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De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia.
Rees E, Han J, Morgan J, Carrera N, Escott-Price V, Pocklington AJ, Duffield M, Hall LS, Legge SE, Pardiñas AF, Richards AL, Roth J, Lezheiko T, Kondratyev N, Kaleda V, Golimbet V, Parellada M, González-Peñas J, Arango C; GROUP Investigators; Gawlik M, Kirov G, Walters JTR, Holmans P, O'Donovan MC, Owen MJ. Rees E, et al. Among authors: duffield m. Nat Neurosci. 2020 Feb;23(2):179-184. doi: 10.1038/s41593-019-0565-2. Epub 2020 Jan 13. Nat Neurosci. 2020. PMID: 31932766 Free PMC article.
Eye-controlled, power wheelchair performs well for ALS patients.
Elliott MA, Malvar H, Maassel LL, Campbell J, Kulkarni H, Spiridonova I, Sophy N, Beavers J, Paradiso A, Needham C, Rifley J, Duffield M, Crawford J, Wood B, Cox EJ, Scanlan JM. Elliott MA, et al. Among authors: duffield m. Muscle Nerve. 2019 Nov;60(5):513-519. doi: 10.1002/mus.26655. Epub 2019 Aug 21. Muscle Nerve. 2019. PMID: 31397910 Free PMC article.
A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes.
Peiris H, Duffield MD, Fadista J, Jessup CF, Kashmir V, Genders AJ, McGee SL, Martin AM, Saiedi M, Morton N, Carter R, Cousin MA, Kokotos AC, Oskolkov N, Volkov P, Hough TA, Fisher EM, Tybulewicz VL, Busciglio J, Coskun PE, Becker A, Belichenko PV, Mobley WC, Ryan MT, Chan JY, Laybutt DR, Coates PT, Yang S, Ling C, Groop L, Pritchard MA, Keating DJ. Peiris H, et al. Among authors: duffield md. PLoS Genet. 2016 May 19;12(5):e1006033. doi: 10.1371/journal.pgen.1006033. eCollection 2016 May. PLoS Genet. 2016. PMID: 27195491 Free PMC article.
69 results