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Title
Clinical whole exome sequencing in child neurology practice
Authors
Keywords
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Journal
ANNALS OF NEUROLOGY
Volume 76, Issue 4, Pages 473-483
Publisher
Wiley
Online
2014-08-18
DOI
10.1002/ana.24251
References
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Related references
Note: Only part of the references are listed.- Laboratory policies on reporting secondary findings in clinical whole exome sequencing: Initial uptake of the ACMG's recommendations
- (2014) Sophia B. Hufnagel et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A Genotype-First Approach to Defining the Subtypes of a Complex Disease
- (2014) Holly A. Stessman et al. CELL
- Making headway with genetic diagnostics of intellectual disabilities
- (2013) M.H. Willemsen et al. CLINICAL GENETICS
- A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome
- (2013) Sonja A de Munnik et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Points to consider for informed consent for genome/exome sequencing
- (2013) GENETICS IN MEDICINE
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
- (2013) Robert C. Green et al. GENETICS IN MEDICINE
- De novo mutations in epileptic encephalopathies
- (2013) et al. NATURE
- Using Whole-Exome Sequencing to Identify Inherited Causes of Autism
- (2013) Timothy W. Yu et al. NEURON
- Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
- (2013) Yaping Yang et al. NEW ENGLAND JOURNAL OF MEDICINE
- The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases
- (2012) William A. Gahl et al. GENETICS IN MEDICINE
- Points to consider in the clinical application of genomic sequencing
- (2012) GENETICS IN MEDICINE
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
- (2012) Anita Rauch et al. LANCET
- Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
- (2012) Joep de Ligt et al. NEW ENGLAND JOURNAL OF MEDICINE
- Exome Sequencing Can Improve Diagnosis and Alter Patient Management
- (2012) T. J. Dixon-Salazar et al. Science Translational Medicine
- Updates in the Genetic Evaluation of the Child with Global Developmental Delay or Intellectual Disability
- (2012) Leigh Anne Flore et al. Seminars in Pediatric Neurology
- Deep sequencing reveals 50 novel genes for recessive cognitive disorders
- (2011) Hossein Najmabadi et al. NATURE
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene
- (2009) Paul Renbaum et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Targeted capture and massively parallel sequencing of 12 human exomes
- (2009) Sarah B. Ng et al. NATURE
- Genetic Evaluation of Intellectual Disabilities
- (2008) John B. Moeschler Seminars in Pediatric Neurology
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