Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2020 | 2 |
2021 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand.
Circ Genom Precis Med. 2021 Jun;14(3):e003229. doi: 10.1161/CIRCGEN.120.003229. Epub 2021 Jun 7.
Circ Genom Precis Med. 2021.
PMID: 34092119
Clinical Trial.
No abstract available.
A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population.
Mauleekoonphairoj J, Tongsima S, Khongphatthanayothin A, Jurgens SJ, Zimmerman DS, Sutjaporn B, Wandee P, Bezzina CR, Nademanee K, Poovorawan Y.
Mauleekoonphairoj J, et al. Among authors: wandee p.
Sci Rep. 2023 Jul 31;13(1):12360. doi: 10.1038/s41598-023-39429-3.
Sci Rep. 2023.
PMID: 37524845
Free PMC article.
Item in Clipboard
Metagenomic analysis of viral genes integrated in whole genome sequencing data of Thai patients with Brugada syndrome.
Chitcharoen S, Phokaew C, Mauleekoonphairoj J, Khongphatthanayothin A, Sutjaporn B, Wandee P, Poovorawan Y, Nademanee K, Payungporn S.
Chitcharoen S, et al. Among authors: wandee p.
Genomics Inform. 2022 Dec;20(4):e44. doi: 10.5808/gi.22047. Epub 2022 Dec 30.
Genomics Inform. 2022.
PMID: 36617651
Free PMC article.
Item in Clipboard
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Makarawate P, Glinge C, Khongphatthanayothin A, Walsh R, Mauleekoonphairoj J, Amnueypol M, Prechawat S, Wongcharoen W, Krittayaphong R, Anannab A, Lichtner P, Meitinger T, Tjong FVY, Lieve KVV, Amin AS, Sahasatas D, Ngarmukos T, Wichadakul D, Payungporn S, Sutjaporn B, Wandee P, Poovorawan Y, Tfelt-Hansen J, Tanck MWT, Tadros R, Wilde AAM, Bezzina CR, Veerakul G, Nademanee K.
Makarawate P, et al. Among authors: wandee p.
Heart Rhythm. 2020 Dec;17(12):2145-2153. doi: 10.1016/j.hrthm.2020.06.027. Epub 2020 Jun 30.
Heart Rhythm. 2020.
PMID: 32619740
Item in Clipboard
Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation.
Mauleekoonphairoj J, Chamnanphon M, Khongphatthanayothin A, Sutjaporn B, Wandee P, Poovorawan Y, Nademanee K, Pongpanich M, Chariyavilaskul P.
Mauleekoonphairoj J, et al. Among authors: wandee p.
Sci Rep. 2020 Nov 3;10(1):18969. doi: 10.1038/s41598-020-76085-3.
Sci Rep. 2020.
PMID: 33144648
Free PMC article.
Item in Clipboard
Genotype and clinical characteristics of congenital long QT syndrome in Thailand.
Saprungruang A, Khongphatthanayothin A, Mauleekoonphairoj J, Wandee P, Kanjanauthai S, Bhuiyan ZA, Wilde AAM, Poovorawan Y.
Saprungruang A, et al. Among authors: wandee p.
Indian Pacing Electrophysiol J. 2018 Sep-Oct;18(5):165-171. doi: 10.1016/j.ipej.2018.07.007. Epub 2018 Jul 20.
Indian Pacing Electrophysiol J. 2018.
PMID: 30036649
Free PMC article.
Item in Clipboard
Cite
Cite