Gorlov IP - Search Results

1

Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans.

Walsh KM, Gorlov IP, Hansen HM, Wu X, Spitz MR, Zhang H, Lu EY, Wenzlaff AS, Sison JD, Wei C, Lloyd SM, Chen W, Frazier ML, Seldin MF, Bierut LJ, Bracci PM, Wrensch MR, Schwartz AG, Wiencke JK, Amos CI. Walsh KM, et al. Among authors: gorlov ip. Cancer Epidemiol Biomarkers Prev. 2013 Feb;22(2):251-60. doi: 10.1158/1055-9965.EPI-12-1007-T. Epub 2012 Dec 5. Cancer Epidemiol Biomarkers Prev. 2013. PMID: 23221128 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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