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

1.   2013 美国国立卫生研究院 FARE Award

2.   2015 美国国立卫生研究院 Orloff Science Award

3.   2017 美国国立卫生研究院 GREAT Award

4.   2019 The International Society for Systemic AutoInflammatory Diseases (ISSAID) 

      Young Investigator Award 

5.   2019 求是科技基金会求是杰出青年学者奖

6.   2019 浙江大学2019年度十大学术进展

7.   2021 中国细胞生物学学会青年女科学家职业发展奖 A 项奖

学术兼职

1. 国际自身炎症疾病学会（ISSAID）委员, 美国医学遗传学与基因组学学院委员（FACMG）

2. 中华医学会医学遗传学分会第十届青委会副主委, 国家卫生健康委遗传咨询能力建设专家委员会委员，中国遗传学会遗传咨询分会委员，美洲华人遗传学会终身会员

主持基金

1.  主持国家自然科学基金-青年基金

2.  主持国家自然科学基金-面上项目2项

3.  主持浙江省杰出青年项目

4.  主持国家重点研发计划重点专项项目课题三(课题组长)

5.  主持浙江省领军型创新团队(首席)

6.  国家自然科学基金-专项项目(骨干)

7.  主持国家自然科学基金-国家杰出青年科学基金

国际学术会议特邀报告

1. The Third International Conference on Deficiency of ADA2, DADA2 cohort in China, Online meeting, 2020

2. ISSAID 10th International Congress,  The NIH Cohort Study of DADA2 Patients: Novel Insights into Pathophysiology and Treatment with the TNF Inhibitors, Mar, 2019, Genoa, Italy.

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

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

5. 23^rd PReS Congress, Biallelic hypomorphic mutations in a   linear deubiquitinase define otulipenia, an early-onset systemic   autoinflammatory disease. Sep, 2016, Genoa, Italy.

6. 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)

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

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

9. 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.

10. 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.

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

12. 7th Congress of ISSAID, Exome sequencing in monogenic   Behçet-like disease. May, 2013, Lausanne, Switzerland.

13. 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.