TY - JOUR
T1 - Common variants of NRXN1, LRP1B and RORA are associated with increased ventricular volumes in psychosis - GWAS findings from the B-SNIP deep phenotyping study
AU - Alliey-Rodriguez, Ney
AU - Grey, Tamar A.
AU - Shafee, Rebecca
AU - Padmanabhan, Jaya
AU - Tandon, Neeraj
AU - Klinger, Madeline
AU - Spring, Jonathan
AU - Coppes, Lucas
AU - Reis, Katherine
AU - Keshavan, Matcheri S.
AU - Gage, Diane
AU - McCarroll, Steven
AU - Bishop, Jeffrey R.
AU - Hill, Scot
AU - Reilly, James L.
AU - Lencer, Rebekka
AU - Clementz, Brett
AU - Buckley, Peter
AU - Meda, Shashwath
AU - Narayanan, Balaji
AU - Glahn, David C.
AU - Pearlson, Godfrey
AU - Ivleva, Elena I.
AU - Tamminga, Carol
AU - Sweeney, John A.
AU - Curtis, David
AU - Keedy, Sarah
AU - Badner, Judith A.
AU - Liu, Chunyu
AU - Gershon, Elliot S.
N1 - Publisher Copyright:
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2017/8/11
Y1 - 2017/8/11
N2 - Schizophrenia, Schizoaffective, and Bipolar Disorders share common illness traits, intermediate phenotypes and a partially overlapping polygenic basis. We performed GWAS on deep phenotyping data, including structural MRI and DTI, clinical, and behavioral scales from 1,115 cases and controls. Significant associations were observed with two cerebrospinal fluid volumes: the temporal horn of left lateral ventricle was associated with NRXN1, and the volume of the cavum septum pellucidum was associated with LRP1B and RORA. Both volumes were associated with illness. Suggestive associations were observed with local gyrification indices, fractional anisotropy and age at onset. The deep phenotyping approach allowed unexpected genetic sharing to be found between phenotypes, including temporal horn of left lateral ventricle and age at onset.
AB - Schizophrenia, Schizoaffective, and Bipolar Disorders share common illness traits, intermediate phenotypes and a partially overlapping polygenic basis. We performed GWAS on deep phenotyping data, including structural MRI and DTI, clinical, and behavioral scales from 1,115 cases and controls. Significant associations were observed with two cerebrospinal fluid volumes: the temporal horn of left lateral ventricle was associated with NRXN1, and the volume of the cavum septum pellucidum was associated with LRP1B and RORA. Both volumes were associated with illness. Suggestive associations were observed with local gyrification indices, fractional anisotropy and age at onset. The deep phenotyping approach allowed unexpected genetic sharing to be found between phenotypes, including temporal horn of left lateral ventricle and age at onset.
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U2 - 10.1101/175489
DO - 10.1101/175489
M3 - Article
AN - SCOPUS:85095634260
JO - Seminars in Fetal and Neonatal Medicine
JF - Seminars in Fetal and Neonatal Medicine
SN - 1744-165X
ER -