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

Year Number of Results
1989 3
1990 4
1991 4
1992 9
1993 4
1994 4
1996 5
1997 1
1998 2
1999 3
2001 1
2002 2
2003 3
2004 2
2005 2
2006 3
2007 2
2008 2
2009 1
2010 3
2011 2
2012 5
2013 2
2014 3
2015 1
2016 3
2017 3
2018 1
2019 1
2020 8
2021 8
2022 4
2023 6
2024 1

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101 results

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Page 1
Mosaicism in Human Health and Disease.
Thorpe J, Osei-Owusu IA, Avigdor BE, Tupler R, Pevsner J. Thorpe J, et al. Among authors: tupler r. Annu Rev Genet. 2020 Nov 23;54:487-510. doi: 10.1146/annurev-genet-041720-093403. Epub 2020 Sep 11. Annu Rev Genet. 2020. PMID: 32916079 Free PMC article. Review.
Does DNA Methylation Matter in FSHD?
Salsi V, Magdinier F, Tupler R. Salsi V, et al. Among authors: tupler r. Genes (Basel). 2020 Feb 28;11(3):258. doi: 10.3390/genes11030258. Genes (Basel). 2020. PMID: 32121044 Free PMC article. Review.
The FSHD jigsaw: are we placing the tiles in the right position?
Salsi V, Vattemi GNA, Tupler RG. Salsi V, et al. Among authors: tupler rg. Curr Opin Neurol. 2023 Oct 1;36(5):455-463. doi: 10.1097/WCO.0000000000001176. Epub 2023 Jun 14. Curr Opin Neurol. 2023. PMID: 37338810 Free PMC article. Review.
Shoulder Injury Related to Vaccine Administration.
Flores C, Choate WS, Tupler R. Flores C, et al. Among authors: tupler r. Ochsner J. 2022 Fall;22(3):261-264. doi: 10.31486/toj.21.0114. Ochsner J. 2022. PMID: 36189092 Free PMC article.
Altered gene silencing and human diseases.
Perini G, Tupler R. Perini G, et al. Among authors: tupler r. Clin Genet. 2006 Jan;69(1):1-7. doi: 10.1111/j.1399-0004.2005.00540.x. Clin Genet. 2006. PMID: 16451126 Review.
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data.
Goselink RJM, Voermans NC, Okkersen K, Brouwer OF, Padberg GW, Nikolic A, Tupler R, Dorobek M, Mah JK, van Engelen BGM, Schreuder THA, Erasmus CE. Goselink RJM, et al. Among authors: tupler r. Neuromuscul Disord. 2017 Dec;27(12):1077-1083. doi: 10.1016/j.nmd.2017.09.007. Epub 2017 Sep 21. Neuromuscul Disord. 2017. PMID: 29102079 Free article. Review.
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.
Dosi C, Rubegni A, Baldacci J, Galatolo D, Doccini S, Astrea G, Berardinelli A, Bruno C, Bruno G, Comi GP, Donati MA, Dotti MT, Filosto M, Fiorillo C, Giannini F, Gigli GL, Grandis M, Lopergolo D, Magri F, Maioli MA, Malandrini A, Massa R, Matà S, Melani F, Messina S, Mignarri A, Moggio M, Pennisi EM, Pegoraro E, Ricci G, Sacchini M, Schenone A, Sampaolo S, Sciacco M, Siciliano G, Tasca G, Tonin P, Tupler R, Valente M, Volpi N, Cassandrini D, Santorelli FM. Dosi C, et al. Among authors: tupler r. Genes (Basel). 2023 Jan 23;14(2):298. doi: 10.3390/genes14020298. Genes (Basel). 2023. PMID: 36833224 Free PMC article.
101 results