Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts
Published 2023 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts
Authors
Keywords
-
Journal
NATURE MEDICINE
Volume 29, Issue 3, Pages 667-678
Publisher
Springer Science and Business Media LLC
Online
2023-03-07
DOI
10.1038/s41591-023-02238-2
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genetic Influence on Neurodevelopment in Nonsyndromic Craniosynostosis
- (2022) Andrew T. Timberlake et al. PLASTIC AND RECONSTRUCTIVE SURGERY
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
- (2021) Daniel Taliun et al. NATURE
- Surgical management of intracranial arachnoid cysts in pediatric patients: radiological and clinical outcome
- (2021) Matthias Schulz et al. Journal of Neurosurgery-Pediatrics
- Intracranial arachnoid cysts and epilepsy in children: Should this be treated surgically? Our 29-year experience and review of the literature
- (2021) Javier Orduna Martínez et al. NEUROCIRUGIA
- DIAPH1 Variants in Non–East Asian Patients With Sporadic Moyamoya Disease
- (2021) Adam J. Kundishora et al. JAMA Neurology
- Chromatin dynamics in human brain development and disease
- (2021) Alfredo M. Valencia et al. TRENDS IN CELL BIOLOGY
- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- Single-Cell Transcriptomic Analyses of the Developing Meninges Reveal Meningeal Fibroblast Diversity and Function
- (2020) John DeSisto et al. DEVELOPMENTAL CELL
- Evidence for 28 genetic disorders discovered by combining healthcare and research data
- (2020) Joanna Kaplanis et al. NATURE
- Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus
- (2020) Sheng Chih Jin et al. NATURE MEDICINE
- STAB: a spatio-temporal cell atlas of the human brain
- (2020) Liting Song et al. NUCLEIC ACIDS RESEARCH
- Rare and de novo coding variants in chromodomain genes in Chiari I malformation
- (2020) Brooke Sadler et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Identification of common genetic risk variants for autism spectrum disorder
- (2019) Jakob Grove et al. NATURE GENETICS
- The single-cell transcriptional landscape of mammalian organogenesis
- (2019) Junyue Cao et al. NATURE
- Malformations of Cerebral Cortex Development: Molecules and Mechanisms
- (2019) Gordana Juric-Sekhar et al. Annual Review of Pathology-Mechanisms of Disease
- Genetic Causes and Modifiers of Autism Spectrum Disorder
- (2019) Lauren Rylaarsdam et al. Frontiers in Cellular Neuroscience
- Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms
- (2019) Rebecca L. Walker et al. CELL
- Structure and Junctional Complexes of Endothelial, Epithelial and Glial Brain Barriers
- (2019) Mariana Castro Dias et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Organoid single-cell genomic atlas uncovers human-specific features of brain development
- (2019) Sabina Kanton et al. NATURE
- Mek1 Y130C mice recapitulate aspects of human cardio-facio-cutaneous syndrome
- (2018) Rifdat Aoidi et al. Disease Models & Mechanisms
- De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus
- (2018) Charuta Gavankar Furey et al. NEURON
- Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation
- (2018) Daniel Duran et al. NEURON
- Spatiotemporal transcriptomic divergence across human and macaque brain development
- (2018) Ying Zhu et al. SCIENCE
- A Review on the Effectiveness of Surgical Intervention for Symptomatic Intracranial Arachnoid Cysts in Adults
- (2018) Madeline J. Hayes et al. World Neurosurgery
- Clinical and radiological outcomes following surgical treatment for intra-cranial arachnoid cysts
- (2018) Samuel Hall et al. CLINICAL NEUROLOGY AND NEUROSURGERY
- Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
- (2017) Sheng Chih Jin et al. NATURE GENETICS
- Chromatin Remodeling BAF (SWI/SNF) Complexes in Neural Development and Disorders
- (2017) Godwin Sokpor et al. Frontiers in Molecular Neuroscience
- Surgery for intracranial arachnoid cysts in children—a prospective long-term study
- (2016) Katrin Rabiei et al. CHILDS NERVOUS SYSTEM
- Enrichr: a comprehensive gene set enrichment analysis web server 2016 update
- (2016) Maxim V. Kuleshov et al. NUCLEIC ACIDS RESEARCH
- DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants
- (2016) Janet Piñero et al. NUCLEIC ACIDS RESEARCH
- Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
- (2016) Andrew T Timberlake et al. eLife
- Outcome of 12 antenatally diagnosed fetal arachnoid cysts: Case series and review of the literature
- (2015) B. De Keersmaecker et al. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
- Clinical application of whole-exome sequencing across clinical indications
- (2015) Kyle Retterer et al. GENETICS IN MEDICINE
- Excess of rare, inherited truncating mutations in autism
- (2015) Niklas Krumm et al. NATURE GENETICS
- Mammalian SWI/SNF chromatin remodeling complexes and cancer: Mechanistic insights gained from human genomics
- (2015) C. Kadoch et al. Science Advances
- Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis
- (2014) R. Chakraborty et al. BLOOD
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors
- (2014) Ketu Mishra-Gorur et al. NEURON
- Causal analysis approaches in Ingenuity Pathway Analysis
- (2013) Andreas Krämer et al. BIOINFORMATICS
- De novo mutations in histone-modifying genes in congenital heart disease
- (2013) Samir Zaidi et al. NATURE
- DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation
- (2013) Eugene Bragin et al. NUCLEIC ACIDS RESEARCH
- Brain and Spinal MR Imaging Findings in Mucopolysaccharidoses: A Review
- (2012) D.I. Zafeiriou et al. AMERICAN JOURNAL OF NEURORADIOLOGY
- Prevalence and natural history of arachnoid cysts in adults
- (2012) Wajd N. Al-Holou et al. JOURNAL OF NEUROSURGERY
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- MEK Is a Key Regulator of Gliogenesis in the Developing Brain
- (2012) Xiaoyan Li et al. NEURON
- Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
- (2012) Joep de Ligt et al. NEW ENGLAND JOURNAL OF MEDICINE
- Natural genetic variation caused by small insertions and deletions in the human genome
- (2011) R. E. Mills et al. GENOME RESEARCH
- Recessive LAMC3 mutations cause malformations of occipital cortical development
- (2011) Tanyeri Barak et al. NATURE GENETICS
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- Prevalence and natural history of arachnoid cysts in children
- (2010) Wajd N. Al-Holou et al. Journal of Neurosurgery-Pediatrics
- Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
- (2010) Kaya Bilgüvar et al. NATURE
- Hundreds of variants clustered in genomic loci and biological pathways affect human height
- (2010) Hana Lango Allen et al. NATURE
- GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists
- (2009) Eran Eden et al. BMC BIOINFORMATICS
- The development of gyrification in childhood and adolescence
- (2009) Tonya White et al. BRAIN AND COGNITION
- Retinoic Acid from the Meninges Regulates Cortical Neuron Generation
- (2009) Julie A. Siegenthaler et al. CELL
- Histone H3 lysine 4 (H3K4) methylation in development and differentiation
- (2009) Joel C. Eissenberg et al. DEVELOPMENTAL BIOLOGY
- Down-regulation of the forkhead transcription factor Foxp1 is required for monocyte differentiation and macrophage function
- (2008) C. Shi et al. BLOOD
- WGCNA: an R package for weighted correlation network analysis
- (2008) Peter Langfelder et al. BMC BIOINFORMATICS
- Sylvian fissure arachnoid cysts: a survey on their diagnostic workout and practical management
- (2008) Gianpiero Tamburrini et al. CHILDS NERVOUS SYSTEM
Publish 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 MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now