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Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders

Genome Biology, 2018-11, Vol.19 (1), p.194-194, Article 194

2018

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Young Offenders’ Emotion Recognition Dysfunction Across Emotion Intensities: Explaining Variation Using Psychopathic Traits, Conduct Disorder and Offense Severity

Journal of psychopathology and behavioral assessment, 2014-03, Vol.36 (1), p.60-73

2014

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Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia

Translational psychiatry, 2021-08, Vol.11 (1), p.433-433, Article 433

2021

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Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing

PloS one, 2014-08, Vol.9 (8), p.e104281-e104281

2014

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Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

American journal of human genetics, 2012-09, Vol.91 (3), p.565-571

2012

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Cardiac malformations and midline skeletal defects in mice lacking filamin A

Human molecular genetics, 2006-08, Vol.15 (16), p.2457-2467

2006

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Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

American journal of human genetics, 2011-09, Vol.89 (3), p.464-473

2011

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Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant-Filtering Interface

Human mutation, 2014-04, Vol.35 (4), p.434-441

2014

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Longitudinal studies examining the impact of prenatal and subsequent episodes of maternal depression on offspring antisocial behaviour

European child & adolescent psychiatry, 2021-01, Vol.30 (1), p.5-40

2021

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The relationship between psychopathy and impulsivity: A multi-impulsivity measurement approach

Personality and individual differences, 2011-09, Vol.51 (4), p.429-434

2011

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The relationship between reward and punishment sensitivity and antisocial behavior in male adolescents

Personality and individual differences, 2014-06, Vol.63, p.122-127

2014

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Genetic diagnosis of familial breast cancer using clonal sequencing

Human mutation, 2010-04, Vol.31 (4), p.484-491

2010

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Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Human molecular genetics, 2012-02, Vol.21 (4), p.776-783

2012

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Genotype-Phenotype Correlation of Mouse Pde6b Mutations

Investigative ophthalmology & visual science, 2005-09, Vol.46 (9), p.3443-3450

2005

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Mutation Detection by Clonal Sequencing of PCR Amplicons and Grouped Read Typing is Applicable to Clinical Diagnostics

Human mutation, 2013-01, Vol.34 (1), p.248-254

2013

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Novel ENU-induced eye mutations in the mouse: models for human eye disease

Human molecular genetics, 2002-04, Vol.11 (7), p.755-767

2002

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Illuminator, a desktop program for mutation detection using short-read clonal sequencing

Genomics (San Diego, Calif.), 2011-10, Vol.98 (4), p.302-309

2011

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Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor

Mammalian genome, 2004-07, Vol.15 (7), p.525-536

2004

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Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome

Human molecular genetics, 2004-07, Vol.13 (14), p.1433-1439

2004

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Illuminator, a desktop program for mutation detection using short-read clonal sequencing: New Genomic Technologies and Applications

Genomics (San Diego, Calif.), 2011, Vol.98 (4), p.302-309

2011

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Antisocial behaviour in adolescence: the role of reward processing

Morgan, Joanne E

2012

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Executive functioning, reward processing, and antisocial behavior in adolescent males

The Routledge International Handbook of Biosocial Criminology, 2015, p.315-327

1, 2015

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Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders

Young Offenders’ Emotion Recognition Dysfunction Across Emotion Intensities: Explaining Variation Using Psychopathic Traits, Conduct Disorder and Offense Severity

Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia

Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

Cardiac malformations and midline skeletal defects in mice lacking filamin A

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant-Filtering Interface

Longitudinal studies examining the impact of prenatal and subsequent episodes of maternal depression on offspring antisocial behaviour

The relationship between psychopathy and impulsivity: A multi-impulsivity measurement approach

The relationship between reward and punishment sensitivity and antisocial behavior in male adolescents

Genetic diagnosis of familial breast cancer using clonal sequencing

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

Genotype-Phenotype Correlation of Mouse Pde6b Mutations

Mutation Detection by Clonal Sequencing of PCR Amplicons and Grouped Read Typing is Applicable to Clinical Diagnostics

Novel ENU-induced eye mutations in the mouse: models for human eye disease

Illuminator, a desktop program for mutation detection using short-read clonal sequencing

Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome

Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

Illuminator, a desktop program for mutation detection using short-read clonal sequencing: New Genomic Technologies and Applications

Antisocial behaviour in adolescence: the role of reward processing

Executive functioning, reward processing, and antisocial behavior in adolescent males

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