A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Current and future applications of genetics in primary care medicine.
Louise S Acheson, Georgia L Wiesner. Prim Care 2004
13
23

The family medical history.
Robin L Bennett. Prim Care 2004
26
11

Efficacy of bilateral prophylactic mastectomy in women with a family history of breast cancer.
L C Hartmann, D J Schaid, J E Woods, T P Crotty, J L Myers, P G Arnold, P M Petty, T A Sellers, J L Johnson, S K McDonnell,[...]. N Engl J Med 1999
914
3

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
3



Genetic education for non-geneticist health professionals.
Rodney Harris, Kirsty Challen, Caroline Benjamin, Hilary Harris. Community Genet 2006
11
27


Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale.
Jean-Marc Calefato, Irma Nippert, Hilary J Harris, Ulf Kristoffersson, Jorg Schmidtke, Leo P Ten Kate, Elizabeth Anionwu, Caroline Benjamin, Kirsty Challen, Anne-Marie Plass,[...]. Genet Med 2008
21
14


Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
Angela Trepanier, Mary Ahrens, Wendy McKinnon, June Peters, Jill Stopfer, Sherry Campbell Grumet, Susan Manley, Julie O Culver, Ronald Acton, Joy Larsen-Haidle,[...]. J Genet Couns 2004
144
3

Clinical genetics issues encountered by family physicians.
Louise S Acheson, Kurt C Stange, Stephen Zyzanski. Genet Med 2005
42
7

Lost in transition: challenges in the expanding field of adult genetics.
Matthew R G Taylor, Janice G Edwards, Lisa Ku. Am J Med Genet C Semin Med Genet 2006
38
7

Genetics in medical practice.
Bruce R Korf. Genet Med 2002
6
50

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
3

Genetic services for familial cancer patients: a follow-up survey of National Cancer Institute Cancer Centers.
Meira Epplein, Ksenia P Koon, Scott D Ramsey, John D Potter. J Clin Oncol 2005
28
10

Cancer genetics evaluation: barriers to and improvements for referral.
Rachael Brandt, Zonera Ali, Allison Sabel, Terri McHugh, Paul Gilman. Genet Test 2008
31
9

Swiss primary care physicians' knowledge, attitudes and perception towards genetic testing for hereditary breast cancer.
Gabriella Pichert, Daniel Dietrich, Peter Moosmann, Marcel Zwahlen, Rolf Arno Stahel, Andr√©-Pascal Sappino. Fam Cancer 2003
26
11

Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs.
Cora M Aalfs, Ellen M A Smets, Hanneke C J M de Haes, Nico J Leschot. Fam Pract 2003
26
11

Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation.
Marieke J H Baars, Albert J J A Scherpbier, Lambert W Schuwirth, Lidewij Henneman, Frits A Beemer, Jan Maarten Cobben, Raoul C M Hennekam, Marian M J J Verweij, Martina C Cornel, Leo P Ten Kate. Genet Med 2005
44
6

Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
Sarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, Peter N Ray, Stephen W Scherer. Pediatr Res 2009
49
6



Physicians' opinion for 'new' genetic testing in Japan.
Takako Ohata, Atsushi Tsuchiya, Maiko Watanabe, Tomohisa Sumida, Fumio Takada. J Hum Genet 2009
23
13

Hereditary breast and ovarian cancers.
June C Carroll, Carol Cremin, Judith Allanson, Sean M Blaine, Heather Dorman, Clare A Gibbons, Jeremy Grimshaw, Christina Honeywell, Wendy S Meschino, Joanne Permaul,[...]. Can Fam Physician 2008
22
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
3

Long-term outcomes of the "Genetics in Primary Care" faculty development initiative.
Anne-Marie Laberge, Kelly Fryer-Edwards, Penny Kyler, Michele A Lloyd-Puryear, Wylie Burke. Fam Med 2009
16
18

The impact of a genetics education program on physicians' knowledge and genetic counseling referral patterns.
Jonathan C Clyman, Fiza Nazir, Sharon Tarolli, Elizabeth Black, Roni Q Lombardi, Joseph J Higgins. Med Teach 2007
19
15

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
59
5



Errors in laboratory medicine.
Pierangelo Bonini, Mario Plebani, Ferruccio Ceriotti, Francesca Rubboli. Clin Chem 2002
394
3


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
52
5

Obstetrics/gynecology residents' knowledge of hereditary breast and ovarian cancer and Lynch syndrome.
Kaylene J Ready, Molly S Daniels, Charlotte C Sun, Susan K Peterson, Hope Northrup, Karen H Lu. J Cancer Educ 2010
16
18

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
112
3

Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA).
Amanda L Laedtke, Suzanne M O'Neill, Wendy S Rubinstein, Kristen J Vogel. J Genet Couns 2012
39
7


The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
213
3


"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.
Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet Med 2012
76
3



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
68
4

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
87
3

General practitioners' attitudes to assessment of genetic risk of common disorders in routine primary care.
D McCahon, R Holder, A Metcalfe, S Clifford, P Gill, T Cole, H V Sleightholme, S Wilson. Clin Genet 2009
18
16

Genetic services and attitudes in primary care pediatrics.
Michael L Rinke, Natalie Mikat-Stevens, Robert Saul, Amy Driscoll, Jill Healy, Beth A Tarini. Am J Med Genet A 2014
23
13

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
336
3


GenetiKit: a randomized controlled trial to enhance delivery of genetics services by family physicians.
June C Carroll, Brenda J Wilson, Judith Allanson, Jeremy Grimshaw, Sean M Blaine, Wendy S Meschino, Joanne A Permaul, Ian D Graham. Fam Pract 2011
30
10


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.