A citation-based method for searching scientific literature

Mark A Hoffman, Marc S Williams. Hum Genet 2011
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity


Crossing the omic chasm: a time for omic ancillary systems.
Justin Starren, Marc S Williams, Erwin P Bottinger. JAMA 2013
53
33

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
259
25

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
323
25

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
53
22

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
22

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
64
19

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
384
19

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
68
19

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
69
19

The genome-enabled electronic medical record.
M A Hoffman. J Biomed Inform 2007
49
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
16

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
Catherine A McCarty, Rex L Chisholm, Christopher G Chute, Iftikhar J Kullo, Gail P Jarvik, Eric B Larson, Rongling Li, Daniel R Masys, Marylyn D Ritchie, Dan M Roden,[...]. BMC Med Genomics 2011
435
16

Clinical decision support for genetically guided personalized medicine: a systematic review.
Brandon M Welch, Kensaku Kawamoto. J Am Med Inform Assoc 2013
61
16

Integrating genetic information resources with an EHR.
Guilherme Del Fiol, Marc S Williams, Naveen Maram, Roberto A Rocha, Grant M Wood, Joyce A Mitchell. AMIA Annu Symp Proc 2006
12
50

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
469
16



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
283
13


Enabling health care decisionmaking through clinical decision support and knowledge management.
David Lobach, Gillian D Sanders, Tiffani J Bright, Anthony Wong, Ravi Dhurjati, Erin Bristow, Lori Bastian, Remy Coeytaux, Gregory Samsa, Vic Hasselblad,[...]. Evid Rep Technol Assess (Full Rep) 2012
87
13

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
13

Genomic and personalized medicine: foundations and applications.
Geoffrey S Ginsburg, Huntington F Willard. Transl Res 2009
260
11


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
33
12

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
61
11

Feasibility of incorporating genomic knowledge into electronic medical records for pharmacogenomic clinical decision support.
Casey Lynnette Overby, Peter Tarczy-Hornoch, James I Hoath, Ira J Kalet, David L Veenstra. BMC Bioinformatics 2010
39
11

The Personalized Medicine Coalition: goals and strategies.
Edward Abrahams, Geoffrey S Ginsburg, Mike Silver. Am J Pharmacogenomics 2005
64
11

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
212
11

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
11

Leveraging the electronic health record to implement genomic medicine.
Iftikhar J Kullo, Gail P Jarvik, Teri A Manolio, Marc S Williams, Dan M Roden. Genet Med 2013
36
11

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
19
21

A novel clinician interface to improve clinician access to up-to-date genetic results.
Allison R Wilcox, Pamela M Neri, Lynn A Volk, Lisa P Newmark, Eugene H Clark, Lawrence J Babb, Matthew Varugheese, Samuel J Aronson, Heidi L Rehm, David W Bates. J Am Med Inform Assoc 2014
13
30

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
123
11

Practical challenges in integrating genomic data into the electronic health record.
Abel N Kho, Luke V Rasmussen, John J Connolly, Peggy L Peissig, Justin Starren, Hakon Hakonarson, M Geoffrey Hayes. Genet Med 2013
46
11

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
11

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
8


Information management to enable personalized medicine: stakeholder roles in building clinical decision support.
Gregory J Downing, Scott N Boyle, Kristin M Brinner, Jerome A Osheroff. BMC Med Inform Decis Mak 2009
28
10

Personalized medicine: progress and promise.
Isaac S Chan, Geoffrey S Ginsburg. Annu Rev Genomics Hum Genet 2011
134
8

Use of electronic health records in U.S. hospitals.
Ashish K Jha, Catherine M DesRoches, Eric G Campbell, Karen Donelan, Sowmya R Rao, Timothy G Ferris, Alexandra Shields, Sara Rosenbaum, David Blumenthal. N Engl J Med 2009
697
8

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group.
Steven M Teutsch, Linda A Bradley, Glenn E Palomaki, James E Haddow, Margaret Piper, Ned Calonge, W David Dotson, Michael P Douglas, Alfred O Berg. Genet Med 2009
458
8

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
79
8

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
8

Grand challenges in clinical decision support.
Dean F Sittig, Adam Wright, Jerome A Osheroff, Blackford Middleton, Jonathan M Teich, Joan S Ash, Emily Campbell, David W Bates. J Biomed Inform 2008
254
8

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
728
8

Taxonomizing, sizing, and overcoming the incidentalome.
Isaac S Kohane, Michael Hsing, Sek Won Kong. Genet Med 2012
89
8

The 1200 patients project: creating a new medical model system for clinical implementation of pharmacogenomics.
P H O'Donnell, A Bush, J Spitz, K Danahey, D Saner, S Das, N J Cox, M J Ratain. Clin Pharmacol Ther 2012
113
8

Inviting patients to read their doctors' notes: a quasi-experimental study and a look ahead.
Tom Delbanco, Jan Walker, Sigall K Bell, Jonathan D Darer, Joann G Elmore, Nadine Farag, Henry J Feldman, Roanne Mejilla, Long Ngo, James D Ralston,[...]. Ann Intern Med 2012
356
8

Clinical decision support in electronic prescribing: recommendations and an action plan: report of the joint clinical decision support workgroup.
Jonathan M Teich, Jerome A Osheroff, Eric A Pifer, Dean F Sittig, Robert A Jenders. J Am Med Inform Assoc 2005
90
8

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
93
8


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.