A citation-based method for searching scientific literature

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, Elizabeth M Yano. Genet Med 2014
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity


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
73
29

Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial.
Wendy S Rubinstein, Louise S Acheson, Suzanne M O'Neill, Mack T Ruffin, Catharine Wang, Jennifer L Beaumont, Nan Rothrock. Genet Med 2011
62
25


Use of a web-based risk appraisal tool for assessing family history and lifestyle factors in primary care.
Heather J Baer, Louise I Schneider, Graham A Colditz, Hank Dart, Analisa Andry, Deborah H Williams, E John Orav, Jennifer S Haas, George Getty, Elizabeth Whittemore,[...]. J Gen Intern Med 2013
25
24

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

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
16

Clinical decision support for genetically guided personalized medicine: a systematic review.
Brandon M Welch, Kensaku Kawamoto. J Am Med Inform Assoc 2013
64
16

Clinical utility of a Web-enabled risk-assessment and clinical decision support program.
Lori A Orlando, R Ryanne Wu, Rachel A Myers, Adam H Buchanan, Vincent C Henrich, Elizabeth R Hauser, Geoffrey S Ginsburg. Genet Med 2016
20
25

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
111
12


Genetics in health care: an overview of current and emerging models.
R N Battista, I Blancquaert, A-M Laberge, N van Schendel, N Leduc. Public Health Genomics 2012
60
12

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
12

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
30

Implementing family health history risk stratification in primary care: impact of guideline criteria on populations and resource demand.
Lori A Orlando, R Ryanne Wu, Chris Beadles, Tiffany Himmel, Adam H Buchanan, Karen P Powell, Elizabeth R Hauser, Vincent C Henrich, Geoffrey S Ginsburg. Am J Med Genet C Semin Med Genet 2014
27
14

Collection and use of cancer family history in primary care.
Nadeem Qureshi, Brenda Wilson, Pasqualina Santaguida, June Carroll, Judith Allanson, Carolina Ruiz Culebro, Melissa Brouwers, Parminder Raina. Evid Rep Technol Assess (Full Rep) 2007
49
12

Effect of preventive messages tailored to family history on health behaviors: the Family Healthware Impact Trial.
Mack T Ruffin, Donald E Nease, Ananda Sen, Wilson D Pace, Catharine Wang, Louise S Acheson, Wendy S Rubinstein, Suzanne O'Neill, Robert Gramling. Ann Fam Med 2011
98
12

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
12

Development and evaluation of a brief self-completed family history screening tool for common chronic disease prevention in primary care.
Fiona M Walter, A Toby Prevost, Linda Birt, Nicola Grehan, Kathy Restarick, Helen C Morris, Stephen Sutton, Peter Rose, Sarah Downing, Jon D Emery. Br J Gen Pract 2013
15
26

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
343
12

Development and validation of a primary care-based family health history and decision support program (MeTree).
Lori A Orlando, Adam H Buchanan, Susan E Hahn, Carol A Christianson, Karen P Powell, Celette Sugg Skinner, Blair Chesnut, Colette Blach, Barbara Due, Geoffrey S Ginsburg,[...]. N C Med J 2013
43
12

Validation of My Family Health Portrait for six common heritable conditions.
Flavia M Facio, W Gregory Feero, Amy Linn, Neal Oden, Kandamurugu Manickam, Leslie G Biesecker. Genet Med 2010
56
12

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
12





Identification and referral of families at high risk for cancer susceptibility.
Kevin M Sweet, Terry L Bradley, Judith A Westman. J Clin Oncol 2002
125
9

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
9

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
331
9

Bringing genetics into primary care: findings from a national evaluation of pilots in England.
Graham Martin, Graeme Currie, Rachael Finn. J Health Serv Res Policy 2009
12
25

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
50
9

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
9

Identification and management of women at high risk for hereditary breast/ovarian cancer syndrome.
Elissa M Ozanne, Andrea Loberg, Sherwood Hughes, Christine Lawrence, Brian Drohan, Alan Semine, Michael Jellinek, Claire Cronin, Frederick Milham, Dana Dowd,[...]. Breast J 2009
37
9

Evaluation of a novel electronic genetic screening and clinical decision support tool in prenatal clinical settings.
Emily A Edelman, Bruce K Lin, Teresa Doksum, Brian Drohan, Vaughn Edelson, Siobhan M Dolan, Kevin Hughes, James O'Leary, Lisa Vasquez, Sara Copeland,[...]. Matern Child Health J 2014
9
33

Validation of a self-administered, computerized tool for collecting and displaying the family history of cancer.
Louise S Acheson, Stephen J Zyzanski, Kurt C Stange, Amy Deptowicz, Georgia L Wiesner. J Clin Oncol 2006
48
9

Meta-analysis of BRCA1 and BRCA2 penetrance.
Sining Chen, Giovanni Parmigiani. J Clin Oncol 2007
9

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

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
225
9

Development and early usage patterns of a consumer-facing family health history tool.
Nathan C Hulse, Pallavi Ranade-Kharkar, Herman Post, Grant M Wood, Marc S Williams, Peter J Haug. AMIA Annu Symp Proc 2011
25
12

The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
340
9

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
Glenn E Palomaki, Monica R McClain, Stephanie Melillo, Heather L Hampel, Stephen N Thibodeau. Genet Med 2009
319
9

Delivery of clinical genetic consultative services in the Veterans Health Administration.
Maren T Scheuner, Nell Marshall, Andrew Lanto, Alison B Hamilton, Sabine Oishi, Barbara Lerner, Martin Lee, Elizabeth M Yano. Genet Med 2014
16
18

Factors influencing organizational adoption and implementation of clinical genetic services.
Alison B Hamilton, Sabine Oishi, Elizabeth M Yano, Cynthia E Gammage, Nell J Marshall, Maren T Scheuner. Genet Med 2014
35
9

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
9

Use of a patient-entered family health history tool with decision support in primary care: impact of identification of increased risk patients on genetic counseling attendance.
Adam H Buchanan, Carol A Christianson, Tiffany Himmel, Karen P Powell, Astrid Agbaje, Geoffrey S Ginsburg, Vincent C Henrich, Lori A Orlando. J Genet Couns 2015
14
21


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
57
9


Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
9

A model for patient-direct screening and referral for familial cancer risk.
Kristin B Niendorf, Melissa A Geller, Rachel Isaksson Vogel, Timothy R Church, Anna Leininger, Angela Bakke, Robert D Madoff. Fam Cancer 2016
11
27


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.