A citation-based method for searching scientific literature

R Ryanne Wu, Rachel A Myers, Nina Sperber, Corrine I Voils, Joan Neuner, Catherine A McCarty, Irina V Haller, Melissa Harry, Kimberly G Fulda, Deanna Cross, David Dimmock, Teji Rakhra-Burris, Adam H Buchanan, Geoffrey S Ginsburg, Lori A Orlando. Genet Med 2019
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


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
62
50

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
48
37

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
32
37

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
38
37

Family health history: underused for actionable risk assessment.
Geoffrey S Ginsburg, R Ryanne Wu, Lori A Orlando. Lancet 2019
30
37

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
31

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
23
31

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
25
31

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
26
31

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
31

10 years later: assessing the impact of public health efforts on the collection of family health history.
Brandon M Welch, Nathaniel O'Connell, Joshua D Schiffman. Am J Med Genet A 2015
31
25

Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial.
R Ryanne Wu, Lori A Orlando, Tiffany L Himmel, Adam H Buchanan, Karen P Powell, Elizabeth R Hauser, Astrid B Agbaje, Vincent C Henrich, Geoffrey S Ginsburg. BMC Fam Pract 2013
40
25

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
18

Acceptability and feasibility of a virtual counselor (VICKY) to collect family health histories.
Catharine Wang, Timothy Bickmore, Deborah J Bowen, Tricia Norkunas, MaryAnn Campion, Howard Cabral, Michael Winter, Michael Paasche-Orlow. Genet Med 2015
26
18

Family physician self-efficacy with screening for inherited cancer risk.
Robert Gramling, Justin Nash, Karen Siren, Charles Eaton, Larry Culpepper. Ann Fam Med 2004
44
18


National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
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,[...]. Ann Intern Med 2009
126
18


Impact of subsidies on cancer genetic testing uptake in Singapore.
Shao-Tzu Li, Jeanette Yuen, Ke Zhou, Nur Diana Binte Ishak, Yanni Chen, Marie Met-Domestici, Sock Hoai Chan, Yee Pin Tan, John Carson Allen, Soon Thye Lim,[...]. J Med Genet 2017
18
18

Providing patient education: impact on quantity and quality of family health history collection.
Chris A Beadles, R Ryanne Wu, Tiffany Himmel, Adam H Buchanan, Karen P Powell, Elizabeth Hauser, Vincent C Henrich, Geoffrey S Ginsburg, Lori A Orlando. Fam Cancer 2014
22
18

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
18

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
967
18

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
55
18

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
70
18

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
18

An Assessment of Family History Information Captured in an Electronic Health Record.
Fernanda Polubriaginof, Nicholas P Tatonetti, David K Vawdrey. AMIA Annu Symp Proc 2015
21
18

The IGNITE network: a model for genomic medicine implementation and research.
Kristin Wiisanen Weitzel, Madeline Alexander, Barbara A Bernhardt, Neil Calman, David J Carey, Larisa H Cavallari, Julie R Field, Diane Hauser, Heather A Junkins, Phillip A Levin,[...]. BMC Med Genomics 2016
139
18

Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey.
Aniwaa Owusu Obeng, Kezhen Fei, Kenneth D Levy, Amanda R Elsey, Toni I Pollin, Andrea H Ramirez, Kristin W Weitzel, Carol R Horowitz. J Pers Med 2018
64
18

Family health history: the case for better tools.
Brandon M Welch, Willard Dere, Joshua D Schiffman. JAMA 2015
33
18

Effect of Sociodemographic Factors on Uptake of a Patient-Facing Information Technology Family Health History Risk Assessment Platform.
R Ryanne Wu, Rachel A Myers, Adam H Buchanan, David Dimmock, Kimberly G Fulda, Irina V Haller, Susanne B Haga, Melissa L Harry, Catherine McCarty, Joan Neuner,[...]. Appl Clin Inform 2019
5
60

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
12


Personalized medicine for prevention: can risk stratified screening decrease colorectal cancer mortality at an acceptable cost?
Sujha Subramanian, Georgiy Bobashev, Robert J Morris, Sonja Hoover. Cancer Causes Control 2017
12
16

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
12

Brief questions to identify patients with inadequate health literacy.
Lisa D Chew, Katharine A Bradley, Edward J Boyko. Fam Med 2004
12

Protocol for the "Implementation, adoption, and utility of family history in diverse care settings" study.
R Ryanne Wu, Rachel A Myers, Catherine A McCarty, David Dimmock, Michael Farrell, Deanna Cross, Troy D Chinevere, Geoffrey S Ginsburg, Lori A Orlando. Implement Sci 2015
15
13

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
852
12

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
918
12

ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N Engl J Med 2015
564
12

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
72
12

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
12

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
107
12

Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing.
Jacqueline Mersch, Nichole Brown, Sara Pirzadeh-Miller, Erin Mundt, Hannah C Cox, Krystal Brown, Melissa Aston, Lisa Esterling, Susan Manley, Theodora Ross. JAMA 2018
100
12

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS.
Clare Turnbull, Richard H Scott, Ellen Thomas, Louise Jones, Nirupa Murugaesu, Freya Boardman Pretty, Dina Halai, Emma Baple, Clare Craig, Angela Hamblin,[...]. BMJ 2018
186
12

American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
Debbie Saslow, Carla Boetes, Wylie Burke, Steven Harms, Martin O Leach, Constance D Lehman, Elizabeth Morris, Etta Pisano, Mitchell Schnall, Stephen Sener,[...]. CA Cancer J Clin 2007
12

Screening for abdominal aortic aneurysm: a consensus statement.
K Craig Kent, Robert M Zwolak, Michael R Jaff, Scott T Hollenbeck, Robert W Thompson, Marc L Schermerhorn, Gregorio A Sicard, Thomas S Riles, Jack L Cronenwett. J Vasc Surg 2004
137
12


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
157
12

Screening of family members of patients with premature coronary heart disease; results from the EUROASPIRE II family survey.
J De Sutter, D De Bacquer, K Kotseva, S Sans, K Pyörälä, D Wood, G De Backer. Eur Heart J 2003
54
12



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.