A citation-based method for searching scientific literature

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: 104



Susan M Wolf, George J Annas, Sherman Elias. Science 2013
Times Cited: 151




List of shared articles



Times cited

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics.
Guido de Wert, Wybo Dondorp, Angus Clarke, Elisabeth M C Dequeker, Christophe Cordier, Zandra Deans, Carla G van El, Florence Fellmann, Ros Hastings, Sabine Hentze,[...]. Eur J Hum Genet 2021
3

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


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
12

Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Wylie Burke, Ellen Wright Clayton, Susan M Wolf, Susan A Berry, Barbara J Evans, James P Evans, Ralph Hall, Diane Korngiebel, Anne-Marie Laberge, Bonnie S LeRoy,[...]. Genet Med 2019
6

"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet Med 2018
25

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.
Michael P Mackley, Edward Blair, Michael Parker, Jenny C Taylor, Hugh Watkins, Elizabeth Ormondroyd. Eur J Hum Genet 2018
9

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
57

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
J A Anderson, M S Meyn, C Shuman, R Zlotnik Shaul, L E Mantella, M J Szego, S Bowdin, N Monfared, R Z Hayeems. J Med Ethics 2017
25