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      <dc:title>The andalusian “multiplex families with bipolar disorder “: a revaluation of the cohort study (1997-2013).</dc:title>
      <dc:creator>Guzmán, José</dc:creator>
      <dc:creator>Mayoral Cleries, Fermín</dc:creator>
      <dc:creator>Moreno-Kustner, Berta</dc:creator>
      <dc:creator>Rivas, Fabio</dc:creator>
      <dc:creator>Romero, Pablo</dc:creator>
      <dc:creator>Gay, Eudoxia</dc:creator>
      <dc:creator>González, María José</dc:creator>
      <dc:creator>Gil, Susana</dc:creator>
      <dc:creator>Cabaleiro, Francisco</dc:creator>
      <dc:creator>Rio, Francisco</dc:creator>
      <dc:creator>Pérez, Fermín</dc:creator>
      <dc:creator>Haro, Jesús</dc:creator>
      <dc:creator>Nöthen, Markus</dc:creator>
      <dc:creator>Streit, Fabian</dc:creator>
      <dc:creator>Strohmaier, Jana</dc:creator>
      <dc:creator>Rietschel, Marcella</dc:creator>
      <dc:subject>Psicosis maniacodepresiva</dc:subject>
      <dc:description>Objectives. &#xd;
Bipolar disorder (BD) is highly heritable, and gene identification will elucidate biological factors and gene-environment interactions. Multiplex families represent a promising resource for identifying rare variants and polygenic effects. However, such families are difficult to recruit.&#xd;
In 1997, >100 multiplex Andalusian BD pedigrees - the largest of which contains >20 affected members- were recruited within an Andalusian-German collaboration study.  Since then, the Andalusian psychiatric network and biobank facilities have been expanded in order to facilitate psychiatric research. Therefore in 2013, the Andalusian-German collaborators initiated a follow-up study of this cohort in order to identify new genetic and environmental factors for BD aetiology and clinical course. &#xd;
&#xd;
Methods.&#xd;
In 1997, BD patients at Andalusian psychiatric hospitals who reported a family history of BD were asked to inform their families about the study. All consenting family members (N= 937; BPI/II=265; Recurrent Mayor Depression=149) were assessed using a structured psychiatric interview for life-time best estimate psychiatric diagnosis (SADS) and the family history method, and blood was obtained for DNA genetic analysis.&#xd;
Follow-up involves reassessment of diagnosis, neuropsychological testing (CANTAB), and the collection of biomaterials (RNA, Plasma, IPS, hair cortisol, etc.). Written informed consent is obtained for all study procedures and analyses.&#xd;
 &#xd;
Results. &#xd;
For the first three families, follow-up assessments and biomaterial-processing have been completed. Follow-up of the remaining families is ongoing.  &#xd;
&#xd;
Conclusion.&#xd;
This cohort represents a unique resource for the investigation of BD aetiology and clinical course, and will be available to international researchers from other sciences.</dc:description>
      <dc:date>2014-12-01T11:40:59Z</dc:date>
      <dc:date>2014-12-01T11:40:59Z</dc:date>
      <dc:date>2014-09-15</dc:date>
      <dc:date>2014-12-01</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>http://hdl.handle.net/10630/8506</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>XVI World Congress of Psychiatry</dc:relation>
      <dc:relation>Madrid</dc:relation>
      <dc:relation>14-18 septiembre 2014</dc:relation>
      <dc:rights>open access</dc:rights>
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