Professor | 姚音 | 数字化转型顾问

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Name	姚音
Contact Information	yin_yao@fudan.edu.cn
Language ability	英语, 中文
Province	上海

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Name

姚音

Contact Information

yin_yao@fudan.edu.cn

Language ability

英语, 中文

Province

上海

University/Lab Affiliation and Title	复旦大学
Faculty	Life Sciences
Academic Background & Achievements	1991.9-1996.7 遗传学博士：哥伦比亚大学 2001：NIH Directors award，约翰霍普金斯大学医学院 2003：The Louis I. and Thomas D. Dublin award，约翰霍普金斯大学公共卫生学院 2006：The Helen Abbey Award for Advising, Mentoring and Teaching Recognition，约翰霍普金斯大学公共卫生学院
Work Experience	1996-1997 - 法国国际癌症研究机构 - 博士后 1997-1998 - 美国匹兹堡大学 - 助理教授 (研究系列) 1998-2004 - 美国约翰·霍普金斯·布隆伯格公共卫生学院 - 助理教授 2004-2007 - 美国约翰·霍普金斯·布隆伯格公共卫生学院 - 副教授 (终身) 2007-2016 - 美国国家精神卫生研究所 - 遗传流行病学研究组负责人 2016-今 - 美国国家精神卫生研究所 - 统计基因组学和数据分析中心主任 2017-今 - 复旦大学 - 特聘教授
Awards	2001：NIH Directors award，约翰霍普金斯大学医学院 2003：The Louis I. and Thomas D. Dublin award，约翰霍普金斯大学公共卫生学院 2006：The Helen Abbey Award for Advising, Mentoring and Teaching Recognition，约翰霍普金斯大学公共卫生学院

University/Lab Affiliation and Title

复旦大学

Faculty

Life Sciences

Academic Background & Achievements

1991.9-1996.7 遗传学博士：哥伦比亚大学
2001：NIH Directors award，约翰霍普金斯大学医学院
2003：The Louis I. and Thomas D. Dublin award，约翰霍普金斯大学公共卫生学院
2006：The Helen Abbey Award for Advising, Mentoring and Teaching Recognition，约翰霍普金斯大学公共卫生学院

Work Experience

1996-1997 - 法国国际癌症研究机构 - 博士后
1997-1998 - 美国匹兹堡大学 - 助理教授 (研究系列)
1998-2004 - 美国约翰·霍普金斯·布隆伯格公共卫生学院 - 助理教授
2004-2007 - 美国约翰·霍普金斯·布隆伯格公共卫生学院 - 副教授 (终身)
2007-2016 - 美国国家精神卫生研究所 - 遗传流行病学研究组负责人
2016-今 - 美国国家精神卫生研究所 - 统计基因组学和数据分析中心主任
2017-今 - 复旦大学 - 特聘教授

Awards

2001：NIH Directors award，约翰霍普金斯大学医学院
2003：The Louis I. and Thomas D. Dublin award，约翰霍普金斯大学公共卫生学院
2006：The Helen Abbey Award for Advising, Mentoring and Teaching Recognition，约翰霍普金斯大学公共卫生学院

Areas of Focus	统计遗传学精神病遗传学计算生物学
Publications	Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4, Bing-Jian, F., Huang, W., Shugart, Y.Y., 2002 Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q, Shugart, Y.Y., 2006 Whole genome association analysis of treatment response in obsessive-compulsive disorder, Qin H, Nestadt G, Shugart, Y.Y., 2016 Comprehensive pathway-based association study of DNA repair gene variants and the risk of nasopharyngeal carcinoma, Qin, H.D., Shugart, Y.Y., Zeng, Y.X., 2011 Anticipation in familial Hodgkin lymphoma, Shugart, Y.Y., 1998 Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis, Qin, H.D., Shugart, Y.Y., Jia WH, 2016 Exploring transcription factors-microRNAs Co-regulation networks in schizophrenia, Xu, Y., Yue, W., Shugart, Y.Y., 2015 Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD), Ritter, M.L., Gerald Nestadt, Shugart, Y.Y., 2017 Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations, Hong, S.E., Shugart, Y.Y., Walsh, C.A., 2000 Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder, Willour, V.L., Shugart, Y.Y., 2004 Common polygenic variation and risk for childhood-onset schizophrenia, Ahn, K., An, S.S., Shugart, Y.Y., Rapoport, J.L., 2016 Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs, Cao, H., Duan, J., Lin, D., Shugart, Y.Y., Calhoun, V., Wang, Y.P., 2014 Exome sequencing and the genetic basis of complex traits, Kiezun, A., Garimella, K., Do, R., Stitziel, N.O., Neale, B.M., McLaren, P.J., Gupta, N., Sklar, P., Sullivan, P.F., Moran, J.L., Hultman, C.M., 2012

Areas of Focus

统计遗传学
精神病遗传学
计算生物学

Publications

Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4, Bing-Jian, F., Huang, W., Shugart, Y.Y., 2002
Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q, Shugart, Y.Y., 2006
Whole genome association analysis of treatment response in obsessive-compulsive disorder, Qin H, Nestadt G, Shugart, Y.Y., 2016
Comprehensive pathway-based association study of DNA repair gene variants and the risk of nasopharyngeal carcinoma, Qin, H.D., Shugart, Y.Y., Zeng, Y.X., 2011
Anticipation in familial Hodgkin lymphoma, Shugart, Y.Y., 1998
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis, Qin, H.D., Shugart, Y.Y., Jia WH, 2016
Exploring transcription factors-microRNAs Co-regulation networks in schizophrenia, Xu, Y., Yue, W., Shugart, Y.Y., 2015
Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD), Ritter, M.L., Gerald Nestadt, Shugart, Y.Y., 2017
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations, Hong, S.E., Shugart, Y.Y., Walsh, C.A., 2000
Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder, Willour, V.L., Shugart, Y.Y., 2004
Common polygenic variation and risk for childhood-onset schizophrenia, Ahn, K., An, S.S., Shugart, Y.Y., Rapoport, J.L., 2016
Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs, Cao, H., Duan, J., Lin, D., Shugart, Y.Y., Calhoun, V., Wang, Y.P., 2014
Exome sequencing and the genetic basis of complex traits, Kiezun, A., Garimella, K., Do, R., Stitziel, N.O., Neale, B.M., McLaren, P.J., Gupta, N., Sklar, P., Sullivan, P.F., Moran, J.L., Hultman, C.M., 2012

遗传学统计学心理健康基因组学数据分析生物信息学流行病学精神病学计算方法疾病研究

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