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

Year Number of Results
1950 4
1951 2
1952 3
1953 2
1954 1
1957 1
1958 1
1959 2
1960 1
1961 4
1963 3
1964 1
1965 3
1966 7
1967 7
1968 1
1969 6
1970 6
1971 3
1972 5
1973 3
1974 1
1975 3
1976 2
1977 2
1978 3
1979 4
1980 2
1981 4
1982 1
1983 1
1984 1
1987 1
1989 1
1992 1
1996 1
2000 1
2001 2
2002 1
2007 1
2008 1
2009 4
2010 4
2011 2
2012 4
2013 4
2014 4
2015 2
2016 2
2017 3
2018 14
2019 10
2020 13
2021 11
2022 7
2023 8
2024 9
2025 13
2026 5

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203 results

Results by year

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Page 1
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A, Nakashima M, Saitsu H, Mizuguchi T, Mitsuhashi S, Takahashi Y, Okamoto N, Osaka H, Nakamura K, Tohyama J, Haginoya K, Takeshita S, Kuki I, Okanishi T, Goto T, Sasaki M, Sakai Y, Miyake N, Miyatake S, Tsuchida N, Iwama K, Minase G, Sekiguchi F, Fujita A, Imagawa E, Koshimizu E, Uchiyama Y, Hamanaka K, Ohba C, Itai T, Aoi H, Saida K, Sakaguchi T, Den K, Takahashi R, Ikeda H, Yamaguchi T, Tsukamoto K, Yoshitomi S, Oboshi T, Imai K, Kimizu T, Kobayashi Y, Kubota M, Kashii H, Baba S, Iai M, Kira R, Hara M, Ohta M, Miyata Y, Miyata R, Takanashi JI, Matsui J, Yokochi K, Shimono M, Amamoto M, Takayama R, Hirabayashi S, Aiba K, Matsumoto H, Nabatame S, Shiihara T, Kato M, Matsumoto N. Takata A, et al. Among authors: iwama k. Nat Commun. 2019 Jun 7;10(1):2506. doi: 10.1038/s41467-019-10482-9. Nat Commun. 2019. PMID: 31175295 Free PMC article.
Clinical and genetic spectrum of patients with IRF2BPL syndrome.
Iwama K, Kato M, Uchiyama Y, Sakamoto M, Miyamoto R, Izumi Y, Ohashi K, Hattori A, Yoshida N, Azuma Y, Watanabe A, Ikeda C, Shimizu-Motohashi Y, Kusabiraki S, Nakagawa E, Sasaki M, Sugai K, Ohori S, Tsuchida N, Hamanaka K, Koshimizu E, Fujita A, Nakashima M, Miyatake S, Sengoku T, Ogata K, Saitoh S, Saitsu H, Ito S, Mizuguchi T, Matsumoto N. Iwama K, et al. J Hum Genet. 2025 Apr;70(4):181-188. doi: 10.1038/s10038-025-01316-2. Epub 2025 Jan 22. J Hum Genet. 2025. PMID: 39843638
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay.
Hamanaka K, Fujita A, Miyatake S, Misawa K, Koshimizu E, Uchiyama Y, Tsuchida N, Seyama R, Sakamoto M, Iwama K, Nishimura N, Utsuno Y, Fu L, Takizawa M, Liang Q, Itai T, Saida K, Ohori S, Kameyama S, Fukuda H, Hayashi Y, Inoue Y, Goto T, Ichikawa K, Kuki I, Fukuoka M, Kim K, Shiohama T, Shimoda K, Otsuka K, Ueda Y, Cho K, Yuge K, Tachi N, Yoshida M, Daida A, Hirasawa K, Yanagishita T, Yamamoto T, Shirai K, Mehr TF, Fattal-Valevski A, Lev D, Yokoyama H, Iwabuchi E, Saito Y, Miura M, Sugai K, Ishiyama A, Sasaki M, Watanabe Y, Takanashi JI, Kim CA, Yokochi K, Tohyama J, Mori T, Izumi Y, Hasegawa Y, Okamoto N, Ikeda T, Osaka H, Kawai Y, Omae Y, Tokunaga K, Kato M, Mizuguchi T, Matsumoto N. Hamanaka K, et al. Among authors: iwama k. NPJ Genom Med. 2025 Aug 26;10(1):60. doi: 10.1038/s41525-025-00521-4. NPJ Genom Med. 2025. PMID: 40858643 Free PMC article.
Monoallelic and biallelic RNU4-2 variants in neurodevelopmental disorders.
Hayashi Y, Kajiwara K, Mizuno S, Okamoto N, Chan MY, Goto T, Hayakawa S, Kato M, Kim CA, Lev D, Moey LH, Taylor J, Gregersen N, Nezer-Kaner I, Keng WT, Okada S, Osaka H, Sagie T, Sakai Y, Tashiro K, Yap P, Fu L, Iwama K, Liang Q, Nishimura N, Saito S, Sakamoto M, Utsuno Y, Tsuchida N, Uchiyama Y, Koshimizu E, Hamanaka K, Miyatake S, Mizuguchi T, Fujita A, Matsumoto N. Hayashi Y, et al. Among authors: iwama k. J Hum Genet. 2025 Dec 17. doi: 10.1038/s10038-025-01442-x. Online ahead of print. J Hum Genet. 2025. PMID: 41408479
Left Atrial Functional Reserve and Recurrence of Atrial Arrhythmias in Patients With Persistent Atrial Fibrillation.
Yoshida Y, Nakanishi K, Daimon M, Hirose K, Iwama K, Mukai Y, Yamamoto Y, Seki H, Hirokawa M, Nakao T, Oshima T, Matsubara T, Shimizu Y, Oguri G, Kojima T, Hasumi E, Fujiu K, Morita H, Kurano M, Takeda N. Yoshida Y, et al. Among authors: iwama k. J Am Soc Echocardiogr. 2025 Nov;38(11):1106-1109. doi: 10.1016/j.echo.2025.08.005. Epub 2025 Aug 14. J Am Soc Echocardiogr. 2025. PMID: 40818511 No abstract available.
Prevalence of albuminuria and its association with left atrial remodelling in patients with atrial fibrillation.
Nakanishi K, Daimon M, Fujiu K, Iwama K, Hirose K, Yoshida Y, Mukai Y, Seki H, Yamamoto Y, Hirokawa M, Nakao T, Oshima T, Matsubara T, Shimizu Y, Oguri G, Kojima T, Hasumi E, Morita H, Kurano M, Takeda N. Nakanishi K, et al. Among authors: iwama k. Eur Heart J Open. 2025 May 14;5(3):oeaf054. doi: 10.1093/ehjopen/oeaf054. eCollection 2025 May. Eur Heart J Open. 2025. PMID: 40444216 Free PMC article.
Total Atrial Conduction Time as a Predictor of Left Atrial Functional Recovery in Atrial Fibrillation.
Seki H, Nakanishi K, Daimon M, Hirose K, Iwama K, Mukai Y, Yoshida Y, Yamamoto Y, Hirokawa M, Nakao T, Oshima T, Matsubara T, Shimizu Y, Oguri G, Kojima T, Hasumi E, Fujiu K, Morita H, Kurano M, Takeda N. Seki H, et al. Among authors: iwama k. JACC Adv. 2025 Oct;4(10 Pt 2):102151. doi: 10.1016/j.jacadv.2025.102151. Epub 2025 Sep 16. JACC Adv. 2025. PMID: 40961735 Free PMC article.
Sex-specific differences in left atrial reverse remodelling after successful catheter ablation for atrial fibrillation.
Yoshida Y, Nakanishi K, Daimon M, Hirose K, Iwama K, Mukai Y, Yamamoto Y, Seki H, Hirokawa M, Nakao T, Oshima T, Matsubara T, Shimizu Y, Oguri G, Kojima T, Hasumi E, Fujiu K, Morita H, Kurano M, Takeda N. Yoshida Y, et al. Among authors: iwama k. Eur Heart J Cardiovasc Imaging. 2026 Feb 27;27(3):480-487. doi: 10.1093/ehjci/jeaf309. Eur Heart J Cardiovasc Imaging. 2026. PMID: 41206217
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.
Sakamoto M, Iwama K, Sasaki M, Ishiyama A, Komaki H, Saito T, Takeshita E, Shimizu-Motohashi Y, Haginoya K, Kobayashi T, Goto T, Tsuyusaki Y, Iai M, Kurosawa K, Osaka H, Tohyama J, Kobayashi Y, Okamoto N, Suzuki Y, Kumada S, Inoue K, Mashimo H, Arisaka A, Kuki I, Saijo H, Yokochi K, Kato M, Inaba Y, Gomi Y, Saitoh S, Shirai K, Morimoto M, Izumi Y, Watanabe Y, Nagamitsu SI, Sakai Y, Fukumura S, Muramatsu K, Ogata T, Yamada K, Ishigaki K, Hirasawa K, Shimoda K, Akasaka M, Kohashi K, Sakakibara T, Ikuno M, Sugino N, Yonekawa T, Gürsoy S, Cinleti T, Kim CA, Teik KW, Yan CM, Haniffa M, Ohba C, Ito S, Saitsu H, Saida K, Tsuchida N, Uchiyama Y, Koshimizu E, Fujita A, Hamanaka K, Misawa K, Miyatake S, Mizuguchi T, Miyake N, Matsumoto N. Sakamoto M, et al. Among authors: iwama k. Genet Med. 2022 Dec;24(12):2453-2463. doi: 10.1016/j.gim.2022.08.007. Epub 2022 Oct 28. Genet Med. 2022. PMID: 36305856 Free article.
203 results