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Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups

Annals of the rheumatic diseases, 2016-08, Vol.75 (8), p.1558-1566

2016

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The CREB1-BDNF-NTRK2 Pathway in Depression: Multiple Gene-Cognition-Environment Interactions

Biological psychiatry (1969), 2011-04, Vol.69 (8), p.762-771

2011

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Immune‐Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA–DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum

Arthritis & rheumatology (Hoboken, N.J.), 2017-05, Vol.69 (5), p.1090-1099

2017

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Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

Neurobiology of aging, 2016-11, Vol.47, p.218.e1-218.e9

2016

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The EuroMyositis registry: an international collaborative tool to facilitate myositis research

Annals of the rheumatic diseases, 2018-01, Vol.77 (1), p.30

2018

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Polymorphisms in the mannose binding lectin (MBL) gene are not associated with radiographic erosions in rheumatoid or inflammatory polyarthritis

Journal of rheumatology, 2004-03, Vol.31 (3), p.442

2004

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Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: Results from the MYONET registry

Rheumatology (Oxford, England), 2024-08, Vol.63 (8), p.2093-2100

2024

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No association between apolipoprotein E or N-Acetyltransferase 2 gene polymorphisms and age-related hearing loss

The Laryngoscope, 2015-01, Vol.125 (1), p.E33-E38

2015

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CNR1 Gene is Associated with High Neuroticism and Low Agreeableness and Interacts with Recent Negative Life Events to Predict Current Depressive Symptoms

Neuropsychopharmacology (New York, N.Y.), 2009-07, Vol.34 (8), p.2019-2027

2009

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Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis

Arthritis research & therapy, 2018-06, Vol.20 (1), p.117-117, Article 117

2018

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Increased Estrogen Rather Than Decreased Androgen Action Is Associated with Longer Androgen Receptor CAG Repeats

The journal of clinical endocrinology and metabolism, 2009-01, Vol.94 (1), p.277-284

2009

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A role for HLA-DRB11101 and DRB10801 in cognitive ability and its decline with age

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2016-03, Vol.171B (2), p.209-214

2016

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Variations in the cannabinoid receptor 1 gene predispose to migraine

Neuroscience letters, 2009-09, Vol.461 (2), p.116-120

2009

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O28Largest Genetic Study to Date in Sporadic Inclusion Body Myositis Confirms the Human Leukocyte Antigen as the Most Associated Region and Suggests a Role for C-C Chemokine Receptor Type 5

Rheumatology (Oxford, England), 2016-04, Vol.55 (suppl_1), p.i48-i48

2016

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Genetic association study of NF-κB genes in UK Caucasian adult and juvenile onset idiopathic inflammatory myopathy

Rheumatology (Oxford, England), 2012-05, Vol.51 (5), p.794-799

2012

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Risk-Taking Behavior in a Gambling Task Associated with Variations in the Tryptophan Hydroxylase 2 Gene: Relevance to Psychiatric Disorders

Neuropsychopharmacology, 2010-04, Vol.35 (5), p.1109-1119

2010

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Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies

Arthritis research & therapy, 2016-07, Vol.18 (1), p.156-156, Article 156

2016

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The HTR1A and HTR1B receptor genes influence stress-related information processing

European neuropsychopharmacology, 2011-01, Vol.21 (1), p.129-139

2011

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Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: Relevance for major depression

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2012-12, Vol.159B (8), p.928-940

2012

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The IFN-λ Genetic Polymorphism Association With the Viral Clearance Induced by Hepatitis C Virus Treatment in Pakistani Patients

Hepatitis monthly, 2014-03, Vol.14 (3), p.e15076-e15076

2014

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Effect of Polymorphisms in Selected Genes Involved in Pituitary-Testicular Function on Reproductive Hormones and Phenotype in Aging Men

The journal of clinical endocrinology and metabolism, 2010-04, Vol.95 (4), p.1898-1908

2010

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The IFN-[lamda] Genetic Polymorphism Association With the Viral Clearance Induced by Hepatitis C Virus Treatment in Pakistani Patients

Hepatitis monthly, 2014-03, Vol.14 (3), p.1

2014

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Genetic Variants in the Catechol-o-Methgltransferase Gene Are Associated With Impulsivity and Executive Function: Relevance for Major Depression

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2012, Vol.159 (8), p.928-940

2012

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Endogenous hormones, androgen receptor CAG repeat length and fluid cognition in middle-aged and older men: results from the European Male Ageing Study

European journal of endocrinology, 2010-06, Vol.162 (6), p.1155

2010

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Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups

The CREB1-BDNF-NTRK2 Pathway in Depression: Multiple Gene-Cognition-Environment Interactions

Immune‐Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA–DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts

The EuroMyositis registry: an international collaborative tool to facilitate myositis research

Polymorphisms in the mannose binding lectin (MBL) gene are not associated with radiographic erosions in rheumatoid or inflammatory polyarthritis

Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: Results from the MYONET registry

No association between apolipoprotein E or N-Acetyltransferase 2 gene polymorphisms and age-related hearing loss

CNR1 Gene is Associated with High Neuroticism and Low Agreeableness and Interacts with Recent Negative Life Events to Predict Current Depressive Symptoms

Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis

Increased Estrogen Rather Than Decreased Androgen Action Is Associated with Longer Androgen Receptor CAG Repeats

A role for HLA-DRB11101 and DRB10801 in cognitive ability and its decline with age

Variations in the cannabinoid receptor 1 gene predispose to migraine

O28Largest Genetic Study to Date in Sporadic Inclusion Body Myositis Confirms the Human Leukocyte Antigen as the Most Associated Region and Suggests a Role for C-C Chemokine Receptor Type 5

Genetic association study of NF-κB genes in UK Caucasian adult and juvenile onset idiopathic inflammatory myopathy

Risk-Taking Behavior in a Gambling Task Associated with Variations in the Tryptophan Hydroxylase 2 Gene: Relevance to Psychiatric Disorders

Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies

The HTR1A and HTR1B receptor genes influence stress-related information processing

Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: Relevance for major depression

The IFN-λ Genetic Polymorphism Association With the Viral Clearance Induced by Hepatitis C Virus Treatment in Pakistani Patients

Effect of Polymorphisms in Selected Genes Involved in Pituitary-Testicular Function on Reproductive Hormones and Phenotype in Aging Men

The IFN-[lamda] Genetic Polymorphism Association With the Viral Clearance Induced by Hepatitis C Virus Treatment in Pakistani Patients

Genetic Variants in the Catechol-o-Methgltransferase Gene Are Associated With Impulsivity and Executive Function: Relevance for Major Depression

Endogenous hormones, androgen receptor CAG repeat length and fluid cognition in middle-aged and older men: results from the European Male Ageing Study

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