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Page 1
Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study Protocol.
Crowley JJ, Cappi C, Ochoa-Panaifo ME, Frederick RM, Kook M, Wiese AD, Rancourt D, Atkinson EG, Giusti-Rodriguez P, Anderberg JL; Latin American Trans-ancestry INitiative for OCD genomics (LATINO), Brazilian Obsessive-Compulsive Spectrum Disorder Working Group (GTTOC); Abramowitz JS, Adorno VR, Aguirre C, Alves GS, Alves GS, Ancalade N, Espinosa AAA, Arnold PD, Ayton DM, Barbosa IG, Castano LMB, Barrera CN, Prieto MB, Berardo MC, Berrones D, Best JR, Bigdeli TB, Burton CL, Callahan JL, Carneiro MCB, Cepeda SL, Chazelle E, Chire JM, Munoz MC, Quiroz PC, Cobite J, Comer JS, Costa DL, Crosbie J, Cruz VO, Dager G, Daza LF, de la Rosa-Gómez A, Del Río D, Delage FZ, Dreher CB, Fay L, Fazio T, Ferrão YA, Ferreira GM, Figueroa EG, Fontenelle LF, Forero DA, Fragoso DT, Gadad BS, Garrison SR, González A, Gonzalez LD, González MA, Gonzalez-Barrios P, Goodman W, Guintivano J, Guttfreund DG, Guzick AG, Halvorsen MW, Hovey JD, Janssen-Aguilar R, Jensen M, Reynolds AZJ, Lujambio JAJ, Khalfe N, Knutsen MA, Lack C, Lanzagorta N, Lima MO, Longhurst MO, Martinez DAL, Luna ES, Marques AH, Martinez M, de Los Angeles Matos M, Maye CE, McGuire JF, Menezes G, Minaya C, Miño T, Mithani SM, de Oca C… See abstract for full author list ➔ Crowley JJ, et al. Among authors: cappi c. medRxiv [Preprint]. 2023 Feb 26:2023.02.23.23286373. doi: 10.1101/2023.02.23.23286373. medRxiv. 2023. PMID: 37131804 Free PMC article. Updated. Preprint.
The drug-naïve OCD patients imaging genetics, cognitive and treatment response study: methods and sample description.
Hoexter MQ, Shavitt RG, D'Alcante CC, Cecconi JP, Diniz JB, Belotto-Silva C, Hounie AG, Borcato S, Moraes I, Joaquim MA, Cappi C, Sampaio AS, Mathis MA, Batistuzzo MC, Lopes AC, Rosa AC, Muniz RK, Marques AH, Santos LC, Taub A, Duran FL, Dougherty DD, Busatto GF, Bressan RA, Miguel EC. Hoexter MQ, et al. Among authors: cappi c. Braz J Psychiatry. 2009 Dec;31(4):349-53. doi: 10.1590/s1516-44462009000400011. Braz J Psychiatry. 2009. PMID: 20098825 Free article.
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, Bloch MH, Blom RM, Bruun RD, Budman CL, Camarena B, Campbell D, Cappi C, Cardona Silgado JC, Cath DC, Cavallini MC, Chavira DA, Chouinard S, Conti DV, Cook EH, Coric V, Cullen BA, Deforce D, Delorme R, Dion Y, Edlund CK, Egberts K, Falkai P, Fernandez TV, Gallagher PJ, Garrido H, Geller D, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Haddad S, Heiman GA, Hemmings SM, Hounie AG, Illmann C, Jankovic J, Jenike MA, Kennedy JL, King RA, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Macciardi F, McCracken JT, McGrath LM, Mesa Restrepo SC, Moessner R, Morgan J, Muller H, Murphy DL, Naarden AL, Ochoa WC, Ophoff RA, Osiecki L, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner TJ, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosàrio MC, Rosenberg D, Rouleau GA, Ruhrmann S, Ruiz-Linares A, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Valencia Duarte AV, Vallada H,… See abstract for full author list ➔ Davis LK, et al. Among authors: cappi c. PLoS Genet. 2013 Oct;9(10):e1003864. doi: 10.1371/journal.pgen.1003864. Epub 2013 Oct 24. PLoS Genet. 2013. PMID: 24204291 Free PMC article.
COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.
Sampaio AS, Hounie AG, Petribú K, Cappi C, Morais I, Vallada H, do Rosário MC, Stewart SE, Fargeness J, Mathews C, Arnold P, Hanna GL, Richter M, Kennedy J, Fontenelle L, de Bragança Pereira CA, Pauls DL, Miguel EC. Sampaio AS, et al. Among authors: cappi c. PLoS One. 2015 Mar 20;10(3):e0119592. doi: 10.1371/journal.pone.0119592. eCollection 2015. PLoS One. 2015. PMID: 25793616 Free PMC article.
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways.
Cappi C, Brentani H, Lima L, Sanders SJ, Zai G, Diniz BJ, Reis VN, Hounie AG, Conceição do Rosário M, Mariani D, Requena GL, Puga R, Souza-Duran FL, Shavitt RG, Pauls DL, Miguel EC, Fernandez TV. Cappi C, et al. Transl Psychiatry. 2016 Mar 29;6(3):e764. doi: 10.1038/tp.2016.30. Transl Psychiatry. 2016. PMID: 27023170 Free PMC article.
Quantifying dimensional severity of obsessive-compulsive disorder for neurobiological research.
Shavitt RG, Requena G, Alonso P, Zai G, Costa DLC, de Bragança Pereira CA, do Rosário MC, Morais I, Fontenelle L, Cappi C, Kennedy J, Menchon JM, Miguel E, Richter PMA. Shavitt RG, et al. Among authors: cappi c. Prog Neuropsychopharmacol Biol Psychiatry. 2017 Oct 3;79(Pt B):206-212. doi: 10.1016/j.pnpbp.2017.06.037. Epub 2017 Jul 1. Prog Neuropsychopharmacol Biol Psychiatry. 2017. PMID: 28673486
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
Cappi C, Oliphant ME, Péter Z, Zai G, Conceição do Rosário M, Sullivan CAW, Gupta AR, Hoffman EJ, Virdee M, Olfson E, Abdallah SB, Willsey AJ, Shavitt RG, Miguel EC, Kennedy JL, Richter MA, Fernandez TV. Cappi C, et al. Biol Psychiatry. 2020 Jun 15;87(12):1035-1044. doi: 10.1016/j.biopsych.2019.09.029. Epub 2019 Oct 16. Biol Psychiatry. 2020. PMID: 31771860 Free PMC article.
56 results