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

Year Number of Results
1971 1
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1993 6
1994 5
1995 3
1996 2
1997 1
1998 7
1999 2
2000 5
2001 6
2002 1
2003 1
2004 1
2006 1
2007 4
2008 3
2009 6
2010 7
2011 7
2012 6
2013 5
2014 6
2015 8
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2017 8
2018 6
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2023 2
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125 results

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Page 1
Determination of Genotype and Phenotypes in Pediatric Patients With Biventricular Noncompaction.
Hirono K, Hata Y, Imamura T, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Ichimata S, Nishida N, Iwasaki H, Urata S, Okada S, Hiratsuji T, Sakaguchi H, Takigiku K, Nakazawa M, Nishihara E, Harada M, Matsuo O, Yasuda K, Yoshida Y, Namiki H, Yasuda K, Ifuku T, Urayama K, Oka H, Ogino K, Kato A, Kan N, Seki S, Seki M, Odanaka Y, Iwashima S, Yoshida S, Miyata T, Miyamoto T, Watanabe K, Kuwabara N, Inuzuka R, Takahashi Y, Sakazaki H, Muneuchi J, Kogaki S, Numano F, Kido S, Nii M, Hoshino S, Ishida H, Maeda J, Hayabuchi Y, Otsubo Y, Ikeda K, Tsukano S, Watanabe M, Momoi N, Fujii T, Fujioka T, Fujino M, Uchiyama H, Baba S, Horigome H, Honda T, Suzuki K, Ichida F. Hirono K, et al. Among authors: hayabuchi y. J Am Heart Assoc. 2024 Nov 5;13(21):e035614. doi: 10.1161/JAHA.124.035614. Epub 2024 Nov 4. J Am Heart Assoc. 2024. PMID: 39494597 Free PMC article.
Clinical Impact of Genetic Testing for Long QT Syndrome　- Evidence From a Nationwide LQTS Registry in Japan.
Aiba T, Ohno S, Takegami M, Kato Y, Sakaguchi H, Shimamoto K, Sonoda K, Ida K, Sumitomo N, Nabeshima T, Murakami T, Ninomiya Y, Kato K, Fukuyama M, Makiyama T, Hayashi K, Ohta K, Morita H, Nakajima T, Kaneko Y, Yagihara N, Otsuki S, Kosho T, Yoshida Y, Takamuro M, Ueno M, Takahashi T, Inden Y, Hayabuchi Y, Muraji S, Watanabe S, Nishimura K, Asano Y, Horigome H, Yoshinaga M, Horie M, Shimizu W, Kusano K. Aiba T, et al. Among authors: hayabuchi y. Circ J. 2025 May 23;89(6):835-844. doi: 10.1253/circj.CJ-25-0105. Epub 2025 Mar 30. Circ J. 2025. PMID: 40159220 Free article.
Sarcomere gene variants did not improve cardiac function in pediatric patients with dilated cardiomyopathy from Japanese cohorts.
Hirono K, Hata Y, Ichimata S, Nishida N, Imamura T, Asano Y, Kuramoto Y, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Muneuchi J, Yasuda K, Urayama K, Oka H, Miyamoto T, Baba K, Kato A, Saiki H, Kuwabara N, Harada M, Baba S, Morikawa M, Iwasaki H, Hirata Y, Ito Y, Sakaguchi H, Urata S, Toda K, Kittaka E, Okada S, Hasebe Y, Hoshino S, Fujii T, Mitsushita N, Nii M, Ogino K, Fujino M, Yoshida Y, Fukuda Y, Iwashima S, Takigiku K, Sakata Y, Inuzuka R, Maeda J, Hayabuchi Y, Fujioka T, Namiki H, Fujita S, Nishida K, Kuraoka A, Kan N, Kido S, Watanabe K, Ichida F. Hirono K, et al. Among authors: hayabuchi y. Sci Rep. 2024 Dec 16;14(1):30469. doi: 10.1038/s41598-024-77360-3. Sci Rep. 2024. PMID: 39681577 Free PMC article.
Reply: To PMID 24814570.
Hayabuchi Y, Sakata M, Kagami S. Hayabuchi Y, et al. Echocardiography. 2015 Oct;32(10):1603-4. doi: 10.1111/echo.13029. Echocardiography. 2015. PMID: 26444453 No abstract available.
Congenital ductus arteriosus aneurysm.
Suzue M, Mori K, Hayabuchi Y. Suzue M, et al. Among authors: hayabuchi y. J Echocardiogr. 2012 Sep;10(3):112-4. doi: 10.1007/s12574-012-0137-x. Epub 2012 Aug 28. J Echocardiogr. 2012. PMID: 27278213 No abstract available.
Detection of 1p36 deletion by clinical exome-first diagnostic approach.
Watanabe M, Hayabuchi Y, Ono A, Naruto T, Horikawa H, Kohmoto T, Masuda K, Nakagawa R, Ito H, Kagami S, Imoto I. Watanabe M, et al. Among authors: hayabuchi y. Hum Genome Var. 2016 May 12;3:16006. doi: 10.1038/hgv.2016.6. eCollection 2016. Hum Genome Var. 2016. PMID: 28428889 Free PMC article.
125 results