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

Year Number of Results
1961 1
1964 1
1965 1
1967 1
1981 1
1982 5
1983 5
1984 5
1985 9
1986 4
1987 2
1989 7
1990 7
1991 2
1994 1
1996 1
1997 1
2001 1
2003 3
2004 1
2010 1
2019 1
2020 4
2021 3
2022 8
2023 6
2024 1

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78 results

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Page 1
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. Among authors: kumaki t. 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.
Extreme genetic signatures of local adaptation during Lotus japonicus colonization of Japan.
Shah N, Wakabayashi T, Kawamura Y, Skovbjerg CK, Wang MZ, Mustamin Y, Isomura Y, Gupta V, Jin H, Mun T, Sandal N, Azuma F, Fukai E, Seren Ü, Kusakabe S, Kikuchi Y, Nitanda S, Kumaki T, Hashiguchi M, Tanaka H, Hayashi A, Sønderkær M, Nielsen KL, Schneeberger K, Vilhjalmsson B, Akashi R, Stougaard J, Sato S, Schierup MH, Andersen SU. Shah N, et al. Among authors: kumaki t. Nat Commun. 2020 Jan 14;11(1):253. doi: 10.1038/s41467-019-14213-y. Nat Commun. 2020. PMID: 31937774 Free PMC article.
Expanding the phenotype of COL4A1-related disorders-Four novel variants.
Nishimura N, Kumaki T, Murakami H, Enomoto Y, Tsurusaki Y, Tsuji M, Tsuyusaki Y, Goto T, Aida N, Kurosawa K. Nishimura N, et al. Among authors: kumaki t. Brain Dev. 2020 Oct;42(9):639-645. doi: 10.1016/j.braindev.2020.05.009. Epub 2020 Jun 19. Brain Dev. 2020. PMID: 32565002
Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing.
Enomoto Y, Yokoi T, Tsurusaki Y, Murakami H, Tominaga M, Minatogawa M, Abe-Hatano C, Kuroda Y, Ohashi I, Ida K, Shiiya S, Kumaki T, Naruto T, Mitsui J, Harada N, Kido Y, Kurosawa K. Enomoto Y, et al. Among authors: kumaki t. Clin Genet. 2022 Mar;101(3):335-345. doi: 10.1111/cge.14103. Epub 2022 Jan 4. Clin Genet. 2022. PMID: 34958122
78 results