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Bridging the gap: Short structural variants in the genetics of anorexia nervosa.
Int J Eat Disord. 2022 Jun;55(6):747-753. doi: 10.1002/eat.23716. Epub 2022 Apr 26.
Int J Eat Disord. 2022.
PMID: 35470453
Free PMC article.
Structural Variants May Be a Source of Missing Heritability in sALS.
Theunissen F, Flynn LL, Anderton RS, Mastaglia F, Pytte J, Jiang L, Hodgetts S, Burns DK, Saunders A, Fletcher S, Wilton SD, Akkari PA.
Theunissen F, et al. Among authors: pytte j.
Front Neurosci. 2020 Jan 31;14:47. doi: 10.3389/fnins.2020.00047. eCollection 2020.
Front Neurosci. 2020.
PMID: 32082115
Free PMC article.
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Association of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis.
Pytte J, Anderton RS, Flynn LL, Theunissen F, Jiang L, Pitout I, James I, Mastaglia FL, Saunders AM, Bedlack R, Siddique T, Siddique N, Akkari PA.
Pytte J, et al.
Neurol Genet. 2020 Feb 27;6(2):e406. doi: 10.1212/NXG.0000000000000406. eCollection 2020 Apr.
Neurol Genet. 2020.
PMID: 32185242
Free PMC article.
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Disease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohort.
Pytte J, Flynn LL, Anderton RS, Mastaglia FL, Theunissen F, James I, Pfaff A, Koks S, Saunders AM, Bedlack R, Burns DK, Lutz MW, Siddique N, Siddique T, Roses AD, Akkari PA.
Pytte J, et al.
Neurol Genet. 2020 Jul 1;6(4):e470. doi: 10.1212/NXG.0000000000000470. eCollection 2020 Aug.
Neurol Genet. 2020.
PMID: 32754644
Free PMC article.
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