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

Year Number of Results
2002 1
2004 3
2005 3
2006 4
2007 1
2008 4
2009 2
2011 3
2012 4
2013 2
2014 7
2015 7
2016 3
2017 5
2018 4
2019 9
2020 4
2021 3
2022 7
2023 8
2024 7

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80 results

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Page 1
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder.
Kuroda Y, Iwata-Otsubo A, Dias KR, Temple SEL, Nagao K, De Hayr L, Zhu Y, Isobe SY, Nishibuchi G, Fiordaliso SK, Fujita Y, Rippert AL, Baker SW, Leung ML, Koboldt DC, Harman A, Keena BA, Kazama I, Subramanian GM, Manickam K, Schmalz B, Latsko M, Zackai EH, Edwards M, Evans CA, Dulik MC, Buckley MF, Yamashita T, O'Brien WT, Harvey RJ, Obuse C, Roscioli T, Izumi K. Kuroda Y, et al. Genet Med. 2023 Jul;25(7):100861. doi: 10.1016/j.gim.2023.100861. Epub 2023 Apr 20. Genet Med. 2023. PMID: 37087635
Regulation of osteoclasts by membrane-derived lipid mediators.
Oikawa T, Kuroda Y, Matsuo K. Oikawa T, et al. Among authors: kuroda y. Cell Mol Life Sci. 2013 Sep;70(18):3341-53. doi: 10.1007/s00018-012-1238-4. Epub 2013 Jan 8. Cell Mol Life Sci. 2013. PMID: 23296124 Free PMC article. Review.
Expanding the phenotypic spectrum of ARCN1-related syndrome.
Ritter AL, Gold J, Hayashi H, Ackermann AM, Hanke S, Skraban C, Cuddapah S, Bhoj E, Li D, Kuroda Y, Wen J, Takeda R, Bibb A, El Chehadeh S, Piton A, Ohl J, Kukolich MK, Nagasaki K, Kato K, Ogi T, Bhatti T, Russo P, Krock B, Murrell JR, Sullivan JA, Shashi V, Stong N, Hakonarson H, Sawano K, Torti E, Willaert R, Si Y, Wilcox WR, Wirgenes KV, Thomassen K, Carlotti K, Erwin A, Lazier J, Marquardt T, He M, Edmondson AC, Izumi K. Ritter AL, et al. Among authors: kuroda y. Genet Med. 2022 Jun;24(6):1227-1237. doi: 10.1016/j.gim.2022.02.005. Epub 2022 Mar 14. Genet Med. 2022. PMID: 35300924 Free PMC article.
A novel variant of ARPC4-related neurodevelopmental disorder.
Kuroda Y, Kumaki T, Saito Y, Enomoto Y, Suzuki H, Takenouchi T, Kosaki K, Kurosawa K. Kuroda Y, et al. Am J Med Genet A. 2023 Mar;191(3):893-895. doi: 10.1002/ajmg.a.63082. Epub 2022 Dec 13. Am J Med Genet A. 2023. PMID: 36513617 No abstract available.
Innervation of the tibial epiphysis through the intercondylar foramen.
Matsuo K, Ji S, Miya A, Yoda M, Hamada Y, Tanaka T, Takao-Kawabata R, Kawaai K, Kuroda Y, Shibata S. Matsuo K, et al. Among authors: kuroda y. Bone. 2019 Mar;120:297-304. doi: 10.1016/j.bone.2018.11.007. Epub 2018 Nov 13. Bone. 2019. PMID: 30439572 Free article.
A Japanese patient with RAD51-associated Fanconi anemia.
Takenaka S, Kuroda Y, Ohta S, Mizuno Y, Hiwatari M, Miyatake S, Matsumoto N, Oka A. Takenaka S, et al. Among authors: kuroda y. Am J Med Genet A. 2019 Jun;179(6):900-902. doi: 10.1002/ajmg.a.61130. Epub 2019 Mar 25. Am J Med Genet A. 2019. PMID: 30907510
80 results