Publications by authors named "Patcharee Lertrit"

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Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber's hereditary optic neuropathy: A case report.
Wanicha Leetiratanai Chuenkongkaew, Buakhwan Chinkulkitnivat, Patcharee Lertrit, Niphon Chirapapaisan, Supannee Kaewsutthi

World J Clin Cases· July 2022

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Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome.
Kirana Veenin, Duangrurdee Wattanasirichaigoon, Bhoom Suktitipat, Saisuda Noojarern, Patcharee Lertrit

Front Pediatr· May 2022

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The prehistoric peopling of Southeast Asia.
Hugh McColl, Fernando Racimo, Lasse Vinner, Fabrice Demeter, Takashi Gakuhari, Patcharee Lertrit

Science· July 2018

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Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.
Worapoj Jinda, Todd D Taylor, Yutaka Suzuki, Wanna Thongnoppakhun, Chanin Limwongse, Patcharee Lertrit

Invest Ophthalmol Vis Sci· April 2017

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A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.
Worapoj Jinda, Naravat Poungvarin, Todd D Taylor, Yutaka Suzuki, Wanna Thongnoppakhun, Patcharee Lertrit

Mol Vis· November 2016

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Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutation.
Aung Win Tun, Sakdithep Chaiyarit, Supannee Kaewsutthi, Wanphen Katanyoo, Wanicha Chuenkongkaew, Patcharee Lertrit

PLoS One· May 2015

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Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai population.
Hathaichanoke Boonyarit, Surakameth Mahasirimongkol, Nuttama Chavalvechakul, Masayuki Aoki, Hanae Amitani, Patcharee Lertrit

Forensic Sci Int Genet· July 2014

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Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes.
Worapoj Jinda, Todd D Taylor, Yutaka Suzuki, Wanna Thongnoppakhun, Chanin Limwongse, Patcharee Lertrit

Invest Ophthalmol Vis Sci· April 2014

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Mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations.
Lanka Ranaweera, Supannee Kaewsutthi, Aung Win Tun, Hathaichanoke Boonyarit, Samerchai Poolsuwan, Patcharee Lertrit

J Hum Genet· January 2014

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Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand.
Rochmy Istikharah, Aung Win Tun, Supannee Kaewsutthi, Pratibha Aryal, Bussaraporn Kunhapan, Patcharee Lertrit

Exp Eye Res· November 2013

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Polyglutamined expanded androgen receptor interacts with chaperonin CCT.
Suttikarn Pongtepaditep, Thawornchai Limjindaporn, Patcharee Lertrit, Chatchawan Srisawat, Chanin Limwongse

Eur J Med Genet· November 2012

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Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye.
Nopasak Phasukkijwatana, Patcharee Lertrit, Sompong Liammongkolkul, Pinnita Prabhasawat

Curr Eye Res· September 2011

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Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.
Supannee Kaewsutthi, Nopasak Phasukkijwatana, Yutthana Joyjinda, Wanicha Chuenkongkaew, Bussaraporn Kunhapan, Patcharee Lertrit

Invest Ophthalmol Vis Sci· July 2011

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Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand.
Nopasak Phasukkijwatana, Bussaraporn Kunhapan, Jim Stankovich, Wanicha L Chuenkongkaew, Russell Thomson, Patcharee Lertrit

Hum Genet· July 2010

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Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis.
Patcharee Lertrit, Samerchai Poolsuwan, Rachanie Thosarat, Thitima Sanpachudayan, Hathaichanoke Boonyarit

Am J Phys Anthropol· December 2008

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Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation.
Komon Luangtrakool, Farrah-Yasmin Tate, Rachael Shepherd, Sarah Campbell, Carolyn M Sue, Patcharee Lertrit

Southeast Asian J Trop Med Public Health· July 2008

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Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.
Nopasak Phasukkijwatana, Wanicha L Chuenkongkaew, Rungnapa Suphavilai, Komon Luangtrakool, Bussaraporn Kunhapan, Patcharee Lertrit

J Hum Genet· February 2007

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Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
Pattamon Tharaphan, Wanicha L Chuenkongkaew, Komon Luangtrakool, Thitima Sanpachudayan, Bhoom Suktitipat, Patcharee Lertrit

J Neuroophthalmol· December 2006

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The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.
Nopasak Phasukkijwatana, Wanicha L Chuenkongkaew, Rungnapa Suphavilai, Bhoom Suktitipat, Sarinee Pingsuthiwong, Patcharee Lertrit

J Hum Genet· May 2006

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Proportion of 11778 mutant mitochondrial DNA and clinical expression in a thai population with leber hereditary optic neuropathy.
Wanicha L Chuenkongkaew, Rungnapa Suphavilai, Lookjan Vaeusorn, Nopasak Phasukkijwatana, Patcharee Lertrit

J Neuroophthalmol· September 2005

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Oculopharyngodistal myopathy in a Thai family.
Rawiphan Witoonpanich, Sriphan Phankhian, Thanyachai Sura, Patcharee Lertrit, Suchart Phudhichareonrat

J Med Assoc Thai· December 2004

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Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
Wanicha Chuenkongkaew, Patcharee Lertrit, Rungnapa Suphavilai

Southeast Asian J Trop Med Public Health· March 2004

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An A-71C substitution in a green gene at the second position in the red/green visual-pigment gene array is associated with deutan color-vision deficiency.
Hisao Ueyama, Yao-Hua Li, Gui-Lian Fu, Patcharee Lertrit, La-ongsri Atchaneeyasakul

Proc Natl Acad Sci U S A· March 2003

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Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
Herawati Sudoyo, Helena Suryadi, Patcharee Lertrit, Patcharin Pramoonjago, Diana Lyrawati

J Hum Genet· January 2003

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