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Results by year

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

Year Number of Results
1920 1
1980 1
1982 1
1983 1
1987 1
1988 2
1990 2
1991 2
1993 1
1994 2
1995 3
1996 3
1997 2
1998 3
1999 1
2000 2
2002 6
2003 7
2004 2
2005 7
2006 2
2008 3
2009 5
2010 8
2011 9
2012 8
2013 11
2014 4
2015 6
2016 4
2017 4
2018 4
2019 3
2020 3
2021 9
2022 5
2023 5

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124 results

Results by year

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Page 1
Fragile sites, chromosomal lesions, tandem repeats, and disease.
Mirceta M, Shum N, Schmidt MHM, Pearson CE. Mirceta M, et al. Among authors: pearson ce. Front Genet. 2022 Nov 17;13:985975. doi: 10.3389/fgene.2022.985975. eCollection 2022. Front Genet. 2022. PMID: 36468036 Free PMC article. Review.
A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo.
Nakamori M, Panigrahi GB, Lanni S, Gall-Duncan T, Hayakawa H, Tanaka H, Luo J, Otabe T, Li J, Sakata A, Caron MC, Joshi N, Prasolava T, Chiang K, Masson JY, Wold MS, Wang X, Lee MYWT, Huddleston J, Munson KM, Davidson S, Layeghifard M, Edward LM, Gallon R, Santibanez-Koref M, Murata A, Takahashi MP, Eichler EE, Shlien A, Nakatani K, Mochizuki H, Pearson CE. Nakamori M, et al. Among authors: pearson ce. Nat Genet. 2020 Feb;52(2):146-159. doi: 10.1038/s41588-019-0575-8. Epub 2020 Feb 14. Nat Genet. 2020. PMID: 32060489 Free PMC article.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, Leib DE, Chen R, Tanaka H, Mason AG, Lévesque D, Khan M, Razzaghi M, Prasolava T, Lanni S, Sato N, Caron MC, Panigrahi GB, Wang P, Lau R, Castel AL, Masson JY, Tippett L, Turner C, Spies M, La Spada AR, Campos EI, Curtis MA, Boisvert FM, Faull RLM, Davidson BL, Nakamori M, Okazawa H, Wold MS, Pearson CE. Gall-Duncan T, et al. Among authors: pearson ce. Cell. 2023 Oct 26;186(22):4898-4919.e25. doi: 10.1016/j.cell.2023.09.008. Epub 2023 Oct 11. Cell. 2023. PMID: 37827155
Molecular genetics of congenital myotonic dystrophy.
Lanni S, Pearson CE. Lanni S, et al. Among authors: pearson ce. Neurobiol Dis. 2019 Dec;132:104533. doi: 10.1016/j.nbd.2019.104533. Epub 2019 Jul 19. Neurobiol Dis. 2019. PMID: 31326502 Free article. Review.
Disease-associated repeat instability and mismatch repair.
Schmidt MHM, Pearson CE. Schmidt MHM, et al. Among authors: pearson ce. DNA Repair (Amst). 2016 Feb;38:117-126. doi: 10.1016/j.dnarep.2015.11.008. Epub 2015 Dec 12. DNA Repair (Amst). 2016. PMID: 26774442 Review.
De novo mutations, genetic mosaicism and human disease.
Mohiuddin M, Kooy RF, Pearson CE. Mohiuddin M, et al. Among authors: pearson ce. Front Genet. 2022 Sep 26;13:983668. doi: 10.3389/fgene.2022.983668. eCollection 2022. Front Genet. 2022. PMID: 36226191 Free PMC article. Review.
Understanding veterinary leadership in practice.
Pearson CE, Butler AJ, Murray YP. Pearson CE, et al. Vet Rec. 2018 Apr 21;182(16):460. doi: 10.1136/vr.104485. Epub 2018 Feb 14. Vet Rec. 2018. PMID: 29445011
Genome-wide tandem repeat expansions contribute to schizophrenia risk.
Mojarad BA, Engchuan W, Trost B, Backstrom I, Yin Y, Thiruvahindrapuram B, Pallotto L, Mitina A, Khan M, Pellecchia G, Haque B, Guo K, Heung T, Costain G, Scherer SW, Marshall CR, Pearson CE, Bassett AS, Yuen RKC. Mojarad BA, et al. Among authors: pearson ce. Mol Psychiatry. 2022 Sep;27(9):3692-3698. doi: 10.1038/s41380-022-01575-x. Epub 2022 May 12. Mol Psychiatry. 2022. PMID: 35546631 Free PMC article.
124 results