Patcharee Lertrit

1.5k citations

41 papers · 770 indexed · h-index 17

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Ophthalmology top 5%

Papers in ⓘ

Clinical Biochemistry 19
- Metabolism and Genetic Disorders 19
Molecular Biology 37
- Mitochondrial Function and Pathology 28
- ATP Synthase and ATPases Research 12
- Metabolomics and Mass Spectrometry Studies 4
- Molecular Biology Techniques and Applications 3

Co-authors: Sangkot Marzuki (11 shared papers)Edward Byrne (10 shared papers)Robert M. I. Kapsa (9 shared papers)A.S. Noer (4 shared papers)Dominic Thyagarajan (6 shared papers)Wanicha Chuenkongkaew (10 shared papers)Nopasak Phasukkijwatana (6 shared papers)Herawati Sudoyo (4 shared papers)
Journals: Human Genetics (5 papers)Investigative Ophthalmology & Visual Science (3 papers)Proceedings of the National Academy of Sciences (1 paper)Frontiers in Pediatrics (1 paper)Human Molecular Genetics (1 paper)
Partner nations: Thailand Australia Japan

In The Last Decade

Patcharee Lertrit

40 papers receiving 756 citations

Peers

Countries citing papers authored by Patcharee Lertrit

Since Specialization

Citations

This map shows the geographic impact of Patcharee Lertrit's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Patcharee Lertrit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patcharee Lertrit more than expected).

Fields of papers citing papers by Patcharee Lertrit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patcharee Lertrit. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Patcharee Lertrit. The network helps show where Patcharee Lertrit may publish in the future.

Co-authors

The 25 scholars most cited alongside Patcharee Lertrit, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Patcharee Lertrit Line = papers co-authored together Patcharee Lertrit links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Normal variants of human mitochondrial DNA and translation products: the building of a reference data base Human Genetics ·Sangkot Marzuki, A.S. Noer, Patcharee Lertrit, Dominic Thyagarajan, Robert M. I. Kapsa, P. Utthanaphol, Edward Byrne	1991	74
2	A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome. Europe PMC (PubMed Central) ·A.S. Noer, Herawati Sudoyo, Patcharee Lertrit, Dominic Thyagarajan, P. Utthanaphol, Robert M. I. Kapsa, Edward Byrne, Sangkot Marzuki	1991	64
3	A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I. PubMed ·Patcharee Lertrit, A.S. Noer, M.J.Bernadette Jean-François, Robert M. I. Kapsa, Xenia Dennett, Dominic Thyagarajan, K Lethlean, Edward Byrne, Sangkot Marzuki	1992	55
4	Whole Exome Sequencing in Thai Patients With Retinitis Pigmentosa Reveals Novel Mutations in Six Genes Investigative Ophthalmology & Visual Science ·Worapoj Jinda, Todd D. Taylor, Yutaka Suzuki, Wanna Thongnoppakhun, Chanin Limwongse, Patcharee Lertrit, Prapat Suriyaphol, Adisak Trinavarat, La‐ongsri Atchaneeyasakul	2014	44
5	Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy Journal of Human Genetics ·Herawati Sudoyo, Helena Suryadi, Patcharee Lertrit, Patcharin Pramoonjago, Diana Lyrawati, Sangkot Marzuki	2002	40
6	Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand Human Genetics ·Nopasak Phasukkijwatana, Bussaraporn Kunhapan, Jim Stankovich, Wanicha Chuenkongkaew, Russell Thomson, Timothy A. Thornton, Melanie Bahlo, Taisei Mushiroda, Yusuke Nakamura, Surakameth Mahasirimongkol, Aung Win Tun, Chatchawan Srisawat, Chanin Limwongse, Chayanon Peerapittayamongkol, Thanyachai Sura, Wichit Suthammarak, Patcharee Lertrit	2010	39
7	Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis American Journal of Physical Anthropology ·Patcharee Lertrit, Samerchai Poolsuwan, Rachanie Thosarat, Thitima Sanpachudayan, Hathaichanoke Boonyarit, Chatchai Chinpaisal, Bhoom Suktitipat	2008	34
8	Mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations Journal of Human Genetics ·Lanka Ranaweera, Supannee Kaewsutthi, Aung Win Tun, Hathaichanoke Boonyarit, Samerchai Poolsuwan, Patcharee Lertrit	2013	29
9	Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (Myoclonic epilepsy with ragged red fibers) encephalomyopathy Human Genetics ·Patcharee Lertrit, A.S. Noer, Edward Byrne, Sangkot Marzuki	1992	28
10	Rapid and noninvasive screening of patients with mitochondrial myopathy Human Mutation ·Nicky Kotsimbos, M.J.Bernadette Jean-François, Marjan Huizing, Robert M. I. Kapsa, Patcharee Lertrit, Nurjati Chairani Siregar, Sangkot Marzuki, Carolyn M. Sue, Edward Byrne	1994	26
11	Stability of Epitheliotrophic Factors in Autologous Serum Eye Drops from Chronic Stevens-Johnson Syndrome Dry Eye Compared to Non-autoimmune Dry Eye Current Eye Research ·Nopasak Phasukkijwatana, Patcharee Lertrit, Sompong Liammongkolkul, Pinnita Prabhasawat	2011	26
12	Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction Human Molecular Genetics ·Patcharee Lertrit, Robert M. I. Kapsa, M.J. Bernadette Jean-FRANCOLS, Dominic Thyagaraian, A.Salfuddin Noer, Sangkopt Marzukil, Edward Byrne	1994	25
13	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 Forensic Science International Genetics ·Hathaichanoke Boonyarit, Surakameth Mahasirimongkol, Nuttama Chavalvechakul, Masayuki Aoki, Hanae Amitani, Naoya Hosono, Naoyuki Kamatani, Michiaki Kubo, Patcharee Lertrit	2014	23
14	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 Proceedings of the National Academy of Sciences ·Hisao Ueyama, Yaohua Li, Guilian Fu, Patcharee Lertrit, La‐ongsri Atchaneeyasakul, Sanae Oda, Shoko Tanabe, Yasuhiro Nishida, Shinichi Yamade, Iwao Ohkubo	2003	21
15	The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees Journal of Human Genetics ·Nopasak Phasukkijwatana, Wanicha Chuenkongkaew, Rungnapa Suphavilai, Bhoom Suktitipat, Sarinee Pingsuthiwong, Ngamkae Ruangvaravate, La‐ongsri Atchaneeyasakul, Sukhuma Warrasak, Anuchit Poonyathalang, Thanyachai Sura, Patcharee Lertrit	2006	20
16	Mitochondrial Haplogroup Background May Influence Southeast Asian G11778A Leber Hereditary Optic Neuropathy Investigative Ophthalmology & Visual Science ·Supannee Kaewsutthi, Nopasak Phasukkijwatana, Yutthana Joyjinda, Wanicha Chuenkongkaew, Bussaraporn Kunhapan, Aung Win Tun, Bhoom Suktitipat, Patcharee Lertrit	2011	20
17	Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA^{Leu (UUR)} gene generally associated with the MELAS subset of mitochondrial encephalomyopathies Australian and New Zealand Journal of Medicine ·M.J.Bernadette Jean-François, Patcharee Lertrit, Samuel F. Berkovic, Denis Crimmins, John G. Morris, Sangkot Marzuki, Edward Byrne	1994	18
18	Mitochondrial DNA polymorphism in substantia nigra Journal of the Neurological Sciences ·Robert M. I. Kapsa, M.J.Bernadette Jean-François, Patcharee Lertrit, Shan Weng, Nurjati Chairani Siregar, Joseline Ojaimi, Geoffrey A. Donnan, Colin L. Masters, Edward Byrne	1996	16
19	Mitochondrial DNA Haplogroup Distribution in Pedigrees of Southeast Asian G11778A Leber Hereditary Optic Neuropathy Journal of Neuro-Ophthalmology ·Pattamon Tharaphan, Wanicha Chuenkongkaew, Komon Luangtrakool, Thitima Sanpachudayan, Bhoom Suktitipat, Rungnapa Suphavilai, Chatchawan Srisawat, Thanyachai Sura, Patcharee Lertrit	2006	15
20	Exome sequencing in Thai patients with familial obesity Genetics and Molecular Research ·Supannee Kaewsutthi, Jeerunda Santiprabhob, Benjaluck Phonrat, Anchalee Tungtrongchitr, Patcharee Lertrit, Rungsunn Tungtrongchitr	2016	15

About Patcharee Lertrit

Patcharee Lertrit is a scholar working on Clinical Biochemistry, Molecular Biology, Ophthalmology, Cellular and Molecular Neuroscience and Nutrition and Dietetics, having authored 41 papers that have together received 770 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (28 papers), Metabolism and Genetic Disorders (19 papers), ATP Synthase and ATPases Research (12 papers), Metabolomics and Mass Spectrometry Studies (4 papers), Genetic Neurodegenerative Diseases (4 papers), Forensic and Genetic Research (3 papers), Molecular Biology Techniques and Applications (3 papers) and Trace Elements in Health (3 papers). The work is most often cited by research in Clinical Biochemistry (254 citations), Ophthalmology (87 citations), Molecular Biology (625 citations), Genetics (131 citations) and Cellular and Molecular Neuroscience (67 citations). Patcharee Lertrit has collaborated with scholars based in Thailand, Australia and Japan. Frequent co-authors include Sangkot Marzuki, Edward Byrne, Robert M. I. Kapsa, A.S. Noer, Dominic Thyagarajan, Wanicha Chuenkongkaew, Nopasak Phasukkijwatana, Herawati Sudoyo, M.J.Bernadette Jean-François and Bhoom Suktitipat. Their work appears in journals such as Human Genetics, Investigative Ophthalmology & Visual Science, Proceedings of the National Academy of Sciences, Frontiers in Pediatrics and Human Molecular Genetics.

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