Patcharee Lertrit

1.5k total citations
41 papers, 770 citations indexed

About

Patcharee Lertrit is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Patcharee Lertrit has authored 41 papers receiving a total of 770 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 19 papers in Clinical Biochemistry and 6 papers in Genetics. Recurrent topics in Patcharee Lertrit's work include Mitochondrial Function and Pathology (28 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (12 papers). Patcharee Lertrit is often cited by papers focused on Mitochondrial Function and Pathology (28 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (12 papers). Patcharee Lertrit collaborates with scholars based in Thailand, Australia and Japan. Patcharee Lertrit's co-authors include Sangkot Marzuki, Edward Byrne, Robert M. I. Kapsa, A.S. Noer, Dominic Thyagarajan, Wanicha Chuenkongkaew, Nopasak Phasukkijwatana, Herawati Sudoyo, Supannee Kaewsutthi and Bhoom Suktitipat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Annals of Neurology.

In The Last Decade

Patcharee Lertrit

40 papers receiving 756 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Patcharee Lertrit Thailand	17	625	254	131	87	67	41	770
Majida Charif Morocco	17	417 0.7×	88 0.3×	114 0.9×	36 0.4×	38 0.6×	51	617
Rajeshwari D. Koilkonda United States	13	818 1.3×	135 0.5×	155 1.2×	172 2.0×	101 1.5×	21	889
Suzanne C.E.H. Sallevelt Netherlands	15	534 0.9×	335 1.3×	170 1.3×	13 0.1×	43 0.6×	24	772
Rebecca McGreal United States	10	537 0.9×	63 0.2×	55 0.4×	87 1.0×	18 0.3×	13	680
Pascal Joset Switzerland	14	412 0.7×	62 0.2×	245 1.9×	19 0.2×	78 1.2×	26	640
Daniel Navarro-Gomez United States	13	495 0.8×	36 0.1×	204 1.6×	178 2.0×	51 0.8×	19	621
Maja Hempel Germany	19	511 0.8×	112 0.4×	342 2.6×	8 0.1×	90 1.3×	58	855
Roberta Tammaro Italy	11	515 0.8×	27 0.1×	180 1.4×	87 1.0×	70 1.0×	12	615
Jonatan Halvardson Sweden	14	584 0.9×	45 0.2×	209 1.6×	7 0.1×	32 0.5×	23	781
J. Bronwyn Bateman United States	16	460 0.7×	18 0.1×	257 2.0×	206 2.4×	44 0.7×	34	680

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-authorship network of co-authors of Patcharee Lertrit

This figure shows the co-authorship network connecting the top 25 collaborators of Patcharee Lertrit. A scholar is included among the top collaborators of Patcharee Lertrit based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Patcharee Lertrit. Patcharee Lertrit is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Wattanasirichaigoon, Duangrurdee, Bhoom Suktitipat, Patcharee Lertrit, et al.. (2022). Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome. Frontiers in Pediatrics. 10. 876436–876436. 2 indexed citations

Lertrit, Patcharee, et al.. (2022). Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report. World Journal of Clinical Cases. 10(20). 6944–6953. 1 indexed citations

Taylor, Todd D., Yutaka Suzuki, Wanna Thongnoppakhun, et al.. (2017). Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes. Investigative Ophthalmology & Visual Science. 58(4). 2413–2413. 10 indexed citations

Kaewsutthi, Supannee, Jeerunda Santiprabhob, Benjaluck Phonrat, et al.. (2016). Exome sequencing in Thai patients with familial obesity. Genetics and Molecular Research. 15(2). 15 indexed citations

Tun, Aung Win, Sakdithep Chaiyarit, Supannee Kaewsutthi, et al.. (2014). 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. PLoS ONE. 9(9). e106779–e106779. 14 indexed citations

Tun, Aung Win, et al.. (2013). Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand. Experimental Eye Research. 116. 55–57. 11 indexed citations

Phasukkijwatana, Nopasak, et al.. (2011). 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. 36(9). 775–781. 26 indexed citations

Thyagarajan, Dominic, et al.. (2009). Significance of mitochondrial DNA deletions in myotonic dystrophy. Acta Neurologica Scandinavica. 87(1). 32–36. 3 indexed citations

Phasukkijwatana, Nopasak, et al.. (2006). Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy. Journal of Human Genetics. 51(12). 1110–1117. 12 indexed citations

10.

Chuenkongkaew, Wanicha, Komon Luangtrakool, Bhoom Suktitipat, et al.. (2006). Mitochondrial DNA Haplogroup Distribution in Pedigrees of Southeast Asian G11778A Leber Hereditary Optic Neuropathy. Journal of Neuro-Ophthalmology. 26(4). 264–267. 15 indexed citations

11.

Phasukkijwatana, Nopasak, Wanicha Chuenkongkaew, Bhoom Suktitipat, et al.. (2006). The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees. Journal of Human Genetics. 51(4). 298–304. 20 indexed citations

12.

Chuenkongkaew, Wanicha, et al.. (2005). Proportion of 11778 Mutant Mitochondrial DNA and Clinical Expression in a Thai Population With Leber Hereditary Optic Neuropathy. Journal of Neuro-Ophthalmology. 25(3). 173–175. 13 indexed citations

13.

Chuenkongkaew, Wanicha, et al.. (2004). Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.. PubMed. 35(1). 167–8. 3 indexed citations

14.

Sudoyo, Herawati, et al.. (2002). Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy. Journal of Human Genetics. 47(11). 594–604. 40 indexed citations

15.

Kapsa, Robert M. I., M.J.Bernadette Jean-François, Patcharee Lertrit, et al.. (1996). Mitochondrial DNA polymorphism in substantia nigra. Journal of the Neurological Sciences. 144(1-2). 204–211. 16 indexed citations

16.

Jean-François, M.J.Bernadette, Patcharee Lertrit, Samuel F. Berkovic, et al.. (1994). 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. 24(2). 188–193. 18 indexed citations

17.

Lertrit, Patcharee, et al.. (1994). Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction. Human Molecular Genetics. 3(11). 1973–1981. 25 indexed citations

18.

Marzuki, Sangkot, Patcharee Lertrit, Robert M. I. Kapsa, et al.. (1992). Reply to Howell et al.: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA. The American Journal of Human Genetics. 50(6). 1337–1340. 9 indexed citations

19.

Lertrit, Patcharee, A.S. Noer, Edward Byrne, & Sangkot Marzuki. (1992). Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (Myoclonic epilepsy with ragged red fibers) encephalomyopathy. Human Genetics. 90(3). 251–4. 28 indexed citations

20.

Noer, A.S., Herawati Sudoyo, Patcharee Lertrit, et al.. (1991). 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). 49(4). 715–22. 64 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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