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Association between the oxytocin receptor (OXTR) gene and children's social cognition at 18 months

Genes, brain and behavior, 2014-09, Vol.13 (7), p.603-610

2014

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Support for EKN1 as the susceptibility locus for dyslexia on 15q21

Molecular psychiatry, 2004-12, Vol.9 (12), p.1111-1121

2004

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Arginine vasopressin 1a receptor gene and maternal behavior: evidence of association and moderation

Genes, brain and behavior, 2012-04, Vol.11 (3), p.262-268

2012

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A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-03, Vol.162B (2), p.146-156

2013

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Association of the ROBO1 gene with reading disabilities in a family‐based analysis

Genes, brain and behavior, 2014-04, Vol.13 (4), p.430-438

2014

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Association of the KCNJ5 gene with Tourette Syndrome and Attention‐Deficit/Hyperactivity Disorder

Genes, brain and behavior, 2014-07, Vol.13 (6), p.535-542

2014

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Association of the glutamate receptor subunit gene GRIN2B with attention‐deficit/hyperactivity disorder

Genes, brain and behavior, 2007-07, Vol.6 (5), p.444-452

2007

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The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder

Molecular psychiatry, 2005-11, Vol.10 (11), p.998-1005

2005

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Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems

Molecular psychiatry, 2007-08, Vol.12 (8), p.776-785

2007

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Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder

Molecular psychiatry, 2000-07, Vol.5 (4), p.405-409

2000

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Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disorders

Neuropsychobiology, 2008-01, Vol.58 (2), p.71-80

2008

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The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder

Molecular psychiatry, 2005-11, Vol.10 (11), p.973-973

2005

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Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor

Molecular psychiatry, 2000-09, Vol.5 (5), p.548-551

2000

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Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention- deficit/hyperactivity disorder in the 16p13 region

Molecular psychiatry, 2004-05, Vol.9 (5), p.494-499

2004

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Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region

Genes, brain and behavior, 2008-11, Vol.7 (8), p.877-886

2008

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Genome scan for linkage to Gilles de la Tourette syndrome

American journal of medical genetics, 1999-08, Vol.88 (4), p.437-445

1999

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Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD)

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2009-09, Vol.150B (6), p.866-873

2009

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Association study between gilles de la tourette syndrome and two genes in the robo-slit pathway located in the chromosome 11q24 linked/associated region

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-01, Vol.147B (1), p.68-72

2008

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Catechol-O-methyltransferase and Gilles de la Tourette syndrome

Molecular psychiatry, 1999-09, Vol.4 (5), p.492-495

1999

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Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder

American journal of medical genetics, 2000-02, Vol.96 (1), p.114-117

2000

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Association study of CREB1 and childhood-onset mood disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-08, Vol.137B (1), p.45-50

2005

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Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder

American journal of medical genetics, 2000-06, Vol.96 (3), p.262-267

2000

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5′-Untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder

American journal of medical genetics, 2001-01, Vol.105 (1), p.84-90

2001

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Attention-deficit hyperactivity disorder and the adrenergic receptors α1C and α2C

Molecular psychiatry, 2001-05, Vol.6 (3), p.334-337

2001

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Association study of the adrenergic receptors and childhood-onset mood disorders in Hungarian families

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-04, Vol.141B (3), p.227-233

2006

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Association between the oxytocin receptor (OXTR) gene and children's social cognition at 18 months

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

Arginine vasopressin 1a receptor gene and maternal behavior: evidence of association and moderation

A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1

Association of the ROBO1 gene with reading disabilities in a family‐based analysis

Association of the KCNJ5 gene with Tourette Syndrome and Attention‐Deficit/Hyperactivity Disorder

Association of the glutamate receptor subunit gene GRIN2B with attention‐deficit/hyperactivity disorder

The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder

Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems

Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder

Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disorders

The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder

Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor

Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention- deficit/hyperactivity disorder in the 16p13 region

Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region

Genome scan for linkage to Gilles de la Tourette syndrome

Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD)

Association study between gilles de la tourette syndrome and two genes in the robo-slit pathway located in the chromosome 11q24 linked/associated region

Catechol-O-methyltransferase and Gilles de la Tourette syndrome

Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder

Association study of CREB1 and childhood-onset mood disorders

Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder

5′-Untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder

Attention-deficit hyperactivity disorder and the adrenergic receptors α1C and α2C

Association study of the adrenergic receptors and childhood-onset mood disorders in Hungarian families

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