A citation-based method for searching scientific literature

Jessica E Baars, Margreet G E M Ausems, Els van Riel, Marijke C Kars, Eveline M A Bleiker. J Genet Couns 2016
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
37
33


The Long and Short of Genetic Counseling Summary Letters: A Case-control Study.
J Roggenbuck, R Temme, D Pond, J Baker, K Jarvis, M Liu, S Dugan, N J Mendelsohn. J Genet Couns 2015
15
33

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
42
33

Long-term satisfaction and quality of life following risk reducing surgery in BRCA1/2 mutation carriers.
Gillian W Hooker, Lesley King, Lauren Vanhusen, Kristi Graves, Beth N Peshkin, Claudine Isaacs, Kathryn L Taylor, Elizabeth Poggi, Marc D Schwartz. Hered Cancer Clin Pract 2014
20
16


Women's constructions of the 'right time' to consider decisions about risk-reducing mastectomy and risk-reducing oophorectomy.
A Fuchsia Howard, Joan L Bottorff, Lynda G Balneaves, Charmaine Kim-Sing. BMC Womens Health 2010
21
16


Fertility intentions following testing for a BRCA1 gene mutation.
Ken R Smith, Lee Ellington, Anna Y Chan, Robert T Croyle, Jeffrey R Botkin. Cancer Epidemiol Biomarkers Prev 2004
43
16

Decision support: helping patients and families to find a balance at the end of life.
Mary Ann Murray, Toba Miller, Valerie Fiset, Annette O'Connor, Mary Jane Jacobsen. Int J Palliat Nurs 2004
40
16

Perceptions of Ashkenazi Jewish breast cancer patients on genetic testing for mutations in BRCA1 and BRCA2.
K A Phillips, E Warner, W S Meschino, J Hunter, M Abdolell, G Glendon, I L Andrulis, P J Goodwin. Clin Genet 2000
38
16

Women's attitudes toward preventive strategies for hereditary breast or ovarian carcinoma differ from one country to another: differences among English, French, and Canadian women.
C M Julian-Reynier, L J Bouchard, D G Evans, F A Eisinger, W D Foulkes, B Kerr, I R Blancquaert, J P Moatti, H H Sobol. Cancer 2001
71
16

Cultural aspects of healthy BRCA carriers from two ethnocultural groups.
Alicia Navarro de Souza, Danielle Groleau, Carmen G Loiselle, William D Foulkes, Nora Wong. Qual Health Res 2014
10
16

What I wish I'd known before surgery: BRCA carriers' perspectives after bilateral salipingo-oophorectomy.
Danielle Campfield Bonadies, Anne Moyer, Ellen T Matloff. Fam Cancer 2011
39
16

Preliminary report of the relationship between experience of death of a relative, illness perception, and psychological outcome among BRCA carriers.
Dikla Samama, Ilanit Hasson-Ohayon, Shlomit Perry, Ofir Morag, Gil Goldzweig. Psychol Health Med 2014
5
20


Sources of uncertainty about daughters' breast cancer risk that emerge during genetic counseling consultations.
Carma L Bylund, Carla L Fisher, Dale Brashers, Shawna Edgerson, Emily A Glogowski, Sherry R Boyar, Yelena Kemel, Sara Spencer, David Kissane. J Genet Couns 2012
28
16

Women receiving news of a family BRCA1/2 mutation: messages of fear and empowerment.
Cheryl B Crotser, Suzanne S Dickerson. J Nurs Scholarsh 2010
14
16

Acceptance of preventive surgeries by Israeli women who had undergone BRCA testing.
Vardit Kram, Tamar Peretz, Michal Sagi. Fam Cancer 2006
24
16

Long-term patient-reported satisfaction after contralateral prophylactic mastectomy and implant reconstruction.
Starr Koslow, Lindsay A Pharmer, Amie M Scott, Michelle Stempel, Monica Morrow, Andrea L Pusic, Tari A King. Ann Surg Oncol 2013
65
16

Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award.
Mary-Claire King, Ephrat Levy-Lahad, Amnon Lahad. JAMA 2014
174
16


Facilitators and Challenges in Psychosocial Adaptation to Being at Increased Familial Risk of Breast Cancer.
Louise Heiniger, Melanie A Price, Margaret Charles, Phyllis N Butow. J Genet Couns 2015
6
16

"I do not want my baby to suffer as I did"; prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: a case report and genetic counseling considerations.
Efrat Dagan, Ruth Gershoni-Baruch, Alina Kurolap, Yael Goldberg, Georgeta Fried. Genet Test Mol Biomarkers 2014
2
50

Reproductive issues for women with BRCA mutations.
Lois C Friedman, Rita M Kramer. J Natl Cancer Inst Monogr 2005
33
16


Rethinking cultural competence.
Laurence J Kirmayer. Transcult Psychiatry 2012
149
16

Patient satisfaction and cancer-related distress among unselected Jewish women undergoing genetic testing for BRCA1 and BRCA2.
K A Metcalfe, A Poll, M Llacuachaqui, S Nanda, A Tulman, N Mian, P Sun, S A Narod. Clin Genet 2010
39
16



International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriers.
Kelly A Metcalfe, Daphna Birenbaum-Carmeli, Jan Lubinski, Jacek Gronwald, Henry Lynch, Pal Moller, Parviz Ghadirian, William D Foulkes, Jan Klijn, Eitan Friedman,[...]. Int J Cancer 2008
246
16

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
14
16

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
30
16


Parents' communication with siblings of children affected by an inherited genetic condition.
Gillian Plumridge, Alison Metcalfe, Jane Coad, Paramjit Gill. J Genet Couns 2011
20
16

Design and Feasibility of an Intervention to Support Cancer Genetic Counselees in Informing their At-Risk Relatives.
Eveline de Geus, Willem Eijzenga, Fred H Menko, Rolf H Sijmons, Hanneke C J M de Haes, Cora M Aalfs, Ellen M A Smets. J Genet Couns 2016
12
16

Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences.
Alison Metcalfe, Gill Plumridge, Jane Coad, Andrew Shanks, Paramjit Gill. Eur J Hum Genet 2011
66
16

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
16


Increased genetic counseling support improves communication of genetic information in families.
Laura E Forrest, Jo Burke, Sonya Bacic, David J Amor. Genet Med 2008
62
16


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
16

Assessment of the Readability of Genetic Counseling Patient Letters.
Emily Brown, Megan Skinner, Stephanie Ashley, Kate Reed, Shannan DeLany Dixon. J Genet Couns 2016
10
16

Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research.
Sandi Dheensa, Angela Fenwick, Shiri Shkedi-Rafid, Gillian Crawford, Anneke Lucassen. Genet Med 2016
45
16


Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery.
Ivan Eisler, Matthew Ellison, Frances Flinter, Jo Grey, Suzanne Hutchison, Carole Jackson, Louise Longworth, Rhona MacLeod, Marion McAllister, Alison Metcalfe,[...]. Eur J Hum Genet 2016
22
16

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
107
16

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
76
16


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
54
16


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.