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

Year Number of Results
1989 1
1993 1
1998 3
1999 1
2000 1
2001 5
2003 4
2004 4
2005 1
2006 4
2007 1
2008 2
2009 1
2010 2
2011 5
2012 7
2013 6
2014 5
2015 3
2016 1
2017 1
2018 4
2019 8
2020 9
2021 11
2022 1
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87 results
Results by year
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Page 1
De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.
Sakamoto M, Sasaki K, Sugie A, Nitta Y, Kimura T, Gürsoy S, Cinleti T, Iai M, Sengoku T, Ogata K, Suzuki A, Okamoto N, Iwama K, Tsuchida N, Uchiyama Y, Koshimizu E, Fujita A, Hamanaka K, Miyatake S, Mizuguchi T, Taguri M, Ito S, Takahashi H, Miyake N, Matsumoto N. Sakamoto M, et al. Among authors: sengoku t. Hum Mol Genet. 2021 Dec 17;31(1):69-81. doi: 10.1093/hmg/ddab224. Hum Mol Genet. 2021. PMID: 34346499
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder.
Nishioka M, Kazuno AA, Nakamura T, Sakai N, Hayama T, Fujii K, Matsuo K, Komori A, Ishiwata M, Watanabe Y, Oka T, Matoba N, Kataoka M, Alkanaq AN, Hamanaka K, Tsuboi T, Sengoku T, Ogata K, Iwata N, Ikeda M, Matsumoto N, Kato T, Takata A. Nishioka M, et al. Among authors: sengoku t. Nat Commun. 2021 Jun 18;12(1):3750. doi: 10.1038/s41467-021-23453-w. Nat Commun. 2021. PMID: 34145229 Free PMC article.
OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation.
Saida K, Fukuda T, Scott DA, Sengoku T, Ogata K, Nicosia A, Hernandez-Garcia A, Lalani SR, Azamian MS, Streff H, Liu P, Dai H, Mizuguchi T, Miyatake S, Asahina M, Ogata T, Miyake N, Matsumoto N. Saida K, et al. Among authors: sengoku t. Front Cell Dev Biol. 2021 Mar 3;9:631428. doi: 10.3389/fcell.2021.631428. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33748114 Free PMC article.
Evaluation of rapid drug safety communication materials for patients in Japan.
Yaguchi-Saito A, Yamamoto K, Sengoku T, Suka M, Sato T, Hinata M, Nakamura T, Nakayama T, Yamamoto M. Yaguchi-Saito A, et al. Among authors: sengoku t. Drug Discov Ther. 2021 May 11;15(2):101-107. doi: 10.5582/ddt.2021.01028. Epub 2021 Apr 30. Drug Discov Ther. 2021. PMID: 33952763 Free article.
Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy.
Saida K, Tamaoki J, Sasaki M, Haniffa M, Koshimizu E, Sengoku T, Maeda H, Kikuchi M, Yokoyama H, Sakamoto M, Iwama K, Sekiguchi F, Hamanaka K, Fujita A, Mizuguchi T, Ogata K, Miyake N, Miyatake S, Kobayashi M, Matsumoto N. Saida K, et al. Among authors: sengoku t. Clin Genet. 2021 Dec;100(6):722-730. doi: 10.1111/cge.14066. Epub 2021 Oct 7. Clin Genet. 2021. PMID: 34569062
Temporary Tracheal Compression by Dilated Functionally Normal Esophagus.
Sengoku T, Sonoo T, Kira K, Takahashi Y, Hashimoto H, Nakamura K. Sengoku T, et al. Clin Pract Cases Emerg Med. 2018 Apr 18;2(2):177-178. doi: 10.5811/cpcem.2018.3.37534. eCollection 2018 May. Clin Pract Cases Emerg Med. 2018. PMID: 29849267 Free PMC article. No abstract available.
87 results