A citation-based method for searching scientific literature

Sandi Dheensa, Angela Fenwick, Shiri Shkedi-Rafid, Gillian Crawford, Anneke Lucassen. Genet Med 2016
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity




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
74
29

Genetic information: a joint account?
Michael Parker, Anneke M Lucassen. BMJ 2004
74
29


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
152
27


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
88
22

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
20


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
54
18

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
20

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
39
20


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
63
14

Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information.
Rebecca D Pentz, Susan K Peterson, Beatty Watts, Sally W Vernon, Patrick M Lynch, Laura M Koehly, Ellen R Gritz. Genet Test 2005
37
18

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
75
14


Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
80
14

Guidelines for disclosing genetic information to family members: from development to use.
Béatrice Godard, Thierry Hurlimann, Martin Letendre, Nathalie Egalité. Fam Cancer 2006
56
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
30
23


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
34
20


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
48
14

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
12

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

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
31
19

Increased genetic counseling support improves communication of genetic information in families.
Laura E Forrest, Jo Burke, Sonya Bacic, David J Amor. Genet Med 2008
66
12


Supporting disclosure of genetic information to family members: professional practice and timelines in cancer genetics.
Benjamin Derbez, Antoine de Pauw, Dominique Stoppa-Lyonnet, Sandrine de Montgolfier. Fam Cancer 2017
15
40




Confidentiality and sharing genetic information with relatives.
Anneke Lucassen, Michael Parker. Lancet 2010
18
27



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
86
10


Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?
Rick D Vavolizza, Isha Kalia, Kathleen Erskine Aaron, Louise B Silverstein, Dorit Barlevy, David Wasserman, Christine Walsh, Robert W Marion, Siobhan M Dolan. J Genet Couns 2015
27
18

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
23

Am I My Family's Keeper? Disclosure Dilemmas in Next-Generation Sequencing.
Roel H P Wouters, Rhodé M Bijlsma, Margreet G E M Ausems, Johannes J M van Delden, Emile E Voest, Annelien L Bredenoord. Hum Mutat 2016
20
25

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
49
10

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
105
10

Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
Fred H Menko, Cora M Aalfs, Lidewij Henneman, Yrrah Stol, Miranda Wijdenes, Ellen Otten, Marleen M J Ploegmakers, Johan Legemaate, Ellen M A Smets, Guido M W R de Wert,[...]. Fam Cancer 2013
25
20

Genetic information and the family: are we our brother's keeper?
Bartha Maria Knoppers. Trends Biotechnol 2002
37
10

Confidentiality versus duty to inform--an empirical study on attitudes towards the handling of genetic information.
Katharina Wolff, Wibecke Brun, Gerd Kvale, Karin Nordin. Am J Med Genet A 2007
10
40

The "duty to warn" a patient's family members about hereditary disease risks.
Kenneth Offit, Elizabeth Groeger, Sam Turner, Eve A Wadsworth, Mary A Weiser. JAMA 2004
156
8

Development of the Informing Relatives Inventory (IRI): Assessing Index Patients' Knowledge, Motivation and Self-Efficacy Regarding the Disclosure of Hereditary Cancer Risk Information to Relatives.
Eveline de Geus, Cora M Aalfs, Fred H Menko, Rolf H Sijmons, Mathilde G E Verdam, Hanneke C J M de Haes, Ellen M A Smets. Int J Behav Med 2015
12
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.