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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 4
2005 2
2006 2
2007 1
2008 2
2010 4
2011 6
2012 6
2013 4
2014 5
2015 3
2016 3
2017 8
2018 7
2019 2
2020 3
2021 1
2022 1
2023 1
2026 0

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54 results

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Page 1
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy.
Ollila HM, Sharon E, Lin L, Sinnott-Armstrong N, Ambati A, Yogeshwar SM, Hillary RP, Jolanki O, Faraco J, Einen M, Luo G, Zhang J, Han F, Yan H, Dong XS, Li J, Zhang J, Hong SC, Kim TW, Dauvilliers Y, Barateau L, Lammers GJ, Fronczek R, Mayer G, Santamaria J, Arnulf I, Knudsen-Heier S, Bredahl MKL, Thorsby PM, Plazzi G, Pizza F, Moresco M, Crowe C, Van den Eeden SK, Lecendreux M, Bourgin P, Kanbayashi T, Martínez-Orozco FJ, Peraita-Adrados R, Benetó A, Montplaisir J, Desautels A, Huang YS; FinnGen; Jennum P, Nevsimalova S, Kemlink D, Iranzo A, Overeem S, Wierzbicka A, Geisler P, Sonka K, Honda M, Högl B, Stefani A, Coelho FM, Mantovani V, Feketeova E, Wadelius M, Eriksson N, Smedje H, Hallberg P, Hesla PE, Rye D, Pelin Z, Ferini-Strambi L, Bassetti CL, Mathis J, Khatami R, Aran A, Nampoothiri S, Olsson T, Kockum I, Partinen M, Perola M, Kornum BR, Rueger S, Winkelmann J, Miyagawa T, Toyoda H, Khor SS, Shimada M, Tokunaga K, Rivas M, Pritchard JK, Risch N, Kutalik Z, O'Hara R, Hallmayer J, Ye CJ, Mignot EJ. Ollila HM, et al. Among authors: mantovani v. Nat Commun. 2023 May 15;14(1):2709. doi: 10.1038/s41467-023-36120-z. Nat Commun. 2023. PMID: 37188663 Free PMC article.
Gene Panel Analysis in a Large Cohort of Patients With Autosomal Dominant Polycystic Kidney Disease Allows the Identification of 80 Potentially Causative Novel Variants and the Characterization of a Complex Genetic Architecture in a Subset of Families.
Mantovani V, Bin S, Graziano C, Capelli I, Minardi R, Aiello V, Ambrosini E, Cristalli CP, Mattiaccio A, Pariali M, De Fanti S, Faletra F, Grosso E, Cantone R, Mancini E, Mencarelli F, Pasini A, Wischmeijer A, Sciascia N, Seri M, La Manna G. Mantovani V, et al. Front Genet. 2020 May 7;11:464. doi: 10.3389/fgene.2020.00464. eCollection 2020. Front Genet. 2020. PMID: 32457805 Free PMC article.
Next Generation Sequencing Analysis of MODY-X Patients: A Case Report Series.
Maltoni G, Franceschi R, Di Natale V, Al-Qaisi R, Greco V, Bertorelli R, De Sanctis V, Quattrone A, Mantovani V, Cauvin V, Zucchini S. Maltoni G, et al. Among authors: mantovani v. J Pers Med. 2022 Sep 30;12(10):1613. doi: 10.3390/jpm12101613. J Pers Med. 2022. PMID: 36294752 Free PMC article.
TRPV1 channels regulate cortical excitability in humans.
Mori F, Ribolsi M, Kusayanagi H, Monteleone F, Mantovani V, Buttari F, Marasco E, Bernardi G, Maccarrone M, Centonze D. Mori F, et al. Among authors: mantovani v. J Neurosci. 2012 Jan 18;32(3):873-9. doi: 10.1523/JNEUROSCI.2531-11.2012. J Neurosci. 2012. PMID: 22262885 Free PMC article.
Genetic variants associated with psychotic symptoms across psychiatric disorders.
Calabrò M, Porcelli S, Crisafulli C, Albani D, Kasper S, Zohar J, Souery D, Montgomery S, Mantovani V, Mendlewicz J, Bonassi S, Vieta E, Frustaci A, Ducci G, Landi S, Boccia S, Bellomo A, Di Nicola M, Janiri L, Colombo R, Benedetti F, Mandelli L, Fabbri C, Serretti A. Calabrò M, et al. Among authors: mantovani v. Neurosci Lett. 2020 Feb 16;720:134754. doi: 10.1016/j.neulet.2020.134754. Epub 2020 Jan 13. Neurosci Lett. 2020. PMID: 31945448
Liquid biopsy in the diagnosis of HPV DNA in breast lesions.
Carolis S, Pellegrini A, Santini D, Ceccarelli C, De Leo A, Alessandrini F, Arienti C, Pignatta S, Tesei A, Mantovani V, Zamagni C, Taffurelli M, Sansone P, Bonafé M, Cricca M. Carolis S, et al. Among authors: mantovani v. Future Microbiol. 2018 Feb;13:187-194. doi: 10.2217/fmb-2017-0145. Epub 2017 Oct 4. Future Microbiol. 2018. PMID: 28975808 Free article.
Mutations of the CFTR gene in pancreatic disease.
Pezzilli R, Morselli-Labate AM, Mantovani V, Romboli E, Selva P, Migliori M, Corinaldesi R, Gullo L. Pezzilli R, et al. Among authors: mantovani v. Pancreas. 2003 Nov;27(4):332-6. doi: 10.1097/00006676-200311000-00011. Pancreas. 2003. PMID: 14576497
Maternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients.
Bonora E, Graziano C, Minopoli F, Bacchelli E, Magini P, Diquigiovanni C, Lomartire S, Bianco F, Vargiolu M, Parchi P, Marasco E, Mantovani V, Rampoldi L, Trudu M, Parmeggiani A, Battaglia A, Mazzone L, Tortora G; IMGSAC; Maestrini E, Seri M, Romeo G. Bonora E, et al. Among authors: mantovani v. EMBO Mol Med. 2014 Jun;6(6):795-809. doi: 10.1002/emmm.201303235. Epub 2014 Apr 6. EMBO Mol Med. 2014. PMID: 24737869 Free PMC article.
54 results