Patcharee Lertrit
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Genetic Neurodegenerative Diseases, Forensic and Genetic Research
Most-Cited Works
- → The prehistoric peopling of Southeast Asia(2018)521 cited
- A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.(1991)
- → Normal variants of human mitochondrial DNA and translation products: the building of a reference data base(1991)81 cited
- A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.(1992)
- → Whole Exome Sequencing in Thai Patients With Retinitis Pigmentosa Reveals Novel Mutations in Six Genes(2014)50 cited
- → Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy(2002)48 cited
- → Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand(2010)48 cited
- → Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis(2008)39 cited
- → Mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations(2013)36 cited
- → Stability of Epitheliotrophic Factors in Autologous Serum Eye Drops from Chronic Stevens-Johnson Syndrome Dry Eye Compared to Non-autoimmune Dry Eye(2011)34 cited