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

Year Number of Results
2002 1
2003 1
2004 3
2005 5
2006 2
2007 3
2008 1
2009 5
2010 4
2011 3
2012 8
2013 10
2014 5
2015 6
2016 9
2017 16
2018 11
2019 9
2020 9
2021 8
2022 3
2023 6
2024 4

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115 results

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Page 1
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel.
Shen J, Oza AM, Del Castillo I, Duzkale H, Matsunaga T, Pandya A, Kang HP, Mar-Heyming R, Guha S, Moyer K, Lo C, Kenna M, Alexander JJ, Zhang Y, Hirsch Y, Luo M, Cao Y, Wai Choy K, Cheng YF, Avraham KB, Hu X, Garrido G, Moreno-Pelayo MA, Greinwald J, Zhang K, Zeng Y, Brownstein Z, Basel-Salmon L, Davidov B, Frydman M, Weiden T, Nagan N, Willis A, Hemphill SE, Grant AR, Siegert RK, DiStefano MT, Amr SS, Rehm HL, Abou Tayoun AN; ClinGen Hearing Loss Working Group. Shen J, et al. Among authors: matsunaga t. Genet Med. 2019 Nov;21(11):2442-2452. doi: 10.1038/s41436-019-0535-9. Epub 2019 Jun 4. Genet Med. 2019. PMID: 31160754 Free PMC article.
Etiology and genes.
Matsunaga T. Matsunaga T. Adv Otorhinolaryngol. 2014;75:2-8. doi: 10.1159/000350491. Epub 2013 Oct 11. Adv Otorhinolaryngol. 2014. PMID: 24135340 Review. No abstract available.
The pathogenic role of the BRCA2 c.7847C>T (p.Ser2616Phe) variant in breast and ovarian cancer predisposition.
Yamazawa K, Sugano K, Tanakaya K, Inoue S, Murakami H, Nakashima M, Adachi M, Oki S, Makabe T, Yamashita H, Ueki A, Sasaoka A, Nakashoji A, Kinoshita T, Matsunaga T, Arai M, Nakamura S, Miyata H, Ikegami M, Mano H, Kohsaka S, Matsui A. Yamazawa K, et al. Among authors: matsunaga t. Cancer Sci. 2023 Jul;114(7):2993-3002. doi: 10.1111/cas.15799. Epub 2023 Apr 17. Cancer Sci. 2023. PMID: 37067535 Free PMC article.
Metacarpophalangeal pattern profile analysis for a 3-month-old infant with Feingold syndrome 2.
Isobe A, Maeda N, Fujita H, Banno S, Kageyama T, Hatabu N, Sato R, Suzuki E, Miharu M, Komiyama O, Nakashima M, Matsunaga T, Nishimura G, Yamazawa K. Isobe A, et al. Among authors: matsunaga t. Am J Med Genet A. 2021 Mar;185(3):952-954. doi: 10.1002/ajmg.a.62038. Epub 2020 Dec 27. Am J Med Genet A. 2021. PMID: 33369046 Review. No abstract available.
Mitochondrial mutations in maternally inherited hearing loss.
Mutai H, Watabe T, Kosaki K, Ogawa K, Matsunaga T. Mutai H, et al. Among authors: matsunaga t. BMC Med Genet. 2017 Mar 20;18(1):32. doi: 10.1186/s12881-017-0389-4. BMC Med Genet. 2017. PMID: 28320335 Free PMC article.
Pax3 deficiency diminishes melanocytes in the developing mouse cochlea.
Udagawa T, Takahashi E, Tatsumi N, Mutai H, Kondo Y, Atkinson PJ, Matsunaga T, Yoshikawa M, Kojima H, Okabe M, Cheng AG. Udagawa T, et al. Among authors: matsunaga t. Res Sq [Preprint]. 2023 Jun 9:rs.3.rs-2990436. doi: 10.21203/rs.3.rs-2990436/v1. Res Sq. 2023. PMID: 37333245 Free PMC article. Updated. Preprint.
Differences between acoustic trauma and other types of acute noise-induced hearing loss in terms of treatment and hearing prognosis.
Wada T, Sano H, Nishio SY, Kitoh R, Ikezono T, Iwasaki S, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Suzuki M, Takahashi H, Tono T, Yamashita H, Hara A, Usami SI. Wada T, et al. Among authors: matsunaga t. Acta Otolaryngol. 2017;137(sup565):S48-S52. doi: 10.1080/00016489.2017.1297899. Epub 2017 Apr 10. Acta Otolaryngol. 2017. PMID: 28394667 Review.
115 results