White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study

SN Hatton, KH Huynh, L Bonilha, E Abela, S Alhusaini… - Brain, 2020 - academic.oup.com
The epilepsies are commonly accompanied by widespread abnormalities in cerebral white
matter. ENIGMA-Epilepsy is a large quantitative brain imaging consortium, aggregating data …

Machine learning for genetic prediction of psychiatric disorders: a systematic review

M Bracher-Smith, K Crawford, V Escott-Price - Molecular Psychiatry, 2021 - nature.com
Abstract Machine learning methods have been employed to make predictions in psychiatry
from genotypes, with the potential to bring improved prediction of outcomes in psychiatric …

[HTML][HTML] Biological and environmental predictors of heterogeneity in neurocognitive ageing: Evidence from Betula and other longitudinal studies

L Nyberg, CJ Boraxbekk, DE Sörman, P Hansson… - Ageing research …, 2020 - Elsevier
Individual differences in cognitive performance increase with advancing age, reflecting
marked cognitive changes in some individuals along with little or no change in others …

Synergistic effects of common schizophrenia risk variants

N Schrode, SM Ho, K Yamamuro, A Dobbyn… - Nature …, 2019 - nature.com
The mechanisms by which common risk variants of small effect interact to contribute to
complex genetic disorders are unclear. Here, we apply a genetic approach, using isogenic …

Distorted neurocomputation by a small number of extra-large spines in psychiatric disorders

K Obi-Nagata, N Suzuki, R Miyake, ML MacDonald… - Science …, 2023 - science.org
Human genetics strongly support the involvement of synaptopathy in psychiatric disorders.
However, trans-scale causality linking synapse pathology to behavioral changes is lacking …

[HTML][HTML] A polygenic p factor for major psychiatric disorders

S Selzam, JRI Coleman, A Caspi, TE Moffitt… - Translational …, 2018 - nature.com
It has recently been proposed that a single dimension, called the p factor, can capture a
person's liability to mental disorder. Relevant to the p hypothesis, recent genetic research …

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

E Rees, J Han, J Morgan, N Carrera… - Nature …, 2020 - nature.com
Schizophrenia is a highly polygenic disorder with important contributions from both common
and rare risk alleles. We analyzed exome sequencing data for de novo variants (DNVs) in a …

Pleiotropy and cross-disorder genetics among psychiatric disorders

PH Lee, YCA Feng, JW Smoller - Biological psychiatry, 2021 - Elsevier
Genome-wide analyses of common and rare genetic variations have documented the
heritability of major psychiatric disorders, established their highly polygenic genetic …

Genetic architecture of abdominal aortic aneurysm in the million veteran program

D Klarin, SS Verma, R Judy, O Dikilitas, BN Wolford… - Circulation, 2020 - Am Heart Assoc
Background: Abdominal aortic aneurysm (AAA) is an important cause of cardiovascular
mortality; however, its genetic determinants remain incompletely defined. In total, 10 …

Genetics of obsessive-compulsive disorder

B Mahjani, K Bey, J Boberg, C Burton - Psychological medicine, 2021 - cambridge.org
BackgroundObsessive-compulsive disorder (OCD) is a psychiatric disorder with multiple
symptom dimensions (eg contamination, symmetry). OCD clusters in families and decades …