标题
Autism spectrum disorders—A genetics review
作者
关键词
-
出版物
GENETICS IN MEDICINE
Volume 13, Issue 4, Pages 278-294
出版商
Springer Nature
发表日期
2011-02-25
DOI
10.1097/gim.0b013e3181ff67ba
参考文献
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。- Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
- (2010) David T. Miller et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Autism and mitochondrial disease
- (2010) Richard H. Haas Developmental Disabilities Research Reviews
- De novo rates and selection of large copy number variation
- (2010) A. Itsara et al. GENOME RESEARCH
- Phenotypic variability and genetic susceptibility to genomic disorders
- (2010) S. Girirajan et al. HUMAN MOLECULAR GENETICS
- An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS)
- (2010) Ryu-ichiro Hashimoto et al. JOURNAL OF PSYCHIATRIC RESEARCH
- A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
- (2010) Santhosh Girirajan et al. NATURE GENETICS
- Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
- (2010) Simone Berkel et al. NATURE GENETICS
- Clinical Genetic Testing for Patients With Autism Spectrum Disorders
- (2010) Y. Shen et al. PEDIATRICS
- Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report
- (2010) Timothy Buie et al. PEDIATRICS
- A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region
- (2010) L McInnes et al. Molecular Autism
- Paternal age increases the risk for autism in an Iranian population sample
- (2010) Roksana Sasanfar et al. Molecular Autism
- The Xp contiguous deletion syndrome and autism
- (2009) Marwan Shinawi et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1
- (2009) Deqiong Ma et al. ANNALS OF HUMAN GENETICS
- Twenty-year outcome for individuals with autism and average or near-average cognitive abilities
- (2009) Megan A. Farley et al. Autism Research
- Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
- (2009) C. G. F. de Kovel et al. BRAIN
- Autism spectrum disorders in children and adolescents with Moebius sequence
- (2009) Wolfgang Briegel et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- Genetics of autistic disorders: review and clinical implications
- (2009) Christine M. Freitag et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
- (2009) Nathalie Van der Aa et al. European Journal of Medical Genetics
- The role of copy number variation in schizophrenia
- (2009) George Kirov Expert Review of Neurotherapeutics
- The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly
- (2009) Elizabeth A Varga et al. GENETICS IN MEDICINE
- Parents’ Perceptions of Autism Spectrum Disorder Etiology and Recurrence Risk and Effects of their Perceptions on Family Planning: Recommendations for Genetic Counselors
- (2009) Christina G. Selkirk et al. Journal of Genetic Counseling
- Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
- (2009) S Ben-Shachar et al. JOURNAL OF MEDICAL GENETICS
- Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
- (2009) B. A. Fernandez et al. JOURNAL OF MEDICAL GENETICS
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
- (2009) M. Shinawi et al. JOURNAL OF MEDICAL GENETICS
- Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications
- (2009) Jill A. Rosenfeld et al. Journal of Neurodevelopmental Disorders
- Common genetic variants on 5p14.1 associate with autism spectrum disorders
- (2009) Kai Wang et al. NATURE
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
- (2009) Marwan Shinawi et al. NATURE GENETICS
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders
- (2009) Sarah J Spence et al. PEDIATRIC RESEARCH
- Prevalence of Parent-Reported Diagnosis of Autism Spectrum Disorder Among Children in the US, 2007
- (2009) M. D. Kogan et al. PEDIATRICS
- Haploinsufficiency forPtenandSerotonin transportercooperatively influences brain size and social behavior
- (2009) Damon T. Page et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
- (2009) Jonathan Sebat et al. TRENDS IN GENETICS
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Development and validation of a measure of dysmorphology: Useful for autism subgroup classification
- (2008) Judith H. Miles et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Nuclear and Mitochondrial Genome Defects in Autisms
- (2008) Moyra Smith et al. Annals of the New York Academy of Sciences
- Continuing Increases in Autism Reported to California's Developmental Services System
- (2008) Robert Schechter et al. ARCHIVES OF GENERAL PSYCHIATRY
- Autism genetics: strategies, challenges, and opportunities
- (2008) Brian J. O'Roak et al. Autism Research
- The methyl-CpG-binding protein MeCP2 and neurological disease
- (2008) Adrian Bird BIOCHEMICAL SOCIETY TRANSACTIONS
- Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
- (2008) Susan L. Christian et al. BIOLOGICAL PSYCHIATRY
- Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15
- (2008) Nicholas J Wang et al. BMC GENETICS
- Behavioural phenotype of Cornelia de Lange syndrome: case–control study
- (2008) Chris Oliver et al. BRITISH JOURNAL OF PSYCHIATRY
- Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism
- (2008) S. Xu et al. CYTOGENETIC AND GENOME RESEARCH
- The Rise in Autism and the Role of Age at Diagnosis
- (2008) Irva Hertz-Picciotto et al. EPIDEMIOLOGY
- Catatonia in autism: implications across the life span
- (2008) Angelina Kakooza-Mwesige et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- A 15q13.3 microdeletion segregating with autism
- (2008) Alistair T Pagnamenta et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Clinical genetics evaluation in identifying the etiology of autism spectrum disorders
- (2008) G Bradley Schaefer et al. GENETICS IN MEDICINE
- Association of common variants in the Joubert syndrome gene (AHI1) with autism
- (2008) Ana I. Alvarez Retuerto et al. HUMAN MOLECULAR GENETICS
- Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
- (2008) D T Miller et al. JOURNAL OF MEDICAL GENETICS
- Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
- (2008) F D Hannes et al. JOURNAL OF MEDICAL GENETICS
- Neuroligins and neurexins link synaptic function to cognitive disease
- (2008) Thomas C. Südhof NATURE
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
- (2008) Andrew J Sharp et al. NATURE GENETICS
- The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
- (2008) Amber Hogart et al. NEUROBIOLOGY OF DISEASE
- AUTISM SPECTRUM DISORDERS FOLLOWING IN UTERO EXPOSURE TO ANTIEPILEPTIC DRUGS
- (2008) R. L. Bromley et al. NEUROLOGY
- Regression in Autistic Spectrum Disorders
- (2008) Gerry A. Stefanatos NEUROPSYCHOLOGY REVIEW
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
- Mitochondrial Disease in Autism Spectrum Disorder Patients: A Cohort Analysis
- (2008) Jacqueline R. Weissman et al. PLoS One
- GENETICS: Insights into the Pathogenesis of Autism
- (2008) J. S. Sutcliffe SCIENCE
- Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry
- (2008) E. M. Morrow et al. SCIENCE
- Diagnosis of autism spectrum disorders in the first 3 years of life
- (2008) Rebecca J Landa Nature clinical practice. Neurology
- Autism and Metabolic Diseases
- (2007) Barbara Manzi et al. JOURNAL OF CHILD NEUROLOGY
- Characterization of Autism in Young Children With Tuberous Sclerosis Complex
- (2007) Shafali S. Jeste et al. JOURNAL OF CHILD NEUROLOGY
Add 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 NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started