A citation-based method for searching scientific literature

Afsaneh Hayat Roshanai, Claudia Lampic, Charlotta Ingvoldstad, Marie Stenmark Askmalm, Chathrine Bjorvatn, Richard Rosenquist, Karin Nordin. J Genet Couns 2012
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


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
40

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
110
30

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

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
30

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
76
30


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
20
30


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
59
30

Guidelines for disclosing genetic information to family members: from development to use.
Béatrice Godard, Thierry Hurlimann, Martin Letendre, Nathalie Egalité. Fam Cancer 2006
55
30

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
30

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
30


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
159
30


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
39
30


CONSORT 2010 statement: Updated guidelines for reporting parallel group randomised trials.
Kenneth F Schulz, Douglas G Altman, David Moher. J Pharmacol Pharmacother 2010
307
20

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
102
20

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
239
20

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
156
20

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
20

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
20


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
74
20

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
20

Training general practitioners in behavior change counseling to improve asthma medication adherence.
Sandra Broers, Ellen Smets, Patrick Bindels, Floor Bennebroek Evertsz', Mart Calff, Hanneke de Haes. Patient Educ Couns 2005
30
20

Information needs about hereditary breast cancer among women with early-onset breast cancer.
Wendy F Cohn, Mary E Ropka, Susan M Jones, Susan Miesfeldt. Cancer Detect Prev 2003
8
25


Prenatal counseling for congenital anomaly tests: parental preferences and perceptions of midwife performance.
L Martin, S Van Dulmen, E Spelten, A De Jonge, P De Cock, E Hutton. Prenat Diagn 2013
22
20

Informing relatives about their hereditary or familial cancer risk: study protocol for a randomized controlled trial.
Eveline de Geus, Cora M Aalfs, Mathilde G E Verdam, Hanneke C J M de Haes, Ellen M A Smets. Trials 2014
12
20

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

The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services.
D Gareth Evans, Julian Barwell, Diana M Eccles, Amanda Collins, Louise Izatt, Chris Jacobs, Alan Donaldson, Angela F Brady, Andrew Cuthbert, Rachel Harrison,[...]. Breast Cancer Res 2014
179
20

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
187
20

Subjective interpretation of inconclusive BRCA1/2 cancer genetic test results and transmission of information to the relatives.
C Cypowyj, F Eisinger, L Huiart, H Sobol, M Morin, C Julian-Reynier. Psychooncology 2009
20
20

Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer.
M Ponz de Leon, P Benatti, C Di Gregorio, M Pedroni, L Losi, M Genuardi, A Viel, M Fornasarig, E Lucci-Cordisco, M Anti,[...]. Br J Cancer 2004
51
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
10


Patients' evaluation of informed consent to postponed information: cohort study.
Han Boter, Johannes J M van Delden, Rob J de Haan, Gabriël J E Rinkel. BMJ 2004
18
10

Modified informed consent procedure: consent to postponed information.
Han Boter, Johannes J M van Delden, Rob J de Haan, Gabriël J E Rinkel. BMJ 2003
41
10


BRCA1 in the family: a case description of the psychological implications.
A C DudokdeWit, A Tibben, P G Frets, E J Meijers-Heijboer, P Devilee, J G Klijn, J C Oosterwijk, M F Niermeijer. Am J Med Genet 1997
67
10

Initial cancer genetic counseling consultation: change in counselees' cognitions and anxiety, and association with addressing their needs and preferences.
Arwen H Pieterse, Margreet G E M Ausems, Alexandra M Van Dulmen, Frits A Beemer, Jozien M Bensing. Am J Med Genet A 2005
61
10

The effects of additional care by a pulmonary nurse for asthma and COPD patients at a respiratory outpatient clinic: results from a double blind, randomized clinical trial.
Geert N Rootmensen, Anton R J van Keimpema, Elske E Looysen, Letty van der Schaaf, Rob J de Haan, Henk M Jansen. Patient Educ Couns 2008
30
10

The effect of a minimal intervention strategy in addition to nicotine replacement therapy to support smoking cessation in cardiovascular outpatients: a randomized clinical trial.
Louise C W Wiggers, Ellen M A Smets, Frans J Oort, Ron J G Peters, Marja N Storm-Versloot, Hester Vermeulen, Hanneke C J M de Haes, Dink A Legemate. Eur J Cardiovasc Prev Rehabil 2006
19
10

Family communication matters: the impact of telling relatives about unclassified variants and uninformative DNA-test results.
Joël Vos, Anna M Jansen, Fred Menko, Christi J van Asperen, Anne M Stiggelbout, Aad Tibben. Genet Med 2011
27
10

Attitudes and misconceptions about predictive genetic testing for cancer risk.
Abigail L Rose, Nikki Peters, Judy A Shea, Katrina Armstrong. Community Genet 2005
33
10

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
10

Attitudes about genetics in underserved, culturally diverse populations.
Diana S Catz, Nancy S Green, Jonathan N Tobin, Michele A Lloyd-Puryear, Penny Kyler, Ann Umemoto, Jennifer Cernoch, Roxane Brown, Fredericka Wolman. Community Genet 2005
109
10

Characteristics of genomic test consumers who spontaneously share results with their health care provider.
Burcu F Darst, Lisa Madlensky, Nicholas J Schork, Eric J Topol, Cinnamon S Bloss. Health Commun 2014
23
10


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.