A citation-based method for searching scientific literature




Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf, Kent D McKelvey, Kelly E Ormond, C Sue Richards, Christopher N Vlangos, Michael Watson, Christa L Martin, David T Miller. Genet Med 2017
Times Cited: 761




List of shared articles



Times cited

Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing.
Lea Godino, Liliana Varesco, William Bruno, Carla Bruzzone, Linda Battistuzzi, Marzena Franiuk, Sara Miccoli, Benedetta Bertonazzi, Claudio Graziano, Marco Seri,[...]. J Genet Couns 2021
1

Clinical Findings and Diagnostic Yield of Arrhythmogenic Cardiomyopathy Through Genomic Screening of Pathogenic or Likely Pathogenic Desmosome Gene Variants.
Eric D Carruth, Dominik Beer, Amro Alsaid, Marci L B Schwartz, Megan McMinn, Melissa A Kelly, Adam H Buchanan, Christopher D Nevius, Hugh Calkins, Cynthia A James,[...]. Circ Genom Precis Med 2021
0


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

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

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

Next-Generation Sequencing to Diagnose Suspected Genetic Disorders.
David R Adams, Christine M Eng. N Engl J Med 2018
80