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Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder

Charney, A. W. (author)
Ruderfer, D. M. (author)
Stahl, E. A. (author)
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Moran, J. L. (author)
Karolinska Institutet
Chambert, K. (author)
Belliveau, R. A. (author)
Forty, L. (author)
Gordon-Smith, K. (author)
Di Florio, A. (author)
Lee, P. H. (author)
Bromet, E. J. (author)
Buckley, P. F. (author)
Escamilla, M. A. (author)
Fanous, A. H. (author)
Fochtmann, L. J. (author)
Lehrer, D. S. (author)
Malaspina, D. (author)
Marder, S. R. (author)
Karolinska Institutet
Morley, C. P. (author)
Nicolini, H. (author)
Perkins, D. O. (author)
Rakofsky, J. J. (author)
Rapaport, M. H. (author)
Medeiros, H. (author)
Karolinska Institutet
Sobell, J. L. (author)
Green, E. K. (author)
Backlund, L. (author)
Karolinska Institutet
Bergen, S. E. (author)
Karolinska Institutet
Jureus, A. (author)
Karolinska Institutet
Schalling, M. (author)
Lichtenstein, P. (author)
Karolinska Institutet
Roussos, P. (author)
Knowles, J. A. (author)
Jones, I. (author)
Jones, L. A. (author)
Hultman, C. M. (author)
Perlis, R. H. (author)
Purcell, S. M. (author)
McCarroll, S. A. (author)
Pato, C. N. (author)
Pato, M. T. (author)
Craddock, N. (author)
Landén, Mikael, 1966 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology
Smoller, J. W. (author)
Sklar, P. (author)
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 (creator_code:org_t)
2017-01-10
2017
English.
In: Translational Psychiatry. - : Springer Science and Business Media LLC. - 2158-3188. ; 7:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We performed a genome-wide association study of 6447 bipolar disorder (BD) cases and 12 639 controls from the International Cohort Collection for Bipolar Disorder (ICCBD). Meta-analysis was performed with prior results from the Psychiatric Genomics Consortium Bipolar Disorder Working Group for a combined sample of 13 902 cases and 19 279 controls. We identified eight genome-wide significant, associated regions, including a novel associated region on chromosome 10 (rs10884920; P = 3.28 x 10(-8)) that includes the brain-enriched cytoskeleton protein adducin 3 (ADD3), a non-coding RNA, and a neuropeptide-specific aminopeptidase P (XPNPEP1). Our large sample size allowed us to test the heritability and genetic correlation of BD subtypes and investigate their genetic overlap with schizophrenia and major depressive disorder. We found a significant difference in heritability of the two most common forms of BD (BD I SNP-h(2) = 0.35; BD II SNP-h(2) = 0.25; P = 0.02). The genetic correlation between BD I and BD II was 0.78, whereas the genetic correlation was 0.97 when BD cohorts containing both types were compared. In addition, we demonstrated a significantly greater load of polygenic risk alleles for schizophrenia and BD in patients with BD I compared with patients with BD II, and a greater load of schizophrenia risk alleles in patients with the bipolar type of schizoaffective disorder compared with patients with either BD I or BD II. These results point to a partial difference in the genetic architecture of BD subtypes as currently defined.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)

Keyword

genome-wide association
spectrum disorder
ii disorder
risk loci
schizophrenia
family
depression
unipolar
illness
susceptibility
Psychiatry
rshon es
1982
archives of general psychiatry
v39
p1157
guffin p
1991
archives of general psychiatry
v48
p764

Publication and Content Type

ref (subject category)
art (subject category)

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