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

Year Number of Results
1985 1
1989 4
1990 4
1991 13
1992 5
1993 13
1994 5
1995 10
1996 10
1997 8
1998 13
1999 10
2000 9
2001 4
2002 10
2003 5
2004 7
2005 8
2006 6
2007 7
2008 11
2009 8
2010 10
2011 12
2012 10
2013 13
2014 11
2015 13
2016 7
2017 12
2018 12
2019 7
2020 8
2021 15
2022 2
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282 results
Results by year
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Page 1
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky MS, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AA, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Yamamoto GL, et al. Among authors: passos bueno mr. J Med Genet. 2015 Jun;52(6):413-21. doi: 10.1136/jmedgenet-2015-103018. Epub 2015 Mar 20. J Med Genet. 2015. PMID: 25795793
Osteogenesis imperfecta in Brazilian patients.
Trancozo M, Moraes MVD, Silva DA, Soares JAM, Barbirato C, Almeida MG, Santos LR, Rebouças MRGO, Akel AN Jr, Sipolatti V, Nunes VRR, Errera FIV, Aguena M, Passos-Bueno MR, Paula F. Trancozo M, et al. Among authors: passos bueno mr. Genet Mol Biol. 2019 Apr-Jun;42(2):344-350. doi: 10.1590/1678-4685-GMB-2018-0043. Epub 2019 Aug 15. Genet Mol Biol. 2019. PMID: 31429852 Free PMC article.
A review of craniofacial disorders caused by spliceosomal defects.
Lehalle D, Wieczorek D, Zechi-Ceide RM, Passos-Bueno MR, Lyonnet S, Amiel J, Gordon CT. Lehalle D, et al. Among authors: passos bueno mr. Clin Genet. 2015 Nov;88(5):405-15. doi: 10.1111/cge.12596. Epub 2015 May 1. Clin Genet. 2015. PMID: 25865758 Review.
Development of a comprehensive noninvasive prenatal test.
Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck I, Passos-Bueno MR. Malcher C, et al. Among authors: passos bueno mr. Genet Mol Biol. 2018 Jul/Sept.;41(3):545-554. doi: 10.1590/1678-4685-GMB-2017-0177. Epub 2018 Jul 16. Genet Mol Biol. 2018. PMID: 30043834 Free PMC article.
Mutations in collagen 18A1 and their relevance to the human phenotype.
Passos-Bueno MR, Suzuki OT, Armelin-Correa LM, Sertié AL, Errera FI, Bagatini K, Kok F, Leite KR. Passos-Bueno MR, et al. An Acad Bras Cienc. 2006 Mar;78(1):123-31. doi: 10.1590/s0001-37652006000100012. Epub 2006 Mar 8. An Acad Bras Cienc. 2006. PMID: 16532212 Free article. Review.
Structural variation of the malaria-associated human glycophorin A-B-E region.
Louzada S, Algady W, Weyell E, Zuccherato LW, Brajer P, Almalki F, Scliar MO, Naslavsky MS, Yamamoto GL, Duarte YAO, Passos-Bueno MR, Zatz M, Yang F, Hollox EJ. Louzada S, et al. Among authors: passos bueno mr. BMC Genomics. 2020 Jun 29;21(1):446. doi: 10.1186/s12864-020-06849-8. BMC Genomics. 2020. PMID: 32600246 Free PMC article.
282 results