Genetic investigation of cognitive development in autistic spectrum disorders.
Genetic investigation of cognitive development in autistic spectrum disorders.
批准号:
8112745
负责人:
Eric M Morrow
金额:
$18.42万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-10 至 2012-06-30
关键词:
AdultAffectAmericanAppointmentAutistic DisorderBioinformaticsBostonBrainCandidate Disease GeneChildChildhoodClinicClinicalClinical ResearchCognition DisordersCognitiveCollaborationsCollectionConsanguinityDNA ResequencingDevelopmentDiagnosticDiseaseDoctor of PhilosophyEarly DiagnosisEnrollmentEnvironmentEthicsFamilyFoundationsFounder GenerationFunctional disorderGenesGeneticGenetic Predisposition to DiseaseGenomicsGenotypeHealth SciencesHealth TechnologyHumanInstitutesInternationalInvestigationK-Series Research Career ProgramsLaboratoriesLeadLinkMapsMedicalMedicineMeleagris gallopavoMentorsMethodsMiddle EastMinorMolecularMutationNeurodevelopmental DisorderNorth AmericaPakistanParentsPatientsPediatric HospitalsPervasive Development DisorderPharmacotherapyPhenotypePopulationProtocols documentationPsychiatryRecessive GenesResearchResearch DesignResearch PersonnelResearch ProposalsResearch TrainingResidenciesResolutionResourcesSamplingTestingTrainingTraining ProgramsTranslational Researchautism spectrum disorderbasecareerclinically significantcognitive neurosciencecohortdensitydisease phenotypegenetic pedigreegenetic resourceimprovedinstructormedical schoolsmorphometrymouse modelneurodevelopmentneuropsychiatrynovelpatient oriented researchpatient populationprogramsresearch in practicetherapy developmenttooltranslational study
中文摘要
描述(由申请人提供):K23职业发展奖的申请题为“自闭症谱系障碍认知发展的遗传调查”。候选人拥有MD和PhD学位。他的博士学位是遗传小鼠模型的分子神经发育。他在麻省理工学院的本科训练,以及他在哈佛医学院哈佛-麻省理工学院健康科学与技术部的医学博士学位涉及定量方法的研究。候选人一直在MGH-姆克林精神病学住院医师的临床培训。他是哈佛医学院的精神病学讲师,在麻省总医院和波士顿儿童医院任职,并在麻省理工学院和哈佛的布罗德研究所担任博士后。如果成功,该申请人的职业轨迹是在MGH领导一个以实验室为基础的分子精神病学项目,重点是自闭症和认知发展相关障碍。链接到这个转化研究实验室,候选人计划直接在MGH精神病学的成人普遍性发展障碍的临床研究计划。候选人的研究计划描述了旨在识别自闭症谱系障碍(ASD)基因的研究。候选人建议研究两个互补的患者群体:1)来自阿拉伯中东,土耳其和巴基斯坦的特殊创始人群体,其中受影响儿童的父母是近亲; 2)北美家庭的大量收集来自AGRE和波士顿自闭症联盟的(>4000个样本),包括候选人建议在MGH儿科精神病学中表征的200个家庭的队列。近亲谱系将作为自闭症国际纯合性作图协作的一部分(候选人担任副主任),目的是发现高度外显的常染色体隐性基因。用于分析的主要工具将是Affytek 500 K SNP微阵列,并且研究将包括基因组拷贝数以及缺失和纯合性作图。将使用大规模重新测序、关联研究和表型-基因型研究在北美患者中研究由此鉴定的基因。导师包括Chris A.沃尔什,医学博士,博士,遗传学主席在儿童医院波士顿和董事波士顿自闭症联盟。沃尔什博士的实验室在国际遗传合作和识别神经发育和认知障碍中的隐性基因方面具有专业知识。此外,布罗德研究所的统计遗传学家Mark J. Daly博士将担任共同导师。候选人正在寻求在人口和统计遗传学,生物信息学的培训。他还在寻求以患者为导向的ASD研究培训,这将通过儿童医院的发育医学中心以及国家尊重的外部自闭症研究专家进行。
英文摘要
DESCRIPTION (provided by applicant): This application for a K23 Career Development Award is entitled "Genetic investigation of cognitive development in autistic spectrum disorders". The candidate has MD and PhD degrees. His PhD is in molecular neurodevelopment in genetic mouse models. His undergraduate training at MIT, and his MD in the Harvard-MIT Division of Health Sciences and Technology at Harvard Medical School involved studies in quantitative methods. The candidate has pursued clinical training through to Chief Residency in the MGH- McLean Psychiatry Residency. He is an Instructor in Psychiatry at Harvard Medical School with appointments at the MGH and Children's Hospital Boston, as well as a postdoctoral affiliation with the Broad Institute of MIT and Harvard. If successful, the career trajectory for this applicant is to lead a laboratory- based program in Molecular Psychiatry at MGH with a focus in autism and related disorders of cognitive development. Linked to this translational research lab, the candidate plans to direct a Clinical Research Program for Adults with Pervasive Development Disorders in MGH Psychiatry. The candidate's research proposal describes studies designed to identify genes in autism spectrum disorders (ASD). The candidate proposes to study two complementary patient populations: 1) a special founder population from the Arabic Middle East, Turkey and Pakistan, wherein parents of affected children are consanguineous; and 2) a large collection of North American families (>4000 samples) from AGRE and the Boston Autism Consortium, including a cohort of 200 families which the candidate proposes to characterized in MGH Pediatric Psychiatry. The consanguineous pedigrees will be enrolled as part of the Autism International Homozygosity Mapping Collaborative (for which the candidate serves as Associate Director) with the aim of discovering highly penetrant autosomal recessive genes. A principal tool for analysis will be the Affymetrix 500K SNP microarray, and studies will include genomic copy number, as well as deletion and homozygosity mapping. Genes thereby identified will be studied in the North American patients using large-scale resequencing, association studies and phenotype-genotype studies. Mentors include Chris A. Walsh, MD, PhD, Chair of Genetics at the Children's Hospital Boston and Director of the Boston Autism Consortium. Dr. Walsh's lab has expertise in international genetic collaborations and identifying recessive genes in neurodevelopmental and cognitive disorders. In addition, Mark J. Daly, PhD, a statistical geneticist at the Broad Institute will serve as co-mentor. The candidate is seeking training in human population and statistical genetics, and bioinformatics. He is also seeking patient- oriented research training in ASD which will be pursued through the Developmental Medicine Center at Children's Hospital, as well as with external autism research experts of national esteem.
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DOI:
10.1002/ajmg.b.31063
发表时间:
2010-06-05
期刊:
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
影响因子:
2.8
作者:
[Ching, Michael S. L., Shen, Yiping, Tan, Wen-Hann, Jeste, Shafali S., Morrow, Eric M., Chen, Xiaoli, Mukaddes, Nahit M., Yoo, Seung-Yun, Hanson, Ellen, Hundley, Rachel, Austin, Christina, Becker, Ronald E., Berry, Gerard T., Driscoll, Katherine, Engle, Elizabeth C., Friedman, Sandra, Gusella, James F., Hisama, Fuki M., Irons, Mira B., Lafiosca, Tina, LeClair, Elaine, Miller, David T., Neessen, Michael, Picker, Jonathan D., Rappaport, Leonard, Rooney, Cynthia M., Sarco, Dean P., Stoler, Joan M., Walsh, Christopher A., Wolff, Robert R., Zhang, Ting, Nasir, Ramzi H., Wu, Bai-Lin]
通讯作者:
Wu, Bai-Lin
Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.
自闭症大脑中内体 NHE6 和 NHE9 的基因被错误调节。
DOI:
10.1038/mp.2013.28
发表时间:
2014
期刊:
Molecular psychiatry
影响因子:
11
作者:
[Schwede,M, Garbett,K, Mirnics,K, Geschwind,DH, Morrow,EM]
通讯作者:
Morrow,EM
DOI:
10.1016/j.jaac.2013.01.003
发表时间:
2013-04
期刊:
Journal of the American Academy of Child and Adolescent Psychiatry
影响因子:
13.3
作者:
[Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM]
通讯作者:
Morrow EM
DOI:
10.1016/j.jaac.2010.08.009
发表时间:
2010-11
期刊:
Journal of the American Academy of Child and Adolescent Psychiatry
影响因子:
13.3
作者:
[Morrow EM]
通讯作者:
Morrow EM
DOI:
10.1093/bioinformatics/bts234
发表时间:
2012-06-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
[Aguiar D, Halldórsson BV, Morrow EM, Istrail S]
通讯作者:
Istrail S
共 7 条
Mechanisms of Disease and Treatments in Novel Metabolic Development Brain Disorders
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批准号:10622084
-
项目类别:
-
资助金额:$2.8万
-
财政年份:2022
-
负责人:Eric M Morrow
-
依托单位:
Mechanisms of disease and treatment in novel metabolic developmental brain disorders
-
批准号:10375639
-
项目类别:
-
资助金额:$57.86万
-
财政年份:2021
-
负责人:Eric M Morrow
-
依托单位:
Mechanisms of Disease and Treatment in Novel Metabolic Developmental Brain Disorders
-
批准号:10527375
-
项目类别:
-
资助金额:$58.01万
-
财政年份:2021
-
负责人:Eric M Morrow
-
依托单位:
Mechanisms of disease and treatment in novel metabolic developmental brain disorders
-
批准号:10712302
-
项目类别:
-
资助金额:$31.42万
-
财政年份:2021
-
负责人:Eric M Morrow
-
依托单位:
Mechanisms of Disease and Treatment in Novel Metabolic Developmental Brain Disorders
-
批准号:10745757
-
项目类别:
-
资助金额:$3.26万
-
财政年份:2021
-
负责人:Eric M Morrow
-
依托单位:
Neurodegenerative mechanisms in Christianson syndrome and NHE6-related disorders
-
批准号:9811045
-
项目类别:
-
资助金额:$96.38万
-
财政年份:2019
-
负责人:Eric M Morrow
-
依托单位:
Neurodegenerative Mechanisms in Christianson Syndrome and NHE6-Related Disorders
-
批准号:10417212
-
项目类别:
-
资助金额:$94.82万
-
财政年份:2019
-
负责人:Eric M Morrow
-
依托单位:
Neurodegenerative mechanisms in Christianson syndrome and NHE6-related disorders
-
批准号:10020810
-
项目类别:
-
资助金额:$94.82万
-
财政年份:2019
-
负责人:Eric M Morrow
-
依托单位:
Neurodegenerative Mechanisms in Christianson Syndrome and NHE6-Related Disorders
-
批准号:10653694
-
项目类别:
-
资助金额:$71.89万
-
财政年份:2019
-
负责人:Eric M Morrow
-
依托单位:
Neurodegenerative Mechanisms in Christianson Syndrome and NHE6-Related Disorders
-
批准号:10213154
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项目类别:
-
资助金额:$94.82万
-
财政年份:2019
-
负责人:Eric M Morrow
-
依托单位:
Neurodegenerative mechanisms in Christianson syndrome and NHE6-related disorders
-
批准号:10164658
-
项目类别:
-
资助金额:$7.93万
-
财政年份:2019
-
负责人:Eric M Morrow
-
依托单位:
Autism-linked endosomal mechanisms in neuronal arborization and connectivity
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批准号:8887441
-
项目类别:
-
资助金额:$40.63万
-
财政年份:2015
-
负责人:Eric M Morrow
-
依托单位:
Support for the 1st International Basic Science and Clinical Conference on Christianson Syndrome
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批准号:8986521
-
项目类别:
-
资助金额:$1.7万
-
财政年份:2015
-
负责人:Eric M Morrow
-
依托单位:
Support for the 1st International Basic Science and Clinical Conference on Christianson Syndrome
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批准号:9197362
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项目类别:
-
资助金额:$0.3万
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财政年份:2015
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负责人:Eric M Morrow
-
依托单位:
Mechanisms of circuit failure and treatments in patient-derived neurons in autism
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批准号:9085416
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项目类别:
-
资助金额:$40.63万
-
财政年份:2014
-
负责人:Eric M Morrow
-
依托单位:
Mechanisms of circuit failure and treatments in patient-derived neurons in autism
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批准号:8797732
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项目类别:
-
资助金额:$40.63万
-
财政年份:2014
-
负责人:Eric M Morrow
-
依托单位:
Mechanisms of circuit failure and treatments in patient-derived neurons in autism
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批准号:8927693
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项目类别:
-
资助金额:$40.63万
-
财政年份:2014
-
负责人:Eric M Morrow
-
依托单位:
Genetic investigation of cognitive development in autistic spectrum disorders.
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批准号:7689266
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项目类别:
-
资助金额:$18.42万
-
财政年份:2007
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负责人:Eric M Morrow
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依托单位:
Genetic investigation of cognitive development in autistic spectrum disorders.
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批准号:7940928
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项目类别:
-
资助金额:$18.42万
-
财政年份:2007
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负责人:Eric M Morrow
-
依托单位:
Genetic investigation of cognitive development in autistic spectrum disorders.
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批准号:7299397
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项目类别:
-
资助金额:$18.3万
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财政年份:2007
-
负责人:Eric M Morrow
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依托单位:
海外基金