Medical Genetics Training Grant
Medical Genetics Training Grant
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
中文摘要
约翰霍普金斯医学遗传学T32博士后培训计划的总体目标是
招募和教育有潜力成为遗传学领域领导者的医生科学家
药我们的计划旨在让学员接触现代医学遗传学和基因组学的各个方面
从研究项目延伸到病人护理。这种博士后培训经验强调指导
研究医学遗传学和基因组学,并为学员在学术医学的职业生涯做好准备。以来
我们的大多数学员都是医生,我们利用医生-科学家培训模式来弥合
遗传学研究和临床医学。
约翰霍普金斯在遗传特征的分类和定位方面发挥了领导作用,
基因组和计算方法的识别和理解基因及其在人类中的作用
疾病,以及临床研究,诊断和治疗孟德尔疾病和多因素疾病
具有重要的遗传贡献。McKusick-Nathans遗传医学系(DGM),
负责监督人类和医学遗传学的临床、教育和研究活动
在约翰霍普金斯大学医学院。
这个T32医学遗传学博士后培训计划是在其第44年的运作与支持
来自NIGMS指导研究培训被整合到医学遗传学住院医师,其目的是
优化利用约翰霍普金斯大学丰富的临床和研究资源以及培训环境
并支持我们的学员作为医生科学家的职业发展。临床遗传学培训如下
通过一段时间的强化研究培训,最大限度地保护研究时间,并通过T32培训提供支持
格兰特.研究培训由精心挑选的研究导师主持,并由
研究委员会。在成功完成该计划后,学员有资格获得
美国医学遗传学委员会在临床遗传学方面拥有丰富的研究经验和专业知识
作为一名独立的物理学家和科学家。我们的培训项目有着出色的记录
教育已经并将继续为该领域做出实质性贡献的医生科学家
医学遗传学在过去的10年里,我们的学员平均有4.5篇来自T32的同行评审出版物
支持培训和我们的毕业生的绝大多数(>80%)采取了以研究为中心或研究相关的
学术机构的职位。URM学员在我们的培训计划中有很好的代表性。我们现在已经
优化整合课程,将医学遗传学的联合收割机临床和研究培训相结合,
多样化的受训人群和培训资源,通过开发与儿科,内部
医学,MFM,REI和NHGRI的培训联盟,并建立了结构化的研究奖学金,
支持个别学员的兴趣和职业目标,以促进他们作为医生科学家的职业生涯。
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
DOI:
10.1111/bjh.12748
发表时间:
2014-05
期刊:
British journal of haematology
影响因子:
6.5
作者:
[Khincha PP, Wentzensen IM, Giri N, Alter BP, Savage SA]
通讯作者:
Savage SA
共 36 条
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
-
批准号:7723453
-
项目类别:
-
资助金额:$1.36万
-
财政年份:2008
-
负责人:TAO WANG
-
依托单位:
X chromosome cDNA microarray Screening and Functional Study of Novel XLMR genes
-
批准号:7305496
-
项目类别:
-
资助金额:$24.4万
-
财政年份:2007
-
负责人:TAO WANG
-
依托单位:
IMPROVING THE POWER OF LINKAGE DISEQULIBRIUM MAPPING
-
批准号:7601010
-
项目类别:
-
资助金额:$0.51万
-
财政年份:2007
-
负责人:TAO WANG
-
依托单位:
X chromosome cDNA microarray Screening and Functional Study of Novel XLMR genes
-
批准号:7683791
-
项目类别:
-
资助金额:$23.91万
-
财政年份:2007
-
负责人:TAO WANG
-
依托单位:
X chromosome cDNA microarray Screening and Functional Study of Novel XLMR genes
-
批准号:7494168
-
项目类别:
-
资助金额:$23.91万
-
财政年份:2007
-
负责人:TAO WANG
-
依托单位:
ID of Genes Responsible for X-Linked Mental Retardation
-
批准号:6798304
-
项目类别:
-
资助金额:$13.39万
-
财政年份:2003
-
负责人:TAO WANG
-
依托单位:
ID of Genes Responsible for X-Linked Mental Retardation
-
批准号:7120091
-
项目类别:
-
资助金额:$13.47万
-
财政年份:2003
-
负责人:TAO WANG
-
依托单位:
ID of Genes Responsible for X-Linked Mental Retardation
-
批准号:6943517
-
项目类别:
-
资助金额:$13.47万
-
财政年份:2003
-
负责人:TAO WANG
-
依托单位:
ID of Genes Responsible for X-Linked Mental Retardation
-
批准号:6674621
-
项目类别:
-
资助金额:$13.31万
-
财政年份:2003
-
负责人:TAO WANG
-
依托单位:
Medical Genetics Training Program
-
批准号:8690856
-
项目类别:
-
资助金额:$32.42万
-
财政年份:1977
-
负责人:TAO WANG
-
依托单位:
Medical Genetics Training Grant
-
批准号:8999108
-
项目类别:
-
资助金额:$36.25万
-
财政年份:1977
-
负责人:TAO WANG
-
依托单位:
Medical Genetics Training Grant
-
批准号:10332129
-
项目类别:
-
资助金额:$43.72万
-
财政年份:1977
-
负责人:TAO WANG
-
依托单位:
海外基金