Bours V - Search Results

1

Evidence of association between interferon regulatory factor 5 gene polymorphisms and asthma.

Wang C, Rose-Zerilli MJ, Koppelman GH, Sandling JK, Holloway JW, Postma DS, Holgate ST, Bours V, Syvänen AC, Dideberg V. Wang C, et al. Among authors: bours v. Gene. 2012 Aug 10;504(2):220-5. doi: 10.1016/j.gene.2012.05.021. Epub 2012 May 18. Gene. 2012. PMID: 22613848

2

An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.

Dideberg V, Kristjansdottir G, Milani L, Libioulle C, Sigurdsson S, Louis E, Wiman AC, Vermeire S, Rutgeerts P, Belaiche J, Franchimont D, Van Gossum A, Bours V, Syvänen AC. Dideberg V, et al. Among authors: bours v. Hum Mol Genet. 2007 Dec 15;16(24):3008-16. doi: 10.1093/hmg/ddm259. Epub 2007 Sep 19. Hum Mol Genet. 2007. PMID: 17881657 Free article.

3

Lymphotoxin alpha gene in Crohn's disease patients: absence of implication in the response to infliximab in a large cohort study.

Dideberg V, Louis E, Farnir F, Bertoli S, Vermeire S, Rutgeerts P, De Vos M, Van Gossum A, Belaiche J, Bours V. Dideberg V, et al. Among authors: bours v. Pharmacogenet Genomics. 2006 May;16(5):369-73. doi: 10.1097/01.fpc.0000204993.91806.b1. Pharmacogenet Genomics. 2006. PMID: 16609369

4

[Integration of pharmacogenetics in the medical practice].

Dideberg V, Bours V. Dideberg V, et al. Among authors: bours v. Rev Med Liege. 2005 Dec;60(12):918-22. Rev Med Liege. 2005. PMID: 16457391 Free article. Review. French.

5

Modulating effect of COMT Val(158)Met polymorphism on interference resolution during a working memory task.

Jaspar M, Dideberg V, Bours V, Maquet P, Collette F. Jaspar M, et al. Among authors: bours v. Brain Cogn. 2015 Apr;95:7-18. doi: 10.1016/j.bandc.2015.01.013. Epub 2015 Feb 12. Brain Cogn. 2015. PMID: 25682348 Free article.

6

The TNF/ADAM 17 system: implication of an ADAM 17 haplotype in the clinical response to infliximab in Crohn's disease.

Dideberg V, Théâtre E, Farnir F, Vermeire S, Rutgeerts P, De Vos M, Belaiche J, Franchimont D, Van Gossum A, Louis E, Bours V. Dideberg V, et al. Among authors: bours v. Pharmacogenet Genomics. 2006 Oct;16(10):727-34. doi: 10.1097/01.fpc.0000230117.26581.a4. Pharmacogenet Genomics. 2006. PMID: 17001292

7

Influence of COMT Genotype on Antero-posterior Cortical Functional Connectivity Underlying Interference Resolution.

Jaspar M, Manard M, Dideberg V, Bours V, Maquet P, Collette F. Jaspar M, et al. Among authors: bours v. Cereb Cortex. 2016 Feb;26(2):498-509. doi: 10.1093/cercor/bhu188. Epub 2014 Sep 8. Cereb Cortex. 2016. PMID: 25205659 Free article.

8

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.

Uwineza A, Caberg JH, Hitayezu J, Hellin AC, Jamar M, Dideberg V, Rusingiza EK, Bours V, Mutesa L. Uwineza A, et al. Among authors: bours v. BMC Med Genet. 2014 Jul 12;15:79. doi: 10.1186/1471-2350-15-79. BMC Med Genet. 2014. PMID: 25016475 Free PMC article.

9

[PHARMACOGENOMICS AND PERSONALIZED MEDICINE: TOWARDS A SYSTEMATIC GENOMIC SCREENING?].

Dideberg V, Segers K, Koopmansch B, Lambert F, Bours V. Dideberg V, et al. Among authors: bours v. Rev Med Liege. 2015 May-Jun;70(5-6):251-6. Rev Med Liege. 2015. PMID: 26285448 Free article. French.

10

Modulating effect of COMT genotype on the brain regions underlying proactive control process during inhibition.

Jaspar M, Genon S, Muto V, Meyer C, Manard M, Dideberg V, Bours V, Salmon E, Maquet P, Collette F. Jaspar M, et al. Among authors: bours v. Cortex. 2014 Jan;50:148-61. doi: 10.1016/j.cortex.2013.06.003. Epub 2013 Jun 19. Cortex. 2014. PMID: 23859480 Free article.

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