Palmer C - Search Results

1

Childhood asthma exacerbations and the Arg16 β2-receptor polymorphism: A meta-analysis stratified by treatment.

Turner S, Francis B, Vijverberg S, Pino-Yanes M, Maitland-van der Zee AH, Basu K, Bignell L, Mukhopadhyay S, Tavendale R, Palmer C, Hawcutt D, Pirmohamed M, Burchard EG, Lipworth B; Pharmacogenomics in Childhood Asthma Consortium. Turner S, et al. Among authors: palmer c. J Allergy Clin Immunol. 2016 Jul;138(1):107-113.e5. doi: 10.1016/j.jaci.2015.10.045. Epub 2016 Jan 7. J Allergy Clin Immunol. 2016. PMID: 26774659 Free PMC article.

2

Overweight and obesity in deltaF508 homozygous cystic fibrosis.

Kastner-Cole D, Palmer CN, Ogston SA, Mehta A, Mukhopadhyay S. Kastner-Cole D, et al. J Pediatr. 2005 Sep;147(3):402-4. doi: 10.1016/j.jpeds.2005.06.003. J Pediatr. 2005. PMID: 16182686

3

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.

Palmer CN, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, Goudie DR, Sandilands A, Campbell LE, Smith FJ, O'Regan GM, Watson RM, Cecil JE, Bale SJ, Compton JG, DiGiovanna JJ, Fleckman P, Lewis-Jones S, Arseculeratne G, Sergeant A, Munro CS, El Houate B, McElreavey K, Halkjaer LB, Bisgaard H, Mukhopadhyay S, McLean WH. Palmer CN, et al. Nat Genet. 2006 Apr;38(4):441-6. doi: 10.1038/ng1767. Epub 2006 Mar 19. Nat Genet. 2006. PMID: 16550169

4

Glutathione S-transferase M1 and P1 genotype, passive smoking, and peak expiratory flow in asthma.

Palmer CN, Doney AS, Lee SP, Murrie I, Ismail T, Macgregor DF, Mukhopadhyay S. Palmer CN, et al. Pediatrics. 2006 Aug;118(2):710-6. doi: 10.1542/peds.2005-3030. Pediatrics. 2006. PMID: 16882827

5

Filaggrin null mutations are associated with increased asthma severity in children and young adults.

Palmer CN, Ismail T, Lee SP, Terron-Kwiatkowski A, Zhao Y, Liao H, Smith FJ, McLean WH, Mukhopadhyay S. Palmer CN, et al. J Allergy Clin Immunol. 2007 Jul;120(1):64-8. doi: 10.1016/j.jaci.2007.04.001. Epub 2007 May 25. J Allergy Clin Immunol. 2007. PMID: 17531295

6

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study.

Henderson J, Northstone K, Lee SP, Liao H, Zhao Y, Pembrey M, Mukhopadhyay S, Smith GD, Palmer CN, McLean WH, Irvine AD. Henderson J, et al. J Allergy Clin Immunol. 2008 Apr;121(4):872-7.e9. doi: 10.1016/j.jaci.2008.01.026. Epub 2008 Mar 5. J Allergy Clin Immunol. 2008. PMID: 18325573

7

A polymorphism controlling ORMDL3 expression is associated with asthma that is poorly controlled by current medications.

Tavendale R, Macgregor DF, Mukhopadhyay S, Palmer CN. Tavendale R, et al. J Allergy Clin Immunol. 2008 Apr;121(4):860-3. doi: 10.1016/j.jaci.2008.01.015. J Allergy Clin Immunol. 2008. PMID: 18395550

8

Gene-environment interaction in the onset of eczema in infancy: filaggrin loss-of-function mutations enhanced by neonatal cat exposure.

Bisgaard H, Simpson A, Palmer CN, Bønnelykke K, McLean I, Mukhopadhyay S, Pipper CB, Halkjaer LB, Lipworth B, Hankinson J, Woodcock A, Custovic A. Bisgaard H, et al. PLoS Med. 2008 Jun 24;5(6):e131. doi: 10.1371/journal.pmed.0050131. PLoS Med. 2008. PMID: 18578563 Free PMC article.

9

Chromosome 17q21 gene variants are associated with asthma and exacerbations but not atopy in early childhood.

Bisgaard H, Bønnelykke K, Sleiman PM, Brasholt M, Chawes B, Kreiner-Møller E, Stage M, Kim C, Tavendale R, Baty F, Pipper CB, Palmer CN, Hakonarsson H. Bisgaard H, et al. Among authors: palmer cn. Am J Respir Crit Care Med. 2009 Feb 1;179(3):179-85. doi: 10.1164/rccm.200809-1436OC. Epub 2008 Nov 21. Am J Respir Crit Care Med. 2009. PMID: 19029000

10

An obesity-associated FTO gene variant and increased energy intake in children.

Cecil JE, Tavendale R, Watt P, Hetherington MM, Palmer CN. Cecil JE, et al. N Engl J Med. 2008 Dec 11;359(24):2558-66. doi: 10.1056/NEJMoa0803839. N Engl J Med. 2008. PMID: 19073975 Free article.

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