kha chin long, norlela sukor, geok chin tan, nor azian abdul murad, morris jonathan brown, elena aisha azizan.  (2023).  elucidating effect of inhibiting aldosterone synthesis on human adrenocortical cells.  - journal of hypertension.  e362. 

khairul anwar zarkasi, nor azian abdul murad, norfazilah ahmad, rahman jamal, noraidatulakma abdullah.  (2022).  coronary heart disease in type 2 diabetes mellitus: genetic factors and their mechanisms, gene-gene, and gene-environment interactions in the asian populations.  - international journal of environmental research and public health.  1-48. 

nor azian abdul murad, siti aishah sulaiman, azlina ahmad-annuar, norlinah mohamed ibrahim, wael mohamed, shahrul azmin md rani, kin ying mok.  (2022).  editorial: genetic and molecular diversity in parkinson's disease.  - frontiers in aging neuroscience.  1-4. 

khairul anwar zarkasi, noraidatulakma abdullah, nor azian abdul murad, norfazilah ahmad, rahman jamal.  (2022).  genetic factors for coronary heart disease and their mechanisms: a meta-analysis and comprehensive review of common variants from genome-wide association studies.  - diagnostics.  1-35. 

abdul khalif adha abd talib, syahrul sazliyana shaharir, nor azian abdul murad, noraidatulakma abdullah, elena aisha azizan, abdul halim abdul gafor, ruslinda mustafar, mohd shahrir mohamed said, sakthiswary rajalingham, abdul rahmaa. jamal, zarina abdul.  (2022).  validation of the sle susceptible gene loci in the multi-ethnic malaysian systemic lupus erythematosus (sle) cohort and their associations with clinical manifestation.  - annals of the rheumatic diseases.  453. 

nurruzanna ismail, noraidatulakma abdullah, nor azian abdul murad, rahman jamal, siti aishah sulaiman.  (2021).  long non-coding rnas (lncrnas) in cardiovascular disease complication of type 2 diabetes.  - diagnostics.  1-27. 

kin y mok, east asian parkinson disease genomics consortium.  (2021).  the east asian parkinson disease genomics consortium.  - the lancet neurology.  982. 

jiann ll, nurul ain mk, jo aan g, hanafi ad, jaclyn ai ct, nor azian am, shamsul azhar s, siti aishah s, shazrul f, shalisah sp, suriati ms, geetha g, thambu m, a. rahman aj, wan zurinah wn, fatimatul syahirah mbs and lai fong c.  (2021).  the role of oxidative stress in suicidal behaviour among bipolar patients: a cross-sectional-study in a malaysian sample.  - frontiers in psychiatry.  1-10. 

vicneswarry dorairaj, siti aishah sulaiman, nadiah abu and nor azian abdul murad.  (2021).  nonalcoholic fatty liver disease (nafld): pathogenesis and noninvasive diagnosis.  - biomedicines.  1-25. 

n. ahmad, s. a. shah, a. h. abdul gafor, n. a. abdul murad, m. a. kamaruddin, n. abd jalal, n. ismail , m. r. alias and r. jamal.  (2020).  gene-environment interaction in chronic kidney disease among people with type 2 diabetes from the malaysian cohort project: a case-control study.  - diabetic medicine.  1890-1901. 

kok beng gan, kim soon chong, anusha devi nawoor, sue-mian then, nor azian abdul murad and a. rahman a. jamal.  (2020).  development of a hla-b*58:01 allele screening system for allopurinol-induced severe cutaneous adverse reactions detection.  - ieee access.  25306-25323. 

vicneswarry dorairaj, siti aishah sulaiman, nadiah abu, nor azian abdul murad.  (2020).  extracellular vesicles in the development of the non-alcoholic fatty liver disease: an update.  - biomolecules.  1-24. 

tamil selvi loganathan, siti aishah sulaiman, nor azian abdul murad, shamsul azhar shah, abdul halim abdul gafor, rahman jamal, noraidatulakma abdullah.  (2020).  interactions among non-coding rnas in diabetic nephropathy.  - frontiers in pharmacology.  1-19. 

noraidatulakma abdullah, nor azian abdul murad, john attia, christopher oldmeadow, mohd arman kamaruddin, nazihah abd jalal, norliza ismail, rahman jamal, rodney j. scott and elizabeth g. holliday.  (2018).  differing contributions of classical risk factors to type 2 diabetes in multi-ethnic malaysian populations.  - international journal of environmental research and public health.  . 

nor idayu a. rahman, nor azian abdul murad, mohammad manir hossain mollah, rahman jamal and roslan harun.  (2017).  nfix as a master regulator for lung cancer progression.  - frontiers in pharmacology.  1-12. 

nor aslina samat, nor azian abdul murad, khairiyah mohamad, mohd ridhwan abdul razak and norlinah mohamed ibrahim.  (2017).  apolipoprotein e4 a biomarker for executive dysfunction among parkinsons disease patients with mild cognitive impairment.  - frontiers in neuroscience.  1-8. 

noraidatulakma abdullah, nor azian abdul murad, ezanee azlina mohd haniff, saiful effendi syafruddin, john attia, christopher oldmeadow, mohd arman kamaruddin, nazihah abd jalal, norliza ismail, muhiddin ishak, rahman jamal, rodney j. scott, elizabeth gh.  (2017).  predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic malaysian cohort.  - public health.  31-38. 

ahmad r. arshad, siti a. sulaiman, amalia a. saperi , rahman jamal, norlinah mohamed ibrahim and nor azian abdul murad.  (2017).  micrornas and target genes as biomarkers for the diagnosis of early onset of parkinson disease.  - frontiers of molecular neuroscience.  1-20. 

bee hong soon, nor azian abdul murad, sue mian then, azizi abu bakar, farizal fadzilb, jegan thanabalan, mohd saffari mohd haspanic, toh charng jeng, azmi mohd tamil, roslan harun, wan zurinah wan ngah, rahman jamal.  (2017).  mitochondrial dna mutations in grade ii and iii glioma cell lines are associated with significant mitochondrial dysfunction and higher oxidative stress.  - frontiers in physiology.  1-14. 

yock-ping chow, nor azian abdul murad, zamzureena mohd rani, jia-shiun khoo, pei-sin chong, loo-ling wu, rahman jamal.  (2017).  exome sequencing identifies slc26a4, gjb2, scarb2 and duox2 mutations in 2 siblings with pendred syndrome in a malaysian family.  - orphanet journal of rare diseases.  40-48. 

jason k cullen,norazian abdul murad,abreyyeo, matthewmckenzie,michealward, kok leongchong,nicolelschieber,robert g parton,yi chieh lim,ernstwolvetang, ghassan j maghzal, roland stocker, martin lavin.  (2016).  aarf domain containing kinase 3 (adck3) mutant cells display signs of oxidative stress, defects in mitochondrial homeostasis and lysosomal accumulation.  - plos one.  e0148213. 

mohd firdaus che mat, nor azian abdul murad, kamariah ibrahim, norfilza mohd mokhtar, wan zurinah wan ngah, roslan harun, rahman jamal.  (2016).  silencing of pros1 induces apoptosis and inhibits migration and invation of glioblastoma multiforme cells.  - international journal of oncology.  2359-2366. 

adeel masood butt, mohd cairul iqbal mohd amin, haliza katas, nor azian abdul murad, rahman jamal, prashant kesharwani.  (2016).  doxorubicin and sirna codelivery via chitosan-coated phresponsive mixed micellar polyplexes for enhanced cancer therapy in multidrug-resistant tumors.  - molecular pharmaceutics.  4179-4190. 

nf mohamad pakarul razy, na abdul murad, se syafruddin, a ahmad-annuar, sy lim, nm ibrahim, r jamal.  (2015).  glucocerebrosidase mutations in malay parkinson`s disease patients.  - public health genomics.  23. 

zainal abidin s, tan el, chan sc, jaafar , lee ax, abd hamid m, abdul murad na, pakarul razy nf, azmin s, ahmad annuar a, lim s, cheah ps, ling kh, mohamed ibrahim n.  (2015).  drd and grin2b polymorphisms and their association with the development of impulse control behaviour among malaysian parkinson`s disease patients.  - bmc neurology.  1-10. 

n abdullah, na abdul murad, j attia, c oldmeadow, ea mohd haniff, se syafruddin, n abd jalal, n ismail, m ishak, r jamal, rj scott and eg holliday.  (2015).  characterizing the genetic risk for type 2 diabetes in a malaysian multi-ethnic cohort.  - diabetic medicine.  1377-1384. 

zz mohd rani, na abdul murad, sm then, sp bernam, a abdullah, s saimun, sn othman, aa raymond, r jamal.  (2015).  hla-b*1502 screening in epileptic patients using a high resolution melting-real tme pcr (hrm-qpcr) method.  - public health genomics.  21. 

murad na, cullen jk, mckenzie m, ryan mt, thorburn d, gueven n, kobayashi j, birrell g, yang j, dork t, becherel o, grattan-smith p, lavin mf..  (2013).  mitochondrial dysfunction in a novel form of autosomal recessive ataxia.  - mitochondrion.  13(3):235-245. 

abdul murad na, othman z, khalid m, abdul razak z, hussain r, nadesan s, sagap i, mohamed rose i, wan ngah wz, jamal r..  (2012).  missense mutations in mlh1, msh2, kras, and apc genes in colorectal cancer patients in malaysia.  - digestive diseases and sciences.  57(11) : 2863-2872.