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Genetic Studies of Clubfoot (ITEV)

Genetic Studies of Clubfoot (ITEV)
马蹄足的遗传学研究 (ITEV)
批准号:
7897782
负责人:
JACQUELINE T HECHT
金额:
$35.5万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-29 至 2012-07-31

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DESCRIPTION (provided by applicant): Clubfoot or idiopathic talipes equinovarus (ITEV) is one of the five most common birth defects, affecting approximately 4,000 newborns each year in the US. While the orthopedic care of these children has improved, longterm problems persist and the health care costs are significant. Studies suggest that ITEV is a complex disorder with segregation analyses and family studies indicating that genetic factors play an important etiologic role in the development of ITEV. Only one environmental factor, maternal smoking during pregnancy, has been implicated. We postulate that a small number of genes account for a substantial fraction of ITEV and that these genes can be identified in a defined population. The challenge now is to identify the genetic loci and, later, the effect of environmental exposures. To accomplish this task, it is important to have a well-defined population and the methodology to detect linkage with and without association. Towards these goals, we have identified and characterized multiplex ITEV families and simplex ITEV trios including two large ITEV families, a resource which is among the largest ITEV population in existence. We will perform a high-density SNP genome scan on our ITEV dataset to identify chromosomal regions that may harbor ITEV genes with subsequent interrogation of these regions and candidate genes. We are in a position with our unique ITEV population and with the methodology in place to undertake this study. The study phases are: 1) continued ascertainment of multiplex families and ethnically diverse parent child trios, 2) high density SNP genome-wide scan 3) collection of confirmatory (simplex trios and case-control) datasets to test newly identified genes. The results of this study will provide data essential to the identification of the gene(s) contributing to the ITEV phenotype. Identification of high-risk genotypes can lead to the development of prevention programs in selected populations and may suggest gene-based prevention strategies.
期刊论文(4)
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会议论文
Genome-wide association study identifies new disease loci for isolated clubfoot.
全基因组关联研究确定了孤立性马蹄内翻足的新疾病位点。
DOI: 10.1136/jmedgenet-2014-102303
发表时间: 2014
期刊: Journal of medical genetics
影响因子: 4
作者: [Zhang,Tian-Xiao, Haller,Gabe, Lin,Peng, Alvarado,DavidM, Hecht,JacquelineT, Blanton,SusanH, StephensRichards,B, Rice,JohnP, Dobbs,MatthewB, Gurnett,ChristinaA]
通讯作者: Gurnett,ChristinaA
DOI: 10.1002/ajmg.a.33130
发表时间: 2009-12
期刊: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
影响因子: 2
作者: [Ester, Audrey R., Weymouth, Katelyn S., Burt, Amber, Wise, Carol A., Scott, Allison, Gurnett, Christina A., Dobbs, Matthew B., Blanton, Susan H., Hecht, Jacqueline T.]
通讯作者: Hecht, Jacqueline T.
DOI: 10.1002/ajmg.a.34167
发表时间: 2011-09
期刊: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
影响因子: 2
作者: [Weymouth, Katelyn S., Blanton, Susan H., Bamshad, Michael J., Beck, Anita E., Alvarez, Christine, Richards, Steve, Gurnett, Christina A., Dobbs, Matthew B., Barnes, Douglas, Mitchell, Laura E., Hecht, Jacqueline T.]
通讯作者: Hecht, Jacqueline T.
Leveraging novel methods to improve nonsyndromic cleft lip/palate gene discovery
Leveraging novel methods to improve nonsyndromic cleft lip/palate gene discovery
Consequences of Mutant COMP Expression and Therapeutic Approaches in Transgenic M
Consequences of Mutant COMP Expression and Therapeutic Approaches in Transgenic M
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