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Page 1
Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.
Husson T, Duboc JB, Quenez O, Charbonnier C, Rotharmel M, Cuenca M, Jegouzo X, Richard AC, Frebourg T, Deleuze JF, Boland A, Genin E, Debette S, Tzourio C, Campion D, Nicolas G, Guillin O; FREX Consortium. Husson T, et al. Among authors: guillin o. Transl Psychiatry. 2018 Dec 5;8(1):268. doi: 10.1038/s41398-018-0291-7. Transl Psychiatry. 2018. PMID: 30518751 Free PMC article.
Frontotemporal dementia phenotype associated with MAPT gene duplication.
Rovelet-Lecrux A, Hannequin D, Guillin O, Legallic S, Jurici S, Wallon D, Frebourg T, Campion D. Rovelet-Lecrux A, et al. Among authors: guillin o. J Alzheimers Dis. 2010;21(3):897-902. doi: 10.3233/JAD-2010-100441. J Alzheimers Dis. 2010. PMID: 20634582
Psychosis revealing familial idiopathic basal ganglia calcification.
Nicolas G, Guillin O, Borden A, Bioux S, Lefaucheur R, Hannequin D. Nicolas G, et al. Among authors: guillin o. Gen Hosp Psychiatry. 2013 Sep-Oct;35(5):575.e3-5. doi: 10.1016/j.genhosppsych.2012.09.008. Epub 2012 Oct 31. Gen Hosp Psychiatry. 2013. PMID: 23122487
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.
Nicolas G, Pottier C, Charbonnier C, Guyant-Maréchal L, Le Ber I, Pariente J, Labauge P, Ayrignac X, Defebvre L, Maltête D, Martinaud O, Lefaucheur R, Guillin O, Wallon D, Chaumette B, Rondepierre P, Derache N, Fromager G, Schaeffer S, Krystkowiak P, Verny C, Jurici S, Sauvée M, Vérin M, Lebouvier T, Rouaud O, Thauvin-Robinet C, Rousseau S, Rovelet-Lecrux A, Frebourg T, Campion D, Hannequin D; French IBGC Study Group. Nicolas G, et al. Among authors: guillin o. Brain. 2013 Nov;136(Pt 11):3395-407. doi: 10.1093/brain/awt255. Epub 2013 Sep 24. Brain. 2013. PMID: 24065723
Dementia in middle-aged patients with schizophrenia.
Nicolas G, Beherec L, Hannequin D, Opolczynski G, Rothärmel M, Wallon D, Véra P, Martinaud O, Guillin O, Campion D. Nicolas G, et al. Among authors: guillin o. J Alzheimers Dis. 2014;39(4):809-22. doi: 10.3233/JAD-131688. J Alzheimers Dis. 2014. PMID: 24284366
Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes.
Guipponi M, Santoni FA, Setola V, Gehrig C, Rotharmel M, Cuenca M, Guillin O, Dikeos D, Georgantopoulos G, Papadimitriou G, Curtis L, Méary A, Schürhoff F, Jamain S, Avramopoulos D, Leboyer M, Rujescu D, Pulver A, Campion D, Siderovski DP, Antonarakis SE. Guipponi M, et al. Among authors: guillin o. PLoS One. 2014 Nov 24;9(11):e112745. doi: 10.1371/journal.pone.0112745. eCollection 2014. PLoS One. 2014. PMID: 25420024 Free PMC article.
Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers.
Nicolas G, Charbonnier C, de Lemos RR, Richard AC, Guillin O, Wallon D, Legati A, Geschwind D, Coppola G, Frebourg T, Campion D, de Oliveira JR, Hannequin D; collaborators from the French IBGC study Group. Nicolas G, et al. Among authors: guillin o. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):586-94. doi: 10.1002/ajmg.b.32336. Epub 2015 Jun 30. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26129893
Correction: Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes.
Guipponi M, Santoni FA, Setola V, Gehrig C, Rotharmel M, Cuenca M, Guillin O, Dikeos D, Georgantopoulos G, Papadimitriou G, Curtis L, Méary A, Schürhoff F, Jamain S, Avramopoulos D, Leboyer M, Rujescu D, Pulver A, Campion D, Siderovski DP, Antonarakis SE. Guipponi M, et al. Among authors: guillin o. PLoS One. 2015 Oct 21;10(10):e0141630. doi: 10.1371/journal.pone.0141630. eCollection 2015. PLoS One. 2015. PMID: 26488584 Free PMC article. No abstract available.
88 results