Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
Times Cited: 363
Times Cited: 363
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond, Heidi L Rehm, Michael S Watson, Marc S Williams, Leslie G Biesecker. Genet Med 2013
Times Cited: 1654
Times Cited: 1654
List of shared articles
Times cited
Challenges Related to the Use of Next-Generation Sequencing for the Optimization of Drug Therapy.
Yitian Zhou, Volker M Lauschke. Handb Exp Pharmacol 2022
Yitian Zhou, Volker M Lauschke. Handb Exp Pharmacol 2022
Clinical geneticists' views on and experiences with unsolicited findings in next-generation sequencing: "A great technology creating new dilemmas".
Vyne van der Schoot, Carlijn Damsté, Helger G Yntema, Han G Brunner, Anke J M Oerlemans. J Genet Couns 2022
Vyne van der Schoot, Carlijn Damsté, Helger G Yntema, Han G Brunner, Anke J M Oerlemans. J Genet Couns 2022
Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics.
Marion Rosier, Myriam Guedj, Patrick Calvas, Sophie Julia, Christelle Garnier, Anne Cambon-Thomsen, Maria Teresa Muñoz Sastre. J Health Psychol 2021
Marion Rosier, Myriam Guedj, Patrick Calvas, Sophie Julia, Christelle Garnier, Anne Cambon-Thomsen, Maria Teresa Muñoz Sastre. J Health Psychol 2021
Public engagement with genomic medicine: a summary of town hall discussions.
Holly Etchegary, Mercy Winsor, Angela Power, Charlene Simmonds. J Community Genet 2021
Holly Etchegary, Mercy Winsor, Angela Power, Charlene Simmonds. J Community Genet 2021
Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial.
Christine Rini, Myra I Roche, Feng-Chang Lin, Ann Katherine M Foreman, Cynthia M Khan, Ida Griesemer, Margaret Waltz, Kristy Lee, Julianne M O'Daniel, James P Evans,[...]. Patient Educ Couns 2021
Christine Rini, Myra I Roche, Feng-Chang Lin, Ann Katherine M Foreman, Cynthia M Khan, Ida Griesemer, Margaret Waltz, Kristy Lee, Julianne M O'Daniel, James P Evans,[...]. Patient Educ Couns 2021
A qualitative study among patients with an inherited retinal disease on the meaning of genomic unsolicited findings.
Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Caroline Van Cauwenbergh, Bart P Leroy, Ignaas Devisch, Elfride De Baere. Sci Rep 2021
Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Caroline Van Cauwenbergh, Bart P Leroy, Ignaas Devisch, Elfride De Baere. Sci Rep 2021
Participants' Preferences and Reasons for Wanting Feedback of Individual Genetic Research Results From an HIV-TB Genomic Study: A Case Study From Botswana.
Dimpho Ralefala, Mary Kasule, Olivia P Matshabane, Ambroise Wonkam, Mogomotsi Matshaba, Jantina de Vries. J Empir Res Hum Res Ethics 2021
Dimpho Ralefala, Mary Kasule, Olivia P Matshabane, Ambroise Wonkam, Mogomotsi Matshaba, Jantina de Vries. J Empir Res Hum Res Ethics 2021
A systematic approach to the disclosure of genomic findings in clinical practice and research: a proposed framework with colored matrix and decision-making pathways.
Kenji Matsui, Keiichiro Yamamoto, Shimon Tashiro, Tomohide Ibuki. BMC Med Ethics 2021
Kenji Matsui, Keiichiro Yamamoto, Shimon Tashiro, Tomohide Ibuki. BMC Med Ethics 2021
Attitudes towards Genetic Information Delivered by High-Throughput Sequencing among Molecular Geneticists, Genetic Counselors, Medical Advisors and Students in France.
Vlad Titerlea, Doulaye Dembélé, Jean-Louis Mandel, Jocelyn Laporte. Eur J Med Genet 2020
Vlad Titerlea, Doulaye Dembélé, Jean-Louis Mandel, Jocelyn Laporte. Eur J Med Genet 2020
Informed Consent in the Genomics Era.
Shannon Rego, Megan E Grove, Mildred K Cho, Kelly E Ormond. Cold Spring Harb Perspect Med 2020
Shannon Rego, Megan E Grove, Mildred K Cho, Kelly E Ormond. Cold Spring Harb Perspect Med 2020
From Genetics to Genomics: Facing the Liability Implications in Clinical Care.
Gary Marchant, Mark Barnes, James P Evans, Bonnie LeRoy, Susan M Wolf. J Law Med Ethics 2020
Gary Marchant, Mark Barnes, James P Evans, Bonnie LeRoy, Susan M Wolf. J Law Med Ethics 2020
Should Researchers Offer Results to Family Members of Cancer Biobank Participants? A Mixed-Methods Study of Proband and Family Preferences.
Deborah R Gordon, Carmen Radecki Breitkopf, Marguerite Robinson, Wesley O Petersen, Jason S Egginton, Kari G Chaffee, Gloria M Petersen, Susan M Wolf, Barbara A Koenig. AJOB Empir Bioeth 2019
Deborah R Gordon, Carmen Radecki Breitkopf, Marguerite Robinson, Wesley O Petersen, Jason S Egginton, Kari G Chaffee, Gloria M Petersen, Susan M Wolf, Barbara A Koenig. AJOB Empir Bioeth 2019
Using the diffusion of innovations model to guide participant engagement in the genomics era.
Katie L Lewis, Flavia M Facio, Courtney D Berrios. J Genet Couns 2019
Katie L Lewis, Flavia M Facio, Courtney D Berrios. J Genet Couns 2019
Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies.
Eleanor McVeigh, Harriet Jones, Graeme Black, Georgina Hall. J Community Genet 2019
Eleanor McVeigh, Harriet Jones, Graeme Black, Georgina Hall. J Community Genet 2019
Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results.
David J Seiffert, Patricia McCarthy Veach, Bonnie LeRoy, Weihua Guan, Heather Zierhut. J Genet Couns 2019
David J Seiffert, Patricia McCarthy Veach, Bonnie LeRoy, Weihua Guan, Heather Zierhut. J Genet Couns 2019
A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.
Melissa Martyn, Anaita Kanga-Parabia, Elly Lynch, Paul A James, Ivan Macciocca, Alison H Trainer, Jane Halliday, Louise Keogh, Janney Wale, Ingrid Winship,[...]. J Genet Couns 2019
Melissa Martyn, Anaita Kanga-Parabia, Elly Lynch, Paul A James, Ivan Macciocca, Alison H Trainer, Jane Halliday, Louise Keogh, Janney Wale, Ingrid Winship,[...]. J Genet Couns 2019
Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
Genetics professionals' attitudes toward prenatal exome sequencing.
Casey E Brew, Brian A Castro, Vivian Pan, Alexa Hart, Bruce Blumberg, Catherine Wicklund. J Genet Couns 2019
Casey E Brew, Brian A Castro, Vivian Pan, Alexa Hart, Bruce Blumberg, Catherine Wicklund. J Genet Couns 2019
Personalized Medicine and the Power of Electronic Health Records.
Noura S Abul-Husn, Eimear E Kenny. Cell 2019
Noura S Abul-Husn, Eimear E Kenny. Cell 2019
Cases in Precision Medicine: Should You Participate in a Study Involving Genomic Sequencing of Your Patients?
Paul S Appelbaum, Deborah F Stiles, Wendy Chung. Ann Intern Med 2019
Paul S Appelbaum, Deborah F Stiles, Wendy Chung. Ann Intern Med 2019
Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.
Ruth Horn, Michael Parker. Prenat Diagn 2018
Ruth Horn, Michael Parker. Prenat Diagn 2018
Improved ethical guidance for the return of results from psychiatric genomics research.
G Lázaro-Muñoz, M S Farrell, J J Crowley, D M Filmyer, R A Shaughnessy, R C Josiassen, P F Sullivan. Mol Psychiatry 2018
G Lázaro-Muñoz, M S Farrell, J J Crowley, D M Filmyer, R A Shaughnessy, R C Josiassen, P F Sullivan. Mol Psychiatry 2018
The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study.
Christine Rini, Cynthia M Khan, Elizabeth Moore, Myra I Roche, James P Evans, Jonathan S Berg, Bradford C Powell, Giselle Corbie-Smith, Ann Katherine M Foreman, Ida Griesemer,[...]. Genet Med 2018
Christine Rini, Cynthia M Khan, Elizabeth Moore, Myra I Roche, James P Evans, Jonathan S Berg, Bradford C Powell, Giselle Corbie-Smith, Ann Katherine M Foreman, Ida Griesemer,[...]. Genet Med 2018
Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.
Clair Morrissey, Rebecca L Walker. J Med Philos 2018
Clair Morrissey, Rebecca L Walker. J Med Philos 2018
Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing.
Susan T Vadaparampil, Deborah Cragun. Transl Behav Med 2018
Susan T Vadaparampil, Deborah Cragun. Transl Behav Med 2018
Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.
Swetha Narayanan, Bruce Blumberg, Marla L Clayman, Vivian Pan, Catherine Wicklund. J Genet Couns 2018
Swetha Narayanan, Bruce Blumberg, Marla L Clayman, Vivian Pan, Catherine Wicklund. J Genet Couns 2018
Genomics for paediatricians: promises and pitfalls.
Carrie Louise Hammond, Josh Matthew Willoughby, Michael James Parker. Arch Dis Child 2018
Carrie Louise Hammond, Josh Matthew Willoughby, Michael James Parker. Arch Dis Child 2018
Strategies to Guide the Return of Genomic Research Findings: An Australian Perspective.
Lisa Eckstein, Margaret Otlowski. J Bioeth Inq 2018
Lisa Eckstein, Margaret Otlowski. J Bioeth Inq 2018
How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis.
D F Vears, E Niemiec, H C Howard, P Borry. Clin Genet 2018
D F Vears, E Niemiec, H C Howard, P Borry. Clin Genet 2018
Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate.
Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
Preference heterogeneity with respect to whole genome sequencing. A discrete choice experiment among parents of children with rare genetic diseases.
Christine Peyron, Aurore Pélissier, Sophie Béjean. Soc Sci Med 2018
Christine Peyron, Aurore Pélissier, Sophie Béjean. Soc Sci Med 2018
Responsibility, identity, and genomic sequencing: A comparison of published recommendations and patient perspectives on accepting or declining incidental findings.
Felicity Boardman, Rachel Hale. Mol Genet Genomic Med 2018
Felicity Boardman, Rachel Hale. Mol Genet Genomic Med 2018
Cost analysis of whole genome sequencing in German clinical practice.
Marika Plöthner, Martin Frank, J-Matthias Graf von der Schulenburg. Eur J Health Econ 2017
Marika Plöthner, Martin Frank, J-Matthias Graf von der Schulenburg. Eur J Health Econ 2017
My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
[Whole-genome sequencing in German clinical practice : Economic impacts of its use in selected areas of application].
Marika Plöthner, Martin Frank, J-Matthias Graf von der Schulenburg. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2017
Marika Plöthner, Martin Frank, J-Matthias Graf von der Schulenburg. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2017
Confidentiality in Biobanking Research: A Comparison of Donor and Nondonor Families' Understanding of Risks.
Laura A Siminoff, Maureen Wilson-Genderson, Maghboeba Mosavel, Laura Barker, Jennifer Trgina, Heather M Traino. Genet Test Mol Biomarkers 2017
Laura A Siminoff, Maureen Wilson-Genderson, Maghboeba Mosavel, Laura Barker, Jennifer Trgina, Heather M Traino. Genet Test Mol Biomarkers 2017
Preferences for the provision of whole genome sequencing services among young adults.
Christopher H Wade, Kailyn R Elliott. PLoS One 2017
Christopher H Wade, Kailyn R Elliott. PLoS One 2017
Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
Expect the unexpected: screening for secondary findings in clinical genomics research.
Michael P Mackley, Benjamin Capps. Br Med Bull 2017
Michael P Mackley, Benjamin Capps. Br Med Bull 2017
Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples.
Kurt D Christensen, Sarah K Savage, Noelle L Huntington, Elissa R Weitzman, Sonja I Ziniel, Phoebe L Bacon, Cara N Cacioppo, Robert C Green, Ingrid A Holm. J Empir Res Hum Res Ethics 2017
Kurt D Christensen, Sarah K Savage, Noelle L Huntington, Elissa R Weitzman, Sonja I Ziniel, Phoebe L Bacon, Cara N Cacioppo, Robert C Green, Ingrid A Holm. J Empir Res Hum Res Ethics 2017
Lost in translation: returning germline genetic results in genome-scale cancer research.
Amber L Johns, Skye H McKay, Jeremy L Humphris, Mark Pinese, Lorraine A Chantrill, R Scott Mead, Katherine Tucker, Lesley Andrews, Annabel Goodwin, Conrad Leonard,[...]. Genome Med 2017
Amber L Johns, Skye H McKay, Jeremy L Humphris, Mark Pinese, Lorraine A Chantrill, R Scott Mead, Katherine Tucker, Lesley Andrews, Annabel Goodwin, Conrad Leonard,[...]. Genome Med 2017