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Association of the NRG1 gene and schizophrenia : a meta-analysis

Molecular psychiatry, 2006-06, Vol.11 (6), p.539-546

2006

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Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample

Molecular psychiatry, 2010-01, Vol.15 (1), p.29-37

2010

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The dystrobrevin-binding protein 1 gene: features and networks

Molecular psychiatry, 2009-01, Vol.14 (1), p.18-29

2009

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Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

Molecular psychiatry, 2011-04, Vol.16 (4), p.429-441

2011

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Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Human molecular genetics, 2012-08, Vol.21 (16), p.3647-3654

2012

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Comparative immunogenetics of autism and schizophrenia

Genes, brain and behavior, 2011-10, Vol.10 (7), p.689-701

2011

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OPA1 , encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

Nature genetics, 2000-10, Vol.26 (2), p.211-215

2000

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No evidence for linkage or association of neuregulin-1 ( ) with disease in the Irish study of high-density schizophrenia families (ISHDSF)

Molecular psychiatry, 2004-08, Vol.9 (8), p.777-783

2004

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Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4

Molecular psychiatry, 2006-06, Vol.11 (6), p.603-611

2006

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Association study of SNAP25 and schizophrenia in Irish family and case-control samples

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-03, Vol.153B (2), p.663-674

2010

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Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS)

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-01, Vol.153B (1), p.323-331

2010

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A region of 35 kb containing the trace amine associate receptor 6 ( ) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families

Molecular psychiatry, 2007-09, Vol.12 (9), p.842-853

2007

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Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy

British journal of ophthalmology, 2003-01, Vol.87 (1), p.48-53

2003

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Alcohol dependence is associated with the ZNF699 gene, a human locus related to Drosophila hangover, in the irish affected sib pair study of alcohol dependence (IASPSAD) sample

Molecular psychiatry, 2006-11, Vol.11 (11), p.1025-1031

2006

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A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population : evidence for a founder effect

Human genetics, 2001-11, Vol.109 (5), p.498-502

2001

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Mutations in the RP2 Gene Cause Disease in 10% of Families with Familial X-Linked Retinitis Pigmentosa Assessed in This Study

American journal of human genetics, 1999-04, Vol.64 (4), p.1210-1215

1999

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Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa

British journal of ophthalmology, 1999-10, Vol.83 (10), p.1144-1148

1999

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An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders

Genomics (San Diego, Calif.), 2002-04, Vol.79 (4), p.560-572

2002

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Evidence for a New Locus for X-Linked Retinitis Pigmentosa (RP23)

Investigative ophthalmology & visual science, 2000-07, Vol.41 (8), p.2080-2086

2000

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Association of the NRG1 gene and schizophrenia: a meta-analysis

Molecular psychiatry, 2006-06, Vol.11 (6), p.613-613

2006

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Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus

Human genetics, 1999-07, Vol.105 (1-2), p.57-62

1999

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Novel frameshift mutations in the RP2 gene and polymorphic variants

Human mutation, 2000-06, Vol.15 (6), p.580-580

2000

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An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Human molecular genetics, 2014-06, Vol.23 (12), p.3316-3326

2014

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Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2 [published erratum appears in Invest Opyhthalmol Vis Sci 1998 Feb;39(2):219]

Investigative ophthalmology & visual science, 1997-08, Vol.38 (9), p.1893-1896

1997

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Dinucleotide repeat polymorphism at the DXS556 locus

Human molecular genetics, 1993-05, Vol.2 (5), p.613-613

1993

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Association of the NRG1 gene and schizophrenia : a meta-analysis

Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample

The dystrobrevin-binding protein 1 gene: features and networks

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Comparative immunogenetics of autism and schizophrenia

OPA1 , encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

No evidence for linkage or association of neuregulin-1 ( ) with disease in the Irish study of high-density schizophrenia families (ISHDSF)

Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4

Association study of SNAP25 and schizophrenia in Irish family and case-control samples

Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS)

A region of 35 kb containing the trace amine associate receptor 6 ( ) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families

Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy

Alcohol dependence is associated with the ZNF699 gene, a human locus related to Drosophila hangover, in the irish affected sib pair study of alcohol dependence (IASPSAD) sample

A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population : evidence for a founder effect

Mutations in the RP2 Gene Cause Disease in 10% of Families with Familial X-Linked Retinitis Pigmentosa Assessed in This Study

Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa

An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders

Evidence for a New Locus for X-Linked Retinitis Pigmentosa (RP23)

Association of the NRG1 gene and schizophrenia: a meta-analysis

Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus

Novel frameshift mutations in the RP2 gene and polymorphic variants

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2 [published erratum appears in Invest Opyhthalmol Vis Sci 1998 Feb;39(2):219]

Dinucleotide repeat polymorphism at the DXS556 locus

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