puan zam zureena binti mohd rani

pegawai penyelidik

institut perubatan molekul (umbi)



   Biografi/ Biography :

  • Zam Zureena Mohd Rani graduated with Diploma (Medical Laboratory Technology) from UiTM in 2004 and Bachelor Science (Biomedical Science) from UKM in 2011. Currently, she is a Senior Research officer and Quality Manager for MS ISO/IEC 17025:2017 in UMBI. Her research interests include non-communicable diseases (NCD) such as diabetes and hypercholesterolemia and rare diseases. Currently, her work focuses on identification of mutations or variants involved in these diseases using whole exome sequencing, targeted sequencing and genotyping using mass spectrometry. She is Technical manager for HLA-B:1502 testing under MS ISO/IEC 17025:2017 (scope: acid nucleic) in UMBI since 2015.

  • zam zureena mohd rani, raja mohd fadhil raja abd rahman, mohd ridhwan abd. razak dan sazuita saidin.  (2023).  pengesanan hla-b*27 berkaitan dengan ankylosing spondylitis (as).  - website umbi.  1. 

     

    zam zureena mohd rani dan fara zela mohd radin.  (2023).  implikasi keabnormalan mitokondria dna (mtdna) pada kesihatan.  - website umbi.  1. 

     

    nor azian abdul murad, yusuf mohammad noor, zam zureena mohd. rani, siti aishah sulaiman, yock ping chow, noraidatulakma abdullah, norfazilah ahmad, norliza ismail, nazihah abdul jalal , mohd. arman kamaruddin, amalia afzan, rahman jamal.  (2023).  hypercholesterolemia in the malaysian cohort participants: genetic and non-genetic risk factors.  - genes.  1-15. 

     

    lina khialida saidi, zam zureena md rani, siti aishah silaiman, ismail aziah, anis amirah alim, sharipah nadzirah syed ahmad ayob, dee chang fu, azrul azlan hamzah, nor azian abdul murad.  (2023).  kaedah diagnostik semasa dan penggunaan ujian titik penjagaan pantas (poc) bagi mendiagnos hiperkolesterolemia famili (fh).  - jurnal sains kesihatan malaysia.  35-45. 

     

    siti aishah sulaiman, chow yock ping, muhammad-redha abdullah zawawi, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal, nor azian abdul murad11.  (2023).  whole exome sequencing (wes) in mullerian agenesis and anorectal anomaly : a case study.  - rcmm & nccr 2023.  49. 

     

    nor azian abdul murad, yusuf mohammad noor, zam zureena mohd. rani, siti aishah sulaiman, yock ping chow, noraidatulakma abdullah, norfazilah ahmad, norliza ismail, nazihah abdul jalal , mohd. arman kamaruddin, amalia afzan, rahman jamal.  (2023).  hypercholesterolemia in the malaysian cohort participants: genetic and non-genetic risk factors.  - genes.  1-15. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    nor azian abdul murad, yusuf mohammad noor, zam zureena mohd. rani, siti aishah sulaiman, yock ping chow, noraidatulakma abdullah, norfazilah ahmad, norliza ismail, nazihah abdul jalal , mohd. arman kamaruddin, amalia afzan, rahman jamal.  (2023).  hypercholesterolemia in the malaysian cohort participants: genetic and non-genetic risk factors.  - genes.  1-15. 

     

    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. 

     

    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. 

     

    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. 

     

    zam zureena mohd rani, raja mohd fadhil raja abd rahman, mohd ridhwan abd. razak dan sazuita saidin.  (2023).  pengesanan hla-b*27 berkaitan dengan ankylosing spondylitis (as).  - website umbi.  1. 

     

    zam zureena mohd rani dan fara zela mohd radin.  (2023).  implikasi keabnormalan mitokondria dna (mtdna) pada kesihatan.  - website umbi.  1. 

     

    siti aishah sulaiman, chow yock ping, muhammad-redha abdullah zawawi, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal, nor azian abdul murad11.  (2023).  whole exome sequencing (wes) in mullerian agenesis and anorectal anomaly : a case study.  - rcmm & nccr 2023.  49. 

     

    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. 

     
    puan zam zureena binti mohd rani

    pegawai penyelidik

    institut biologi molekul perubatan ukm (umbi)

     zureena@ukm.edu.my



       Biografi/ Biography :

  • PEGAWAI PENYELIDIK

  • zam zureena mohd rani, raja mohd fadhil raja abd rahman, mohd ridhwan abd. razak dan sazuita saidin.  (2023).  pengesanan hla-b*27 berkaitan dengan ankylosing spondylitis (as).  - website umbi.  1. 

     

    zam zureena mohd rani dan fara zela mohd radin.  (2023).  implikasi keabnormalan mitokondria dna (mtdna) pada kesihatan.  - website umbi.  1. 

     

    nor azian abdul murad, yusuf mohammad noor, zam zureena mohd. rani, siti aishah sulaiman, yock ping chow, noraidatulakma abdullah, norfazilah ahmad, norliza ismail, nazihah abdul jalal , mohd. arman kamaruddin, amalia afzan, rahman jamal.  (2023).  hypercholesterolemia in the malaysian cohort participants: genetic and non-genetic risk factors.  - genes.  1-15. 

     

    lina khialida saidi, zam zureena md rani, siti aishah silaiman, ismail aziah, anis amirah alim, sharipah nadzirah syed ahmad ayob, dee chang fu, azrul azlan hamzah, nor azian abdul murad.  (2023).  kaedah diagnostik semasa dan penggunaan ujian titik penjagaan pantas (poc) bagi mendiagnos hiperkolesterolemia famili (fh).  - jurnal sains kesihatan malaysia.  35-45. 

     

    siti aishah sulaiman, chow yock ping, muhammad-redha abdullah zawawi, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal, nor azian abdul murad11.  (2023).  whole exome sequencing (wes) in mullerian agenesis and anorectal anomaly : a case study.  - rcmm & nccr 2023.  49. 

     

    nor azian abdul murad, yusuf mohammad noor, zam zureena mohd. rani, siti aishah sulaiman, yock ping chow, noraidatulakma abdullah, norfazilah ahmad, norliza ismail, nazihah abdul jalal , mohd. arman kamaruddin, amalia afzan, rahman jamal.  (2023).  hypercholesterolemia in the malaysian cohort participants: genetic and non-genetic risk factors.  - genes.  1-15. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    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. 

     

    nor azian abdul murad, yusuf mohammad noor, zam zureena mohd. rani, siti aishah sulaiman, yock ping chow, noraidatulakma abdullah, norfazilah ahmad, norliza ismail, nazihah abdul jalal , mohd. arman kamaruddin, amalia afzan, rahman jamal.  (2023).  hypercholesterolemia in the malaysian cohort participants: genetic and non-genetic risk factors.  - genes.  1-15. 

     

    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. 

     

    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. 

     

    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. 

     

    zam zureena mohd rani, raja mohd fadhil raja abd rahman, mohd ridhwan abd. razak dan sazuita saidin.  (2023).  pengesanan hla-b*27 berkaitan dengan ankylosing spondylitis (as).  - website umbi.  1. 

     

    zam zureena mohd rani dan fara zela mohd radin.  (2023).  implikasi keabnormalan mitokondria dna (mtdna) pada kesihatan.  - website umbi.  1. 

     

    siti aishah sulaiman, chow yock ping, muhammad-redha abdullah zawawi, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal, nor azian abdul murad11.  (2023).  whole exome sequencing (wes) in mullerian agenesis and anorectal anomaly : a case study.  - rcmm & nccr 2023.  49. 

     

    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.