Anderson B - Search Results

1

Predicting and preventing the cardiotoxicity of cancer therapy.

Anderson B, Sawyer DB. Anderson B, et al. Expert Rev Cardiovasc Ther. 2008 Aug;6(7):1023-33. doi: 10.1586/14779072.6.7.1023. Expert Rev Cardiovasc Ther. 2008. PMID: 18666852 Review.

2

Circulating neuregulin-1β levels vary according to the angiographic severity of coronary artery disease and ischemia.

Geisberg CA, Wang G, Safa RN, Smith HM, Anderson B, Peng XY, Veerkamp B, Zhao DX, Blakemore D, Yu C, Sawyer DB. Geisberg CA, et al. Among authors: anderson b. Coron Artery Dis. 2011 Dec;22(8):577-82. doi: 10.1097/MCA.0b013e32834d3346. Coron Artery Dis. 2011. PMID: 22027878 Free PMC article.

3

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. Dement Geriatr Cogn Disord. 2007;23(2):126-32. doi: 10.1159/000097857. Epub 2006 Dec 8. Dement Geriatr Cogn Disord. 2007. PMID: 17159347

4

Examination of tetrahydrobiopterin pathway genes in autism.

Schnetz-Boutaud NC, Anderson BM, Brown KD, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Schnetz-Boutaud NC, et al. Among authors: anderson bm. Genes Brain Behav. 2009 Nov;8(8):753-7. doi: 10.1111/j.1601-183X.2009.00521.x. Epub 2009 Jul 14. Genes Brain Behav. 2009. PMID: 19674121 Free PMC article.

5

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: anderson b. Hum Mutat. 2009 Mar;30(3):463-71. doi: 10.1002/humu.20953. Hum Mutat. 2009. PMID: 19241460 Free PMC article.

6

C3 R102G polymorphism increases risk of age-related macular degeneration.

Spencer KL, Olson LM, Anderson BM, Schnetz-Boutaud N, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Spencer KL, et al. Hum Mol Genet. 2008 Jun 15;17(12):1821-4. doi: 10.1093/hmg/ddn075. Epub 2008 Mar 6. Hum Mol Genet. 2008. PMID: 18325906 Free PMC article.

7

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. 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.

8

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: anderson b. Hum Mutat. 2007 Nov;28(11):1065-73. doi: 10.1002/humu.20567. Hum Mutat. 2007. PMID: 17573676

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. Autism Res. 2008 Dec;1(6):364-9. doi: 10.1002/aur.55. Autism Res. 2008. PMID: 19360691 Free PMC article.

10

Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration.

Canter JA, Olson LM, Spencer K, Schnetz-Boutaud N, Anderson B, Hauser MA, Schmidt S, Postel EA, Agarwal A, Pericak-Vance MA, Sternberg P Jr, Haines JL. Canter JA, et al. Among authors: anderson b. PLoS One. 2008 May 7;3(5):e2091. doi: 10.1371/journal.pone.0002091. PLoS One. 2008. PMID: 18461138 Free PMC article.

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