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Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus.
Zhang Y, Wang YF, Yang J, Zhang J, Sun L, Hirankarn N, Pan HF, Lau CS, Chan TM, Lee TL, Leung AM, Mok CC, Zhang L, Shen JJ, Wong SN, Lee KW, Ho MH, Lee PP, Chung BH, Chong CY, Wong RW, Mok MY, Wong WH, Tong KL, Tse NK, Li XP, Avihingsanon Y, Rianthavorn P, Deekajorndej T, Suphapeetiporn K, Shotelersuk V, Ying SK, Fung SK, Lai WM, Wong CM, Ng IO, Garcia-Barcelo MM, Cherny SS, Tam PK, Sham PC, Yang S, Ye DQ, Cui Y, Zhang XJ, Yang W, Lau YL. Zhang Y, et al. Among authors: suphapeetiporn k. Arthritis Res Ther. 2015 Mar 20;17(1):67. doi: 10.1186/s13075-015-0577-6. Arthritis Res Ther. 2015. PMID: 25880549 Free PMC article.
Quantitative assessment of glomerular basement membrane collagen IV α chains in paraffin sections from patients with focal segmental glomerulosclerosis and Alport gene variants.
Puapatanakul P, Isaranuwatchai S, Chanakul A, Surintrspanont J, Iampenkhae K, Kanjanabuch T, Suphapeetiporn K, Charu V, Suleiman HY, Praditpornsilpa K, Miner JH. Puapatanakul P, et al. Among authors: suphapeetiporn k. Kidney Int. 2024 May;105(5):1049-1057. doi: 10.1016/j.kint.2024.01.036. Epub 2024 Feb 22. Kidney Int. 2024. PMID: 38401706
F8 variants and their genotype-phenotype correlations in Thai patients with haemophilia A: a nationwide multicentre study.
Trirut C, Sosothikul D, Ittiwut R, Ittiwut C, Pongsewalak S, Songthawee N, Natesirinilkul R, Banjerdlak P, Na Songkhla P, Komvilaisak P, Moonla C, Suphapeetiporn K. Trirut C, et al. Among authors: suphapeetiporn k. J Clin Pathol. 2024 Jul 9:jcp-2024-209542. doi: 10.1136/jcp-2024-209542. Online ahead of print. J Clin Pathol. 2024. PMID: 38981663
Prevalence and clinical outcomes of germline variants among patients with myeloid neoplasms.
Kongkiatkamon S, Niparuck P, Rattanathammethee T, Kobbuaklee S, Suksusut A, Wudhikarn K, Ittiwut C, Chetruengchai W, Chuncharunee S, Bunworasate U, Suphapeetiporn K, Rojnuckarin P, Polprasert C. Kongkiatkamon S, et al. Among authors: suphapeetiporn k. J Clin Pathol. 2024 May 22:jcp-2023-209264. doi: 10.1136/jcp-2023-209264. Online ahead of print. J Clin Pathol. 2024. PMID: 38777570
Novel PLEC variants associated with infantile cholestasis.
Kor-Anantakul P, Chen HL, Chen YH, Ittiwut C, Ittiwut R, Chaijitraruch N, Suphapeetiporn K, Chongsrisawat V. Kor-Anantakul P, et al. Among authors: suphapeetiporn k. Clin Genet. 2024 Dec;106(6):769-775. doi: 10.1111/cge.14611. Epub 2024 Aug 21. Clin Genet. 2024. PMID: 39168815
A Novel NR5A1 Mutation in a Thai Boy with 46, XY DSD.
Wacharasindhu S, Ittiwut C, Ittiwut R, Aroonparkmongkol S, Suphapeetiporn K. Wacharasindhu S, et al. Among authors: suphapeetiporn k. J Pediatr Genet. 2023 Mar 20;13(3):181-184. doi: 10.1055/s-0043-1764480. eCollection 2024 Sep. J Pediatr Genet. 2023. PMID: 39086445 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.
Expanding the phenotypic spectrum of Caffey disease.
Suphapeetiporn K, Tongkobpetch S, Mahayosnond A, Shotelersuk V. Suphapeetiporn K, et al. Clin Genet. 2007 Mar;71(3):280-4. doi: 10.1111/j.1399-0004.2007.00768.x. Clin Genet. 2007. PMID: 17309652
150 results