A citation-based method for searching scientific literature

Arian W Plat, Abraham A Kroon, Constant P Van Schayck, Peter W De Leeuw, Henri E J H Stoffers. Eur J Gen Pract 2009
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


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
158
47

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
71
41

The comprehensiveness of family cancer history assessments in primary care.
Harvey J Murff, Robert A Greevy, Sapna Syngal. Community Genet 2007
81
41

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
238
35

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
104
29

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
56
29


Systematic review: family history in risk assessment for common diseases.
Brenda J Wilson, Nadeem Qureshi, Pasqualina Santaguida, Julian Little, June C Carroll, Judith Allanson, Parminder Raina. Ann Intern Med 2009
85
23

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
158
23

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
62
23

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
105
23

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
37
23

Family history: still relevant in the genomics era.
Megan Doerr, Kathryn Teng. Cleve Clin J Med 2012
39
23

Comparing electronic health record portals to obtain patient-entered family health history in primary care.
Michael F Murray, Monica A Giovanni, Elissa Klinger, Elise George, Lucas Marinacci, George Getty, Phyllis Brawarsky, Beatriz Rocha, E John Orav, David W Bates,[...]. J Gen Intern Med 2013
27
23

Family history tools for primary care are not ready yet to be implemented. A systematic review.
Céline L M M de Hoog, Piet J M Portegijs, Henri E J H Stoffers. Eur J Gen Pract 2014
26
23

Quality of family history collection with use of a patient facing family history assessment tool.
R Ryanne Wu, Tiffany L Himmel, Adam H Buchanan, Karen P Powell, Elizabeth R Hauser, Geoffrey S Ginsburg, Vincent C Henrich, Lori A Orlando. BMC Fam Pract 2014
26
23

Cancer risk assessment: quality and impact of the family history interview.
Harvey J Murff, Daniel Byrne, Sapna Syngal. Am J Prev Med 2004
83
23

Primary care physicians' use of family history for cancer risk assessment.
Brian S Flynn, Marie E Wood, Takamaru Ashikaga, Alan Stockdale, Greg S Dana, Shelly Naud. BMC Fam Pract 2010
48
23

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
50
17

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
17

Collecting genetic information in primary care: evaluating a new family history tool.
Nadeem Qureshi, Jane Bethea, Bernadette Modell, Paul Brennan, Alexia Papageorgiou, Sandy Raeburn, Rhydian Hapgood, Michael Modell. Fam Pract 2005
65
17

Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence.
Liesbeth Claassen, Lidewij Henneman, A Cecile J W Janssens, Miranda Wijdenes-Pijl, Nadeem Qureshi, Fiona M Walter, Paula W Yoon, Danielle R M Timmermans. BMC Public Health 2010
74
17

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
83
17

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
63
17

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
76
17

The genetic family history as a risk assessment tool in internal medicine.
Theresa M Frezzo, Wendy S Rubinstein, Daniel Dunham, Kelly E Ormond. Genet Med 2003
75
17


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
65
17

American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
Karen H Lu, Marie E Wood, Molly Daniels, Cathy Burke, James Ford, Noah D Kauff, Wendy Kohlmann, Noralane M Lindor, Therese M Mulvey, Linda Robinson,[...]. J Clin Oncol 2014
160
17

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
49
17

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
17
17

Development and validation of a family history screening questionnaire in Australian primary care.
Jon D Emery, Gabrielle Reid, A Toby Prevost, David Ravine, Fiona M Walter. Ann Fam Med 2014
17
17

Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™).
Cecelia Bellcross, April Hermstad, Christine Tallo, Christine Stanislaw. Genet Med 2019
17
17

Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.
Fay Kastrinos, Hajime Uno, Chinedu Ukaegbu, Carmelita Alvero, Ashley McFarland, Matthew B Yurgelun, Matthew H Kulke, Deborah Schrag, Jeffrey A Meyerhardt, Charles S Fuchs,[...]. J Clin Oncol 2017
81
17

Automatic Genetic Risk Assessment Calculation Using Breast Cancer Family History Data from the EHR compared to Self-Report.
Margaret Sin, Julia E McGuinness, Meghna S Trivedi, Alejandro Vanegas, Thomas B Silverman, Katherine D Crew, Rita Kukafka. AMIA Annu Symp Proc 2018
7
42

A systematic review of factors that act as barriers to patient referral to genetic services.
Türem Delikurt, Graham R Williamson, Violetta Anastasiadou, Heather Skirton. Eur J Hum Genet 2015
91
17

Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.
Deborah Cragun, Anne Weidner, Courtney Lewis, Devon Bonner, Jongphil Kim, Susan T Vadaparampil, Tuya Pal. Cancer 2017
108
17

Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities.
Larissa A Meyer, Meaghan E Anderson, Robin A Lacour, Anuj Suri, Molly S Daniels, Diana L Urbauer, Graciela M Nogueras-Gonzalez, Kathleen M Schmeler, David M Gershenson, Karen H Lu. Obstet Gynecol 2010
89
17

Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.
Anne Marie McCarthy, Mirar Bristol, Susan M Domchek, Peter W Groeneveld, Younji Kim, U Nkiru Motanya, Judy A Shea, Katrina Armstrong. J Clin Oncol 2016
92
17

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Laura M Amendola, Jonathan S Berg, Carol R Horowitz, Frank Angelo, Jeannette T Bensen, Barbara B Biesecker, Leslie G Biesecker, Gregory M Cooper, Kelly East, Kelly Filipski,[...]. Am J Hum Genet 2018
59
17

Review and Comparison of Electronic Patient-Facing Family Health History Tools.
Brandon M Welch, Kevin Wiley, Lance Pflieger, Rosaline Achiangia, Karen Baker, Chanita Hughes-Halbert, Heath Morrison, Joshua Schiffman, Megan Doerr. J Genet Couns 2018
39
17


Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine.
Jeffrey N Weitzel, Kathleen R Blazer, Deborah J MacDonald, Julie O Culver, Kenneth Offit. CA Cancer J Clin 2011
154
11

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom.
Simon Sanderson, Ron Zimmern, Mark Kroese, Julian Higgins, Christine Patch, Jon Emery. Genet Med 2005
73
11

Assessing women at high risk of breast cancer: a review of risk assessment models.
Eitan Amir, Orit C Freedman, Bostjan Seruga, D Gareth Evans. J Natl Cancer Inst 2010
269
11

Healthy choices through family history: a community approach to family history awareness.
Claudia Petruccio, Kenna R Mills Shaw, Joann Boughman, Carlos Fernandez, Ilana Harlow, Margaret Kruesi, Penny Kyler, Michele A Lloyd-Puryear, James O'Leary, Amy Skillman,[...]. Community Genet 2008
25
11

National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009.
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,[...]. NIH Consens State Sci Statements 2009
11
18

Family history in primary care: understanding GPs' resistance to clinical genetics--qualitative study.
Jonathan Mathers, Sheila Greenfield, Alison Metcalfe, Trevor Cole, Sarah Flanagan, Sue Wilson. Br J Gen Pract 2010
25
11

The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
356
11

Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood.
M T Scheuner, S J Wang, L J Raffel, S K Larabell, J I Rotter. Am J Med Genet 1997
189
11


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.