| P50 | author | George Davey Smith | Q21003878 |
| | Esther Crawley | Q90579200 |
| P2860 | cites work | Utility of the blood for gene expression profiling and biomarker discovery in chronic fatigue syndrome | Q21342986 |
| | ‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?* | Q22066036 |
| | Childhood predictors of self reported chronic fatigue syndrome/myalgic encephalomyelitis in adults: national birth cohort study | Q24562785 |
| | Epidemiology of chronic fatigue syndrome and self reported myalgic encephalomyelitis in 5-15 year olds: cross sectional study | Q24671215 |
| | Gene expression in peripheral blood mononuclear cells from patients with chronic fatigue syndrome | Q24672120 |
| | An integrative genomics approach to infer causal associations between gene expression and disease | Q29616385 |
| | Gene expression profile of empirically delineated classes of unexplained chronic fatigue | Q33239752 |
| | Risk factors associated with chronic fatigue syndrome in a cluster of pediatric cases | Q34102535 |
| | Problems of reporting genetic associations with complex outcomes | Q34184173 |
| | Chronic fatigue syndrome and other fatiguing illnesses in adolescents: a population-based study | Q34326578 |
| | Primary juvenile fibromyalgia syndrome and chronic fatigue syndrome in adolescents | Q34338918 |
| | Association between chronic fatigue syndrome and the corticosteroid-binding globulin gene ALA SER224 polymorphism | Q34369519 |
| | The validity of an empirical delineation of heterogeneity in chronic unexplained fatigue | Q34513057 |
| | Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue. | Q34513067 |
| | Gene expression profile exploration of a large dataset on chronic fatigue syndrome | Q34513076 |
| | Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome | Q34513090 |
| | A first study of cytokine genomic polymorphisms in CFS: Positive association of TNF-857 and IFNgamma 874 rare alleles. | Q34536139 |
| | Association of chronic fatigue syndrome with human leucocyte antigen class II alleles | Q35589069 |
| | What can mendelian randomisation tell us about modifiable behavioural and environmental exposures? | Q36119363 |
| | Gene expression correlates of unexplained fatigue | Q40334663 |
| | Relationship between disabling fatigue and depression in children: genetic study | Q42597178 |
| | Is disabling fatigue in childhood influenced by genes? | Q42599979 |
| | Familial corticosteroid-binding globulin deficiency due to a novel null mutation: association with fatigue and relative hypotension | Q43705647 |
| | Identifying illness parameters in fatiguing syndromes using classical projection methods | Q48505258 |
| | An empirical delineation of the heterogeneity of chronic unexplained fatigue in women. | Q48505283 |
| | Prevalence of chronic disabling fatigue in children and adolescents. | Q52089309 |
| | A Twin Study of the Etiology of Prolonged Fatigue and Immune Activation | Q57269030 |
| | Complex genetic and environmental relationships between psychological distress, fatigue and immune functioning: a twin study | Q57269112 |
| | Unique genetic and environmental determinants of prolonged fatigue: a twin study | Q57269137 |
| | Identification of novel expressed sequences, up-regulated in the leucocytes of chronic fatigue syndrome patients | Q59569190 |
| | Lack of association between HLA genotype and chronic fatigue syndrome | Q59745208 |
| | Epidemiology--is it time to call it a day? | Q73426385 |
| | A twin study of chronic fatigue | Q77221201 |
| | Chronic fatigue syndrome | Q82407941 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | chronic fatigue syndrome | Q209733 |
| P304 | page(s) | 1058-1061 | |
| P577 | publication date | 2007-09-05 | |
| P1433 | published in | Archives of Disease in Childhood | Q4787296 |
| P1476 | title | Is chronic fatigue syndrome (CFS/ME) heritable in children, and if so, why does it matter? | |
| P478 | volume | 92 | |