课题基金 / 基金详情

MOLECULAR GENETIC STUDIES OF CHILD PSYCHOPATHOLOGY

MOLECULAR GENETIC STUDIES OF CHILD PSYCHOPATHOLOGY
儿童心理病理学的分子遗传学研究
批准号:
6351647
负责人:
Edwin H Cook
金额:
$10.04万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-02-01 至 2002-01-31

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DESCRIPTION (Adapted from applicant's abstract): For several years, several child and adolescent onset disorders, including autistic disorder, attention-deficit hyperactivity disorder, obsessive-compulsive disorder, and major depressive disorder, have been shown to have varying degrees of genetic influence. However, there has been no consistent evidence that they are explained by single genes, or by genetic factors alone. Recent developments in molecular and statistical aspects of genetics have made the study of such complex disorders feasible. The first research component of the independent scientist award is to collect 350 carefully diagnosed subjects with autistic disorder. The Autism Diagnostic Interview and Autism Diagnostic Observation Schedule will be used in addition to diagnosis of autistic disorder by both the examining child and adolescent psychologist and child and adolescent psychiatrist. Cross-site reliability will be maintained. DNA will be collected from both the proband and his/her parents. The transmission/disequilibrium test (TdT) will be used to determine whether alleles at candidate loci are preferentially transmitted. In addition, this data base will be available for replication of any susceptibility loci identified in other samples. In a previous study, linkage disequilibrium between attention-deficit/hyperactivity disorder and a genetic marker at the dopamine transporter locus has been identified. A second research component of the independent scientist development plan will be a study designed to replicate the initial study with addition of a structured diagnostic interview. In collaboration with other colleagues, genetic analyses of childhood onset major depressive disorder (TdT of candidate genes) will be conducted. An emphasis will be placed on collecting DNA from subjects with reliably and valid diagnoses to provide a data base for molecular genetic studies severe disorders of children and adolescents. Consultants in diagnostic methodology and genetic analysis will meet regularly with the candidate to provide guidance for ongoing research career development.
期刊论文(30)
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科研奖励(0)
会议论文
DOI: 10.1176/ajp.2006.163.12.2148
发表时间: 2006-12
期刊: The American journal of psychiatry
影响因子: --
作者: [Camille W. Brune;Soo-Jeong Kim;Jeff Salt;B. Leventhal;C. Lord;E. Cook]
通讯作者: Camille W. Brune;Soo-Jeong Kim;Jeff Salt;B. Leventhal;C. Lord;E. Cook
Are the arginine vasopressin V1a receptor microsatellites related to hypersexuality in children with a prepubertal and early adolescent bipolar disorder phenotype?
精氨酸加压素 V1a 受体微卫星是否与青春期前和青春期早期双相情感障碍表型儿童的性欲亢进有关?
DOI: 10.1111/j.1399-5618.2005.00259.x
发表时间: 2005
期刊: Bipolar disorders
影响因子: 5.4
作者: [Geller,Barbara, Tillman,Rebecca, Badner,JudithA, CookJr,EdwinH]
通讯作者: CookJr,EdwinH
Deletion polymorphism in the coding region of the human NESP55 alternative transcript of GNAS1.
GNAS1 的人类 NESP55 替代转录物编码区的缺失多态性。
DOI: 10.1006/mcpr.2000.0300
发表时间: 2000
期刊: Molecular and cellular probes
影响因子: 3.3
作者: [Kim,SJ, Gonen,D, Hanna,GL, Leventhal,BL, CookJr,EH]
通讯作者: CookJr,EH
Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism.
自闭症血清素 5-HT2A 受体基因 (HTR2A) 的传递不平衡研究。
DOI: 10.1002/ajmg.10192
发表时间: 2002
期刊: American journal of medical genetics
影响因子: --
作者: [Veenstra-VanderWeele,Jeremy, Kim,Soo-Jeong, Lord,Catherine, Courchesne,Rachel, Akshoomoff,Natasha, Leventhal,BennettL, Courchesne,Eric, CookJr,EdwinH]
通讯作者: CookJr,EdwinH
6
    GENETICS OF SEROTONIN IN AUTISM: NEUROCHEMICAL AND CLINICAL
    ACE: Translational Studies of Insistence on Sameness in Autism
    ACE: Translational Studies of Insistence on Sameness in Autism
    GENETICS OF SEROTONIN IN AUTISM: NEUROCHEMICAL AND CLINICAL ENDOPHENOTYPES
    海外基金