Cousin E - Search Results

1

Modeling the effect of a genetic factor for a complex trait in a simulated population.

Bourgey M, Leutenegger AL, Cousin E, Bourgain C, Babron MC, Clerget-Darpoux F. Bourgey M, et al. Among authors: cousin e. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S87. doi: 10.1186/1471-2156-6-S1-S87. BMC Genet. 2005. PMID: 16451702 Free PMC article.

2

Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effects.

Cousin E, Deleuze JF, Genin E. Cousin E, et al. BMC Genet. 2006 Apr 5;7:20. doi: 10.1186/1471-2156-7-20. BMC Genet. 2006. PMID: 16597333 Free PMC article.

3

Association studies in candidate genes: strategies to select SNPs to be tested.

Cousin E, Genin E, Mace S, Ricard S, Chansac C, del Zompo M, Deleuze JF. Cousin E, et al. Hum Hered. 2003;56(4):151-9. doi: 10.1159/000073200. Hum Hered. 2003. PMID: 15031617

4

ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease.

Macé S, Cousin E, Ricard S, Génin E, Spanakis E, Lafargue-Soubigou C, Génin B, Fournel R, Roche S, Haussy G, Massey F, Soubigou S, Bréfort G, Benoit P, Brice A, Campion D, Hollis M, Pradier L, Benavides J, Deleuze JF. Macé S, et al. Among authors: cousin e. Neurobiol Dis. 2005 Feb;18(1):119-25. doi: 10.1016/j.nbd.2004.09.011. Neurobiol Dis. 2005. PMID: 15649702

5

Association study of the GAB2 gene with the risk of developing Alzheimer's disease.

Chapuis J, Hannequin D, Pasquier F, Bentham P, Brice A, Leber I, Frebourg T, Deleuze JF, Cousin E, Thaker U, Amouyel P, Mann D, Lendon C, Campion D, Lambert JC. Chapuis J, et al. Among authors: cousin e. Neurobiol Dis. 2008 Apr;30(1):103-6. doi: 10.1016/j.nbd.2007.12.006. Epub 2008 Jan 5. Neurobiol Dis. 2008. PMID: 18272374

6

No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease.

Cousin E, Hannequin D, Macé S, Dubois B, Ricard S, Génin E, Brun C, Chansac C, Pradier L, Frebourg T, Brice A, Campion D, Deleuze JF. Cousin E, et al. Neurosci Lett. 2003 Dec 19;353(2):153-5. doi: 10.1016/s0304-3940(03)01105-4. Neurosci Lett. 2003. PMID: 14664923

7

No replication of genetic association between candidate polymorphisms and Alzheimer's disease.

Cousin E, Macé S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Génin E, Brice A, Campion D. Cousin E, et al. Neurobiol Aging. 2011 Aug;32(8):1443-51. doi: 10.1016/j.neurobiolaging.2009.09.004. Epub 2009 Nov 3. Neurobiol Aging. 2011. PMID: 19889475

8

A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism.

Cousin E, Hannequin D, Ricard S, Macé S, Génin E, Chansac C, Brice A, Dubois B, Frebourg T, Mercken L, Benavides J, Pradier L, Campion D, Deleuze JF. Cousin E, et al. Neurosci Lett. 2003 May 15;342(1-2):5-8. doi: 10.1016/s0304-3940(03)00225-8. Neurosci Lett. 2003. PMID: 12727304

9

Association between the Thr325Ile polymorphism of the thrombin-activatable fibrinolysis inhibitor and stroke in the Ludwigshafen Risk and Cardiovascular Health Study.

Kozian DH, Lorenz M, März W, Cousin E, Mace S, Deleuze JF. Kozian DH, et al. Among authors: cousin e. Thromb Haemost. 2010 May;103(5):976-83. doi: 10.1160/TH09-10-0682. Epub 2010 Mar 9. Thromb Haemost. 2010. PMID: 20216989

10

Variations in the APP gene promoter region and risk of Alzheimer disease.

Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert JC, Campion D. Guyant-Maréchal L, et al. Among authors: cousin e. Neurology. 2007 Feb 27;68(9):684-7. doi: 10.1212/01.wnl.0000255938.33739.46. Neurology. 2007. PMID: 17325276

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