Honda S - Search Results

1

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: honda s. J Hum Genet. 2007;52(5):397-405. doi: 10.1007/s10038-007-0127-4. Epub 2007 Apr 4. J Hum Genet. 2007. PMID: 17406783

2

Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.

Honda S, Orii KO, Kobayashi J, Hayashi S, Imamura A, Imoto I, Nakagawa E, Goto Y, Inazawa J. Honda S, et al. J Hum Genet. 2010 Apr;55(4):244-7. doi: 10.1038/jhg.2010.14. Epub 2010 Mar 26. J Hum Genet. 2010. PMID: 20339384

3

Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.

Honda S, Hayashi S, Imoto I, Toyama J, Okazawa H, Nakagawa E, Goto Y, Inazawa J. Honda S, et al. J Hum Genet. 2010 Sep;55(9):590-9. doi: 10.1038/jhg.2010.74. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613765

4

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.

Hayashi S, Imoto I, Aizu Y, Okamoto N, Mizuno S, Kurosawa K, Okamoto N, Honda S, Araki S, Mizutani S, Numabe H, Saitoh S, Kosho T, Fukushima Y, Mitsubuchi H, Endo F, Chinen Y, Kosaki R, Okuyama T, Ohki H, Yoshihashi H, Ono M, Takada F, Ono H, Yagi M, Matsumoto H, Makita Y, Hata A, Inazawa J. Hayashi S, et al. Among authors: honda s. J Hum Genet. 2011 Feb;56(2):110-24. doi: 10.1038/jhg.2010.129. Epub 2010 Oct 28. J Hum Genet. 2011. PMID: 20981036

5

Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.

Honda S, Satomura S, Hayashi S, Imoto I, Nakagawa E, Goto Y, Inazawa J; Japanese Mental Retardation Consortium. Honda S, et al. J Hum Genet. 2012 Jan;57(1):73-7. doi: 10.1038/jhg.2011.131. Epub 2011 Dec 1. J Hum Genet. 2012. PMID: 22129561

6

Clinical and molecular cytogenetic characterization of two patients with non-mutational aberrations of the FMR2 gene.

Honda S, Hayashi S, Kato M, Niida Y, Hayasaka K, Okuyama T, Imoto I, Mizutani S, Inazawa J. Honda S, et al. Am J Med Genet A. 2007 Apr 1;143A(7):687-93. doi: 10.1002/ajmg.a.31638. Am J Med Genet A. 2007. PMID: 17343270

7

The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpoints.

Honda S, Hayashi S, Nakane T, Imoto I, Kurosawa K, Mizuno S, Okamoto N, Kato M, Yoshihashi H, Kubota T, Nakagawa E, Goto Y, Inazawa J. Honda S, et al. Am J Med Genet A. 2012 Jun;158A(6):1292-303. doi: 10.1002/ajmg.a.35321. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22528406

8

Anticipation in Japanese families with schizophrenia.

Imamura A, Honda S, Nakane Y, Okazaki Y. Imamura A, et al. Among authors: honda s. J Hum Genet. 1998;43(4):217-23. doi: 10.1007/s100380050076. J Hum Genet. 1998. PMID: 9852670

9

Predictive models of in-hospital deterioration of Society of Cardiovascular Angiography and Intervention shock stage in patients with acute myocardial infarction initially presenting with stable hemodynamic condition.

Mukaida T, Kataoka Y, Murai K, Sawada K, Iwai T, Matama H, Honda S, Fujino M, Yoneda S, Takagi K, Nakao K, Otsuka F, Tahara Y, Asaumi Y, Noguchi T. Mukaida T, et al. Among authors: honda s. Cardiovasc Diagn Ther. 2024 Dec 31;14(6):1148-1160. doi: 10.21037/cdt-24-226. Epub 2024 Nov 12. Cardiovasc Diagn Ther. 2024. PMID: 39790208 Free PMC article.

10

Colorectal Cancer Screening and Social Needs.

Franklin IR, Gambatese R, Duggan MC, Green BB, Nocon RS, Coronado GD, Hahn EE, Honda SA, Koplan K, Levin TR, Steiner CA, Ngo-Metzger Q. Franklin IR, et al. Among authors: honda sa. J Am Board Fam Med. 2025 Jan 2:jabfm.2023.230497R1. doi: 10.3122/jabfm.2023.230497R1. Online ahead of print. J Am Board Fam Med. 2025. PMID: 39746817

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