A citation-based method for searching scientific literature

Kathryn A Phillips, Patricia A Deverka, Gillian W Hooker, Michael P Douglas. Health Aff (Millwood) 2018
Times Cited: 87







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



Times Cited
  Times     Co-cited
Similarity


Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
132
13

Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing.
Christine E Miller, Patti Krautscheid, Erin E Baldwin, Tatiana Tvrdik, Amanda S Openshaw, Kim Hart, Danielle Lagrave. Am J Med Genet A 2014
75
9

Current conditions in medical genetics practice.
Deborah R Maiese, Alisha Keehn, Megan Lyon, David Flannery, Michael Watson. Genet Med 2019
53
11

Precision Medicine: From Science To Value.
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
165
6

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
26
19

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
11
45


The Global State of the Genetic Counseling Profession.
MaryAnn Abacan, Lamia Alsubaie, Kristine Barlow-Stewart, Beppy Caanen, Christophe Cordier, Eliza Courtney, Emeline Davoine, Janice Edwards, Niby J Elackatt, Kate Gardiner,[...]. Eur J Hum Genet 2019
92
5

Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast Cancer.
Allison W Kurian, Yun Li, Ann S Hamilton, Kevin C Ward, Sarah T Hawley, Monica Morrow, M Chandler McLeod, Reshma Jagsi, Steven J Katz. J Clin Oncol 2017
146
5

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
32
12

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
564
4

Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.
Diane Hauser, Aniwaa Owusu Obeng, Kezhen Fei, Michelle A Ramos, Carol R Horowitz. Health Aff (Millwood) 2018
32
12


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
4



Payer Coverage for Hereditary Cancer Panels: Barriers, Opportunities, and Implications for the Precision Medicine Initiative.
Julia R Trosman, Christine B Weldon, Michael P Douglas, Allison W Kurian, R Kate Kelley, Patricia A Deverka, Kathryn A Phillips. J Natl Compr Canc Netw 2017
26
15

Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States.
Caryn Kseniya Rubanovich, Cynthia Cheung, Jess Mandel, Cinnamon S Bloss. Hum Mol Genet 2018
44
9

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
4


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
918
4

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
122
4


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
19
21

Improving the value of costly genetic reference laboratory testing with active utilization management.
Jane A Dickerson, Bonnie Cole, Jessie H Conta, Monica Wellner, Stephanie E Wallace, Rhona M Jack, Joe Rutledge, Michael L Astion. Arch Pathol Lab Med 2014
38
10

Genetic Testing and Results in a Population-Based Cohort of Breast Cancer Patients and Ovarian Cancer Patients.
Allison W Kurian, Kevin C Ward, Nadia Howlader, Dennis Deapen, Ann S Hamilton, Angela Mariotto, Daniel Miller, Lynne S Penberthy, Steven J Katz. J Clin Oncol 2019
131
4

Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.
Erin Crellin, Belinda McClaren, Amy Nisselle, Stephanie Best, Clara Gaff, Sylvia Metcalfe. Front Genet 2019
26
15

Growth of molecular diagnostics and genetic testing in the USA, 2008-2011: analysis and implications.
Jeanne De Sa, Brantley Carlson, Nadine Caputo, Deneen Vojta, Lewis Sandy, Simon Stevens. Per Med 2013
9
44

Genomic education for the next generation of health-care providers.
MaryAnn Campion, Constance Goldgar, Robert J Hopkin, Cynthia A Prows, Shoumita Dasgupta. Genet Med 2019
32
12

Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010.
Lidewij Henneman, Eric Vermeulen, Carla G van El, Liesbeth Claassen, Danielle R M Timmermans, Martina C Cornel. Eur J Hum Genet 2013
70
5

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
386
3

Strategies for integrating personalized medicine into healthcare practice.
Daryl E Pritchard, Franziska Moeckel, Mary Susan Villa, Laura T Housman, Catherine A McCarty, Howard L McLeod. Per Med 2017
42
7


Genetic Counseling Assistants: an Integral Piece of the Evolving Genetic Counseling Service Delivery Model.
Sara Pirzadeh-Miller, Linda S Robinson, Parker Read, Theodora S Ross. J Genet Couns 2017
21
14

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
62
4

A novel approach in pediatric telegenetic services: geneticist, pediatrician and genetic counselor team.
Shobana Kubendran, Siddharthan Sivamurthy, Gerald Bradley Schaefer. Genet Med 2017
31
9

Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices.
Brandie Heald, Lisa Rybicki, Diane Clements, Jessica Marquard, Jessica Mester, Ryan Noss, Monica Nardini, Jill Polk, Brittany Psensky, Christina Rigelsky,[...]. NPJ Genom Med 2016
19
15

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
C Alexander Valencia, Ammar Husami, Jennifer Holle, Judith A Johnson, Yaping Qian, Abhinav Mathur, Chao Wei, Subba Rao Indugula, Fanggeng Zou, Haiying Meng,[...]. Front Pediatr 2015
111
3

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
162
3

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
82
3


Training future physicians in the era of genomic medicine: trends in undergraduate medical genetics education.
Jevon Plunkett-Rondeau, Katherine Hyland, Shoumita Dasgupta. Genet Med 2015
44
6

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
643
3

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
350
3

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
967
3

Challenges of coverage policy development for next-generation tumor sequencing panels: experts and payers weigh in.
Julia R Trosman, Christine B Weldon, R Kate Kelley, Kathryn A Phillips. J Natl Compr Canc Netw 2015
29
10

From helices to health: undergraduate medical education in genetics and genomics.
Katherine Hyland, Kathryn Garber, Shoumita Dasgupta. Per Med 2019
11
27

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
Susanne B Haga, Madeline M Carrig, Julianne M O'Daniel, Lori A Orlando, Ley A Killeya-Jones, Geoffrey S Ginsburg, Alex Cho. J Gen Intern Med 2011
58
5

Public knowledge of and attitudes toward genetics and genetic testing.
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
140
3

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
3


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.