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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2004 1
2006 1
2007 6
2008 9
2009 5
2010 4
2011 7
2012 8
2013 11
2014 10
2015 12
2016 10
2017 10
2018 15
2019 17
2020 17
2021 8
2022 9
2023 7
2024 2

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141 results

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Page 1
A germline STAT6 gain-of-function variant is associated with early-onset allergies.
Suratannon N, Ittiwut C, Dik WA, Ittiwut R, Meesilpavikkai K, Israsena N, Ingrungruanglert P, Dalm VASH, van Daele PLA, Sanpavat A, Chaijitraruch N, Schrijver B, Buranapraditkun S, Porntaveetus T, Swagemakers SMA, IJspeert H, Palaga T, Suphapeetiporn K, van der Spek PJ, Hirankarn N, Chatchatee P, Martin van Hagen P, Shotelersuk V. Suratannon N, et al. Among authors: suphapeetiporn k. J Allergy Clin Immunol. 2023 Feb;151(2):565-571.e9. doi: 10.1016/j.jaci.2022.09.028. Epub 2022 Oct 7. J Allergy Clin Immunol. 2023. PMID: 36216080
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: suphapeetiporn k. Clin Genet. 2021 Dec;100(6):703-712. doi: 10.1111/cge.14060. Epub 2021 Sep 22. Clin Genet. 2021. PMID: 34496037
Genetic, metabolic and clinical delineation of an MRPS23-associated mitochondrial disorder.
Ittiwut C, Ittiwut R, Kuptanon C, Matsuhashi T, Shimura M, Sugiyama Y, Onuki T, Ohtake A, Murayama K, Vatanavicharn N, Dejputtawat W, Tantisirivit N, Kor-Anantakul P, Kamolvisit W, Suphapeetiporn K, Shotelersuk V. Ittiwut C, et al. Among authors: suphapeetiporn k. Sci Rep. 2023 Dec 12;13(1):22005. doi: 10.1038/s41598-023-49161-7. Sci Rep. 2023. PMID: 38086984 Free PMC article.
Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study.
Ozen A, Chongsrisawat V, Sefer AP, Kolukisa B, Jalbert JJ, Meagher KA, Brackin T, Feldman HB, Baris S, Karakoc-Aydiner E, Ergelen R, Fuss IJ, Moorman H, Suratannon N, Suphapeetiporn K, Perlee L, Harari OA, Yancopoulos GD, Lenardo MJ; Pozelimab CHAPLE Working Group. Ozen A, et al. Among authors: suphapeetiporn k. Lancet. 2024 Feb 17;403(10427):645-656. doi: 10.1016/S0140-6736(23)02358-9. Epub 2024 Jan 23. Lancet. 2024. PMID: 38278170 Clinical Trial.
Whole exome sequencing for diagnosis of hereditary thrombocytopenia.
Mekchay P, Ittiwut C, Ittiwut R, Akkawat B, Le Grand SM, Leela-Adisorn N, Muanpetch S, Khovidhunkit W, Sosothikul D, Shotelersuk V, Suphapeetiporn K, Rojnuckarin P. Mekchay P, et al. Among authors: suphapeetiporn k. Medicine (Baltimore). 2020 Nov 20;99(47):e23275. doi: 10.1097/MD.0000000000023275. Medicine (Baltimore). 2020. PMID: 33217855 Free PMC article.
Expanding phenotypic spectrum of familial comedones.
Rerknimitr P, Korkij W, Wititsuwannakul J, Panmontha W, Suphapeetiporn K, Shotelersuk V. Rerknimitr P, et al. Among authors: suphapeetiporn k. Dermatology. 2014;228(3):215-9. doi: 10.1159/000358170. Epub 2014 May 6. Dermatology. 2014. PMID: 24818872
A novel PITX2 mutation in non-syndromic orodental anomalies.
Intarak N, Theerapanon T, Ittiwut C, Suphapeetiporn K, Porntaveetus T, Shotelersuk V. Intarak N, et al. Among authors: suphapeetiporn k. Oral Dis. 2018 May;24(4):611-618. doi: 10.1111/odi.12804. Epub 2018 Mar 13. Oral Dis. 2018. PMID: 29121437
Whole-Exome Sequencing Solved over 2-Decade Kidney Disease Enigma.
Isaranuwatchai S, Chanakul A, Ittiwut C, Srichomthong C, Shotelersuk V, Praditpornsilpa K, Suphapeetiporn K. Isaranuwatchai S, et al. Among authors: suphapeetiporn k. Nephron. 2021;145(3):311-316. doi: 10.1159/000514293. Epub 2021 Mar 16. Nephron. 2021. PMID: 33725694
141 results