A citation-based method for searching scientific literature




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: 1486




List of shared articles



Times cited

Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment.
Shan Jiang, Aslam H Anis, Ian Cromwell, Tima Mohammadi, Kasmintan A Schrader, Janet Lucas, Christine M Armour, Marc Clausen, Yvonne Bombard, Dean A Regier. Genet Med 2020
0

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

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
125

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
29

Associations of perceived norms with intentions to learn genomic sequencing results: Roles for attitudes and ambivalence.
Allecia E Reid, Jennifer M Taber, Rebecca A Ferrer, Barbara B Biesecker, Katie L Lewis, Leslie G Biesecker, William M P Klein. Health Psychol 2018
3

Genomic information and a person's right not to know: A closer look at variations in hypothetical informational preferences in a German sample.
Laura Flatau, Markus Reitt, Gunnar Duttge, Christian Lenk, Barbara Zoll, Wolfgang Poser, Alexandra Weber, Urs Heilbronner, Marcella Rietschel, Jana Strohmaier,[...]. PLoS One 2018
4

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance.
Wylie Burke, Laura M Beskow, Susan Brown Trinidad, Stephanie M Fullerton, Kathleen Brelsford. J Law Med Ethics 2018
10

Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.
Josephine Johnston, John D Lantos, Aaron Goldenberg, Flavia Chen, Erik Parens, Barbara A Koenig. Hastings Cent Rep 2018
26


The Gene Pool: The Ethics of Genetics in Primary Care.
Karen J Whitt, McKenna Hughes, Elizabeth Betsy S Hopkins, Ann Maradiegue. Annu Rev Nurs Res 2016
2

Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered.
Rhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, Martijn Pj Lolkema, Stefan Sleijfer, Emile E Voest, Margreet Gem Ausems, Neeltje Steeghs. Eur J Hum Genet 2016
18

A comparative assessment of clinical whole exome and transcriptome profiling across sequencing centers: implications for precision cancer medicine.
Eliezer M Van Allen, Dan Robinson, Colm Morrissey, Colin Pritchard, Alma Imamovic, Scott Carter, Mara Rosenberg, Aaron McKenna, Yi-Mi Wu, Xuhong Cao,[...]. Oncotarget 2016
13

Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders.
S Fokstuen, P Makrythanasis, E Hammar, M Guipponi, E Ranza, K Varvagiannis, F A Santoni, M Albarca-Aguilera, M E Poleggi, F Couchepin,[...]. Hum Genomics 2016
17

WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases.
Amélie Pinard, David Salgado, Jean-Pierre Desvignes, Ghadi Rai, Nadine Hanna, Pauline Arnaud, Céline Guien, Maria Martinez, Laurence Faivre, Guillaume Jondeau,[...]. Hum Mutat 2016
2

Tay-Sachs disease: current perspectives from Australia.
Raelia M Lew, Leslie Burnett, Anné L Proos, Martin B Delatycki. Appl Clin Genet 2015
14

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.
Dean A Regier, Stuart J Peacock, Reka Pataky, Kimberly van der Hoek, Gail P Jarvik, Jeffrey Hoch, David Veenstra. CMAJ 2015
47