A citation-based method for searching scientific literature

Deborah O Himes, Margaret F Clayton, Gary W Donaldson, Lee Ellington, Saundra S Buys, Anita Y Kinney. J Genet Couns 2016
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


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
120
21

Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.
Anita Y Kinney, Karin M Butler, Marc D Schwartz, Jeanne S Mandelblatt, Kenneth M Boucher, Lisa M Pappas, Amanda Gammon, Wendy Kohlmann, Sandra L Edwards, Antoinette M Stroup,[...]. J Natl Cancer Inst 2014
73
21

Young adult daughters of BRCA1/2 positive mothers: what do they know about hereditary cancer and how much do they worry?
Andrea F Patenaude, Nadine Tung, Paula D Ryan, Leif W Ellisen, Larissa Hewitt, Katherine A Schneider, Kenneth P Tercyak, Julie Aldridge, Judy E Garber. Psychooncology 2013
29
21

Awareness of cancer susceptibility genetic testing: the 2000, 2005, and 2010 National Health Interview Surveys.
Phuong L Mai, Susan Thomas Vadaparampil, Nancy Breen, Timothy S McNeel, Louise Wideroff, Barry I Graubard. Am J Prev Med 2014
69
21


Randomized controlled trial of a psychosocial telephone counseling intervention in BRCA1 and BRCA2 mutation carriers.
Kristi D Graves, Lari Wenzel, Marc D Schwartz, George Luta, Paul Wileyto, Steven Narod, Beth N Peshkin, Alfred Marcus, David Cella, Susan Powell Emsbo,[...]. Cancer Epidemiol Biomarkers Prev 2010
33
14

Factors associated with genetic counseling and BRCA testing in a population-based sample of young Black women with breast cancer.
D Cragun, D Bonner, J Kim, M R Akbari, S A Narod, A Gomez-Fuego, J D Garcia, S T Vadaparampil, Tuya Pal. Breast Cancer Res Treat 2015
50
14

Interest in genetic testing for modest changes in breast cancer risk: implications for SNP testing.
K D Graves, B N Peshkin, G Luta, W Tuong, M D Schwartz. Public Health Genomics 2011
41
14

Dispositional cancer worry: convergent, divergent, and predictive validity of existing scales.
Jakob D Jensen, Jennifer K Bernat, LaShara A Davis, Robert Yale. J Psychosoc Oncol 2010
30
14

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
Andrea Desmond, Allison W Kurian, Michele Gabree, Meredith A Mills, Michael J Anderson, Yuya Kobayashi, Nora Horick, Shan Yang, Kristen M Shannon, Nadine Tung,[...]. JAMA Oncol 2015
197
14

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
14



Can risk and illness perceptions predict breast cancer worry in healthy women?
Andrea Gibbons, AnnMarie Groarke. J Health Psychol 2016
10
20

Parental communication of BRCA1/2 genetic test results to children.
K P Tercyak, C Hughes, D Main, C Snyder, J F Lynch, H T Lynch, C Lerman. Patient Educ Couns 2001
77
14

How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults.
Angela R Bradbury, James J Dignam, Comfort N Ibe, Sogyong L Auh, Fay J Hlubocky, Shelly A Cummings, Melody White, Olufunmilayo I Olopade, Christopher K Daugherty. J Clin Oncol 2007
60
14


Talking to children about maternal BRCA1/2 genetic test results: a qualitative study of parental perceptions and advice.
Andrea Farkas Patenaude, Tiffani A DeMarco, Beth N Peshkin, Heiddis Valdimarsdottir, Judy E Garber, Katherine A Schneider, Larissa Hewitt, Jennifer Hamilton, Kenneth P Tercyak. J Genet Couns 2013
21
14

Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
Joanne Armstrong, Michele Toscano, Nancy Kotchko, Sue Friedman, Marc D Schwartz, Katherine S Virgo, Kristian Lynch, James E Andrews, Claudia X Aguado Loi, Joseph E Bauer,[...]. JAMA Oncol 2015
78
14


Clinical characteristics affect the impact of an uninformative DNA test result: the course of worry and distress experienced by women who apply for genetic testing for breast cancer.
Sandra van Dijk, Daniëlle R M Timmermans, Hanne Meijers-Heijboer, Aad Tibben, Christi J van Asperen, Wilma Otten. J Clin Oncol 2006
60
14


Public knowledge of and attitudes toward genetics and genetic testing.
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
125
14

Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling.
Morgan Butrick, Scott Kelly, Beth N Peshkin, George Luta, Rachel Nusbaum, Gillian W Hooker, Kristi Graves, Lisa Feeley, Claudine Isaacs, Heiddis B Valdimarsdottir,[...]. Genet Med 2015
58
14

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
136
14

Health disparities: the importance of culture and health communication.
Stephen B Thomas, Michael J Fine, Said A Ibrahim. Am J Public Health 2004
71
14

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
57
14

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
14

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
34
14

Projecting individualized probabilities of developing breast cancer for white females who are being examined annually.
M H Gail, L A Brinton, D P Byar, D K Corle, S B Green, C Schairer, J J Mulvihill. J Natl Cancer Inst 1989
14


Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer.
Tasha R Smith, Mark Steven Miller, Kurt Lohman, Ethan M Lange, L Douglas Case, Harvey W Mohrenweiser, Jennifer J Hu. Cancer Lett 2003
149
7

Variants in DNA double-strand break repair genes and breast cancer susceptibility.
Bettina Kuschel, Annika Auranen, Simon McBride, Karen L Novik, Antonis Antoniou, Julian M Lipscombe, Nicholas E Day, Douglas F Easton, Bruce A J Ponder, Paul D P Pharoah,[...]. Hum Mol Genet 2002
313
7

Genetic regulation of ionizing radiation sensitivity and breast cancer risk.
Jennifer J Hu, Tasha R Smith, Mark Steven Miller, Kurt Lohman, L Douglas Case. Environ Mol Mutagen 2002
97
7

DNA damage processing defects and disease.
R E Moses. Annu Rev Genomics Hum Genet 2001
31
7

A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer.
S L Winsey, N A Haldar, H P Marsh, M Bunce, S E Marshall, A L Harris, F Wojnarowska, K I Welsh. Cancer Res 2000
223
7

Polymorphisms XRCC1-R399Q and XRCC3-T241M and the risk of breast cancer at the Ontario site of the Breast Cancer Family Registry.
Jane C Figueiredo, Julia A Knight, Laurent Briollais, Irene L Andrulis, Hilmi Ozcelik. Cancer Epidemiol Biomarkers Prev 2004
77
7


Polymorphisms in XRCC1 modify the association between polycyclic aromatic hydrocarbon-DNA adducts, cigarette smoking, dietary antioxidants, and breast cancer risk.
Jing Shen, Marilie D Gammon, Mary Beth Terry, Lianwen Wang, Qiao Wang, Fangfang Zhang, Susan L Teitelbaum, Sybil M Eng, Sharon K Sagiv, Mia M Gaudet,[...]. Cancer Epidemiol Biomarkers Prev 2005
74
7

DNA repair gene XRCC3 241Met variant is not associated with risk of cutaneous malignant melanoma.
Zhigang Duan, Hongbing Shen, Jeffrey E Lee, Jeffrey E Gershenwald, Merrick I Ross, Paul F Mansfield, Madeleine Duvic, Sara S Strom, Margaret R Spitz, Qingyi Wei. Cancer Epidemiol Biomarkers Prev 2002
42
7


Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.
Jacques Ferlay, Isabelle Soerjomataram, Rajesh Dikshit, Sultan Eser, Colin Mathers, Marise Rebelo, Donald Maxwell Parkin, David Forman, Freddie Bray. Int J Cancer 2015
7


Genetic polymorphisms of XRCC1 and risk of gastric cancer.
Seong-Gene Lee, Byungsik Kim, Jaewon Choi, Changhoon Kim, Inchul Lee, Kyuyoung Song. Cancer Lett 2002
86
7

DNA Repair Gene Polymorphisms in Relation to Non-Small Cell Lung Cancer Survival.
Yuliang Su, Huan Zhang, Fangxiu Xu, Jinyu Kong, Herbert Yu, Biyun Qian. Cell Physiol Biochem 2015
13
7

Inheritance of the 194Trp and the 399Gln variant alleles of the DNA repair gene XRCC1 are associated with increased risk of early-onset colorectal carcinoma in Egypt.
S Z Abdel-Rahman, A S Soliman, M L Bondy, S Omar, S A El-Badawy, H M Khaled, I A Seifeldin, B Levin. Cancer Lett 2000
160
7

XRCC3 5'-UTR and IVS5-14 polymorphisms and breast cancer susceptibility: a meta-analysis.
Li-Xin Qiu, Chen Mao, Lei Yao, Ke-Da Yu, Ping Zhan, Bo Chen, Hai-Guang Liu, Hui Yuan, Jian Zhang, Kai Xue,[...]. Breast Cancer Res Treat 2010
15
7

Genetic polymorphisms in DNA repair genes and risk of lung cancer.
D Butkiewicz, M Rusin, L Enewold, P G Shields, M Chorazy, C C Harris. Carcinogenesis 2001
272
7

Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers.
Stefan Michiels, Patrick Danoy, Philippe Dessen, Alex Bera, Thomas Boulet, Christine Bouchardy, Mark Lathrop, Alain Sarasin, Simone Benhamou. Carcinogenesis 2007
58
7

XPD codon 751 polymorphism, metabolism genes, smoking, and bladder cancer risk.
Mariana C Stern, Laura R Johnson, Douglas A Bell, Jack A Taylor. Cancer Epidemiol Biomarkers Prev 2002
80
7


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.