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Allergy|October 3, 2012
The CRTH2 antagonist OC000459 reduces nasal and ocular symptoms in allergic subjects exposed to grass pollen, a randomised, placebo-controlled, double-blind trialF Horak, P Zieglmayer, R Zieglmayer, et al.
Molecular Psychiatry|October 14, 2000
A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorderJ Holmes, A Payton, J H Barrett, et al.
Plos One|February 26, 2009
Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesisTimothy A Graubert, Michelle A Payton, Jin Shao, et al.
American Journal of Medical Genetics|July 13, 2001
Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based studyA Payton, J Holmes, J H Barrett, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 19, 2013
Predicting cognitive ability in ageing cohorts using Type 2 diabetes genetic riskM Luciano, R Mõttus, S E Harris, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 13, 2013
IGF2 gene polymorphisms and IGF-II concentration are determinants of longitudinal weight trends in type 2 diabetesR P Narayanan, B Fu, A Payton, et al.
Plos One|August 8, 2015
Antileukemic Efficacy of Continuous vs Discontinuous Dexamethasone in Murine Models of Acute Lymphoblastic LeukemiaLaura B Ramsey, Laura J Janke, Monique A Payton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in malesR Srinivasan, Y Davidson, L Gibbons, et al.
Genes, Brain, and Behavior|December 17, 2008
Variation in the dysbindin gene and normal cognitive function in three independent population samplesM Luciano, F Miyajima, P A Lind, et al.
Intelligence|February 26, 2016
Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differencesW D Hill, G Davies, D C Liewald, et al.
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