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Artigo de periodico
Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder (2016)
Cappi, Carolina; Diniz, Juliana Belo; Requena, Guaraci de Lima; Lourenço, Tiaya; Lisboa, Bianca Cristina Garcia; Batistuzzo, Marcelo Camargo; Marques, Andrea Horvath; Hoexter, Marcelo Queiroz; Pereira, Carlos Alberto de Bragança ; Miguel, Eurípedes Constantino; Brentani, Helena
Source: BMC Neuroscience. Unidades: IME, FM
Assunto: BIOESTATÍSTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAPPI, Carolina et al. Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder. BMC Neuroscience, v. 17, n. 1, p. [8 ], 2016Tradução . . Disponível em: https://doi.org/10.1186/s12868-016-0313-4. Acesso em: 16 nov. 2024.
APA
Cappi, C., Diniz, J. B., Requena, G. de L., Lourenço, T., Lisboa, B. C. G., Batistuzzo, M. C., et al. (2016). Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder. BMC Neuroscience, 17( 1), [8 ]. doi:10.1186/s12868-016-0313-4
NLM
Cappi C, Diniz JB, Requena G de L, Lourenço T, Lisboa BCG, Batistuzzo MC, Marques AH, Hoexter MQ, Pereira CA de B, Miguel EC, Brentani H. Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder [Internet]. BMC Neuroscience. 2016 ; 17( 1): [8 ].[citado 2024 nov. 16 ] Available from: https://doi.org/10.1186/s12868-016-0313-4
Vancouver
Cappi C, Diniz JB, Requena G de L, Lourenço T, Lisboa BCG, Batistuzzo MC, Marques AH, Hoexter MQ, Pereira CA de B, Miguel EC, Brentani H. Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder [Internet]. BMC Neuroscience. 2016 ; 17( 1): [8 ].[citado 2024 nov. 16 ] Available from: https://doi.org/10.1186/s12868-016-0313-4
Artigo de periodico
An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder (2016)
Lima, Leandro de Araújo; Feio-dos-Santos, Ana Cecília; Belangero, Sintia Iole; Gadelha, Ary; Bressan, Rodrigo Affonseca; Salum, Giovanni Abrahão; Pan, Pedro Mario; Moriyama, Tais Silveira; Graeff-Martins, Ana Soledade; Tamanaha, Ana Carina; Alvarenga, Pedro; Krieger, Fernanda Valle; Fleitlich-Bilyk, Bacy; Jackowski, Andrea Parolin; Brietzke, Elisa; Sato, João Ricardo; Polanczyk, Guilherme Vanoni; Mari, Jair de Jesus; Manfro, Gisele Gus; Rosário, Maria Conceição do; Miguel, Eurípedes Constantino; Puga, Renato David; Tahira, Ana Carolina; Souza, Viviane Neri; Chile, Thais; Gouveia, Gisele Rodrigues; Simões, Sérgio Nery; Chang, Xiao; Pellegrino, Renata; Tian, Lifeng; Glessner, Joseph T.; Hashimoto, Ronaldo Fumio ; Rohde, Luis Augusto; Sleiman, Patrick M. A.; Hakonarson, Hakon; Brentani, Helena
Source: Scientific Reports. Unidades: FM, IME
Subjects: DOENÇAS GENÉTICAS, CRIANÇAS, ADOLESCENTES, HIPERATIVIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Leandro de Araújo et al. An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder. Scientific Reports, v. 6, n. 22851, p. 14 , 2016Tradução . . Disponível em: https://doi.org/10.1038/srep22851. Acesso em: 16 nov. 2024.
APA
Lima, L. de A., Feio-dos-Santos, A. C., Belangero, S. I., Gadelha, A., Bressan, R. A., Salum, G. A., et al. (2016). An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder. Scientific Reports, 6( 22851), 14 . doi:10.1038/srep22851
NLM
Lima L de A, Feio-dos-Santos AC, Belangero SI, Gadelha A, Bressan RA, Salum GA, Pan PM, Moriyama TS, Graeff-Martins AS, Tamanaha AC, Alvarenga P, Krieger FV, Fleitlich-Bilyk B, Jackowski AP, Brietzke E, Sato JR, Polanczyk GV, Mari J de J, Manfro GG, Rosário MC do, Miguel EC, Puga RD, Tahira AC, Souza VN, Chile T, Gouveia GR, Simões SN, Chang X, Pellegrino R, Tian L, Glessner JT, Hashimoto RF, Rohde LA, Sleiman PMA, Hakonarson H, Brentani H. An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder [Internet]. Scientific Reports. 2016 ; 6( 22851): 14 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/srep22851
Vancouver
Lima L de A, Feio-dos-Santos AC, Belangero SI, Gadelha A, Bressan RA, Salum GA, Pan PM, Moriyama TS, Graeff-Martins AS, Tamanaha AC, Alvarenga P, Krieger FV, Fleitlich-Bilyk B, Jackowski AP, Brietzke E, Sato JR, Polanczyk GV, Mari J de J, Manfro GG, Rosário MC do, Miguel EC, Puga RD, Tahira AC, Souza VN, Chile T, Gouveia GR, Simões SN, Chang X, Pellegrino R, Tian L, Glessner JT, Hashimoto RF, Rohde LA, Sleiman PMA, Hakonarson H, Brentani H. An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder [Internet]. Scientific Reports. 2016 ; 6( 22851): 14 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/srep22851
Artigo de periodico
An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder (2014)
Cappi, Carolina; Hounie, Ana Gabriela; Mariani, Daniel B; Diniz, Juliana Belo; Silva, Aderbal R. T; Reis, Viviane N. S; Busso, Ariane F; Silva, Amanda Gonçalves; Fidalgo, Felipe; Rogatto, Silvia Regina; Miguel, Eurípedes Constantino; Krepischi, Ana Cristina Victorino ; Brentani, Helena
Source: PLOS ONE. Unidades: FM, IB
Subjects: TRANSTORNO OBSESSIVO-COMPULSIVO, SEROTONINA, TRANSTORNOS MENTAIS, GENOMAS, NEUROPSIQUIATRIA, EXPRESSÃO GÊNICA, GENÉTICA (FATORES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAPPI, Carolina et al. An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder. PLOS ONE, v. 9, n. 10, 2014Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0110198. Acesso em: 16 nov. 2024.
APA
Cappi, C., Hounie, A. G., Mariani, D. B., Diniz, J. B., Silva, A. R. T., Reis, V. N. S., et al. (2014). An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder. PLOS ONE, 9( 10). doi:10.1371/journal.pone.0110198
NLM
Cappi C, Hounie AG, Mariani DB, Diniz JB, Silva ART, Reis VNS, Busso AF, Silva AG, Fidalgo F, Rogatto SR, Miguel EC, Krepischi ACV, Brentani H. An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder [Internet]. PLOS ONE. 2014 ;9( 10):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1371/journal.pone.0110198
Vancouver
Cappi C, Hounie AG, Mariani DB, Diniz JB, Silva ART, Reis VNS, Busso AF, Silva AG, Fidalgo F, Rogatto SR, Miguel EC, Krepischi ACV, Brentani H. An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder [Internet]. PLOS ONE. 2014 ;9( 10):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1371/journal.pone.0110198
Artigo de periodico
Association study between functional polymorphisms in the TNF-alpha gene and obsessive-compulsive disorder (2012)
Cappi, Carolina; Muniz, Renan Kawano; Sampaio, Aline Santos; Cordeiro, Quirino; Brentani, Helena; Palácios, Selma A.; Marques, Andrea H.; Vallada, Homero; Miguel, Eurípedes Constantino; Guilherme, Luiza; Hounie, Ana Gabriela
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: POLIMORFISMO, GENES, MARCADOR MOLECULAR, TRANSTORNOS MENTAIS (GENÉTICA), TRANSTORNO OBSESSIVO-COMPULSIVO (GENÉTICA), CITOCINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAPPI, Carolina et al. Association study between functional polymorphisms in the TNF-alpha gene and obsessive-compulsive disorder. Arquivos de Neuro-Psiquiatria, v. 70, n. 2, p. 87-90, 2012Tradução . . Disponível em: https://doi.org/10.1590/s0004-282x2012000200003. Acesso em: 16 nov. 2024.
APA
Cappi, C., Muniz, R. K., Sampaio, A. S., Cordeiro, Q., Brentani, H., Palácios, S. A., et al. (2012). Association study between functional polymorphisms in the TNF-alpha gene and obsessive-compulsive disorder. Arquivos de Neuro-Psiquiatria, 70( 2), 87-90. doi:10.1590/s0004-282x2012000200003
NLM
Cappi C, Muniz RK, Sampaio AS, Cordeiro Q, Brentani H, Palácios SA, Marques AH, Vallada H, Miguel EC, Guilherme L, Hounie AG. Association study between functional polymorphisms in the TNF-alpha gene and obsessive-compulsive disorder [Internet]. Arquivos de Neuro-Psiquiatria. 2012 ; 70( 2): 87-90.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0004-282x2012000200003
Vancouver
Cappi C, Muniz RK, Sampaio AS, Cordeiro Q, Brentani H, Palácios SA, Marques AH, Vallada H, Miguel EC, Guilherme L, Hounie AG. Association study between functional polymorphisms in the TNF-alpha gene and obsessive-compulsive disorder [Internet]. Arquivos de Neuro-Psiquiatria. 2012 ; 70( 2): 87-90.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1590/s0004-282x2012000200003

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