Gorlov IP - Search Results

1

Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans.

Walsh KM, Amos CI, Wenzlaff AS, Gorlov IP, Sison JD, Wu X, Spitz MR, Hansen HM, Lu EY, Wei C, Zhang H, Chen W, Lloyd SM, Frazier ML, Bracci PM, Seldin MF, Wrensch MR, Schwartz AG, Wiencke JK. Walsh KM, et al. Among authors: gorlov ip. Oncotarget. 2012 Nov;3(11):1428-38. doi: 10.18632/oncotarget.746. Oncotarget. 2012. PMID: 23232035 Free PMC article.

2

Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancers.

Gorlov IP, Gorlova OY, Frazier ML, Amos CI. Gorlov IP, et al. Am J Hum Genet. 2003 Nov;73(5):1157-61. doi: 10.1086/378819. Epub 2003 Oct 1. Am J Hum Genet. 2003. PMID: 14526391 Free PMC article.

3

Polymorphisms of folate metabolic genes and susceptibility to bladder cancer: a case-control study.

Lin J, Spitz MR, Wang Y, Schabath MB, Gorlov IP, Hernandez LM, Pillow PC, Grossman HB, Wu X. Lin J, et al. Among authors: gorlov ip. Carcinogenesis. 2004 Sep;25(9):1639-47. doi: 10.1093/carcin/bgh175. Epub 2004 Apr 29. Carcinogenesis. 2004. PMID: 15117811

4

Missense mutations in cancer suppressor gene TP53 are colocalized with exonic splicing enhancers (ESEs).

Gorlov IP, Gorlova OY, Frazier ML, Amos CI. Gorlov IP, et al. Mutat Res. 2004 Oct 4;554(1-2):175-83. doi: 10.1016/j.mrfmmm.2004.04.014. Mutat Res. 2004. PMID: 15450416

5

Predicting the oncogenicity of missense mutations reported in the International Agency for Cancer Research (IARC) mutation database on p53.

Gorlov IP, Gorlova OY, Amos CI. Gorlov IP, et al. Hum Mutat. 2005 Nov;26(5):446-54. doi: 10.1002/humu.20242. Hum Mutat. 2005. PMID: 16173033

6

Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genome.

Gorlov IP, Kimmel M, Amos CI. Gorlov IP, et al. Hum Mol Genet. 2006 Apr 1;15(7):1143-50. doi: 10.1093/hmg/ddl029. Epub 2006 Feb 24. Hum Mol Genet. 2006. PMID: 16500998

7

ATM sequence variants associate with susceptibility to non-small cell lung cancer.

Yang H, Spitz MR, Stewart DJ, Lu C, Gorlov IP, Wu X. Yang H, et al. Among authors: gorlov ip. Int J Cancer. 2007 Nov 15;121(10):2254-9. doi: 10.1002/ijc.22918. Int J Cancer. 2007. PMID: 17582598 Free PMC article.

8

Seizure 6-like (SEZ6L) gene and risk for lung cancer.

Gorlov IP, Meyer P, Liloglou T, Myles J, Boettger MB, Cassidy A, Girard L, Minna JD, Fischer R, Duffy S, Spitz MR, Haeussinger K, Kammerer S, Cantor C, Dierkesmann R, Field JK, Amos CI. Gorlov IP, et al. Cancer Res. 2007 Sep 1;67(17):8406-11. doi: 10.1158/0008-5472.CAN-06-4784. Cancer Res. 2007. PMID: 17804757 Free article.

9

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.

Gorlov IP, Gorlova OY, Sunyaev SR, Spitz MR, Amos CI. Gorlov IP, et al. Am J Hum Genet. 2008 Jan;82(1):100-12. doi: 10.1016/j.ajhg.2007.09.006. Am J Hum Genet. 2008. PMID: 18179889 Free PMC article.

10

Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.

Amos CI, Wu X, Broderick P, Gorlov IP, Gu J, Eisen T, Dong Q, Zhang Q, Gu X, Vijayakrishnan J, Sullivan K, Matakidou A, Wang Y, Mills G, Doheny K, Tsai YY, Chen WV, Shete S, Spitz MR, Houlston RS. Amos CI, et al. Among authors: gorlov ip. Nat Genet. 2008 May;40(5):616-22. doi: 10.1038/ng.109. Epub 2008 Apr 2. Nat Genet. 2008. PMID: 18385676 Free PMC article.

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