Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents von She, Chun Hing, Tsang, Hing Wai, Yang, Xingtian, Tsao, Sabrina Sl, Tang, Clara Sm, Chan, Sophelia Hs, Kwan, Mike Yw, Chua, Gilbert T, Yang, Wanling, Ip, Patrick

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Severity of SARS-CoV-2 Omicron BA.2 infection in unvaccinated hospitalized children: comparison to influenza and parainfluenza infections von Tso, Winnie W.Y., Kwan, Mike Y.W., Wang, Yu Liang, Leung, Lok Kan, Leung, Daniel, Chua, Gilbert T., Ip, Patrick, Fong, Daniel Y.T., Wong, Wilfred H.S., Chan, Sophelia H.S., Chan, Jasper F.W., Peiris, Malik, Lau, Yu Lung, Rosa Duque, Jaime S.

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Mental health & maltreatment risk of children with special educational needs during COVID-19 von Tso, Winnie W.Y., Chan, Ko Ling, Lee, Tatia M.C., Rao, Nirmala, Lee, S.L., Jiang, Fan, Chan, Sophelia H.S., Wong, Wilfred H.S., Wong, Rosa S., Tung, Keith T.S., Yam, Jason C., Liu, Anthony P.Y., Chua, Gilbert T., Rosa Duque, Jaime S., Lam, Almen L.N., Yip, K.M., Leung, L.K., Wang, Yuliang, Sun, Jin, Wang, Guanghai, Chan, Godfrey C.F., Wong, Ian C.K., Ip, Patrick

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Limb girdle muscular dystrophy due to LAMA2 mutations: Diagnostic difficulties due to associated peripheral neuropathy von Chan, Sophelia H.S, Foley, A. Reghan, Phadke, Rahul, Mathew, Ann Agnes, Pitt, Matthew, Sewry, Caroline, Muntoni, Francesco

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Congenital muscular dystrophies in China von Ge, Lin, Zhang, Cheng, Wang, Zhaoxia, Chan, Sophelia H.S., Zhu, Wenhua, Han, Chunxi, Zhang, Xiaoli, Zheng, Hong, Wu, Liwen, Jin, Bo, Shan, Jingli, Mao, Bing, Zhong, Jianmin, Peng, Xiaoyin, Cheng, Yaying, Hu, Jun, Sun, Yan, Lu, Junlan, Hua, Ying, Zhu, Sainan, Wei, Cuijie, Wang, Shuo, Jiao, Hui, Yang, Haipo, Fu, Xiaona, Fan, Yanbin, Chang, Xingzhi, Wang, Shuang, Bao, Xinhua, Zhang, Yuehua, Wang, Jingmin, Wu, Ye, Jiang, Yuwu, Yuan, Yun, Rutkowski, Anne, Bönnemann, Carsten G., Wei, Wei, Wu, Xiru, Xiong, Hui

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Collagen VI-related myopathies: clinical variability, phenotype-genotype correlation and exploratory transcriptome study von Kwong, Anna KY, Zhang, Yanmin, Ho, Ronnie SL, Gao, Yuan, Ling, Xu, Tsang, Mandy HY, Luk, HM, Chung, Brian HY, Bönnemann, Carsten G, Javed, Asif, Chan, Sophelia HS

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Megaconial congenital muscular dystrophy: Same novel homozygous mutation in CHKB gene in two unrelated Chinese patients von Chan, Sophelia HS, Ho, Ronnie SL, Khong, PL, Chung, Brian HY, Tsang, Mandy HY, Yu, Mullin HC, Yeung, Matthew CW, Chan, Angel OK, Fung, CW

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Cytoplasmic body pathology in severe ACTA1 -related myopathy in the absence of typical nemaline rods von Donkervoort, Sandra, Chan, Sophelia HS, Hotchkiss, Leslie, Bradley, Nathaniel, Nguyen, David, Leach, Meganne E, Mohassel, Payam, Hu, Ying, Thangarajh, Mathula, Bharucha-Goebel, Diana, Kan, Amanda, Ho, Ronnie SL, Reyes, Christine, Nance, Jessica, Moore, Steven A, Foley, A. Reghan, Bönnemann, Carsten G

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Infantile to late adulthood onset facioscapulohumeral dystrophy type 1 a case series von Leung, W. Y., Luk, H. M., Vardhanabhuti, Varut, Gao, Y., Hui, K. F., Lau, W. Y., Young, Terence P. H., Li, Jessica T. C., Fung, Eva L. W., Chiu, Annie T. G., Lo, Ivan F. M., Chung, Brian H. Y., Cheung, Y. F., Chan, Sophelia H. S.

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Spinal Primitive Neuroectodermal Tumor Mimicking as Chronic Inflammatory Demyelination Polyneuropathy: A Case Report and Review of Literature von Chan, Sophelia H. S., Tsang, Dickson S. F., Wong, Virginia C. N., Chan, Godfrey C. F.

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Anti-NMDA Receptor Encephalitis With Atypical Brain Changes on MRI von Chan, Sophelia H.S., MD, Wong, Virginia C.N., MD, Fung, Cheuk-wing, MD, Dale, Russell C., PhD, Vincent, Angela, PhD

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Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey von Mak, Christopher CY, Leung, Gordon KC, Mok, Gary TK, Yeung, Kit San, Yang, Wanling, Fung, Cheuk-Wing, Chan, Sophelia HS, Lee, So-Lun, Lee, Ni-Chung, Pfundt, Rolph, Lau, Yu-Lung, Chung, Brian HY

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Additional file 2 of Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents von She, Chun Hing, Tsang, Hing Wai, Yang, Xingtian, Tsao, Sabrina SL, Tang, Clara SM, Chan, Sophelia HS, Kwan, Mike YW, Chua, Gilbert T, Yang, Wanling, Ip, Patrick

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Additional file 3 of Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents von She, Chun Hing, Tsang, Hing Wai, Yang, Xingtian, Tsao, Sabrina SL, Tang, Clara SM, Chan, Sophelia HS, Kwan, Mike YW, Chua, Gilbert T, Yang, Wanling, Ip, Patrick

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Additional file 1 of Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents von She, Chun Hing, Tsang, Hing Wai, Yang, Xingtian, Tsao, Sabrina SL, Tang, Clara SM, Chan, Sophelia HS, Kwan, Mike YW, Chua, Gilbert T, Yang, Wanling, Ip, Patrick

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Megaconial congenital muscular dystrophy: Same novel homozygous mutation in CHKB gene in two unrelated Chinese patients von Chan, Sophelia Hs, Ho, Ronnie Sl, Khong, P L, Chung, Brian Hy, Tsang, Mandy Hy, Yu, Mullin Hc, Yeung, Matthew Cw, Chan, Angel Ok, Fung, C W

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