Z.A.M.H. Zabidi-Hussin

Author

Also Known As

H. Nishio, Z A M H Zabidi-Hussin, Z. A. M. H. Zabidi-Hussin, Z.A.M.H. Zabidi-Hussin, Zabidi AMH Zabidi‐Hussin, Zabidi Azhar Mohd Hussin Zabidi-Hussin, Zabidi Zabidi-Hussin

Publications

223

Citations

H-Index

Concepts

All Affiliations

Universiti Sains Malaysia Sultanah Aminah Hospital Hospital Kuala Lumpur

About

Z.A.M.H. Zabidi-Hussin is an author at Universiti Sains Malaysia specializing in pathology, medicine, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	80
2	Molecular Genetics	2	2	26
3	Public Health	1	1	15
4	Cell Biology	1	1	13
5	Immunology	1	1	15

Z.A.M.H. Zabidi-Hussin

Publications

115

Citations

H-Index

Page 1

	Year	Citations
Biochemical profiling to predict disease severity in metachromatic leukodystrophy Mohd Adi Firdaus Tan, Maria Fuller, Z.A.M.H. Zabidi-Hussin, Molecular Genetics and Metabolism RheumatologyAutoimmune DiseaseMedicinePathologyBiomarkers	2009	30
Curricular Trends in Malaysian Medical Schools: Innovations Within Nor Azila, Rogayah Ja'afar, Z.A.M.H. Zabidi-Hussin Annals of the Academy of Medicine Singapore	2006	25
Two Novel Gross Deletions of TSC2 in Malaysian Patients with Tuberous Sclerosis Complex and TSC2/PKD1 Contiguous Deletion Syndrome Nur Farrah Dila Ismail, Nik Mohd Ariff Nik Abdul Malik, Jafar Mohseni, Japanese Journal of Clinical Oncology Malaysian PatientsGeneticsImmunologyPathologyMolecular Genetics	2014	15
Transcript, methylation and molecular docking analyses of the effects of HDAC inhibitors, SAHA and Dacinostat, on SMN2 expression in fibroblasts of SMA patients Jafar Mohseni, Belal O. Al‐Najjar, Habibah A. Wahab, Journal of Human Genetics Hdac InhibitorsSmn2 ExpressionOncogenic AgentMedicineMolecular Docking Analyses	2016	13
Mutation Spectrum of<i>Dystrophin</i>Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy Abdul Qawee Rani, Teguh Haryo Sasongko, Sarina Sulong, Journal of Neurogenetics Genetic DiseasesExon DuplicationMendelian DisorderGenetic DisorderMedicine	2013	11
Combination of Multiple Ligation-Dependent Probe Amplification and Illumina MiSeq Amplicon Sequencing for TSC1/TSC2 Gene Analyses in Patients with Tuberous Sclerosis Complex Nur Farrah Dila Ismail, Abdul Qawee Rani, Nik Mohd Ariff Nik Abdul Malik, Journal of Molecular Diagnostics Tuberous Sclerosis ComplexGenetic DisorderMedicineGeneticsNext-generation Sequencing	2017	11
Practical way of creating differential diagnoses through an expanded VITAMINSABCDEK mnemonic Z.A.M.H. Zabidi-Hussin Advances in Medical Education and Practice	2016	10

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