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1.
Am J Med Genet B Neuropsychiatr Genet ; 162B(2): 96-121, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23341144

RESUMO

The XXth World Congress of Psychiatric Genetics (WCPG), sponsored by The International Society of Psychiatric Genetics (ISPG) took place in Hamburg, Germany on October 14-18, 2012. Approximately 600 participants gathered to discuss the latest findings in this rapidly advancing field. The following report was written by student travel awardees. Each was assigned sessions as rapporteurs. This manuscript represents topics covered in most, but not all, oral presentations during the conference, and some of the major notable new findings reported at this 2012 WCPG.


Assuntos
Transtornos Mentais/genética , Animais , Encéfalo/patologia , Modelos Animais de Doenças , Descoberta de Drogas , Endofenótipos , Epigênese Genética , Testes Genéticos , Variação Genética , Genoma Humano/genética , Estudo de Associação Genômica Ampla , Alemanha , Humanos , Padrões de Herança/genética , Imageamento por Ressonância Magnética , Camundongos , Análise de Sequência de DNA
2.
Mol Neuropsychiatry ; 5(Suppl 1): 72-84, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32399471

RESUMO

Bipolar disorder (BD) is a neuropsychiatric mood disorder characterized by recurrent episodes of mania and depression in addition to disruptions in sleep, energy, appetite, and cognitive functions-rhythmic behaviors that typically change on daily cycles. BD symptoms can also be provoked by seasonal changes, sleep, and/or circadian disruption, indicating that chronobiological factors linked to the circadian clock may be a common feature in the disorder. Research indicates that BD exists on a clinical spectrum, with distinct subtypes often intersecting with other psychiatric disorders. This heterogeneity has been a major challenge to BD research and contributes to problems in diagnostic stability and treatment outcomes. To address this heterogeneity, we propose that chronobiologically related biomarkers could be useful in classifying BD into objectively measurable phenotypes to establish better diagnoses, inform treatments, and perhaps lead to better clinical outcomes. Presently, we review the biological basis of circadian time keeping in humans, discuss the links of BD to the circadian clock, and pre-sent recent studies that evaluated chronobiological measures as a basis for establishing BD phenotypes. We conclude that chronobiology may inform future research using other novel techniques such as genomics, cell biology, and advanced behavioral analyses to establish new and more biologically based BD phenotypes.

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