dr. siti aishah binti sulaiman

pensyarah universiti

institut perubatan molekul (umbi)

No. Telefon Rasmi :  0391459070

No. rasmi:
UKM : 03 8921 5555



   Biografi/ Biography :

  • Dr. Siti Aishah Sulaiman completed her Ph.D. in Medicine in 2015 with a thesis title of Early Life Determinants of β-Cell Function in The Sheep. In her Ph.D. project, she investigated the role of early life factor, the intrauterine growth restriction (IUGR) in the development of β-cells dysregulation and insulin resistance, in an animal model of IUGR. She also determined the window of an early life intervention for IUGR-induced β-cells dysregulation, by a post-natal treatment of an anti-diabetic drug, Exendin-4. In 2016, she joined the UKM Medical Molecular Biology Institute (UMBI) as a postdoctoral research fellow. Here in UMBI, she performed the genome sequencing of colorectal and breast cancer patients. At the same time, she also worked together with a psychiatrist to determine the expression profile of oxidative stress markers in Bipolar Disorder patients. Upon completing her postdoctoral fellowship, she was offered to be a research fellow in UMBI and is currently doing the research on non-coding RNA regulation of disease development, with a particular interest in the role of long non-coding RNAs (lncRNAs) in diabetes complications, such as Diabetic Nephropathy and Diabetic Cardiomyopathy as well as the Non-alcoholic Fatty Liver Disease. Since 2015 till now, she has published many articles, and have acquired RM 1,449,400 of research grants. Dr Siti Aishah has numerous experiences in designing and performing the molecular experiments and data analysis.

  • 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. 

     

    azrul azlan bin hamzah;a. rahman bin a. jamal;norlaila binti mustafa;nor azian binti abdul murad;jumril yunas;siti aishah binti sulaiman.  (2023).  development of mems-based lateral flow assay for detection of ldlr gene mutations for familial hypercholesterolemia (fh).  -

     

    rafhanah izzati razali, vicneswarry dorairaj, muhammad nafiz haidi adrus, siti aishah sulaiman.  (2023).  lncrna-mirna-mrna network identification in the non-alcoholic steatohepatitis (nash).  - international meeting - 47th annual conference of the malaysian society for biochemistry and molecular biology.  39. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2023).  population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.  - frontiers in genetics.  1-11. 

     

    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. 

     

    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. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2023).  population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.  - frontiers in genetics.  1-11. 

     

    siti aishah sulaiman, vicneswarry dorairaj, muhammad nafiz haidi adrus.  (2022).  genetic polymorphisms and diversity in nonalcoholic fatty liver disease (nafld): a mini review.  - biomedicines.  1-23. 

     

    johannes jun wei low, siti aishah sulaiman, nor adzimah johdi and nadiah abu.  (2022).  immunomodulatory effects of extracellular vesicles in glioblastoma.  - frontiers in cell and developmental biology.  1-11. 

     

    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. 

     

    nor azila ma, nor azian am, azmawati mn, sharifah azura s, petrick p, najma k, mohd rohaizat h, norfazilah a, anita s, hanita o, tuti ningseh md, nurul syakima am, ezanee azlina, siti aishah, nurul syeefa', abdul rashid, abdul halim, hanafiah hr, rahman j.  (2021).  covid-19 in malaysia: exposure assessment and prevention practices among healthcare workers at a teaching hospital.  - journal of infection in developing countries.  1816-1824. 

     

    siti aishah sulaiman,nor ilham ainaa muhsin,ahmad rasyadan arshad, wan fahmi wan mohamad nazarie,rahman jamal,norlinah mohamed ibrahim,nor azian abdul murad.  (2020).  differential expression of circulating mirnas in parkinsons disease patients: potential early biomarker?.  - neurology asia.  319-329. 

     

    siti a sulaiman, nadiah abu, nurul-syakima ab mutalib, teck yew low, rahman jamal.  (2019).  signatures of gene expression, dna methylation and micrornas of hepatocellular carcinoma with vascular invasion.  - future oncology.  2603-2617. 

     

    maimiza zahari, siti aishah sulaiman, zulhabri othman, yasmin ayob, faraizah abd karim, rahman jamal.  (2018).  mutational profiles of f8 and f9 in a cohort of haemophilia a and haemophilia b patients in the multi-ethnic malaysian population.  - the mediterranean journal of hematology and infectious diseases. 

     

    tamil selvi loganathan, siti aishah sulaiman, noraidatulakma abdullah, rahman jamal.  (2018).  detection and confirmation of the presence of long non-coding rna in archival frozen whole urine samples.  - medicine & health.  328. 

     

    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. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2023).  population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.  - frontiers in genetics.  1-11. 

     

    siti aishah sulaiman, vicneswarry dorairaj, muhammad nafiz haidi adrus.  (2022).  genetic polymorphisms and diversity in nonalcoholic fatty liver disease (nafld): a mini review.  - biomedicines.  1-23. 

     

    johannes jun wei low, siti aishah sulaiman, nor adzimah johdi and nadiah abu.  (2022).  immunomodulatory effects of extracellular vesicles in glioblastoma.  - frontiers in cell and developmental biology.  1-11. 

     

    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. 

     

    nurul-syakima ab mutalib, siti aishah sulaiman and rahman jamal.  (2019).  computational epigenetics and diseases.  - 452. 

     

    siti aishah sulaiman, nor azian abdul murad, ezanee azlina mohamad hanif, nadiah abu, and rahman jamal.  (2018).  circular rna: biogenesis and function.  - 370. 

     

    azrul azlan bin hamzah;a. rahman bin a. jamal;norlaila binti mustafa;nor azian binti abdul murad;jumril yunas;siti aishah binti sulaiman.  (2023).  development of mems-based lateral flow assay for detection of ldlr gene mutations for familial hypercholesterolemia (fh).  -

     

    rafhanah izzati razali, vicneswarry dorairaj, muhammad nafiz haidi adrus, siti aishah sulaiman.  (2023).  lncrna-mirna-mrna network identification in the non-alcoholic steatohepatitis (nash).  - international meeting - 47th annual conference of the malaysian society for biochemistry and molecular biology.  39. 

     

    mohamed afiq hidayat zailani, raja zahratulazma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2022).  genetic variants of g6pd deficiency in southeast asian countries and future directions of genomic medicine..  - the 19th annual scientific meeting malaysian society of haematology.  1. 

     

    mira farzana mohamad mokhtar, muhammad redha abdullah zawawi & siti aishah sulaiman.  (2022).  prediction tools and databases of mirna targets in research.  - website umbi.  1. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, hafiza alauddin, azlin ithnin, siti aishah sulaiman, endom ismail, ainoon othman.  (2022).  point-of-care genetic testing for glucose-6-phosphate dehydrogenase (g6pd) deficiency as a novel molecular diagnostic approach: challenges and opportunities.  - medical genetics conference kuala lumpur 2022: the future is now.  1. 

     
    dr. siti aishah binti sulaiman

    pensyarah universiti

    institut biologi molekul perubatan ukm (umbi)

     sitiaishahsulaiman@ukm.edu.my

    No. Telefon Rasmi :  9070

    No. rasmi:
    UKM : 03 8921 5555



       Biografi/ Biography :

  • PENSYARAH UNIVERSITI

  • 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. 

     

    azrul azlan bin hamzah;a. rahman bin a. jamal;norlaila binti mustafa;nor azian binti abdul murad;jumril yunas;siti aishah binti sulaiman.  (2023).  development of mems-based lateral flow assay for detection of ldlr gene mutations for familial hypercholesterolemia (fh).  -

     

    rafhanah izzati razali, vicneswarry dorairaj, muhammad nafiz haidi adrus, siti aishah sulaiman.  (2023).  lncrna-mirna-mrna network identification in the non-alcoholic steatohepatitis (nash).  - international meeting - 47th annual conference of the malaysian society for biochemistry and molecular biology.  39. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2023).  population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.  - frontiers in genetics.  1-11. 

     

    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. 

     

    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. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2023).  population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.  - frontiers in genetics.  1-11. 

     

    siti aishah sulaiman, vicneswarry dorairaj, muhammad nafiz haidi adrus.  (2022).  genetic polymorphisms and diversity in nonalcoholic fatty liver disease (nafld): a mini review.  - biomedicines.  1-23. 

     

    johannes jun wei low, siti aishah sulaiman, nor adzimah johdi and nadiah abu.  (2022).  immunomodulatory effects of extracellular vesicles in glioblastoma.  - frontiers in cell and developmental biology.  1-11. 

     

    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. 

     

    nor azila ma, nor azian am, azmawati mn, sharifah azura s, petrick p, najma k, mohd rohaizat h, norfazilah a, anita s, hanita o, tuti ningseh md, nurul syakima am, ezanee azlina, siti aishah, nurul syeefa', abdul rashid, abdul halim, hanafiah hr, rahman j.  (2021).  covid-19 in malaysia: exposure assessment and prevention practices among healthcare workers at a teaching hospital.  - journal of infection in developing countries.  1816-1824. 

     

    siti aishah sulaiman,nor ilham ainaa muhsin,ahmad rasyadan arshad, wan fahmi wan mohamad nazarie,rahman jamal,norlinah mohamed ibrahim,nor azian abdul murad.  (2020).  differential expression of circulating mirnas in parkinsons disease patients: potential early biomarker?.  - neurology asia.  319-329. 

     

    siti a sulaiman, nadiah abu, nurul-syakima ab mutalib, teck yew low, rahman jamal.  (2019).  signatures of gene expression, dna methylation and micrornas of hepatocellular carcinoma with vascular invasion.  - future oncology.  2603-2617. 

     

    maimiza zahari, siti aishah sulaiman, zulhabri othman, yasmin ayob, faraizah abd karim, rahman jamal.  (2018).  mutational profiles of f8 and f9 in a cohort of haemophilia a and haemophilia b patients in the multi-ethnic malaysian population.  - the mediterranean journal of hematology and infectious diseases. 

     

    tamil selvi loganathan, siti aishah sulaiman, noraidatulakma abdullah, rahman jamal.  (2018).  detection and confirmation of the presence of long non-coding rna in archival frozen whole urine samples.  - medicine & health.  328. 

     

    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. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2023).  population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review.  - frontiers in genetics.  1-11. 

     

    siti aishah sulaiman, vicneswarry dorairaj, muhammad nafiz haidi adrus.  (2022).  genetic polymorphisms and diversity in nonalcoholic fatty liver disease (nafld): a mini review.  - biomedicines.  1-23. 

     

    johannes jun wei low, siti aishah sulaiman, nor adzimah johdi and nadiah abu.  (2022).  immunomodulatory effects of extracellular vesicles in glioblastoma.  - frontiers in cell and developmental biology.  1-11. 

     

    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. 

     

    nurul-syakima ab mutalib, siti aishah sulaiman and rahman jamal.  (2019).  computational epigenetics and diseases.  - 452. 

     

    siti aishah sulaiman, nor azian abdul murad, ezanee azlina mohamad hanif, nadiah abu, and rahman jamal.  (2018).  circular rna: biogenesis and function.  - 370. 

     

    azrul azlan bin hamzah;a. rahman bin a. jamal;norlaila binti mustafa;nor azian binti abdul murad;jumril yunas;siti aishah binti sulaiman.  (2023).  development of mems-based lateral flow assay for detection of ldlr gene mutations for familial hypercholesterolemia (fh).  -

     

    rafhanah izzati razali, vicneswarry dorairaj, muhammad nafiz haidi adrus, siti aishah sulaiman.  (2023).  lncrna-mirna-mrna network identification in the non-alcoholic steatohepatitis (nash).  - international meeting - 47th annual conference of the malaysian society for biochemistry and molecular biology.  39. 

     

    mohamed afiq hidayat zailani, raja zahratulazma raja sabudin, azlin ithnin, hafiza alauddin, siti aishah sulaiman, endom ismail, ainoon othman.  (2022).  genetic variants of g6pd deficiency in southeast asian countries and future directions of genomic medicine..  - the 19th annual scientific meeting malaysian society of haematology.  1. 

     

    mira farzana mohamad mokhtar, muhammad redha abdullah zawawi & siti aishah sulaiman.  (2022).  prediction tools and databases of mirna targets in research.  - website umbi.  1. 

     

    mohamed afiq hidayat zailani, raja zahratul azma raja sabudin, hafiza alauddin, azlin ithnin, siti aishah sulaiman, endom ismail, ainoon othman.  (2022).  point-of-care genetic testing for glucose-6-phosphate dehydrogenase (g6pd) deficiency as a novel molecular diagnostic approach: challenges and opportunities.  - medical genetics conference kuala lumpur 2022: the future is now.  1.