The genetic architecture of the human cerebral cortex

…, FM Rashid, WR Reay, R Redlich, CS Reinbold… - Science, 2020 - science.org
INTRODUCTION The cerebral cortex underlies our complex cognitive capabilities.
Variations in human cortical surface area and thickness are associated with neurological, …

[HTML][HTML] Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

…, M Jungkunz, J Frank, S Awasthi, CS Reinbold… - Translational …, 2017 - nature.com
Borderline personality disorder (BOR) is determined by environmental and genetic factors,
and characterized by affective instability and impulsivity, diagnostic symptoms also observed …

[HTML][HTML] Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

…, J Hecker, A Hofmann, A Maaser, CS Reinbold… - PloS one, 2017 - journals.plos.org
Bipolar disorder (BD) is a highly heritable neuropsychiatric disease characterized by recurrent
episodes of mania and depression. BD shows substantial clinical and genetic overlap …

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs

…, C Prieto, A Ragothaman, CS Reinbold… - Human brain …, 2022 - Wiley Online Library
The Enhancing NeuroImaging Genetics through Meta‐Analysis copy number variant (ENIGMA‐CNV)
and 22q11.2 Deletion Syndrome Working Groups (22q‐ENIGMA WGs) were …

[HTML][HTML] Dose response of the 16p11. 2 distal copy number variant on intracranial volume and basal ganglia

…, S Pudas, E Quinlan, DS Quintana, CS Reinbold… - Molecular …, 2020 - nature.com
Carriers of large recurrent copy number variants (CNVs) have a higher risk of developing
neurodevelopmental disorders. The 16p11.2 distal CNV predisposes carriers to eg, autism …

Association of copy number variation of the 15q11. 2 BP1-BP2 region with cortical and subcortical morphology and cognition

…, B Pike, C Prieto, EB Quinlan, CS Reinbold… - JAMA …, 2020 - jamanetwork.com
Importance Recurrent microdeletions and duplications in the genomic region 15q11.2
between breakpoints 1 (BP1) and 2 (BP2) are associated with neurodevelopmental disorders. …

[HTML][HTML] 1q21. 1 distal copy number variants are associated with cerebral and cognitive alterations in humans

…, GB Pike, C Prieto, EB Quinlan, CS Reinbold… - Translational …, 2021 - nature.com
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers
are predisposed to multiple neurodevelopmental disorders, including schizophrenia, autism …

Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan

…, Ø Sørensen, AM Mowinckel, CS Reinbold… - Neurology …, 2020 - AAN Enterprises
Objective To test the hypothesis that genetic risk for Alzheimer disease (AD) may represent
a stable influence on the brain from early in life, rather than being primarily age dependent, …

[HTML][HTML] Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

…, J Strohmaier, A Maaser-Hecker, CS Reinbold… - Translational …, 2020 - nature.com
Bipolar disorder (BD) is a highly heritable neuropsychiatric disease characterized by recurrent
episodes of depression and mania. Research suggests that the cumulative impact of …

[HTML][HTML] Analysis of the influence of microRNAs in lithium response in bipolar disorder

CS Reinbold, AJ Forstner, J Hecker… - Frontiers in …, 2018 - frontiersin.org
Bipolar disorder (BD) is a common, highly heritable neuropsychiatric disease characterized
by recurrent episodes of mania and depression. Lithium is the best-established long-term …