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Comprehensive genome assembly reveals genetic diversity and carcass consumption insights in critically endangered Asian king vultures.
Sci Rep. 2024 Apr 24;14(1):9455. doi: 10.1038/s41598-024-59990-9.
Sci Rep. 2024.
PMID: 38658744
Free PMC article.
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Yeetong P, Dembélé ME, Pongpanich M, Cissé L, Srichomthong C, Maiga AB, Dembélé K, Assawapitaksakul A, Bamba S, Yalcouyé A, Diarra S, Mefoung SE, Rakwongkhachon S, Traoré O, Tongkobpetch S, Fischbeck KH, Gahl WA, Guinto CO, Shotelersuk V, Landouré G.
Yeetong P, et al. Among authors: assawapitaksakul a.
Mov Disord. 2024 Jan;39(1):164-172. doi: 10.1002/mds.29654. Epub 2023 Nov 22.
Mov Disord. 2024.
PMID: 37994247
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A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases.
Sinthuwiwat T, Buranapraditkun S, Kamolvisit W, Tongkobpetch S, Chetruengchai W, Srichomthong C, Assawapitaksakul A, Phokaew C, Kueanjinda P, Palaga T, Boonpiyathad T, Suphapeetiporn K, Hirankarn N, Shotelersuk V.
Sinthuwiwat T, et al. Among authors: assawapitaksakul a.
Sci Rep. 2022 Sep 14;12(1):15420. doi: 10.1038/s41598-022-19334-x.
Sci Rep. 2022.
PMID: 36104364
Free PMC article.
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Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency.
Tantirukdham N, Sahakitrungruang T, Chaisiwamongkol R, Pongpanich M, Srichomthong C, Assawapitaksakul A, Buasong A, Tongkobpetch S, Yeetong P, Shotelersuk V.
Tantirukdham N, et al. Among authors: assawapitaksakul a.
J Clin Endocrinol Metab. 2022 Jun 16;107(7):1939-1947. doi: 10.1210/clinem/dgac187.
J Clin Endocrinol Metab. 2022.
PMID: 35363313
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Genotypic and phenotypic landscapes of 51 pharmacogenes derived from whole-genome sequencing in a Thai population.
Wankaew N, Chariyavilaskul P, Chamnanphon M, Assawapitaksakul A, Chetruengchai W, Pongpanich M, Shotelersuk V.
Wankaew N, et al. Among authors: assawapitaksakul a.
PLoS One. 2022 Feb 17;17(2):e0263621. doi: 10.1371/journal.pone.0263621. eCollection 2022.
PLoS One. 2022.
PMID: 35176049
Free PMC article.
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The Thai reference exome (T-REx) variant database.
Shotelersuk V, Wichadakul D, Ngamphiw C, Srichomthong C, Phokaew C, Wilantho A, Pakchuen S, Nakhonsri V, Shaw PJ, Wasitthankasem R, Piriyapongsa J, Wangkumhang P, Assawapitaksakul A, Chetruengchai W, Lapphra K, Khuninthong A, Makarawate P, Suphapeetiporn K, Mahasirimongkol S, Satproedprai N, Porntaveetus T, Pisitkun P, Praphanphoj V, Kantaputra P, Tassaneeyakul W, Tongsima S.
Shotelersuk V, et al. Among authors: assawapitaksakul a.
Clin Genet. 2021 Dec;100(6):703-712. doi: 10.1111/cge.14060. Epub 2021 Sep 22.
Clin Genet. 2021.
PMID: 34496037
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Rapid exome sequencing as the first-tier investigation for diagnosis of acutely and severely ill children and adults in Thailand.
Kamolvisit W, Phowthongkum P, Boonsimma P, Kuptanon C, Rojnueangnit K, Wattanasirichaigoon D, Chanvanichtrakool M, Phuaksaman C, Wiromrat P, Srichomthong C, Ittiwut C, Phokaew C, Ittiwut R, Assawapitaksakul A, Chetruengchai W, Buasong A, Suphapeetiporn K, Shotelersuk V.
Kamolvisit W, et al. Among authors: assawapitaksakul a.
Clin Genet. 2021 Jul;100(1):100-105. doi: 10.1111/cge.13963. Epub 2021 Apr 13.
Clin Genet. 2021.
PMID: 33822359
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TTTCA repeat insertions in an intron of YEATS2 in benign adult familial myoclonic epilepsy type 4.
Yeetong P, Pongpanich M, Srichomthong C, Assawapitaksakul A, Shotelersuk V, Tantirukdham N, Chunharas C, Suphapeetiporn K, Shotelersuk V.
Yeetong P, et al. Among authors: assawapitaksakul a.
Brain. 2019 Nov 1;142(11):3360-3366. doi: 10.1093/brain/awz267.
Brain. 2019.
PMID: 31539032
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