A citation-based method for searching scientific literature

T Rigter, C J A van Aart, M W Elting, Q Waisfisz, M C Cornel, L Henneman. Clin Genet 2014
Times Cited: 30



J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
Times Cited: 86




List of shared articles



Times cited

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
14

An approach to pediatric exome and genome sequencing.
Leslie G Biesecker, Barbara B Biesecker. Curr Opin Pediatr 2014
20

Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.
Candice Cornelis, Aad Tibben, Wybo Dondorp, Mieke van Haelst, Annelien L Bredenoord, Nine Knoers, Marcus Düwell, Ineke Bolt, Marieke van Summeren. Eur J Hum Genet 2016
13


Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.
Lotte Krabbenborg, L E L M Vissers, J Schieving, T Kleefstra, E J Kamsteeg, J A Veltman, M A Willemsen, S Van der Burg. J Genet Couns 2016
42

Evaluating a counselling strategy for diagnostic WES in paediatric neurology: an exploration of parents' information and communication needs.
L Krabbenborg, J Schieving, T Kleefstra, L E L M Vissers, M A Willemsen, J A Veltman, S van der Burg. Clin Genet 2016
17

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

Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.
Leandra K Tolusso, Kathleen Collins, Xue Zhang, Jennifer R Holle, C Alexander Valencia, Melanie F Myers. J Genet Couns 2017
10

Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.
Emma C Hitchcock, Causes Study, Alison M Elliott. Mol Genet Genomic Med 2020
3

Defining and managing incidental findings in genetic and genomic practice.
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J Med Genet 2014
37

Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings.
Amanda L Bergner, Juli Bollinger, Karen S Raraigh, Crystal Tichnell, Brittney Murray, Carrie Lynn Blout, Aida Bytyci Telegrafi, Cynthia A James. Am J Med Genet A 2014
28

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

Patients' views on incidental findings from clinical exome sequencing.
Kristin E Clift, Colin M E Halverson, Alexander S Fiksdal, Ashok Kumbamu, Richard R Sharp, Jennifer B McCormick. Appl Transl Genom 2015
57