A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
211
16


Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
224
15


Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
195
14


Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians.
Cecelia A Bellcross, Katherine Kolor, Katrina A B Goddard, Ralph J Coates, Michele Reyes, Muin J Khoury. Am J Prev Med 2011
109
12

The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
339
11

Primary care physicians' utilization and perceptions of genetics services.
S J Hayflick, M P Eiff, L Carpenter, J Steinberger. Genet Med 1998
103
11

Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives.
Elisa Jf Houwink, Scheltus J van Luijk, Lidewij Henneman, Cees van der Vleuten, Geert Jan Dinant, Martina C Cornel. BMC Fam Pract 2011
79
13


US physicians' attitudes toward genetic testing for cancer susceptibility.
A N Freedman, L Wideroff, L Olson, W Davis, C Klabunde, K P Srinath, B B Reeve, R T Croyle, R Ballard-Barbash. Am J Med Genet A 2003
134
10

The 'new genetics' and primary care: GPs' views on their role and their educational needs.
E K Watson, D Shickle, N Qureshi, J Emery, J Austoker. Fam Pract 1999
136
9

Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions.
Erin K Harvey, Chana E Fogel, Mark Peyrot, Kurt D Christensen, Sharon F Terry, Joseph D McInerney. Genet Med 2007
55
16


Family history questionnaires designed for clinical use: a systematic review.
G T Reid, F M Walter, J M Brisbane, J D Emery. Public Health Genomics 2009
53
15

Developing Family Healthware, a family history screening tool to prevent common chronic diseases.
Paula W Yoon, Maren T Scheuner, Cynthia Jorgensen, Muin J Khoury. Prev Chronic Dis 2009
102
8

Physicians' knowledge of genetics and genetic tests.
K J Hofman, E S Tambor, G A Chase, G Geller, R R Faden, N A Holtzman. Acad Med 1993
154
8

Reported referral for genetic counseling or BRCA 1/2 testing among United States physicians: a vignette-based study.
Katrina F Trivers, Laura-Mae Baldwin, Jacqueline W Miller, Barbara Matthews, C Holly A Andrilla, Denise M Lishner, Barbara A Goff. Cancer 2011
76
10

Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians.
L Wideroff, S T Vadaparampil, M H Greene, S Taplin, L Olson, A N Freedman. J Med Genet 2005
109
8

Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system.
Lori A Orlando, Elizabeth R Hauser, Carol Christianson, Karen P Powell, Adam H Buchanan, Blair Chesnut, Astrid B Agbaje, Vincent C Henrich, Geoffrey Ginsburg. BMC Health Serv Res 2011
33
24

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
327
8

Research priorities for evaluating family history in the prevention of common chronic diseases.
Paula W Yoon, Maren T Scheuner, Muin J Khoury. Am J Prev Med 2003
155
7

Can family history be used as a tool for public health and preventive medicine?
Paula W Yoon, Maren T Scheuner, Kris L Peterson-Oehlke, Marta Gwinn, Andrew Faucett, Muin J Khoury. Genet Med 2002
235
7

Integrating genetics as practices of primary care.
Rosemary Robins, Sylvia Metcalfe. Soc Sci Med 2004
37
18

Familial risk for common diseases in primary care: the Family Healthware Impact Trial.
Suzanne M O'Neill, Wendy S Rubinstein, Catharine Wang, Paula W Yoon, Louise S Acheson, Nan Rothrock, Erin J Starzyk, Jennifer L Beaumont, James M Galliher, Mack T Ruffin. Am J Prev Med 2009
86
8

Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics.
R T Acton, N M Burst, L Casebeer, S M Ferguson, P Greene, B L Laird, L Leviton. Acad Med 2000
111
7


Errors in delivery of cancer genetics services: implications for practice.
Karina L Brierley, Danielle Campfield, Whitney Ducaine, Lindsay Dohany, Talia Donenberg, Kristen Shannon, Robin C Schwartz, Ellen T Matloff. Conn Med 2010
65
10

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.
Irmgard Nippert, Hilary J Harris, Claire Julian-Reynier, Ulf Kristoffersson, Leo P Ten Kate, Elizabeth Anionwu, Caroline Benjamin, Kirsty Challen, Jörg Schmidtke, R Peter Nippert,[...]. J Community Genet 2011
58
12

Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
104
7

Effect of adding systematic family history enquiry to cardiovascular disease risk assessment in primary care: a matched-pair, cluster randomized trial.
Nadeem Qureshi, Sarah Armstrong, Paula Dhiman, Paula Saukko, Joan Middlemass, Philip H Evans, Joe Kai. Ann Intern Med 2012
79
8

Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine.
Katherine Bonter, Clarissa Desjardins, Nathan Currier, Jason Pun, Fredrick D Ashbury. BMJ Open 2011
56
12

Needs assessment study of genetics education for general practitioners in Australia.
Sylvia Metcalfe, Rosalind Hurworth, Jennifer Newstead, Rosemary Robins. Genet Med 2002
69
8

National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
Alfred O Berg, Macaran A Baird, Jeffrey R Botkin, Deborah A Driscoll, Paul A Fishman, Peter D Guarino, Robert A Hiatt, Gail P Jarvik, Sandra Millon-Underwood, Thomas M Morgan,[...]. Ann Intern Med 2009
123
6

The current state of cancer family history collection tools in primary care: a systematic review.
Nadeem Qureshi, June C Carroll, Brenda Wilson, Pasqualina Santaguida, Judith Allanson, Melissa Brouwers, Parminder Raina. Genet Med 2009
67
8

Family history-taking in community family practice: implications for genetic screening.
L S Acheson, G L Wiesner, S J Zyzanski, M A Goodwin, K C Stange. Genet Med 2000
174
6

Family history in public health practice: a genomic tool for disease prevention and health promotion.
Rodolfo Valdez, Paula W Yoon, Nadeem Qureshi, Ridgely Fisk Green, Muin J Khoury. Annu Rev Public Health 2010
148
6

Cancer risk assessment from family history: gaps in primary care practice.
Randa D Sifri, Richard Wender, Nina Paynter. J Fam Pract 2002
37
16

Genetics in primary care: a USA faculty development initiative.
Wylie Burke, Louise Acheson, Jeffery Botkin, Kenneth Bridges, Ardis Davis, James Evans, Jaime Frias, James Hanson, Norman Kahn, Ruth Kahn,[...]. Community Genet 2002
40
15

Genetic susceptibility to cancer. Family physicians' experience.
June C Carroll, Judith Belle Brown, Sean Blaine, Gord Glendon, Patricia Pugh, Wendy Medved. Can Fam Physician 2003
51
11

Physician use of genetic testing for cancer susceptibility: results of a national survey.
Louise Wideroff, Andrew N Freedman, Lorayn Olson, Carrie N Klabunde, William Davis, Kadaba P Srinath, Robert T Croyle, Rachel Ballard-Barbash. Cancer Epidemiol Biomarkers Prev 2003
103
6

Health Heritage© a web-based tool for the collection and assessment of family health history: initial user experience and analytic validity.
W F Cohn, M E Ropka, S L Pelletier, J R Barrett, M B Kinzie, M B Harrison, Z Liu, S Miesfeldt, A L Tucker, B B Worrall,[...]. Public Health Genomics 2010
56
10

GPs' views on their role in cancer genetics services and current practice.
A Fry, H Campbell, H Gudmunsdottir, R Rush, M Porteous, D Gorman, A Cull. Fam Pract 1999
107
6

Educational needs in genetic medicine: primary care perspectives.
Susan B Trinidad, Kelly Fryer-Edwards, Anthony Crest, Penny Kyler, Michele A Lloyd-Puryear, Wylie Burke. Community Genet 2008
29
20

Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients.
Shilpa Grover, Elena M Stoffel, Laoti Bussone, Elizabeth Tschoegl, Sapna Syngal. Clin Gastroenterol Hepatol 2004
120
6


Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey.
E J Stanek, C L Sanders, K A Johansen Taber, M Khalid, A Patel, R R Verbrugge, B C Agatep, R E Aubert, R S Epstein, F W Frueh. Clin Pharmacol Ther 2012
260
6

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
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.