A citation-based method for searching scientific literature

Alexandra Suttman, Robert Pilarski, Doreen M Agnese, Leigha Senter. J Genet Couns 2018
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity



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
33
35

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017
28


Germline BRCA1 mutations increase prostate cancer risk.
D Leongamornlert, N Mahmud, M Tymrakiewicz, E Saunders, T Dadaev, E Castro, C Goh, K Govindasami, M Guy, L O'Brien,[...]. Br J Cancer 2012
184
21

Stigmatization and male identity: Norwegian males' experience after identification as BRCA1/2 mutation carriers.
Nina Strømsvik, Målfrid Råheim, Nina Oyen, Lars Fredrik Engebretsen, Eva Gjengedal. J Genet Couns 2010
20
21

Guilt, blame and responsibility: men's understanding of their role in the transmission of BRCA1/2 mutations within their family.
Nina Hallowell, Audrey Arden-Jones, Ros Eeles, Claire Foster, Anneke Lucassen, Clare Moynihan, Maggie Watson. Sociol Health Illn 2006
75
21

"Guys Don't Have Breasts": The Lived Experience of Men Who Have BRCA Gene Mutations and Are at Risk for Male Breast Cancer.
Michelle Skop, Justin Lorentz, Mobin Jassi, Danny Vesprini, Gillian Einstein. Am J Mens Health 2018
12
25

"When information is not enough": A model for understanding BRCA-positive previvors' information needs regarding hereditary breast and ovarian cancer risk.
Marleah Dean, Courtney L Scherr, Meredith Clements, Rachel Koruo, Jennifer Martinez, Amy Ross. Patient Educ Couns 2017
25
21

Men in the women's world of hereditary breast and ovarian cancer--a systematic review.
Nina Strømsvik, Målfrid Råheim, Nina Oyen, Eva Gjengedal. Fam Cancer 2009
25
21


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
87
21

Cancer risks for men with BRCA1/2 mutations
Suzanne M Mahon. Oncol Nurs Forum 2014
9
33

Ambiguity in a masculine world: Being a BRCA1/2 mutation carrier and a man with prostate cancer.
C Moynihan, E K Bancroft, A Mitra, A Ardern-Jones, E Castro, E C Page, R A Eeles. Psychooncology 2017
9
33

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
53
21

Breast cancer risk among male BRCA1 and BRCA2 mutation carriers.
Yu Chuan Tai, Susan Domchek, Giovanni Parmigiani, Sining Chen. J Natl Cancer Inst 2007
201
21

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
21
21

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
28
21

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
53
21


BRCA1/2 genetic testing uptake and psychosocial outcomes in men.
Kristi D Graves, Rhoda Gatammah, Beth N Peshkin, Ayelet Krieger, Christy Gell, Heiddis B Valdimarsdottir, Marc D Schwartz. Fam Cancer 2011
19
21

Communication of Information about Genetic Risks: Putting Families at the Center.
Álvaro Mendes, Alison Metcalfe, Milena Paneque, Liliana Sousa, Angus J Clarke, Jorge Sequeiros. Fam Process 2018
21
14


Skin cancer risk in BRCA1/2 mutation carriers.
P V Gumaste, L A Penn, R M Cymerman, T Kirchhoff, D Polsky, B McLellan. Br J Dermatol 2015
33
14

'Cancer doesn't have an age': genetic testing and cancer risk management in BRCA1/2 mutation-positive women aged 18-24.
Allison Werner-Lin, Lindsey M Hoskins, Maya H Doyle, Mark H Greene. Health (London) 2012
31
14


To tell or not to tell: barriers and facilitators in family communication about genetic risk.
K Forrest, S A Simpson, B J Wilson, E R van Teijlingen, L McKee, N Haites, E Matthews. Clin Genet 2003
244
14

Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication.
Jan Hodgson, Sylvia Metcalfe, Clara Gaff, Susan Donath, Martin B Delatycki, Ingrid Winship, Loane Skene, MaryAnne Aitken, Jane Halliday. Eur J Hum Genet 2016
44
14

Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling.
Alvaro Mendes, Raquel Chiquelho, Teresa Almeida Santos, Liliana Sousa. J Community Genet 2010
19
14


Characteristics of health information gatherers, disseminators, and blockers within families at risk of hereditary cancer: implications for family health communication interventions.
Laura M Koehly, June A Peters, Regina Kenen, Lindsey M Hoskins, Anne L Ersig, Natalia R Kuhn, Jennifer T Loud, Mark H Greene. Am J Public Health 2009
109
14

Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study.
Lea Godino, Leigh Jackson, Daniela Turchetti, Catherine Hennessy, Heather Skirton. Eur J Hum Genet 2018
20
14

Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors.
Robin L Bennett, Kathryn Steinhaus French, Robert G Resta, Debra Lochner Doyle. J Genet Couns 2008
119
14

The impact of proband mediated information dissemination in families with a BRCA1/2 gene mutation.
E Sermijn, G Goelen, E Teugels, L Kaufman, M Bonduelle, B Neyns, B Poppe, A De Paepe, J De Grève. J Med Genet 2004
46
14

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
62
14

Genetic health professionals and the communication of genetic information in families: Practice during and after a genetic consultation.
Laura E Forrest, Martin B Delatycki, Lisette Curnow, Loane Skene, Maryanne Aitken. Am J Med Genet A 2010
31
14

Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research.
Alison Metcalfe, Jane Coad, Gill M Plumridge, Paramjit Gill, Peter Farndon. Eur J Hum Genet 2008
96
14

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
51
14

Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population.
Suzanne C O'Neill, Chalanda Evans, Rebekah J Hamilton, Beth N Peshkin, Claudine Isaacs, Sue Friedman, Kenneth P Tercyak. Fam Cancer 2018
9
22

Role of Genetic Testing for Inherited Prostate Cancer Risk: Philadelphia Prostate Cancer Consensus Conference 2017.
Veda N Giri, Karen E Knudsen, William K Kelly, Wassim Abida, Gerald L Andriole, Chris H Bangma, Justin E Bekelman, Mitchell C Benson, Amie Blanco, Arthur Burnett,[...]. J Clin Oncol 2018
109
14

Cost-effectiveness analysis of germ-line BRCA testing in women with breast cancer and cascade testing in family members of mutation carriers.
Haitham W Tuffaha, Andrew Mitchell, Robyn L Ward, Luke Connelly, James R G Butler, Sarah Norris, Paul A Scuffham. Genet Med 2018
43
14


Germline genetic testing for inherited prostate cancer in practice: Implications for genetic testing, precision therapy, and cascade testing.
Veda N Giri, Sarah E Hegarty, Colette Hyatt, Erin O'Leary, John Garcia, Karen E Knudsen, William K Kelly, Leonard G Gomella. Prostate 2019
38
14

Understanding of multigene test results among males undergoing germline testing for inherited prostate cancer: Implications for genetic counseling.
Veda N Giri, Elias Obeid, Sarah E Hegarty, Laura Gross, Lisa Bealin, Colette Hyatt, Carolyn Y Fang, Amy Leader. Prostate 2018
10
20

Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.
Elena Castro, Chee Goh, David Olmos, Ed Saunders, Daniel Leongamornlert, Malgorzata Tymrakiewicz, Nadiya Mahmud, Tokhir Dadaev, Koveela Govindasami, Michelle Guy,[...]. J Clin Oncol 2013
423
14


Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.
Bronson D Riley, Julie O Culver, Cécile Skrzynia, Leigha A Senter, June A Peters, Josephine W Costalas, Faith Callif-Daley, Sherry C Grumet, Katherine S Hunt, Rebecca S Nagy,[...]. J Genet Couns 2012
198
14

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
14

Unmet support needs and distress among women with a BRCA1/2 mutation.
Ashley Farrelly, Victoria White, Bettina Meiser, Michael Jefford, Mary-Anne Young, Sandra Ieropoli, Ingrid Winship, Jessica Duffy. Fam Cancer 2013
18
14

Young adult daughters of BRCA1/2 positive mothers: what do they know about hereditary cancer and how much do they worry?
Andrea F Patenaude, Nadine Tung, Paula D Ryan, Leif W Ellisen, Larissa Hewitt, Katherine A Schneider, Kenneth P Tercyak, Julie Aldridge, Judy E Garber. Psychooncology 2013
33
14


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.