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List of works by Bin Alwi Zilfalil

A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population

scientific article published on 01 April 2010

A simple and rapid genotyping method for beta-2 receptor (beta2 AR) gene using allele specific multiplex PCR.

scientific article

A whole genome analyses of genetic variants in two Kelantan Malay individuals

scientific article

Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.

scientific article published in January 2012

An improved rapid genotyping method for the study of beta-2 adrenergic receptor gene polymorphisms using single tube allele specific multiplex PCR.

scientific article

Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia

scientific article

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization ⬇️

scientific article published on December 1, 2010

Clinical manifestations in trisomy 9

scientific article (publication date: July 2009)

Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy

scientific article

Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1

scientific article published in March 2011

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

scientific article published on 10 August 2011

De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features

scientific article published on 25 March 2011

Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients

scientific article published on 01 February 2007

Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy

scientific article published on 22 February 2011

Dissecting the genetic structure and admixture of four geographical Malay populations.

scientific article

Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies

scientific article published on 22 July 2015

Gastric precancerous lesions are associated with gene variants in Helicobacter pylori-susceptible ethnic Malays.

scientific article published on June 2013

Genetic polymorphism of CYP2D6 in patients with cardiovascular disease -- a cohort study.

scientific article published in December 2004

Harmonizing the interpretation of genetic variants across the world: the Malaysian experience

scientific article

Human Variome Project country nodes: documenting genetic information within a country

scientific article published on 18 July 2012

Mapping human genetic diversity in Asia

scientific article

Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate.

scientific article published in July 2010

Molecular description of familial defective APOB-100 in Malaysia.

scientific article published on 18 June 2013

Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.

scientific article published on 26 February 2013

Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia

scientific article published on 5 October 2013

Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy

scientific article

Population genetic structure of peninsular Malaysia Malay sub-ethnic groups

scientific article published in 2011

Prevalence and molecular study of G6PD deficiency in Malaysian Orang Asli

scientific article published on 01 April 2011

RB pocket domain B mutation frequency in Malaysia.

scientific article published in September 2010

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies.

scientific article published on 17 August 2017

Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography.

scientific article published on 20 March 2008

The first Malay database toward the ethnic-specific target molecular variation

scientific article published on 30 April 2015

The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia

scientific article published on 11 June 2014

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.

scientific article

Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate or cleft palate only in Kelantan, Malaysia

scientific article published on 06 January 2008

Two closely spaced nonsense mutations in the DMD gene in a Malaysian family

scientific article published on 08 April 2011

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