Teguh Haryo Sasongko



Salutation
Associate Professor Dr

School/Centre
School of Medicine

Department
Human Biology

Appointment
Deputy Director, Commercialisation & Support

Position
Associate Professor

Email
teguhharyosasongko@imu.edu.my



Education

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PhD (Medical Sciences (Human Molecular Genetics)), 2008 Kobe University Graduate School of Medicine
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MD (Medicine), 2003 Universitas Gadjah Mada School of Medicine

Memberships

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The Cochrane Collaboration Cochrane Staff Member 2018 - Present
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Forum for Ethical Review Committees in the Asian and Western Pacific Region (FERCAP) Member 2013 - Present

Research Funding
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Systematic Review and Meta-Analysis of the association between miRNA-126 and Diabetic Retinopathy IMU Internal Research Grant | 02 Sep 2024 - 31 Dec 2025
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Childhood Emotional Abuse and Mental Health among Young Adults in Asia: A Scoping Review IMU Internal Research Grant | 01 Mar 2024 - 28 Feb 2026
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The psychological interventions for non-suicidal self-injury among young adults: A scoping review IMU Internal Research Grant | 01 Mar 2024 - 28 Feb 2026
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Role of EGFR exon 20 insertion mutation in non-small cell lung carcinoma: An updated meta-analysis of prognostic factor studies IMU Internal Research Grant | 01 Jul 2023 - 30 Jun 2024
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Barriers to Psychological Help-Seeking among University Students: A Scoping Review IMU Internal Research Grant | 01 Mar 2023 - 31 Aug 2023
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A Survey on Genomic Literacy of Students in Medicine and Other Allied Health Sciences in Malaysia Perdana University - MMA Foundation Grant | 01 Oct 2021 - 31 May 2022
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Surveillance System to observe seroconversion to SARS-CoV-2 in Human: Combining Hospital Based and Population Based Longitudinal Study in Sleman HDSS (Health and Demographic Surveillance System) RISPRO-Diaspora | 01 Feb 2021 - 31 Jan 2024
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Elucidating the regulatory effect of miRNA on survival motor neuron (SMN) protein in spinal muscular atropy (SMA) Human iPSC-Derived Fibroblast FRGS | 01 Jan 2019 - 31 Mar 2022
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Development of AI-powered Clinical Decision-Support System based on Big-Data Analytics for Molecular Genetic Diagnosis Prototype Research Grant Scheme | 01 Jan 2019 - 01 Jan 2022
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Genetic Host Susceptibility Factors to Severe Dengue Infection – A Systematic Review IMU Internal Funding (BMedSc Research Project) | 01 Jul 2018 - 31 Dec 2022
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Cell-Based Bioassays and Virtual Molecular Docking for Elucidating The Effects Of Malaysian-Derived mTOR Inhibitor Substances On A Tuberous On A Tuberous-Sclerosis-Complex-Derived Tumor Cells USM Research University (Individual) Grant | 01 Jan 2014 - 31 Dec 2017
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Community Outreach for the Promotion of Public Awareness on Genetic Disorders; Targeting General Public and Patients/Families. Knowledge Transfer Program - MOE | 01 Jan 2014 - 31 Dec 2016
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Genome Wide Gene Promoter DNA Methylation Study On Response To Oral Anti-Diabetics In Malay Male Patients With Type 2 Diabetes Mellitus (T2DM) USM Research University (Individual) Grant | 01 Jan 2014 - 31 Dec 2017
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Novel Approaches To Detection Of Disease Recurrence, Risk Reduction And Improved Management Of Breast Cancer USM Research University (Team) Grant | 01 Jan 2013 - 31 Dec 2016
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Influence of ACE I/D Polymorphism on the Performance of Malay Male School Children in Endurance Type Sport USM Short Term Grant | 01 Jan 2012 - 31 Dec 2015
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A Study on Isodiospyrin Putative Inhibitory actions against exonic splicing enhancers of dystrophin gene exon skipping in Duchenne Muscular Dystrophy USM Research University (Individual) Grant | 01 Jan 2012 - 31 Dec 2016
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Study on the Association Among ACTN3 R577X Polymorphism, Sprint Achievement and Academic Performance in Malay Male School Children USM Short Term Grant | 01 Jan 2012 - 31 Dec 2015
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Neurology & Psychiatry - Pediatric Neurology Ministry of Education, Malaysia | 01 Jan 2012 - 31 Dec 2015
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Analysis of Genetic Polymorphism as Risk Factors for Type 2 Diabetes Mellitus Among Malaysian Malay : A Pharmacogenetic Study USM Research University (Individual) Grant | 01 Jan 2011 - 31 Dec 2015
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Qualitative and Quantitative Analyses Of SMN 2 Gene Expression Upon Expression with Histone De-acetylase Inhibitors and Polyphenols USM Research University (Individual) Grant | 01 Jan 2010 - 31 Dec 2014
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Development Of Mutation Screening For The Molecular Diagnosis Of Tuberous Sclerosis Complex USM Research University (Individual) Grant | 01 Jan 2010 - 31 Dec 2013
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Codon-Correction-Inframing Approach For The Repair Of Dystrophin Gene Mutation In Duchenne Muscular Dystrophy Patients USM Research University (Individual) Grant | 01 Jan 2010 - 31 Dec 2014
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Significance of Exonic Splicing Enhancer (ESE) Motifs in The Splicing Mechanism within Internal Exons of SMN Genes USM Short Term Grant | 01 Jan 2009 - 31 Dec 2011

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Publications

Research Articles

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Profiling circulating microRNA and regulatory pathways in transfusion-dependent thalassemia and thalassemia trait compared to healthy controls: a preliminary study ExRNA 2024
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Differentially gene expression profiling reveals effect similarities of everolimus, asiaticoside, and asiatic acid on TSC-derived renal angiomyolipoma JOURNAL OF APPLIED PHARMACEUTICAL SCIENCE 2024
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Bibliometric analysis and network visualization on Tuberous Sclerosis Complex. BANGLADESH JOURNAL OF MEDICAL SCIENCE 2024
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Potential Use of MicroRNA Technology in Thalassemia Therapy JOURNAL OF CLINICAL MEDICINE RESEARCH 2024
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Parental stature as a risk factor for stunting in Indonesia: A systematic review and meta-analysis NARRA J 2023
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Research on children in the developing world. Quo Vadis? MALAYSIAN JOURNAL OF PAEDIATRICS AND CHILD HEALTH 2023
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Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization PSYCHIATRIC GENETICS 2023
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Angiotensin‐converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease COCHRANE DATABASE OF SYSTEMATIC REVIEWS 2021
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Disease Monitoring Parameters for Autoimmune Diseases ASIAN PAC. J. HEALTH SCI 2021
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The role of mTOR signalling pathway in hypoxia-induced cognitive impairment INTERNATIONAL JOURNAL OF NEUROSCIENCE 2021
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In silico analyses and cytotoxicity study of asiaticoside and asiatic acid from malaysian plant as potential mTOR inhibitors MOLECULES 2020
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Antiphospholipid antibodies in epilepsy: a systematic review and meta-analysis AUTOIMMUNITY REVIEWS 2018
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Commercializing oocytes in the era of therapeutic cloning; an extension of pro-life vs pro-choice debates JKKI: JURNAL KEDOKTERAN DAN KESEHATAN INDONESIA 2018
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Genetic background of β thalassemia modifier: recent update JOURNAL OF BIOMEDICINE AND TRANSLATIONAL RESEARCH 2018
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Four nucleotide deletions of exon 47 in Dystrophin gene: A case report of a Kelantanese Duchenne Muscular Dystrophy patient JOURNAL OF BIOMEDICAL AND CLINICAL SCIENCES (JBCS) 2018
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Human Genetics and Genetic Disorders HUMAN GENETICS 2017
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Placebo Controlled Trials: Interests of Subjects versus Interests of Drug Regulators THE MALAYSIAN JOURNAL OF MEDICAL SCIENCES: MJMS 2017
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Presence of anticardiolipin antibodies in patients with dementia: a systematic review and meta-analysis FRONTIERS IN AGING NEUROSCIENCE 2017
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Therapeutic suppression of nonsense mutation: an emerging target in multiple diseases and thrombotic disorders CURRENT PHARMACEUTICAL DESIGN 2017
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A 15-year single centre retrospective study of antiphospholipid syndrome patients from Northern Malaysia THE MALAYSIAN JOURNAL OF PATHOLOGY 2017
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Social and communicative functions of informed consent forms in East Asia and beyond FRONTIERS IN GENETICS 2017
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Combination of multiple ligation-dependent probe amplification and illumina MiSeq amplicon sequencing for TSC1/TSC2 gene analyses in patients with tuberous sclerosis complex THE JOURNAL OF MOLECULAR DIAGNOSTICS 2017
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Rapamycin and rapalogs for tuberous sclerosis complex COCHRANE DATABASE OF SYSTEMATIC REVIEWS 2016
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Natural products towards the discovery of potential future antithrombotic drugs CURRENT PHARMACEUTICAL DESIGN 2016
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Type 2 diabetes mellitus and Alzheimer’s disease: bridging the pathophysiology and management CURRENT PHARMACEUTICAL DESIGN 2016
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Familial primary antiphospholipid syndrome: A report of co-occurrence in three Malaysian family members EUROPEAN JOURNAL OF RHEUMATOLOGY 2016
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Transcript, methylation and molecular docking analyses of the effects of HDAC inhibitors, SAHA and Dacinostat, on SMN2 expression in fibroblasts of SMA patients JOURNAL OF HUMAN GENETICS 2016
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Antiplatelet and anticoagulant agents for preventing recurrence of peripheral vascular thrombosis in patients with Antiphospholipid syndrome COCHRANE DATABASE OF SYSTEMATIC REVIEWS 2016
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DNA methylation: an epigenetic insight into type 2 diabetes mellitus CURRENT PHARMACEUTICAL DESIGN 2016
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Antiphospholipid antibody-mediated thrombotic mechanisms in antiphospholipid syndrome: towards pathophysiology-based treatment CURRENT PHARMACEUTICAL DESIGN 2016
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‘Non-criteria’neurologic manifestations of antiphospholipid syndrome: a hidden kingdom to be discovered CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS (FORMERLY CURRENT DRUG TARGETS-CNS & NEUROLOGICAL DISORDERS) 2016
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Promoting Public Awareness in Genetic Disorder through Social Media OE(TM),NLG"Y'**NLGSH 2016
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A study on optimal concentrations of isodiospyrin putative inhibitory actions against exonic splicing enhancers of Dystrophin gene exon 53 skipping in Duchenne Muscular Dystrophy CONFERENCE ABSTRACT: 14 TH MEETING OF THE ASIAN-PACIFIC SOCIETY FOR NEUROCHEMISTRY. DOI: 10.3389/CONF. FNCEL 2016
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Rapamycin and its analogues (rapalogs) for Tuberous Sclerosis Complex-associated tumors: a systematic review on non-randomized studies using meta-analysis ORPHANET JOURNAL OF RARE DISEASES 2015
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Nomenclature Confusion in Deletion Mutations Involving Repetitive Nucleotides: A Lesson from HBB Gene Codon 35 (–C) vs. Codon 36 (–C) HEMOGLOBIN 2015
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Informed consent template and guidelines on the ethical practice in human genetics and human genomic research; initiatives of the Universiti Sains Malaysia THE MALAYSIAN JOURNAL OF MEDICAL SCIENCES: MJMS 2015
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Two novel gross deletions of TSC2 in Malaysian patients with tuberous sclerosis complex and TSC2/PKD1 contiguous deletion syndrome JAPANESE JOURNAL OF CLINICAL ONCOLOGY 2014
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Efficacy and safety of sitagliptin as a third therapeutic agent in the treatment of type 2 diabetes mellitus J DIABETES RES CLIN METAB 2014
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Macrodactyly and poliosis in tuberous sclerosis complex JAPANESE JOURNAL OF CLINICAL ONCOLOGY 2014
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Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia GENE 2014
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Bioinformatics and Biotechnology in Human Genetic Research: A Current Scenario BIOTECHNOLOGY AND BIOINFORMATICS: ADVANCES AND APPLICATIONS FOR BIOENERGY, BIOREMEDIATION AND BIOPHARMACEUTICAL RESEARCH 2014
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Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy JOURNAL OF NEUROGENETICS 2013
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Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy GENETICS AND MOLECULAR BIOLOGY 2013
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Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy THE INDIAN JOURNAL OF MEDICAL RESEARCH 2012
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Two-Cycle Ethanol Precipitation May Be Necessary for DNA Extracted from Amniotic Fluid Using Salting-Out Procedure. INTERNATIONAL MEDICAL JOURNAL 2012
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Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy JOURNAL OF NEUROGENETICS 2011
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Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia BMC MEDICAL GENETICS 2011
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Tuberous Sclerosis Complex NOVEL ASPECTS ON EPILEPSY 2011
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Two closely spaced nonsense mutations in the DMD gene in a Malaysian family MOLECULAR GENETICS AND METABOLISM 2011
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Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder BRAIN AND DEVELOPMENT 2010
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Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy ANNALS OF SAUDI MEDICINE 2010
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MERCI: a useful systematic'aide memoir'to help clinicians teach ethics MEDICAL EDUCATION 2009
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Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy BRAIN AND DEVELOPMENT 2009
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Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy BRAIN AND DEVELOPMENT 2009
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Hypomutability at the Polyadenine Tract in SMN Intron 3 Shows the Invariability of the a‐SMN Protein Structure ANNALS OF HUMAN GENETICS 2008
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Novel mutations in 21 patients with tuberous sclerosis complex and variation of tandem splice-acceptor sites in TSC1 exon 14 KOBE J MED SCI 2008
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Germ‐line mutation of KCNQ2, p. R213W, in a Japanese family with benign familial neonatal convulsion PEDIATRICS INTERNATIONAL 2008
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SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy PEDIATRICS INTERNATIONAL 2008
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C117T variant in the SMN1 gene found in the Japanese population PEDIATRICS INTERNATIONAL 2007
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Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome KOBE J MED SCI 2007
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A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins JOURNAL OF NEUROLOGY 2007
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QUANTIFICATION OF SMN GENE COPY NUMBER USING REAL-TIME PCR. MALAYSIAN JOURNAL OF MEDICAL SCIENCES 2006
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ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population KOBE JOURNAL OF MEDICAL SCIENCES 2005

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Other Publications

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Setting Research Priority for The Rural Region in Developing Nations; An Ethical Obligation International Conference on Multidisciplinary Approaches for Sustainable Rural Development (ICMA-SURE) 2023 | 19 Oct 2023
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SMN gene copy number analysis of malaysian spinal muscular atrophy (SMA) patients. Journal of Medical Genetics | 01 Jan 2005

Medias

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Potensi Selingkuh Mengintai Dalam Genetika? CNN Indonesia | 02 Jul 2023
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Kisah Cochrane: sumber rujukan informasi medis kepercayaan WHO The Conversation Indonesia | 16 Aug 2021
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COVID-19 in Southeast Asia: all eyes on Indonesia The Conversation Indonesia | 15 Jul 2021
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Mengapa pemerintah mesti segera beri vaksin COVID-19 untuk ibu hamil The Conversation Indonesia | 05 Jul 2021
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Kasus COVID-19 dan kematian di Asia Tenggara meningkat tajam, apa penyebabnya? The Conversation Indonesia | 15 Jun 2021
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Campur tangan DPR dalam riset vaksin Nusantara merusak sistem pengawasan obat dan makanan The Conversation Indonesia | 06 May 2021
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Mengapa vaksinasi COVID-19 swasta di Indonesia perlu kita dukung? The Conversation Indonesia | 26 Mar 2021
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Indonesian-made COVID-19 breathalyser sensitivity comparable to RT-PCR The Conversation Indonesia | 02 Mar 2021
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Riset: GeNose C19, hidung elekronik pendeteksi virus corona sensitivitasnya sebanding tes PCR The Conversation Indonesia | 17 Feb 2021
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4 prinsip kebijakan pengendalian pandemi COVID-19 cukup jelas: mengapa sulit terwujud di Indonesia The Conversation Indonesia | 22 Dec 2020
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Skandal riset Unair: bolehkah KSAD perintahkan prajurit jadi “kelinci percobaan” uji klinik obat COVID-19? The Conversation Indonesia | 06 Oct 2020
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7 persoalan serius dalam uji klinik calon obat COVID-19 dari riset Unair, BIN, dan TNI AD The Conversation Indonesia | 28 Aug 2020
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Science literacy as part of the pandemic new norms BERNAMA | 01 Jul 2020

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Supervisions
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Sandra Michael James Michael, Jocelyn Tan Xin Yi, Amritesh Singh A/L Malkit Singh, Chee Yuein Choy | Undergraduate | 01 Jan 2020 - 31 Dec 2020 Thesis: Risk of Bias Assessment of studies included for the Cochrane Systematic Review on the efficacy and safety of Rapamycin for Tuberous Sclerosis Complex
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Stanley Chai Soon Hou | Undergraduate | 01 Jan 2020 Thesis: Rapamycin and Rapalogs for Tuberous Sclerosis Complex; Review Update for Cochrane (Meta Analysis Part)
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Jocelyn Tan Xin Yi | Undergraduate | 01 Jan 2020 Thesis: Rapamycin and Rapalogs for Tuberous Sclerosis Complex; Review Update for Cochrane (Risk of Bias Assessment Part)
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Zu Hazzin Azim Bin Zamri, Thavaneshan A/L Kunasekaran, Adeline Ong, S.Jaiyaswiny A/P S.Sivakumar | Undergraduate | 01 Jan 2020 - 31 Dec 2020 Thesis: Characterizing systematically reviewed intervention management of genetically inherited disorders; A secondary data analysis of Cochrane Database of Systematic Reviews
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Siti Safura Jaapar | Doctorate | 01 Jan 2018 Thesis: Investigation of gut microbiome changes in neurodegenerative diseases using spinal muscular atrophy as a study model. Perdana University
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Ninie Nadia Binti Zulkipli | Doctorate | 01 Jan 2018 - 31 Dec 2021 Thesis: Elucidating the Effects of Malaysian-Derived mTOR Inhibitor on a Tuberous-Sclerosis-Complex-Derived Tumor Cells. Universiti Sains Malaysia
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Fakhrurrazi Yahaya | Doctorate | 01 Jan 2018 Thesis: Study of Application of Maqasid Shariah in Prenatal Diagnosis Issues in Malaysian Context
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Priyaah A/P Sekar | Undergraduate | 01 Jan 2018 - 31 Dec 2020 Thesis: Genetic Host Susceptibility Factors to Dengue Haemorrhagic Fever; A Systematic Review
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Nur Atikah Binti Nor Azhar | Master (Research) | 01 Jan 2017 - 31 Dec 2021 Thesis: Whole Exome Sequencing (WES) Analysis On Cerebral Palsy Patients With Underlying Genetic Factors
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Siti Nabilahuda Mohd Azlan | Undergraduate | 01 Jul 2016 - 30 Sep 2016 Thesis: Validation of TSC genes MiSeq Amplicon Sequencing
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Nur Atikah Binti Nor Azhar | Undergraduate | 01 Jul 2015 - 30 Sep 2015 Thesis: Analysis of ACE polymorphisms in Male School Children with Sprinter Capacity
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Fahmida Alam | Doctorate | 01 Jan 2015 - 31 Dec 2019 Thesis: Genome-wide gene promoter DNA methylation study on response to oral anti-diabetics in Malay male patients with Type 2 Diabetes Mellitus. Universiti Sains Malaysia
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Hussain Saad Alzahrani | Master (Mixed Mode) | 01 Jan 2015 - 31 Dec 2017 Thesis: A Study on Optimal Concentrations of Isodiospyrin Putative Inhibitory Actions Against Exonic Splicing Enhancers of Dystrophin Gene Exon 53 Skipping in Duchenne Muscular Dystrophy
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Hamshawagini A/P Chandra | Undergraduate | 01 Jul 2014 - 30 Sep 2014 Thesis: Compound heterozygous mutations in ARSA gene in a Malay family with Metachromatic Leukodystrophy (MLD)
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Thanga Ganapathy A/L Suprumanian, Prevena A/P Subramaniam, Tabitha Shirani, Vinodh A/L Puspalingam | Undergraduate | 01 Jan 2014 - 31 Dec 2016 Thesis: Identification of SMN Hybrid breakpoint in a Malaysian patient with Spinal Muscular Atrophy
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Roslina Rashid | Doctorate | 01 Jan 2014 - 31 Dec 2018 Thesis: A study on Isodiospyrin putative inhibitory actions against exonic splicing enhancers of Dystrophin gene exon skipping in Duchenne Muscular Dystrophy
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Chia Boon Hock | Master (Research) | 01 Jan 2014 - 31 Dec 2017 Thesis: A study on the influence of ACTN3 R577X and ACE I/D Polymorpshisms on the physical and academic performance of Malay male school children
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Najlaa Maddin | Undergraduate | 01 Jul 2013 - 30 Sep 2013 Thesis: Optimization of TSC2 Amplicons Amplifications
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Md Asiful Islam | Doctorate | 01 Jan 2012 - 31 Dec 2017 Thesis: Elucidation of Clinical And Laboratory Features, Comorbidity Risks, Treatment Options and Molecular Pathophysiology of Antiphospholipid Syndrome (APS) Patients
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Syah Nor Iman Othman | Undergraduate | 01 Jul 2011 - 30 Sep 2011 Thesis: Identification of deletion breakpoint in ARG1 gene of a Malaysian patient with Hyperargininemia
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Jafar Mohseni | Doctorate | 01 Jan 2011 - 31 Dec 2014 Thesis: Analysis of SMN2 expression modulation upon exposure with histone deacetylase inhibitors and polyphenols; An in-vitro cell-based assay for the therapy for Spinal Muscular Atrophy
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Nur Farrah Dila Ismail | Master (Research) | 01 Jan 2011 - 31 Dec 2013 Thesis: MSc in Human Genetics. Genotype-Phenotype Study of Tuberous Sclerosis Complex in selected cohort of Malaysian patients with TSC2 mutations
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Fatemeh Hayati | Doctorate | 01 Jan 2011 - 31 Dec 2015 Thesis: Analysis of genetic polymorphisms as risk factor for Type 2 Diabetes Mellitus among Malaysian Malay: A Pharmacogenetic Study. Universiti Sains Malaysia
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Nik Mohd Ariff Nik Abd Malik | Undergraduate | 01 Jul 2010 - 30 Sep 2010 Thesis: Development of minigenes for splicing assay of SMN exon 3 using overlapping extension PCR
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Syarifah Aqumi Seyd Mah Aziz | Undergraduate | 01 Jul 2010 - 30 Sep 2010 Thesis: Optimization of DNA extraction method from amniotic fluid
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Nurul Syuhada Mohamad @ Ishak | Undergraduate | 01 Jul 2010 - 30 Sep 2010 Thesis: Optimization of DNA extraction from saliva using OG-500 kit (ORA gene – DNA self-collection kit)
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Rani Abdulqawee Al-Mahyoob | Doctorate | 01 Jan 2009 - 31 Dec 2013 Thesis: Reconstruction of Protein Synthesis Through Codon Unique Revision (RESCUER) For DMD Gene Mutation Correction In Malaysian Patients With Duchenne Muscular Dystrophy

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