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

Year Number of Results
1955 2
1959 1
1960 1
1961 1
1963 2
1964 3
1965 1
1966 1
1967 2
1968 4
1969 1
1970 4
1971 4
1972 1
1973 7
1974 4
1975 5
1976 5
1977 5
1978 4
1979 3
1980 10
1981 8
1982 20
1983 8
1984 14
1985 10
1986 10
1987 4
1988 3
1989 6
1990 9
1991 13
1992 13
1993 13
1994 16
1995 4
1996 9
1997 10
1998 12
1999 12
2000 8
2001 18
2002 9
2003 12
2004 15
2005 14
2006 18
2007 31
2008 36
2009 52
2010 55
2011 53
2012 46
2013 38
2014 65
2015 95
2016 92
2017 73
2018 71
2019 56
2020 55
2021 56
2022 49
2023 57
2024 71
2025 22

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1,317 results

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Page 1
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, Kuniyoshi K, Hayashi T, Mizobuchi K, Ueno S, Terasaki H, Kominami T, Nao-I N, Mawatari G, Mizota A, Shinoda K, Kondo M, Kato K, Sekiryu T, Nakamura M, Kusuhara S, Yamamoto H, Yamamoto S, Mochizuki K, Kondo H, Matsushita I, Kameya S, Fukuchi T, Hatase T, Horiguchi M, Shimada Y, Tanikawa A, Yamamoto S, Miura G, Ito N, Murakami A, Fujimaki T, Hotta Y, Tanaka K, Iwata T. Suga A, et al. Among authors: mochizuki k. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
Solvent-derived defects suppress adsorption in MOF-74.
Fu Y, Yao Y, Forse AC, Li J, Mochizuki K, Long JR, Reimer JA, De Paëpe G, Kong X. Fu Y, et al. Among authors: mochizuki k. Nat Commun. 2023 Apr 25;14(1):2386. doi: 10.1038/s41467-023-38155-8. Nat Commun. 2023. PMID: 37185270 Free PMC article.
1,317 results