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。Astrocyte-synapse interactions and cell adhesion molecules
Margaux Saint-Martin et al.
FEBS JOURNAL (2023)
The genomic landscape across 474 surgically accessible epileptogenic human brain lesions
Javier A. Lopez-Rivera et al.
BRAIN (2023)
Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene
Carmen Barba et al.
NEUROLOGY (2023)
Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene
Carmen Barba et al.
NEUROLOGY (2023)
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations
Dulcie Lai et al.
BRAIN (2022)
Somatic genomic changes in single Alzheimer's disease neurons
Michael B. Miller et al.
NATURE (2022)
Detection of brain somatic variation in epilepsy-associated developmental lesions
Tracy A. Bedrosian et al.
EPILEPSIA (2022)
High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy
Balagopal Pai et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2022)
Inherent mosaicism and extensive mutation of human placentas
Tim H. H. Coorens et al.
NATURE (2021)
PTEN somatic mutations contribute to spectrum or cerebral overgrowth
Daniel C. Koboldt et al.
BRAIN (2021)
Integrated analysis of multimodal single-cell data
Yuhan Hao et al.
CELL (2021)
Filamin A-negative hyaline astrocytic inclusions in pediatric patients with intractable epilepsy: report of 2 cases
Grant M. Fischer et al.
JOURNAL OF NEUROSURGERY-PEDIATRICS (2020)
Somatic SLC35A2 mosaicism correlates with clinical findings in epilepsy brain tissue
Katherine E. Miller et al.
NEUROLOGY-GENETICS (2020)
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay
Katja Kobow et al.
ACTA NEUROPATHOLOGICA (2020)
Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo
Narges Zare Mehrjardi et al.
CELL PROLIFERATION (2020)
Astrocytes as Guardians of Neuronal Excitability: Mechanisms Underlying Epileptogenesis
Quirijn P. Verhoog et al.
FRONTIERS IN NEUROLOGY (2020)
Childhood cerebellar tumours mirror conserved fetal transcriptional programs
Maria C. Vladoiu et al.
NATURE (2019)
DoubletFinder: Doublet Detection in Single-Cell RNA Sequencing Data Using Artificial Nearest Neighbors
Christopher S. McGinnis et al.
CELL SYSTEMS (2019)
Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis
Taejeong Bae et al.
SCIENCE (2018)
Somatic mosaicism and neurodevelopmental disease
Alissa M. D'Gama et al.
NATURE NEUROSCIENCE (2018)
Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups
Kristian W. Pajtler et al.
CANCER CELL (2015)
Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain (vol 8, pg 1280, 2014)
Xuyu Cai et al.
CELL REPORTS (2015)
Churchill: an ultra-fast, deterministic, highly scalable and balanced parallelization strategy for the discovery of human genetic variation in clinical and population-scale genomics
Benjamin J. Kelly et al.
GENOME BIOLOGY (2015)
MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data
Greg Finak et al.
GENOME BIOLOGY (2015)
Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma
Anoop P. Patel et al.
SCIENCE (2014)
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
Daniel C. Koboldt et al.
GENOME RESEARCH (2012)
Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells
Christine Varela et al.
JOURNAL OF CLINICAL INVESTIGATION (2012)
Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations
Annapurna Poduri et al.
NEURON (2012)
Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism
Caroline Robberecht et al.
MOLECULAR CYTOGENETICS (2012)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
Laura K. Conlin et al.
HUMAN MOLECULAR GENETICS (2010)
Distinct Functions of Glial and Neuronal Dystroglycan in the Developing and Adult Mouse Brain
Jakob S. Satz et al.
JOURNAL OF NEUROSCIENCE (2010)
MOSAIC TETRASOMY 12P WITH DISCREPANCY BETWEEN FETAL TISSUES AND EXTRAEMBRYONIC TISSUES: MOLECULAR ANALYSIS AND POSSIBLE MECHANISM OF FORMATION
Chih-Ping Chen et al.
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Hyaline Protoplasmic Astrocytopathy of Neocortex
E. Tessa Hedley-Whyte et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2009)
Mosaic Trisomy la Due to a de novo Translocation in a Foetus with Early Developmental Abnormalities (Karyotype 46,XY,der(14),t(1;14)(p11;p11.2)/46,XY) Delineation of Parent and Cell Stage of Origin
Thomas Eggermann et al.
INTERNATIONAL JOURNAL OF HUMAN GENETICS (2008)
Trisomy recurrence: A reconsideration based on North American data
D Warburton et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Presence of filamin in the astrocytic inclusions of Aicardi syndrome
IB Van den Veyver et al.
PEDIATRIC NEUROLOGY (2004)
Compilation of published comparative genomic hybridization studies
S Struski et al.
CANCER GENETICS AND CYTOGENETICS (2002)
Genetic abnormalities detected in genomic hybridisation epenclymomas by comparative
M Carter et al.
BRITISH JOURNAL OF CANCER (2002)
Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma
S Ward et al.
GENES CHROMOSOMES & CANCER (2001)