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European Journal of Medical Genetics|May 1, 2014
Genotype-phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletionIsabella Fanizza, Sara Bertuzzo, Silvana Beri, et al.Molecular Psychiatry|August 4, 2023
Prenatal exposure to environmental air pollution and psychosocial stress jointly contribute to the epigenetic regulation of the serotonin transporter gene in newbornsSarah Nazzari, Lucia Cagliero, Serena Grumi, et al.Frontiers in Psychiatry|September 30, 2017
Maternal Sensitivity Buffers the Association between SLC6A4 Methylation and Socio-Emotional Stress Response in 3-Month-Old Full Term, but not very Preterm InfantsLivio Provenzi, Monica Fumagalli, Roberto Giorda, et al.Development and Psychopathology|October 13, 2007
Socioeconomic status mediates the genetic contribution of the dopamine receptor D4 and serotonin transporter linked promoter region repeat polymorphisms to externalization in preadolescenceMaria Nobile, Roberto Giorda, Cecilia Marino, et al.Development and Psychopathology|March 1, 2023
Sex-dimorphic pathways in the associations between maternal trait anxiety, infant <i>BDNF</i> methylation, and negative emotionalitySarah Nazzari, Serena Grumi, Fabiana Mambretti, et al.European Child & Adolescent Psychiatry|December 1, 2009
COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10-14Maria Nobile, Marianna Rusconi, Monica Bellina, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|August 9, 2016
Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samplesSara Mascheretti, Vittoria Trezzi, Roberto Giorda, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|January 30, 2009
The influence of family structure, the TPH2 G-703T and the 5-HTTLPR serotonergic genes upon affective problems in children aged 10-14 yearsMaria Nobile, Marianna Rusconi, Monica Bellina, et al.Epilepsia Open|March 29, 2018
Partial deletion of <i>DEPDC5</i> in a child with focal epilepsyMaria Clara Bonaglia, Roberto Giorda, Roberta Epifanio, et al.European Journal of Human Genetics : EJHG|February 28, 2008
Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1)Roberto Giorda, M Clara Bonaglia, Greta Milani, et al.Pageof 13