A citation-based method for searching scientific literature

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, Rebecca A Campo, Kristina G Flores, Jeanne S Mandelblatt, Marc D Schwartz. J Clin Oncol 2016
Times Cited: 57







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



Times Cited
  Times     Co-cited
Similarity


Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
11

The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.
Caroline S Bennette, Carlos J Gallego, Wylie Burke, Gail P Jarvik, David L Veenstra. Genet Med 2015
61
3

Use of Cancer Genetics Services in African-American Young Breast Cancer Survivors.
Tarsha Jones, Joan S Lockhart, Kari E Mendelsohn-Victor, Debra Duquette, Laurel L Northouse, Sonia A Duffy, Rosemary Donley, Sofia D Merajver, Kara J Milliron, J Scott Roberts,[...]. Am J Prev Med 2016
28
7

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
19
10

The evolution of cancer risk assessment in the era of next generation sequencing.
Heather Fecteau, Kristen J Vogel, Kristen Hanson, Shannon Morrill-Cornelius. J Genet Couns 2014
42
4

Cancer risk assessment using genetic panel testing: considerations for clinical application.
Susan Hiraki, Erica S Rinella, Freya Schnabel, Ruth Oratz, Harry Ostrer. J Genet Couns 2014
27
7


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
40
5

Concerns about cancer risk and experiences with genetic testing in a diverse population of patients with breast cancer.
Reshma Jagsi, Kent A Griffith, Allison W Kurian, Monica Morrow, Ann S Hamilton, John J Graff, Steven J Katz, Sarah T Hawley. J Clin Oncol 2015
57
3

Development of the clinical next-generation sequencing industry in a shifting policy climate.
Margaret A Curnutte, Karen L Frumovitz, Juli M Bollinger, Amy L McGuire, David J Kaufman. Nat Biotechnol 2014
20
10



Communication of BRCA results and family testing in 1,103 high-risk women.
Eleanor L Cheung, Ashley D Olson, Tina M Yu, Pamela Z Han, Mary S Beattie. Cancer Epidemiol Biomarkers Prev 2010
53
3

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
3

Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.
Ravi N Sharaf, Parvathi Myer, Christopher D Stave, Lisa C Diamond, Uri Ladabaum. Clin Gastroenterol Hepatol 2013
73
3

Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results.
Laura C Beamer, Marcia L Grant, Carin R Espenschied, Kathleen R Blazer, Heather L Hampel, Jeffrey N Weitzel, Deborah J MacDonald. J Clin Oncol 2012
141
3

Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial.
Susan V Montgomery, Andrea M Barsevick, Brian L Egleston, Ruth Bingler, Karen Ruth, Suzanne M Miller, John Malick, Terrence P Cescon, Mary B Daly. Fam Cancer 2013
43
4

Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical center.
Brandie Heald, Thomas Plesec, Xiuli Liu, Rish Pai, Deepa Patil, Jessica Moline, Richard R Sharp, Carol A Burke, Matthew F Kalady, James Church,[...]. J Clin Oncol 2013
115
3

Coriell Personalized Medicine Collaborative®: a prospective study of the utility of personalized medicine.
Margaret A Keller, Erynn S Gordon, Catharine B Stack, Neda Gharani, Courtney J Sill, Tara J Schmidlen, Mintzer Joseph, John Pallies, Norman P Gerry, Michael F Christman. Per Med 2010
41
4

Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer.
Lisa R Susswein, Cécile Skrzynia, Leslie A Lange, Jessica K Booker, Mark L Graham, James P Evans. J Clin Oncol 2008
42
4

BRCA genetic counseling among at-risk Latinas in New York City: new beliefs shape new generation.
Katarina M Sussner, Tiffany Edwards, Cristina Villagra, M Carina Rodriguez, Hayley S Thompson, Lina Jandorf, Heiddis B Valdimarsdottir. J Genet Couns 2015
28
7


Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?
Deborah Cragun, Courtney Scherr, Lucia Camperlengo, Susan T Vadaparampil, Tuya Pal. Genet Test Mol Biomarkers 2016
11
18

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
323
3

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


Barriers to the use of personalized medicine in breast cancer.
Christine B Weldon, Julia R Trosman, William J Gradishar, Al B Benson, Julian C Schink. J Oncol Pract 2012
44
4


An evidence-based approach to managing women's decisional conflict.
Annette M O'Connor, Mary Jane Jacobsen, Dawn Stacey. J Obstet Gynecol Neonatal Nurs 2002
143
3

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
Mary B Daly, Robert Pilarski, Jennifer E Axilbund, Michael Berry, Saundra S Buys, Beth Crawford, Meagan Farmer, Susan Friedman, Judy E Garber, Seema Khan,[...]. J Natl Compr Canc Netw 2016
108
3


My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
17
11

Genetic testing and cancer risk management recommendations by physicians for at-risk relatives.
Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
77
3

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
230
3

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
4

Measuring numeracy without a math test: development of the Subjective Numeracy Scale.
Angela Fagerlin, Brian J Zikmund-Fisher, Peter A Ubel, Aleksandra Jankovic, Holly A Derry, Dylan M Smith. Med Decis Making 2007
402
3

Recommendations for Telephone Counseling.
K E Ormond, J Haun, L Cook, D Duquette, C Ludowese, A L Matthews. J Genet Couns 2000
24
8

Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing.
Courtney Doughty Rice, Jennifer Gamm Ruschman, Lisa J Martin, Jennifer B Manders, Erin Miller. Fam Cancer 2010
18
11


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
947
3

The Activities and Impact of State Programs to Address Hereditary Breast and Ovarian Cancer, 2011-2014.
Katrina F Trivers, Juan L Rodriguez, Summer L Cox, Barbara E Crane, Debra Duquette. Healthcare (Basel) 2015
11
18


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
8

Use of BRCA Mutation Test in the U.S., 2004-2014.
Fangjian Guo, Jacqueline M Hirth, Yu-Li Lin, Gwyn Richardson, Lyuba Levine, Abbey B Berenson, Yong-Fang Kuo. Am J Prev Med 2017
32
6

Analysis of Reimbursement of Genetic Counseling Services at a Single Institution in a State Requiring Licensure.
Jennifer R Leonhard, Paul J Munson, Jason D Flanagan, Kristen L De Berg, Paul A Thompson, Lori W Dean, Quinn P Stein. J Genet Couns 2017
9
22

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
8

The Deceptive Appeal of Direct-to-Consumer Genetics.
Wylie Burke, Susan Brown Trinidad. Ann Intern Med 2016
14
14

Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
Kara N Maxwell, Bradley Wubbenhorst, Kurt D'Andrea, Bradley Garman, Jessica M Long, Jacquelyn Powers, Katherine Rathbun, Jill E Stopfer, Jiajun Zhu, Angela R Bradbury,[...]. Genet Med 2015
89
3

Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic Testing.
Cathelijne H van der Wouden, Deanna Alexis Carere, Anke H Maitland-van der Zee, Mack T Ruffin, J Scott Roberts, Robert C Green. Ann Intern Med 2016
64
3

NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer.
Janice L Berliner, Angela Musial Fay, Shelly A Cummings, Brittany Burnett, Todd Tillmanns. J Genet Couns 2013
78
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.