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Scopus Click arrow to expand the list of publications
Ismail R, K Teh L, Amir J, Alwi Z, Lopez CG. Genetic polymorphism of CYP2D6 in Chinese subjects in Malaysia. J Clin Pharm Ther 2003;28(4):279–84.
Romaino SMN, Teh LK, Zilfalil BA, Thong CP, Ismail AA, Amir J, et al. A simple and rapid genotyping method for beta-2 receptor (β2 AR) gene using allele specific multiplex PCR. J Clin Pharm Ther. 2004;29(1):47–52.
Zilfalil BA, Zabidi-Hussin AMH, Watihayati MS, Rozainah MY, Naing L, Sutomo R, et al. Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in Malay patients with spinal muscular atrophy. Medical Journal of Malaysia. 2004;59(4):512–4.
Teh LK, Zilfalil BA, Marina I, Rosemi BS, Ismail R. Genetic polymorphism of CYP2D6 in patients with cardiovascular disease - A cohort study. J Clin Pharm Ther. 2004;29(6):559–64.
Liza-Sharmini AT, Azlan ZN, Zilfalil BA. Ocular findings in Malaysian children with Down syndrome. Singapore Med J. 2006;47(1):14–9.
Zilfalil BA, Sarina S, Liza-Sharmini AT, Oldfield NJ, Stenhouse SA. Detection of F508del mutation in cystic fibrosis transmembrane conductance regulator gene mutation among Malays. Singapore Med J. 2006;47(2):129–33.
Bhuiyan ZA, Zilfalil BA, Hennekam RCM. A Malay boy with the Cornelia de Lange syndrome: Clinical and molecular findings. Singapore Med J. 2006;47(8):724–7.
Zilfalil BA, Hoh BP, Nizam MZ, Liza-Sharmini AT, Teh LK, Ismail R. An improved rapid genotyping method for the study of beta-2 adrenergic receptor gene polymorphisms using single tube allele specific multiplex PCR. J Clin Pharm Ther. 2006;31(6):637–40.
Rajion ZA, Alwi Z. Genetics of cleft lip and palate: A review. Malaysian Journal of Medical Sciences. 2007;14(1):4–9.
Watihayati MS, Zabidi-Hussin AMH, Tang TH, Matsuo M, Nishio H, Zilfalil BA. Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients. Pediatrics International. 2007;49(1):11–4.
Watihayati MS, Zabidi-Hussin AMH, Tang TH, Matsuo M, Nishio H, Zilfalil BA. Erratum: Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients (Pediatrics International (2007) 49, (11-14)). Pediatrics International. 2007;49(2):303.
Pal S, Siti MI, Ankathil R, Zilfalil BA. Two cases of isochromosome 18q syndrome. Singapore Med J 2007;48(5):e146–50.
Azman BZ, Ankathil R, Siti Mariam I, Suhaida MA, Norhashimah M, Tarmizi AB, et al. Cytogenetic and clinical profile of Down syndrome in Northeast Malaysia. Singapore Med J. 2007;48(6):550–4.
Zahari MN, Peng HB, Ling CL, Tet CM, Tajudin LSA, Alwi Z. A report of a SNP EX3 1209A>G of prostaglandin F receptor gene among Malaysians. International Medical Journal. 2007;14(2):89–91.
Hoh BP, Zahary MN, Tajudin LSA, Chieng LL, Cheong MT, Sidek MR, et al. A novel single nucleotide polymorphism, IVS2 -97A>T, in the prostaglandin F2α receptor gene was identified among the Malaysian patients with glaucoma. Kobe Journal of Medical Sciences. 2007;53(2):49–52.
Watihayati MS, Zabidi-Hussin AMH, Tang TH, Nishio H, Zilfalil BA. NAIP-deletion analysis in Malaysian patients with spinal muscular atrophy. Kobe Journal of Medical Sciences. 2007;53(4):171–5.
Hassan R, Ramli M, Abdullah WZ, Mustaffa R, Ghazali S, Ankathil R, et al. Short communication One-Step Multiplex RT-PCR for detection of BCR/ABL gene in Malay patients with chronic myeloid leukaemia. Asia Pac J Mol Biol Biotechnol. 2008;16(2):41–4.
Peng HB, Rajab NSA, Gin OK, Alwi Z. Y-chromosomal STR variation in malays of kelantan and minang. Pertanika J Trop Agric Sci. 2008;31(1):135–40.
Marini M, Salmi AA, Watihayati MS, Mardziah MDS, Zahri MK, Hoh BP, et al. Screening of dystrophin gene deletions in Malaysian patients with Duchenne Muscular Dystrophy. Medical Journal of Malaysia. 2008;63(1):31–4.
Mohamad N, Rashidi A, Aaasim WAW, Kamaruddin J, Bakar NHA, Nizam MZ, et al. Beta-2 adrenergic receptor polymorphisms and acute exacerbation of bronchial asthma. International Medical Journal. 2008;15(1):7–11.
Azman BZ, Akhir SM, Zilfalil BA, Ankathil R. Two cases of deletion 5p syndrome: One with paternal involvement and another with atypical presentation. Singapore Med J. 2008;49(4):e98–100.
Cheong MT, Kodisvary M, Raja VS, Azhany Y, Zilfalil BA, Liza-Sharmini AT. Response to Latanoprost monotherapy among Malay patients with glaucoma. Asian Journal of Ophthalmology. 2008;10(2):118–22.
Kannan TP, Azman BZ, Ahmad Tarmizi AB, Suhaida MA, Siti Mariam I, Ravindran A, et al. Turner syndrome diagnosed in northeastern Malaysia. Singapore Med J. 2008;49(5):400–4.
Rahman RA, Ahmad A, Rahman ZAA, Mokhtar KI, Lah NASN, Zilfalil BA, et al. Transforming growth factor-α and nonsyndromic cleft lip with or without palate or cleft palate only in Kelantan, Malaysia. Cleft Palate-Craniofacial Journal. 2008;45(6):583–6.
Watihayati MS, Zabidi AMH, Tang TH, Nishio H, Zilfalil BA. NAIP-deletion analysis in Malaysian patients with spinal muscular atrophy (Kobe Journal of Medical Sciences 53, 4, (171-175)). Kobe Journal of Medical Sciences. 2008;54(4).
Aishah ZS, Khairi MDM, Normastura AR, Zafarina Z, Zilfalil BA. Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography. Journal of Laryngology and Otology. 2008;122(12):1284–8.
Akhir SM, Ismail SM, Zulkifli A, Hassan R, Zilfalil BA, Ankathil R. Cytogenetic analysis of 104 acute myeloid leukemia (AML) patients at Human Genome Center, Universiti Sains Malaysia, Kelantan. International Medical Journal. 2008;15(5):363–5.
Rozitah R, Nizam MZ, Nur Shafawati AR, Nor Atifah MA, Dewi M, Kannan TP, et al. Detection of beta-globin gene mutations among Kelantan Malay thalassaemia patients by polymerase chain reaction restriction fragment length polymorphism. Singapore Med J. 2008;49(12):1046–9.
Watihayati MS, Fatemeh H, Marini M, Atif AB, Zahiruddin WM, Sasongko TH, et al. Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy. Brain Dev. 2009;31(1):42–5.
Kannan TP, Hemlatha S, Ankathil R, Zilfalil BA. Clinical manifestations in trisomy 9. Indian J Pediatr. 2009;76(7):745–6.
Al-khateeb A, Mohamed MS, Ibrahim S, Yusof Z, Zilfalil BA. A review of the genetic aspects of familial hypercholestrolemia in Malaysia. International Medical Journal. 2009;16(3):183–8.
Abdulla MA, Ahmed I, Assawamakin A, Bhak J, Brahmachari SK, Calacal GC, et al. Mapping human genetic diversity in Asia. Science (1979). 2009;326(5959):1541–5.
Pal S, Ma SO, Norhasimah M, Suhaida MA, Siti Mariam I, Ankathil R, et al. Chromosomal abnormalities and reproductive outcome in Malaysian couples with miscarriages. Singapore Med J . 2009;50(10):1008–12. Available from: Kannan TP, Zilfalil BA. Cytogenetics: Past, present and future. Malaysian Journal of Medical Sciences. 2009;16(2):4–9.
Arffah KS, Yusuf SM, Rasool AHG, Halim AS, Zilfalil BA. Effect of Tocotrienol Rich Fraction (TRF) on fibroblasts from normal and hypertrophic scar tissues in vitro. International Medical Journal. 2009;16(4):247–50.
Salahshourifar I, Halim AS, Sulaiman WAW, Zilfalil BA. Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate. Am J Med Genet A. 2010;152(7):1818–21.
Yusoff S, Takeuchi A, Ashi C, Tsukada M, Ma’Amor NH, Zilfalil BA, et al. A polymorphic mutation, c.-3279t>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the malay population. Pediatr Res. 2010;67(4):401–6.
Sasongko TH, Gunadi, Yusoff S, Atif AB, Fatemeh H, Rani A, et al. Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder. Brain Dev. 2010;32(5):385–9.
Yusof HA, Ramlee N, Ishak SR, Ab Rajab NS, Ghani SA, Bachok NS, et al. Identification of single nucleotide polymorphism (SNP) 153104 (A to G) of RB1 gene in Malaysian retinoblastoma children and its association with laterality and staging of the disease. International Medical Journal. 2010;17(2):129–33.
Hikmah EM, Norhashimah M, Mariam IS, Razak S, Sudhikaran W, Limprasert P, et al. Divergence in cytogenetic and molecular genetic analysis results: A case report of fragile X syndrome among siblings. International Medical Journal. 2010;17(2):135–9.
Ishak SR, Hanafi H, Alagaratnam J V, Zilfalil BA, Tajudin LSA. RB pocket domain B mutation frequency in Malaysia. Ophthalmic Genet. 2010;31(3):159–61.
Sasongko TH, Salmi AR, Zilfalil BA, Albar MA, Mohd Hussin ZA. Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: Type 1 spinal muscular atrophy. Ann Saudi Med. 2010;30(6):427–31.
Ahzad HA, Ramli SF, Loong TM, Salahshourifar I, Zilfalil BA, Yusoff NM. De novo ring chromosome 6 in a child with multiple congenital anomalies. Kobe Journal of Medical Sciences. 2010;56(2):E79–84.
Natasya Naili MN, Hasnita CH, Shamim AK, Hasnan J, Fauziah MI, Narazah MY, et al. Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization. Cancer Genet Cytogenet. 2010;203(2):309–12.
Al-Khateeb A, Mohamed MS, Imran K, Ibrahim S, Zilfalil BA, Yusof Z. Low-density lipoprotein cholesterol goal attainment among Malaysian dyslipidemic patients. Southeast Asian Journal of Tropical Medicine and Public Health. 2011;42(2):388–94.
Salahshourifar I, Halim AS, Sulaiman WAW, Zilfalil BA. Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: Association of variants in OFC1. J Dent Res. 2011;90(3):387–91.
Sasongko TH, Gunadi, Zilfalil BA, Zabidi-Hussin Z. Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy. J Neurogenet . 2011;25(1–2):15–6.
Al-Khateeb A, Zahri MK, Mohamed MS, Sasongko TH, Ibrahim S, Yusof Z, et al. Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia. BMC Med Genet. 2011;12.
Amini F, Ismail E, Zilfalil BA. Prevalence and molecular study of G6PD deficiency in Malaysian Orang Asli. Intern Med J. 2011;41(4):351–3.
Hatin WI, Nur-Shafawati AR, Zahri MK, Xu S, Jin L, Tan SG, et al. Population genetic structure of peninsular Malaysia Malay sub-ethnic groups. PLoS One. 2011;6(4).
Salahshourifar I, Halim AS, Sulaiman WAW, Ariffin R, Naili Muhamad Nor N, Zilfalil BA. De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features. Cytogenet Genome Res. 2011;134(2):83–7.
Elias MH, Ankathil R, Salmi AR, Sudhikaran W, Limprasert P, Zilfalil BA. A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction. Genet Test Mol Biomarkers. 2011;15(6):387–93.
Rani AQ, Malueka RG, Sasongko TH, Awano H, Lee T, Yagi M, et al. Two closely spaced nonsense mutations in the DMD gene in a Malaysian family. Mol Genet Metab. 2011;103(3):303–4.
Salahshourifar I, Sulaiman WAW, Zilfalil BA, Halim AS. Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population. Am J Med Genet A. 2011;155(9):2302–7.
Salahshourifar I, Halim AS, Wan Sulaiman WA, Zilfalil BA. Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population. J Hum Genet. 2011;56(11):755–8.
Hikmah EM, Ankathil R, Peng HB, Zilfalil BA. Addition of low-cost additives improves real time PCR assay of GC rich FMR1 region utilizing taqman probe. International Medical Journal. 2011;18(4):272–4.
Marini M, Sasongko TH, Watihayati MS, Atif AB, Hayati F, Gunadi, et al. Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy. Indian Journal of Medical Research. 2012;135(1):31–5.
Al-Khateeb A, Mohamed MS, Imran K, Ibrahim S, Zilfalil BA, Yusof Z. Lipid profile parameters in Malaysian dyslipidemic patients. Kobe Journal of Medical Sciences. 2011;57(2):E38–48.
Salahshourifar I, Wan Sulaiman WA, Halim AS, Zilfalil BA. Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: Review of the literature. Eur J Med Genet. 2012;55(6–7):389–93.
Patrinos GP, Smith TD, Howard H, Al-Mulla F, Chouchane L, Hadjisavvas A, et al. Human variome project country nodes: Documenting genetic information within a country. Hum Mutat. 2012;33(11):1513–9.
Zainal SA, Md Daud MK, Abd Rahman N, Zainuddin Z, Alwi Z. Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss. Int J Pediatr Otorhinolaryngol. 2012;76(8):1175–9.
Al-Khateeb A, Al-Talib H, Mohamed MS, Yusof Z, Zilfalil BA. Phenotype-genotype analyses of clinically diagnosed Malaysian familial hypercholestrolemic patients. Advances in Clinical and Experimental Medicine. 2013;22(1):57–67.
Maran S, Lee YY, Xu S, Rajab NS, Hasan N, Mustaffa N, et al. Deleted in Colorectal Cancer (DCC) gene polymorphism is associated with H. pylori infection among susceptible Malays from the North-Eastern Region of Peninsular Malaysia. Hepatogastroenterology. 2013;60(122):124–8.
Maran S, Lee YY, Xu SH, Raj MS, Abdul Majid N, Choo KE, et al. Towards understanding the low prevalence of Helicobacter pylori in Malays: Genetic variants among Helicobacter pylori-negative ethnic Malays in the north-eastern region of Peninsular Malaysia and Han Chinese and South Indians. J Dig Dis. 2013;14(4):196–202.
Rani AQ, Sasongko TH, Sulong S, Bunyan D, Salmi AR, Zilfalil BA, et al. Mutation spectrum of Dystrophin gene in Malaysian patients with duchenne/becker muscular dystrophy. J Neurogenet. 2013;27(1–2):11–5.
AL-Khateeb AR, Al-Talib H, Mohd MS, Yusof Z, Zilfalil BA. The role of lipid lowering therapy in the achievement of therapeutic goal among malaysian hyperlipidemic patients. International Medical Journal. 2013;20(3):272–5.
Maran S, Lee YY, Xu S, Rajab NS, Hasan N, Aziz SHSA, et al. Gastric precancerous lesions are associated with gene variants in Helicobacter pylori-susceptible ethnic Malays. World J Gastroenterol. 2013;19(23):3615–22.
Mohseni J, Boon Hock C, Abdul Razak C, Othman SNI, Hayati F, PeiTee WO, et al. Novel complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia. Gene. 2014;533(1):240–5.
Al-Khateeb AR, Sapawi Mohd M, Yusof Z, Zilfalil BA. Molecular description of familial defective APOB-100 in Malaysia. Biochem Genet. 2013;51(9–10):811–23.
Elmi OS, Hasan H, Abdullah S, Mat Jeab MZ, Zilfalil BA, Naing NN. Prevalence and associated factors with transmission of latent tuberculosis among household contacts of multi-drug resistant tuberculosis patients in Malaysia. World Journal of Medical Sciences. 2014;10(3):285–94.
Osman HA, Hasan H, Suppian R, Bahar N, Che Hussin NS, Rahim AA, et al. Evaluation of the Atlas Helicobacter pylori stool antigen test for diagnosis of infection in adult patients. Asian Pacific Journal of Cancer Prevention. 2014;15(13):5245–7.
Hanafi S, Hassan R, Bahar R, Abdullah WZ, Johan MF, Rashid ND, et al. Multiplex amplification refractory mutation system (MARMA) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia. Am J Blood Res. 2014;4(1):33–40.
Atif AB, Chan YY, Ravichandran M, Zilfalil BA. Molecular analysis of the camp- response element [CRE] elements in the promoter region and exon 1 of the survival of motor neuron 2 [SMN2] gene in Malaysian spinal muscular atrophy patients; to elucidate their role in circumscribing the clinical severity of SMA. Int J Pharm Pharm Sci. 2014;6(11):437–9.
Deng L, Hoh BP, Lu D, Fu R, Phipps ME, Li S, et al. The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia. Hum Genet. 2014;133(9):1169–85.
Hatin WI, Nur-Shafawati AR, Etemad A, Jin W, Qin P, Xu S, et al. A genome wide pattern of population structure and admixture in peninsular Malaysia Malays. HUGO Journal. 2014;8(1):1–18.
Wan Juhari WK, Md Tamrin NA, Mat Daud MHR, Isa HW, Mohd Nasir N, Maran S, et al. A whole genome analyses of genetic variants in two Kelantan Malay individuals. HUGO Journal. 2014;8(1):1–5.
Atif AB, Zahri MK, Nordin S, Esa AR, Zilfalil BA, Mahadeva Rao US. Comparative analysis of the antibacterial, antifungal, antiproliferative and cyclic response element (CRE) induced expression of downstream luc gene activities of Monopterus albus and Channa straitus extracts. J Appl Pharm Sci . 2015;5(1):42–7.
Hoh BP, Deng L, Julia-Ashazila MJ, Zuraihan Z, Nur-Hasnah M, Nur-Shafawati AR, et al. Research open access fine-scale population structure of Malays in peninsular Malaysia and Singapore and implications for association studies. Hum Genomics . 2015;9.
Juhari WKW, Rahman WFWA, Sidek ASM, Hassan MRA, Noordin KBAA, Zakaria AD, et al. Analysis of hereditary nonpolyposis colorectal cancer in malay cohorts using immunohistochemical screening. Asian Pacific Journal of Cancer Prevention. 2015;16(9):3767–71.
Osman HA, Hasan H, Suppian R, Arjunan S, Zilfalil BA. Genotyping of Helicobacter pylori cagA gene from a patient who failed eradication therapy: A case report and review of the literature. International Medical Journal. 2015;22(2):90–1.
Jamal R, Syed Zakaria SZ, Kamaruddin MA, Abd Jalal N, Ismail N, Mohd Kamil N, et al. Cohort Profile: The Malaysian Cohort (TMC) project: A prospective study of non-communicable diseases in a multi-ethnic population. Int J Epidemiol. 2015;44(2):423–31.
Halim-Fikri H, Etemad A, Latif AZA, Merican AF, Baig AA, Annuar AA, et al. The first Malay database toward the ethnic-specific target molecular variation. BMC Res Notes. 2015;8(1).
Osman HA, Hasan H, Suppian R, Hassan S, Andee DZ, Abdul Majid N, et al. Prevalence of Helicobacter pylori cagA, babA2, and dupA genotypes and correlation with clinical outcome in Malaysian patients with dyspepsia. Turk J Med Sci. 2015;45(4):940–6.
Deng L, Hoh BP, Lu D, Saw WY, Twee-Hee Ong R, Kasturiratne A, et al. Dissecting the genetic structure and admixture of four geographical Malay populations. Sci Rep. 2015;5.
Elmi OS, Hasan H, Abdullah S, Jeab MZM, Alwi ZB, Naing NN. Multidrug-resistant tuberculosis and risk factors associated with its development: A retrospective study. J Infect Dev Ctries. 2015;9(10):1076–85.
Zainal SA, Daud MKM, Rahman NA, Zainuddin Z, Zilfalil BA. Absence of GJB6 coding region deletion in non-syndromic hearing loss in Malay population. International Medical Journal. 2016;23(5):504–5.
Nik Hassan NN, Plazzer JP, Smith TD, Halim-Fikri H, MacRae F, Zubaidi Al A, et al. Harmonizing the interpretation of genetic variants across the world: The Malaysian experience. BMC Res Notes. 2016;9(1).
Azman NF, Abdullah WZ, Mohamad N, Bahar R, Johan MF, Diana R, et al. Practice of iron chelation therapy for transfusion-dependent thalassemia in Southeast Asia. Asian Biomedicine. 2016;10(6):537–47.
Buang SN, Diana R, Jaafar S, Muhammad DI, Daud MSM, Jamaluddin J, et al. A review on thalassemia profile in Malaysia and the challenges of its prevention and control programme. Malaysian Journal of Public Health Medicine. 2017;17(3):15–26.
Shang X, Peng Z, Ye Y, Asan, Zhang X, Chen Y, et al. Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies. EBioMedicine. 2017;23:150–9.
Yahya P, Sulong S, Harun A, Wan Isa H, Ab Rajab NS, Wangkumhang P, et al. Analysis of the genetic structure of the Malay population: Ancestry-informative marker SNPs in the Malay of Peninsular Malaysia. Forensic Sci Int Genet. 2017;30:152–9.
Li X, Ooi FK, Zilfalil BA, Yusoff S. The influence of angiotensin-converting enzyme gene ID polymorphism on human physical fitness performance in European and other populations. Sport Sci Health. 2017;13(3):495–506.
Yusof W, Halim-Fikri H, Zilfalil BA. The human variome project and global globin challenge. Pakistan Paediatric Journal . 2017;41(4):202–6.
Juhari WKW, Noordin KBAA, Rahman WFWA, Zakaria AD, Sidek ASM, Hassan MRA, et al. MLH1 and MSH2 gene mutations and polymorphisms in six malay families with hereditary nonpolyposis colorectal cancer. International Medical Journal Malaysia . 2018;17(1):71–8.
Khoo EJ, Chua SH, Thong MK, Zilfalil BA, Lantos J. Introducing clinical ethics consultation service in Malaysia: A SWOT analysis. Clin Ethics. 2019;14(1):26–32.
Abdullah UYH, Ibrahim HM, Mahmud NB, Salleh MZ, Kek TL, Noorizhab MNFB, et al. Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β-Thalassemias. Hemoglobin. 2019;43(3):182–7.
Abdullah UYH, Ibrahim HM, Jassim HM, Salleh MZ, Kek TL, Fakhruzzaman bin Noorizhab MN, et al. Relative proteome quantification of alpha, beta, gamma and delta globin chains in early eluting peaks of Bio-Rad variant II® CE-HPLC of hemoglobin from healthy and beta-thalassemia subjects in Malaysia. Biochem Biophys Rep . 2019;18.
Zilfalil BA. Global Globin 2020 Challenge: The Past, Present and Future. Hemoglobin. 2019;43(6):302.
Yahya P, Sulong S, Harun A, Wangkumhang P, Wilantho A, Ngamphiw C, et al. Ancestry-informative marker (AIM) SNP panel for the Malay population. Int J Legal Med. 2020;134(1):123–34.
Bhattarai M, Wan Juhari WK, Lama R, Pun CB, Yusof W, Rahman WFWA, et al. MLH1 and MSH2 mismatch repair protein profile using immunohistochemistry in Nepalese colorectal cancer patients. Medical Journal of Indonesia. 2020;29(2):183–9.
Abdullah UYH, Simbak N, Azzubaidi MS, Osman R, Ibrahim HM, Jassim HM, et al. Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. J Hematop. 2020;13(1):33–40.
Azman NF, Abdullah WZ, Hanafi S, Diana R, Bahar R, Johan MF, et al. Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity. Ann Hematol. 2020;99(4):729–35.
Abdullah UYH, Ibrahim HM, Mahmud NB, Salleh MZ, Teh LK, Noorizhab MNFB, et al. Genotype-Phenotype Correlation of β-Thalassemia in Malaysian Population: Toward Effective Genetic Counseling. Hemoglobin . 2020;44(3):184–9.
Lama R, Yusof W, Shrestha TR, Hanafi S, Bhattarai M, Hassan R, et al. Prevalence and distribution of major β-thalassemia mutations and HbE/β-thalassemia variant in Nepalese ethnic groups. Hematology/ Oncology and Stem Cell Therapy . 2021;
Juhari WKW, Noordin KBAA, Zakaria AD, Rahman WFWA, Mokhter WMMWM, Hassan MRA, et al. Whole-genome profiles of malay colorectal cancer patients with intact mmr proteins. Genes (Basel) . 2021;12(9).
Kountouris P, Stephanou C, Archer N, Bonifazi F, Giannuzzi V, Kuo KHM, et al. The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies. Am J Hematol . 2021;96(11):E416–20.
Lazim NM, Lah CIC, Juhari WKW, Sulong S, Zilfalil BA, Abdullah B. The role of genetic pathways in the development of chemoradiation resistance in nasopharyngeal carcinoma (NPC) patients. Genes (Basel) . 2021;12(11).
Alwi ZB, Syed-Hassan SNRK. Thalassemia in Malaysia. Hemoglobin. 2022;46(1):45–52.
Halim-Fikri BH, Lederer CW, Baig AA, Mat-Ghani SNA, Syed-Hassan SNRK, Yusof W, et al. Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries. J Pers Med. 2022;12(4).
Tamana S, Xenophontos M, Minaidou A, Stephanou C, Harteveld CL, Bento C, et al. Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies. Elife. 2022;11.
Ankathil R, Zakaria WNA, Van ROSTENBERGHE H, Ibrahim NR, Ramli N, Ismail SM, et al. Karyotype patterns, clinical features, and parental ages of three predominant live born autosomal trisomies of Northeast Malaysia. Malaysian Journal of Pathology. 2022;44(2):235–44.
Kountouris P, Stephanou C, Lederer CW, Traeger-Synodinos J, Bento C, Harteveld CL, et al. Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert Panel. Hum Mutat. 2022;43(8):1089–96.
*As of April 20, 2023
Web of Science Click arrow to expand the list of publications
Web of Science Click arrow to expand the list of publications
Rajion ZA, Alwi Z. Genetics Of Cleft Lip And Palate : A Review. MALAYSIAN JOURNAL OF MEDICAL SCIENCES. 2007;14(1):4–9.
Yusof HA, Ramlee N, Ishak SR, Ab Rajab NS, Ghani SA, Bachok NS, et al. Identification of Single Nucleotide Polymorphism (SNP) 153104 (A to G) of RB1 Gene in Malaysian Retinoblastoma Children and Its Association with Laterality and Staging of the Disease. INTERNATIONAL MEDICAL JOURNAL. 2010;17(2):129–33.
Maran S, Ismail AW, Lee YY, Mustaffa N, Majid NA, Choo KE, et al. A low prevalence of Helicobacter pylori among Malays in the north-eastern region of Peninsular Malaysia can be explained by diet and genetic polymorphisms. J Gastroenterol Hepatol. 2012;27:24.
Maran S, Ismail AW, Lee YY, Mustaffa N, Majid NA, Choo KE, et al. A low prevalence of Helicobacter pylori among Malays in the north-eastern region of Peninsular Malaysia can be explained by diet and genetic polymorphisms. J Gastroenterol Hepatol. 2012;27:4–5.
Zainal SA, Daud MKM, Abd Rahman N, Zainuddin Z, Alwi Z. Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss. Int J Pediatr Otorhinolaryngol. 2012;76(8):1175–9.
Hashim SN, Hanafi H, Ishak SR, Rahmat J, Nasir A, Ismail S, et al. Mutational Analysis in N- and C- Termini of RB1 Gene among Sporadic Retinoblastoma Patients in Malaysia. INTERNATIONAL MEDICAL JOURNAL. 2012;19(4):369–72.
Ooi FK, Li X, Chen CK, Hanapi MH, Alwi Z, Yusoff S, et al. Relationship Between Quantitative Ultrasound Measurements Of Bone And Muscular Peak Torque Of The Lower Limbs In Malay Males. OSTEOPOROSIS INTERNATIONAL. 2014;25(IOF Regionals-5h Asia-Pacific Osteoporosis Meeting):598.
Yahya P, Sulong S, Harun A, Isa HW, Ab Rajab NS, Wangkumhang P, et al. Analysis of the genetic structure of the Malay population: Ancestry-informative marker SNPs in the Malay of Peninsular Malaysia. FORENSIC SCIENCE INTERNATIONAL-GENETICS. 2017;30:152–9.
Abdullah UYH, Simbak N, Azzubaidi MS, Osman R, Ibrahim HM, Jassim HM, et al. Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. J Hematop. 2020;13(1):33–40
Ankathil R, Zakaria WNA, Van Rostenberghe H, Ibrahim NR, Ramli N, Ismail SM, et al. Karyotype patterns, clinical features, and parental ages of three predominant live born autosomal trisomies of Northeast Malaysia. MALAYSIAN JOURNAL OF PATHOLOGY. 2022;44(2):235–44.
Alwi ZB, Syed-Hassan S. Thalassemia in Malaysia. Hemoglobin. 2022;46(1):45–52.
*As of April 20, 2023
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*As of April 20, 2023
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1) Penyakit genetik atrofi muskular spina / Zilfalil Alwi, Zabidi Azhar Mohd Hussin
2) A Handbook on Medical Ethnics and Law in Malaysia / Zilfalil Alwi & Majdah Zawawi
3) Polymerase Chain Reaction: Types And Applications / Faheem Mustafa FM (Author), Mohammad Hassan (Editor), Mubashir Munir (Editor), Khalid Muhammad (Editor), Zilfalil Alwi (Editor), Hassan Rathore (Editor), Tanzeel Huma (Editor), Hassanain Al Talib (Editor), Zilfalil Bin Alwi (Editor), Atif Amin Baig (Editor)
4) Genetic Diseases for the Common Man Paperback – November 30, 2015 / Dr Atif A Baig AAB (Author), Dr Afrasiab Khan SB (Author), Dr Shoaib Bhati AK (Author), Dr Mohammad Naveed Afzal MNA (Editor), Dr Humayun Iqbal Khan HIK (Editor), Dr Zilfalil Bin Alwi ZBA (Editor)
5) Spinal Muscular Atrophy; a Molecular Insight Molecular Atrophies and Promoter Region of SMN Genes / Atif Baig, Thant Zin, Zilfalil Alwi
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Mapping human genetic diversity in Asia HUGO Pan-Asian SNP Consortium, MA Abdulla, I Ahmed, ...Science 326 (5959), 1541-1545
Rapid targeted next-generation sequencing platform for molecular screening and clinical genotyping in subjects with hemoglobinopathies X Shang, Z Peng, Y Ye, X Zhang, Y Chen, B Zhu, W Cai, S Chen, R Cai, ...EBioMedicine 23, 150-159
Ocular findings in Malaysian children with Down syndrome AT Liza-Sharmini, ZN Azlan, BA Zilfalil Singapore medical journal 47 (1), 14
Population Genetic Structure of Peninsular Malaysia Malay Sub-Ethnic Groups WI Hatin, MK Zahri, S Xu, L Jin, SG Tan, M Rizman-Idid, BA Zilfalil PloS one 6 (4), e18312
THE USE OF SNPS IN PHARMACOGENOMICS STUDIES ZB Alwi Malaysian Journal of Medical Sciences 12 (2), 4-12
Cytogenetic and clinical profile of Down syndrome in Northeast Malaysia BZ Azman, R Ankathil, I Siti Mariam, MA Suhaida, M Norhashimah, ...Singapore medical journal 48 (6), 550
Multidrug-resistant tuberculosis and risk factors associated with its development: a retrospective study OS Elmi, H Hasan, S Abdullah, MZM Jeab, ZB Alwi, NN Naing The Journal of Infection in Developing Countries 9 (10), 1076-1085
Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy MS Watihayati, H Fatemeh, M Marini, AB Atif, WM Zahiruddin, ...Brain and Development 31 (1), 42-45
Cytogenetics: Past, present and future TP Kannan, ZB Alwi Malaysian Journal of Medical Sciences 16 (2), 4-9
The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia L Deng, BP Hoh, D Lu, R Fu, ME Phipps, S Li, AR Nur-Shafawati, WI Hatin, ...Human genetics 133, 1169-1185
Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia A Al-Khateeb, MK Zahri, MS Mohamed, TH Sasongko, S Ibrahim, Z Yusof, ...BMC medical genetics 12, 1-11
Chromosomal abnormalities and reproductive outcome in Malaysian couples with miscarriages S Pal, SO Ma, M Norhasimah, MA Suhaida, I Siti Mariam, R Ankathil, ...Singapore medical journal 50 (10), 1008
A polymorphic mutation, c.-3279T> G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population S Yusoff, A Takeuchi, C Ashi, M Tsukada, NH Ma'Amor, BA Zilfalil, ...Pediatric research 67 (4), 401-406
Dissecting the genetic structure and admixture of four geographical Malay populations L Deng, BP Hoh, D Lu, WY Saw, R Twee-Hee Ong, A Kasturiratne, ...Scientific reports 5 (1), 14375
Genetic polymorphism of CYP2D6 in Chinese subjects in Malaysia R Ismail, LK Teh, J Amir, Z Alwi, CG Lopez Journal of clinical pharmacy and therapeutics 28 (4), 279-284
Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population I Salahshourifar, AS Halim, WA Wan Sulaiman, BA Zilfalil Journal of human genetics 56 (11), 755-758
S Maran, YY Lee, S Xu, NS Rajab, N Hasan, SAA SH, NA Majid, BA Zilfalil World Journal of Gastroenterology 19 (23), 3615-3622
Mutation screening of< i> IFR6</i> among families with non-syndromic oral clefts and identification of two novel variants: Review of the literature I Salahshourifar, WA Wan Sulaiman, AS Halim, BA Zilfalil European Journal of Medical Genetics
Mutation detection in< i> GJB2</i> gene among Malays with non-syndromic hearing loss SA Zainal, MK Md Daud, N Abd Rahman, Z Zainuddin, Z Alwi International Journal of Pediatric Otorhinolaryngology
Genetics of Cleft Lip and Palate: A Review ZA Rajion, Z Alwi Malaysian Journal of Medical Sciences 14 (1), 4-9
The first Malay database toward the ethnic-specific target molecular variation H Halim-Fikri, A Etemad, AZA Latif, AF Merican, AA Baig, AA Annuar, ...BMC research notes 8, 1-6
Evaluation of the Atlas Helicobacter pylori stool antigen test for diagnosis of infection in adult patientsHA Osman, H Hasan, R Suppian, N Bahar, NS Che Hussin, AA Rahim, ...Asian Pacific Journal of Cancer Prevention 15 (13), 5245-5247
A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction MH Elias, R Ankathil, AR Salmi, W Sudhikaran, P Limprasert, BA Zilfalil Genetic testing and molecular biomarkers 15 (6), 387-393
A genome wide pattern of population structure and admixture in peninsular Malaysia Malays WI Hatin, AR Nur-Shafawati, A Etemad, W Jin, P Qin, S Xu, L Jin, SG Tan, ...The HUGO journal 8 (1), 1-18
Prevalence and molecular study of G6PD deficiency in Malaysian Orang Asli F Amini, E Ismail, BA Zilfalil Internal Medicine Journal 41 (4), 351-353
Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy TH Sasongko, AR Salmi, BA Zilfalil, MA Albar, ZA Mohd Hussin Annals of Saudi medicine 30 (6), 427-431
Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients MS WATIHAYATI, AMH ZABIDI‐HUSSIN, TH TANG, M Matsuo, H Nishio Pediatrics International 49 (1), 11-14
Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan …S Hanafi, R Hassan, R Bahar, WZ Abdullah, MF Johan, ND Rashid, ...American journal of blood research 4 (1), 33
Towards understanding the low prevalence of Helicobacter pylori in Malays: Genetic variants among Helicobacter pylori‐negative ethnic Malays in the north …S Maran, YY Lee, SH Xu, MS Raj, N Abdul Majid, KE Choo, BA Zilfalil, ...Journal of digestive diseases 14 (4), 196-202
Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate I Salahshourifar, AS Halim, WAW Sulaiman, BA Zilfalil American Journal of Medical Genetics Part A 152 (7), 1818-1821
Two cases of isochromosome 18q syndrome S Pal, MI Siti, R Ankathil, BA Zilfalil Singapore medical journal 48, e146
Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy AQ Rani, TH Sasongko, S Sulong, D Bunyan, AR Salmi, BA Zilfalil, ...Journal of neurogenetics 27 (1-2), 11-15
Human variome project country nodes: Documenting genetic information within a country GP Patrinos, TD Smith, H Howard, F Al‐Mulla, L Chouchane, ...Human Mutation
De Novo Interstitial Deletion of 1q32. 2–q32. 3 Including the Entire< i> IRF6</i> Gene in a Patient with Oral Cleft and Other Dysmorphic Features I Salahshourifar, AS Halim, WAW Sulaiman, R Ariffin, ...Cytogenetic and genome research 134 (2), 83-87
Prevalence of Helicobacter pylori cagA, babA2, and dupA genotypes andcorrelation with clinical outcome in Malaysian patients with dyspepsia HA Osman, H Hasan, R Suppian, S Hassan, DZ Andee, NA Majid, ...Turkish journal of medical sciences 45 (4), 940-946
De novo Ring Chromosome 6 in a Child with Multiple Congenital Anomalies HA AHZAD, SF RAMLI, T LOONG, I SALAHSHOURIFAR, BINA ZILFALIL, ...The Kobe journal of the medical sciences 56 (2), 79-84
Turner syndrome diagnosed in northeastern Malaysia TP Kannan, BZ Azman, AB Ahmad Tarmizi, MA Suhaida, I Siti Mariam, ...Singapore medical journal 49 (5)
One-step multiplex RT-PCR for detection of BCR/ABL gene in Malay patients with chronic myeloid leukaemia R Hassan, M Ramli, WZ Abdullah, R Mustaffa, S Ghazali, R Ankathil, ...Asia Pacific Journal of Molecular Biology & Biotechnology 16 (2), 41-44
Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy M Marini, TH Sasongko, MS Watihayati, AB Atif, F Hayati, Z Zabidi-Hussin, ...The Indian Journal of Medical Research 135 (1), 31
Detection of beta-globin gene mutations among Kelantan Malay thalassaemia patients by polymerase chain reaction restriction fragment length polymorphism R Rozitah, MZ Nizam, AR Nur Shafawati, MA Nor Atifah, M Dewi, ...Singapore Medical Journal 49 (12), 1046
Practice of iron chelation therapy for transfusion-dependent thalassemia in Southeast Asia NF Azman, WZ Abdullah, N Mohamad, R Bahar, MF Johan, R Diana, ...Asian Biomedicine 10 (6), 537-547
Clinical manifestations in trisomy 9 TP Kannan, S Hemlatha, R Ankathil, BA Zilfalil Indian journal of pediatrics 76 (7), 745-746
NAIP-deletion analysis in Malaysian patients with spinal muscular atrophy ZH AMH, T TH, Z BA Kobe J. Med. Sci 53 (4), 171-175
A novel single nucleotide polymorphism, IVS2-97A> T, in the prostaglandin F2alpha receptor gene was identified among the Malaysian patients with glaucoma HB Peng, MN Zahary, LS Tajudin, CL Lin, CM Teck, MR Sidek, ...Kobe J Med Sci 53 (1-2), 49-52
A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findings ZA Bhuiyan, BA Zilfalil, RCM Hennekam Singapore medical journal 47 (8), 724
Genotype-phenotype correlation of β-thalassemia in Malaysian population: Toward effective genetic counseling UYH Abdullah, HM Ibrahim, NB Mahmud, MZ Salleh, LK Teh, ...Hemoglobin 44 (3), 184-189
Analysis of the genetic structure of the Malay population: Ancestry-informative marker SNPs in the Malay of Peninsular Malaysia P Yahya, S Sulong, A Harun, HW Isa, NS Ab Rajab, P Wangkumhang, ...Forensic Science International: Genetics 30, 152-159
Phenotype-genotype analyses of clinically diagnosed Malaysian familial hypercholestrolemic patients A Al-Khateeb, H Al-Talib, MS Mohamed, Z Yusof, BA Zilfalil Advances in Clinical and Experimental Medicine 22 (1), 57-67
Deleted in Colorectal Cancer (DCC) gene polymorphism is associated with H. pylori infection among susceptible Malays from the north-eastern region of Peninsular Malaysia. S Maran, YY Lee, S Xu, NS Rajab, N Hasan, N Mustaffa Hepato-gastroenterology 60 (121), 124-128
Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population I Salahshourifar, WAW Sulaiman, BA Zilfalil, AS HalimAmerican Journal of Medical Genetics Part A
Transforming growth factor-α and nonsyndromic cleft lip with or without palate or cleft palate only in Kelantan, Malaysia RA Rahman, A Ahmad, ZAA Rahman, KI Mokhtar, NASN Lah, BA Zilfalil, ...The Cleft palate-craniofacial journal 45 (6), 583-586
Genetic polymorphism of CYP2D6 in patients with cardiovascular disease–a cohort study LK Teh, BA Zilfalil, I Marina, BS Rosemi, R Ismail Journal of clinical pharmacy and therapeutics 29 (6), 559-564
Consortium SNP (2011) Population genetic structure of Peninsular Malaysia Malay sub-ethnic groups WI Hatin, AR Nur-Shafawati, MK Zahri, S Xu, L Jin, SG Tan, ...PloS one 6 (4), e18312
Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert Panel P Kountouris, C Stephanou, CW Lederer, J Traeger‐Synodinos, C Bento, ...Human Mutation 43 (8), 1089-1096
The influence of angiotensin-converting enzyme gene ID polymorphism on human physical fitness performance in European and other populationsX Li, FK Ooi, BA Zilfalil, S Yusoff Sport Sciences for Health 13, 495-506
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies BP Hoh, L Deng, MJ Julia-Ashazila, Z Zuraihan, M Nur-Hasnah, ...Human genomics 9, 1-9
Molecular Description of Familial Defective APOB-100 in Malaysia AR Al-Khateeb, M Sapawi Mohd, Z Yusof, BA ZilfalilBiochemical genetics 51, 811-823
Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation BZ Azman, SM Akhir, BA Zilfalil, R Ankathil Singapore Med J 49 (4), e98-e100
A simple and rapid genotyping method for beta‐2 receptor (β2 AR) gene using allele specific multiplex PCR SMN Romaino, LK Teh, BA Zilfalil, CP Thong, AA Ismail, J Amir, ...Journal of clinical pharmacy and therapeutics 29 (1), 47-52
ITHANET: Information and database community portal for haemoglobinopathies P Kountouris, C Stephanou, C Bento, P Fanis, J Elion, RS Ramesar, ...bioRxiv, 209361
A whole genome analyses of genetic variants in two Kelantan Malay individuals WK Wan Juhari, NA Md Tamrin, MHR Mat Daud, HW Isa, N Mohd Nasir, ...The HUGO journal 8, 1-5
Development and validation of a questionnaire on the knowledge of tuberculosis and the perception of tuberculosis treatment among tuberculosis patients in Malaysia. OS Elmi, H Hasan, S Abdullah, MZM Jeab, WA Nadiah, BA Zilfalil, ...
Peninsular Malaysia’s Negrito Orang Asli and its theory of African origin E Ismail, F Amini, A Razak, Z Alwi, R FarhourSains Malaysiana 42, 921-926
The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies P Kountouris, C Stephanou, NM Archer, F Bonifazi, V Giannuzzi, ...Blood 138, 948
Comparative analysis of the antibacterial, antifungal, antiproliferative and cyclic response element (CRE) induced expression of downstream luc gene activities of Monopterus …AB Atif, MK Zahri, AR Esa, BA Zilfalil, USM Rao, S Nordin Journal of Applied Pharmaceutical Science 5 (1), 042-047
Prevalence and associated factors with transmission of latent tuberculosis among household contacts of multi-drug resistant tuberculosis patients in Malaysia OS Elmi, H Hasan, S Abdullah, MZM Jeab, BA Zilfalil, NN Naing World Journal of Medical Sciences 10 (3), 285-294
Novel complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia J Mohseni, CB Hock, CA Razak, SNI Othman, F Hayati, WO PeiTee, ... Gene 533 (1), 240-245
Low-density lipoprotein cholesterol goal attainment among Malaysian dyslipidemic patients A Al-Khateeb, MS Mohamed, K Imran, S Ibrahim, BA ZILFALIL, Z Yusof Southeast Asian journal of tropical medicine and public health 42 (2), 388-394
Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization N Naili, CH Hasnita, AK Shamim, J Hasnan, MI Fauziah, MY Narazah, ...Cancer Genetics and Cytogenetics 203 (2), 309-312
Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography ZS Aishah, MDM Khairi, AR Normastura, Z Zafarina, BA Zilfalil The Journal of Laryngology & Otology 122 (12), 1284-1288
Y-chromosomal STR Variation in Malays of Kelantan and Minang HB Peng, NSA Rajab, OK Gin, Z Alwi Pertanika J Trop Agric Sci 31 (1), 135-40
Detection of F508del mutation in cystic fibrosis transmembrane conductance regulator gene mutation among Malays BA Zilfalil, S Sarina, AT Liza-Sharmini, NJ Oldfield, SA Stenhouse Singapore medical journal 47 (2), 129
The free alpha-hemoglobin: A promising biomarker for β-thalassemia H Uday Younis, F Ahmed Ghazi, AB Atif Molecular Biomarkers & Diagnosis 5 (5), 1-7
Lipid Profile Parameters in Malaysian Dyslipidemic Patients A Al-Khateeb, MS Mohamed, K Imran, S Ibrahim, BA Zilfalil, Z Yusof The Kobe journal of the medical sciences 57 (2), 38-48
Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity NF Azman, WZ Abdullah, S Hanafi, R Diana, R Bahar, MF Johan, ...Annals of hematology 99, 729-735
Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy M Marini, AA Salmi, MS Watihayati, MD SMardziah, MK Zahri, BP Hoh, ...Med. J. Malaysia 63 (1), 31-34
Clinical and Genetic Analysis of Long QT Syndrome in two Malay Children ZA Bhuiyan, ND Din, BA Zilfalil, AR Wong
The role of genetic pathways in the development of chemoradiation resistance in nasopharyngeal carcinoma (NPC) patients N Mat Lazim, CI Che Lah, WK Wan Juhari, S Sulong, BA Zilfalil, ...Genes 12 (11), 1835
Whole-genome profiles of Malay Colorectal Cancer patients with intact MMR proteins WKW Juhari, KB Ahmad Amin Noordin, AD Zakaria, WFWA Rahman, ...Genes 12 (9), 1448
A review on thalassemia profile in Malaysia and the challenges of its prevention and control programme SN Buang, R Diana, S Jaafar, DI Muhammad, MSM Daud, J Jamaluddin, ...Malaysian Journal of Public Health Medicine 17 (3), 15-26
Cardiovascular Risk Factors among Malaysian Diabetic Patients A Al-Khateeb, MS Mohd, Z Yusof, H Al-Talib, BA Zilfalil International Archives of Medicine 9
Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in malay patients with spinal muscular atroph BA Zilfalil, AM Zabidi-Hussin, MS Watihayati, MY Rozainah, L Naing, ...Med J Malaysia 59 (4), 512-514
Thalassemia in Malaysia ZB Alwi, SNRK Syed-Hassan Hemoglobin 46 (1), 45-52
Ancestry-informative marker (AIM) SNP panel for the Malay population P Yahya, S Sulong, A Harun, P Wangkumhang, A Wilantho, C Ngamphiw, ...International journal of legal medicine 134, 123-134 Introducing clinical ethics consultation service in Malaysia: A SWOT analysis EJ Khoo, SH Chua, MK Thong, BA Zilfalil, J Lantos Clinical Ethics 14 (1), 26-32
Computational characterization of the promoter region of SMN2 (Survival of Motor Neuron) Gene AA Baig, CY Yean, MA Tengku, AL Zubaidi, N Simbak, Z Alwi Research Journal of Pharmacy and Technology 11 (7), 2729-2736
Harmonizing the interpretation of genetic variants across the world: the Malaysian experience NN Nik Hassan, JP Plazzer, TD Smith, H Halim-Fikri, F Macrae, ... BMC Research Notes 9 (1), 1-7
Indicators of anaerobic capacity and muscular performance in Malay female athletes and non-athletes with ACE gene I/D polymorphism X Li, FK Ooi, BA Zilfalil, S Yusoff Inter J Sports Sci 5, 201-208
Analysis of hereditary nonpolyposis colorectal cancer in Malay cohorts using immunohistochemical screening WKW Juhari, WFWA Rahman, ASM Sidek, MRA Hassan, KBAA Noordin, ... Asian Pacific Journal of Cancer Prevention 16 (9), 3767-3771
Two closely spaced nonsense mutations in the DMD gene in a Malaysian family AQ Rani, RG Malueka, TH Sasongko, H Awano, T Lee, M Yagi, BA Zilfalil, ...Molecular Genetics and Metabolism
Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1 I Salahshourifar, AS Halim, WAW Sulaiman, BA Zilfalil Journal of dental research 90 (3), 387-391
Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy TH Sasongko, BA Zilfalil, Z Zabidi-Hussin Journal of Neurogenetics, 25 1 (2), 15-16
RB pocket domain B mutation frequency in Malaysia. SR Ishak, H Hanafi, JV Alagaratnam, BA Zilfalil, LS Tajudin Ophthalmic genetics 31 (3), 159
Relative proteome quantification of alpha, beta, gamma and delta globin chains in early eluting peaks of Bio-Rad variant II® CE-HPLC of hemoglobin from healthy and beta …UYH Abdullah, HM Ibrahim, HM Jassim, MZ Salleh, TL Kek, ...Biochemistry and biophysics reports 18, 100635
Low density lipoprotein receptor (LDLR) gene and ocular manifestation in Malay patients with familial hypercholesterolaemia AT Liza-Sharmini, NIM Nur, AR Al-Khateeb, WHW Hitam, ZB Alwi Malaysian Journal of Ophthalmology 1 (2), 98-113
Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β …UYH Abdullah, HM Ibrahim, NB Mahmud, MZ Salleh, TL Kek, ...Hemoglobin 43 (3), 182-187
Isolation of nucleated red blood cell from peripheral blood of β-thalassemia major patients using CD71 magnetic beads and future application MY Haiyuni, S Aziee, S Hanafi, AS Heba, R Diana, NF Azman, R Hassan, ...Journal of Biomedical and Clinical Sciences (JBCS) 3 (1), 25-30
Factors affecting health-related quality of life among paediatric patients with thalassemia: A review of literature WA Wan-Nor-Asyikeen, MM Zulkifli, BA Zilfalil Malaysian Journal of Paediatrics and Child Health 23 (1), 1-15
The Human Variome Project and Global Globin Challenge W Yusof, H Halim-Fikri, BA Zilfalil Pak. Pediatr. J 41, 202-206
Genotype-phenotype association of HbE/β-thalassemia disease and the role of genetic modifiers SB Hanafi, WZ Abdullah, RA Adnan, R Bahar, MF Johan, NF Azman, ...Malaysian Journal of Paediatrics and Child Health 22, 1-16
Association of ocular biometry and PTGFR gene in primary angle closure KR Maharajah, NY Ling, N Zahary, LSA Tajudin International Medical Journal 22 (6), 478-483
The characteristics of Helicobacter pylori infection and clinical outcomes of patient with upper gastrointestinal bleeding admitted at hospital Universiti Sains Malaysia HA Osman, H Hasan, R Suppian, NAC Hamzah, SET Sharif, NA Majid, ...World Applied Sciences Journal
An improved rapid genotyping method for the study of beta‐2 adrenergic receptor gene polymorphisms using single tube allele specific multiplex PCR BA Zilfalil, BP Hoh, MZ Nizam, AT Liza‐Sharmini, LK Teh, R Ismail Journal of clinical pharmacy and therapeutics 31 (6), 637-640
Genetically confirmed spinal muscular atrophy type 3 with epilepsy in a Malay patient, a case report BA Zilfalil, MS Watihayati, MY Rozainah, L Naing, R Sutomo, H Nishio, ...Neurol J Southeast Asia 8, 113-5
A NEW PARADIGM IN MEDICINE: GENOME WIDE ASSOCIATION STUDIES S MARAN, YY LEE, BA ZILFALIL, AM NOORIZAN Jilid 18 No. 1 &2/ISSN 1394-5750 Jan & July 2011, 3
Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies S Tamana, M Xenophontos, A Minaidou, C Stephanou, CL Harteveld, ...Elife 11, e79713
Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries BH Halim-Fikri, CW Lederer, AA Baig, SNA Mat-Ghani, ...Journal of Personalized Medicine 12 (4), 552
Non-compliance to iron chelation therapy in patients with transfusion-dependent thalassaemia ASC Chai, N Draman, SSM Yusoff, NF Azman, MM Zulkifli, NM Yaacob, ...Pediatric Hematology Oncology Journal 6 (4), 207-215
Prevalence and distribution of major β-thalassemia mutations and HbE/β-thalassemia variant in Nepalese ethnic groups R Lama, W Yusof, TR Shrestha, S Hanafi, M Bhattarai, R Hassan, ...Hematology/oncology and stem cell therapy
M Bhattarai, WKW Juhari, R Lama, CB Pun, W Yusof, WFWA Rahman, ..Medical Journal of Indonesia 29 (2), 183-9
A Review of Molecular Testing for Hereditary Nonpolyposis Colorectal Cancer
WKW Juhari, WFWA Rahman, AD Zakaria, KBAA Noordin, BA Zilfalil Malaysian Journal of Human Genetics 1 (1), 18-25
Factors affecting health-related quality of life and its association with the Xmn1-Gγ polymorphism among adolescents with transfusion-dependent beta thalassemia and HbE/β …W Yusof, MM Zulkifli, NF Azman, SA Ab Hamid, A Othman, N Draman, ...Pediatric Hematology Oncology Journal 5 (2), 30-36
COVID-19 and SARS-CoV-2: A Virus of Sexism? SNRK SyedHassan, NM Yusoff, BA Zilfalil Malaysian Journal of Human Genetics 1 (1), 1-3
A liveborn double aneuploidy with simultaneous occurrence of Edwards and Klinefelter syndromes-A rare case report A Zakaria, SM Ismail, ZA Bakar, NMZM Zin, NAM Nawi, NM Yunus, ...The Malaysian Journal of Medical Sciences 27, 28-28
Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience UYH Abdullah, N Simbak, MS Azzubaidi, R Osman, HM Ibrahim, ... Journal of Hematopathology 13, 33-40
The ITHANET-Human Variome Project: Moving Functional Annotation Forward P Kountouris, C Stephanou, CW Lederer, S Tamana, A Minaidou, ...Hemoglobin 43 (6), 327-327
Global Globin 2020 Challenge: The Past, Present and Future BA Zilfalil Hemoglobin 43 (6), 302-302
Factors Affecting Health Related Quality of Life and Its Association with Xmn1 Gene Modifier among Transfusion-Dependent β-Thalassemia and HbE/β-Thalassemia Adolescent in East …MM Zulkifli, W Yusof, NF Azman, SA Ab Hamid, WNAW Adnan, A Othman, ...Asian Journal of Medicine and Biomedicine, 19-19
Detection of XMN1-Gγ Polymorphism Among Patients with HbE/Βeta Thalassaemia in North East Malaysia RA Adnan, NS Hanafi, Z Alwi, S Sulong Journal of Biomedical and Clinical Sciences (JBCS) 2 (2), 42-43
Four nucleotide deletions of exon 47 in Dystrophin gene: A case report of a Kelantanese Duchenne Muscular Dystrophy patient F Azman, RA Adnan, NCA Razak, R Abdullah, NM Yunus, TH Sasongko, ...Journal of Biomedical and Clinical Sciences (JBCS) 2 (2), 11-13
Relationships between the quantitative ultrasound measurement of the of lower limb bones, muscular performance and anaerobic capacities in Malay university students X Li, FK Ooi, CK Chen, MH MUHAMADJournal of Physical Education and Sport 17 (3), 2097-2104
Bone health, ACE gene I/D and ACTN3 gene R577X polymorphisms in Spanish and different Asian populations F Ooi, Z BA, X Li J Osteopor Phys Act 3 (3)
TAQI POLYMORPHISM OF VITAMIN D RECEPTOR GENE AS A POTENTIAL MARKER FOR BONE COMPLICATIONS IN TRANSFUSION DEPENDENT THALASSEMIA PATIENTS: MANAGEMENT IMPLICATIONS D Rashid, WZ Abdullah, A Nasir, R Bahar, NF Azman, S Hanafi, MF Johan, ...EDITORIAL BOARD, 21
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Optimizing Multiplex PCR for a Set of Malay Ancestry Informative Marker-Single Nucleotide Polymorphisms (AIM-SNPs) and Preliminary Analysis of Genotypes Between Malay and non …YT Cheng, SNRK Syed-Hassan, P Yahya, A Harun, NM Yunus, S Sulong, ...Asian Journal of Medicine and Biomedicine 5 (2), 52-61
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Knockdown by MSH2 and EPCAM siRNA suppress Wnt/β-Catenin Pathway in HCT116 Cell Line WKW Juhari, KBAA Noordin, WFWA Rahman, AD Zakaria, ...
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An Infrequent Gonosome-Autosome Mosaicism Co-Existent with Constitutional Telomeric Association C Yi-Ting, NMZM Zin, NAM Nawi, SM Ismail, NM Yunus, S Sulong, ...The Malaysian Journal of Medical Sciences 27, 35-35
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Genotype pattern of VDR gene in transfusion dependent HbE/β thalassemia with osteoporosis D Rashid, A Nasir, R Hassan, MF Johan, R Bahar, NF Azman, S Hanafi, ...Asian Journal of Medicine and Biomedicine, 6-6
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For online access to this journal via your library Y Goto, K Hatakeyama, T Kitama, Y Sato, H Kanemura, K Aoyagi, ...
Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia AK Alyaa, Z Mohd, M Mohd, S Teguh, I Suhairi, Y Zurkurnai, Z Bin BMC Medical Genetics 12
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EXON SPLICING ENHANCER: MUTATION AND DISEASE INDUCTION IN SPINAL MUSCULAR ATROPHY
H FATEMEH, AA BAIG, T HS, Z BA
Jilid 18 No. 1 &2/ISSN 1394-5750 Jan & July 2011, 26
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