A citation-based method for searching scientific literature

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.
Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
Times Cited: 363



ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
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




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
0

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
0

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
0

Public engagement with genomic medicine: a summary of town hall discussions.
Holly Etchegary, Mercy Winsor, Angela Power, Charlene Simmonds. J Community Genet 2021
1

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
0

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
3

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
0

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
1

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
0

Informed Consent in the Genomics Era.
Shannon Rego, Megan E Grove, Mildred K Cho, Kelly E Ormond. Cold Spring Harb Perspect Med 2020
5

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
24

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
9

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
1

Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
36

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
1

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
3

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
8

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
17

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
11

Personalized Medicine and the Power of Electronic Health Records.
Noura S Abul-Husn, Eimear E Kenny. Cell 2019
78

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
0

Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.
Ruth Horn, Michael Parker. Prenat Diagn 2018
55

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
20

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
19

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
71

The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.
Clair Morrissey, Rebecca L Walker. J Med Philos 2018
8

Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing.
Susan T Vadaparampil, Deborah Cragun. Transl Behav Med 2018
3

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
10

Genomics for paediatricians: promises and pitfalls.
Carrie Louise Hammond, Josh Matthew Willoughby, Michael James Parker. Arch Dis Child 2018
2

Strategies to Guide the Return of Genomic Research Findings: An Australian Perspective.
Lisa Eckstein, Margaret Otlowski. J Bioeth Inq 2018
1

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
11

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
16

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
12

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
14

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
19

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
21

[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
1

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
12

Preferences for the provision of whole genome sequencing services among young adults.
Christopher H Wade, Kailyn R Elliott. PLoS One 2017
2

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
15

Expect the unexpected: screening for secondary findings in clinical genomics research.
Michael P Mackley, Benjamin Capps. Br Med Bull 2017
12

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
15

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
22


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