A citation-based method for searching scientific literature

Marleah Dean, Ann L Tezak, Sabrina Johnson, Joy K Pierce, Anne Weidner, Kate Clouse, Tuya Pal, Deborah Cragun. Patient Educ Couns 2021
Times Cited: 7

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

Times Cited
  Times     Co-cited

Familial communication and cascade testing among relatives of BRCA population screening participants.
Sari Lieberman, Amnon Lahad, Ariela Tomer, Sivan Koka, Malka BenUziyahu, Aviad Raz, Ephrat Levy-Lahad. Genet Med 2018

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

Assessing relatives' readiness for hereditary cancer cascade genetic testing.
Erica M Bednar, Charlotte C Sun, Sheryl McCurdy, Sally W Vernon. Genet Med 2020

Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families.
Emma Healey, Natalie Taylor, Sian Greening, Claire E Wakefield, Linda Warwick, Rachel Williams, Kathy Tucker. Genet Med 2017

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

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

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

Breast cancer in the personal genomics era.
Rachel E Ellsworth, David J Decewicz, Craig D Shriver, Darrell L Ellsworth. Curr Genomics 2010

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?
Deborah J Bowen, Sukh Makhnoon, Brian H Shirts, Stephanie M Fullerton, Eric Larson, James D Ralston, Kathleen Leppig, David R Crosslin, David Veenstra, Gail P Jarvik. Patient Educ Couns 2021

Meta-analysis of BRCA1 and BRCA2 penetrance.
Sining Chen, Giovanni Parmigiani. J Clin Oncol 2007

Communication about genetic testing in families of male BRCA1/2 carriers and non-carriers: patterns, priorities and problems.
N Hallowell, A Ardern-Jones, R Eeles, C Foster, A Lucassen, C Moynihan, M Watson. Clin Genet 2005

Psychosocial and clinical factors of probands impacting intrafamilial disclosure and uptake of genetic testing among families with BRCA1/2 or MMR gene mutations.
Nathalie Alegre, Pierre Vande Perre, Yves Jean Bignon, Aude Michel, Virginie Galibert, Ornellia Mophawe, Carole Corsini, Isabelle Coupier, Jean Chiesa, Laura Robert,[...]. Psychooncology 2019

Sharing BRCA1/2 test results with first-degree relatives: factors predicting who women tell.
Andrea Farkas Patenaude, Michel Dorval, Lisa S DiGianni, Katherine A Schneider, Anu Chittenden, Judy E Garber. J Clin Oncol 2006

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

Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review.
Alison L Young, Phyllis N Butow, Janine Vetsch, Veronica F Quinn, Andrea F Patenaude, Katherine M Tucker, Claire E Wakefield. J Genet Couns 2017

A Web-Based Tool to Automate Portions of Pretest Genetic Counseling for Inherited Cancer.
Deborah Cragun, Anne Weidner, Ann Tezak, Brenda Zuniga, Georgia L Wiesner, Tuya Pal. J Natl Compr Canc Netw 2020

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

Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.
Susan M Domchek, Tara M Friebel, Christian F Singer, D Gareth Evans, Henry T Lynch, Claudine Isaacs, Judy E Garber, Susan L Neuhausen, Ellen Matloff, Rosalind Eeles,[...]. JAMA 2010

Low rates of cascade genetic testing among families with hereditary gynecologic cancer: An opportunity to improve cancer prevention.
Natalie E Griffin, Tommy R Buchanan, Stephanie H Smith, Andrea A Leon, Melissa F Meyer, Jingxia Liu, Rachel G Tabak, Katherine C Fuh, Premal H Thaker, Matthew A Powell,[...]. Gynecol Oncol 2020

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

Family communication of genetic test results among women with inherited breast cancer genes.
Deborah Cragun, Anne Weidner, Ann Tezak, Kate Clouse, Tuya Pal. J Genet Couns 2021

Talazoparib in Patients with Advanced Breast Cancer and a Germline BRCA Mutation.
Jennifer K Litton, Hope S Rugo, Johannes Ettl, Sara A Hurvitz, Anthony Gonçalves, Kyung-Hun Lee, Louis Fehrenbacher, Rinat Yerushalmi, Lida A Mina, Miguel Martin,[...]. N Engl J Med 2018

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial.
Willem Eijzenga, Eveline de Geus, Cora M Aalfs, Fred H Menko, Rolf H Sijmons, Hanneke C J M de Haes, Ellen M A Smets. Patient Educ Couns 2018

Cancer risk management among female BRCA1/2, PALB2, CHEK2, and ATM carriers.
Deborah Cragun, Anne Weidner, Ann Tezak, Kate Clouse, Tuya Pal. Breast Cancer Res Treat 2020

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

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010

Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.
Jan M Hodgson, Sylvia A Metcalfe, Maryanne Aitken, Susan M Donath, Clara L Gaff, Ingrid M Winship, Martin B Delatycki, Loane L C Skene, Belinda J McClaren, Jean L Paul,[...]. BMC Med Genet 2014

Family communication of BRCA1/2 results and family uptake of BRCA1/2 testing in a diverse population of BRCA1/2 carriers.
Julia Fehniger, Feng Lin, Mary S Beattie, Galen Joseph, Celia Kaplan. J Genet Couns 2013

Association of Germline Genetic Testing Results With Locoregional and Systemic Therapy in Patients With Breast Cancer.
Allison W Kurian, Kevin C Ward, Paul Abrahamse, Ann S Hamilton, Dennis Deapen, Monica Morrow, Reshma Jagsi, Steven J Katz. JAMA Oncol 2020

Impact of oophorectomy on cancer incidence and mortality in women with a BRCA1 or BRCA2 mutation.
Amy P M Finch, Jan Lubinski, Pål Møller, Christian F Singer, Beth Karlan, Leigha Senter, Barry Rosen, Lovise Maehle, Parviz Ghadirian, Cezary Cybulski,[...]. J Clin Oncol 2014

Precision Public Health for the Era of Precision Medicine.
Muin J Khoury, Michael F Iademarco, William T Riley. Am J Prev Med 2016

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

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

Multigene Panel Testing Detects Equal Rates of Pathogenic BRCA1/2 Mutations and has a Higher Diagnostic Yield Compared to Limited BRCA1/2 Analysis Alone in Patients at Risk for Hereditary Breast Cancer.
Nimmi S Kapoor, Lisa D Curcio, Carlee A Blakemore, Amy K Bremner, Rachel E McFarland, John G West, Kimberly C Banks. Ann Surg Oncol 2015

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study.
I van Oostrom, H Meijers-Heijboer, H J Duivenvoorden, A H J T Bröcker-Vriends, C J van Asperen, R H Sijmons, C Seynaeve, A R van Gool, J G M Klijn, A Tibben. Clin Genet 2007

Screening for fragile X syndrome: a literature review and modelling study.
F J Song, P Barton, V Sleightholme, G L Yao, A Fry-Smith. Health Technol Assess 2003

How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults.
Angela R Bradbury, James J Dignam, Comfort N Ibe, Sogyong L Auh, Fay J Hlubocky, Shelly A Cummings, Melody White, Olufunmilayo I Olopade, Christopher K Daugherty. J Clin Oncol 2007

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

Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening.
Kenneth Offit, Kaitlyn A Tkachuk, Zsofia K Stadler, Michael F Walsh, Hector Diaz-Zabala, Jeffrey D Levin, Zoe Steinsnyder, Vignesh Ravichandran, Ravi N Sharaf, Melissa K Frey,[...]. J Clin Oncol 2020

Precision Medicine: Familiarity, Perceived Health Drivers, and Genetic Testing Considerations Across Health Literacy Levels in a Diverse Sample.
Jessica R Williams, Vivian M Yeh, Marino A Bruce, Carolyn Szetela, Flora Ukoli, Consuelo H Wilkins, Sunil Kripalani. J Genet Couns 2018

Peer Support for the Hardly Reached: A Systematic Review.
Rebeccah Sokol, Edwin Fisher. Am J Public Health 2016

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.