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。Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Disruption of neurexin 1 associated with autism spectrum disorder
Hyung-Goo Kim et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
Susan L. Christian et al.
BIOLOGICAL PSYCHIATRY (2008)
Genome-wide linkage analyses of quantitative and categorical autism subphenotypes
Xiao-Qing Liu et al.
BIOLOGICAL PSYCHIATRY (2008)
Advances in autism genetics: on the threshold of a new neurobiology
Brett S. Abrahams et al.
NATURE REVIEWS GENETICS (2008)
Diagnosis of autism spectrum disorders in the first 3 years of life
Rebecca J. Landa
NATURE CLINICAL PRACTICE NEUROLOGY (2008)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Disruption of cerebral cortex MET signaling in autism spectrum disorder
Daniel B. Campbell et al.
ANNALS OF NEUROLOGY (2007)
Social and communication development in toddlers with early and later diagnosis of autism spectrum disorders
Rebecca J. Landa et al.
ARCHIVES OF GENERAL PSYCHIATRY (2007)
Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees
G. B. Christensen et al.
PROSTATE (2007)
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients
Tetsushi Sadakata et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
E. Rajcan-Separovic et al.
JOURNAL OF MEDICAL GENETICS (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
A genetic variant that disrupts MET transcription is associated with autism
Daniel B. Campbell et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Evidence for multiple loci from a genome scan of autism kindreds
G. D. Schellenberg et al.
MOLECULAR PSYCHIATRY (2006)
A heterogeneity-based genome search meta-analysis for autism-spectrum disorders
TA Trikalinos et al.
MOLECULAR PSYCHIATRY (2006)
Association of Reelin gene polymorphisms with autism
FJ Serajee et al.
GENOMICS (2006)
The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees
DF Levinson et al.
BMC GENETICS (2005)
Analysis of the RELN gene as a genetic risk factor for autism
DA Skaar et al.
MOLECULAR PSYCHIATRY (2005)
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects
JA Lamb et al.
JOURNAL OF MEDICAL GENETICS (2005)
Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree
H Coon et al.
HUMAN HEREDITY (2005)
Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels
EL Goode et al.
GENETIC EPIDEMIOLOGY (2005)
Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis
QQ Huang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment
CW Bartlett et al.
HUMAN HEREDITY (2004)
Novel family-based approaches to genetic risk in thrombosis
J Blangero et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2003)
The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism
D Castermans et al.
JOURNAL OF MEDICAL GENETICS (2003)
Analysis of reelin as a candidate gene for autism
E Bonora et al.
MOLECULAR PSYCHIATRY (2003)
A bias-ed assessment of the use of SNPs in human complex traits
JD Terwilliger et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2002)
A major susceptibility locus for specific language impairment is located on 13q21
CW Bartlett et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
A high-resolution recombination map of the human genome
A Kong et al.
NATURE GENETICS (2002)
Linkage of body mass index to chromosome 20 in Utah pedigrees
SC Hunt et al.
HUMAN GENETICS (2001)
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
AM Persico et al.
MOLECULAR PSYCHIATRY (2001)
Consanguinity and prereproductive mortality in the Utah Mormon population
LB Jorde
HUMAN HEREDITY (2001)
A convergent validity study of the differential ability scales and the Wechsler intelligence scale for children-third edition with Hispanic children
KE DiCerbo et al.
JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT (2000)
Multilocus linkage analysis by blocked Gibbs sampling
A Thomas et al.
STATISTICS AND COMPUTING (2000)
The Autism Diagnostic Observation Schedule-Generic: A standard measure of social and communication deficits associated with the spectrum of autism
C Lord et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2000)
Linkage analysis in the presence of errors I: Complex-valued recombination fractions and complex phenotypes
HHH Goring et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
分享论文
