Genome-wide association analysis identifies genetic variations in subjects with myalgic encephalomyelitis/chronic fatigue syndrome

Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

(2015) Ellen Wright Clayton   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Using theRPackagecrlmmfor Genotyping and Copy Number Estimation

(2015) Robert B. Scharpf et al.   Journal of Statistical Software

Genetic and epigenetic fine mapping of causal autoimmune disease variants

(2014) Kyle Kai-How Farh et al.   NATURE

Statistical power and significance testing in large-scale genetic studies

(2014) Pak C. Sham et al.   NATURE REVIEWS GENETICS

Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system

(2014) Elisa Docampo et al.   PAIN

Polymorphisms in STK17A gene are associated with systemic lupus erythematosus and its clinical manifestations

(2013) Andréia Maria da Silva Fonseca et al.   GENE

Association of RNASEL and 8q24 variants with the presence and aggressiveness of hereditary and sporadic prostate cancer in a hispanic population

(2013) Ignacio F. San Francisco et al.   JOURNAL OF CELLULAR AND MOLECULAR MEDICINE

A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults

(2013) K U Ludwig et al.   Translational Psychiatry

A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome

(2012) Mohammad Al-Haggar et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The association of attempted suicide with genetic variants in the SLC6A4 and TPH genes depends on the definition of suicidal behavior: a systematic review and meta-analysis

(2012) R C Clayden et al.   Translational Psychiatry

Evidence for a heritable predisposition to Chronic Fatigue Syndrome

(2011) Frederick Albright et al.   BMC Neurology

Increased IgA responses to the LPS of commensal bacteria is associated with inflammation and activation of cell-mediated immunity in chronic fatigue syndrome

(2011) Michael Maes et al.   JOURNAL OF AFFECTIVE DISORDERS

Myalgic encephalomyelitis: International Consensus Criteria

(2011) B. M. Carruthers et al.   JOURNAL OF INTERNAL MEDICINE

CFTR mutation analysis and haplotype associations in CF patients

(2011) S.K. Cordovado et al.   MOLECULAR GENETICS AND METABOLISM

Convergent Genomic Studies Identify Association of GRIK2 and NPAS2 with Chronic Fatigue Syndrome

(2011) Alicia K. Smith et al.   NEUROPSYCHOBIOLOGY

From SNPs to Genes: Disease Association at the Gene Level

(2011) Benjamin Lehne et al.   PLoS One

Dissociation of accumulated genetic risk and disease severity in patients with schizophrenia

(2011) S Papiol et al.   Translational Psychiatry

The genetics of multiple sclerosis: An update 2010

(2010) Sabine Hoffjan et al.   MOLECULAR AND CELLULAR PROBES

RECK Negatively Regulates Matrix Metalloproteinase-9 Transcription

(2009) Satoshi Takagi et al.   CANCER RESEARCH

Toll-like Receptor 2 and DC-SIGNR1 Differentially Regulate Suppressors of Cytokine Signaling 1 in Dendritic Cells duringMycobacterium tuberculosisInfection

(2009) Varsha Srivastava et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Acute enterovirus infection followed by myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and viral persistence

(2009) J. Chia et al.   JOURNAL OF CLINICAL PATHOLOGY

Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotype

(2009) Taku Miyagawa et al.   JOURNAL OF HUMAN GENETICS

Plasma cytokines in women with chronic fatigue syndrome

(2009) Mary Fletcher et al.   Journal of Translational Medicine

Narcolepsy is strongly associated with the T-cell receptor alpha locus

(2009) Joachim Hallmayer et al.   NATURE GENETICS