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Individualized pretest risk estimates to guide treatment decisions in patients with clinical high risk for psychotic disorders.
Sprüngli-Toffel E, Studerus E, Curtis L, Conchon C, Alameda L, Bailey B, Caron C, Haase C, Gros J, Herbrecht E, Huber CG, Riecher-Rössler A, Conus P, Solida A, Armando M, Kapsaridi A, Ducommun MM, Klauser P, Plessen KJ, Urben S, Edan A, Nanzer N, Navarro AL, Schneider M, Genoud D, Michel C, Kindler J, Kaess M, Oliver D, Fusar-Poli P, Borgwardt S, Andreou C. Sprüngli-Toffel E, et al. Among authors: schneider m. Span J Psychiatry Ment Health. 2024 Sep 18:S2950-2853(24)00052-8. doi: 10.1016/j.sjpmh.2024.09.001. Online ahead of print. Span J Psychiatry Ment Health. 2024. PMID: 39303874 Free article.
No age effect in the prevalence and clinical significance of ultra-high risk symptoms and criteria for psychosis in 22q11 deletion syndrome: Confirmation of the genetically driven risk for psychosis?
Armando M, Schneider M, Pontillo M, Vicari S, Debbané M, Schultze-Lutter F, Eliez S. Armando M, et al. Among authors: schneider m. PLoS One. 2017 Apr 13;12(4):e0174797. doi: 10.1371/journal.pone.0174797. eCollection 2017. PLoS One. 2017. PMID: 28406913 Free PMC article. Clinical Trial.
Characterization and prediction of clinical pathways of vulnerability to psychosis through graph signal processing.
Sandini C, Zöller D, Schneider M, Tarun A, Armando M, Nelson B, Amminger PG, Yuen HP, Markulev C, Schäffer MR, Mossaheb N, Schlögelhofer M, Smesny S, Hickie IB, Berger GE, Chen EY, de Haan L, Nieman DH, Nordentoft M, Riecher-Rössler A, Verma S, Thompson A, Yung AR, McGorry PD, Van De Ville D, Eliez S. Sandini C, et al. Among authors: schneider m. Elife. 2021 Sep 27;10:e59811. doi: 10.7554/eLife.59811. Elife. 2021. PMID: 34569937 Free PMC article.
No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.
Guipponi M, Santoni F, Schneider M, Gehrig C, Bustillo XB, Kates WR, Morrow B, Armando M, Vicari S, Sloan-Béna F, Gagnebin M, Shashi V, Hooper SR, Eliez S, Antonarakis SE. Guipponi M, et al. Among authors: schneider m. Transl Psychiatry. 2017 Feb 21;7(2):e1039. doi: 10.1038/tp.2016.258. Transl Psychiatry. 2017. PMID: 28221368 Free PMC article.
Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Fiksinski AM, Schneider M, Murphy CM, Armando M, Vicari S, Canyelles JM, Gothelf D, Eliez S, Breetvelt EJ, Arango C, Vorstman JAS. Fiksinski AM, et al. Among authors: schneider m. Am J Med Genet A. 2018 Oct;176(10):2182-2191. doi: 10.1002/ajmg.a.40387. Epub 2018 Sep 8. Am J Med Genet A. 2018. PMID: 30194907 Free PMC article. Review.
7,450 results