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Interaction between Chromatin Proteins MECP2 and ATRX Is Disrupted by Mutations That Cause Inherited Mental Retardation

Proceedings of the National Academy of Sciences - PNAS, 2007-02, Vol.104 (8), p.2709-2714

2007

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A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

American journal of human genetics, 2009-12, Vol.85 (6), p.833-846

2009

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Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population

Neuroscience letters, 2010-05, Vol.475 (3), p.169-173

2010

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Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature, 2008-09, Vol.455 (7210), p.237-241

2008

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Genome-wide association study identifies five new schizophrenia loci

Nature genetics, 2011-10, Vol.43 (10), p.969-976

2011

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Nature (London), 2009-08, Vol.460 (7256), p.748-752

2009

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Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial

The lancet respiratory medicine, 2015-09, Vol.3 (9), p.684-691

2015

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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

PLoS genetics, 2009-06, Vol.5 (6), p.e1000534

2009

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Quantitative T1 brain mapping in early relapsing-remitting multiple sclerosis: longitudinal changes, lesion heterogeneity and disability

European radiology, 2024-06, Vol.34 (6), p.3826-3839

2024

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Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

Molecular psychiatry, 2011-03, Vol.16 (3), p.286-292

2011

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent

American journal of human genetics, 2013-09, Vol.93 (3), p.463-470

2013

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Genetic Schizophrenia Risk Variants Jointly Modulate Total Brain and White Matter Volume

Biological psychiatry (1969), 2013-03, Vol.73 (6), p.525-531

2013

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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor

PLoS genetics, 2012-04, Vol.8 (4), p.e1002656-e1002656

2012

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Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia

PLoS computational biology, 2012-07, Vol.8 (7), p.e1002587-e1002587

2012

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Homozygosity mapping of depressive disorder in a large family from Pakistan: Significant linkage on chromosome 6 and 9

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-03, Vol.162B (2), p.157-162

2013

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Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

PLoS genetics, 2010-09, Vol.6 (9), p.e1001097

2010

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Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

Molecular psychiatry, 2012-02, Vol.17 (2), p.193-201

2012

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Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis

PloS one, 2012-06, Vol.7 (6), p.e37852

2012

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A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

Journal of medical genetics, 2012-02, Vol.49 (2), p.96-103

2012

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 ( ) as a risk gene for schizophrenia

Molecular psychiatry, 2011-11, Vol.16 (11), p.1117-1129

2011

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Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms

Molecular psychiatry, 2012-08, Vol.17 (8), p.818-826

2012

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Nature genetics, 2008-09, Vol.40 (9), p.1056-1058

2008

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A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-12, Vol.162B (8), p.847-854

2013

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Start listening: Study guide incl. workbook

MacLean, Alan C

1981

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MacLean, Alan C

1981

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Interaction between Chromatin Proteins MECP2 and ATRX Is Disrupted by Mutations That Cause Inherited Mental Retardation

A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population

Rare chromosomal deletions and duplications increase risk of schizophrenia

Genome-wide association study identifies five new schizophrenia loci

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial

Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

Quantitative T1 brain mapping in early relapsing-remitting multiple sclerosis: longitudinal changes, lesion heterogeneity and disability

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent

Genetic Schizophrenia Risk Variants Jointly Modulate Total Brain and White Matter Volume

Runs of homozygosity implicate autozygosity as a schizophrenia risk factor

Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia

Homozygosity mapping of depressive disorder in a large family from Pakistan: Significant linkage on chromosome 6 and 9

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis

A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

GWA study data mining and independent replication identify cardiomyopathy-associated 5 ( ) as a risk gene for schizophrenia

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability

Start listening: Study guide incl. workbook

Start listening: Workbook

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