A citation-based method for searching scientific literature

Layla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, Melissa C Parra, Sha Tang, Kelly D Farwell Gonzalez. Genet Med 2014
Times Cited: 74



Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers, Anne-Marie Laberge, Jacek Majewski, Roberto Mendoza-Londono, M Stephen Meyn, Jacques L Michaud, Tanya N Nelson, Julie Richer, Bekim Sadikovic, David L Skidmore, Tracy Stockley, Sherry Taylor, Clara van Karnebeek, Ma'n H Zawati, Julie Lauzon, Christine M Armour. J Med Genet 2015
Times Cited: 118




List of shared articles



Times cited

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

Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Joon-Ho Yu, Paul S Appelbaum, Kyle B Brothers, Steven Joffe, Tia L Kauffman, Barbara A Koenig, Anya Er Prince, Sarah Scollon, Susan M Wolf, Barbara A Bernhardt,[...]. Per Med 2019
5

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.
Emmanuelle Souzeau, Kathryn P Burdon, David A Mackey, Alex W Hewitt, Ravi Savarirayan, Margaret Otlowski, Jamie E Craig.  2016
7

Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
F Houdayer, O Putois, M L Babonneau, H Chaumet, L Joly, C Juif, C C Michon, S Staraci, E Cretin, S Delanoue,[...]. Eur J Med Genet 2019
8

Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
Salma Shickh, Marc Clausen, Chloe Mighton, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Rita Kodida, Emma Reble, Christine Elser, Andrea Eisen, Seema Panchal,[...]. BMJ Open 2019
4

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
71

Whether, when, how, and how much? General public's and cancer patients' views about the disclosure of genomic secondary findings.
Jude Emmanuel ClĂ©ophat, Michel Dorval, Zaki El Haffaf, Jocelyne Chiquette, Stephanie Collins, Benjamin Malo, Vincent Fradet, Yann Joly, Hermann Nabi. BMC Med Genomics 2021
0

Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.
Emma E Smith, Christèle du Souich, Nick Dragojlovic, Alison M Elliott. J Genet Couns 2019
15

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
3