A citation-based method for searching scientific literature

Kaylene J Ready, Molly S Daniels, Charlotte C Sun, Susan K Peterson, Hope Northrup, Karen H Lu. J Cancer Educ 2010
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
101
53

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
104
46


Genetic testing and cancer risk management recommendations by physicians for at-risk relatives.
Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
74
30


Genetic assessment of breast cancer risk in primary care practice.
Wylie Burke, Julie Culver, Linda Pinsky, Sarah Hall, Susan E Reynolds, Yutaka Yasui, Nancy Press. Am J Med Genet A 2009
48
23

Too many referrals of low-risk women for BRCA1/2 genetic services by family physicians.
Della Brown White, Vence L Bonham, Jean Jenkins, Nancy Stevens, Colleen M McBride. Cancer Epidemiol Biomarkers Prev 2008
33
23

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
23

Gynecologists' training, knowledge, and experiences in genetics: a survey.
L Wilkins-Haug, L D Hill, M L Power, G B Holzman, J Schulkin. Obstet Gynecol 2000
42
23


Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels.
Katarina Domanska, Christina Carlsson, Pär-Ola Bendahl, Mef Nilbert. BMC Med Genet 2009
20
23

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
63
23


Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications.
Karina L Brierley, Erica Blouch, Whitney Cogswell, Jeanne P Homer, Debbie Pencarinha, Christine L Stanislaw, Ellen T Matloff. Cancer J 2012
62
23

Primary care physicians' utilization and perceptions of genetics services.
S J Hayflick, M P Eiff, L Carpenter, J Steinberger. Genet Med 1998
90
23

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
126
23

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
99
23


The comprehensiveness of family cancer history assessments in primary care.
Harvey J Murff, Robert A Greevy, Sapna Syngal. Community Genet 2007
70
15

Education and experience with breast health maintenance and breast cancer care: a study of obstetricians and gynecologists.
Andrew W Menzin, Britta L Anderson, Sterling B Williams, Jay Schulkin. J Cancer Educ 2010
3
66

Meta-analysis of BRCA1 and BRCA2 penetrance.
Sining Chen, Giovanni Parmigiani. J Clin Oncol 2007
980
15


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
102
15


An analysis of the causes of adverse events from the Quality in Australian Health Care Study.
R M Wilson, B T Harrison, R W Gibberd, J D Hamilton. Med J Aust 1999
165
15


Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians.
Katrina J Lowstuter, Sharon Sand, Kathleen R Blazer, Deborah J MacDonald, Kimberly C Banks, Carol A Lee, Barbara U Schwerin, Margaret Juarez, Gwen C Uman, Jeffrey N Weitzel. Genet Med 2008
34
15

Understanding adverse events: human factors.
J Reason. Qual Health Care 1995
256
15


Familial risk of cancer and knowledge and use of genetic testing.
Heather J Baer, Phyllis Brawarsky, Michael F Murray, Jennifer S Haas. J Gen Intern Med 2010
21
15

Cancer risk in mutation carriers of DNA-mismatch-repair genes.
M Aarnio, R Sankila, E Pukkala, R Salovaara, L A Aaltonen, A de la Chapelle, P Peltomäki, J P Mecklin, H J Järvinen. Int J Cancer 1999
686
15

Underdiagnosis of Lynch syndrome involves more than family history criteria.
Hardeep Singh, Rachel Schiesser, Gobind Anand, Peter A Richardson, Hashem B El-Serag. Clin Gastroenterol Hepatol 2010
46
15

Cancer risk assessment from family history: gaps in primary care practice.
Randa D Sifri, Richard Wender, Nina Paynter. J Fam Pract 2002
37
15

Family history and colorectal cancer screening: a survey of physician knowledge and practice patterns.
Paul C Schroy, Adam F Barrison, Bruce S Ling, Sheila Wilson, Adam C Geller. Am J Gastroenterol 2002
100
15

Awareness of genetic testing for colorectal cancer predisposition among specialists in gastroenterology.
Shivani Batra, Heiddis Valdimarsdottir, Margaret McGovern, Steven Itzkowitz, Karen Brown. Am J Gastroenterol 2002
52
15

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol 2011
227
15

Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome.
Steve Heymann, Suzette Delaloge, Arslane Rahal, Olivier Caron, Thierry Frebourg, Lise Barreau, Corinne Pachet, Marie-Christine Mathieu, Hugo Marsiglia, Céline Bourgier. Radiat Oncol 2010
99
15

Patterns of cancer genetic testing: a randomized survey of Oregon clinicians.
Summer L Cox, Amy I Zlot, Kerry Silvey, Debi Elliott, Tara Horn, Amber Johnson, Richard F Leman. J Cancer Epidemiol 2012
22
15

Physician Risk Assessment Knowledge Regarding BRCA Genetics Testing.
Jason Cohn, William Blazey, David Tegay, Brian Harper, Sharon Koehler, Brookshield Laurent, Vivian Chan, Min-Kyung Jung, Bhuma Krishnamachari. J Cancer Educ 2015
8
25

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
74
15

Impact of oophorectomy on cancer incidence and mortality in women with a BRCA1 or BRCA2 mutation.
Amy P M Finch, Jan Lubinski, Pål Møller, Christian F Singer, Beth Karlan, Leigha Senter, Barry Rosen, Lovise Maehle, Parviz Ghadirian, Cezary Cybulski,[...]. J Clin Oncol 2014
308
15

Educational needs and preferred methods of learning among Florida practitioners who order genetic testing for hereditary breast and ovarian cancer.
Deborah Cragun, Andrea Doty Besharat, Courtney Lewis, Susan T Vadaparampil, Tuya Pal. J Cancer Educ 2013
12
16

Surveying the current landscape of clinical genetics residency training.
Caleb P Bupp, Laurie A Demmer, Robert A Saul. Genet Med 2015
6
33


Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
73
15

Implementation and evaluation of a genetics curriculum to improve obstetrician-gynecologist residents' knowledge and skills in genetic diagnosis and counseling.
Charles J Macri, Nancy D Gaba, Lauren M Sitzer, Lisa Freese, Susanne L Bathgate, John W Larsen. Am J Obstet Gynecol 2005
10
20

Patients' interest in discussing cancer risk and risk management with primary care physicians.
Adam H Buchanan, Celette Sugg Skinner, Susan M Rawl, Barry K Moser, Victoria L Champion, Linda L Scott, Tara S Strigo, Lori Bastian. Patient Educ Couns 2005
14
7

Identification and referral of families at high risk for cancer susceptibility.
Kevin M Sweet, Terry L Bradley, Judith A Westman. J Clin Oncol 2002
92
7

Common hereditary cancers and implications for primary care.
J Emery, A Lucassen, M Murphy. Lancet 2001
42
7

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
204
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.