Kathryn A Phillips, Patricia A Deverka, Gillian W Hooker, Michael P Douglas. Health Aff (Millwood) 2018
Times Cited: 87
Times Cited: 87
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
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
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
Christine E Miller, Patti Krautscheid, Erin E Baldwin, Tatiana Tvrdik, Amanda S Openshaw, Kim Hart, Danielle Lagrave. Am J Med Genet A 2014
9
Current conditions in medical genetics practice.
Deborah R Maiese, Alisha Keehn, Megan Lyon, David Flannery, Michael Watson. Genet Med 2019
Deborah R Maiese, Alisha Keehn, Megan Lyon, David Flannery, Michael Watson. Genet Med 2019
11
Precision Medicine: From Science To Value.
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
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
Kathryn A Phillips, Patricia A Deverka, Julia R Trosman, Michael P Douglas, James D Chambers, Christine B Weldon, Andrew P Dervan. Nat Biotechnol 2017
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
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
45
Opportunities to improve recruitment into medical genetics residency programs: survey results of program directors and medical genetics residents.
Michelle Cichon, Gerald L Feldman. Genet Med 2014
Michelle Cichon, Gerald L Feldman. Genet Med 2014
25
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
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
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
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
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
Kathryn A Phillips, Julia R Trosman, Robin K Kelley, Mark J Pletcher, Michael P Douglas, Christine B Weldon. Health Aff (Millwood) 2014
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
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
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
Diane Hauser, Aniwaa Owusu Obeng, Kezhen Fei, Michelle A Ramos, Carol R Horowitz. Health Aff (Millwood) 2018
12
Evolving Payer Coverage Policies on Genomic Sequencing Tests: Beginning of the End or End of the Beginning?
Kathryn A Phillips. JAMA 2018
Kathryn A Phillips. JAMA 2018
25
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
Zornitza Stark, Deborah Schofield, Khurshid Alam, William Wilson, Nessie Mupfeki, Ivan Macciocca, Rupendra Shrestha, Susan M White, Clara Gaff. Genet Med 2017
4
Primary-care providers' perceived barriers to integration of genetics services: a systematic review of the literature.
Natalie A Mikat-Stevens, Ingrid A Larson, Beth A Tarini. Genet Med 2015
Natalie A Mikat-Stevens, Ingrid A Larson, Beth A Tarini. Genet Med 2015
4
Expanding the genetic counseling workforce: program directors' views on increasing the size of genetic counseling graduate programs.
Vivian Pan, Beverly M Yashar, Rachel Pothast, Catherine Wicklund. Genet Med 2016
Vivian Pan, Beverly M Yashar, Rachel Pothast, Catherine Wicklund. Genet Med 2016
9
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
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
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
Caryn Kseniya Rubanovich, Cynthia Cheung, Jess Mandel, Cinnamon S Bloss. Hum Mol Genet 2018
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
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
Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics.
. Genet Med 2015
. 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
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
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
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
4
Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS).
Julia R Trosman, Christine B Weldon, Anne Slavotinek, Mary E Norton, Michael P Douglas, Kathryn A Phillips. Genet Med 2020
Julia R Trosman, Christine B Weldon, Anne Slavotinek, Mary E Norton, Michael P Douglas, Kathryn A Phillips. Genet Med 2020
17
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
Michael P Douglas, Stephanie L Parker, Julia R Trosman, Anne M Slavotinek, Kathryn A Phillips. Genet Med 2019
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
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
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
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
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
Erin Crellin, Belinda McClaren, Amy Nisselle, Stephanie Best, Clara Gaff, Sylvia Metcalfe. Front Genet 2019
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
Jeanne De Sa, Brantley Carlson, Nadine Caputo, Deneen Vojta, Lewis Sandy, Simon Stevens. Per Med 2013
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
MaryAnn Campion, Constance Goldgar, Robert J Hopkin, Cynthia A Prows, Shoumita Dasgupta. Genet Med 2019
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
Lidewij Henneman, Eric Vermeulen, Carla G van El, Liesbeth Claassen, Danielle R M Timmermans, Martina C Cornel. Eur J Hum Genet 2013
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
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
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
Daryl E Pritchard, Franziska Moeckel, Mary Susan Villa, Laura T Housman, Catherine A McCarty, Howard L McLeod. Per Med 2017
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
Sara Pirzadeh-Miller, Linda S Robinson, Parker Read, Theodora S Ross. J Genet Couns 2017
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
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
4
A novel approach in pediatric telegenetic services: geneticist, pediatrician and genetic counselor team.
Shobana Kubendran, Siddharthan Sivamurthy, Gerald Bradley Schaefer. Genet Med 2017
Shobana Kubendran, Siddharthan Sivamurthy, Gerald Bradley Schaefer. Genet Med 2017
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
Brandie Heald, Lisa Rybicki, Diane Clements, Jessica Marquard, Jessica Mester, Ryan Noss, Monica Nardini, Jill Polk, Brittany Psensky, Christina Rigelsky,[...]. NPJ Genom Med 2016
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
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
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
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
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
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
3
The state of the medical geneticist workforce: findings of the 2003 survey of American Board of Medical Genetics certified geneticists.
Judith A Cooksey, Gaetano Forte, Judith Benkendorf, Miriam G Blitzer. Genet Med 2005
Judith A Cooksey, Gaetano Forte, Judith Benkendorf, Miriam G Blitzer. Genet Med 2005
4
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
Jevon Plunkett-Rondeau, Katherine Hyland, Shoumita Dasgupta. Genet Med 2015
6
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
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
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
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
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
Julia R Trosman, Christine B Weldon, R Kate Kelley, Kathryn A Phillips. J Natl Compr Canc Netw 2015
10
From helices to health: undergraduate medical education in genetics and genomics.
Katherine Hyland, Kathryn Garber, Shoumita Dasgupta. Per Med 2019
Katherine Hyland, Kathryn Garber, Shoumita Dasgupta. Per Med 2019
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
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
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
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
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
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.