Matches in SemOpenAlex for { <https://semopenalex.org/work/W2105201620> ?p ?o ?g. }
- W2105201620 endingPage "781" @default.
- W2105201620 startingPage "781" @default.
- W2105201620 abstract "<h3>Context</h3>Cortical thickness is a highly heritable structural brain measurement, and reduced thickness has been associated with schizophrenia, bipolar disorder, and decreased cognitive performance among healthy control individuals. Identifying genes that contribute to variation in cortical thickness provides a means to elucidate some of the biological mechanisms underlying these diseases and general cognitive abilities.<h3>Objectives</h3>To identify common genetic variants that affect cortical thickness in patients with schizophrenia, patients with bipolar disorder, and controls and to test these variants for association with cognitive performance.<h3>Design</h3>A total of 597 198 single-nucleotide polymorphisms were tested for association with average cortical thickness in a genome-wide association study. Significantly associated single-nucleotide polymorphisms were tested for their effect on several measures of cognitive performance.<h3>Setting</h3>Four major hospitals in Oslo, Norway.<h3>Participants</h3>A total of 1054 case individuals and controls were analyzed in the genome-wide association study and follow-up cognitive study. The genome-wide association study included controls (n = 181) and individuals with DSM-IV–diagnosed schizophrenia spectrum disorder (n = 94), bipolar spectrum disorder (n = 97), and other psychotic and affective disorders (n = 49).<h3>Main Outcome Measures</h3>Cortical thickness measured with magnetic resonance imaging and cognitive performance as assessed by several neuropsychological tests.<h3>Results</h3>Two closely linked genetic variants (rs4906844 and rs11633924) within the Prader-Willi and Angelman syndrome region on chromosome 15q12 showed a genome-wide significant association (P = 1.1 10<sup>8</sup>) with average cortical thickness and modest association with cognitive performance (permuted P = .03) specifically among patients diagnosed as having schizophrenia.<h3>Conclusion</h3>This genome-wide association study identifies a common genetic variant that contributes to the heritable reduction of cortical thickness in schizophrenia. These results highlight the usefulness of cortical thickness as an intermediate phenotype for neuropsychiatric diseases. Future independent replication studies are required to confirm these findings." @default.
- W2105201620 created "2016-06-24" @default.
- W2105201620 creator A5014429025 @default.
- W2105201620 creator A5038692125 @default.
- W2105201620 creator A5052074090 @default.
- W2105201620 creator A5052633022 @default.
- W2105201620 creator A5052826567 @default.
- W2105201620 creator A5061544197 @default.
- W2105201620 creator A5063840815 @default.
- W2105201620 creator A5064324947 @default.
- W2105201620 creator A5069816019 @default.
- W2105201620 creator A5077225971 @default.
- W2105201620 creator A5087626511 @default.
- W2105201620 creator A5090399778 @default.
- W2105201620 date "2011-08-01" @default.
- W2105201620 modified "2023-10-10" @default.
- W2105201620 title "Association of Genetic Variants on 15q12 With Cortical Thickness and Cognition in Schizophrenia" @default.
- W2105201620 cites W1546698346 @default.
- W2105201620 cites W1583327662 @default.
- W2105201620 cites W1963673462 @default.
- W2105201620 cites W1967111730 @default.
- W2105201620 cites W1968763887 @default.
- W2105201620 cites W1974435463 @default.
- W2105201620 cites W1977411337 @default.
- W2105201620 cites W1979315240 @default.
- W2105201620 cites W1979981225 @default.
- W2105201620 cites W1981833273 @default.
- W2105201620 cites W1988011968 @default.
- W2105201620 cites W1988672159 @default.
- W2105201620 cites W1990436516 @default.
- W2105201620 cites W1991873855 @default.
- W2105201620 cites W1997031801 @default.
- W2105201620 cites W1998446689 @default.
- W2105201620 cites W1999384062 @default.
- W2105201620 cites W2005585817 @default.
- W2105201620 cites W2007298996 @default.
- W2105201620 cites W2013373204 @default.
- W2105201620 cites W2013859768 @default.
- W2105201620 cites W2014596655 @default.
- W2105201620 cites W2018851857 @default.
- W2105201620 cites W2019465651 @default.
- W2105201620 cites W2021377987 @default.
- W2105201620 cites W2023069923 @default.
- W2105201620 cites W2023171821 @default.
- W2105201620 cites W2024386053 @default.
- W2105201620 cites W2029759605 @default.
- W2105201620 cites W2031746153 @default.
- W2105201620 cites W2037674765 @default.
- W2105201620 cites W2043758434 @default.
- W2105201620 cites W2049409353 @default.
- W2105201620 cites W2052998051 @default.
- W2105201620 cites W2055503620 @default.
- W2105201620 cites W2058069331 @default.
- W2105201620 cites W2066185347 @default.
- W2105201620 cites W2075123043 @default.
- W2105201620 cites W2080287250 @default.
- W2105201620 cites W2090823243 @default.
- W2105201620 cites W2097330821 @default.
- W2105201620 cites W2098597355 @default.
- W2105201620 cites W2100910260 @default.
- W2105201620 cites W2106887445 @default.
- W2105201620 cites W2111884236 @default.
- W2105201620 cites W2113054165 @default.
- W2105201620 cites W2116928980 @default.
- W2105201620 cites W2118196858 @default.
- W2105201620 cites W2119128125 @default.
- W2105201620 cites W2122701285 @default.
- W2105201620 cites W2126549748 @default.
- W2105201620 cites W2127205775 @default.
- W2105201620 cites W2128476271 @default.
- W2105201620 cites W2131564374 @default.
- W2105201620 cites W2141704631 @default.
- W2105201620 cites W2143956675 @default.
- W2105201620 cites W2145240519 @default.
- W2105201620 cites W2147410970 @default.
- W2105201620 cites W2147621924 @default.
- W2105201620 cites W2148953407 @default.
- W2105201620 cites W2156947770 @default.
- W2105201620 cites W2158991820 @default.
- W2105201620 cites W2160983331 @default.
- W2105201620 cites W2161633633 @default.
- W2105201620 cites W2031442248 @default.
- W2105201620 cites W2110558605 @default.
- W2105201620 doi "https://doi.org/10.1001/archgenpsychiatry.2011.81" @default.
- W2105201620 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3375053" @default.
- W2105201620 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21810643" @default.
- W2105201620 hasPublicationYear "2011" @default.
- W2105201620 type Work @default.
- W2105201620 sameAs 2105201620 @default.
- W2105201620 citedByCount "23" @default.
- W2105201620 countsByYear W21052016202012 @default.
- W2105201620 countsByYear W21052016202013 @default.
- W2105201620 countsByYear W21052016202014 @default.
- W2105201620 countsByYear W21052016202015 @default.
- W2105201620 countsByYear W21052016202016 @default.
- W2105201620 countsByYear W21052016202017 @default.
- W2105201620 countsByYear W21052016202018 @default.
- W2105201620 countsByYear W21052016202019 @default.