MYT1L : A systematic review of genetic variation encompassing schizophrenia and autism

MYT1L mutation in a patient causes intellectual disability and early onset of obesity: a case report and review of the literature

(2019) Abeer Al Tuwaijri et al.   JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM

Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders

(2018) Aditi Deshpande et al.   Developmental Neurobiology

Myt1L Promotes Differentiation of Oligodendrocyte Precursor Cells and is Necessary for Remyelination After Lysolecithin-Induced Demyelination

(2018) Yanqing Shi et al.   Neuroscience Bulletin

Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity

(2018) Carla Sustek D’Angelo et al.   Molecular Cytogenetics

A novel MYT1L mutation in a patient with severe early-onset obesity and intellectual disability

(2018) Petra Loid et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates

(2017) Moritz Mall et al.   NATURE

MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus

(2017) Patricia Blanchet et al.   PLoS Genetics

Analysis of protein-coding genetic variation in 60,706 humans

(2016) Monkol Lek et al.   NATURE

Mice with Shank3 Mutations Associated with ASD and Schizophrenia Display Both Shared and Distinct Defects

(2016) Yang Zhou et al.   NEURON

De novo genic mutations among a Chinese autism spectrum disorder cohort

(2016) Tianyun Wang et al.   Nature Communications

Haploinsufficiency of the MYT1L gene causes intellectual disability frequently associated with behavioral disorder

(2015) Sonia Mayo et al.   GENETICS IN MEDICINE

Genetic studies in intellectual disability and related disorders

(2015) Lisenka E. L. M. Vissers et al.   NATURE REVIEWS GENETICS

Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

(2014) Nina De Rocker et al.   GENETICS IN MEDICINE

Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

Refining analyses of copy number variation identifies specific genes associated with developmental delay

(2014) Bradley P Coe et al.   NATURE GENETICS

Copy Number Variation in Thai Population

(2014) Bhoom Suktitipat et al.   PLoS One

A new patient with a terminal de novo 2p25.3 deletion of 1.9 Mb associated with early-onset of obesity, intellectual disabilities and hyperkinetic disorder

(2014) Maria Bonaglia et al.   Molecular Cytogenetics

Generation of Induced Neuronal Cells by the Single Reprogramming Factor ASCL1

(2014) Soham Chanda et al.   Stem Cell Reports

Identification of rare copy number variants in high burden schizophrenia families

(2013) Maarten J. Van Den Bossche et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

(2013) Jennifer Gladys Mulle et al.   BIOLOGICAL PSYCHIATRY

Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes

(2013) Martine Doco-Fenzy et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The Database of Genomic Variants: a curated collection of structural variation in the human genome

(2013) Jeffrey R. MacDonald et al.   NUCLEIC ACIDS RESEARCH

Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH

(2012) M Rio et al.   CLINICAL GENETICS

Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia

(2012) Yohan Lee et al.   PSYCHIATRIC GENETICS

MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions

(2011) Servi J.C. Stevens et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Induction of human neuronal cells by defined transcription factors

(2011) Zhiping P. Pang et al.   NATURE

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism

(2011) Kacie J. Meyer et al.   PSYCHIATRIC GENETICS

Direct conversion of fibroblasts to functional neurons by defined factors

(2010) Thomas Vierbuchen et al.   NATURE

Copy Number Variation in Schizophrenia in the Japanese Population

(2009) Masashi Ikeda et al.   BIOLOGICAL PSYCHIATRY

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

(2009) George Kirov et al.   HUMAN MOLECULAR GENETICS

Comparative genomics of autism and schizophrenia

(2009) B. Crespi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

(2008) Terry Vrijenhoek et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Genotype, haplotype and copy-number variation in worldwide human populations

(2008) Mattias Jakobsson et al.   NATURE

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE