A citation-based method for searching scientific literature

S C Sanderson, S C O'Neill, L A Bastian, G Bepler, C M McBride. Public Health Genomics 2010
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity



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
113
20

Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours.
Theresa M Marteau, David P French, Simon J Griffin, A T Prevost, Stephen Sutton, Clare Watkinson, Sophie Attwood, Gareth J Hollands. Cochrane Database Syst Rev 2010
195
18

Incorporating genetic susceptibility feedback into a smoking cessation program for African-American smokers with low income.
Colleen M McBride, Gerold Bepler, Isaac M Lipkus, Pauline Lyna, Greg Samsa, Jennifer Albright, Santanu Datta, Barbara K Rimer. Cancer Epidemiol Biomarkers Prev 2002
141
16

Social networkers' attitudes toward direct-to-consumer personal genome testing.
Amy L McGuire, Christina M Diaz, Tao Wang, Susan G Hilsenbeck. Am J Bioeth 2009
152
16

Psychological and behavioural impact of genetic testing smokers for lung cancer risk: a phase II exploratory trial.
Saskia C Sanderson, Steve E Humphries, Christina Hubbart, Eluned Hughes, Martin J Jarvis, Jane Wardle. J Health Psychol 2008
53
18

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
345
16

Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.
Colleen M McBride, Sharon Hensley Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2009
87
15

Genetic testing: psychological aspects and implications.
Caryn Lerman, Robert T Croyle, Kenneth P Tercyak, Heidi Hamann. J Consult Clin Psychol 2002
175
15

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.
Muin J Khoury, Colleen M McBride, Sheri D Schully, John P A Ioannidis, W Gregory Feero, A Cecile J W Janssens, Marta Gwinn, Denise G Simons-Morton, Jay M Bernhardt, Michele Cargill,[...]. Genet Med 2009
151
13

Health behavior changes after genetic risk assessment for Alzheimer disease: The REVEAL Study.
Serena Chao, J Scott Roberts, Theresa M Marteau, Rebecca Silliman, L Adrienne Cupples, Robert C Green. Alzheimer Dis Assoc Disord 2008
156
11

Responses to online GSTM1 genetic test results among smokers related to patients with lung cancer: a pilot study.
Saskia C Sanderson, Suzanne C O'Neill, Della Brown White, Gerold Bepler, Lori Bastian, Isaac M Lipkus, Colleen M McBride. Cancer Epidemiol Biomarkers Prev 2009
41
17

Genetic susceptibility testing in smoking-cessation treatment: one-year outcomes of a randomized trial.
J Audrain, N R Boyd, J Roth, D Main, N F Caporaso, C Lerman. Addict Behav 1997
81
11

A survey of UK public interest in internet-based personal genome testing.
Lynn F Cherkas, Juliette M Harris, Elana Levinson, Tim D Spector, Barbara Prainsack. PLoS One 2010
75
11

An intervention study of smoking cessation with feedback on genetic cancer susceptibility in Japan.
Hidemi Ito, Keitaro Matsuo, Kenji Wakai, Toshiko Saito, Hiroshi Kumimoto, Katashi Okuma, Kazuo Tajima, Nobuyuki Hamajima. Prev Med 2006
41
14

Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
77
10


Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
96
10

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
122
10

An agenda for personalized medicine.
Pauline C Ng, Sarah S Murray, Samuel Levy, J Craig Venter. Nature 2009
195
8

Consumer perceptions of direct-to-consumer personalized genomic risk assessments.
Cinnamon S Bloss, Laura Ornowski, Elana Silver, Michele Cargill, Vance Vanier, Nicholas J Schork, Eric J Topol. Genet Med 2010
89
8


Personal genomics and individual identities: motivations and moral imperatives of early users.
Michelle L McGowan, Jennifer R Fishman, Marcie A Lambrix. New Genet Soc 2010
69
8

Incorporating biomarkers of exposure and genetic susceptibility into smoking cessation treatment: effects on smoking-related cognitions, emotions, and behavior change.
C Lerman, K Gold, J Audrain, T H Lin, N R Boyd, C T Orleans, B Wilfond, G Louben, N Caporaso. Health Psychol 1997
115
8

Does genetic testing result in behavioral health change? Changes in smoking behavior following testing for alpha-1 antitrypsin deficiency.
Matthew J Carpenter, Charlie Strange, Yonge Jones, Marguerite R Dickson, Cindy Carter, M Allison Moseley, Gregory E Gilbert. Ann Behav Med 2007
57
8

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
110
8

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
42
11

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
8

Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families.
Nadine A Kasparian, Bettina Meiser, Phyllis N Butow, Judy M Simpson, Graham J Mann. Genet Med 2009
64
8

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
831
8

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
6

Public interest in genetic testing for susceptibility to heart disease and cancer: a population-based survey in the UK.
Saskia C Sanderson, Jane Wardle, Martin J Jarvis, Steve E Humphries. Prev Med 2004
60
6


Assessing hypothetical scenario methodology in genetic susceptibility testing analog studies: a quantitative review.
Susan Persky, Kimberly A Kaphingst, Celeste M Condit, Colleen M McBride. Genet Med 2007
67
6

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
102
6


Genetics and smoking cessation improving outcomes in smokers at risk.
Caryn E Lerman, Robert A Schnoll, Marcus R Munafò. Am J Prev Med 2007
65
6




Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial.
Richard W Grant, Kelsey E O'Brien, Jessica L Waxler, Jason L Vassy, Linda M Delahanty, Laurie G Bissett, Robert C Green, Katherine G Stember, Candace Guiducci, Elyse R Park,[...]. Diabetes Care 2013
87
6

Effects of informed consent for individual genome sequencing on relevant knowledge.
K A Kaphingst, F M Facio, M-R Cheng, S Brooks, H Eidem, A Linn, B B Biesecker, L G Biesecker. Clin Genet 2012
81
6

Changing their minds with time: a comparison of hypothetical and actual reproductive behaviors in parents of children with cystic fibrosis.
Susan M Sawyer, Belinda Cerritelli, Lucy S Carter, Mary Cooke, Judith A Glazner, John Massie. Pediatrics 2006
56
7

Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer.
O Bratt, J E Damber, M Emanuelsson, U Kristoffersson, R Lundgren, H Olsson, H Grönberg. Eur J Cancer 2000
92
6

Update on procedure-related risks for prenatal diagnosis techniques.
Ann Tabor, Zarko Alfirevic. Fetal Diagn Ther 2010
226
6

Non-invasive prenatal testing for single gene disorders: exploring the ethics.
Zuzana Deans, Melissa Hill, Lyn S Chitty, Celine Lewis. Eur J Hum Genet 2013
29
13


Letting the genome out of the bottle--will we get our wish?
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N Engl J Med 2008
258
5




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.