- Home
- Publications
- Publication Search
- Publication Details
Title
Prospective and detailed behavioral phenotyping in DDX3X syndrome
Authors
Keywords
-
Journal
Molecular Autism
Volume 12, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2021-05-17
DOI
10.1186/s13229-021-00431-z
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development
- (2020) Ashley L. Lennox et al. NEURON
- De novo DDX3X missense variants in males appear viable and contribute to syndromic intellectual disability
- (2019) Pantelis Nicola et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Expansion of phenotype of DDX3X syndrome
- (2019) Bryony Beal et al. CLINICAL DYSMORPHOLOGY
- Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
- (2019) Elizabeth K. Ruzzo et al. CELL
- Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
- (2018) Anke Van Dijck et al. BIOLOGICAL PSYCHIATRY
- Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder
- (2018) Atsushi Takata et al. Cell Reports
- Phenotypic expansion in DDX3X - a common cause of intellectual disability in females
- (2018) Xia Wang et al. Annals of Clinical and Translational Neurology
- Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts
- (2018) Marco Garieri et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The RNA helicase DDX3X is an essential mediator of innate antimicrobial immunity
- (2018) Daniel Szappanos et al. PLoS Pathogens
- Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
- (2017) Ryan K C Yuen et al. NATURE NEUROSCIENCE
- DDX3 Modulates Neurite Development via Translationally Activating an RNA Regulon Involved in Rac1 Activation
- (2016) H.-H. Chen et al. JOURNAL OF NEUROSCIENCE
- Genome-wide characteristics of de novo mutations in autism
- (2016) Ryan KC Yuen et al. npj Genomic Medicine
- Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
- (2015) Lot Snijders Blok et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- RNA helicase DDX3: at the crossroad of viral replication and antiviral immunity
- (2015) Fernando Valiente-Echeverría et al. REVIEWS IN MEDICAL VIROLOGY
- The Ded1/DDX3 subfamily of DEAD-box RNA helicases
- (2014) Deepak Sharma et al. CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY
- The contribution of de novo coding mutations to autism spectrum disorder
- (2014) Ivan Iossifov et al. NATURE
- The role of the DEAD-box RNA helicase DDX3 in mRNA metabolism
- (2013) Ricardo Soto-Rifo et al. Wiley Interdisciplinary Reviews-RNA
- Psychometric Properties of the Revised Developmental Coordination Disorder Questionnaire
- (2009) Brenda N. Wilson et al. PHYSICAL & OCCUPATIONAL THERAPY IN PEDIATRICS
- The DEAD-Box RNA Helicase DDX3 Associates with Export Messenger Ribonucleoproteins as well asTip-associated Protein and Participates in Translational Control
- (2008) Ming-Chih Lai et al. MOLECULAR BIOLOGY OF THE CELL
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now