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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hernández I, Montrreal L, Antúnez C, Antonell A, Tankard RM, Bis JC, Sims R, Bellenguez C, Quintela I, González-Perez A, Calero M, Franco-Macías E, Macías J, Blesa R, Cervera-Carles L, Menéndez-González M, Frank-García A, Royo JL, Moreno F, Huerto Vilas R, Baquero M, Diez-Fairen M, Lage C, García-Madrona S, García-González P, Alarcón-Martín E, Valero S, Sotolongo-Grau O, Ullgren A, Naj AC, Lemstra AW, Benaque A, Pérez-Cordón A, Benussi A, Rábano A, Padovani A, Squassina A, de Mendonça A, Arias Pastor A, Kok AAL, Meggy A, Pastor AB, Espinosa A, Corma-Gómez A, Martín Montes A, Sanabria Á, DeStefano AL, Schneider A, Haapasalo A, Kinhult Ståhlbom A, Tybjærg-Hansen A, Hartmann AM, Spottke A, Corbatón-Anchuelo A, Rongve A, Borroni B, Arosio B, Nacmias B, Nordestgaard BG, Kunkle BW, Charbonnier C, Abdelnour C, Masullo C, Martínez Rodríguez C, Muñoz-Fernandez C, Dufouil C, Graff C, Ferreira CB, Chillotti C, Reynolds CA, Fenoglio C, Van Broeckhoven C, Clark C, Pisanu C, Satizabal CL, Holmes C, Buiza-Rueda D, Aarsland D, Rujescu D, Alcolea D, Galimberti D, Wallon D, Seripa D, Grün… See abstract for full author list ➔ de Rojas I, et al. Among authors: boschi s. Nat Commun. 2021 Jun 7;12(1):3417. doi: 10.1038/s41467-021-22491-8. Nat Commun. 2021. PMID: 34099642 Free PMC article.
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Rubino E, Rainero I, Chiò A, Rogaeva E, Galimberti D, Fenoglio P, Grinberg Y, Isaia G, Calvo A, Gentile S, Bruni AC, St George-Hyslop PH, Scarpini E, Gallone S, Pinessi L; TODEM Study Group. Rubino E, et al. Neurology. 2012 Oct 9;79(15):1556-62. doi: 10.1212/WNL.0b013e31826e25df. Epub 2012 Sep 12. Neurology. 2012. PMID: 22972638 Free PMC article.
Genetic variants in the NOTCH4 gene influence the clinical features of migraine.
Rubino E, Fenoglio P, Gallone S, Govone F, Vacca A, De Martino P, Giobbe ML, Boschi S, Pinessi L, Gentile S, Rainero I. Rubino E, et al. Among authors: boschi s. J Headache Pain. 2013 Mar 26;14(1):28. doi: 10.1186/1129-2377-14-28. J Headache Pain. 2013. PMID: 23566281 Free PMC article.
Is HCRTR2 a genetic risk factor for Alzheimer's disease?
Gallone S, Boschi S, Rubino E, De Martino P, Scarpini E, Galimberti D, Fenoglio C, Acutis PL, Maniaci MG, Pinessi L, Rainero I. Gallone S, et al. Among authors: boschi s. Dement Geriatr Cogn Disord. 2014;38(3-4):245-53. doi: 10.1159/000359964. Epub 2014 Jun 25. Dement Geriatr Cogn Disord. 2014. PMID: 24969517
KCNK18 (TRESK) genetic variants in Italian patients with migraine.
Rainero I, Rubino E, Gallone S, Zavarise P, Carli D, Boschi S, Fenoglio P, Savi L, Gentile S, Benna P, Pinessi L, Dalla Volta G. Rainero I, et al. Among authors: boschi s. Headache. 2014 Oct;54(9):1515-22. doi: 10.1111/head.12439. Headache. 2014. PMID: 25324165
Investigating the role of adipokines in chronic migraine.
Rubino E, Vacca A, Govone F, Gai A, Boschi S, Zucca M, De Martino P, Gentile S, Pinessi L, Rainero I. Rubino E, et al. Among authors: boschi s. Cephalalgia. 2017 Oct;37(11):1067-1073. doi: 10.1177/0333102416665871. Epub 2016 Aug 22. Cephalalgia. 2017. PMID: 27553954 Free article.
O057. Altered plasma adipokines concentrations in chronic migraine.
Rubino E, Govone F, Vacca A, Gai A, Boschi S, Zucca M, Pinessi L, Rainero I. Rubino E, et al. Among authors: boschi s. J Headache Pain. 2015 Dec;16(Suppl 1):A56. doi: 10.1186/1129-2377-16-S1-A56. J Headache Pain. 2015. PMID: 28132332 Free PMC article. No abstract available.
Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy.
Rubino E, Zhang M, Mongini T, Boschi S, Vercelli L, Vacca A, Govone F, Gai A, Giordana MT, Grinberg M, Rogaeva E, Rainero I. Rubino E, et al. Among authors: boschi s. Neurobiol Aging. 2018 Jun;66:181.e1-181.e2. doi: 10.1016/j.neurobiolaging.2018.02.007. Epub 2018 Feb 14. Neurobiol Aging. 2018. PMID: 29519717 Free article.
271 results