Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases

Biological Psychiatry - Netherlands
doi 10.1016/j.biopsych.2018.12.009
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

Copy Number Variants Encompassing Mendelian Disease Genes in a Large Multigenerational Family Segregating Bipolar Disorder

BMC Genetics
Genetics
2015English

A Genome-Wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases

American Journal of Human Genetics
Genetics
2010English

High Resolution Analysis of Rare Copy Number Variants in Patients With Autism Spectrum Disorder From Taiwan

Scientific Reports
Multidisciplinary
2017English

Copy Number Variation at 22q11.2: From Rare Variants to Common Mechanisms of Developmental Neuropsychiatric Disorders

Molecular Psychiatry
PsychiatryMolecular NeuroscienceMental HealthMolecular BiologyCellular
2013English

Rare Copy Number Variants Are an Important Cause of Epileptic Encephalopathies

Annals of Neurology
Neurology
2011English

A New Method for Detecting Associations With Rare Copy-Number Variants

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2015English

Tourette Syndrome Is Associated With Recurrent Exonic Copy Number Variants

Neurology
Neurology
2010English

Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes

American Journal of Human Genetics
Genetics
2012English

From Rare Copy Number Variations to Biological Processes in ADHD

2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy