Evaluating a counselling strategy for diagnostic WES in paediatric neurology: an exploration of parents' information and communication needs

scientific article published on 28 April 2015

Evaluating a counselling strategy for diagnostic WES in paediatric neurology: an exploration of parents' information and communication needs is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/CGE.12601
P698PubMed publication ID25916247

P50authorJoris A VeltmanQ57687954
P2093author name stringM A Willemsen
T Kleefstra
J Schieving
L E L M Vissers
L Krabbenborg
S van der Burg
P2860cites workNext generation genetic counseling: introduction to the special issueQ33894048
Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patientsQ34507484
Lynch syndrome patients' views of and preferences for return of results following whole exome sequencingQ35671138
What is ideal genetic counselling? A survey of current international guidelinesQ37057830
Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consentQ37360685
Parental attitudes, values, and beliefs toward the return of results from exome sequencing in childrenQ37595586
Informed consent for return of incidental findings in genomic researchQ37722733
SUDEP: what do parents want to know?Q42625453
Feedback of individual genetic results to research participants: in favor of a qualified disclosure policyQ44166679
The usefulness of whole-exome sequencing in routine clinical practice.Q50657606
A de novo paradigm for mental retardation.Q51828800
Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice.Q55520912
Diagnostic exome sequencing in persons with severe intellectual disabilityQ55670486
Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.Q55711624
P433issue2
P304page(s)244-250
P577publication date2015-04-28
P1433published inClinical GeneticsQ5133760
P1476titleEvaluating a counselling strategy for diagnostic WES in paediatric neurology: an exploration of parents' information and communication needs
P478volume89

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cites work (P2860)
Q38883296A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology
Q90274646Challenges to informed consent for exome sequencing: A best-worst scaling experiment
Q64040878Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study)
Q49720670Genetic Counseling in the Era of Genomics: What's all the Fuss about?
Q41686977How do providers discuss the results of pediatric exome sequencing with families?
Q91856722Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort
Q56527776Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate
Q92141652Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing
Q47632310Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders
Q57055341Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study
Q97905170Parental experiences of ultrarapid genomic testing for their critically unwell infants and children
Q53869120Patient perspectives on whole-genome sequencing for undiagnosed diseases.
Q37421261Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases