A citation-based method for searching scientific literature

Megan C Roberts, Jennifer M Taber, William M Klein. J Cancer Educ 2018
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
71
37

Interventions to improve risk communication in clinical genetics: systematic review.
A Edwards, J Gray, A Clarke, J Dundon, G Elwyn, C Gaff, K Hood, R Iredale, S Sivell, C Shaw,[...]. Patient Educ Couns 2008
76
25

Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
37
25

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
25

Public Awareness of Direct-to-Consumer Genetic Tests: Findings from the 2013 U.S. Health Information National Trends Survey.
Tanya Agurs-Collins, Rebecca Ferrer, Allison Ottenbacher, Erika A Waters, Mary E O'Connell, Jada G Hamilton. J Cancer Educ 2015
32
25

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.
Mary B Daly, Robert Pilarski, Michael Berry, Saundra S Buys, Meagan Farmer, Susan Friedman, Judy E Garber, Noah D Kauff, Seema Khan, Catherine Klein,[...]. J Natl Compr Canc Netw 2017
296
25

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
244
25

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
25

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
60
25

Age differences in genetic knowledge, health literacy and causal beliefs for health conditions.
S Ashida, M Goodman, C Pandya, L M Koehly, C Lachance, J Stafford, K A Kaphingst. Public Health Genomics 2011
59
25

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
25

Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review.
Tatiane Yanes, Amanda M Willis, Bettina Meiser, Katherine M Tucker, Megan Best. Eur J Hum Genet 2019
28
25

A systematic review and economic evaluation of diagnostic strategies for Lynch syndrome.
Tristan Snowsill, Nicola Huxley, Martin Hoyle, Tracey Jones-Hughes, Helen Coelho, Chris Cooper, Ian Frayling, Chris Hyde. Health Technol Assess 2014
79
12

Improving subjective perception of personal cancer risk: systematic review and meta-analysis of educational interventions for people with cancer or at high risk of cancer.
Mbathio Dieng, Caroline G Watts, Nadine A Kasparian, Rachael L Morton, Graham J Mann, Anne E Cust. Psychooncology 2014
23
12

Transforming Cancer Prevention through Precision Medicine and Immune-oncology.
Thomas W Kensler, Avrum Spira, Judy E Garber, Eva Szabo, J Jack Lee, Zigang Dong, Andrew J Dannenberg, William N Hait, Elizabeth Blackburn, Nancy E Davidson,[...]. Cancer Prev Res (Phila) 2016
86
12


Has the revolution arrived?
Francis Collins. Nature 2010
165
12


Specific psychosocial issues of individuals undergoing genetic counseling for cancer - a literature review.
Willem Eijzenga, Daniela E E Hahn, Neil K Aaronson, Irma Kluijt, Eveline M A Bleiker. J Genet Couns 2014
29
12


Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.
Kathryn A Phillips, Patricia A Deverka, Harold C Sox, Muin J Khoury, Lewis G Sandy, Geoffrey S Ginsburg, Sean R Tunis, Lori A Orlando, Michael P Douglas. Genet Med 2017
37
12

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
57
12


Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results.
Laura C Beamer, Marcia L Grant, Carin R Espenschied, Kathleen R Blazer, Heather L Hampel, Jeffrey N Weitzel, Deborah J MacDonald. J Clin Oncol 2012
147
12

Patient compliance based on genetic medicine: a literature review.
Kai Insa Schneider, Jörg Schmidtke. J Community Genet 2014
24
12

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
37
12

Keeping pace with the times--the Genetic Information Nondiscrimination Act of 2008.
Kathy L Hudson, M K Holohan, Francis S Collins. N Engl J Med 2008
131
12

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
12

The role of the genetic counsellor: a systematic review of research evidence.
Heather Skirton, Christophe Cordier, Charlotta Ingvoldstad, Nicolas Taris, Caroline Benjamin. Eur J Hum Genet 2015
31
12



Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.
Sharon E Plon, Diana M Eccles, Douglas Easton, William D Foulkes, Maurizio Genuardi, Marc S Greenblatt, Frans B L Hogervorst, Nicoline Hoogerbrugge, Amanda B Spurdle, Sean V Tavtigian. Hum Mutat 2008
560
12

Educating underserved Latino communities about family health history using lay health advisors.
K A Kaphingst, C R Lachance, A Gepp, L Hoyt D'Anna, B Rios-Ellis. Public Health Genomics 2011
31
12

Impact of presymptomatic genetic testing on young adults: a systematic review.
Lea Godino, Daniela Turchetti, Leigh Jackson, Catherine Hennessy, Heather Skirton. Eur J Hum Genet 2016
32
12

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
12


Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review.
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
60
12

Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing.
Christine Stanislaw, Yuan Xue, William R Wilcox. Cancer Biol Med 2016
22
12

Primary care physicians' awareness, experience and opinions of direct-to-consumer genetic testing.
Karen P Powell, Whitney A Cogswell, Carol A Christianson, Gaurav Dave, Amit Verma, Sonja Eubanks, Vincent C Henrich. J Genet Couns 2012
64
12

Genetic counseling for hereditary breast and ovarian cancer among Puerto Rican women living in the United States.
Courtney L Scherr, Elsa Vasquez, Gwendolyn P Quinn, Susan T Vadaparampil. Rev Recent Clin Trials 2014
11
12


Values and options in cancer care (VOICE): study design and rationale for a patient-centered communication and decision-making intervention for physicians, patients with advanced cancer, and their caregivers.
Michael Hoerger, Ronald M Epstein, Paul C Winters, Kevin Fiscella, Paul R Duberstein, Robert Gramling, Phyllis N Butow, Supriya G Mohile, Paul R Kaesberg, Wan Tang,[...]. BMC Cancer 2013
90
12

Primary care providers' cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda.
Jada G Hamilton, Ekland Abdiwahab, Heather M Edwards, Min-Lin Fang, Andrew Jdayani, Erica S Breslau. J Gen Intern Med 2017
50
12

Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology.
Dawn Provenzale, Samir Gupta, Dennis J Ahnen, Travis Bray, Jamie A Cannon, Gregory Cooper, Donald S David, Dayna S Early, Deborah Erwin, James M Ford,[...]. J Natl Compr Canc Netw 2016
120
12

Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians.
Barbara A Bernhardt, Cara Zayac, Erynn S Gordon, Lisa Wawak, Reed E Pyeritz, Sarah E Gollust. Per Med 2012
28
12

American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.
Mark E Robson, Angela R Bradbury, Banu Arun, Susan M Domchek, James M Ford, Heather L Hampel, Stephen M Lipkin, Sapna Syngal, Dana S Wollins, Noralane M Lindor. J Clin Oncol 2015
309
12


Informed consent for human genetic and genomic studies: a systematic review.
A Khan, B J Capps, M Y Sum, C N Kuswanto, K Sim. Clin Genet 2014
22
12

Effective Referral of Low-Income Women at Risk for Hereditary Breast and Ovarian Cancer to Genetic Counseling: A Randomized Delayed Intervention Control Trial.
Rena J Pasick, Galen Joseph, Susan Stewart, Celia Kaplan, Robin Lee, Judith Luce, Sharon Davis, Titas Marquez, Tung Nguyen, Claudia Guerra. Am J Public Health 2016
14
12



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.