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Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.
Brain. 2022 Apr 29;145(3):1029-1037. doi: 10.1093/brain/awab386.
Brain. 2022.
PMID: 34983064
Free article.
Detection of a pathogenic Alu element insertion in PALB2 gene from targeted NGS diagnostic data.
Eyries M, Ariste O, Legrand G, Basset N, Guillerm E, Perrier A, Duros C, Cohen-Haguenauer O, de la Grange P, Coulet F.
Eyries M, et al. Among authors: ariste o.
Eur J Hum Genet. 2022 Oct;30(10):1187-1190. doi: 10.1038/s41431-022-01064-3. Epub 2022 Mar 11.
Eur J Hum Genet. 2022.
PMID: 35277653
Free PMC article.
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Recurrent missense variants in clonal hematopoiesis-related genes present in the general population.
Ariste O, de la Grange P, Veitia RA.
Ariste O, et al.
Clin Genet. 2023 Feb;103(2):247-251. doi: 10.1111/cge.14259. Epub 2022 Nov 27.
Clin Genet. 2023.
PMID: 36353970
Free PMC article.
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Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.
Auguste A, Bessière L, Todeschini AL, Caburet S, Sarnacki S, Prat J, D'angelo E, De La Grange P, Ariste O, Lemoine F, Legois B, Sultan C, Zider A, Galmiche L, Kalfa N, Veitia RA.
Auguste A, et al. Among authors: ariste o.
Hum Mol Genet. 2015 Dec 1;24(23):6687-98. doi: 10.1093/hmg/ddv373. Epub 2015 Sep 11.
Hum Mol Genet. 2015.
PMID: 26362254
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