A citation-based method for searching scientific literature

Christine E Koil, Jessica N Everett, Leah Hoechstetter, Rick E Ricer, Karen M Huelsman. Genet Med 2003
Times Cited: 34







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



Times Cited
  Times     Co-cited
Similarity


Why do physicians vary so widely in their referral rates?
P Franks, G C Williams, J Zwanziger, C Mooney, M Sorbero. J Gen Intern Med 2000
120
5


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
5

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
49
5

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
67
5

Knowledge, attitudes, and utilization of BRCA1/2 testing among women with early-onset breast cancer.
Nikki Peters, Susan M Domchek, Abigail Rose, Rachael Polis, Jill Stopfer, Katrina Armstrong. Genet Test 2005
39
5

Factors determining dissemination of results and uptake of genetic testing in families with known BRCA1/2 mutations.
Esme Finlay, Jill E Stopfer, Eric Burlingame, Katherine Goldfeder Evans, Katherine L Nathanson, Barbara L Weber, Katrina Armstrong, Timothy R Rebbeck, Susan M Domchek. Genet Test 2008
100
5

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
Thomas S Frank, Amie M Deffenbaugh, Julia E Reid, Mark Hulick, Brian E Ward, Beth Lingenfelter, Kathi L Gumpper, Thomas Scholl, Sean V Tavtigian, Dmitry R Pruss,[...]. J Clin Oncol 2002
628
5

Genetic testing in young women with breast cancer: results from a Web-based survey.
K J Ruddy, S Gelber, J Shin, J E Garber, R Rosenberg, M Przypysny, A H Partridge. Ann Oncol 2010
17
11


Referral and experience with genetic testing among women with early onset breast cancer.
Karen L Brown, Robin Hutchison, Randi E Zinberg, Margaret M McGovern. Genet Test 2005
27
7

Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.
M Cappelli, L Surh, L Humphreys, S Verma, D Logan, A Hunter, J Allanson. Clin Genet 1999
91
5

Genetic/familial high-risk assessment: breast and ovarian.
Mary B Daly, Jennifer E Axilbund, Saundra Buys, Beth Crawford, Carolyn D Farrell, Susan Friedman, Judy E Garber, Salil Goorha, Stephen B Gruber, Heather Hampel,[...]. J Natl Compr Canc Netw 2010
161
5

Cancer genetic risk assessment and referral patterns in primary care.
Hetal S Vig, Joanne Armstrong, Brian L Egleston, Carla Mazar, Michele Toscano, Angela R Bradbury, Mary B Daly, Neal J Meropol. Genet Test Mol Biomarkers 2009
42
5

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
77
5

Significant differences among physician specialties in management recommendations of BRCA1 mutation carriers.
S U Dhar, H P Cooper, T Wang, B Parks, S A Staggs, S Hilsenbeck, S E Plon. Breast Cancer Res Treat 2011
21
9

The virtual consultation: practitioners' experiences of genetic counseling by videoconferencing in Australia.
Elvira Zilliacus, Bettina Meiser, Elizabeth Lobb, Tracey E Dudding, Kristine Barlow-Stewart, Katherine Tucker. Telemed J E Health 2010
29
6

The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees' outcome.
Ulla Platten, Johanna Rantala, Annika Lindblom, Yvonne Brandberg, Gunilla Lindgren, Brita Arver. Fam Cancer 2012
31
6

The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary care.
J Emery, H Morris, R Goodchild, T Fanshawe, A T Prevost, M Bobrow, A L Kinmonth. Br J Cancer 2007
75
5

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
5

A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians.
Maren T Scheuner, Alison B Hamilton, Jane Peredo, Taylor J Sale, Colletta Austin, Stuart C Gilman, M Scott Bowen, Caroline Lubick Goldzweig, Martin Lee, Brian S Mittman,[...]. Genet Med 2014
32
6

Telegenetics: a systematic review of telemedicine in genetics services.
Jennifer S Hilgart, Julie A Hayward, Bernadette Coles, Rachel Iredale. Genet Med 2012
89
5

Cancer risk assessment by rural and Appalachian family medicine physicians.
Kimberly M Kelly, Margaret M Love, Kevin A Pearce, Kyle Porter, Mary A Barron, Michael Andrykowski. J Rural Health 2009
13
15

The use by Alabama pediatricians of genetics consultation in the evaluation of developmental delay.
Min-Jye Chen, Cheryl L Holt, Edward J Lose, Nathaniel H Robin. Am J Med Genet A 2008
8
25

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
7

Barriers to access: results from focus groups to identify genetic service needs in the community.
Rosalyn Y Beene-Harris, Catharine Wang, Janice V Bach. Community Genet 2007
22
9

Human genetics and genomics a decade after the release of the draft sequence of the human genome.
Nasheen Naidoo, Yudi Pawitan, Richie Soong, David N Cooper, Chee-Seng Ku. Hum Genomics 2011
41
5

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
60
5

What Predicts the Use of Genetic Counseling Services After the Birth of a Child with Down Syndrome?
Veronica Collins, Jane Halliday, Robert Williamson. J Genet Couns 2003
7
28

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
23
8

Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing.
Courtney Doughty Rice, Jennifer Gamm Ruschman, Lisa J Martin, Jennifer B Manders, Erin Miller. Fam Cancer 2010
18
11


Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
50
5

Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance.
Adam H Buchanan, Santanu K Datta, Celette Sugg Skinner, Gail P Hollowell, Henry F Beresford, Thomas Freeland, Benjamin Rogers, John Boling, P Kelly Marcom, Martha B Adams. J Genet Couns 2015
87
5



Physicians' attitudes about multiplex tumor genomic testing.
Stacy W Gray, Katherine Hicks-Courant, Angel Cronin, Barrett J Rollins, Jane C Weeks. J Clin Oncol 2014
145
5

Prioritization of future genetics education for general practitioners: a Delphi study.
Elisa J F Houwink, Lidewij Henneman, Myrte Westerneng, Scheltus J van Luijk, Martina C Cornel, Jan Geert Dinant, Cees van der Vleuten. Genet Med 2012
31
6

Primary care physicians' knowledge of and experience with pharmacogenetic testing.
S B Haga, W Burke, G S Ginsburg, R Mills, R Agans. Clin Genet 2012
160
5

Cancer genetics education in a low- to middle-income country: evaluation of an interactive workshop for clinicians in Kenya.
Jessica A Hill, Su Yeon Lee, Lucy Njambi, Timothy W Corson, Helen Dimaras. PLoS One 2015
11
18


A primary care specialist genetics service: a cluster-randomised factorial trial.
Greta Westwood, Ruth Pickering, Sue Latter, Paul Little, Karen Gerard, Anneke Lucassen, I Karen Temple. Br J Gen Pract 2012
7
28

Cluster randomized trial of a multifaceted primary care decision-support intervention for inherited breast cancer risk.
Brenda J Wilson, Nicola Torrance, Jill Mollison, M Stuart Watson, Alison Douglas, Zosia Miedzybrodzka, Richard Gordon, Sarah Wordsworth, Marion Campbell, Neva Haites,[...]. Fam Pract 2006
19
10

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
5

The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review.
Nick Dragojlovic, Kennedy Borle, Nicola Kopac, Ursula Ellis, Patricia Birch, Shelin Adam, Jan M Friedman, Amy Nisselle, Alison M Elliott, Larry D Lynd. Genet Med 2020
12
16

A theory-informed systematic review of clinicians' genetic testing practices.
Jean L Paul, Hanna Leslie, Alison H Trainer, Clara Gaff. Eur J Hum Genet 2018
9
22

The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017
65
5


Family physicians' perspectives on ovarian cancer.
R E Gray, P Chart, J C Carroll, M I Fitch, D Cloutier-Fisher. Cancer Prev Control 1999
6
16



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.