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

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants

(2013) Carla Sustek D'Angelo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

Spatiotemporal expression pattern of Myt/NZF family zinc finger transcription factors during mouse nervous system development

(2013) Fumio Matsushita et al.   DEVELOPMENTAL DYNAMICS

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

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

(2012) M Rio et al.   CLINICAL GENETICS

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

(2012) Joep de Ligt et al.   NEW ENGLAND JOURNAL OF MEDICINE

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

(2012) Yohan Lee et al.   PSYCHIATRIC GENETICS

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

(2012) B. J. O'Roak et al.   SCIENCE

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

Direct conversion of human fibroblasts to dopaminergic neurons

(2011) U. Pfisterer et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Direct conversion of fibroblasts to functional neurons by defined factors

(2010) Thomas Vierbuchen et al.   NATURE

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

(2009) Helen V. Firth et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden

(2009) Frida Renström et al.   HUMAN MOLECULAR GENETICS

Secondary neurogenesis and telencephalic organization in zebrafish and mice: a brief review

(2009) Mario F. WULLIMANN   Integrative Zoology

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

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

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

(2008) Gudmar Thorleifsson et al.   NATURE GENETICS

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

(2008) Cristen J Willer et al.   NATURE GENETICS

High-resolution in situ hybridization to whole-mount zebrafish embryos

(2007) Christine Thisse et al.   Nature Protocols