S. Zain

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The role of single nucleotide polymorphisms and copy number variations in the spectrum of non-alcoholic fatty liver disease / Shamsul bin Mohd Zain

S. Zain, 2013 .

Susceptibility and Gene Interaction Study of the Angiotensin II Type 1 Receptor (AGTR1) Gene Polymorphisms with Non-Alcoholic Fatty Liver Disease in a Multi-Ethnic Population

S. Rampal, R. Mohamed, Agus Salim, 2013, PloS one.

Genome-Wide Analysis of Copy Number Variation Identifies Candidate Gene Loci Associated with the Progression of Non-Alcoholic Fatty Liver Disease

D. Cooper, S. Rampal, R. Mohamed, 2014, PloS one.

Phosphatidylethanolamine N-methyltransferase gene rs7946 polymorphism plays a role in risk of nonalcoholic fatty liver disease: evidence from meta-analysis

R. Mohamed, S. Zain, Z. Mohamed, 2016, Pharmacogenetics and genomics.

A multi-ethnic study of a PNPLA3 gene variant and its association with disease severity in non-alcoholic fatty liver disease

S. Rampal, R. Mohamed, P. Cheah, 2012, Human Genetics.

Use of simple scoring systems for a public health approach in the management of non‐alcoholic fatty liver disease patients

R. Mohamed, S. Zain, S. Mahadeva, 2020, JGH open : an open access journal of gastroenterology and hepatology.

Protein Profiling of Women with Spontaneous Preterm Birth

S. Zain, S. Omar, Z. Mohamed, 2015, Pharmacology.

Downregulation of hsa‐miR‐548d‐3p and overexpression of HOXA9 in diffuse large B‐cell lymphoma patients and the risk of R‐CHOP chemotherapy resistance and disease progression

S. Zain, S. Tan, Y. Pung, 2022, International journal of laboratory hematology.

Copy number variation in exportin-4 (XPO4) gene and its association with histological severity of non-alcoholic fatty liver disease

M. Pirmohamed, R. Mohamed, S. Zain, 2015, Scientific Reports.

Analysis of serum circulating MicroRNAs level in Malaysian patients with gestational diabetes mellitus

H. Kamyab, S. Zain, S. Omar, 2022, Scientific Reports.

Intracellular and exosomal microRNAome profiling of human vascular smooth muscle cells during replicative senescence.

S. Zain, W. Chilian, T. Low, 2021, American journal of physiology. Heart and circulatory physiology.

Association of vaspin rs2236242 with type 2 diabetes mellitus and obesity: a meta-analysis of case-control studies

S. Zain, Y. Pung, R. Mohamed, 2022, Journal of Diabetes & Metabolic Disorders.

Genetic association of LMAN2L gene in schizophrenia and bipolar disorder and its interaction with ANK3 gene polymorphism

G. Reynolds, N. Zainal, S. Zain, 2014, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

HLA-DQB1*06 reduces fibrosis score in patients with non-alcoholic fatty liver disease.

R. Mohamed, S. Zain, S. Mahadeva, 2020, Hepatology research : the official journal of the Japan Society of Hepatology.

Genetic Polymorphisms in LDLR, APOB, PCSK9 and Other Lipid Related Genes Associated with Familial Hypercholesterolemia in Malaysia

R. Mohamed, J. Vadivelu, S. Zain, 2013, PloS one.

KIR genotype and haplotype frequencies in the multi-ethnic population of Malaysia.

S. Zain, W. Wen, Y. Pung, 2022, Human immunology.

Genetic polymorphisms in the one-carbon metabolism pathway genes and susceptibility to non-Hodgkin lymphoma

K. Chang, S. Zain, Z. Mohamed, 2015, Tumor Biology.

Genetic association of LMAN 2 L gene in schizophrenia and bipolar disorder and its interaction with ANK 3 gene polymorphism

G. Reynolds, N. Zainal, S. Zain, 2014 .

Association of glucokinase regulatory gene polymorphisms with risk and severity of non-alcoholic fatty liver disease: an interaction study with adiponutrin gene

S. Rampal, R. Mohamed, P. Cheah, 2014, Journal of Gastroenterology.

Effect of polymorphisms within methotrexate pathway genes on methotrexate toxicity and plasma levels in adults with hematological malignancies.

K. Chang, S. Zain, Z. Mohamed, 2014, Pharmacogenomics.

Polymorphisms in methylenetetrahydrofolate reductase gene and risk of non-Hodgkin lymphoma in a multi-ethnic population

K. Chang, S. Zain, Z. Mohamed, 2014, Journal of Human Genetics.

Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm)

T. Mushiroda, N. S. Vo, G. Patrinos, 2021, Human genome variation.

Southeast Asian Pharmacogenomics Research Network (SEAPharm): Current Status and Perspectives

W. Chantratita, T. M. Hlaing, R. Yuliwulandari, 2019, Public Health Genomics.

Circulating cytokines and small molecules follow distinct expression patterns in acute myeloid leukaemia

Y. M. Yusoff, Y. Assenov, S. Zain, 2017, British Journal of Cancer.

Loss-of-function HSD17B13 variants, non-alcoholic steatohepatitis and adverse liver outcomes: Results from a multi-ethnic Asian cohort

R. Mohamed, S. Zain, Z. Mohamed, 2021, Clinical and molecular hepatology.

A case-control study and meta-analysis confirm glucokinase regulatory gene rs780094 is a risk factor for gestational diabetes mellitus.

S. Zain, S. Omar, Z. Mohamed, 2018, Gene.

Health motivations and perceived barriers are determinants of self-care behaviour for the prevention of hypertension in a Malaysian community

Faiz Daud, N. Tan, S. Zain, 2022, PloS one.

Preliminary examination of microRNA expression profiling in bipolar disorder I patients during antipsychotic treatment

N. Zainal, S. Zain, Z. Mohamed, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A common variant in the glucokinase regulatory gene rs780094 and risk of nonalcoholic fatty liver disease: A meta‐analysis

R. Mohamed, S. Zain, Z. Mohamed, 2015, Journal of gastroenterology and hepatology.

Comparison Between Dichloroacetate and Phenylbutyrate Treatment for Pyruvate Dehydrogenase Deficiency

Timothy Simpson, S. Dawson, S. Zain, 2022, British Journal of Biomedical Science.

A multi-ethnic study of a PNPLA3 gene variant and its association with disease severity in non-alcoholic fatty liver disease

S. Rampal, R. Mohamed, P. Cheah, 2012, Human Genetics.

Impact of leptin receptor gene variants on risk of non‐alcoholic fatty liver disease and its interaction with adiponutrin gene

S. Rampal, R. Mohamed, P. Cheah, 2013, Journal of gastroenterology and hepatology.

Comprehensive evaluation of the neuropeptide-Y gene variants in the risk of obesity: a case–control study and meta-analysis

A. Hamidi, S. Zain, Z. Mohamed, 2015, Pharmacogenetics and genomics.

Micro-RNA Regulation of Vascular Smooth Muscle Cells and Its Significance in Cardiovascular Diseases.

S. Zain, W. Chilian, Y. Pung, 2021, Canadian journal of physiology and pharmacology.

Comprehensive evaluation of the neuropeptide-y gene variants in risk of obesity: A case-control study and meta-analysis Short title: Meta-analysis of NPY variants and obesity

A. Hamidi, S. Zain, Z. Mohamed, 2015 .

Analysis of serum circulating MicroRNAs level in Malaysian patients with gestational diabetes mellitus

H. Kamyab, S. Zain, S. Omar, 2022, Scientific Reports.

Renin-Angiotensin System Gene Variants and Type 2 Diabetes Mellitus: Influence of Angiotensinogen

S. Zain, N. Abdullah, Munavvar Zubaid Abdul Sattar, 2015, Journal of diabetes research.

Association of glucokinase regulatory gene polymorphisms with risk and severity of non-alcoholic fatty liver disease: an interaction study with adiponutrin gene

S. Rampal, R. Mohamed, P. Cheah, 2014, Journal of Gastroenterology.

Carbamazepine 10,11-epoxidation in human liver microsomes: influence of the CYP3A5*3 polymorphism.

S. Zain, N. Hanioka, T. Isobe, 2017, Die Pharmazie.

Preliminary examination of microRNA expression profiling in bipolar disorder I patients during antipsychotic treatment

N. Zainal, S. Zain, Z. Mohamed, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.