A citation-based method for searching scientific literature

Maria C Katapodi, Laurel Northouse, Penny Pierce, Kara J Milliron, Guipeng Liu, Sofia D Merajver. Oncol Nurs Forum 2011
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


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
26

Cognitive and emotional factors predicting decisional conflict among high-risk breast cancer survivors who receive uninformative BRCA1/2 results.
Christine Rini, Suzanne C O'Neill, Heiddis Valdimarsdottir, Rachel E Goldsmith, Lina Jandorf, Karen Brown, Tiffani A DeMarco, Beth N Peshkin, Marc D Schwartz. Health Psychol 2009
31
20


Decision-making about genetic testing among women at familial risk for breast cancer.
P B Jacobsen, H B Valdimarsdottier, K L Brown, K Offit. Psychosom Med 1997
127
13

Genetic testing: psychological aspects and implications.
Caryn Lerman, Robert T Croyle, Kenneth P Tercyak, Heidi Hamann. J Consult Clin Psychol 2002
177
13

Uptake rates for breast cancer genetic testing: a systematic review.
Mary E Ropka, Jennifer Wenzel, Elayne K Phillips, Mir Siadaty, John T Philbrick. Cancer Epidemiol Biomarkers Prev 2006
114
13

Validation of a decisional conflict scale.
A M O'Connor. Med Decis Making 1995
13

Randomized trial of a portable, self-administered decision aid for postmenopausal women considering long-term preventive hormone therapy.
A M O'Connor, P Tugwell, G A Wells, T Elmslie, E Jolly, G Hollingworth, R McPherson, E Drake, W Hopman, T Mackenzie. Med Decis Making 1998
185
13

Underestimation of breast cancer risk: influence on screening behavior.
Maria C Katapodi, Marylin J Dodd, Kathryn A Lee, Noreen C Facione. Oncol Nurs Forum 2009
49
13


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

Family issues in a psychoeducation group for women with a BRCA mutation.
J Speice, S H McDaniel, P T Rowley, S Loader. Clin Genet 2002
35
13

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
13

Long-term psychological impact of carrying a BRCA1/2 mutation and prophylactic surgery: a 5-year follow-up study.
Iris van Oostrom, Hanne Meijers-Heijboer, Litanja N Lodder, Hugo J Duivenvoorden, Arthur R van Gool, Caroline Seynaeve, Conny A van der Meer, Jan G M Klijn, Bert N van Geel, Curt W Burger,[...]. J Clin Oncol 2003
193
13

The emotional effects of genetic diseases: implications for clinical genetics.
Marion McAllister, Linda Davies, Katherine Payne, Stuart Nicholls, Dian Donnai, Rhona MacLeod. Am J Med Genet A 2007
45
13

Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.
Susan M Domchek, Tara M Friebel, Christian F Singer, D Gareth Evans, Henry T Lynch, Claudine Isaacs, Judy E Garber, Susan L Neuhausen, Ellen Matloff, Rosalind Eeles,[...]. JAMA 2010
849
13

Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine.
Jeffrey N Weitzel, Kathleen R Blazer, Deborah J MacDonald, Julie O Culver, Kenneth Offit. CA Cancer J Clin 2011
146
13

Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.
Beth Anderson, Jennifer McLosky, Elizabeth Wasilevich, Sarah Lyon-Callo, Debra Duquette, Glenn Copeland. J Cancer Epidemiol 2012
63
13

Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
Katrina Armstrong, Ellyn Micco, Amy Carney, Jill Stopfer, Mary Putt. JAMA 2005
288
13

Risk-reducing salpingo-oophorectomy for the prevention of BRCA1- and BRCA2-associated breast and gynecologic cancer: a multicenter, prospective study.
Noah D Kauff, Susan M Domchek, Tara M Friebel, Mark E Robson, Johanna Lee, Judy E Garber, Claudine Isaacs, D Gareth Evans, Henry Lynch, Rosalind A Eeles,[...]. J Clin Oncol 2008
359
13

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
13

Future health applications of genomics: priorities for communication, behavioral, and social sciences research.
Colleen M McBride, Deborah Bowen, Lawrence C Brody, Celeste M Condit, Robert T Croyle, Marta Gwinn, Muin J Khoury, Laura M Koehly, Bruce R Korf, Theresa M Marteau,[...]. Am J Prev Med 2010
105
13

Cancer genetic risk assessment for individuals at risk of familial breast cancer.
Jennifer S Hilgart, Bernadette Coles, Rachel Iredale. Cochrane Database Syst Rev 2012
49
13

Long-term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance.
Marc D Schwartz, Claudine Isaacs, Kristi D Graves, Elizabeth Poggi, Beth N Peshkin, Christy Gell, Clinton Finch, Scott Kelly, Kathryn L Taylor, Lauren Perley. Cancer 2012
93
13



Communicating genetic and genomic information: health literacy and numeracy considerations.
D H Lea, K A Kaphingst, D Bowen, I Lipkus, D W Hadley. Public Health Genomics 2011
142
13

The role of numeracy on client knowledge in BRCA genetic counseling.
David B Portnoy, Debra Roter, Lori H Erby. Patient Educ Couns 2010
24
13

Public awareness of genetic influence on chronic disease risk: are genetic and lifestyle causal beliefs compatible?
Saskia C Sanderson, Jo Waller, Steve E Humphries, Jane Wardle. Public Health Genomics 2011
18
13


A systematic review of perceived risks, psychological and behavioral impacts of genetic testing.
Jodi T Heshka, Crystal Palleschi, Heather Howley, Brenda Wilson, Philip S Wells. Genet Med 2008
223
13

Cancer-related direct-to-consumer advertising: a critical review.
Emily Z Kontos, K Viswanath. Nat Rev Cancer 2011
40
13

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
13

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
13

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
13

Parents' attitudes toward pediatric genetic testing for common disease risk.
Kenneth P Tercyak, Sharon Hensley Alford, Karen M Emmons, Isaac M Lipkus, Benjamin S Wilfond, Colleen M McBride. Pediatrics 2011
51
13

"Is it really worth it to get tested?": primary care patients' impressions of predictive SNP testing for colon cancer.
Kara-Grace Leventhal, William Tuong, Beth N Peshkin, Yasmin Salehizadeh, Mary B Fishman, Susan Eggly, Kevin FitzGerald, Marc D Schwartz, Kristi D Graves. J Genet Couns 2013
26
13

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
13


Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes.
Aisha S Sie, Judith B Prins, Liesbeth Spruijt, C Marleen Kets, Nicoline Hoogerbrugge. Fam Cancer 2013
14
14

Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information.
Serena Oliveri, Gabriella Pravettoni, Chiara Fioretti, Mats G Hansson. Public Health Genomics 2016
9
22

Genetic testing for hereditary melanoma and pancreatic cancer: a longitudinal study of psychological outcome.
Lisa G Aspinwall, Jennifer M Taber, Samantha L Leaf, Wendy Kohlmann, Sancy A Leachman. Psychooncology 2013
27
13

A follow-up study on men tested for BRCA1/BRCA2 mutations: impacts and coping processes.
Shoshana Shiloh, Efrat Dagan, Irit Friedman, Natalie Blank, Eitan Friedman. Psychooncology 2013
14
14

Living at Risk: Factors That Affect the Experience of Direct-to-Consumer Genetic Testing.
Serena Oliveri, Chiara Renzi, Marianna Masiero, Gabriella Pravettoni. Mayo Clin Proc 2015
13
15

Exploring the short-term impact of DNA-testing in breast cancer patients: the counselees' perception matters, but the actual BRCA1/2 result does not.
Joël Vos, Jan C Oosterwijk, Encarna Gomez-Garcia, Fred H Menko, Margriet J Collee, Christi J van Asperen, Anna M Jansen, Anne M Stiggelbout, Aad Tibben. Patient Educ Couns 2012
23
13

Impact of a patient decision aid on care among patients with nonvalvular atrial fibrillation: a cluster randomized trial.
Finlay A McAlister, Malcolm Man-Son-Hing, Sharon E Straus, William A Ghali, David Anderson, Sumit R Majumdar, Paul Gibson, Jafna L Cox, Miriam Fradette. CMAJ 2005
71
6

Evaluation of a decision aid for families considering p53 genetic counseling and testing.
Susan K Peterson, Rebecca D Pentz, Amie M Blanco, Patricia A Ward, Beatty G Watts, Salma K Marani, Leslie Colvin James, Louise C Strong. Genet Med 2006
15
6

Making choices for childbirth: a randomized controlled trial of a decision-aid for informed birth after cesarean.
Allison Shorten, Brett Shorten, John Keogh, Sandra West, Jonathan Morris. Birth 2005
115
6


A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patients.
A G W Hunter, M Cappelli, L Humphreys, J E Allanson, T T Chiu, C Peeters, D Moher, A Zimak. Clin Genet 2005
70
6


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.