课题基金 / 基金详情

Medical Genetics Training Grant

Medical Genetics Training Grant
医学遗传学培训补助金
批准号:
10647632
负责人:
TAO WANG
金额:
$44.89万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1977
资助国家:
美国
项目状态:
未结题
起止时间:
1977-07-01 至 2027-06-30

项目摘要

项目成果

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中文摘要
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英文摘要
The overall goals of the T32 Postdoctoral Training Program in Medical Genetics at Johns Hopkins are to recruit and educate physician-scientists who have the potentials to become leaders in the field of Genetic Medicine. Our program is designed to expose trainees to all facets of modern medical genetics and genomics extending from research programs to patient care. This postdoctoral training experience emphasizes mentored research in medical genetics and genomics, and prepares trainees for a career in academic medicine. Since the majority of our trainees are physicians, we utilize a physician-scientist training model to bridge the gap between genetics research and clinical medicine. Johns Hopkins provides leadership in the categorization and mapping of inherited traits, the application of genomic and computational methods to the identification and understanding of genes and their roles in human diseases, and in clinical research, diagnosis, and treatment of Mendelian disorders and multifactorial disorders with significant genetic contributions. The McKusick-Nathans Department of Genetic Medicine (DGM), the home of this training program, oversees the clinical, educational, and research activities in human and medical genetics at the Johns Hopkins University School of Medicine. This T32 postdoctoral training program in medical genetics is in its 44th year of operation with supports from NIGMS. The mentored research training is integrated into a medical genetics residency, which is designed to optimize the utilization of the rich clinical and research resources and training environments at Johns Hopkins and support the career development as physician scientists for our trainees. Clinical genetics training is followed by a period of intensive research training with maximally protected research time supported by this T32 training grant. The research training is under the auspices of a carefully selected research mentors and monitored by a research committee. After a successfully completion of this program, trainees are eligible for certification by the American Board of Medical Genetics in clinical genetics and possess strong research experiences and expertise to embark on independent career as physician-scientists. Our training program has an outstanding track record of educating physician-scientists who have made and continue to make substantial contributions to the field of medical genetics. Over the last 10 years, our trainees had an average 4.5 peer-reviewed publications from T32 supported training and the vast majority (>80%) of our graduates took research-centered or research-related positions at academic institutions. URM trainees are well represented in our training program. We have now optimized integrated curriculums that combine clinical and research training in medical genetics, expanded diversified trainee populations and training resources by developing combined programs with pediatrics, internal medicine, MFM, REI, and a training consortium with NHGRI, and established structured research fellowships to support the interests and career goals of individual trainees to advance their careers as physician scientists.
期刊论文(56)
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DOI: 10.1016/j.ymgmr.2017.07.004
发表时间: 2017-12
期刊: Molecular genetics and metabolism reports
影响因子: 1.9
作者: [Muriello MJ, Viall S, Bottiglieri T, Cusmano-Ozog K, Ferreira CR]
通讯作者: Ferreira CR
DOI: 10.1002/ajmg.a.36548
发表时间: 2014-08
期刊: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
影响因子: 2
作者: [Hudson, Cindy, Schwanke, Corbin, Johnson, John P., Elias, Abdallah F., Phillips, Sandy, Schwalbe, Tammy, Tunby, Mary, Xu, Dongbin]
通讯作者: Xu, Dongbin
Albinism and developmental delay: the need to test for 15q11-q13 deletion.
白化病和发育迟缓:需要检测15q11-q13缺失。
DOI: 10.1016/j.pediatrneurol.2007.06.024
发表时间: 2007
期刊: Pediatric neurology
影响因子: 3.8
作者: [Saadeh,Reem, Lisi,EmilyC, Batista,DeniseAS, McIntosh,Iain, Hoover-Fong,JulieE]
通讯作者: Hoover-Fong,JulieE
Prenatal ABO/RHD Genotyping: A New Paradigm to Allow for Fresh Whole Blood for Cardiopulmonary Bypass in the Immediate Newborn Period.
产前 ABO/RHD 基因分型:一种新范式,允许在新生儿早期进行心肺搭桥术时使用新鲜全血。
DOI: 10.1159/000487592
发表时间: 2018
期刊: Fetal diagnosis and therapy
影响因子: 2.2
作者: [Bishop,JulietChhay, Blakemore,Karin, Vricella,Luca, Sekar,Priya, Sagaser,Katelynn, Crino,Jude, Ness,Paul, Kogutt,BenjaminK, Boyd,Joan, Aucott,Susan, Jelin,AngieC, Chiu,Joanne, Gehrie,Eric, McMillan,KristenNelson]
通讯作者: McMillan,KristenNelson
36
    Functional characterization of a FRMPD4 mutation in a UDP family
    • 批准号:
      8680443
    • 项目类别:
    • 资助金额:
      $24.3万
    • 财政年份:
      2014
    • 负责人:
      TAO WANG
    • 依托单位:
    DHHC 15 palmitoylation modulates striatal dopamine system
    • 批准号:
      8770451
    • 项目类别:
    • 资助金额:
      $24.3万
    • 财政年份:
      2014
    • 负责人:
      TAO WANG
    • 依托单位:
    Functional characterization of a FRMPD4 mutation in a UDP family
    • 批准号:
      8927658
    • 项目类别:
    • 资助金额:
      $24.3万
    • 财政年份:
      2014
    • 负责人:
      TAO WANG
    • 依托单位:
    IMPROVING THE POWER OF LINKAGE DISEQULIBRIUM MAPPING
    海外基金