A citation-based method for searching scientific literature

Christine Y Lu, Stephanie Loomer, Rachel Ceccarelli, Kathleen M Mazor, James Sabin, Ellen Wright Clayton, Geoffrey S Ginsburg, Ann Chen Wu. J Pers Med 2018
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


Insurance coverage policies for personalized medicine.
Andrew Hresko, Susanne B Haga. J Pers Med 2012
58
21


Access to Guideline-Recommended Pharmacogenomic Tests for Cancer Treatments: Experience of Providers and Patients.
Ann Chen Wu, Kathleen M Mazor, Rachel Ceccarelli, Stephanie Loomer, Christine Y Lu. J Pers Med 2017
5
60

Genetic testing insurance coverage trends: a review of publicly available policies from the largest US payers.
Michael D Graf, Denise F Needham, Nicole Teed, Trisha Brown. Per Med 2013
31
15

Development of a Streamlined Work Flow for Handling Patients' Genetic Testing Insurance Authorizations.
Wendy R Uhlmann, Katie Schwalm, Victoria M Raymond. J Genet Couns 2017
12
25


Pharmacogenomics in the clinic.
Mary V Relling, William E Evans. Nature 2015
353
15

Payer decision making for next-generation sequencing-based genetic tests: insights from cell-free DNA prenatal screening.
Andrew P Dervan, Patricia A Deverka, Julia R Trosman, Christine B Weldon, Michael P Douglas, Kathryn A Phillips. Genet Med 2017
14
21

Precision Medicine: From Science To Value.
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
118
15

Payer coverage policies for multigene tests.
Kathryn A Phillips, Patricia A Deverka, Julia R Trosman, Michael P Douglas, James D Chambers, Christine B Weldon, Andrew P Dervan. Nat Biotechnol 2017
25
15

Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?
Kathryn A Phillips, Patricia A Deverka, Gillian W Hooker, Michael P Douglas. Health Aff (Millwood) 2018
67
15

Private payer coverage policies for exome sequencing (ES) in pediatric patients: trends over time and analysis of evidence cited.
Michael P Douglas, Stephanie L Parker, Julia R Trosman, Anne M Slavotinek, Kathryn A Phillips. Genet Med 2019
14
21



A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
10

Personalized medicine: factors influencing reimbursement.
Lisa M Meckley, Peter J Neumann. Health Policy 2010
82
10

Clinical and economic challenges facing pharmacogenomics.
J Cohen, A Wilson, K Manzolillo. Pharmacogenomics J 2013
41
10

Estimating the prevalence of heterozygous familial hypercholesterolaemia: a systematic review and meta-analysis.
Leo E Akioyamen, Jacques Genest, Shubham D Shan, Rachel L Reel, Jordan M Albaum, Anna Chu, Jack V Tu. BMJ Open 2017
137
10

Familial Hypercholesterolemia: Cascade Screening in Children and Relatives of the Affected.
Nitika Setia, Renu Saxena, J P S Sawhney, Ishwar C Verma. Indian J Pediatr 2018
6
33

Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia.
Anne C Goldberg, Paul N Hopkins, Peter P Toth, Christie M Ballantyne, Daniel J Rader, Jennifer G Robinson, Stephen R Daniels, Samuel S Gidding, Sarah D de Ferranti, Matthew K Ito,[...]. J Clin Lipidol 2011
288
10

Genetic identification of familial hypercholesterolemia within a single U.S. health care system.
Noura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, Eric A Wright, Dustin N Hartzel, Claudia Gonzaga-Jauregui, Colm O'Dushlaine, Joseph B Leader, H Lester Kirchner, D'Andra M Lindbuchler,[...]. Science 2016
186
10

A novel approach to screening for familial hypercholesterolemia in a large public venue.
Megan Campbell, Jessa Humanki, Heather Zierhut. J Community Genet 2017
8
25

Prevalence of Familial Hypercholesterolemia in the 1999 to 2012 United States National Health and Nutrition Examination Surveys (NHANES).
Sarah D de Ferranti, Angie Mae Rodday, Michael M Mendelson, John B Wong, Laurel K Leslie, R Christopher Sheldrick. Circulation 2016
200
10

Parent-child genetic testing for familial hypercholesterolaemia in an Australian context.
Jing Pang, Andrew C Martin, Timothy R Bates, Amanda J Hooper, Damon A Bell, John R Burnett, Richard Norman, Gerald F Watts. J Paediatr Child Health 2018
11
18

Genetically confirmed familial hypercholesterolemia in outpatients with hypercholesterolemia.
Xu Wang, Long Jiang, Li-Yuan Sun, Yue Wu, Wen-Hui Wen, Xi-Fu Wang, Wei Liu, Yu-Jie Zhou, Lu-Ya Wang. J Geriatr Cardiol 2018
8
25


Familial Hypercholesterolemia: A Systematic Review of Guidelines on Genetic Testing and Patient Management.
Giuseppe Migliara, Valentina Baccolini, Annalisa Rosso, Elvira D'Andrea, Azzurra Massimi, Paolo Villari, Corrado De Vito.  2017
14
14

Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel.
Amy C Sturm, Joshua W Knowles, Samuel S Gidding, Zahid S Ahmad, Catherine D Ahmed, Christie M Ballantyne, Seth J Baum, Mafalda Bourbon, Alain Carrié, Marina Cuchel,[...]. J Am Coll Cardiol 2018
141
10

Genetic diagnosis of familial hypercholesterolemia is associated with a premature and high coronary heart disease risk.
Florent Séguro, Jean-Pierre Rabès, Dorota Taraszkiewicz, Jean-Bernard Ruidavets, Vanina Bongard, Jean Ferrières. Clin Cardiol 2018
11
18

Analysis of Children and Adolescents with Familial Hypercholesterolemia.
Ilenia Minicocci, Simone Pozzessere, Cristina Prisco, Anna Montali, Alessia di Costanzo, Eliana Martino, Francesco Martino, Marcello Arca. J Pediatr 2017
11
18

Barriers to the identification of familial hypercholesterolemia among primary care providers.
John Zimmerman, Daniel Duprez, Patricia McCarthy Veach, Heather A Zierhut. J Community Genet 2019
11
18

Genetically Confirmed Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome.
Almudena Amor-Salamanca, Sergio Castillo, Emiliano Gonzalez-Vioque, Fernando Dominguez, Lucía Quintana, Carla Lluís-Ganella, Juan Manuel Escudier, Javier Ortega, Enrique Lara-Pezzi, Luis Alonso-Pulpon,[...]. J Am Coll Cardiol 2017
67
10

Genetic testing of familial hypercholesterolemia in a real clinical setting.
Branislav Vohnout, Dominika Gabcova, Miroslava Huckova, Iwar Klimes, Daniela Gasperikova, Katarina Raslova. Wien Klin Wochenschr 2016
5
40

Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.
Kenneth D Levy, Kathryn Blake, Colette Fletcher-Hoppe, James Franciosi, Daisuke Goto, James K Hicks, Ann M Holmes, Sri Harsha Kanuri, Ebony B Madden, Michael D Musty,[...]. Genet Med 2019
21
10


Utilization of genetic tests: analysis of gene-specific billing in Medicare claims data.
Julie A Lynch, Brygida Berse, W David Dotson, Muin J Khoury, Nicole Coomer, John Kautter. Genet Med 2017
22
10

Precision oncology in advanced cancer patients improves overall survival with lower weekly healthcare costs.
Derrick S Haslem, Ingo Chakravarty, Gail Fulde, Heather Gilbert, Brian P Tudor, Karen Lin, James M Ford, Lincoln D Nadauld. Oncotarget 2018
15
13

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
10

Direct-to-Consumer Testing 2.0: Emerging Models of Direct-to-Consumer Genetic Testing.
Megan A Allyse, David H Robinson, Matthew J Ferber, Richard R Sharp. Mayo Clin Proc 2018
53
10

Genomic sequencing: assessing the health care system, policy, and big-data implications.
Kathryn A Phillips, Julia R Trosman, Robin K Kelley, Mark J Pletcher, Michael P Douglas, Christine B Weldon. Health Aff (Millwood) 2014
29
10

Health technology assessment and private payers' coverage of personalized medicine.
Julia R Trosman, Stephanie L Van Bebber, Kathryn A Phillips. J Oncol Pract 2011
26
10

EXAMINING EVIDENCE IN U.S. PAYER COVERAGE POLICIES FOR MULTI-GENE PANELS AND SEQUENCING TESTS.
James D Chambers, Cayla J Saret, Jordan E Anderson, Patricia A Deverka, Michael P Douglas, Kathryn A Phillips. Int J Technol Assess Health Care 2017
14
14

Preemptive pharmacogenetic testing: exploring the knowledge and perspectives of US payers.
Nicholas J Keeling, Meagen M Rosenthal, Donna West-Strum, Amit S Patel, Cyrine E Haidar, James M Hoffman. Genet Med 2019
27
10

From the Past to the Present: Insurer Coverage Frameworks for Next-Generation Tumor Sequencing.
Julia R Trosman, Christine B Weldon, William J Gradishar, Al B Benson, Massimo Cristofanilli, Allison W Kurian, James M Ford, Alan Balch, John Watkins, Kathryn A Phillips. Value Health 2018
9
22

Association of Broad-Based Genomic Sequencing With Survival Among Patients With Advanced Non-Small Cell Lung Cancer in the Community Oncology Setting.
Carolyn J Presley, Daiwei Tang, Pamela R Soulos, Anne C Chiang, Janina A Longtine, Kerin B Adelson, Roy S Herbst, Weiwei Zhu, Nathan C Nussbaum, Rachael A Sorg,[...]. JAMA 2018
57
10

Cost-effectiveness of pharmacogenetic-guided treatment: are we there yet?
M Verbelen, M E Weale, C M Lewis. Pharmacogenomics J 2017
90
10


Private payers disagree with Medicare over medical device coverage about half the time.
James D Chambers, Matthew Chenoweth, Teja Thorat, Peter J Neumann. Health Aff (Millwood) 2015
21
10


Genesurance Counseling: Patient Perspectives.
Chelsea Wagner, Lauren Murphy, Jacqueline Harkenrider, Sandra Darilek, Eleazar Soto-Torres, Quinn Stein, Jennifer Hoskovec. J Genet Couns 2018
8
25


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.