Bartlett J - Search Results

1

A single-nucleotide polymorphism in the fetal catechol-O-methyltransferase gene is associated with spontaneous preterm birth in African Americans.

Thota C, Menon R, Wentz MJ, Fortunato SJ, Bartlett J, Drobek CO, Nair S, Al-Hendy A. Thota C, et al. Among authors: bartlett j. Reprod Sci. 2012 Feb;19(2):135-42. doi: 10.1177/1933719111417885. Epub 2011 Dec 6. Reprod Sci. 2012. PMID: 22158829 Free PMC article.

2

Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease.

Liang X, Schnetz-Boutaud N, Bartlett J, Anderson BM, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: bartlett j. Dement Geriatr Cogn Disord. 2007;23(2):126-32. doi: 10.1159/000097857. Epub 2006 Dec 8. Dement Geriatr Cogn Disord. 2007. PMID: 17159347

3

No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasets.

Liang X, Schnetz-Boutaud N, Bartlett J, Allen MJ, Gwirtsman H, Schmechel DE, Carney RM, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: bartlett j. Ann Hum Genet. 2008 Jan;72(Pt 1):141-4. doi: 10.1111/j.1469-1809.2007.00394.x. Epub 2007 Aug 24. Ann Hum Genet. 2008. PMID: 17725684

4

Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.

Liang X, Slifer M, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: bartlett j. Hum Mutat. 2009 Mar;30(3):463-71. doi: 10.1002/humu.20953. Hum Mutat. 2009. PMID: 19241460 Free PMC article.

5

Examination of association of genes in the serotonin system to autism.

Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Anderson BM, et al. Among authors: bartlett j. Neurogenetics. 2009 Jul;10(3):209-16. doi: 10.1007/s10048-009-0171-7. Epub 2009 Jan 28. Neurogenetics. 2009. PMID: 19184136 Free PMC article.

6

Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease.

Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: bartlett j. Hum Mutat. 2007 Nov;28(11):1065-73. doi: 10.1002/humu.20567. Hum Mutat. 2007. PMID: 17573676

7

Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.

Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: bartlett j. Mol Psychiatry. 2006 Mar;11(3):280-5. doi: 10.1038/sj.mp.4001766. Mol Psychiatry. 2006. PMID: 16222332

8

Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease.

Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Martin ER, et al. Among authors: bartlett j. J Med Genet. 2005 Oct;42(10):787-92. doi: 10.1136/jmg.2004.029553. J Med Genet. 2005. PMID: 16199552 Free PMC article.

9

Examination of association to autism of common genetic variationin genes related to dopamine.

Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Anderson BM, et al. Among authors: bartlett j. Autism Res. 2008 Dec;1(6):364-9. doi: 10.1002/aur.55. Autism Res. 2008. PMID: 19360691 Free PMC article.

10

Consanguinity mapping of congenital heart disease in a South Indian population.

McGregor TL, Misri A, Bartlett J, Orabona G, Friedman RD, Sexton D, Maheshwari S, Morgan TM. McGregor TL, et al. Among authors: bartlett j. PLoS One. 2010 Apr 21;5(4):e10286. doi: 10.1371/journal.pone.0010286. PLoS One. 2010. PMID: 20422016 Free PMC article.

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