Identification of Novel X-linked Intellectual Disability Genes
Identification of Novel X-linked Intellectual Disability Genes
批准号:
8471801
负责人:
Charles E Schwartz
金额:
$46.8万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-06-01 至 2014-05-31
关键词:
3&apos Untranslated RegionsAffectBioinformaticsBirthCandidate Disease GeneCaringCell LineChronicClinical ManagementCollectionCounselingDNA SequenceDataDefectDetectionDevelopmentDiseaseEtiologyEventExonsFamilyFunctional RNAGene Expression ProfilingGene MutationGeneral PopulationGenesGeneticGenetic PolymorphismGenomicsGenotypeGoalsGrantHuman DevelopmentIndividualIntellectual functioning disabilityLarge-Scale SequencingLeadLinkMapsMedicalMethodsMicroRNAsMolecularMolecular Diagnostic TechniquesMutationParentsPathogenesisPatientsPhenotypePreventionResearchResearch Project GrantsSocial ImpactsSocial WorkSocietiesSyndromeVariantX Chromosomebaseclinical Diagnosiscognitive functioncohortcostdisabilitydisorder preventioneconomic impactfollow-upgene discoverygenetic elementindexinginnovationinsightmalenext generation sequencingnovelprobandpromoterresearch clinical testingscreeningsegregation
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Intellectual disability (ID) is a common disability affecting 2-3% of the general population. X-linked ID (XLID) disorders, caused by defects of genes on the X chromosome, affect 1.7 of 1,000 males. Patients with ID require long-term family involvement, medical care and social services with enormous attendant burden and cost. XLID is a medically important and biologically significant group of disorders for which the prospects for further progress on the understanding of their molecular basis using traditional genetic approaches are low. The availability of finished sequence for the X chromosome and the enormous capability of the next generation sequencing methods offer an exciting new opportunity to identify the genetic bases of this highly heterogeneous group of disorders. The fact that males have a single X chromosome makes these disorders especially attractive targets for a large scale sequencing approach. Using next generation sequencing and gene expression analysis, this study intends to (1) obtain DNA sequence of all recognized, functionally important segments of the euchromatic portion of the X chromosome in probands from 35 known X-linked ID entities, (2) identify a minimum of 15 novel XLID genes, and (3) establish genotype/phenotype correlations for the novel XLID genes discovered in this project. Identification of genes that cause XLID is essential for clinical diagnosis, counseling, prevention, clinical management, and a rational development of effective novel treatments. Understanding the pathogenesis of ID will provide valuable insight into the mechanisms for normal development of human cognitive functions. We anticipate that the results of this study will lead to (1) new research projects to understand the function of these XLID genes in intellectual function; (2) novel molecular diagnostic methods; (3) innovative strategies for disease prevention and treatment; and (4) major and lasting economic and social impacts on the affected individuals, their families, and society.
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Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome.
成骨细胞和破骨细胞功能受损,表征了斯奈德 - 鲁滨逊综合征的骨质疏松症。
DOI:
10.1186/s13023-015-0235-8
发表时间:
2015-03-07
期刊:
Orphanet journal of rare diseases
影响因子:
3.7
作者:
[Albert JS, Bhattacharyya N, Wolfe LA, Bone WP, Maduro V, Accardi J, Adams DR, Schwartz CE, Norris J, Wood T, Gafni RI, Collins MT, Tosi LL, Markello TC, Gahl WA, Boerkoel CF]
通讯作者:
Boerkoel CF
ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons.
ZC4H2是Xlid基因,是CNS中间神经元特定子集的产生所必需的。
DOI:
10.1093/hmg/ddv208
发表时间:
2015-09-01
期刊:
Human molecular genetics
影响因子:
3.5
作者:
[May M, Hwang KS, Miles J, Williams C, Niranjan T, Kahler SG, Chiurazzi P, Steindl K, Van Der Spek PJ, Swagemakers S, Mueller J, Stefl S, Alexov E, Ryu JI, Choi JH, Kim HT, Tarpey P, Neri G, Holloway L, Skinner C, Stevenson RE, Dorsky RI, Wang T, Schwartz CE, Kim CH]
通讯作者:
Kim CH
Protein sector analysis for the clustering of disease-associated mutations.
用于疾病相关突变聚类的蛋白质扇区分析。
DOI:
10.1186/1471-2164-15-s11-s4
发表时间:
2014
期刊:
BMC genomics
影响因子:
4.4
作者:
[Guevara-Coto,Jose, Schwartz,CharlesE, Wang,Liangjiang]
通讯作者:
Wang,Liangjiang
DOI:
10.1097/mcd.0000000000000242
发表时间:
2019-01
期刊:
Clinical dysmorphology
影响因子:
0.7
作者:
[Stevenson RE, Chudley AE, Srivastava AK, Rodriguez J, Friez MJ, Schwartz CE]
通讯作者:
Schwartz CE
DOI:
10.1371/journal.pone.0116454
发表时间:
2015
期刊:
PloS one
影响因子:
3.7
作者:
[Niranjan TS, Skinner C, May M, Turner T, Rose R, Stevenson R, Schwartz CE, Wang T]
通讯作者:
Wang T
共 7 条
Novel Metabolic Biomarker for Autism Spectrum Disorder
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批准号:8285545
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项目类别:
-
资助金额:$14.83万
-
财政年份:2012
-
负责人:Charles E Schwartz
-
依托单位:
Novel Metabolic Biomarker for Autism Spectrum Disorder
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批准号:8440742
-
项目类别:
-
资助金额:$12.16万
-
财政年份:2012
-
负责人:Charles E Schwartz
-
依托单位:
Identification of Novel X-linked Intellectual Disability Genes
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批准号:8269854
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项目类别:
-
资助金额:$50.22万
-
财政年份:2011
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负责人:Charles E Schwartz
-
依托单位:
Identification of Novel X-linked Intellectual Disability Genes
-
批准号:8084989
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项目类别:
-
资助金额:$46.3万
-
财政年份:2011
-
负责人:Charles E Schwartz
-
依托单位:
CHOLESTEROL METABOLISM IN PLASMA LIPOPROTEINS AND LIVER
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批准号:6114899
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项目类别:
-
资助金额:$3.45万
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财政年份:1998
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负责人:Charles E Schwartz
-
依托单位:
CHOLESTEROL METABOLISM IN PLASMA LIPOPROTEINS & LIVER: STUDIES IN TWO
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批准号:6264248
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项目类别:
-
资助金额:$0.06万
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财政年份:1998
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负责人:Charles E Schwartz
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依托单位:
CHOLESTEROL METABOLISM IN PLASMA LIPOPROTEINS AND LIVER
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批准号:6246015
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项目类别:
-
资助金额:$2.76万
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财政年份:1997
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负责人:Charles E Schwartz
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依托单位:
CHOLESTEROL METABOLISM IN PLASMA LIPOPROTEINS AND LIVER
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批准号:6276134
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项目类别:
-
资助金额:$3.31万
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财政年份:1997
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负责人:Charles E Schwartz
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依托单位:
X-Linked Mental Retardation-Linkage
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批准号:6886823
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项目类别:
-
资助金额:$146.04万
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财政年份:1990
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负责人:Charles E Schwartz
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依托单位:
X-Linked Mental Retardation-Linkage
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批准号:6438256
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项目类别:
-
资助金额:$147.92万
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财政年份:1990
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负责人:Charles E Schwartz
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依托单位:
X-Linked Mental Retardation-Linkage
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批准号:7048579
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项目类别:
-
资助金额:$146.67万
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财政年份:1990
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负责人:Charles E Schwartz
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依托单位:
X-Linked Mental Retardation-Linkage
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批准号:6622012
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项目类别:
-
资助金额:$140.18万
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财政年份:1990
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负责人:Charles E Schwartz
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依托单位:
X-Linked Mental Retardation-Linkage
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批准号:6719519
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项目类别:
-
资助金额:$143.75万
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财政年份:1990
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负责人:Charles E Schwartz
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依托单位:
CHOLESTEROL METABOLISM IN PLASMA LIPOPROTEINS & LIVER: STUDIES IN TWO
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批准号:6304935
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项目类别:
-
资助金额:$0.06万
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财政年份:--
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负责人:Charles E Schwartz
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依托单位:
CHOLESTEROL AND PHOSPHATIDYLCHOLINE METABOLISM IN PLASMA LIPOPROTEINS AND LIVER
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批准号:5218704
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项目类别:
-
资助金额:$0.0万
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财政年份:--
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负责人:Charles E Schwartz
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依托单位:--
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