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。Abnormal functional connectivity in autism spectrum disorders during face processing
Natalia M. Kleinhans et al.
BRAIN (2008)
Severe congenital encephalopathy caused by MECP2 null mutations in males:: central hypoxia and reduced neuronal dendritic structure
B. Schule et al.
CLINICAL GENETICS (2008)
Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism
C. S. Loat et al.
GENES BRAIN AND BEHAVIOR (2008)
Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome
Nadia P. Belichenko et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2008)
Brain-derived neurotrophic factor polymorphisms and frontal cortex morphology in schizophrenia
Katarina Varnas et al.
PSYCHIATRIC GENETICS (2008)
MeCP2, a key contributor to neurological disease, activates and represses transcription
Maria Chahrour et al.
SCIENCE (2008)
Selective cerebral volume reduction in Rett syndrome: A multiple-approach MR imaging study
J. C. Carter et al.
AMERICAN JOURNAL OF NEURORADIOLOGY (2008)
Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language
Timothy C. Bates et al.
INTELLIGENCE (2008)
Role of intermediate progenitor cells in cerebral cortex development
Adria Pontious et al.
DEVELOPMENTAL NEUROSCIENCE (2008)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Sex difference in Mecp2 expression during a critical period of rat brain development
Joseph R. Kurian et al.
EPIGENETICS (2007)
Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis
Lekbir Baala et al.
NATURE GENETICS (2007)
The odyssey of MeCP2 and parental imprinting
Janine M. LaSalle
EPIGENETICS (2007)
Gait function in newly diagnosed children with autism: cerebellar and basal ganglia related motor disorder
Nicole J. Rinehart et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2006)
Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation
Raman P. Nagarajan et al.
EPIGENETICS (2006)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
Early progressive encephalopathy in boys and MECP2 mutations
P. Kankirawatana et al.
NEUROLOGY (2006)
Identification of cis-regulatory elements for MECP2 expression
Jinglan Liu et al.
HUMAN MOLECULAR GENETICS (2006)
A map of recent positive selection in the human genome (vol 4, pg 154, 2006)
BF Voight et al.
PLOS BIOLOGY (2006)
A map of recent positive selection in the human genome
BF Voight et al.
PLOS BIOLOGY (2006)
Global landscape of recent inferred Darwinian selection for Homo sapiens
ET Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
A haplotype map of the human genome
D Altshuler et al.
NATURE (2005)
Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans
PD Evans et al.
SCIENCE (2005)
Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens
N Mekel-Bobrov et al.
SCIENCE (2005)
Adaptive evolution of ASPM, a major determinant of cerebral cortical size in humans
PD Evans et al.
HUMAN MOLECULAR GENETICS (2004)
Language-association cortex asymmetry in autism and specific language impairment
L De Fossé et al.
ANNALS OF NEUROLOGY (2004)
Brain development in autism: Early overgrowth followed by premature arrest of growth
E Courchesne
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2004)
The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells
BP Jung et al.
JOURNAL OF NEUROBIOLOGY (2003)
Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous
SL Lake et al.
HUMAN HEREDITY (2003)
Mutation analysis of the coding sequence of the MECP2 gene in infantile autism
KS Beyer et al.
HUMAN GENETICS (2002)
Regulation of cerebral cortical size by control of cell cycle exit in neural precursors
A Chenn et al.
SCIENCE (2002)
MeCP2 mutations in children with and without the phenotype of Rett syndrome
K Hoffbuhr et al.
NEUROLOGY (2001)
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations
MD Shahbazian et al.
CURRENT OPINION IN NEUROLOGY (2001)
分享论文
