A citation-based method for searching scientific literature

Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
Times Cited: 74







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



Times Cited
  Times     Co-cited
Similarity



Process and outcome in communication of genetic information within families: a systematic review.
Clara L Gaff, Angus J Clarke, Paul Atkinson, Stephanie Sivell, Glyn Elwyn, Rachel Iredale, Hazel Thornton, Joanna Dundon, Chris Shaw, Adrian Edwards. Eur J Hum Genet 2007
147
41

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
237
29



Family communication about genetic risk: the little that is known.
Brenda J Wilson, Karen Forrest, Edwin R van Teijlingen, Lorna McKee, Neva Haites, Eric Matthews, Sheila A Simpson. Community Genet 2004
114
24

Family communication about positive BRCA1 and BRCA2 genetic test results.
Bobbi McGivern, Jessica Everett, Geoffrey G Yager, Robert C Baumiller, Amanda Hafertepen, Howard M Saal. Genet Med 2004
89
22

Factors determining dissemination of results and uptake of genetic testing in families with known BRCA1/2 mutations.
Esme Finlay, Jill E Stopfer, Eric Burlingame, Katherine Goldfeder Evans, Katherine L Nathanson, Barbara L Weber, Katrina Armstrong, Timothy R Rebbeck, Susan M Domchek. Genet Test 2008
100
20

Guidelines for disclosing genetic information to family members: from development to use.
Béatrice Godard, Thierry Hurlimann, Martin Letendre, Nathalie Egalité. Fam Cancer 2006
55
27

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
104
18

Increased genetic counseling support improves communication of genetic information in families.
Laura E Forrest, Jo Burke, Sonya Bacic, David J Amor. Genet Med 2008
61
22

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
46
30



All in the family: evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results.
Chanita Hughes, Caryn Lerman, Marc Schwartz, Beth N Peshkin, Lari Wenzel, Steven Narod, Camille Corio, Kenneth P Tercyak, Danielle Hanna, Claudine Isaacs,[...]. Am J Med Genet 2002
155
17

A social network analysis of communication about hereditary nonpolyposis colorectal cancer genetic testing and family functioning.
Laura M Koehly, Susan K Peterson, Beatty G Watts, Kari K G Kempf, Sally W Vernon, Ellen R Gritz. Cancer Epidemiol Biomarkers Prev 2003
109
17

Communicating BRCA1/2 genetic test results within the family: a qualitative analysis.
Caroline Dancyger, Mel Wiseman, Chris Jacobs, Jonathan A Smith, Melissa Wallace, Susan Michie. Psychol Health 2011
37
35

Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients.
Erna Claes, Gerry Evers-Kiebooms, Andrea Boogaerts, Marleen Decruyenaere, Lieve Denayer, Eric Legius. Am J Med Genet A 2003
158
17

Communicating genetic information in families--a review of guidelines and position papers.
Laura E Forrest, Martin B Delatycki, Loane Skene, MaryAnne Aitken. Eur J Hum Genet 2007
84
17

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
57
22

How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence.
Álvaro Mendes, Milena Paneque, Liliana Sousa, Angus Clarke, Jorge Sequeiros. Eur J Hum Genet 2016
36
33

Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessment.
Deborah J MacDonald, Linda Sarna, Gwen van Servellen, Roshan Bastani, Joyce Newman Giger, Jeffrey N Weitzel. Genet Med 2007
48
22

Family communication regarding inherited high cholesterol: why and how do patients disclose genetic risk?
Hélène W P van den Nieuwenhoff, Ilse Mesters, Caroline Gielen, Nanne K de Vries. Soc Sci Med 2007
38
28

A family genetic risk communication framework: guiding tool development in genetics health services.
Miriam E Wiens, Brenda J Wilson, Christina Honeywell, Holly Etchegary. J Community Genet 2013
29
37

An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations.
Paboda Ratnayake, Claire E Wakefield, Bettina Meiser, Graeme Suthers, Melanie A Price, Jessica Duffy, Kathy Tucker. Fam Cancer 2011
23
43

Family letters are an effective way to inform relatives about inherited cardiac disease.
Wilma P van der Roest, José M Pennings, Marian Bakker, Maarten P van den Berg, J Peter van Tintelen. Am J Med Genet A 2009
53
18

Facilitating family communication about predictive genetic testing: probands' perceptions.
Clara L Gaff, Veronica Collins, Tiffany Symes, Jane Halliday. J Genet Couns 2005
72
13

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
32


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
79
13

Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing.
K Aktan-Collan, A Haukkala, K Pylvänäinen, H J Järvinen, L A Aaltonen, P Peltomäki, E Rantanen, H Kääriäinen, J-P Mecklin. J Med Genet 2007
51
17

Genetic professionals' reports of nondisclosure of genetic risk information within families.
Angus Clarke, Martin Richards, Lauren Kerzin-Storrar, Jane Halliday, Mary Anne Young, Sheila A Simpson, Katie Featherstone, Karen Forrest, Anneke Lucassen, Patrick J Morrison,[...]. Eur J Hum Genet 2005
71
12

How families communicate about HNPCC genetic testing: findings from a qualitative study.
Susan K Peterson, Beatty G Watts, Laura M Koehly, Sally W Vernon, Walter F Baile, Wendy K Kohlmann, Ellen R Gritz. Am J Med Genet C Semin Med Genet 2003
109
12

Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.
R Beth Dugan, Georgia L Wiesner, Eric T Juengst, Maryann O'Riordan, Anne L Matthews, Nathaniel H Robin. Am J Med Genet C Semin Med Genet 2003
73
12

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
38
23

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
122
10

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
85
10


A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome.
Ani Kardashian, Julia Fehniger, Jennifer Creasman, Eleanor Cheung, Mary Stanley Beattie. Hered Cancer Clin Pract 2012
21
38

Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives.
Afsaneh Hayat Roshanai, Claudia Lampic, Richard Rosenquist, Karin Nordin. Fam Cancer 2010
13
53

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
62
11


Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy.
Imke Christiaans, Erwin Birnie, Gouke J Bonsel, Arthur Am Wilde, Irene M van Langen. Eur J Hum Genet 2008
70
10

Medical Geneticists' duty to warn at-risk relatives for genetic disease.
Marni J Falk, R Beth Dugan, Mary Ann O'Riordan, Anne L Matthews, Nathaniel H Robin. Am J Med Genet A 2003
62
11

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
46
15

Family Communication in Inherited Cardiovascular Conditions in Ireland.
Sinead Whyte, Andrew Green, Marion McAllister, Hannah Shipman. J Genet Couns 2016
11
63


Openness to discuss cancer in the nuclear family: scale, development, and validation.
I Mesters, H van den Borne, L McCormick, J Pruyn, M de Boer, T Imbos. Psychosom Med 1997
77
8

Toward a biopsychosocial model for 21st-century genetics.
John S Rolland, Janet K Williams. Fam Process 2005
120
8

Intention to communicate BRCA1/BRCA2 genetic test results to the family.
Andrea M Barsevick, Susan V Montgomery, Karen Ruth, Eric A Ross, Brian L Egleston, Ruth Bingler, John Malick, Suzanne M Miller, Terrence P Cescon, Mary B Daly. J Fam Psychol 2008
27
22


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.