testing among an ethnically diverse cohort of women with endometrial cancer.
Jessica Lee, Lindsay R Gubernick, Allison L Brodsky, Julia E Fehniger, Douglas A Levine, Deanna Gerber, Shabnam A Asgari, Anna Cantor, Jessica T Martineau, Ophira M Ginsburg,[...]. Gynecol Oncol 2018
12
50

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.
Holly K Tabor, Benjamin E Berkman, Sara Chandros Hull, Michael J Bamshad. Am J Med Genet A 2011
93
50


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
50

Telegenetics in Maine: Successful clinical and educational service delivery model developed from a 3-year pilot project.
Dale Halsey Lea, Judith L Johnson, Sara Ellingwood, Walter Allan, Arvind Patel, Rosemarie Smith. Genet Med 2005
52
50

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
50

A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment.
Erica M Bednar, Holly D Oakley, Charlotte C Sun, Catherine C Burke, Mark F Munsell, Shannon N Westin, Karen H Lu. Gynecol Oncol 2017
26
50

Genetics/genomics education for nongenetic health professionals: a systematic literature review.
Divya Talwar, Tung-Sung Tseng, Margaret Foster, Lei Xu, Lei-Shih Chen. Genet Med 2017
38
50

Telegenetics use in presymptomatic genetic counselling: patient evaluations on satisfaction and quality of care.
Ellen Otten, Erwin Birnie, Adelita V Ranchor, Irene M van Langen. Eur J Hum Genet 2016
23
50

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
50

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
50


Underuse of BRCA testing in patients with breast and ovarian cancer.
Jason D Wright, Ling Chen, Ana I Tergas, Melissa Accordino, Cande V Ananth, Alfred I Neugut, Dawn L Hershman. Am J Obstet Gynecol 2016
25
50


Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results.
Angela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, Michael J Hall, Susan M Domchek, Mary B Daly, Pamela Ganschow, Generosa Grana, Olufunmilayo I Olopade, Dominique Fetzer,[...]. J Natl Cancer Inst 2018
20
50


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.