Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility
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Title
Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility
Authors
Keywords
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Journal
Translational Psychiatry
Volume 8, Issue 1, Pages -
Publisher
Springer Nature
Online
2018-01-09
DOI
10.1038/s41398-017-0061-y
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Note: Only part of the references are listed.- Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
- (2017) Andrew S Allen et al. LANCET NEUROLOGY
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- (2016) M Kataoka et al. MOLECULAR PSYCHIATRY
- A spectral approach integrating functional genomic annotations for coding and noncoding variants
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- (2016) Tarjinder Singh et al. NATURE NEUROSCIENCE
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- (2016) Giulio Genovese et al. NATURE NEUROSCIENCE
- Loss-of-function variants — not always what they seem
- (2016) Darren J. Burgess NATURE REVIEWS GENETICS
- A network of synaptic genes associated with schizophrenia and bipolar disorder
- (2016) Diego A. Forero et al. SCHIZOPHRENIA RESEARCH
- Rare mutations and hypermethylation of the ARC gene associated with schizophrenia
- (2016) Yang-An Chuang et al. SCHIZOPHRENIA RESEARCH
- Anti-NMDA receptor encephalitis, autoimmunity, and psychosis
- (2016) Matthew S. Kayser et al. SCHIZOPHRENIA RESEARCH
- Health and population effects of rare gene knockouts in adult humans with related parents
- (2016) V. M. Narasimhan et al. SCIENCE
- Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population
- (2016) Yuto Takasaki et al. Scientific Reports
- NMDA receptor subunit mutations in neurodevelopmental disorders
- (2015) Nail Burnashev et al. CURRENT OPINION IN PHARMACOLOGY
- Genome-wide burden of deleterious coding variants increased in schizophrenia
- (2015) Loes M. Olde Loohuis et al. Nature Communications
- Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample
- (2015) Emma Colvert et al. JAMA Psychiatry
- Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies
- (2015) C. Dong et al. HUMAN MOLECULAR GENETICS
- The Familial Risk of Autism
- (2014) Sven Sandin et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- A general framework for estimating the relative pathogenicity of human genetic variants
- (2014) Martin Kircher et al. NATURE GENETICS
- MutationTaster2: mutation prediction for the deep-sequencing age
- (2014) Jana Marie Schwarz et al. NATURE METHODS
- A recently-discovered NMDA receptor gene, GRIN3B, is associated with duration mismatch negativity
- (2014) Yi-Ting Lin et al. PSYCHIATRY RESEARCH
- The genomics of schizophrenia: update and implications
- (2013) Paola Giusti-Rodríguez et al. JOURNAL OF CLINICAL INVESTIGATION
- Autism
- (2013) Meng-Chuan Lai et al. LANCET
- NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease
- (2013) Pierre Paoletti et al. NATURE REVIEWS NEUROSCIENCE
- Dopamine and glutamate receptor genes interactively influence episodic memory in old age
- (2013) Goran Papenberg et al. NEUROBIOLOGY OF AGING
- A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
- (2012) D. G. MacArthur et al. SCIENCE
- Rare structural variation of synapse and neurotransmission genes in autism
- (2011) X Gai et al. MOLECULAR PSYCHIATRY
- Behavioral analysis of NR2C knockout mouse reveals deficit in acquisition of conditioned fear and working memory
- (2011) Brandon G. Hillman et al. NEUROBIOLOGY OF LEARNING AND MEMORY
- Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia
- (2011) J Tarabeux et al. Translational Psychiatry
- A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders
- (2010) A M Addington et al. MOLECULAR PSYCHIATRY
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder
- (2010) Wenjia Song et al. NEUROSCIENCE LETTERS
- Postnatal NMDA receptor ablation in corticolimbic interneurons confers schizophrenia-like phenotypes
- (2009) Juan E Belforte et al. NATURE NEUROSCIENCE
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- Human Splicing Finder: an online bioinformatics tool to predict splicing signals
- (2009) François-Olivier Desmet et al. NUCLEIC ACIDS RESEARCH
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