A citation-based method for searching scientific literature

D Max Smith, Tarlan Namvar, Ryan P Brown, T Blaise Springfield, Beth N Peshkin, Richard J Walsh, James C Welsh, Bonnie Levin, Nicole Brandt, Sandra M Swain. Pharmacogenomics 2020
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
262
50


Pharmacogenomics.
Dan M Roden, Howard L McLeod, Mary V Relling, Marc S Williams, George A Mensah, Josh F Peterson, Sara L Van Driest. Lancet 2019
102
37

Knowledge and attitudes on pharmacogenetics among pediatricians.
Shahad Rahawi, Hetanshi Naik, Kathryn V Blake, Aniwaa Owusu Obeng, Rachel M Wasserman, Yoshinori Seki, Vicky L Funanage, Kimihiko Oishi, Stuart A Scott. J Hum Genet 2020
14
37

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
153
37

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
162
37

Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).
James M Hoffman, Henry M Dunnenberger, J Kevin Hicks, Kelly E Caudle, Michelle Whirl Carrillo, Robert R Freimuth, Marc S Williams, Teri E Klein, Josh F Peterson. J Am Med Inform Assoc 2016
53
25

Practical considerations in genomic decision support: The eMERGE experience.
Timothy M Herr, Suzette J Bielinski, Erwin Bottinger, Ariel Brautbar, Murray Brilliant, Christopher G Chute, Beth L Cobb, Joshua C Denny, Hakon Hakonarson, Andrea L Hartzler,[...]. J Pathol Inform 2015
34
25

Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.
Galen Joseph, Flavia Chen, Julie Harris-Wai, Jennifer M Puck, Charlotte Young, Barbara A Koenig. Pediatrics 2016
21
25

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
129
25

Clinical Pharmacogenetics Implementation Consortium Guideline for Thiopurine Dosing Based on TPMT and NUDT15 Genotypes: 2018 Update.
Mary V Relling, Matthias Schwab, Michelle Whirl-Carrillo, Guilherme Suarez-Kurtz, Ching-Hon Pui, Charles M Stein, Ann M Moyer, William E Evans, Teri E Klein, Federico Guillermo Antillon-Klussmann,[...]. Clin Pharmacol Ther 2019
176
25

PARC report: a health-systems focus on reimbursement and patient access to pharmacogenomics testing.
Sara L Rogers, Nicholas J Keeling, Jyothsna Giri, Nina Gonzaludo, J Shawn Jones, Emily Glogowski, Christine M Formea. Pharmacogenomics 2020
5
40

How to Transition from Single-Gene Pharmacogenetic Testing to Preemptive Panel-Based Testing: A Tutorial.
Richard J Marrero, Emily J Cicali, Meghan J Arwood, Elizabeth Eddy, David DeRemer, Brian H Ramnaraign, Karen C Daily, Dennie Jones, Kelsey J Cook, Larisa H Cavallari,[...]. Clin Pharmacol Ther 2020
11
25

The Clinical Pharmacogenetics Implementation Consortium: 10 Years Later.
Mary V Relling, Teri E Klein, Roseann S Gammal, Michelle Whirl-Carrillo, James M Hoffman, Kelly E Caudle. Clin Pharmacol Ther 2020
50
25

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Pharmacogenetics-Guided Warfarin Dosing: 2017 Update.
J A Johnson, K E Caudle, L Gong, M Whirl-Carrillo, C M Stein, S A Scott, M T Lee, B F Gage, S E Kimmel, M A Perera,[...]. Clin Pharmacol Ther 2017
255
25

Clinical implementation of pharmacogenomics via a health system-wide research biobank: the University of Colorado experience.
Christina L Aquilante, David P Kao, Katy E Trinkley, Chen-Tan Lin, Kristy R Crooks, Emily C Hearst, Steven J Hess, Elizabeth L Kudron, Yee Ming Lee, Ina Liko,[...]. Pharmacogenomics 2020
12
25

Implementing Pharmacogenomics at Your Institution: Establishment and Overcoming Implementation Challenges.
M J Arwood, S Chumnumwat, L H Cavallari, E A Nutescu, J D Duarte. Clin Transl Sci 2016
43
25

Integrating pharmacogenomics into electronic health records with clinical decision support.
J Kevin Hicks, Henry M Dunnenberger, Karl F Gumpper, Cyrine E Haidar, James M Hoffman. Am J Health Syst Pharm 2016
67
25

Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects.
Simona Volpi, Carol J Bult, Rex L Chisholm, Patricia A Deverka, Geoffrey S Ginsburg, Howard J Jacob, Melpomeni Kasapi, Howard L McLeod, Dan M Roden, Marc S Williams,[...]. Clin Pharmacol Ther 2018
59
25

Implementation of Pharmacogenetics at Cincinnati Children's Hospital Medical Center: Lessons Learned Over 14 Years of Personalizing Medicine.
Laura B Ramsey, Cynthia A Prows, Kejian Zhang, Shannon N Saldaña, Michael T Sorter, John P Pestian, Richard J Wenstrup, Alexander A Vinks, Tracy A Glauser. Clin Pharmacol Ther 2019
30
25

A Tutorial for Pharmacogenomics Implementation Through End-to-End Clinical Decision Support Based on Ten Years of Experience from PREDICT.
Michelle Liu, Cindy L Vnencak-Jones, Bartholomew P Roland, Cheryl L Gatto, Janos L Mathe, Shari L Just, Josh F Peterson, Sara L Van Driest, Asli O Weitkamp. Clin Pharmacol Ther 2021
11
25

Pharmacogenomic knowledge gaps and educational resource needs among physicians in selected specialties.
Katherine A Johansen Taber, Barry D Dickinson. Pharmgenomics Pers Med 2014
76
25

Acceptability, Feasibility, and Utility of Integrating Pharmacogenetic Testing into a Child Psychiatry Clinic.
Karla Claudio-Campos, Adaixa Padrón, Gabriel Jerkins, Jaison Nainaparampil, Robyn Nelson, Anna Martin, Kristin Wiisanen, D Max Smith, Yulia Strekalova, Michael Marsiske,[...]. Clin Transl Sci 2021
3
66

Primary care physician experiences with integrated pharmacogenomic testing in a community health system.
Amy A Lemke, Christina G Hutten Selkirk, Nicole S Glaser, Annette W Sereika, Dyson T Wake, Peter J Hulick, Henry M Dunnenberger. Per Med 2017
25
25

Creating a scalable clinical pharmacogenomics service with automated interpretation and medical record result integration - experience from a pediatric tertiary care facility.
Shannon F Manzi, Vincent A Fusaro, Laura Chadwick, Catherine Brownstein, Catherine Clinton, Kenneth D Mandl, Wendy A Wolf, Jared B Hawkins. J Am Med Inform Assoc 2017
24
25

Implementation of Standardized Clinical Processes for TPMT Testing in a Diverse Multidisciplinary Population: Challenges and Lessons Learned.
Kristin W Weitzel, D Max Smith, Amanda R Elsey, Benjamin Q Duong, Benjamin Burkley, Michael Clare-Salzler, Yan Gong, Tara A Higgins, Benjamin Kong, Taimour Langaee,[...]. Clin Transl Sci 2018
13
25

Pharmacogenomics education in medical and pharmacy schools: conclusions of a global survey.
Nataša Karas Kuželički, Irena Prodan Žitnik, David Gurwitz, Adrian Llerena, Ingolf Cascorbi, Sofia Siest, Maurizio Simmaco, Marc Ansari, Mario Pazzagli, Chiara Di Resta,[...]. Pharmacogenomics 2019
27
25

Clinical Pharmacogenetics Implementation Consortium Guideline for Cytochrome P450 (CYP)2D6 Genotype and Atomoxetine Therapy.
Jacob T Brown, Jeffrey R Bishop, Katrin Sangkuhl, Erika L Nurmi, Daniel J Mueller, Jean C Dinh, Andrea Gaedigk, Teri E Klein, Kelly E Caudle, James T McCracken,[...]. Clin Pharmacol Ther 2019
57
25

Pharmacogenetics for Safe Codeine Use in Sickle Cell Disease.
Roseann S Gammal, Kristine R Crews, Cyrine E Haidar, James M Hoffman, Donald K Baker, Patricia J Barker, Jeremie H Estepp, Deqing Pei, Ulrich Broeckel, Winfred Wang,[...]. Pediatrics 2016
49
25

Hmong participants' reactions to return of individual and community pharmacogenetic research results: "A positive light for our community".
K Holzer, K A Culhane-Pera, R J Straka, Y F Wen, M Lo, K Lee, T Xiong, K Peng, J Bishop, B Thyagarajan,[...]. J Community Genet 2021
4
50

Primary care and mental health providers' perceptions of implementation of pharmacogenetics testing for depression prescribing.
Bonnie M Vest, Laura O Wray, Laura A Brady, Michael E Thase, Gregory P Beehler, Sara R Chapman, Leland E Hull, David W Oslin. BMC Psychiatry 2020
8
25

Leveraging the utility of pharmacogenomics in psychiatry through clinical decision support: a focus group study.
Andrew Goodspeed, Nicolas Kostman, Trenton E Kriete, Joel W Longtine, Sean M Smith, Peregrin Marshall, Wesley Williams, Cheryl Clark, Weston W Blakeslee. Ann Gen Psychiatry 2019
6
33

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
186
25

Pharmacogenetic testing in primary care practice: opinions of physicians, pharmacists and patients.
Marie-Pier Frigon, Marie-Ève Blackburn, Camélia Dubois-Bouchard, Ann-Lorie Gagnon, Suzie Tardif, Karine Tremblay. Pharmacogenomics 2019
21
25

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
593
25

Telehealth as a Bright Spot of the COVID-19 Pandemic: Recommendations From the Virtual Frontlines ("Frontweb").
J Nwando Olayiwola, Candy Magaña, Ashley Harmon, Shalina Nair, Erica Esposito, Christine Harsh, L Arick Forrest, Randy Wexler. JMIR Public Health Surveill 2020
29
12

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Ozge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, Matthew S Lebo, Timothy W Yu, Shawn Fayer, Casie A Genetti, Talia S Schwartz, Pankaj B Agrawal, Richard B Parad,[...]. Am J Hum Genet 2019
61
12

Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019
12
12

Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
40
12


Awareness of family health history in a predominantly young adult population.
Sarina Madhavan, Emily Bullis, Rachel Myers, Chris J Zhou, Elise M Cai, Anu Sharma, Shreya Bhatia, Lori A Orlando, Susanne B Haga. PLoS One 2019
4
25


Improving Utilization of the Family History in the Electronic Health Record.
Kathleen T Hickey, Maria C Katapodi, Bernice Coleman, Karin Reuter-Rice, Angela R Starkweather. J Nurs Scholarsh 2017
12
12

Comparing Outcomes of Genetic Counseling Options in Breast and Ovarian Cancer: An Integrative Review
.
Danielle M Fournier, Angela F Bazzell, Joyce E Dains. Oncol Nurs Forum 2018
14
12

Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
Jeanna M McCuaig, Susan Randall Armel, Melanie Care, Alexandra Volenik, Raymond H Kim, Kelly A Metcalfe. Cancers (Basel) 2018
37
12

Impact of patient education videos on genetic counseling outcomes after exome sequencing.
Rebecca Hernan, Megan T Cho, Ashley L Wilson, Priyanka Ahimaz, Catherine Au, Sara M Berger, Edwin Guzman, Michelle Primiano, Jessica E Shaw, Meredith Ross,[...]. Patient Educ Couns 2020
6
16

Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.
Josephine Johnston, John D Lantos, Aaron Goldenberg, Flavia Chen, Erik Parens, Barbara A Koenig. Hastings Cent Rep 2018
31
12

Genetics professionals' opinions of whole-genome sequencing in the newborn period.
Elizabeth Ulm, W Gregory Feero, Richard Dineen, Joel Charrow, Catherine Wicklund. J Genet Couns 2015
8
12

Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Kiran Musunuru, Ray E Hershberger, Sharlene M Day, N Jennifer Klinedinst, Andrew P Landstrom, Victoria N Parikh, Siddharth Prakash, Christopher Semsarian, Amy C Sturm. Circ Genom Precis Med 2020
45
12

Genetics workforce: distribution of genetics services and challenges to health care in California.
Monica Penon-Portmann, Jiyoo Chang, Mira Cheng, Joseph T Shieh. Genet Med 2020
13
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.