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15 results on '"Camerini, Laísa"'

1. Genetic Variations in Elements of the Oxytocinergic Pathway are Associated with Attention/Hyperactivity Problems and Anxiety Problems in Childhood

Author

Camerini, Laísa, Zurchimitten, Gabriel, Bock, Bertha, Xavier, Janaína, Bastos, Clarissa Ribeiro, Martins, Evânia, Ardais, Ana Paula, dos Santos Motta, Janaína Vieira, Pires, Andressa Jacondino, de Matos, Mariana Bonati, de Ávila Quevedo, Luciana, Pinheiro, Ricardo Tavares, and Ghisleni, Gabriele

Published
2024
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2. Temperament traits mediate the relationship between CACNA1C polymorphisms and bipolar disorder in cisgender women

Author

Bastos, Clarissa Ribeiro, Bock, Bertha Bueno, Xavier, Janaina, Camerini, Laísa, Dewes, Samantha Seibt, Grellert, Mateus, de Carvalho, Hudson Wander, Jansen, Karen, da Silva, Ricardo Azevedo, Pinheiro, Ricardo Tavares, de Mattos Souza, Luciano, Oses, Jean Pierre, Portela, Luis Valmor, Lara, Diogo Rizzato, Tovo-Rodrigues, Luciana, and Ghisleni, Gabriele

Published
2023
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3. BDNF Levels According to Variations in the CACNA1C Gene: Sex-Based Disparity

Author

Bastos, Clarissa Ribeiro, Xavier, Janaina, Camerini, Laísa, Dewes, Samantha Seibt, Moreira, Fernanda Pedrotti, Wiener, Carolina David, Jansen, Karen, Kaster, Manuella Pinto, de Mattos Souza, Luciano Dias, da Silva, Ricardo Azevedo, Oses, Jean Pierre, Portela, Luis Valmor, Lara, Diogo Rizzato, Tovo-Rodrigues, Luciana, and Ghisleni, Gabriele

Published
2023
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4. Gene – maltreatment interplay in adult ADHD symptoms: main role of a gene–environment correlation effect in a Brazilian population longitudinal study

Author

Tovo-Rodrigues, Luciana, primary, Camerini, Laísa, additional, Martins-Silva, Thais, additional, Carpena, Marina Xavier, additional, Bonilla, Carolina, additional, Oliveira, Isabel Oliveira, additional, de Paula, Cristiane Silvestre, additional, Murray, Joseph, additional, Barros, Aluísio J. D., additional, Santos, Iná S., additional, Rohde, Luis Augusto, additional, Hutz, Mara Helena, additional, Genro, Julia Pasqualini, additional, and Matijasevich, Alicia, additional

Published
2024
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7. T52. GENETICS – CHILDHOOD MALTREATMENT CORRELATION EFFECT IN ATTENTION DEFICIT HYPERACTIVITY DISORDER SYMPTOMS IN EARLY ADULTHOOD: EVIDENCE FROM THE 2004 PELOTAS (BRAZIL) BIRTH COHORT

Author

Tovo-Rodrigues, Luciana, primary, Hutz, Mara, additional, Camerini, Laísa, additional, Martins-Silva, Thais, additional, Carpena, Marina X, additional, Bonilla, Carolina, additional, Oliveira, Isabel O, additional, de Paula, Cristiane Silvestre, additional, Murray, Joseph, additional, Barros, Aluísio JD, additional, Santos, Iná S., additional, Rohde, Luis A, additional, Genro, Julia P, additional, and Matijasevich, Alicia, additional

Published
2023
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8. COMT Val 158 Met polymorphism protects the impact of a mother's history of childhood trauma on emotional and behavioral problems in preschool children

Author

Xavier, Janaína, primary, Bastos, Clarissa Ribeiro, additional, Marins, Thayane Moreira, additional, Camerini, Laísa, additional, Mello, Daniele Behling, additional, Antunes, Bruna, additional, Quevedo, Luciana de Ávila, additional, Matos, Mariana Bonati, additional, Pinheiro, Ricardo Tavares, additional, and Ghisleni, Gabriele, additional

Published
2023
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9. Temperament traits mediate the relationship between CACNA1C polymorphisms and bipolar disorder in cisgender women

Author

Bastos, Clarissa Ribeiro, primary, Bock, Bertha Bueno, additional, Xavier, Janaina, additional, Camerini, Laísa, additional, Dewes, Samantha Seibt, additional, Grellert, Mateus, additional, de Carvalho, Hudson Wander, additional, Jansen, Karen, additional, da Silva, Ricardo Azevedo, additional, Pinheiro, Ricardo Tavares, additional, de Mattos Souza, Luciano, additional, Oses, Jean Pierre, additional, Portela, Luis Valmor, additional, Lara, Diogo Rizzato, additional, Tovo-Rodrigues, Luciana, additional, and Ghisleni, Gabriele, additional

Published
2022
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10. Genetic Variations in Elements of the Oxytocinergic Pathway are Associated with Attention/Hyperactivity Problems and Anxiety Problems in Childhood

Author

Camerini, Laísa, primary, Zurchimitten, Gabriel, additional, Bock, Bertha, additional, Xavier, Janaína, additional, Bastos, Clarissa Ribeiro, additional, Martins, Evânia, additional, Ardais, Ana Paula, additional, dos Santos Motta, Janaína Vieira, additional, Pires, Andressa Jacondino, additional, de Matos, Mariana Bonati, additional, de Ávila Quevedo, Luciana, additional, Pinheiro, Ricardo Tavares, additional, and Ghisleni, Gabriele, additional

Published
2022
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11. Interaction between COMT Val158Met polymorphism and childhood trauma predicts risk for depression in men

Author

Xavier, Janaína, primary, Bastos, Clarissa Ribeiro, additional, Camerini, Laísa, additional, Amaral, Paola Bajadares, additional, Jansen, Karen, additional, de Mattos Souza, Luciano Dias, additional, da Silva, Ricardo Azevedo, additional, Pinheiro, Ricardo Tavares, additional, Lara, Diogo Rizzato, additional, and Ghisleni, Gabriele, additional

Published
2022
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12. BDNF Levels According to Variations in the CACNA1C Gene: Sex-Based Disparity

Author

Bastos, Clarissa Ribeiro, primary, Xavier, Janaina, additional, Camerini, Laísa, additional, Dewes, Samantha Seibt, additional, Moreira, Fernanda Pedrotti, additional, Wiener, Carolina David, additional, Jansen, Karen, additional, Kaster, Manuella Pinto, additional, de Mattos Souza, Luciano Dias, additional, da Silva, Ricardo Azevedo, additional, Oses, Jean Pierre, additional, Portela, Luis Valmor, additional, Lara, Diogo Rizzato, additional, Tovo-Rodrigues, Luciana, additional, and Ghisleni, Gabriele, additional

Published
2022
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14. Inosine prevents hyperlocomotion in a ketamine-induced model of mania in rats

Author

Camerini, Laísa, primary, Ardais, Ana Paula, additional, Xavier, Janaína, additional, Bastos, Clarissa Ribeiro, additional, Oliveira, Sílvia, additional, Soares, Mayara Sandrielly Pereira, additional, de Mattos, Bruna da Silveira, additional, Ávila, Anita Almeida, additional, do Couto, Carlus Augustu Tavares, additional, Spanevello, Roselia Maria, additional, Pochmann, Daniela, additional, Moritz, Cesar Eduardo Jacinto, additional, Porciúncula, Lisiane Oliveira, additional, Figueiró, Fabrício, additional, Kaster, Manuella Pinto, additional, and Ghisleni, Gabriele, additional

Published
2020
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15. Interaction between COMT Val 158 Met polymorphism and childhood trauma predicts risk for depression in men.

Author

Xavier J, Bastos CR, Camerini L, Amaral PB, Jansen K, de Mattos Souza LD, da Silva RA, Pinheiro RT, Lara DR, and Ghisleni G

Subjects
Female, Genotype, Humans, Male, Polymorphism, Single Nucleotide, Young Adult, Adverse Childhood Experiences, Catechol O-Methyltransferase genetics, Depression genetics
Abstract

Depression is a disabling illness with complex etiology. While the catechol-O-methyltransferase (COMT) gene, in particular the functional Val 158 Met polymorphism, has been related to depression, the mechanisms underlying this gene-disease association are not completely understood. Therefore, we explore the association of COMT Val 158 Met polymorphism with depression as well as its interaction with childhood trauma in 1136 young adults from a population-based study carried out in the city of Pelotas, Brazil. The diagnosis was performed through the Mini International Neuropsychiatric Interview 5.0 (MINI 5.0), and trauma was assessed with the Childhood Trauma Questionnaire (CTQ). Total DNA was extracted and genotyped by real-time PCR, and the QTLbase dataset was queried to perform large-scale quantitative trait locus (QTL) analysis. Our research showed no direct association between the Val 158 Met polymorphism and the diagnosis of depression (women: χ 2  = 0.10, d = 1, p = 0.751; men: χ 2  = 0.003, df = 1, p = 0.956). However, the Met-allele of the Val 158 Met polymorphism modified the effect of childhood trauma in men (OR = 2.58 [95% CI: 1.05-6.29]; p = 0.038) conferring risk for depression only on those who suffer from trauma. The conditional effect from moderation analysis showed that trauma impacts the risk of depression only in men carrying the Met-allele (effect: 0.9490, standard error [SE]: 0.2570; p = 0.0002). QTLbase and dataset for Val 158 Met polymorphism were consistent for markers that influence chromatin accessibility transcription capacity including histone methylation and acetylation. The changes caused in gene regulation by childhood trauma exposure and polymorphism may serve as evidence of the mechanism whereby the interaction increases susceptibility to this disorder in men., (© 2022 International Society for Developmental Neuroscience.)

Published
2022
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