Items where Subject is "Human Genome"
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APOB gene
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
Academic achievement
Association of COMT polymorphism and academic achievement among female undergraduate students. Science Letters, 15 (2). pp. 90-101. ISSN 2682-8626 (2021)
Academic performance
Predictor of academic performance: personality traits and catechol-O-methyltransferase polymorphisms. International Journal of Evaluation and Research in Education (IJERE), 13 (2). pp. 979-986. ISSN 2252-8822 (2024)
Adverse drug reactions
Moving forward with precision medicine: detection of hypersensitivity to drug reactions using HLA-B*15:02 genetic test kit. [Video] (2017)
Allele
Development of a PCR test for detection of warfarin resistance based on the polymorphism of VKORC1 genes. Degree thesis, Universiti Teknologi MARA, Shah Alam. (2012)
Annealing
Development of a PCR test for detection of warfarin resistance based on the polymorphism of VKORC1 genes. Degree thesis, Universiti Teknologi MARA, Shah Alam. (2012)
Antiepileptic drugs (AEDs)
The gene that turns epilepsy treatment deadly. [Website]
Aspirin
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
Awareness
Securing DNA information from selective attacks on humans. Journal of Media and Information Warfare, 4. pp. 93-104. ISSN 2821-3394 (2011)
BP Healthcare Group
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
BRCA1/2 gene
Knowledge and awareness of genetic test available for risk of breast cancer among female students in UiTM. Al-Rafidain Journal of Medical Sciences, 1 (2). pp. 14-18. ISSN 2789-3219 (2021)
Biodiversity characterization
Genetics Research In Malaysia: Suggested Priorities. Buletin Persatuan Genetik Malaysia, 10 (2). pp. 5-6. ISSN 1394-5750 (2004)
Biomarker
MicroRNA methylome signature and their functional roles in colorectal cancer diagnosis, prognosis, and chemoresistance. International Journal of Molecular Sciences, 23 (13). pp. 1-16. ISSN 1422-0067 (2022)
Blood group profiles
Genomic map of blood group alleles in Malaysian indigenous Orang Asli population from whole genome sequences. medRxiv. pp. 1-31. (Unpublished) (2021)
Body Mass Index
A review on the association of Fat Mass Obesity Associated (FTO) gene marker rs9939609 with obesity and Body Mass Index(BMI). Buletin Sains Kesihatan (BSK), 5 (1). pp. 11-20. ISSN 2550-1852 (2021)
Body Mass Index (BMI)
Development of PCR-based genotyping method for Fat Mass Obesity-Associated (FTO) gene polymorphism RS9939609. Journal of Health and Translational Medicine (JUMMEC), 2 (SI). pp. 51-54. ISSN 2289-392X (2023)
Breast Cancer
Knowledge and awareness of genetic test available for risk of breast cancer among female students in UiTM. Al-Rafidain Journal of Medical Sciences, 1 (2). pp. 14-18. ISSN 2789-3219 (2021)
Breast cancer
Mitochondrial DNA mutations in Malaysian female breast cancer patients. PLOS ONE, 15 (5). pp. 1-18. ISSN 1932-6203 (2020)
CACNB2 Mutation
Sudden cardiac arrest in a patient with malignant mitral valve prolapse with CACNB2 gene mutation: a simple coincidence or coexistence?—a case report. European Heart Journal, 7 (4). pp. 1-6. ISSN 2514-2119 (2023)
COMT polymorphism
Association of COMT polymorphism and academic achievement among female undergraduate students. Science Letters, 15 (2). pp. 90-101. ISSN 2682-8626 (2021)
COMT rs4680 polymorphism
Predictor of academic performance: personality traits and catechol-O-methyltransferase polymorphisms. International Journal of Evaluation and Research in Education (IJERE), 13 (2). pp. 979-986. ISSN 2252-8822 (2024)
COX-1
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
CYP2C9
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
Capillary sequencing
Development of PCR-based genotyping method for Fat Mass Obesity-Associated (FTO) gene polymorphism RS9939609. Journal of Health and Translational Medicine (JUMMEC), 2 (SI). pp. 51-54. ISSN 2289-392X (2023)
Carbamazepine
The gene that turns epilepsy treatment deadly. [Website]
Case Report
Sudden cardiac arrest in a patient with malignant mitral valve prolapse with CACNB2 gene mutation: a simple coincidence or coexistence?—a case report. European Heart Journal, 7 (4). pp. 1-6. ISSN 2514-2119 (2023)
Catalpol
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
Catechol-O-methyltransferase
Predictor of academic performance: personality traits and catechol-O-methyltransferase polymorphisms. International Journal of Evaluation and Research in Education (IJERE), 13 (2). pp. 979-986. ISSN 2252-8822 (2024)
Center for Computer Science Studies
Towards Development of Clustering Applications for Large-Scale Comparative Genotyping and Kinship Analysis Using Y-Short Tandem Repeats. OMICS A Journal of Integrative Biology, 19 (6). pp. 361-367. ISSN 1557-8100 (2015)
Cholesterol levels
The effects of genetic variants towards weight and biochemical changes in weight management program. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 269-277. ISSN 2289-392X (2023)
Chromosome
Karyotype pattern and maternal age distribution in down syndrome patients analyzed at Human Genome Center, University Sains Malaysia, Kelantan. Buletin Persatuan Genetik Malaysia, 12 (2). p. 1. ISSN 1394-5750 (2006)
Cognitive functions
Association of COMT polymorphism and academic achievement among female undergraduate students. Science Letters, 15 (2). pp. 90-101. ISSN 2682-8626 (2021)
Colorectal Cancer (CRC)
Dysbiosis and the chemopreventive role of prebiotics in colorectal cancer. Journal of Applied Biotechnology Reports, 10 (2). pp. 943-957. ISSN 2423-5784 (2023)
Colorectal cancer
MicroRNA methylome signature and their functional roles in colorectal cancer diagnosis, prognosis, and chemoresistance. International Journal of Molecular Sciences, 23 (13). pp. 1-16. ISSN 1422-0067 (2022)
Combination
Combinatorial Cytotoxic Effects of Damnacanthal and Doxorubicin against Human Breast Cancer MCF-7 Cells in Vitro. Molecules, 21 (9). ISSN 1420-3049 (2016)
Complex diseases
Live research webinar series 2.0: the right nutrients and drugs for you (the promises of precision health). [Video] (2020)
Confidence interval
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Conscientiousness
Predictor of academic performance: personality traits and catechol-O-methyltransferase polymorphisms. International Journal of Evaluation and Research in Education (IJERE), 13 (2). pp. 979-986. ISSN 2252-8822 (2024)
Copy Number Variants (CNVs)
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy. PLOS ONE. pp. 1-16. ISSN 1932-6203 (2016)
Coronary Artery Disease (CAD)
Genetic analysis of a young adult presented with acute myocardial infarction with no traditional risk factors: a novel case report. Malaysian Journal of Medicine and Health Sciences, 18 (1). pp. 349-352. ISSN 2636-9346 (2022)
Covid-19
Cystic Fibrosis
The molecular genetics and pathogenesis of cystic fibrosis lung disease. Buletin Persatuan Genetik Malaysia, 12 (2). pp. 10-17. ISSN 1394-5750 (2006)
Cystic Fibrosis Transmembrane Conductance Regulator
The molecular genetics and pathogenesis of cystic fibrosis lung disease. Buletin Persatuan Genetik Malaysia, 12 (2). pp. 10-17. ISSN 1394-5750 (2006)
Damnacanthal
Combinatorial Cytotoxic Effects of Damnacanthal and Doxorubicin against Human Breast Cancer MCF-7 Cells in Vitro. Molecules, 21 (9). ISSN 1420-3049 (2016)
Deoxyribonucleic acid
Securing DNA information from selective attacks on humans. Journal of Media and Information Warfare, 4. pp. 93-104. ISSN 2821-3394 (2011)
Diet
The effects of genetic variants towards weight and biochemical changes in weight management program. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 269-277. ISSN 2289-392X (2023)
Doctor2U
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
Dopaminergic pathway
Association of COMT polymorphism and academic achievement among female undergraduate students. Science Letters, 15 (2). pp. 90-101. ISSN 2682-8626 (2021)
Down Syndrome
Karyotype pattern and maternal age distribution in down syndrome patients analyzed at Human Genome Center, University Sains Malaysia, Kelantan. Buletin Persatuan Genetik Malaysia, 12 (2). p. 1. ISSN 1394-5750 (2006)
Doxorubicin
Combinatorial Cytotoxic Effects of Damnacanthal and Doxorubicin against Human Breast Cancer MCF-7 Cells in Vitro. Molecules, 21 (9). ISSN 1420-3049 (2016)
Drug-induced hypersensitivity reactions (DIHRs)
The gene that turns epilepsy treatment deadly. [Website]
Dysbiosis
Dysbiosis and the chemopreventive role of prebiotics in colorectal cancer. Journal of Applied Biotechnology Reports, 10 (2). pp. 943-957. ISSN 2423-5784 (2023)
ELSI
A review of human genome project (HGP) from ethical perspectives. International Journal of Advanced and Applied Sciences, 4 (12). pp. 125-132. ISSN 2313-3724 (2017)
Ecological
Appreciating the richness of nature through genetics: discovering new genetic species. Buletin Persatuan Genetik Malaysia, 19 (1 & 2). ISSN 1394-5750 (2012)
Ellitus
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
Environmental diseases
Live research webinar series 2.0: the right nutrients and drugs for you (the promises of precision health). [Video] (2020)
Epigenetics
MicroRNA methylome signature and their functional roles in colorectal cancer diagnosis, prognosis, and chemoresistance. International Journal of Molecular Sciences, 23 (13). pp. 1-16. ISSN 1422-0067 (2022)
FH
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
FTO gene variant rs9939609
Development of PCR-based genotyping method for Fat Mass Obesity-Associated (FTO) gene polymorphism RS9939609. Journal of Health and Translational Medicine (JUMMEC), 2 (SI). pp. 51-54. ISSN 2289-392X (2023)
Fat Mass Obesity Associated (FTO) gene
A review on the association of Fat Mass Obesity Associated (FTO) gene marker rs9939609 with obesity and Body Mass Index(BMI). Buletin Sains Kesihatan (BSK), 5 (1). pp. 11-20. ISSN 2550-1852 (2021)
Fatty acid desaturase 1 gene
Interaction of dietary linoleic acid and α-linolenic acids with rs174547 in FADS1 gene on metabolic syndrome components among vegetarians. Nutrients, 11 (7). pp. 1-16. ISSN 2072-6643 (2019)
Gastritis
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
Gene Expression
Acquired radioresistance in EMT6 mouse mammary carcinoma cell line is mediated by CTLA-4 and PD-1 through JAK/STAT/PI3K pathway. scientific reports, 13. ISSN 2045-2322 (2023)
Genes
Live research webinar series 2.0: the right nutrients and drugs for you (the promises of precision health). [Video] (2020)
Genetic Mutations
Acquired radioresistance in EMT6 mouse mammary carcinoma cell line is mediated by CTLA-4 and PD-1 through JAK/STAT/PI3K pathway. scientific reports, 13. ISSN 2045-2322 (2023)
Genetic Testing
Podcast Ubat atau Tabu Ep 3: Ujian Genetik | Genetic Testing. [Website] (2024)
Genetic Variation
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy. PLOS ONE. pp. 1-16. ISSN 1932-6203 (2016)
Genetic disease
Karyotype pattern and maternal age distribution in down syndrome patients analyzed at Human Genome Center, University Sains Malaysia, Kelantan. Buletin Persatuan Genetik Malaysia, 12 (2). p. 1. ISSN 1394-5750 (2006)
Genetic diseases
Live research webinar series 2.0: the right nutrients and drugs for you (the promises of precision health). [Video] (2020)
Genetic disorders
The molecular genetics and pathogenesis of cystic fibrosis lung disease. Buletin Persatuan Genetik Malaysia, 12 (2). pp. 10-17. ISSN 1394-5750 (2006)
Genetic studies
The genetic perspektif on human diversity in Malaysia. Buletin Persatuan Genetik Malaysia, 11 (1). pp. 14-16. ISSN 1394-5750 (2005)
Genetic test
Knowledge and awareness of genetic test available for risk of breast cancer among female students in UiTM. Al-Rafidain Journal of Medical Sciences, 1 (2). pp. 14-18. ISSN 2789-3219 (2021)
Genetic test kit
Moving forward with precision medicine: detection of hypersensitivity to drug reactions using HLA-B*15:02 genetic test kit. [Video] (2017)
Genetic variants
Genetic analysis of a young adult presented with acute myocardial infarction with no traditional risk factors: a novel case report. Malaysian Journal of Medicine and Health Sciences, 18 (1). pp. 349-352. ISSN 2636-9346 (2022)
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Genetic variation
Live research webinar series 2.0: the right nutrients and drugs for you (the promises of precision health). [Video] (2020)
Genetics
Appreciating the richness of nature through genetics: discovering new genetic species. Buletin Persatuan Genetik Malaysia, 19 (1 & 2). ISSN 1394-5750 (2012)
The predictive ability of total genotype score and serum metabolite markers in power-based sports performance following different strength training intensities — a pilot study. Pertanika Journal of Science & Technology, 31 (2). pp. 1087-1103. ISSN 2231-8526 (2022)
Predictor of academic performance: personality traits and catechol-O-methyltransferase polymorphisms. International Journal of Evaluation and Research in Education (IJERE), 13 (2). pp. 979-986. ISSN 2252-8822 (2024)
Genetik Manusia
Podcast Ubat atau Tabu Ep 3: Ujian Genetik | Genetic Testing. [Website] (2024)
Genom manusia
Penyelidikan Genom Melayu di Malaysia: Konsep, pencapaian & kajian lanjutan dari perspektif Islam. In: TeSSHI 2014- Technology, Science Social Sciences, Humanities, 5-6 November 2014, One Helang Hotel, Langkawi. (2014)
Genome
Moving forward with precision medicine: detection of hypersensitivity to drug reactions using HLA-B*15:02 genetic test kit. [Video] (2017)
Genome Mapping
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy. PLOS ONE. pp. 1-16. ISSN 1932-6203 (2016)
Genome sequence
Genomic map of blood group alleles in Malaysian indigenous Orang Asli population from whole genome sequences. medRxiv. pp. 1-31. (Unpublished) (2021)
Genome surveillance
Genomic Alterations
Acquired radioresistance in EMT6 mouse mammary carcinoma cell line is mediated by CTLA-4 and PD-1 through JAK/STAT/PI3K pathway. scientific reports, 13. ISSN 2045-2322 (2023)
Genomic DNA
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy. PLOS ONE. pp. 1-16. ISSN 1932-6203 (2016)
Genomic Profiling
Acquired radioresistance in EMT6 mouse mammary carcinoma cell line is mediated by CTLA-4 and PD-1 through JAK/STAT/PI3K pathway. scientific reports, 13. ISSN 2045-2322 (2023)
Genomic traits
Securing DNA information from selective attacks on humans. Journal of Media and Information Warfare, 4. pp. 93-104. ISSN 2821-3394 (2011)
Genotypic Data
Towards Development of Clustering Applications for Large-Scale Comparative Genotyping and Kinship Analysis Using Y-Short Tandem Repeats. OMICS A Journal of Integrative Biology, 19 (6). pp. 361-367. ISSN 1557-8100 (2015)
Genotyping
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy. PLOS ONE. pp. 1-16. ISSN 1932-6203 (2016)
The effects of genetic variants towards weight and biochemical changes in weight management program. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 269-277. ISSN 2289-392X (2023)
Gestational Diabetes Mellitus (GDM)
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Glucose Homeostasis
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
Grade point average
Association of COMT polymorphism and academic achievement among female undergraduate students. Science Letters, 15 (2). pp. 90-101. ISSN 2682-8626 (2021)
HGP
A review of human genome project (HGP) from ethical perspectives. International Journal of Advanced and Applied Sciences, 4 (12). pp. 125-132. ISSN 2313-3724 (2017)
HLA-B*15:02
Moving forward with precision medicine: detection of hypersensitivity to drug reactions using HLA-B*15:02 genetic test kit. [Video] (2017)
The gene that turns epilepsy treatment deadly. [Website]
Hepcidin levels
TMPRSS6 gene polymorphisms associated with iron deficiency anaemia among global population. Egyptian Journal of Medical Human Genetics, 23: 147. pp. 1-16. ISSN 2090-2441 (2022)
Hugo pan-asia snp inisiative
The genetic perspektif on human diversity in Malaysia. Buletin Persatuan Genetik Malaysia, 11 (1). pp. 14-16. ISSN 1394-5750 (2005)
Human Genetic
A review of human genome project (HGP) from ethical perspectives. International Journal of Advanced and Applied Sciences, 4 (12). pp. 125-132. ISSN 2313-3724 (2017)
Human attack
Securing DNA information from selective attacks on humans. Journal of Media and Information Warfare, 4. pp. 93-104. ISSN 2821-3394 (2011)
Human diversity
The genetic perspektif on human diversity in Malaysia. Buletin Persatuan Genetik Malaysia, 11 (1). pp. 14-16. ISSN 1394-5750 (2005)
Infinium asian screening array
Genetic analysis of a young adult presented with acute myocardial infarction with no traditional risk factors: a novel case report. Malaysian Journal of Medicine and Health Sciences, 18 (1). pp. 349-352. ISSN 2636-9346 (2022)
Information security
Securing DNA information from selective attacks on humans. Journal of Media and Information Warfare, 4. pp. 93-104. ISSN 2821-3394 (2011)
Insulin Sensitivity
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
Insulin Signaling Pathway
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
Integrative Pharmacogenomics Institute (iPROMISE)
Towards Development of Clustering Applications for Large-Scale Comparative Genotyping and Kinship Analysis Using Y-Short Tandem Repeats. OMICS A Journal of Integrative Biology, 19 (6). pp. 361-367. ISSN 1557-8100 (2015)
Iron defciency
TMPRSS6 gene polymorphisms associated with iron deficiency anaemia among global population. Egyptian Journal of Medical Human Genetics, 23: 147. pp. 1-16. ISSN 2090-2441 (2022)
Iron defciency anaemia
TMPRSS6 gene polymorphisms associated with iron deficiency anaemia among global population. Egyptian Journal of Medical Human Genetics, 23: 147. pp. 1-16. ISSN 2090-2441 (2022)
Karyotypes
Karyotype pattern and maternal age distribution in down syndrome patients analyzed at Human Genome Center, University Sains Malaysia, Kelantan. Buletin Persatuan Genetik Malaysia, 12 (2). p. 1. ISSN 1394-5750 (2006)
LDLR gene
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
Lifestyle
Lifestyle Causes of Male Infertility. Arab Journal of Urology, 16 (1). pp. 10-20. ISSN 2090-5998 (2018)
Lifestyle causes of male infertility. Arab Journal of Urology, 16 (1). ISSN 2090-5998 (2018)
Linoleic acid
Interaction of dietary linoleic acid and α-linolenic acids with rs174547 in FADS1 gene on metabolic syndrome components among vegetarians. Nutrients, 11 (7). pp. 1-16. ISSN 2072-6643 (2019)
MCF-7
Combinatorial Cytotoxic Effects of Damnacanthal and Doxorubicin against Human Breast Cancer MCF-7 Cells in Vitro. Molecules, 21 (9). ISSN 1420-3049 (2016)
Malaysia dan Islam
Penyelidikan Genom Melayu di Malaysia: Konsep, pencapaian & kajian lanjutan dari perspektif Islam. In: TeSSHI 2014- Technology, Science Social Sciences, Humanities, 5-6 November 2014, One Helang Hotel, Langkawi. (2014)
Malaysian population
Mitochondrial DNA mutations in Malaysian female breast cancer patients. PLOS ONE, 15 (5). pp. 1-18. ISSN 1932-6203 (2020)
Male Infertility
Lifestyle Causes of Male Infertility. Arab Journal of Urology, 16 (1). pp. 10-20. ISSN 2090-5998 (2018)
Lifestyle causes of male infertility. Arab Journal of Urology, 16 (1). ISSN 2090-5998 (2018)
Melayu
Penyelidikan Genom Melayu di Malaysia: Konsep, pencapaian & kajian lanjutan dari perspektif Islam. In: TeSSHI 2014- Technology, Science Social Sciences, Humanities, 5-6 November 2014, One Helang Hotel, Langkawi. (2014)
Meta-analysis
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Metabolic syndromes
Interaction of dietary linoleic acid and α-linolenic acids with rs174547 in FADS1 gene on metabolic syndrome components among vegetarians. Nutrients, 11 (7). pp. 1-16. ISSN 2072-6643 (2019)
Metabolomics
The predictive ability of total genotype score and serum metabolite markers in power-based sports performance following different strength training intensities — a pilot study. Pertanika Journal of Science & Technology, 31 (2). pp. 1087-1103. ISSN 2231-8526 (2022)
Methylation
MicroRNA methylome signature and their functional roles in colorectal cancer diagnosis, prognosis, and chemoresistance. International Journal of Molecular Sciences, 23 (13). pp. 1-16. ISSN 1422-0067 (2022)
MicroRNA
MicroRNA methylome signature and their functional roles in colorectal cancer diagnosis, prognosis, and chemoresistance. International Journal of Molecular Sciences, 23 (13). pp. 1-16. ISSN 1422-0067 (2022)
Microbiota
Dysbiosis and the chemopreventive role of prebiotics in colorectal cancer. Journal of Applied Biotechnology Reports, 10 (2). pp. 943-957. ISSN 2423-5784 (2023)
Mitochondrial DNA (mtDNA)
Mitochondrial DNA mutations in Malaysian female breast cancer patients. PLOS ONE, 15 (5). pp. 1-18. ISSN 1932-6203 (2020)
Mitochondrial Respiration
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
Mitral Valve Prolapse
Sudden cardiac arrest in a patient with malignant mitral valve prolapse with CACNB2 gene mutation: a simple coincidence or coexistence?—a case report. European Heart Journal, 7 (4). pp. 1-6. ISSN 2514-2119 (2023)
Next-generation sequencing (NGS)
Mitochondrial DNA mutations in Malaysian female breast cancer patients. PLOS ONE, 15 (5). pp. 1-18. ISSN 1932-6203 (2020)
Obesity
A review on the association of Fat Mass Obesity Associated (FTO) gene marker rs9939609 with obesity and Body Mass Index(BMI). Buletin Sains Kesihatan (BSK), 5 (1). pp. 11-20. ISSN 2550-1852 (2021)
The effects of genetic variants towards weight and biochemical changes in weight management program. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 269-277. ISSN 2289-392X (2023)
Development of PCR-based genotyping method for Fat Mass Obesity-Associated (FTO) gene polymorphism RS9939609. Journal of Health and Translational Medicine (JUMMEC), 2 (SI). pp. 51-54. ISSN 2289-392X (2023)
Odds ratio
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Orang Asli
The genetic perspektif on human diversity in Malaysia. Buletin Persatuan Genetik Malaysia, 11 (1). pp. 14-16. ISSN 1394-5750 (2005)
Genomic map of blood group alleles in Malaysian indigenous Orang Asli population from whole genome sequences. medRxiv. pp. 1-31. (Unpublished) (2021)
Oxygen Consumption Rate
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
PCR method
Development of a PCR test for detection of warfarin resistance based on the polymorphism of VKORC1 genes. Degree thesis, Universiti Teknologi MARA, Shah Alam. (2012)
PCSK9 gene
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
Personality traits
Predictor of academic performance: personality traits and catechol-O-methyltransferase polymorphisms. International Journal of Evaluation and Research in Education (IJERE), 13 (2). pp. 979-986. ISSN 2252-8822 (2024)
Personalized medicine
The gene that turns epilepsy treatment deadly. [Website]
Pharmacokinetics
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
Phole Genome Sequence
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
Polymorphism
Development of a PCR test for detection of warfarin resistance based on the polymorphism of VKORC1 genes. Degree thesis, Universiti Teknologi MARA, Shah Alam. (2012)
Polymorphisms
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
Prebiotics
Dysbiosis and the chemopreventive role of prebiotics in colorectal cancer. Journal of Applied Biotechnology Reports, 10 (2). pp. 943-957. ISSN 2423-5784 (2023)
Precision Health
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
Precision Medicine
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
Preventive and personalised medicine
Genetic analysis of a young adult presented with acute myocardial infarction with no traditional risk factors: a novel case report. Malaysian Journal of Medicine and Health Sciences, 18 (1). pp. 349-352. ISSN 2636-9346 (2022)
Probiotics
Dysbiosis and the chemopreventive role of prebiotics in colorectal cancer. Journal of Applied Biotechnology Reports, 10 (2). pp. 943-957. ISSN 2423-5784 (2023)
RBC antigens
Genomic map of blood group alleles in Malaysian indigenous Orang Asli population from whole genome sequences. medRxiv. pp. 1-31. (Unpublished) (2021)
RT-PCR (Reverse Transcription Polymerase Chain Reaction)
Acquired radioresistance in EMT6 mouse mammary carcinoma cell line is mediated by CTLA-4 and PD-1 through JAK/STAT/PI3K pathway. scientific reports, 13. ISSN 2045-2322 (2023)
Risk Factors
Lifestyle Causes of Male Infertility. Arab Journal of Urology, 16 (1). pp. 10-20. ISSN 2090-5998 (2018)
Lifestyle causes of male infertility. Arab Journal of Urology, 16 (1). ISSN 2090-5998 (2018)
Risk alleles
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Rs9939609
A review on the association of Fat Mass Obesity Associated (FTO) gene marker rs9939609 with obesity and Body Mass Index(BMI). Buletin Sains Kesihatan (BSK), 5 (1). pp. 11-20. ISSN 2550-1852 (2021)
ST-elevation
Genetic analysis of a young adult presented with acute myocardial infarction with no traditional risk factors: a novel case report. Malaysian Journal of Medicine and Health Sciences, 18 (1). pp. 349-352. ISSN 2636-9346 (2022)
Semen Quality
Lifestyle Causes of Male Infertility. Arab Journal of Urology, 16 (1). pp. 10-20. ISSN 2090-5998 (2018)
Lifestyle causes of male infertility. Arab Journal of Urology, 16 (1). ISSN 2090-5998 (2018)
Single Nucleotide Polymorphism (SNP)
A review on the association of Fat Mass Obesity Associated (FTO) gene marker rs9939609 with obesity and Body Mass Index(BMI). Buletin Sains Kesihatan (BSK), 5 (1). pp. 11-20. ISSN 2550-1852 (2021)
Single Nucleotide Polymorphisms (SNPs)
Meta-analysis of the genetic factors that predisposed asian women to gestational diabetes mellitus. Malaysian Journal of Pharmaceutical Sciences, 19 (2). pp. 131-152. ISSN 2180-429X (2021)
Single nucleotide polymorphism
Interaction of dietary linoleic acid and α-linolenic acids with rs174547 in FADS1 gene on metabolic syndrome components among vegetarians. Nutrients, 11 (7). pp. 1-16. ISSN 2072-6643 (2019)
The predictive ability of total genotype score and serum metabolite markers in power-based sports performance following different strength training intensities — a pilot study. Pertanika Journal of Science & Technology, 31 (2). pp. 1087-1103. ISSN 2231-8526 (2022)
Somatic mutations
Mitochondrial DNA mutations in Malaysian female breast cancer patients. PLOS ONE, 15 (5). pp. 1-18. ISSN 1932-6203 (2020)
Sperm DNA Fragmen-tation
Lifestyle causes of male infertility. Arab Journal of Urology, 16 (1). ISSN 2090-5998 (2018)
Sperm DNA Fragmentation
Lifestyle Causes of Male Infertility. Arab Journal of Urology, 16 (1). pp. 10-20. ISSN 2090-5998 (2018)
Strength training
The predictive ability of total genotype score and serum metabolite markers in power-based sports performance following different strength training intensities — a pilot study. Pertanika Journal of Science & Technology, 31 (2). pp. 1087-1103. ISSN 2231-8526 (2022)
Sudden Cardiac Death
Sudden cardiac arrest in a patient with malignant mitral valve prolapse with CACNB2 gene mutation: a simple coincidence or coexistence?—a case report. European Heart Journal, 7 (4). pp. 1-6. ISSN 2514-2119 (2023)
Sunda Shelf region
Appreciating the richness of nature through genetics: discovering new genetic species. Buletin Persatuan Genetik Malaysia, 19 (1 & 2). ISSN 1394-5750 (2012)
Surveillance program
Synbiotics
Dysbiosis and the chemopreventive role of prebiotics in colorectal cancer. Journal of Applied Biotechnology Reports, 10 (2). pp. 943-957. ISSN 2423-5784 (2023)
TMPRSS6 gene and single nucleotide polymorphisms
TMPRSS6 gene polymorphisms associated with iron deficiency anaemia among global population. Egyptian Journal of Medical Human Genetics, 23: 147. pp. 1-16. ISSN 2090-2441 (2022)
Training response
The predictive ability of total genotype score and serum metabolite markers in power-based sports performance following different strength training intensities — a pilot study. Pertanika Journal of Science & Technology, 31 (2). pp. 1087-1103. ISSN 2231-8526 (2022)
Type-2 Diabetes
Catalpol Ameliorates Insulin Sensitivity and Mitochondrial Respiration in Skeletal Muscle of Type-2 Diabetic Mice Through Insulin Signaling Pathway and AMPK/SIRT1/PGC-1α/PPAR-γ Activation. Biomolecules, 10 (10). ISSN 2218-273X (2020)
UGT1A6
The implication of the polymorphisms of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease patients treated with aspirin. The Journal of Pharmacy and Pharmaceutical Sciences (JPPS), 18 (3). pp. 474-483. ISSN 1482-1826 (2015)
UiTM’s Genomic Testing Services
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
Ujian Genetik
Podcast Ubat atau Tabu Ep 3: Ujian Genetik | Genetic Testing. [Website] (2024)
Universiti Teknologi MARA (UiTM)
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
Towards Development of Clustering Applications for Large-Scale Comparative Genotyping and Kinship Analysis Using Y-Short Tandem Repeats. OMICS A Journal of Integrative Biology, 19 (6). pp. 361-367. ISSN 1557-8100 (2015)
Up-Regulated Genes
Acquired radioresistance in EMT6 mouse mammary carcinoma cell line is mediated by CTLA-4 and PD-1 through JAK/STAT/PI3K pathway. scientific reports, 13. ISSN 2045-2322 (2023)
VKORCI
Development of a PCR test for detection of warfarin resistance based on the polymorphism of VKORC1 genes. Degree thesis, Universiti Teknologi MARA, Shah Alam. (2012)
Vegetarians
Interaction of dietary linoleic acid and α-linolenic acids with rs174547 in FADS1 gene on metabolic syndrome components among vegetarians. Nutrients, 11 (7). pp. 1-16. ISSN 2072-6643 (2019)
Warfarin therapy
Development of a PCR test for detection of warfarin resistance based on the polymorphism of VKORC1 genes. Degree thesis, Universiti Teknologi MARA, Shah Alam. (2012)
Weight Management Program
The effects of genetic variants towards weight and biochemical changes in weight management program. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 269-277. ISSN 2289-392X (2023)
Y-chromosome Short Tandem Repeats (Y-STRs)
Towards Development of Clustering Applications for Large-Scale Comparative Genotyping and Kinship Analysis Using Y-Short Tandem Repeats. OMICS A Journal of Integrative Biology, 19 (6). pp. 361-367. ISSN 1557-8100 (2015)
Young onset myocardial infarction
Genetic analysis of a young adult presented with acute myocardial infarction with no traditional risk factors: a novel case report. Malaysian Journal of Medicine and Health Sciences, 18 (1). pp. 349-352. ISSN 2636-9346 (2022)
Zakesy Biotech Sdn. Bhd.
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
animals
Genetics Research In Malaysia: Suggested Priorities. Buletin Persatuan Genetik Malaysia, 10 (2). pp. 5-6. ISSN 1394-5750 (2004)
cryptic species identification
Genetics Research In Malaysia: Suggested Priorities. Buletin Persatuan Genetik Malaysia, 10 (2). pp. 5-6. ISSN 1394-5750 (2004)
familial hypercholesterolaemia
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
genetic testing
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
humans, plants
Genetics Research In Malaysia: Suggested Priorities. Buletin Persatuan Genetik Malaysia, 10 (2). pp. 5-6. ISSN 1394-5750 (2004)
iPROMISE
UiTM And BP Healthcare Group Launch New Genomic Testing In Malaysia. [Website]
k-Approximate Modal Haplotype (k-AMH)
Towards Development of Clustering Applications for Large-Scale Comparative Genotyping and Kinship Analysis Using Y-Short Tandem Repeats. OMICS A Journal of Integrative Biology, 19 (6). pp. 361-367. ISSN 1557-8100 (2015)
mtDNA alterations
Mitochondrial DNA mutations in Malaysian female breast cancer patients. PLOS ONE, 15 (5). pp. 1-18. ISSN 1932-6203 (2020)
next generation sequencing
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
pathogenic variants
Genetic spectrum of familial hypercholesterolaemia in the Malaysian community: identification of pathogenic gene variants using targeted next-generation sequencing. International Journal of Molecular Sciences, 23. pp. 1-25. ISSN 1422-0067 (2022)
rs4680
Association of COMT polymorphism and academic achievement among female undergraduate students. Science Letters, 15 (2). pp. 90-101. ISSN 2682-8626 (2021)
α-linolenic acid
Interaction of dietary linoleic acid and α-linolenic acids with rs174547 in FADS1 gene on metabolic syndrome components among vegetarians. Nutrients, 11 (7). pp. 1-16. ISSN 2072-6643 (2019)