nor azian abdul murad, wan fahmi wan mohamad nazarie, zam zureena mohd rani, muhammad redha abdullah zawawi, norazlin kamal nor, fara zela mohd radin, rahman jamal, juriza ismail.  (2022).  an integrative bioinformatics meta-analysis of microarray data for identifying hub genes as biomarkers of autism spectrum disorder (asd).  - asian journal of medicine and biomedicine.  84-97. 

zam zureena mohd rani, raja mohd fadhil raja abd rahman, mohd ridhwan abd. razak dan sazuita saidin.  (2022).  farmakogenomik: pendekatan genetik dna bagi rawatan ubatan secara spesifik.  - .  1-4. 

zam zureena mohd rani dan fara zela mohd radin.  (2022).  penyakit jarang jumpa : pengesanan genetik abnormal di kalangan pesakit.  - website umbi.  1. 

zam zureena mohd rani.  (2021).  kitaran pdca dan pemikiran berasaskan risiko: kepentingan di dalam sistem pengurusan kualiti organisasi.  - .  1-4. 

siti aishah sulaiman, zamzureena mohd rani, fara zela mohd radin, nor azian abdul murad.  (2020).  advancement in the diagnosis of mitochondrial diseases.  - journal of translational genetics and genomics (jtgg).  159-187. 

nor azian abdul murad & zam zureena mohd rani.  (2019).  hiperkolesterolemia di malaysia: frekuansi, faktor genetik dan impak farmakogenetik.  - .  . 

nor azian abdul murad & zam zureena mohd rani.  (2019).  penyaringan polimorfisme hla-b*15:02 untuk pesakit epilepsi di hospital canselor tuanku muhriz, ukm oleh umbi.  - .  . 

nor azian abdul murad, chow yock ping, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita a aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, ang mia yang, rahman jamal.  (2019).  digenic inheritance of heterozygous fanca and brca2 mutations in a vacterl-h patient.  - asian journal of medicine and biomedicine.  1-11. 

zam zureena mohd rani, nor azian abdul murad, sue-mian then, suthashini panja bernam,asmaa abdullah, saberi saimun, sri noraima othman, raymond azman ali, rahman jamal.  (2018).  hla-b*15:02 screening in epileptic patients using a high resolution melting-real time pcr (hrm-qpcr) method.  - neurology asia.  . 

chan l.f., sulaiman s.a., abdullah n., mohamad kamal n.a., loo j.l., abdul murad n.a., goon j.a., damanhuri h., mohd rani z.z., tan j.a.c., abdul rahman n.a., wan ngah w.z., jamal r..  (2018).  discovery phase of oxidative stress gene expression and suicidal ideation in bipolar disorder.  - european symposium on suicide & suicidal behaviour.  . 

siti aishah sulaiman, nor azian abdul murad, yock ping chow, zam zureena mohd rani, salwati shuib, dayang anita a. aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal.  (2018).  mutations in kif27, gnas and ift140 genes in a patient with vacterl association: a case report.  - asia pacific journal of molecular medicine.  . 

siti aishah sulaiman, nor azian abdul murad, chow yock ping, zam zureena mohd rani, salwati shuib, dayang anita a. aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal.  (2017).  mutations in kif27, gnas and ift140 genes are associated with vacterl association.  - 7th regional conference on molecular medicine (rcmm) in conjunction with 3rd national conference for cancer research.  . 

nor azian abdul murad, chow yock ping, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita, hana azhari, syarifah azween, zarina abdul latif, rahman jamal.  (2017).  digenic inheritance of heterozygous fanca and brca2 mutations in a vacterl-h patient.  - 7th regional conference on molecular medicine (rcmm) in conjunction with 3rd national conference for cancer research 2017.  . 

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. 

nor azian abdul murad, chow yock ping, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita, hana azhari, syarifah azween, zarina abdul latif, rahman jamal.  (2017).  identification of novel mutations in vacterl-h patient via exome sequencing.  - 7th regional conference on molecular medicine (rcmm) in conjunction with 3rd national conference for cancer research.  . 

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. 

sameh magdeldin, shymaa enany, yutaka yoshida, bo xu, ying zhang, zam zureena, illambarthi lokamani, eishin yaoita, tadashi yamamoto.  (2014).  basics and recent advances of two dimensional-polyacrylamide gel electrophoresis.  - clinical proteomics.  16. 

then, s.-m., rani, z.z.m., raymond, a.a., jamal, r..  (2013).  pharmacogenomics screening of hla-b*1502 in epilepsy patients: how we do it in the ukm medical centre, malaysia.  - neurology asia.  18(SUPPL. 1):27-29. 

mr zam zureena, sf chin, bh soon, a abu bakar, cj toh, f fadzil, j thanabalan, ms mohd haspani, r kumar, h roslan, wz wan ngah, nm mokhtar, r jamal.  (2013).  differential protein profiles in meningioma and glioma: a preliminary glimpse.  - 1st national conference for cancer research & 5th regional conference on molecular medicine (rcmm).  . 

sue-mian then, zam zureena mohd rani, azman ali raymond, safrina ratnaningrum and rahman jamal.  (2011).  frequency of the hla-b*1502 allele contributing to carbamazepine-induced hypersensitivity reactions in a cohort of malaysian epilepsy patients.  - asian pacific journal of allergy and immunology.  29(3):290-293. 

then sue mian, zam zureena binti mohd rani, safrina d ratnaningrum, raymond azman ali, a rahman a jamal.  (2009).  rapid pcr protocol to detect hla-b*1502 polymorphism in epileptic patients with cutaneous adverse drug reactions (cadrs) towards carbamazepine (cbz).  - 3rd regional confenrence on molecular medicine, kota bharu, kelantan.  .