个人简历
Zheng LI博士目前就职于新加坡基因研究院（Genome Institute of Singapore），人类遗传学部门的副研究员。2006年取得英国纽卡斯尔大学的医学博士学位，在读期间曾获得英国国务卿对教育和科学领域设立的海外研究学者奖励计划（Overseas Research Students Awards Scheme）资助。后在国内外多个著名研究所从事遗传学方面的研究，在人类遗传学、复杂病遗传学方面具有丰富的遗传学分析经验。先后在Nature Genetics、 American Journal of Human Genetics等杂志正式发表论文25篇。
研究领域
在人类遗传学、复杂病遗传学方面具有丰富的遗传学分析经验。
近期论文
1.A common variant mapping toCACNA1A is associated with susceptibility to exfoliation syndrome. Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, Nilgün Y, Zarnowski T, Pakravan M, Safieh LA, Jia L, Wang YX, Williams S, PaoliD, Schlottmann PG, Huang L, Sim KS, Foo JN, Nakano M, Ikeda Y, Kumar RS, Ueno M, Manabe S, Hayashi K, Kazama S, Ideta R, Mori Y, Miyata K, Sugiyama K, HigashideT, Chihara E, Inoue K, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Aihara M, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Matsuda F, Yamashiro K, Gotoh N, Miyake M,Astakhov SY, Osman EA, Al-Obeidan SA, Owaidhah O, Al-Jasim L, Al Shahwan S,Fogarty RA, Leo P, Yetkin Y, O?uz Ç, Kanavi MR, Beni AN, Yazdani S, Akopov EL,Toh KY, Howell GR, Orr AC, Goh Y, Meah WY, Peh SQ, Kosior-Jarecka E, Lukasik U,Krumbiegel M, Vithana EN, Wong TY, Liu Y, Koch AE, Challa P, Rautenbach RM,Mackey DA, Hewitt AW, Mitchell P, Wang JJ, Ziskind A, Carmichael T,Ramakrishnan R, Narendran K, Venkatesh R, Vijayan S, Zhao P, Chen X, Guadarrama-Vallejo D,Cheng CY, Perera SA, Husain R, Ho SL, Welge-Luessen UC, Mardin C,Schloetzer-Schrehardt U, Hillmer AM, Herms S, Moebus S, Nöthen MM, Weisschuh N,Shetty R, Ghosh A, Teo YY, Brown MA, Lischinsky I; Blue Mountains Eye Study GWAS Team; Wellcome Trust Case Control Consortium 2, Crowston JG, Coote M, Zhao B,Sang J, Zhang N, You Q, Vysochinskaya V, Founti P, Chatzikyriakidou A,Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH,May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM,Chowbay B, Schaeffeler E, Schwab M, Lerner F, Wang N, Yang Z, Frezzotti P,Kinoshita S, Fingert JH, Inatani M, Tashiro K, Reis A, Edward DP, Pasquale LR,Kubota T, Wiggs JL, Pasutto F, Topouzis F, Dubina M, Craig JE, Yoshimura N,Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC.. Nat Genet.2015 Apr;47(4):387-92. 2.Common variants near ABCA1 and in PMM2 are associated with primary open-angleglaucoma. Dunstan SJ, Hue NT, Han B, Li Z, Tram TT, Sim KS, Parry CM, Chinh NT, Vinh H, Lan NP, Thieu NT, Vinh PV, Koirala S, Dongol S, Arjyal A, Karkey A, Shilpakar O, Dolecek C, Foo JN, Phuong le T, Lanh MN, Do T, Aung T, Hon do N, Teo YY, Hibberd ML, Anders KL, Okada Y, Raychaudhuri S, Simmons CP, Baker S, de Bakker PI,Basnyat B, Hien TT, Farrar JJ, Khor CC. Variation at HLA-DRB1 is associated with resistance to enteric fever. Nat Genet. 2014 Dec;46(12):1333-6. doi:10.1038/ng.3143. Epub 2014 Nov 10. PubMed PMID: 25383971.6: Chen Y, Lin Y, Vithana EN, Jia L, Zuo X, Wong TY, Chen LJ, Zhu X, Tam PO, GongB, Qian S, Li Z, Liu X, Mani B, Luo Q, Guzman C, Leung CK, Li X, Cao W, Yang Q,Tham CC, Cheng Y, Zhang X, Wang N, Aung T, Khor CC, Pang CP, Sun X, Yang Z Nat Genet. 2014 Oct;46(10):1115-9. 3.“Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis.” Sergouniotis PI, Davidson AE, Mackay DS, Li Z, Yang X, Plagnol V, Moore AT, Webster AR. Am J Hum Genet. 2011 Jul 15;89(1):183-90.
