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Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP. Cameron-Christie SR, et al. Among authors: takei r. Am J Hum Genet. 2018 Jun 7;102(6):1115-1125. doi: 10.1016/j.ajhg.2018.04.008. Epub 2018 May 24. Am J Hum Genet. 2018. PMID: 29805041 Free PMC article.
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP. Cameron-Christie SR, et al. Among authors: takei r. Am J Hum Genet. 2019 Sep 5;105(3):669. doi: 10.1016/j.ajhg.2019.08.007. Am J Hum Genet. 2019. PMID: 31491409 Free PMC article. No abstract available.
Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects.
Takei R, Cadzow M, Markie D, Bixley M, Phipps-Green A, Major TJ, Li C, Choi HK, Li Z, Hu H; Eurogout Consortium; Guo H, He M, Shi Y, Stamp LK, Dalbeth N, Merriman TR, Wei WH. Takei R, et al. J Hum Genet. 2021 Feb;66(2):225. doi: 10.1038/s10038-020-00833-6. J Hum Genet. 2021. PMID: 32901114 No abstract available.
A Polynesian-specific copy number variant encompassing the MICA gene associates with gout.
Wang K, Cadzow M, Bixley M, Leask MP, Merriman ME, Yang Q, Li Z, Takei R, Phipps-Green A, Major TJ, Topless R, Dalbeth N, King F, Murphy R, Stamp LK, de Zoysa J, Wang Z, Shi Y, Merriman TR. Wang K, et al. Among authors: takei r. Hum Mol Genet. 2022 Oct 28;31(21):3757-3768. doi: 10.1093/hmg/ddac094. Hum Mol Genet. 2022. PMID: 35451026 Free PMC article.
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations.
Emde AK, Phipps-Green A, Cadzow M, Gallagher CS, Major TJ, Merriman ME, Topless RK, Takei R, Dalbeth N, Murphy R, Stamp LK, de Zoysa J, Wilcox PL, Fox K, Wasik KA, Merriman TR, Castel SE. Emde AK, et al. Among authors: takei r. BMC Genomics. 2021 Nov 1;22(1):666. doi: 10.1186/s12864-021-07949-9. BMC Genomics. 2021. PMID: 34719381 Free PMC article.
Correspondence on 'Variants in urate transporters, ADH1B, GCKR and MEPE genes associated with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank'.
Takei R, Sumpter NA, Phipps-Green A, Cadzow M, Topless RK, Reynolds RJ, Merriman TR. Takei R, et al. Ann Rheum Dis. 2023 Jul;82(7):e174. doi: 10.1136/annrheumdis-2021-220769. Epub 2021 Jun 10. Ann Rheum Dis. 2023. PMID: 34112655 No abstract available.
Pulmonary function and chest CT abnormalities 3 months after discharge from COVID-19, 2020-2021: A nation-wide multicenter prospective cohort study from the Japanese respiratory society.
Kamata H, Takamatsu K, Fukunaga K, Chubachi S, Nakagawara K, Namkoong H, Terai H, Tanaka K, Sato S, Hagiwara E, Takei R, Kondoh Y, Takazono T, Hashimoto M, Tasaka S, Ohrui T, Tanino Y, Mineshita M, Komase Y, Miyazaki K, Nishikawa M, Ando A, Kita H, Ichihara E, Ohshimo S, Murata Y, Ishida M, Kobayashi S, Uchida T, Tateno H, Ikari J, Terashima T, Kozu Y, Tateishi T, Shinkai M, Sagara H, To Y, Ito Y, Yamamoto M, Yamamoto Y, Kita T, Ito Y, Tomii K, Fujita Y, Funaki Y, Yatera K, Yamasue M, Komiya K, Kozawa S, Manabe H, Hozumi H, Horiguchi T, Kitajima T, Nakano Y, Nagaoka T, Hojo M, Ebihara A, Kobayashi M, Takayama K, Jinta T, Sawai T, Fukuda Y, Kaneko T, Chin K, Ogura T, Mukae H, Ishii M, Yokoyama A. Kamata H, et al. Among authors: takei r. Respir Investig. 2024 Apr 25;62(4):572-579. doi: 10.1016/j.resinv.2024.02.009. Online ahead of print. Respir Investig. 2024. PMID: 38669898
160 results