Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.
about
Mutation screening of melatonin-related genes in patients with autism spectrum disordersPolymorphisms in melatonin synthesis pathways: possible influences on depressionMultiple rare variants in the etiology of autism spectrum disordersClinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concernsMelatonin in children with autism spectrum disorders: endogenous and pharmacokinetic profiles in relation to sleep.Sequencing ASMT identifies rare mutations in Chinese Han patients with autismAdvances in the research of melatonin in autism spectrum disorders: literature review and new perspectivesCopy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse modelOver-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceSept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in miceGenome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorderDisruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders.Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern.Bio-collections in autism research.Mouse Models of 22q11.2-Associated Autism Spectrum DisorderGenetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay.Autism: an emerging 'neuroimmune disorder' in search of therapy.Pseudohypoparathyroidism type Ib associated with novel duplications in the GNAS locusIntegrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.Melatonin in Children with Autism Spectrum Disorders: How Does the Evidence Fit Together?Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.Social deficits in male children and adolescents with sex chromosome aneuploidy: a comparison of XXY, XYY, and XXYY syndromesAlterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brainHippocampal Transcriptomic and Proteomic Alterations in the BTBR Mouse Model of Autism Spectrum Disorder.Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses.Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.Biochemical and cellular functions of P4 ATPases.Diagnostic yield of array comparative genomic hybridization in adults with autism spectrum disorders.Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.Sleep in Autism Spectrum Disorders.Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boyAutistic disorder phenotype associated to a complex 15q intrachromosomal rearrangement.Prediction of autism susceptibility genes based on association rules.The Relationship between Sleep Problems, Neurobiological Alterations, Core Symptoms of Autism Spectrum Disorder, and Psychiatric Comorbidities.Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disordersComplex autism spectrum disorder in a patient with a 17q12 microduplication
P2860
Q21202036-30C0995D-761E-413F-B2E6-4145D90AC729Q24288941-E8E1C651-7BCB-4C75-849F-3F2E478528CEQ24635522-F4477CF2-81DE-4B8D-8EC1-02D3625789C2Q26859057-7ACCBEE7-F409-4BE8-9681-4A5BD95D694BQ28390468-2EDB3CEA-45B8-49C4-8150-BE8628D8E120Q28485180-D0C9498D-77C2-4813-898A-5A16E978CF31Q28661706-9C80AAC0-F186-401B-8661-BF24A363DADAQ30439224-BE8ADA3F-3E44-402E-A8B5-D22519299802Q30459881-2EC08ECA-D0A9-43DB-8128-E70399631F4FQ30479118-894C3746-9F07-4131-8A8D-41DA1852530BQ30481665-A1D1DC20-E114-485C-B84B-7F1A84016B34Q33474877-A27B508C-A91D-4620-9A48-7175FC506602Q33611367-177C3F62-33EC-4BFC-95C4-E3FD89B64D8DQ33704992-FC00F7A0-7471-4E1F-8C20-A8D4A367675FQ33792567-650ADEE6-10EF-4178-8E97-1D952699B19FQ33892169-D1C8FEE1-0037-4FAD-840D-E6545C155B27Q33988040-5D6138ED-B8E9-45A3-91EA-029903F37EBDQ34430684-2053FE69-0D9B-44E2-84BD-9DCF58AABAD4Q34994653-76C75F5A-F573-4977-8578-A7353859F314Q35116923-4D69EC6D-FDDB-464B-B46F-88CA0274CFAAQ35595321-664EA8B3-80DF-4BF9-BE32-B41930FEC26DQ35774172-4DE9DF11-9B02-410D-A88F-DA0A99FF024FQ35888762-E6B8D619-E3B7-4063-B991-7D8614611E56Q35895357-E03B6BB5-C461-4299-8FA9-99717F819444Q36083149-DE06386D-1623-4465-8757-19E39721C304Q36309626-6274FAED-6DDD-448A-AC04-83DC8F18D520Q37068738-4B4336E0-8FF2-44B9-8182-07D5A6F7377AQ37705088-F5DC26FD-6CA1-4D6F-9D3C-40D208B5F300Q37788277-E6C0183E-238C-4A85-8957-69E86C06A73BQ38114326-280122F8-FD20-454D-88D8-F56CC1A961E5Q39037201-928C7FF0-C660-4CA2-97DC-B6E24252D4C5Q41486105-A7AFC7CD-0472-47C4-A897-1BA1AF353B78Q42693517-BCF2B0BF-4C8F-42E1-859E-88C7FFDC4095Q50305599-05B3BBC6-F64D-4DE7-BA05-FD38296BAE9EQ50341355-4E18D096-AF18-44D9-92B6-1D40F8A68406Q55070961-5EC3E66D-CEFD-4C9B-AED6-6FFB1DFE0A0AQ57093573-EA834928-784E-4172-BAF1-1539A86B0872Q57279132-A754DA89-1F72-404F-ABCB-950A5778318C
P2860
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@ast
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@en
type
label
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@ast
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@en
prefLabel
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@ast
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@en
P2093
P2860
P356
P1433
P1476
Multiplex ligation-dependent p ...... ovel microduplication in ASMT.
@en
P2093
Alisa Nakamine
Danielle M Zurawiecki
Ellen J Hoffman
Eric Hollander
Guiqing Cai
Jennifer G Reichert
Jeremy M Silverman
Joseph D Buxbaum
Juliet E Goldsmith
Latha Soorya
P2860
P2888
P356
10.1186/1755-8794-1-50
P577
2008-10-16T00:00:00Z
P5875
P6179
1031236829