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    周   青 

     浙江大学生命科学研究院研究员、博士生导师

     美国临床分子遗传学执业主任医师 (DABMGG)

    (美国医学遗传学与基因组学学会ABMGG认证)                                     

教育背景

2000 - 2004     西北大学生命科学学院               学士

2004 - 2009     中国科学院北京基因组研究所     博士


工作背景

2009 - 2010     中国科学院北京基因组研究所     助理研究员

2010 - 2015     美国国立人类基因组研究所         博士后

2015 - 2017     美国国立人类基因组研究所         研究人员

2015 - 2017     美国国立人类基因组研究所         临床分子遗传诊断人员

2017至今         浙江大学生命科学研究院             研究员     

           

学术荣誉

  • 2013 美国国立卫生研究院 Fellows Award for Research Excellence (FARE)

  • 2015 美国国立卫生研究院 Orloff Science Award

  • 2017 国家“千人计划”青年人才 

  • 2017 美国国立卫生研究院 Genome Recognition of Employee Accomplishments and Talents (GREAT) Award


学术兼职

  • Oncogene, Scientific ReportsGenomicsGeneThe Journal of RheumatologyBMC Evolutionary BiologyInternational Journal of Chronic Obstructive Pulmonary DiseaseResearch and Reports in BiologyAdvances in Genomics and Genetics,Biodata mining等学术期刊独立审稿人

     

国际学术会议特邀报告

1.   ACR/ARHP Annual Meeting, Biallelic Hypomorphic Mutations in a Linear Deubiquitinase Define Otulipenia, an Early-Onset Systemic Autoinflammatory Disease. Nov, 2016, Washington, DC, USA.

2.      ASHG 2016 Annual Meeting, Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset systemic autoinflammatory disease. Oct, 2016, Vancouver, Canada.

3.    23rd PReS Congress, Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset systemic autoinflammatory disease. Sep, 2016, Genoa, Italy.

4.      ACR/ARHP Annual Meeting, HA20: A Novel Autoinflammatory Disease Caused By Haploinsufficiency of A20, Encoded By TNFAIP3. Nov, 2015, San Francisco, USA.  (全会报告)

5.      ISSAID Congress, A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein. Sep, 2015, Dresden, Germany.

6.      The National Human Genome Research Institute symposium, Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2. Dec, 2013, Bethesda, USA.

7.   ACR/ARHP Annual Meeting, Intermittent Fever, Immune Dysregulation, And Systemic Vasculopathy Due To Loss-Of-Function Mutations In Adenosine Deaminase2. Oct, 2013, San Diego, USA.

8.      ASHG 2013 Annual Meeting, Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes. Oct, 2013, Boston, USA.

9.      The National Institute of Arthritis and Musculoskeletal and Skin Diseases symposium, Exome sequencing identified CECR1 causing early onset stroke. June, 2013, Bethesda, USA.

10.    7th Congress of ISSAID, Exome sequencing in monogenic Behçet-like disease. May, 2013, Lausanne, Switzerland.

11.    7th Congress of ISSAID, Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes. May, 2013, Lausanne, Switzerland.