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。Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
Vladimir Vacic et al.
NATURE (2011)
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
Brian J. O'Roak et al.
NATURE GENETICS (2011)
Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex
Karine Fenelon et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Type 7 adenylyl cyclase is involved in the ethanol and CRF sensitivity of GABAergic synapses in mouse central amygdala
Maureen T. Cruz et al.
FRONTIERS IN NEUROSCIENCE (2011)
Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
Philip Awadalla et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Detection of nonneutral substitution rates on mammalian phylogenies
Katherine S. Pollard et al.
GENOME RESEARCH (2010)
Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia
Torfi Sigurdsson et al.
NATURE (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
Yingrui Li et al.
NATURE GENETICS (2010)
A de novo paradigm for mental retardation
Lisenka E. L. M. Vissers et al.
NATURE GENETICS (2010)
Uncovering the roles of rare variants in common disease through whole-genome sequencing
Elizabeth T. Cirulli et al.
NATURE REVIEWS GENETICS (2010)
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia
Maria Karayiorgou et al.
NATURE REVIEWS NEUROSCIENCE (2010)
Rate, molecular spectrum, and consequences of human mutation
Michael Lynch
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Cognition in Mouse Models of Schizophrenia Susceptibility Genes
P. Alexander Arguello et al.
SCHIZOPHRENIA BULLETIN (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
Paul Lichtenstein et al.
LANCET (2009)
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
Andreas Gnirke et al.
NATURE BIOTECHNOLOGY (2009)
Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans
Bin Xu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Rare chromosomal deletions and duplications increase risk of schizophrenia
Jennifer L. Stone et al.
NATURE (2008)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson et al.
NATURE (2008)
Accurate whole human genome sequencing using reversible terminator chemistry
David R. Bentley et al.
NATURE (2008)
Strong association of de novo copy number mutations with sporadic schizophrenia
Bin Xu et al.
NATURE GENETICS (2008)
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Tom Walsh et al.
SCIENCE (2008)
Genomic rearrangements and sporadic disease
James R. Lupski
NATURE GENETICS (2007)
Modeling madness in mice: One piece at a time
P. Alexander Arguello et al.
NEURON (2006)
Nine new human Rhodopsin family G-protein coupled receptors:: Identification, sequence characterisation and evolutionary relationship
DEI Gloriam et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2005)
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1
GR Abecasis et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
The human and mouse repertoire of the adhesion family of G-protein-coupled receptors
TK Bjarnadóttir et al.
GENOMICS (2004)
Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database
M Karayiorgou et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2004)
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
D Botstein et al.
NATURE GENETICS (2003)
Schizophrenia as a complex trait - Evidence from a meta-analysis of twin studies
PF Sullivan et al.
ARCHIVES OF GENERAL PSYCHIATRY (2003)
分享论文
