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Nur Afiqah Mohamad

Observed names: Mohamad N.A., Mohamad, Nur Afiqah, Nur Afiqa Mohamad
ORCID: 0000-0002-9015-0525
Observed ORCID: 0000-0002-9015-0525
OpenAlex ID: A5067533695
Deciduous DPSCs Ameliorate MPTP-Mediated Neurotoxicity, Sensorimotor Coordination and Olfactory Function in Parkinsonian Mice
2019 · Christopher Simon, Quan Fu Gan, et al. · International Journal of Molecular Sciences · 36
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Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects
2019 · Nur Afiqah Mohamad, Vasudevan Ramachandran, et al. · Human Genomics · 21
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High-frequency repetitive transcranial magnetic stimulation at dorsolateral prefrontal cortex for migraine prevention: A systematic review and meta-analysis
2022 · Nabil Izzaatie Mohamad Safiai, Nur Afiqah Mohamad, et al. · Cephalalgia · 16
Association of GCK (rs1799884), GCKR (rs780094), and G6PC2 (rs560887) Gene Polymorphisms with Type 2 Diabetes among Malay Ethnics
2023 · Neda Ansari, Vasudevan Ramachandran, et al. · Global Medical Genetics · 14
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In Vitro Blood-Brain Barrier Models for Neuroinfectious Diseases: A Narrative Review
2023 · Ahmad Hussein Badawi, Nur Afiqah Mohamad, et al. · Current Neuropharmacology · 13
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Analysis of OCT1, OCT2 and OCT3 gene polymorphisms among Type 2 diabetes mellitus subjects in Indian ethnicity, Malaysia
2021 · Sabah Ghasan Abood Al-Ashoor, Vasudevan Ramachandran, et al. · Saudi Journal of Biological Sciences · 12
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High-frequency repetitive transcranial magnetic stimulation at dorsolateral prefrontal cortex for migraine prevention: A protocol for a systematic review of controlled trials
2021 · Nabil Izzaatie Mohamad Safiai, Nur Afiqah Mohamad, et al. · PLoS ONE · 10
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Association of Endothelin-Converting Enzyme and Endothelin-1 Gene Polymorphisms with Essential Hypertension in Malay Ethnics
2022 · Elnaz Salim, Vasudevan Ramachandran, et al. · Genetics Research · 7
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Successful Aspects and Impacts of Diabetic Foot Exercise Among Indonesian Type 2 Diabetes Mellitus Patients: A Literature Review
2024 · Healthy Seventina Sirait, Faridah Mohd Said, et al. · International Journal of Advancement in Life Sciences Research · 6
Analysis of homocysteine metabolism enzyme gene polymorphisms in non-syndromic congenital heart disease patients among Malaysians
2014 · Nur Afiqah Mohamad, Vasudevan Ramachandran, et al. · Universiti Putra Malaysia Institutional Repository (Universiti Putra Malaysia) · 6
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A review of the neuroprotective effects of andrographolide in Alzheimer's disease
2021 · Zahra Abedi, Hamidon Basri, et al. · Oriental Pharmacy and Experimental Medicine · 5
Analysis of Angiotensin Converting Enzyme, Endothelial Nitric Oxide Synthase & Serotonin Gene Polymorphisms among Atrial Septal Defect Subjects with and without Pulmonary Arterial Hypertension
2018 · Nur Ilyana Jaafar, Ramachandran Vasudevan, et al. · Journal of Cardiovascular Development and Disease · 5
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Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian family
2023 · Nurul Huda Musa, Karuppiah Thilakavathy, et al. · Frontiers in Genetics · 4
Analysis of the association between CFH Y402H polymorphism and response to intravitreal ranibizumab in patients with neovascular age-related macular degeneration (nAMD)
2018 · Nur Afiqah Mohamad, Vasudevan Ramachandran, et al. · Biomolecules and Biomedicine · 4
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Genotyping of GATA4 Gene Variant (G296S) in Malaysian Congenital Heart Disease Subjects by Real-Time PCR High Resolution Melting Analysis
2013 · Nora Fawzi, Ramachandran Vasudevan, et al. · Journal of Medical Biochemistry · 4
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Transcranial direct current stimulation with multiple oral re-reading therapy for pure alexia without agraphia: a case report
2021 · Nur Afiqah Mohamad, Siti Nadia Che Adinan, et al. · Neurocase · 3
Prevalence and treatment patterns of ranibizumab and photodynamic therapy in a tertiary care setting in Malaysia
2017 · Nur Afiqah Mohamad, Vasudevan Ramachandran, et al. · International Journal of Ophthalmology · 3
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Analysis of Human Bradykinin Receptor Gene and Endothelial Nitric Oxide Synthase Gene Polymorphisms in End-Stage Renal Disease Among Malaysians
2014 · Vasudevan R., Ismail P., et al. · Balkan Journal of Medical Genetics · 3
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A Review of the Social Participation of Stroke Survivors
2024 · Xu Yirong, Nur Afiqah Mohamad, et al. · International journal of Emerging Issues in Social Science Arts and Humanities · 2
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VEGF Polymorphisms Among Neovascular Age-Related Macular Degenerative Subjects in a Multiethnic Population
2017 · Nur Afiqah Mohamad, Vasudevan Ramachandran, et al. · Genetic Testing and Molecular Biomarkers · 2
Association of copy number variations in complement factor H‐Related genes among age‐related macular degenerative subjects
2017 · Norshakimah Md Bakri, Vasudevan Ramachandran, et al. · The Kaohsiung Journal of Medical Sciences · 2
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Application of Capability-Opportunity-Motivation-Behavior Model in the Study of Influencing Factors of Social Participation in Stroke
2024 · Xu Yirong, Nur Afiqah Mohamad, et al. · International Journal of Biotechnology and Biomedicine · 1
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Establishing a hyperacute stroke service during the COVID-19 pandemic: our institution’s one year experience
2023 · Anna Misya’il Abdul Rashid, Mohamad Syafeeq Faeez Md Noh, et al. · BMC Neurology · 1
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Copy number variation in VEGF gene as a biomarker of susceptibility to age-related macular degeneration
2017 · Norshakimah Md Bakri, Vasudevan Ramachandran, et al. · Egyptian Journal of Medical Human Genetics · 1
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R102G polymorphism of the complement component 3 gene in Malaysian subjects with neovascular age-related macular degeneration
2017 · Nur Afiqah Mohamad, Vasudevan Ramachandran, et al. · Egyptian Journal of Medical Human Genetics · 1
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Works count: 33
Citation count: 182
H-index: 7
I10-index: 7
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