Eu-ahsunthornwattana J - Search Results

1

Noonan syndrome, metabolic syndrome and stroke-in-the-young: coincidence, causal or contribution?

Eu-ahsunthornwattana J, Trachoo O, Dejsuphong D, Tunteeratum A, Srichan K, Sura T. Eu-ahsunthornwattana J, et al. J Med Assoc Thai. 2010 Sep;93(9):1084-7. J Med Assoc Thai. 2010. PMID: 20873082

2

Sensitivity and frequencies of dystrophin gene mutations in Thai DMD/BMD patients as detected by multiplex PCR.

Sura T, Eu-ahsunthornwattana J, Pingsuthiwong S, Busabaratana M. Sura T, et al. Dis Markers. 2008;25(2):115-21. doi: 10.1155/2008/521568. Dis Markers. 2008. PMID: 18957722 Free PMC article.

3

Frequencies of spinocerebellar ataxia subtypes in Thailand: window to the population history?

Sura T, Eu-Ahsunthornwattana J, Youngcharoen S, Busabaratana M, Dejsuphong D, Trachoo O, Theerasasawat S, Tunteeratum A, Noparutchanodom C, Tunlayadechanont S. Sura T, et al. J Hum Genet. 2009 May;54(5):284-8. doi: 10.1038/jhg.2009.27. Epub 2009 Mar 27. J Hum Genet. 2009. PMID: 19329990

4

Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of Duchenne muscular dystrophy with duplication of dystrophin gene.

Tunteeratum A, Witoonpanich R, Phudhichareonrat S, Eu-ahsunthornwattana J, Pingsuthiwong S, Srichan K, Sura T. Tunteeratum A, et al. J Clin Neuromuscul Dis. 2009 Sep;11(1):49-53. doi: 10.1097/CND.0b013e3181adcda7. J Clin Neuromuscul Dis. 2009. PMID: 19730022

5

Association of estrogen receptor-alpha single-nucleotide polymorphism (codon 594 G-->A) and Thai patients affected by knee osteoarthritis.

Tawonsawatruk T, Trachoo O, Channoom T, Sura T, Eu-ahsunthornwattana J, Woratanarat P, Wajanavisit W. Tawonsawatruk T, et al. J Med Assoc Thai. 2009 Dec;92 Suppl 6:S45-50. J Med Assoc Thai. 2009. PMID: 20128071

6

A comprehensive Thai pharmacogenomics database (TPGxD-1): Phenotype prediction and variants identification in 942 whole-genome sequencing data.

John S, Klumsathian S, Own-Eium P, Eu-Ahsunthornwattana J, Sura T, Dejsuphong D, Sritara P, Vathesatogkit P, Thongchompoo N, Thabthimthong W, Teerakulkittipong N, Chantratita W, Sukasem C. John S, et al. Among authors: eu ahsunthornwattana j. Clin Transl Sci. 2024 Jun;17(6):e13830. doi: 10.1111/cts.13830. Clin Transl Sci. 2024. PMID: 38853370 Free PMC article.

7

Investigating common mutations in ATP7B gene and the prevalence of Wilson's disease in the Thai population using population-based genome-wide datasets.

Own-Eium P, Dejsuphong D, Vathesatogkit P, Sritara P, Sura T, Aekplakorn W, Suktitipat B, Eu-Ahsunthornwattana J. Own-Eium P, et al. Among authors: eu ahsunthornwattana j. J Hum Genet. 2025 Jan;70(1):17-24. doi: 10.1038/s10038-024-01292-z. Epub 2024 Aug 28. J Hum Genet. 2025. PMID: 39198578

8

PROC Promoter Single Nucleotide Polymorphisms Associated With Low Protein C Activity But Not Increased Risk of Thromboembolism in Pediatric Population.

Udomkittivorakul N, Sasanakul W, Eu-Ahsunthornwattana J, Chuansumrit A, Komwilaisak P, Songdej D, Sirachainan N. Udomkittivorakul N, et al. Among authors: eu ahsunthornwattana j. Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620935206. doi: 10.1177/1076029620935206. Clin Appl Thromb Hemost. 2020. PMID: 32609543 Free PMC article.

9

Precision medicine in Thailand.

Shotelersuk V, Tongsima S, Pithukpakorn M, Eu-Ahsunthornwattana J, Mahasirimongkol S. Shotelersuk V, et al. Among authors: eu ahsunthornwattana j. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):245-253. doi: 10.1002/ajmg.c.31694. Epub 2019 Mar 19. Am J Med Genet C Semin Med Genet. 2019. PMID: 30888117 Review.

10

Comparison of methods to account for relatedness in genome-wide association studies with family-based data.

Eu-Ahsunthornwattana J, Miller EN, Fakiola M; Wellcome Trust Case Control Consortium 2; Jeronimo SM, Blackwell JM, Cordell HJ. Eu-Ahsunthornwattana J, et al. PLoS Genet. 2014 Jul 17;10(7):e1004445. doi: 10.1371/journal.pgen.1004445. eCollection 2014 Jul. PLoS Genet. 2014. PMID: 25033443 Free PMC article.

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