A citation-based method for searching scientific literature

Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
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




List of shared articles



Times cited


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



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



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



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



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



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


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


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