A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy

Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databases

(2018) Tharani Sundararajan et al.   GENE

Prioritization and functional assessment of noncoding variants associated with complex diseases

(2018) Lin Zhou et al.   Genome Medicine

Exploring the Wnt signaling pathway in schizophrenia and bipolar disorder

(2018) Eva Z. Hoseth et al.   Translational Psychiatry

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

(2017) Ingrid E. Scheffer et al.   EPILEPSIA

Models for discovery of targeted therapy in genetic epileptic encephalopathies

(2017) Snezana Maljevic et al.   JOURNAL OF NEUROCHEMISTRY

24-hour rhythmicity of seizures in refractory focal epilepsy

(2016) Hipólito Nzwalo et al.   EPILEPSY & BEHAVIOR

The genetic landscape of the epileptic encephalopathies of infancy and childhood

(2016) Amy McTague et al.   LANCET NEUROLOGY

Altered CSNK1E, FABP4 and NEFH protein levels in the dorsolateral prefrontal cortex in schizophrenia

(2016) Raquel Pinacho et al.   SCHIZOPHRENIA RESEARCH

Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE GENETICS

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

(2014) Caroline Nava et al.   NATURE GENETICS

The methylation hypothesis of pharmacoresistance in epilepsy

(2013) Katja Kobow et al.   EPILEPSIA

De novo mutations in epileptic encephalopathies

(2013) et al.   NATURE

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

(2013) Gemma L Carvill et al.   NATURE GENETICS

Association Between a Casein Kinase 1 Epsilon Gene Polymorphism and Schizophrenia in a Chinese Han Population

(2012) Yinglin Huang et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

FMRP targets distinct mRNA sequence elements to regulate protein expression

(2012) Manuel Ascano et al.   NATURE

FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

(2011) Jennifer C. Darnell et al.   CELL

CHRONOTYPES AND SUBJECTIVE SLEEP PARAMETERS IN EPILEPSY PATIENTS: A LARGE QUESTIONNAIRE STUDY

(2010) Wytske A. Hofstra et al.   CHRONOBIOLOGY INTERNATIONAL

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

(2010) L. Deprez et al.   NEUROLOGY

Analysis of Cell Type-specific Expression of CK1ε in Various Tissues of Young Adult BALB/c Mice and in Mammary Tumors of SV40 T-Ag-transgenic Mice

(2009) Anja C. Utz et al.   JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY

Infantile Spasms and Down Syndrome: A New Animal Model

(2009) Miguel A Cortez et al.   PEDIATRIC RESEARCH

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

(2009) Nanda A. Singh et al.   PLoS Genetics