A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017
76
36

Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.
Kathryn A Phillips, Patricia A Deverka, Harold C Sox, Muin J Khoury, Lewis G Sandy, Geoffrey S Ginsburg, Sean R Tunis, Lori A Orlando, Michael P Douglas. Genet Med 2017
38
18

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
18

Evidence based medicine: what it is and what it isn't.
D L Sackett, W M Rosenberg, J A Gray, R B Haynes, W S Richardson. BMJ 1996
13

Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur J Hum Genet 2017
67
13

What is the clinical utility of genetic testing?
Scott D Grosse, Muin J Khoury. Genet Med 2006
182
13

Defining personal utility in genomics: A Delphi study.
J N Kohler, E Turbitt, K L Lewis, B S Wilfond, L Jamal, H L Peay, L G Biesecker, B B Biesecker. Clin Genet 2017
42
13


Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
Nina R Sperber, Janet S Carpenter, Larisa H Cavallari, Laura J Damschroder, Rhonda M Cooper-DeHoff, Joshua C Denny, Geoffrey S Ginsburg, Yue Guan, Carol R Horowitz, Kenneth D Levy,[...]. BMC Med Genomics 2017
64
13

Will Precision Medicine Improve Population Health?
Muin J Khoury, Sandro Galea. JAMA 2016
111
9

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
261
9


Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.
Zornitza Stark, Deborah Schofield, Melissa Martyn, Luke Rynehart, Rupendra Shrestha, Khurshid Alam, Sebastian Lunke, Tiong Y Tan, Clara L Gaff, Susan M White. Genet Med 2019
81
9

Personal utility in genomic testing: is there such a thing?
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. J Med Ethics 2015
69
9

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
354
9

Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement.
Zornitza Stark, Deborah Schofield, Khurshid Alam, William Wilson, Nessie Mupfeki, Ivan Macciocca, Rupendra Shrestha, Susan M White, Clara Gaff. Genet Med 2017
123
9

Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet Med 2018
85
9

Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.
Tiong Yang Tan, Oliver James Dillon, Zornitza Stark, Deborah Schofield, Khurshid Alam, Rupendra Shrestha, Belinda Chong, Dean Phelan, Gemma R Brett, Emma Creed,[...]. JAMA Pediatr 2017
165
9

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
573
9

A proposed approach to accelerate evidence generation for genomic-based technologies in the context of a learning health system.
Christine Y Lu, Marc S Williams, Geoffrey S Ginsburg, Sengwee Toh, Jeff S Brown, Muin J Khoury. Genet Med 2018
13
15


Translational research is a key to nongeneticist physicians' genomics education.
W Gregory Feero, Teri A Manolio, Muin J Khoury. Genet Med 2014
25
9

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
108
9

Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing.
Joshua W Knowles, Daniel J Rader, Muin J Khoury. JAMA 2017
96
9

Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.
W D Dotson, M P Douglas, K Kolor, A C Stewart, M S Bowen, M Gwinn, A Wulf, H M Anders, C Q Chang, M Clyne,[...]. Clin Pharmacol Ther 2014
41
9

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
100
9

Preparing for precision medicine.
Reza Mirnezami, Jeremy Nicholson, Ara Darzi. N Engl J Med 2012
369
9

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
349
9

Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
Lori A Orlando, Nina R Sperber, Corrine Voils, Marshall Nichols, Rachel A Myers, R Ryanne Wu, Tejinder Rakhra-Burris, Kenneth D Levy, Mia Levy, Toni I Pollin,[...]. Genet Med 2018
33
9

Horizon scanning for translational genomic research beyond bench to bedside.
Mindy Clyne, Sheri D Schully, W David Dotson, Michael P Douglas, Marta Gwinn, Katherine Kolor, Anja Wulf, M Scott Bowen, Muin J Khoury. Genet Med 2014
24
9

Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda.
Enola Proctor, Hiie Silmere, Ramesh Raghavan, Peter Hovmand, Greg Aarons, Alicia Bunger, Richard Griffey, Melissa Hensley. Adm Policy Ment Health 2011
9

Addressing core challenges for the next generation of type 2 translation research and systems: the translation science to population impact (TSci Impact) framework.
Richard Spoth, Louise A Rohrbach, Mark Greenberg, Philip Leaf, C Hendricks Brown, Abigail Fagan, Richard F Catalano, Mary Ann Pentz, Zili Sloboda, J David Hawkins. Prev Sci 2013
133
9


Demystifying theory and its use in improvement.
Frank Davidoff, Mary Dixon-Woods, Laura Leviton, Susan Michie. BMJ Qual Saf 2015
307
9

Genetic tests: clinical validity and clinical utility.
Wylie Burke. Curr Protoc Hum Genet 2014
54
9

Clinical utility of genetic and genomic services: context matters.
W David Dotson, M Scott Bowen, Katherine Kolor, Muin J Khoury. Genet Med 2016
10
20


The policy of public health genomics in Italy.
Benedetto Simone, Walter Mazzucco, Maria Rosaria Gualano, Antonella Agodi, Domenico Coviello, Francesca Dagna Bricarelli, Bruno Dallapiccola, Emilio Di Maria, Antonio Federici, Maurizio Genuardi,[...]. Health Policy 2013
20
10

How is genetic testing evaluated? A systematic review of the literature.
Erica Pitini, Corrado De Vito, Carolina Marzuillo, Elvira D'Andrea, Annalisa Rosso, Antonio Federici, Emilio Di Maria, Paolo Villari. Eur J Hum Genet 2018
38
9

Current state of genomic policies in healthcare among EU member states: results of a survey of chief medical officers.
W Mazzucco, R Pastorino, T Lagerberg, M Colotto, E d'Andrea, C Marotta, C Marzuillo, P Villari, A Federici, W Ricciardi,[...]. Eur J Public Health 2017
13
15

From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
64
9

A proposal of a new evaluation framework towards implementation of genetic tests.
Erica Pitini, Elvira D'Andrea, Corrado De Vito, Annalisa Rosso, Brigid Unim, Carolina Marzuillo, Antonio Federici, Emilio Di Maria, Paolo Villari. PLoS One 2019
10
20

Impact of a diet and activity health promotion intervention on regional patterns of DNA methylation.
Elizabeth Hibler, Lei Huang, Jorge Andrade, Bonnie Spring. Clin Epigenetics 2019
14
14

Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts.
Alanna Kulchak Rahm, Deborah Cragun, Jessica Ezzell Hunter, Mara M Epstein, Jan Lowery, Christine Y Lu, Pamala A Pawloski, Ravi N Sharaf, Su-Ying Liang, Andrea N Burnett-Hartman,[...]. BMC Health Serv Res 2018
20
10

Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors.
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018
16
6

Heart disease risk information, encouragement, and physical activity among Mexican-origin couples: Self- or spouse-driven change?
Kaley F Skapinsky, Susan Persky, Megan Lewis, Andrea Goergen, Sato Ashida, Hendrik D de Heer, Donald Hadley, Anna V Wilkinson, Laura M Koehly. Transl Behav Med 2018
6
16

Patient communication of cancer genetic test results in a diverse population.
Charit√© N Ricker, Rachel B Koff, Chenxu Qu, Julie Culver, Duveen Sturgeon, Kerry E Kingham, Katrina Lowstuter, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra Lebensohn,[...]. Transl Behav Med 2018
17
5

Genetic test reporting of CDKN2A provides informational and motivational benefits for managing melanoma risk.
Lisa G Aspinwall, Tammy K Stump, Jennifer M Taber, Danielle M Drummond, Wendy Kohlmann, Marjan Champine, Sancy A Leachman. Transl Behav Med 2018
14
7

Introduction to the special series on health disparities in genomic medicine.
Kristi D Graves, Kenneth P Tercyak. Health Psychol 2015
2
50

The impact of raw DNA availability and corresponding online interpretation services: A mixed-methods study.
Caitlin G Allen, Jazmine Gabriel, Maureen Flynn, Tricia N Cunningham, Catharine Wang. Transl Behav Med 2018
16
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.