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

Year Number of Results
1968 1
1970 1
1974 1
1975 1
1976 2
1977 2
1978 1
1980 5
1981 4
1985 3
1986 1
1988 2
1989 1
1990 1
1991 2
1992 1
1994 2
1996 2
1998 4
1999 3
2000 6
2001 2
2002 2
2003 2
2004 5
2005 2
2006 6
2007 3
2008 3
2009 6
2010 5
2011 2
2012 2
2013 3
2014 3
2015 3
2016 2
2017 1
2018 7
2019 2
2020 4
2021 1
2022 4
2023 3
2024 1

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113 results

Results by year

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Page 1
SCAF4-related syndromic intellectual disability.
Carvalho LML, Pinto CF, de Oliveira Scliar M, Otto PA, Krepischi ACV, Rosenberg C. Carvalho LML, et al. Among authors: otto pa. Am J Med Genet A. 2023 Feb;191(2):570-574. doi: 10.1002/ajmg.a.63032. Epub 2022 Nov 5. Am J Med Genet A. 2023. PMID: 36333968
Elementary Atlas of Drosophila melanogaster Mutations.
Otto PA. Otto PA. Genet Mol Biol. 2022 Oct 17;45(4):e20220211. doi: 10.1590/1678-4685-GMB-2022-0211. eCollection 2022. Genet Mol Biol. 2022. PMID: 36264083 Free PMC article. No abstract available.
The structure of first-cousin marriages in Brazil.
Otto PA, Lemes RB, Farias AA, Weller M, Lima SOA, Albino VA, Marques-Alves YK, Pardono E, Bocangel MAP, Santos S. Otto PA, et al. Sci Rep. 2020 Sep 23;10(1):15573. doi: 10.1038/s41598-020-72366-z. Sci Rep. 2020. PMID: 32968083 Free PMC article.
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Caldas Rosa ECC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban-Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Lima AR, et al. Among authors: otto pa. Hum Mutat. 2022 Jul;43(7):900-918. doi: 10.1002/humu.24375. Epub 2022 May 10. Hum Mutat. 2022. PMID: 35344616 Free PMC article.
Skewed X-chromosome Inactivation in Women with Idiopathic Intellectual Disability is Indicative of Pathogenic Variants.
Chaves LD, Carvalho LML, Tolezano GC, Pires SF, Costa SS, de Scliar MO, Giuliani LR, Bertola DR, Santos-Rebouças CB, Seo GH, Otto PA, Rosenberg C, Vianna-Morgante AM, Krepischi ACV. Chaves LD, et al. Among authors: otto pa. Mol Neurobiol. 2023 Jul;60(7):3758-3769. doi: 10.1007/s12035-023-03311-0. Epub 2023 Mar 21. Mol Neurobiol. 2023. PMID: 36943625
Men are the main COVID-19 transmitters: behavior or biology?
Silva MVR, de Castro MV, Passos-Bueno MR, Otto PA, Naslavsky MS, Zatz M. Silva MVR, et al. Among authors: otto pa. Discov Ment Health. 2022;2(1):1. doi: 10.1007/s44192-022-00004-3. Epub 2022 Jan 24. Discov Ment Health. 2022. PMID: 35174362 Free PMC article.
Haploid selection drives new gene male germline expression.
Raices JB, Otto PA, Vibranovski MD. Raices JB, et al. Among authors: otto pa. Genome Res. 2019 Jul;29(7):1115-1122. doi: 10.1101/gr.238824.118. Epub 2019 Jun 20. Genome Res. 2019. PMID: 31221725 Free PMC article.
Santos syndrome is caused by mutation in the WNT7A gene.
Alves LU, Santos S, Musso CM, Ezquina SA, Opitz JM, Kok F, Otto PA, Mingroni-Netto RC. Alves LU, et al. Among authors: otto pa. J Hum Genet. 2017 Dec;62(12):1073-1078. doi: 10.1038/jhg.2017.86. Epub 2017 Aug 31. J Hum Genet. 2017. PMID: 28855715
113 results