Cerebral small vessel disease genomics and its implications across the lifespan

M Sargurupremraj, H Suzuki, X Jian… - Nature …, 2020 - nature.com
White matter hyperintensities (WMH) are the most common brain-imaging feature of cerebral
small vessel disease (SVD), hypertension being the main known risk factor. Here, we …

Voxel-based meta-analytical evidence of structural disconnectivity in major depression and bipolar disorder

T Wise, J Radua, G Nortje, AJ Cleare, AH Young… - Biological …, 2016 - Elsevier
Background Identification of white matter microstructure differences and similarities between
major depression and bipolar disorder is a necessary step to better understand the …

Statistical genetic approaches to investigate genotype-by-environment interaction: Review and novel extension of models

VP Diego, EG Manusov, M Almeida, S Laston, D Ortiz… - Genes, 2024 - mdpi.com
Statistical genetic models of genotype-by-environment (G× E) interaction can be divided into
two general classes, one on G× E interaction in response to dichotomous environments (eg …

Enhancing the informativeness and replicability of imaging genomics studies

CS Carter, CE Bearden, ET Bullmore, DH Geschwind… - Biological …, 2017 - Elsevier
Imaging genomics is a new field of investigation that seeks to gain insights into the impact of
human genetic variation on the structure, chemistry, and function of neural systems in health …

Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data

P Kochunov, N Jahanshad, D Marcus, A Winkler… - Neuroimage, 2015 - Elsevier
The degree to which genetic factors influence brain connectivity is beginning to be
understood. Large-scale efforts are underway to map the profile of genetic effects in various …

Association of white matter with core cognitive deficits in patients with schizophrenia

P Kochunov, TR Coyle, LM Rowland… - JAMA …, 2017 - jamanetwork.com
Importance Efforts to remediate the multiple cognitive function impairments in schizophrenia
should consider white matter as one of the underlying neural mechanisms. Objective To …

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

PK Chakraborty, K Schmitz-Abe… - Blood, The Journal …, 2014 - ashpublications.org
Mutations in genes encoding proteins that are involved in mitochondrial heme synthesis,
iron-sulfur cluster biogenesis, and mitochondrial protein synthesis have previously been …

Functional network connectivity impairments and core cognitive deficits in schizophrenia

BM Adhikari, LE Hong, H Sampath… - Human brain …, 2019 - Wiley Online Library
Cognitive deficits contribute to functional disability in patients with schizophrenia and may
be related to altered functional networks that serve cognition. We evaluated the integrity of …

A white matter connection of schizophrenia and Alzheimer's disease

P Kochunov, A Zavaliangos-Petropulu… - Schizophrenia …, 2021 - academic.oup.com
Schizophrenia (SZ) is a severe psychiatric illness associated with an elevated risk for
develo** Alzheimer's disease (AD). Both SZ and AD have white matter abnormalities and …

Neurodevelopmental model of schizophrenia revisited: similarity in individual deviation and idiosyncrasy from the normative model of whole-brain white matter tracts …

YL Chien, HY Lin, YH Tung, TJ Hwang, CL Chen… - Molecular …, 2022 - nature.com
The neurodevelopmental model of schizophrenia is supported by multi-level impairments
shared among schizophrenia and neurodevelopmental disorders. Despite schizophrenia …