Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders
出版年份 2017 全文链接
标题
Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders
作者
关键词
Copy number variation, <em class=EmphasisTypeItalic >DOCK8</em>, Gene-based analysis, Meta-analysis, Neuropsychiatric disorders, Quantitative PCR
出版物
Genome Medicine
Volume 9, Issue 1, Pages -
出版商
Springer Nature
发表日期
2017-11-30
DOI
10.1186/s13073-017-0494-1
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Genetics of Depression: Progress at Last
- (2017) Niamh Mullins et al. Current Psychiatry Reports
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses
- (2016) Aysu Okbay et al. NATURE GENETICS
- Identification of 15 genetic loci associated with risk of major depression in individuals of European descent
- (2016) Craig L Hyde et al. NATURE GENETICS
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
- (2016) Christian R Marshall et al. NATURE GENETICS
- The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
- (2016) Jacqueline MacArthur et al. NUCLEIC ACIDS RESEARCH
- A pilot study on commonality and specificity of copy number variants in schizophrenia and bipolar disorder
- (2016) J Chen et al. Translational Psychiatry
- Copy number variation in bipolar disorder
- (2015) E K Green et al. MOLECULAR PSYCHIATRY
- Integrative analysis of 111 reference human epigenomes
- (2015) Anshul Kundaje et al. NATURE
- Sparse whole-genome sequencing identifies two loci for major depressive disorder
- (2015) Na Cai et al. NATURE
- A gene-based association method for mapping traits using reference transcriptome data
- (2015) Eric R Gamazon et al. NATURE GENETICS
- Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
- (2015) Yun R Li et al. NATURE MEDICINE
- Genetic studies in intellectual disability and related disorders
- (2015) Lisenka E. L. M. Vissers et al. NATURE REVIEWS GENETICS
- The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
- (2015) et al. SCIENCE
- Efficient Test and Visualization of Multi-Set Intersections
- (2015) Minghui Wang et al. Scientific Reports
- The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease
- (2015) Loukas Moutsianas et al. PLoS Genetics
- Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
- (2014) Maude Schneider et al. AMERICAN JOURNAL OF PSYCHIATRY
- GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database
- (2014) R. Leslie et al. BIOINFORMATICS
- Copy number variation in schizophrenia in Sweden
- (2014) J P Szatkiewicz et al. MOLECULAR PSYCHIATRY
- De novo mutations in schizophrenia implicate synaptic networks
- (2014) Menachem Fromer et al. NATURE
- Refining analyses of copy number variation identifies specific genes associated with developmental delay
- (2014) Bradley P Coe et al. NATURE GENETICS
- Efficient multivariate linear mixed model algorithms for genome-wide association studies
- (2014) Xiang Zhou et al. NATURE METHODS
- The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
- (2014) Dexter Hadley et al. Nature Communications
- Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
- (2013) Suleyman Gulsuner et al. CELL
- CFEOM1-Associated Kinesin KIF21A Is a Cortical Microtubule Growth Inhibitor
- (2013) Babet van der Vaart et al. DEVELOPMENTAL CELL
- Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
- (2013) LANCET
- Evidence that duplications of 22q11.2 protect against schizophrenia
- (2013) E Rees et al. MOLECULAR PSYCHIATRY
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
- (2013) S Hong Lee et al. NATURE 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
- ParseCNV integrative copy number variation association software with quality tracking
- (2013) Joseph T. Glessner et al. NUCLEIC ACIDS RESEARCH
- GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus
- (2013) Patrick Sleiman et al. Scientific Reports
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
- (2012) Robert A Scott et al. NATURE GENETICS
- Exome sequencing supports a de novo mutational paradigm for schizophrenia
- (2011) Bin Xu et al. NATURE GENETICS
- Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
- (2011) Josephine Elia et al. NATURE GENETICS
- Genome-wide association study identifies five new schizophrenia loci
- (2011) NATURE GENETICS
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
- (2011) NATURE GENETICS
- A copy number variation morbidity map of developmental delay
- (2011) Gregory M Cooper et al. NATURE GENETICS
- A Versatile Gene-Based Test for Genome-wide Association Studies
- (2010) Jimmy Z. Liu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- METAL: fast and efficient meta-analysis of genomewide association scans
- (2010) C. J. Willer et al. BIOINFORMATICS
- Dedicator of cytokinesis 8 (DOCK8) deficiency
- (2010) Helen C Su Current Opinion in Allergy and Clinical Immunology
- Analysing biological pathways in genome-wide association studies
- (2010) Kai Wang et al. NATURE REVIEWS GENETICS
- Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
- (2010) Joseph T. Glessner et al. PLoS One
- Strong synaptic transmission impact by copy number variations in schizophrenia
- (2010) J. T. Glessner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
- (2009) Helen V. Firth et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane
- (2009) Naoto Kakinuma et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Kank proteins: structure, functions and diseases
- (2009) N. Kakinuma et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- Kank attenuates actin remodeling by preventing interaction between IRSp53 and Rac1
- (2009) Badal Chandra Roy et al. JOURNAL OF CELL BIOLOGY
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects
- (2008) Dorret I Boomsma et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Kank regulates RhoA-dependent formation of actin stress fibers and cell migration via 14-3-3 in PI3K–Akt signaling
- (2008) Naoto Kakinuma et al. JOURNAL OF CELL BIOLOGY
- Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities
- (2007) Bradley L. Griggs et al. GENOMICS
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationPublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More