Area of research
Molecular Biology · Materials Chemistry
Research interest
Research interests include PI3K/AKT/mTOR signaling in cancer, Crystallization and Solubility Studies, X-ray Diffraction in Crystallography, and Chemical Synthesis and Analysis.
The Case for Neurosurgical Intervention in Cancer Neuroscience
Landmine Injury Resulting in Comminuted Lumbar Facet Fracture as a Cause of Lumbar Stenosis and Spondylolisthesis.
Delayed Rupture of an Anterior Communicating Artery Aneurysm After Elective Woven Endobridge Embolization, Re-Treated With Microsurgical Clipping: Operative Technique and Systematic Review.
Transcranial MR-Guided Focused Ultrasound and Hyperostosis Calvariae Diffusa: Case Report and Systematic Review of the Literature.
Metformin Attenuates Renal Fibrosis in a Mouse Model of Adenine-Induced Renal Injury Through Inhibiting TGF-β1 Signaling Pathways
Artificial Intelligence in the Management of Glioma: Era of Personalized Medicine
A Rare Mutation of β1-Adrenergic Receptor Affects Sleep/Wake Behaviors
Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy.
Treatment-refractory Escherichia coli subdural empyema caused by infection of a chronic subdural hematoma in an infant.
Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases
Biochemical and Epigenetic Insights into L-2-Hydroxyglutarate, a Potential Therapeutic Target in Renal Cancer
Neurodegenerative disease biomarkers Aβ<sub>1–40</sub>, Aβ<sub>1–42</sub>, tau, and p‐tau<sub>181</sub> in the vervet monkey cerebrospinal fluid: Relation to normal aging, genetic influences, and cerebral amyloid angiopathy
Cerebellar tonsil ectopia measurement in type I Chiari malformation patients show poor inter-operator reliability
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction
Machine learning for large‐scale wearable sensor data in Parkinson's disease: Concepts, promises, pitfalls, and futures
Intratumoral heterogeneity identified at the epigenetic, genetic and transcriptional level in glioblastoma
Mouse Models of Diabetes, Obesity and Related Kidney Disease
SIRT1 Deficiency in Microglia Contributes to Cognitive Decline in Aging and Neurodegeneration via Epigenetic Regulation of IL-1β
The Emerging Picture of Autism Spectrum Disorder: Genetics and Pathology
A Multiancestral Genome-Wide Exome Array Study of Alzheimer Disease, Frontotemporal Dementia, and Progressive Supranuclear Palsy
Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
An Epigenetic Signature in Peripheral Blood Associated with the Haplotype on 17q21.31, a Risk Factor for Neurodegenerative Tauopathy
Reductions in Brain 5-HT1B Receptor Availability in Primarily Cocaine-Dependent Humans
Blockade of KCa3.1 Ameliorates Renal Fibrosis Through the TGF-β1/Smad Pathway in Diabetic Mice
Succinate dehydrogenase-deficient GISTs are characterized by IGF1R overexpression