A Genome-Wide Investigation of Copy Number Variation in Patients with Sporadic Brain Arteriovenous Malformation
出版年份 2013 全文链接
标题
A Genome-Wide Investigation of Copy Number Variation in Patients with Sporadic Brain Arteriovenous Malformation
作者
关键词
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出版物
PLoS One
Volume 8, Issue 10, Pages e71434
出版商
Public Library of Science (PLoS)
发表日期
2013-10-04
DOI
10.1371/journal.pone.0071434
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations: where do we stand?
- (2012) C. L. Sturiale et al. BRAIN
- Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform
- (2011) Jeanette E Eckel-Passow et al. BMC BIOINFORMATICS
- Comparative analysis of copy number variation detection methods and database construction
- (2011) Asako Koike et al. BMC GENETICS
- Angiopoietin-Like 4 (ANGPTL4) Gene Polymorphisms and Risk of Brain Arteriovenous Malformations
- (2011) Bahar Mikhak et al. CEREBROVASCULAR DISEASES
- Hereditary hemorrhagic telangiectasia: An overview of diagnosis, management, and pathogenesis
- (2011) Jamie McDonald et al. GENETICS IN MEDICINE
- The effects of cadmium on VEGF-mediated angiogenesis in HUVECs
- (2011) Jisun Kim et al. JOURNAL OF APPLIED TOXICOLOGY
- Accuracy of CNV Detection from GWAS Data
- (2011) Dandan Zhang et al. PLoS One
- Copy number variation characteristics in subpopulations of patients with autism spectrum disorders
- (2010) Anna Bremer et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Structural Variation in the Human Genome and its Role in Disease
- (2010) Paweł Stankiewicz et al. Annual Review of Medicine
- Familial brain arteriovenous malformation maps to 5p13–q14, 15q11–q13 or 18p11: Linkage analysis with clipped fingernail DNA on high-density SNP array
- (2010) Masahiro Oikawa et al. European Journal of Medical Genetics
- Chibby interacts with NBPF1 and clusterin, two candidate tumor suppressors linked to neuroblastoma
- (2010) Karl Vandepoele et al. EXPERIMENTAL CELL RESEARCH
- Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study
- (2010) Gaëlle Marenne et al. HUMAN MUTATION
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- The UCSC Genome Browser database: update 2011
- (2010) P. A. Fujita et al. NUCLEIC ACIDS RESEARCH
- The Effect of Algorithms on Copy Number Variant Detection
- (2010) Debby W. Tsuang 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
- VEGF Induces More Severe Cerebrovascular Dysplasia in Eng+/− than in Alk1+/− Mice
- (2010) Qi Hao et al. Translational Stroke Research
- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
- (2009) Andy Itsara et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Reduced Expression of Integrin αvβ8 Is Associated with Brain Arteriovenous Malformation Pathogenesis
- (2009) Hua Su et al. AMERICAN JOURNAL OF PATHOLOGY
- Notch-1 signalling is activated in brain arteriovenous malformations in humans
- (2009) Q. ZhuGe et al. BRAIN
- Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
- (2009) M Mamtani et al. GENES AND IMMUNITY
- Copy number variation at 1q21.1 associated with neuroblastoma
- (2009) Sharon J. Diskin et al. NATURE
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Narcolepsy is strongly associated with the T-cell receptor alpha locus
- (2009) Joachim Hallmayer et al. NATURE GENETICS
- The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci
- (2009) Louise V. Wain et al. PLoS One
- A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia
- (2009) Anna C. Need et al. PLoS Genetics
- Common Variants in Interleukin-1-Beta Gene Are Associated with Intracranial Hemorrhage and Susceptibility to Brain Arteriovenous Malformation
- (2008) Helen Kim et al. CEREBROVASCULAR DISEASES
- Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patients
- (2008) Gaetan Lesca et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen
- (2008) Hylke M Blauw et al. LANCET NEUROLOGY
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Integrated detection and population-genetic analysis of SNPs and copy number variation
- (2008) Steven A McCarroll et al. NATURE GENETICS
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn et al. NATURE GENETICS
- Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
- (2008) Sharon J. Diskin et al. NUCLEIC ACIDS RESEARCH
- Endothelial Notch4 signaling induces hallmarks of brain arteriovenous malformations in mice
- (2008) P. A. Murphy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Brain Arteriovenous Malformation Biology Relevant to Hemorrhage and Implication for Therapeutic Development
- (2008) H. Kim et al. STROKE
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