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: 328



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: 1309




List of shared articles



Times cited

Public engagement with genomic medicine: a summary of town hall discussions.
Holly Etchegary, Mercy Winsor, Angela Power, Charlene Simmonds.  2020
0

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
3

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
0

Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
17

The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies.
Eleanor McVeigh, Harriet Jones, Graeme Black, Georgina Hall.  2019
0

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
0

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
0

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
4

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
1

Personalized Medicine and the Power of Electronic Health Records.
Noura S Abul-Husn, Eimear E Kenny. Cell 2019
14

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

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 2019
0

Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.
Ruth Horn, Michael Parker. Prenat. Diagn. 2018
29

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
14

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
8

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
30

The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.
Clair Morrissey, Rebecca L Walker. J Med Philos 2018
5

Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing.
Susan T Vadaparampil, Deborah Cragun. Transl Behav Med 2018
4

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
3

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
7

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
4

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
8

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
10

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
16

[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
9

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
11

Expect the unexpected: screening for secondary findings in clinical genomics research.
Michael P Mackley, Benjamin Capps. Br. Med. Bull. 2017
7

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
5

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
16

Interest and Attitudes of Patients With Advanced Cancer With Regard to Secondary Germline Findings From Tumor Genomic Profiling.
Jada G Hamilton, Elyse Shuk, Margaux C Genoff, Vivian M Rodríguez, Jennifer L Hay, Kenneth Offit, Mark E Robson. J Oncol Pract 2017
11

Review of Clinical Next-Generation Sequencing.
Sophia Yohe, Bharat Thyagarajan. Arch. Pathol. Lab. Med. 2017
60

When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing.
Leila Jamal, Jill O Robinson, Kurt D Christensen, Jennifer Blumenthal-Barby, Melody J Slashinski, Denise Lautenbach Perry, Jason L Vassy, Julia Wycliff, Robert C Green, Amy L McGuire. AJOB Empir Bioeth 2017
18

The price of whole-genome sequencing may be decreasing, but who will be sequenced?
Deborah A Marshall, Karen V MacDonald, Jill Oliver Robinson, Lisa F Barcellos, Milena Gianfrancesco, Monica Helm, Amy McGuire, Robert C Green, Michael P Douglas, Michael A Goldman,[...]. Per Med 2017
2

Analysis and Annotation of Whole-Genome or Whole-Exome Sequencing Derived Variants for Clinical Diagnosis.
Elizabeth A Worthey. Curr Protoc Hum Genet 2017
6

The Continuing Evolution of Ethical Standards for Genomic Sequencing in Clinical Care: Restoring Patient Choice.
Susan M Wolf. J Law Med Ethics 2017
3

Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.
K A Kaphingst, J Ivanovich, B B Biesecker, R Dresser, J Seo, L G Dressler, P J Goodfellow, M S Goodman. Clin. Genet. 2016
20

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur. J. Hum. Genet. 2016
84

Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing.
Elli G Gourna, Natalie Armstrong, Susan E Wallace. Eur. J. Hum. Genet. 2016
5

Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing.
Julia Wynn. J Genet Couns 2016
12

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study.
Bettina Meiser, Ben Storey, Veronica Quinn, Belinda Rahman, Lesley Andrews. J Genet Couns 2016
7

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe, Timothy Carey, Kristy R Crooks, Brian C Jensen, Eric T Juengst, Kristy Lee,[...]. Genet. Med. 2016
41

Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned.
Bich-Thu Duong, Ravi Savarirayan, Ingrid Winship. Fam. Cancer 2016
2

Genomic intensive care: should we perform genome testing in critically ill newborns?
Dominic J C Wilkinson, Christopher Barnett, Julian Savulescu, Ainsley J Newson. Arch. Dis. Child. Fetal Neonatal Ed. 2016
8

Patient hopes for diagnostic genomic sequencing: roles of uncertainty and social status.
Cynthia M Khan, Elizabeth G Moore, Cristina Leos, Christine Rini. Eur. J. Hum. Genet. 2016
9


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