A citation-based method for searching scientific literature

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
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
100

Improving referral for genetic risk assessment in ovarian cancer using an electronic medical record system.
Sue V Petzel, Rachel Isaksson Vogel, Jena McNiel, Anna Leininger, Peter A Argenta, Melissa A Geller. Int J Gynecol Cancer 2014
21
100

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
66

Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.
Goli Samimi, Marcus Q Bernardini, Lawrence C Brody, Charlisse F Caga-Anan, Ian G Campbell, Georgia Chenevix-Trench, Fergus J Couch, Michael Dean, Joanne A de Hullu, Susan M Domchek,[...]. J Clin Oncol 2017
33
66

Does the diagnosis of breast or ovarian cancer trigger referral to genetic counseling?
C Bethan Powell, Ramey Littell, Elizabeth Hoodfar, Fiona Sinclair, Alice Pressman. Int J Gynecol Cancer 2013
37
66

Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda.
Enola Proctor, Hiie Silmere, Ramesh Raghavan, Peter Hovmand, Greg Aarons, Alicia Bunger, Richard Griffey, Melissa Hensley. Adm Policy Ment Health 2011
66

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
66

Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer.
F G J Kallenberg, C M Aalfs, F O The, C A Wientjes, A C Depla, M W Mundt, P M M Bossuyt, E Dekker. Fam Cancer 2018
7
66

Using behaviour change and implementation science to address low referral rates in oncology.
Janet C Long, Deborah Debono, Rachel Williams, Elizabeth Salisbury, Sharron O'Neill, Elizabeth Eykman, Jordan Butler, Robert Rawson, Kim-Chi Phan-Thien, Stephen R Thompson,[...]. BMC Health Serv Res 2018
11
66

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
66

Genetic consultation embedded in a gynecologic oncology clinic improves compliance with guideline-based care.
Leigha Senter, David M O'Malley, Floor J Backes, Larry J Copeland, Jeffery M Fowler, Ritu Salani, David E Cohn. Gynecol Oncol 2017
21
66

Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing.
Paul A Cohen, Cassandra B Nichols, Lyn Schofield, Steven Van Der Werf, Nicholas Pachter. Int J Gynecol Cancer 2016
18
66

Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis.
Casey L Swanson, Amanika Kumar, Joy M Maharaj, Jennifer L Kemppainen, Brittany C Thomas, Megan R Weinhold, Kristine M Slaby, Kristin C Mara, Myra J Wick, Jamie N Bakkum-Gamez. Gynecol Oncol 2018
13
66

Association of patient navigation with care coordination in an Lynch syndrome screening program.
Susan Miesfeldt, W Gregory Feero, Frances L Lucas, Karen Rasmussen. Transl Behav Med 2018
7
66

Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice.
Stacey A Cohen, Mercy Laurino, Deborah J Bowen, Melissa P Upton, Colin Pritchard, Fuki Hisama, Gail Jarvik, Alessandro Fichera, Britta Sjoding, Robin L Bennett,[...]. Cancer 2016
19
66

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
33


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
33

Physician interpretation of variants of uncertain significance.
Sarah K Macklin, Jessica L Jackson, Paldeep S Atwal, Stephanie L Hines. Fam Cancer 2019
25
33

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
33

Exploring barriers to payer utilization of genetic counselors.
Nan Doyle, Allison Cirino, Amber Trivedi, Maureen Flynn. J Genet Couns 2015
7
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

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
33

Telegenetics: a systematic review of telemedicine in genetics services.
Jennifer S Hilgart, Julie A Hayward, Bernadette Coles, Rachel Iredale. Genet Med 2012
85
33

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
33

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
33

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
33

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
33

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
33

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
33


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
33

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
33


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
33

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
33

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
33

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
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.