Published in J Child Psychol Psychiatry on October 01, 2005
Candidate gene studies of ADHD: a meta-analytic review. Hum Genet (2009) 3.56
Hubris and NEMESIS in heads of government. J R Soc Med (2006) 2.05
Familial association and frequency of learning disabilities in ADHD sibling pair families. J Abnorm Child Psychol (2006) 1.18
Finding genes in child psychology and psychiatry: when are we going to be there? J Child Psychol Psychiatry (2005) 1.07
Time perception, phonological skills and executive function in children with dyslexia and/or ADHD symptoms. J Child Psychol Psychiatry (2010) 0.99
Aetiology for the covariation between combined type ADHD and reading difficulties in a family study: the role of IQ. J Child Psychol Psychiatry (2012) 0.89
Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults. J Neural Transm (Vienna) (2007) 0.85
The Colorado Longitudinal Twin Study of Reading Difficulties and ADHD: Etiologies of Comorbidity and Stability. Twin Res Hum Genet (2015) 0.81
Adrenergic neurotransmitter system transporter and receptor genes associated with atomoxetine response in attention-deficit hyperactivity disorder children. J Neural Transm (Vienna) (2012) 0.79
Phonological short-term memory and central executive processing in attention-deficit/hyperactivity disorder with/without dyslexia--evidence of cognitive overlap. J Neural Transm (Vienna) (2007) 0.79
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder. Neurol Sci (2013) 0.79
Latent class analysis of reading, decoding, and writing performance using the Academic Performance Test: concurrent and discriminating validity. Neuropsychiatr Dis Treat (2013) 0.78
Interpatient variability in dexmedetomidine response: a survey of the literature. ScientificWorldJournal (2014) 0.78
Identifying predictors of high quality care in English general practice: observational study. BMJ (2001) 9.34
The Canadian CT Head Rule for patients with minor head injury. Lancet (2001) 7.91
The Canadian C-spine rule for radiography in alert and stable trauma patients. JAMA (2001) 7.48
Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Mol Psychiatry (2011) 4.16
The effects of aging on reaction time in a signal detection task. Psychol Aging (2001) 2.82
Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm. Nat Genet (1996) 2.80
Variation in emergency department use of cervical spine radiography for alert, stable trauma patients. CMAJ (1997) 2.79
CD226 Gly307Ser association with multiple autoimmune diseases. Genes Immun (2008) 2.76
Association of rheumatoid factor and anti-cyclic citrullinated peptide positivity, but not carriage of shared epitope or PTPN22 susceptibility variants, with anti-tumour necrosis factor response in rheumatoid arthritis. Ann Rheum Dis (2008) 2.01
Genetic variation in the interleukin 10 gene promoter and systemic lupus erythematosus. J Rheumatol (1997) 1.90
Quality assessment for three common conditions in primary care: validity and reliability of review criteria developed by expert panels for angina, asthma and type 2 diabetes. Qual Saf Health Care (2002) 1.89
The impact of gestational stress and prenatal growth on emotional problems in offspring: a review. Acta Psychiatr Scand (2007) 1.89
Maternal smoking during pregnancy as an environmental risk factor for attention deficit hyperactivity disorder behaviour. A review. Minerva Pediatr (2005) 1.69
HLA and rheumatoid arthritis: a combined analysis of 440 British patients. Ann Rheum Dis (1986) 1.66
The Canadian CT Head Rule Study for patients with minor head injury: rationale, objectives, and methodology for phase I (derivation). Ann Emerg Med (2001) 1.65
Relationship between antisocial behaviour, attention-deficit hyperactivity disorder and maternal prenatal smoking. Br J Psychiatry (2005) 1.60
HLA-DRB1*0401/0404 genotype and rheumatoid arthritis: increased association in men, young age at onset, and disease severity. J Rheumatol (1995) 1.58
The effects of catabolic and anabolic steroids on amino acid incorporation by skeletal-muscle ribosomes. Biochem J (1968) 1.57
Association of tumor necrosis factor microsatellite polymorphisms with HLA-DRB1*04-bearing haplotypes in rheumatoid arthritis patients. Arthritis Rheum (1996) 1.56
Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Transl Psychiatry (2012) 1.52
Attitudes of general practitioners to caring for people with learning disability. Br J Gen Pract (1996) 1.51
Effect of cold ischemic time and HLA matching in kidneys coming from "young" and "old" donors: do not leave for tomorrow what you can do tonight. Transplantation (2001) 1.50
Brain-derived neurotrophic factor polymorphism Val66Met influences cognitive abilities in the elderly. Genes Brain Behav (2007) 1.47
Investigating the role of the HLA-Cw*06 and HLA-DRB1 genes in susceptibility to psoriatic arthritis: comparison with psoriasis and undifferentiated inflammatory arthritis. Ann Rheum Dis (2007) 1.47
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease. J Med Genet (2007) 1.44
Biochemical changes in skin and muscle after thermal injury. Br J Exp Pathol (1970) 1.42
Chymase cleavage of stem cell factor yields a bioactive, soluble product. Proc Natl Acad Sci U S A (1997) 1.39
Genetic basis of bad behaviour in adolescents. Lancet (1997) 1.39
The association of PTPN22 with rheumatoid arthritis and juvenile idiopathic arthritis. Rheumatology (Oxford) (2006) 1.36
The links between prenatal stress and offspring development and psychopathology: disentangling environmental and inherited influences. Psychol Med (2009) 1.33
Variation in ED use of computed tomography for patients with minor head injury. Ann Emerg Med (1997) 1.29
Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. Molecular genetic study. Br J Psychiatry (2003) 1.27
A rapid method for the quantitative extraction of bile acids and their conjugates from serum using commercially available reverse-phase octadecylsilane bonded silica cartridges. Clin Chim Acta (1982) 1.26
A study of tremor in multiple sclerosis. Brain (2001) 1.26
Familial transmission of depression and antisocial behavior symptoms: disentangling the contribution of inherited and environmental factors and testing the mediating role of parenting. Psychol Med (2010) 1.25
HLA antigen associations with extra-articular rheumatoid arthritis. Tissue Antigens (1984) 1.22
A surface marker for murine vascular endothelial cells defined by monoclonal antibody. J Histochem Cytochem (1982) 1.21
Stem cell factor induces proliferation and differentiation of highly enriched murine hematopoietic cells. Proc Natl Acad Sci U S A (1991) 1.19
Absence of rheumatoid arthritis in a rural Nigerian population. J Rheumatol (1993) 1.19
Macrophage migration inhibitory factor (MIF) gene polymorphism is associated with susceptibility to but not severity of inflammatory polyarthritis. Genes Immun (2003) 1.18
Clustering of activating mutations in c-KIT's juxtamembrane coding region in canine mast cell neoplasms. J Invest Dermatol (1999) 1.17
A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder. Mol Psychiatry (2000) 1.16
Orthopaedic intervention in early rheumatoid arthritis. Occurrence and predictive factors in an inception cohort of 1064 patients followed for 5 years. Rheumatology (Oxford) (2004) 1.16
Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint maps to an 11-cM region on chromosome 4q35. Am J Hum Genet (1999) 1.14
Expression of hippocampal brain-derived neurotrophic factor and its receptors in Stanley consortium brains. J Psychiatr Res (2009) 1.13
Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis. Genes Immun (2010) 1.13
A spectrum of susceptibility to rheumatoid arthritis within HLA-DRB1: stratification by autoantibody status in a large UK population. Genes Immun (2011) 1.12
Differential contribution of CDKAL1 variants to psoriasis, Crohn's disease and type II diabetes. Genes Immun (2009) 1.12
New HLA DNA polymorphisms associated with autoimmune diseases. Nature (1986) 1.11
Association between rheumatoid arthritis and polymorphism of tumor necrosis factor receptor II, but not tumor necrosis factor receptor I, in Caucasians. Arthritis Rheum (2001) 1.09
High resolution linkage and association mapping identifies a novel rheumatoid arthritis susceptibility locus homologous to one linked to two rat models of inflammatory arthritis. Hum Mol Genet (2001) 1.08
Cathepsin D exon 2 polymorphism associated with general intelligence in a healthy older population. Mol Psychiatry (2003) 1.08
Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies. Mol Psychiatry (2006) 1.08
Free and serum testosterone levels in 276 males: a comparative study of rheumatoid arthritis, ankylosing spondylitis and healthy controls. Clin Rheumatol (1989) 1.07
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Mol Psychiatry (2005) 1.07
Investigation of polymorphisms in the PADI4 gene in determining severity of inflammatory polyarthritis. Ann Rheum Dis (2005) 1.07
Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior. Am J Med Genet B Neuropsychiatr Genet (2008) 1.07
'The risks of playing it safe': a prospective longitudinal study of response to reward in the adolescent offspring of depressed parents. Psychol Med (2012) 1.06
Absence of an association between HLA-DRB1*04 and rheumatoid arthritis in newly diagnosed cases from the community. Ann Rheum Dis (1993) 1.05
Fine mapping the TAGAP risk locus in rheumatoid arthritis. Genes Immun (2011) 1.04
Psychological sequelae of miscarriage: a controlled study using the general health questionnaire and the hospital anxiety and depression scale. Br J Gen Pract (1992) 1.04
Influence of serotonin transporter gene polymorphisms on cognitive decline and cognitive abilities in a nondemented elderly population. Mol Psychiatry (2005) 1.04
Immunogenetic heterogeneity in rheumatoid disease as illustrated by different MHC associations (DQ, Dw and C4) in articular and extra-articular subsets. Br J Rheumatol (1991) 1.03
Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes Brain Behav (2008) 1.03
Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis. Ann Rheum Dis (2010) 1.02
Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD. Mol Psychiatry (2004) 1.02
Attitudes of general practitioners towards health care for people with intellectual disability and the factors underlying these attitudes. J Intellect Disabil Res (1997) 1.02
Evidence for linkage of the HLA-B locus in Behçet's disease, obtained using the transmission disequilibrium test. Arthritis Rheum (2001) 1.01
No support for association between the dopamine transporter (DAT1) gene and ADHD. Am J Med Genet B Neuropsychiatr Genet (2005) 1.01
Association of protein kinase C alpha (PRKCA) gene with multiple sclerosis in a UK population. Brain (2004) 1.00
Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Mol Psychiatry (2002) 1.00
Cultured glial cells express the SNAP-25 analogue SNAP-23. Glia (1999) 0.99
HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party. Thromb Haemost (1997) 0.99
Interruptions during general practice consultations--the patients' view. Fam Pract (1996) 0.99
Hypertension and the post-carotid endarterectomy cerebral hyperperfusion syndrome. Eur J Vasc Endovasc Surg (2010) 0.98
Enteroendocrine cells: neglected players in gastrointestinal disorders? Therap Adv Gastroenterol (2008) 0.98
Physiological aspects of exocytosis in chromaffin cells of the adrenal medulla. Acta Physiol Scand (1999) 0.98
Characterization of a prolactin gene polymorphism and its associations with systemic lupus erythematosus. Arthritis Rheum (2001) 0.98
Evaluation of three different ways of assessing tremor in multiple sclerosis. J Neurol Neurosurg Psychiatry (2000) 0.97
NK1 (TACR1) receptor gene 'knockout' mouse phenotype predicts genetic association with ADHD. J Psychopharmacol (2009) 0.97
Positive association of HLA-DRB1*15 with Dupuytren's disease in Caucasians. Tissue Antigens (2008) 0.96
Variations in serum sCD23 in conditions with either enhanced humoral or cell-mediated immunity. Immunology (1993) 0.96
Differential expression of SNAP-25 isoforms and SNAP-23 in the adrenal gland. J Neurochem (1999) 0.96
Linkage of rheumatoid arthritis to insulin-dependent diabetes mellitus loci: evidence supporting a hypothesis for the existence of common autoimmune susceptibility loci. Arthritis Rheum (2000) 0.96
Association of the CCR5 gene with juvenile idiopathic arthritis. Genes Immun (2010) 0.95
Antibodies to SS-A/Ro-52kD and centromere in autoimmune liver disease: a clue to diagnosis and prognosis of primary biliary cirrhosis. Aliment Pharmacol Ther (2007) 0.95
A large multicentre analysis of CTGF -945 promoter polymorphism does not confirm association with systemic sclerosis susceptibility or phenotype. Ann Rheum Dis (2008) 0.95
Attention deficit hyperactivity disorder: unravelling the molecular genetics. Mol Psychiatry (1998) 0.95