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Article: The usual suspects: Tyrosine hydroxylase and the serotonin transporter in affective disorders

TitleThe usual suspects: Tyrosine hydroxylase and the serotonin transporter in affective disorders
Authors
Issue Date1998
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/mp
Citation
Molecular Psychiatry, 1998, v. 3 n. 2, p. 103-105 How to Cite?
AbstractCandidate gene studies of single polymorphisms in affective disorders and psychosis have produced many intriguing results, but will they ever be definitive? We predict that in the future there will be a convergence of linkage and association analysis to genome-wide linkage disequilibrium studies using overlapping haplotypes.
Persistent Identifierhttp://hdl.handle.net/10722/175782
ISSN
2015 Impact Factor: 13.314
2015 SCImago Journal Rankings: 6.790
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorCollier, DAen_US
dc.contributor.authorSham, PCen_US
dc.date.accessioned2012-11-26T09:01:15Z-
dc.date.available2012-11-26T09:01:15Z-
dc.date.issued1998en_US
dc.identifier.citationMolecular Psychiatry, 1998, v. 3 n. 2, p. 103-105en_US
dc.identifier.issn1359-4184en_US
dc.identifier.urihttp://hdl.handle.net/10722/175782-
dc.description.abstractCandidate gene studies of single polymorphisms in affective disorders and psychosis have produced many intriguing results, but will they ever be definitive? We predict that in the future there will be a convergence of linkage and association analysis to genome-wide linkage disequilibrium studies using overlapping haplotypes.en_US
dc.languageengen_US
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/mpen_US
dc.relation.ispartofMolecular Psychiatryen_US
dc.subject.meshAllelesen_US
dc.subject.meshBipolar Disorder - Geneticsen_US
dc.subject.meshCarrier Proteins - Genetics - Physiologyen_US
dc.subject.meshDepressive Disorder - Geneticsen_US
dc.subject.meshDisease Susceptibilityen_US
dc.subject.meshEpistasis, Geneticen_US
dc.subject.meshGenetic Heterogeneityen_US
dc.subject.meshHaplotypes - Geneticsen_US
dc.subject.meshHumansen_US
dc.subject.meshIntrons - Geneticsen_US
dc.subject.meshLinkage Disequilibriumen_US
dc.subject.meshMembrane Glycoproteins - Genetics - Physiologyen_US
dc.subject.meshMembrane Transport Proteinsen_US
dc.subject.meshMicrosatellite Repeatsen_US
dc.subject.meshMinisatellite Repeatsen_US
dc.subject.meshMood Disorders - Epidemiology - Genetics - Metabolismen_US
dc.subject.meshNerve Tissue Proteinsen_US
dc.subject.meshPromoter Regions, Genetic - Geneticsen_US
dc.subject.meshReproducibility Of Resultsen_US
dc.subject.meshRisken_US
dc.subject.meshSeasonal Affective Disorder - Geneticsen_US
dc.subject.meshSerotonin Plasma Membrane Transport Proteinsen_US
dc.subject.meshTyrosine 3-Monooxygenase - Deficiency - Genetics - Physiologyen_US
dc.titleThe usual suspects: Tyrosine hydroxylase and the serotonin transporter in affective disordersen_US
dc.typeArticleen_US
dc.identifier.emailSham, PC: pcsham@hku.hken_US
dc.identifier.authoritySham, PC=rp00459en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1038/sj.mp.4000384-
dc.identifier.pmid9577831-
dc.identifier.scopuseid_2-s2.0-0031897337en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0031897337&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume3en_US
dc.identifier.issue2en_US
dc.identifier.spage103en_US
dc.identifier.epage105en_US
dc.identifier.isiWOS:000073470500004-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridCollier, DA=26642980600en_US
dc.identifier.scopusauthoridSham, PC=34573429300en_US

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