bioRxivGeneticsPreprint
Common variants of NRXN1, LRP1B and RORA are associated with increased ventricular volumes in psychosis - GWAS findings from the B-SNIP deep phenotyping study
Ney Alliey‐RodrigueziD, Tamar A Grey, Rebecca ShafeeiD, Jaya L. PadmanabhaniD, Neeraj TandoniD, Madeline KlingeriD, Jonathan Spring, Lucas Coppes, Katherine S. ReisiD, Matcheri S. KeshavaniD, Diane Gage, Steven A. McCarrolliD, Jeffrey R. BishopiD, Scot Kristian HilliD, James L. Reilly, Rebekka LenceriD, Brett A. ClementziD, P.F. BuckleyiD, Shashwath A. MedaiD, Balaji NarayananiD, David C. GlahniD, Godfrey D. PearlsoniD, Elena I Ivleva, Carol A. TammingaiD, John A. SweeneyiD, , Elliot S. GershoniD
Abstract
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.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
- Citations
- 9
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