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

Year Number of Results
1955 1
1956 1
1962 1
1963 1
1964 6
1965 4
1966 4
1967 5
1968 1
1969 5
1970 7
1971 3
1972 6
1973 2
1974 2
1975 2
1976 1
1977 3
1978 5
1979 4
1980 4
1981 6
1982 3
1983 6
1984 11
1985 21
1986 16
1987 17
1988 28
1989 28
1990 25
1991 20
1992 23
1993 16
1994 28
1995 13
1996 21
1997 18
1998 28
1999 22
2000 25
2001 23
2002 26
2003 26
2004 30
2005 26
2006 25
2007 18
2008 31
2009 29
2010 41
2011 41
2012 36
2013 43
2014 44
2015 52
2016 48
2017 57
2018 41
2019 61
2020 71
2021 36
Text availability
Article attribute
Article type
Publication date

Search Results

1,156 results
Results by year
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Page 1
Neuroblastoma.
Nakagawara A, Li Y, Izumi H, Muramori K, Inada H, Nishi M. Nakagawara A, et al. Among authors: nishi m. Jpn J Clin Oncol. 2018 Mar 1;48(3):214-241. doi: 10.1093/jjco/hyx176. Jpn J Clin Oncol. 2018. PMID: 29378002 Review.
Androgen insensitivity syndrome: a review.
Batista RL, Costa EMF, Rodrigues AS, Gomes NL, Faria JA Jr, Nishi MY, Arnhold IJP, Domenice S, Mendonca BB. Batista RL, et al. Among authors: nishi my. Arch Endocrinol Metab. 2018 Mar-Apr;62(2):227-235. doi: 10.20945/2359-3997000000031. Arch Endocrinol Metab. 2018. PMID: 29768628 Review.
Wide spectrum of NR5A1-related phenotypes in 46,XY and 46,XX individuals.
Domenice S, Machado AZ, Ferreira FM, Ferraz-de-Souza B, Lerario AM, Lin L, Nishi MY, Gomes NL, da Silva TE, Silva RB, Correa RV, Montenegro LR, Narciso A, Costa EM, Achermann JC, Mendonca BB. Domenice S, et al. Among authors: nishi my. Birth Defects Res C Embryo Today. 2016 Dec;108(4):309-320. doi: 10.1002/bdrc.21145. Birth Defects Res C Embryo Today. 2016. PMID: 28033660 Free PMC article. Review.
Prevalence of disease-causing genes in Japanese patients with BRCA1/2-wildtype hereditary breast and ovarian cancer syndrome.
Kaneyasu T, Mori S, Yamauchi H, Ohsumi S, Ohno S, Aoki D, Baba S, Kawano J, Miki Y, Matsumoto N, Nagasaki M, Yoshida R, Akashi-Tanaka S, Iwase T, Kitagawa D, Masuda K, Hirasawa A, Arai M, Takei J, Ide Y, Gotoh O, Yaguchi N, Nishi M, Kaneko K, Matsuyama Y, Okawa M, Suzuki M, Nezu A, Yokoyama S, Amino S, Inuzuka M, Noda T, Nakamura S. Kaneyasu T, et al. Among authors: nishi m. NPJ Breast Cancer. 2020 Jun 12;6:25. doi: 10.1038/s41523-020-0163-1. eCollection 2020. NPJ Breast Cancer. 2020. PMID: 32566746 Free PMC article.
A tumor profile in Patau syndrome (trisomy 13).
Satgé D, Nishi M, Sirvent N, Vekemans M, Chenard MP, Barnes A. Satgé D, et al. Among authors: nishi m. Am J Med Genet A. 2017 Aug;173(8):2088-2096. doi: 10.1002/ajmg.a.38294. Epub 2017 May 25. Am J Med Genet A. 2017. PMID: 28544599 Review.
Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing.
Homma TK, Freire BL, Honjo Kawahira RS, Dauber A, Funari MFA, Lerario AM, Nishi MY, Albuquerque EV, Vasques GA, Collett-Solberg PF, Miura Sugayama SM, Bertola DR, Kim CA, Arnhold IJP, Malaquias AC, Jorge AAL. Homma TK, et al. Among authors: nishi my. J Pediatr. 2019 Dec;215:192-198. doi: 10.1016/j.jpeds.2019.08.024. Epub 2019 Oct 17. J Pediatr. 2019. PMID: 31630891
A tumor profile in Edwards syndrome (trisomy 18).
Satgé D, Nishi M, Sirvent N, Vekemans M. Satgé D, et al. Among authors: nishi m. Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):296-306. doi: 10.1002/ajmg.c.31511. Epub 2016 Jul 30. Am J Med Genet C Semin Med Genet. 2016. PMID: 27474103 Review.
1,156 results
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