A citation-based method for searching scientific literature

Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
Times Cited: 73







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



Times Cited
  Times     Co-cited
Similarity


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
149
32

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
246
32


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
311
15

Pharmacogenomic knowledge gaps and educational resource needs among physicians in selected specialties.
Katherine A Johansen Taber, Barry D Dickinson. Pharmgenomics Pers Med 2014
71
15

Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
64
17

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
13

Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
99
13

Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
201
10

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.
Irmgard Nippert, Hilary J Harris, Claire Julian-Reynier, Ulf Kristoffersson, Leo P Ten Kate, Elizabeth Anionwu, Caroline Benjamin, Kirsty Challen, Jörg Schmidtke, R Peter Nippert,[...]. J Community Genet 2011
54
14

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Jason L Vassy, Denise M Lautenbach, Heather M McLaughlin, Sek Won Kong, Kurt D Christensen, Joel Krier, Isaac S Kohane, Lindsay Z Feuerman, Jennifer Blumenthal-Barby, J Scott Roberts,[...]. Trials 2014
94
10

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
327
10


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
129
9


Pharmacogenomics instruction in US and Canadian medical schools: implications for personalized medicine.
James S Green, Travis J O'Brien, Vincent A Chiappinelli, Arthur F Harralson. Pharmacogenomics 2010
50
14

Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.
Bruce R Korf, Anna B Berry, Melvin Limson, Ali J Marian, Michael F Murray, P Pearl O'Rourke, Eugene R Passamani, Mary V Relling, John Tooker, Gregory J Tsongalis,[...]. Genet Med 2014
72
9

Physicians' attitudes about multiplex tumor genomic testing.
Stacy W Gray, Katherine Hicks-Courant, Angel Cronin, Barrett J Rollins, Jane C Weeks. J Clin Oncol 2014
133
9

Clinician Perspectives on Using Pharmacogenomics in Clinical Practice.
Kim M Unertl, Habiba Jaffa, Julie R Field, Lisa Price, Josh F Peterson. Per Med 2015
36
19

Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol.
Suzette J Bielinski, Janet E Olson, Jyotishman Pathak, Richard M Weinshilboum, Liewei Wang, Kelly J Lyke, Euijung Ryu, Paul V Targonski, Michael D Van Norstrand, Matthew A Hathcock,[...]. Mayo Clin Proc 2014
174
9

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Robert C Green, Katrina A B Goddard, Gail P Jarvik, Laura M Amendola, Paul S Appelbaum, Jonathan S Berg, Barbara A Bernhardt, Leslie G Biesecker, Sawona Biswas, Carrie L Blout,[...]. Am J Hum Genet 2016
93
9

Development and evaluation of a pharmacogenomics educational program for pharmacists.
Christine M Formea, Wayne T Nicholson, Kristen B McCullough, Kevin D Berg, Melody L Berg, Julie L Cunningham, Julianna A Merten, Narith N Ou, Joanna L Stollings. Am J Pharm Educ 2013
50
12

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
64
9

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
249
8

Genomic medicine: a decade of successes, challenges, and opportunities.
Jeanette J McCarthy, Howard L McLeod, Geoffrey S Ginsburg. Sci Transl Med 2013
131
8

Assessment of the pharmacogenomics educational needs of pharmacists.
Kristen B McCullough, Christine M Formea, Kevin D Berg, Julianna A Burzynski, Julie L Cunningham, Narith N Ou, Maria I Rudis, Joanna L Stollings, Wayne T Nicholson. Am J Pharm Educ 2011
108
8

A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
Heather M McLaughlin, Ozge Ceyhan-Birsoy, Kurt D Christensen, Isaac S Kohane, Joel Krier, William J Lane, Denise Lautenbach, Matthew S Lebo, Kalotina Machini, Calum A MacRae,[...]. BMC Med Genet 2014
60
10

Gynecologists' training, knowledge, and experiences in genetics: a survey.
L Wilkins-Haug, L D Hill, M L Power, G B Holzman, J Schulkin. Obstet Gynecol 2000
42
14

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
118
8

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
740
8

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
94
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
109
6


The current and future state of pharmacogenomics medical education in the USA.
Tracey J Nickola, James S Green, Arthur F Harralson, Travis J O'Brien. Pharmacogenomics 2012
30
16

Genetic testing and cancer risk management recommendations by physicians for at-risk relatives.
Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
74
6

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
6

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
6


Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine.
Katherine Bonter, Clarissa Desjardins, Nathan Currier, Jason Pun, Fredrick D Ashbury. BMJ Open 2011
48
10

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
122
6

Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
182
6

Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives.
Elisa Jf Houwink, Scheltus J van Luijk, Lidewij Henneman, Cees van der Vleuten, Geert Jan Dinant, Martina C Cornel. BMC Fam Pract 2011
74
6

Clinical pharmacogenetics implementation: approaches, successes, and challenges.
Kristin W Weitzel, Amanda R Elsey, Taimour Y Langaee, Benjamin Burkley, David R Nessl, Aniwaa Owusu Obeng, Benjamin J Staley, Hui-Jia Dong, Robert W Allan, J Felix Liu,[...]. Am J Med Genet C Semin Med Genet 2014
120
6

Personal genome testing in medical education: student experiences with genotyping in the classroom.
Simone Lucia Vernez, Keyan Salari, Kelly E Ormond, Sandra Soo-Jin Lee. Genome Med 2013
37
13

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
138
6

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
Brian H Shirts, Joseph S Salama, Samuel J Aronson, Wendy K Chung, Stacy W Gray, Lucia A Hindorff, Gail P Jarvik, Sharon E Plon, Elena M Stoffel, Peter Z Tarczy-Hornoch,[...]. J Am Med Inform Assoc 2015
54
9

Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine.
Keyan Salari, Konrad J Karczewski, Louanne Hudgins, Kelly E Ormond. PLoS One 2013
55
9

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
44
11

Patients' and physicians' perspectives on pharmacogenetic testing.
Anja Rogausch, Daniela Prause, Anne Schallenberg, Jürgen Brockmöller, Wolfgang Himmel. Pharmacogenomics 2006
72
6

Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.
L J Rasmussen-Torvik, S C Stallings, A S Gordon, B Almoguera, M A Basford, S J Bielinski, A Brautbar, M H Brilliant, D S Carrell, J J Connolly,[...]. Clin Pharmacol Ther 2014
138
6


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.