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Chear, Chai Teng and El Farran, Bader Abdul Kader and Sham, Marina and Ramalingam, Kavetha and Noh, Lokman Mohd and Ismail, Intan Hakimah and Chiow, Mei Yee and Baharin, Mohd Farid and Ripen, Adiratna Mat and Mohamad, Saharuddin (2022) A Novel De Novo NFKBIA missense mutation associated to ectodermal dysplasia with dysgammaglobulinemia. Genes, 13 (10). ISSN 2073-4425, DOI https://doi.org/10.3390/genes13101900.
Chear, Chai Teng and Ripen, Adiratna Mat and Mohamad, Saharuddin (2022) Deciphering the structural and functional impact of Q657L mutation in NLRC4 using computational methods. Molecular Simulation, 48 (14). pp. 1240-1255. ISSN 0892-7022, DOI https://doi.org/10.1080/08927022.2022.2080822.
Ripen, Adiratna Mat and Chear, Chai Teng and Baharin, Mohd Farid and Nallusamy, Revathy and Chan, Kwai Cheng and Kassim, Asiah and Choo, Chong Ming and Wong, Ke Juin and Fong, Siew Moy and Tan, Kah Kee and Nachiappan, Jeyaseelan P. and Teo, Kai Ru and Chiow, Mei Yee and Hishamshah, Munirah and Ghani, Hamidah and Muralitharan, Rikeish R. and Bin Mohamad, Saharuddin (2021) A single-center pilot study in Malaysia on the clinical utility of whole-exome sequencing for inborn errors of immunity. Clinical and Experimental Immunology, 206 (2). pp. 119-128. ISSN 0009-9104, DOI https://doi.org/10.1111/cei.13626.
Chear, Chai Teng and Nallusamy, Revathy and Chan, Kwai Cheng and Mohd Tap, Ratna and Baharin, Mohd Farid and Syed Yahya, Sharifah Nurul Husna and Krishnan, Prasobhan Bala and Bin Mohamad, Saharuddin and Ripen, Adiratna Mat (2021) Atypical presentation of severe fungal necrotizing fasciitis in a patient with X-Linked Agammaglobulinemia. Journal of Clinical Immunology, 41 (6). pp. 1178-1186. ISSN 0271-9142, DOI https://doi.org/10.1007/s10875-021-01017-3.
Chear, Chai Teng and Nallusamy, Revathy and Canna, Scott W. and Chan, Kwai Cheng and Baharin, Mohd Farid and Hishamshah, Munirah and Ghani, Hamidah and Ripen, Adiratna Mat and Bin Mohamad, Saharuddin (2020) A novel de novo NLRC4 mutation reinforces the likely pathogenicity of specific LRR domain mutation. CLINICAL IMMUNOLOGY, 211. ISSN 15216616, DOI https://doi.org/10.1016/j.clim.2019.108328.
