ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries
This review summarizes the last decade of work by the ENIGMA (E nhancing N euro I
maging G enetics through M eta A nalysis) Consortium, a global alliance of over 1400 …
maging G enetics through M eta A nalysis) Consortium, a global alliance of over 1400 …
Cross disorder comparisons of brain structure in schizophrenia, bipolar disorder, major depressive disorder, and 22q11. 2 deletion syndrome: a review of ENIGMA …
This review compares the main brain abnormalities in schizophrenia (SZ), bipolar disorder
(BD), major depressive disorder (MDD), and 22q11. 2 Deletion Syndrome (22q11DS) …
(BD), major depressive disorder (MDD), and 22q11. 2 Deletion Syndrome (22q11DS) …
An overview of the first 5 years of the ENIGMA obsessive–compulsive disorder working group: The power of worldwide collaboration
OA Van den Heuvel, PSW Boedhoe… - Human brain …, 2022 - Wiley Online Library
Neuroimaging has played an important part in advancing our understanding of the
neurobiology of obsessive–compulsive disorder (OCD). At the same time, neuroimaging …
neurobiology of obsessive–compulsive disorder (OCD). At the same time, neuroimaging …
Prader–Willi syndrome and chromosome 15q11. 2 BP1-BP2 region: a review
MG Butler - International Journal of Molecular Sciences, 2023 - mdpi.com
Prader–Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular
genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism …
genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism …
Mapping the genetic architecture of cortical morphology through neuroimaging: progress and perspectives
D van der Meer, T Kaufmann - Translational Psychiatry, 2022 - nature.com
Cortical morphology is a key determinant of cognitive ability and mental health. Its
development is a highly intricate process spanning decades, involving the coordinated …
development is a highly intricate process spanning decades, involving the coordinated …
Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs
Abstract The Enhancing NeuroImaging Genetics through Meta‐Analysis copy number
variant (ENIGMA‐CNV) and 22q11. 2 Deletion Syndrome Working Groups (22q‐ENIGMA …
variant (ENIGMA‐CNV) and 22q11. 2 Deletion Syndrome Working Groups (22q‐ENIGMA …
The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with …
SK Rafi, MG Butler - International Journal of Molecular Sciences, 2020 - mdpi.com
The 15q11. 2 BP1-BP2 microdeletion (Burnside–Butler) syndrome is emerging as the most
frequent pathogenic copy number variation (CNV) in humans associated with …
frequent pathogenic copy number variation (CNV) in humans associated with …
Effects of eight neuropsychiatric copy number variants on human brain structure
Many copy number variants (CNVs) confer risk for the same range of neurodevelopmental
symptoms and psychiatric conditions including autism and schizophrenia. Yet, to date …
symptoms and psychiatric conditions including autism and schizophrenia. Yet, to date …
[HTML][HTML] Lessons learned from neuroimaging studies of copy number variants: a systematic review
C Modenato, S Martin-Brevet, CA Moreau… - Biological …, 2021 - Elsevier
Pathogenic copy number variants (CNVs) and aneuploidies alter gene dosage and are
associated with neurodevelopmental psychiatric disorders such as autism spectrum disorder …
associated with neurodevelopmental psychiatric disorders such as autism spectrum disorder …
Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies
Copy number variants (CNVs), defined as genome sequences of≥ 50 bp that differ in copy
number from that in a reference genome, are a common form of structural variation …
number from that in a reference genome, are a common form of structural variation …