A citation-based method for searching scientific literature

Brandon M Welch, Kensaku Kawamoto. J Am Med Inform Assoc 2013
Times Cited: 68







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



Times Cited
  Times     Co-cited
Similarity


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
304
23

Development and use of active clinical decision support for preemptive pharmacogenomics.
Gillian C Bell, Kristine R Crews, Mark R Wilkinson, Cyrine E Haidar, J Kevin Hicks, Donald K Baker, Nancy M Kornegay, Wenjian Yang, Shane J Cross, Scott C Howard,[...]. J Am Med Inform Assoc 2014
133
20

Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.
J M Pulley, J C Denny, J F Peterson, G R Bernard, C L Vnencak-Jones, A H Ramirez, J T Delaney, E Bowton, K Brothers, K Johnson,[...]. Clin Pharmacol Ther 2012
273
19


Effect of clinical decision-support systems: a systematic review.
Tiffani J Bright, Anthony Wong, Ravi Dhurjati, Erin Bristow, Lori Bastian, Remy R Coeytaux, Gregory Samsa, Vic Hasselblad, John W Williams, Michael D Musty,[...]. Ann Intern Med 2012
544
16

Technical desiderata for the integration of genomic data into Electronic Health Records.
Daniel R Masys, Gail P Jarvik, Neil F Abernethy, Nicholas R Anderson, George J Papanicolaou, Dina N Paltoo, Mark A Hoffman, Isaac S Kohane, Howard P Levy. J Biomed Inform 2012
65
16


Electronic health record design and implementation for pharmacogenomics: a local perspective.
Josh F Peterson, Erica Bowton, Julie R Field, Marc Beller, Jennifer Mitchell, Jonathan Schildcrout, William Gregg, Kevin Johnson, Jim N Jirjis, Dan M Roden,[...]. Genet Med 2013
67
13

Opportunities for genomic clinical decision support interventions.
Casey Lynnette Overby, Isaac Kohane, Joseph L Kannry, Marc S Williams, Justin Starren, Erwin Bottinger, Omri Gottesman, Joshua C Denny, Chunhua Weng, Peter Tarczy-Hornoch,[...]. Genet Med 2013
43
20

A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine.
Kensaku Kawamoto, David F Lobach, Huntington F Willard, Geoffrey S Ginsburg. BMC Med Inform Decis Mak 2009
68
11

Genomic and personalized medicine: foundations and applications.
Geoffrey S Ginsburg, Huntington F Willard. Transl Res 2009
265
11


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
343
11

Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach.
Emily Beth Devine, Chia-Ju Lee, Casey L Overby, Neil Abernethy, Jeannine McCune, Joe W Smith, Peter Tarczy-Hornoch. Int J Med Inform 2014
48
16

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
10

The CLIPMERGE PGx Program: clinical implementation of personalized medicine through electronic health records and genomics-pharmacogenomics.
O Gottesman, S A Scott, S B Ellis, C L Overby, A Ludtke, J-S Hulot, J Hall, K Chatani, K Myers, J L Kannry,[...]. Clin Pharmacol Ther 2013
101
10

Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey.
E J Stanek, C L Sanders, K A Johansen Taber, M Khalid, A Patel, R R Verbrugge, B C Agatep, R E Aubert, R S Epstein, F W Frueh. Clin Pharmacol Ther 2012
283
10

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
Peter Tarczy-Hornoch, Laura Amendola, Samuel J Aronson, Levi Garraway, Stacy Gray, Robert W Grundmeier, Lucia A Hindorff, Gail Jarvik, Dean Karavite, Matthew Lebo,[...]. Genet Med 2013
49
14

PG4KDS: a model for the clinical implementation of pre-emptive pharmacogenetics.
James M Hoffman, Cyrine E Haidar, Mark R Wilkinson, Kristine R Crews, Donald K Baker, Nancy M Kornegay, Wenjian Yang, Ching-Hon Pui, Ulrike M Reiss, Aditya H Gaur,[...]. Am J Med Genet C Semin Med Genet 2014
159
10

Integrating pharmacogenetic information and clinical decision support into the electronic health record.
Barry R Goldspiel, Willy A Flegel, Gary DiPatrizio, Tristan Sissung, Sharon D Adams, Scott R Penzak, Leslie G Biesecker, Thomas A Fleisher, Jharana J Patel, David Herion,[...]. J Am Med Inform Assoc 2014
41
17

Electronic medical records and personalized medicine.
Mark A Hoffman, Marc S Williams. Hum Genet 2011
37
16

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
14

Ten commandments for effective clinical decision support: making the practice of evidence-based medicine a reality.
David W Bates, Gilad J Kuperman, Samuel Wang, Tejal Gandhi, Anne Kittler, Lynn Volk, Cynthia Spurr, Ramin Khorasani, Milenko Tanasijevic, Blackford Middleton. J Am Med Inform Assoc 2003
769
8

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
61
9

The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
354
8

Communicating new knowledge on previously reported genetic variants.
Samuel J Aronson, Eugene H Clark, Matthew Varugheese, Samantha Baxter, Lawrence J Babb, Heidi L Rehm. Genet Med 2012
70
8

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
236
8

Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers.
Henry M Dunnenberger, Kristine R Crews, James M Hoffman, Kelly E Caudle, Ulrich Broeckel, Scott C Howard, Robert J Hunkler, Teri E Klein, William E Evans, Mary V Relling. Annu Rev Pharmacol Toxicol 2015
275
8




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
7

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
36
13

A clinician-driven automated system for integration of pharmacogenetic interpretations into an electronic medical record.
J K Hicks, K R Crews, J M Hoffman, N M Kornegay, M R Wilkinson, R Lorier, A Stoddard, W Yang, C Smith, C A Fernandez,[...]. Clin Pharmacol Ther 2012
72
7

Overriding of drug safety alerts in computerized physician order entry.
Heleen van der Sijs, Jos Aarts, Arnold Vulto, Marc Berg. J Am Med Inform Assoc 2006
690
7

Pharmacogenomics and individualized medicine: translating science into practice.
K R Crews, J K Hicks, C-H Pui, M V Relling, W E Evans. Clin Pharmacol Ther 2012
140
7

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
61
8

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
33
15

Pharmacogenetics: from bench to byte--an update of guidelines.
J J Swen, M Nijenhuis, A de Boer, L Grandia, A H Maitland-van der Zee, H Mulder, G A P J M Rongen, R H N van Schaik, T Schalekamp, D J Touw,[...]. Clin Pharmacol Ther 2011
612
7

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
7

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W Andrew Faucett, Rongling Li, Teri A Manolio, Saskia C Sanderson, Joseph Kannry, Randi Zinberg, Melissa A Basford,[...]. Genet Med 2013
413
7

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
168
7

Technical desiderata for the integration of genomic data with clinical decision support.
Brandon M Welch, Karen Eilbeck, Guilherme Del Fiol, Laurence J Meyer, Kensaku Kawamoto. J Biomed Inform 2014
21
23

A proposed clinical decision support architecture capable of supporting whole genome sequence information.
Brandon M Welch, Salvador Rodriguez Loya, Karen Eilbeck, Kensaku Kawamoto. J Pers Med 2014
6
83

Pharmacogenomic knowledge gaps and educational resource needs among physicians in selected specialties.
Katherine A Johansen Taber, Barry D Dickinson. Pharmgenomics Pers Med 2014
84
7

Making pharmacogenomic-based prescribing alerts more effective: A scenario-based pilot study with physicians.
Casey Lynnette Overby, Emily Beth Devine, Neil Abernethy, Jeannine S McCune, Peter Tarczy-Hornoch. J Biomed Inform 2015
20
25

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
7

The Personalized Medicine Coalition: goals and strategies.
Edward Abrahams, Geoffrey S Ginsburg, Mike Silver. Am J Pharmacogenomics 2005
65
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

The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.
Samuel J Aronson, Eugene H Clark, Lawrence J Babb, Samantha Baxter, Lisa M Farwell, Birgit H Funke, Amy Lovelette Hernandez, Victoria A Joshi, Elaine Lyon, Andrew R Parthum,[...]. Hum Mutat 2011
56
7


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.