A citation-based method for searching scientific literature

Fernanda Polubriaginof, Nicholas P Tatonetti, David K Vawdrey. AMIA Annu Symp Proc 2015
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
356
31

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
27

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
22

Automated extraction of family history information from clinical notes.
Robert Bill, Serguei Pakhomov, Elizabeth S Chen, Tamara J Winden, Elizabeth W Carter, Genevieve B Melton. AMIA Annu Symp Proc 2014
21
23

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
22

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

Identification and extraction of family history information from clinical reports.
Sergey Goryachev, Hyeoneui Kim, Qing Zeng-Treitler. AMIA Annu Symp Proc 2008
31
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

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
18

Collection of family health history for assessment of chronic disease risk in primary care.
Karen P Powell, Carol A Christianson, Susan E Hahn, Gaurav Dave, Leslie R Evans, Susan H Blanton, Elizabeth Hauser, Astrid Agbaje, Lori A Orlando, Geoffrey S Ginsburg,[...]. N C Med J 2013
25
13

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
179
13

Family history tools in primary care: does one size fit all?
B J Wilson, J C Carroll, J Allanson, J Little, H Etchegary, D Avard, B K Potter, D Castle, J M Grimshaw, P Chakraborty. Public Health Genomics 2012
15
20

Family history intake: a challenge to personalized approaches in health promotion and disease prevention.
Ronit Endevelt, Iris Goren, Tal Sela, Varda Shalev. Isr J Health Policy Res 2015
9
33


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
13

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
13

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
13

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
13

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
13

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
13

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
13

Family history tools for primary care are not ready yet to be implemented. A systematic review.
C√©line L M M de Hoog, Piet J M Portegijs, Henri E J H Stoffers. Eur J Gen Pract 2014
26
13

Implementation, adoption, and utility of family health history risk assessment in diverse care settings: evaluating implementation processes and impact with an implementation framework.
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,[...]. Genet Med 2019
17
17

Determining Onset for Familial Breast and Colorectal Cancer from Family History Comments in the Electronic Health Record.
Danielle L Mowery, Kensaku Kawamoto, Rick Bradshaw, Wendy Kohlmann, Joshua D Schiffman, Charlene Weir, Damian Borbolla, Wendy W Chapman, Guilherme Del Fiol. AMIA Jt Summits Transl Sci Proc 2019
13
23


Effects of computerized clinical decision support systems on practitioner performance and patient outcomes: a systematic review.
Amit X Garg, Neill K J Adhikari, Heather McDonald, M Patricia Rosas-Arellano, P J Devereaux, Joseph Beyene, Justina Sam, R Brian Haynes. JAMA 2005
9

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
9



Clinical decision support and appropriateness of antimicrobial prescribing: a randomized trial.
Matthew H Samore, Kim Bateman, Stephen C Alder, Elizabeth Hannah, Sharon Donnelly, Gregory J Stoddard, Bassam Haddadin, Michael A Rubin, Jacquelyn Williamson, Barry Stults,[...]. JAMA 2005
150
9

Assessing race and ethnicity data quality across cancer registries and EMRs in two hospitals.
Simon J Craddock Lee, James E Grobe, Jasmin A Tiro. J Am Med Inform Assoc 2016
19
10

Missed policy opportunities to advance health equity by recording demographic data in electronic health records.
Megan Daugherty Douglas, Daniel E Dawes, Kisha B Holden, Dominic Mack. Am J Public Health 2015
21
9

Accuracy of race, ethnicity, and language preference in an electronic health record.
Elissa V Klinger, Sara V Carlini, Irina Gonzalez, Stella St Hubert, Jeffrey A Linder, Nancy A Rigotti, Emily Z Kontos, Elyse R Park, Lucas X Marinacci, Jennifer S Haas. J Gen Intern Med 2015
69
9


Effects of tamoxifen vs raloxifene on the risk of developing invasive breast cancer and other disease outcomes: the NSABP Study of Tamoxifen and Raloxifene (STAR) P-2 trial.
Victor G Vogel, Joseph P Costantino, D Lawrence Wickerham, Walter M Cronin, Reena S Cecchini, James N Atkins, Therese B Bevers, Louis Fehrenbacher, Eduardo R Pajon, James L Wade,[...]. JAMA 2006
9


Patient and physician reminders to promote colorectal cancer screening: a randomized controlled trial.
Thomas D Sequist, Alan M Zaslavsky, Richard Marshall, Robert H Fletcher, John Z Ayanian. Arch Intern Med 2009
161
9

Disease Heritability Inferred from Familial Relationships Reported in Medical Records.
Fernanda C G Polubriaginof, Rami Vanguri, Kayla Quinnies, Gillian M Belbin, Alexandre Yahi, Hojjat Salmasian, Tal Lorberbaum, Victor Nwankwo, Li Li, Mark M Shervey,[...]. Cell 2018
47
9

Are electronic health records ready for genomic medicine?
Maren T Scheuner, Han de Vries, Benjamin Kim, Robin C Meili, Sarah H Olmstead, Stephanie Teleki. Genet Med 2009
41
9


The variant call format and VCFtools.
Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A Albers, Eric Banks, Mark A DePristo, Robert E Handsaker, Gerton Lunter, Gabor T Marth, Stephen T Sherry,[...]. Bioinformatics 2011
9

Empowering Mayo Clinic Individualized Medicine with Genomic Data Warehousing.
Iain Horton, Yaxiong Lin, Gay Reed, Mathieu Wiepert, Steven Hart. J Pers Med 2017
11
18

SMART on FHIR: a standards-based, interoperable apps platform for electronic health records.
Joshua C Mandel, David A Kreda, Kenneth D Mandl, Isaac S Kohane, Rachel B Ramoni. J Am Med Inform Assoc 2016
243
9


A roadmap for national action on clinical decision support.
Jerome A Osheroff, Jonathan M Teich, Blackford Middleton, Elaine B Steen, Adam Wright, Don E Detmer. J Am Med Inform Assoc 2007
309
9

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention.
Michael Inouye, Gad Abraham, Christopher P Nelson, Angela M Wood, Michael J Sweeting, Frank Dudbridge, Florence Y Lai, Stephen Kaptoge, Marta Brozynska, Tingting Wang,[...]. J Am Coll Cardiol 2018
268
9

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
9

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
9

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
138
9

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
990
9


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.