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Molecular linkage studies of bipolar disorder

Linkage studies have defined at least five bipolar (BP) disorder susceptibility loci that meet suggested guidelines for initial identification and subsequent confirmation. These loci, found on 18p11, 18q22, 21q21, 4p16, and Xq26, are targets for BP candidate gene investigations. Molecular dissection...

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Detalles Bibliográficos
Autor principal: Berrettini, Wade H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181563/
https://www.ncbi.nlm.nih.gov/pubmed/22033545
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author Berrettini, Wade H.
author_facet Berrettini, Wade H.
author_sort Berrettini, Wade H.
collection PubMed
description Linkage studies have defined at least five bipolar (BP) disorder susceptibility loci that meet suggested guidelines for initial identification and subsequent confirmation. These loci, found on 18p11, 18q22, 21q21, 4p16, and Xq26, are targets for BP candidate gene investigations. Molecular dissection of expressed sequences for these regions is likely to yield specific BP susceptibility alleles in most cases, in all probability, these BP susceptibility alleles will be common in the general population, and, individually, will be neither necessary nor sufficient for manifestation syndrome. Additive or multiplicative oligogenic models involving several susceptibility loci appear most reasonable at present, it is hoped thai these BP susceptibility genes will increase understanding of many mysteries surrounding these disorders, including drug response, cycling patterns, age-of-onset, and modes of transmission.
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spelling pubmed-31815632011-10-27 Molecular linkage studies of bipolar disorder Berrettini, Wade H. Dialogues Clin Neurosci Basic Research Linkage studies have defined at least five bipolar (BP) disorder susceptibility loci that meet suggested guidelines for initial identification and subsequent confirmation. These loci, found on 18p11, 18q22, 21q21, 4p16, and Xq26, are targets for BP candidate gene investigations. Molecular dissection of expressed sequences for these regions is likely to yield specific BP susceptibility alleles in most cases, in all probability, these BP susceptibility alleles will be common in the general population, and, individually, will be neither necessary nor sufficient for manifestation syndrome. Additive or multiplicative oligogenic models involving several susceptibility loci appear most reasonable at present, it is hoped thai these BP susceptibility genes will increase understanding of many mysteries surrounding these disorders, including drug response, cycling patterns, age-of-onset, and modes of transmission. Les Laboratoires Servier 1999-06 /pmc/articles/PMC3181563/ /pubmed/22033545 Text en http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Berrettini, Wade H.
Molecular linkage studies of bipolar disorder
title Molecular linkage studies of bipolar disorder
title_full Molecular linkage studies of bipolar disorder
title_fullStr Molecular linkage studies of bipolar disorder
title_full_unstemmed Molecular linkage studies of bipolar disorder
title_short Molecular linkage studies of bipolar disorder
title_sort molecular linkage studies of bipolar disorder
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181563/
https://www.ncbi.nlm.nih.gov/pubmed/22033545
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