A citation-based method for searching scientific literature

Laura E Forrest, Jo Burke, Sonya Bacic, David J Amor. Genet Med 2008
Times Cited: 61







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



Times Cited
  Times     Co-cited
Similarity



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
36

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
52


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
26

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
26

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
24

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
32

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
74
22

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
19

The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.
Erica Sermijn, Liesbeth Delesie, Ellen Deschepper, Ingrid Pauwels, Maryse Bonduelle, Erik Teugels, Jacques De Grève. Fam Cancer 2016
29
41

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
18

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
35

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
21

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
16


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
45
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
14

Guidelines for disclosing genetic information to family members: from development to use.
Béatrice Godard, Thierry Hurlimann, Martin Letendre, Nathalie Egalité. Fam Cancer 2006
55
16

Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients.
Karin Landsbergen, Chris Verhaak, Floor Kraaimaat, Nicoline Hoogerbrugge. Fam Cancer 2005
53
16

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
39


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
42

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
16

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
13

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
21

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
13

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
13

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
27

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

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
11

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
39
17

Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.
N Hallowell, C Foster, R Eeles, A Ardern-Jones, V Murday, M Watson. J Med Ethics 2003
119
9

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
367
9

Health first, genetics second: exploring families' experiences of communicating genetic information.
Laura E Forrest, Lisette Curnow, Martin B Delatycki, Loane Skene, Maryanne Aitken. Eur J Hum Genet 2008
30
20

Comparison of genetic services with and without genetic registers: access and attitudes to genetic counselling services among relatives of genetic clinic patients.
L Kerzin-Storrar, C Wright, P R Williamson, A Fryer, A Njindou, O Quarrell, D Donnai, D Craufurd. J Med Genet 2002
21
28

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
9

Communicating genetic test results to the family: a six-step, skills-building strategy.
M B Daly, A Barsevick, S M Miller, R Buckman, J Costalas, S Montgomery, R Bingler. Fam Community Health 2001
59
10

Communication of BRCA1 and BRCA2 results to at-risk relatives: a cancer risk assessment program's experience.
Josephine Wagner Costalas, Mark Itzen, John Malick, James S Babb, Betsy Bove, Andrew K Godwin, Mary B Daly. Am J Med Genet C Semin Med Genet 2003
96
9

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
12

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
16

Informing family members about a hereditary predisposition to cancer: attitudes and practices among clinical geneticists.
Yrrah H Stol, Fred H Menko, Marjan J Westerman, Rien M J P A Janssens. J Med Ethics 2010
18
33

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
10

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
18
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.