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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 3
2025 9

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111 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.
Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form.
Ricci G, Torri F, Ruggiero L, Vercelli L, Gadaleta G, Rolle E, Risi B, Carraro E, Evangelista T, Bugiardini E, Dubuisson N, Voermans N, Siciliano G, Mongini T, Filosto M; Italian Clinical Network for FSHD. Ricci G, et al. Neurol Sci. 2025 Sep;46(9):4633-4643. doi: 10.1007/s10072-025-08276-7. Epub 2025 Jun 13. Neurol Sci. 2025. PMID: 40506648
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.
111 results