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Showing results 1 to 7 of 7

	Title	Author(s)	Issue Date
	Diagnosing Titinopathy: lessons from a multi-omics pilot study in Hong Kong Proceeding/Conference:World Muscle Society 2022 Congress	Zhang, Y Xue, L Lei, Y Chan, HSS Javed, A	2022
	Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus Journal:Rheumatology	Song, Q LEI, Y Shao, L Li, W Kong, Q Lin, Z Qin, X Wei, W Hou, F Li, J Guo, X Mao, Y CAO, Y LIU, Z ZHENG, L LIANG, R Jiang, Y Liu, Y Zhang, L Yang, J Lau, YL Zhang, Y Ban, B Wang, YF Yang, W	2021
	Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups Journal:Nature Communications	Wang, YF Zhang, Y Lin, Z ZHANG, H Wang, TY CAO, Y Morris, DL Sheng, Y Yin, X Zhong, SL Gu, X LEI, Y He, J Wu, Q SHEN, J Yang, J Lam, TH Lin, JH Mai, Z GUO, M Tang, Y Chen, Y Song, Q Ban, B Mok, CC Cui, Y Lu, L Shen, N Sham, PC Lau, CS Smith, DK Vyse, TJ Zhang, X Lau, YL Yang, W	2021
	Identification of Shared and Asian-Specific Loci for Systemic Lupus Erythematosus and Evidence for Roles of Type III Interferon Signaling and Lysosomal Function in the Disease: A Multi-Ancestral Genome-Wide Association Study. Journal:Arthritis & Rheumatology	Wang, Y Wei, W Tangtanatakul, P ZHENG, L LEI, Y Lin, Z Qian, C Qin, X Hou, F Zhang, X Shao, L Satproedprai, N MahasirimongkoL, S Pisitkun, P Song, Q Lau, YL Zhang, Y Hirankarn, N Yang, W	2022
	Ranking variant pathogenicity using Exomiser facilitated the identification of the missing second mutation in three recessive cases of congenital myopathy Proceeding/Conference:The 20th Asian and Oceanian Myopathy Center (AOMC) Meeting in conjunction with the National Scientific Meeting of Indonesian Neurological Association (PERDOSSI) Jun 9th-12th 2022	Lei, Y Yang, W Chan, HSS	2022
	Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity Journal:Frontiers in Immunology	Chan, KW Wong, CYA LEUNG, D Yang, X Fok, SFS Mak, HS Lei, Y Ma, W Mao, H Zhao, X Liang, W Singh, S Barbouche, MR He, JX Jiang, LP Liew, WK Le, MHT Muktiarti, D Santos-Ocamo, FH Djidjik, R Belaid, B Ismail, IH Abdul Latiff, AH Lee, WS Chen, TX Liu, J Jin, R Wang, X Chen, YH Yu, HH Rai, D Raj, R Vaughan, J Urban, M Berg, S VAN DEN Eley, B Lee, ACW Isa, MS Ang, EY Lee, BW Yeoh, AEJ Shek, LP Quynh Le, NN Nguyen, VAT Phan Nguyen Lien, A Capulong, RD Mallillin, JM Villanueva, JCMM Camonayan, KAB Vera, MD Casis-Hao, RJ Lobo, RCM Foronda, R Binas, VWE Boushaki, S Kechout, N Phongsamart, G Wongwaree, S Jiratchaya, C Lao-Araya, M Trakultivakorn, M Suratannon, N Jirapongsananuruk, O Chantveerawong, T Kamchaisatian, W Chan, LL Koh, MT Wong, KJ Fong, SM Thong, MK Latiff, AZ Noh, LM Silva, R DE Jouhadi, Z Al-Saad, K Vignesh, P Jindal, AK Rawat, A Gupta, A Suri, D Yang, J Au, EYL Kwok, JSY Chan, SY Hui, WYF Chua, GT Sou Da Rosa Duque, J Cheong, KN Chong, CY Ho, MHK Lee, TL Wong, WHS Yang, W Lee, PPW Tu, W Yang, XQ Lau, YL	2022
	TTN mutations in limb girdle muscular dystrophy with calpainopathy-like presentation in 2 siblings Proceeding/Conference:19th Asian-Oceanian Myology Center Meeting (AOMC2021)	LEI, Y Yang, W Chan, HSS	2021

Showing results 1 to 7 of 7