Shete SS - Search Results

1

Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk.

Li Y, Xiao X, Li J, Byun J, Cheng C, Bossé Y, McKay J, Albanes D, Lam S, Tardon A, Chen C, Bojesen SE, Landi MT, Johansson M, Risch A, Bickeböller H, Wichmann HE, Christiani DC, Rennert G, Arnold S, Goodman G, Field JK, Davies MPA, Shete SS, Le Marchand L, Melander O, Brunnström H, Liu G, Hung RJ, Andrew AS, Kiemeney LA, Shen H, Sun R, Zienolddiny S, Grankvist K, Johansson M, Caporaso N, Teare DM, Hong YC, Lazarus P, Schabath MB, Aldrich MC, Schwartz AG, Gorlov I, Purrington K, Yang P, Liu Y, Han Y, Bailey-Wilson JE, Pinney SM, Mandal D, Willey JC, Gaba C, Brennan P, Amos CI; INTEGRAL-ILCCO lung cancer consortium. Li Y, et al. Among authors: shete ss. Hum Mol Genet. 2022 Aug 23;31(16):2831-2843. doi: 10.1093/hmg/ddac030. Hum Mol Genet. 2022. PMID: 35138370 Free PMC article.

2

Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients.

Spitz MR, Wu X, Wang Y, Wang LE, Shete S, Amos CI, Guo Z, Lei L, Mohrenweiser H, Wei Q. Spitz MR, et al. Cancer Res. 2001 Feb 15;61(4):1354-7. Cancer Res. 2001. PMID: 11245433

3

Variance components analysis for genetic linkage of time to onset for disease.

Amos CI, Shete S, Gu X. Amos CI, et al. Genet Epidemiol. 2001;21 Suppl 1:S768-73. doi: 10.1002/gepi.2001.21.s1.s768. Genet Epidemiol. 2001. PMID: 11793775

4

Modeling age x major gene interaction by a variance component approach.

Shete SS, Chen J, Zhou X, Amos CI. Shete SS, et al. Genet Epidemiol. 2001;21 Suppl 1:S849-53. doi: 10.1002/gepi.2001.21.s1.s849. Genet Epidemiol. 2001. PMID: 11793791

5

Adaptations of linkage and association methods for the study of asthma, a complex trait.

Bosken CH, Ko YC, Shete S, Wang TN, Chen J, Amos CI, Cheng LS. Bosken CH, et al. Genet Epidemiol. 2001;21 Suppl 1:S89-96. doi: 10.1002/gepi.2001.21.s1.s89. Genet Epidemiol. 2001. PMID: 11793792

6

Individual-specific liability groups in genetic linkage, with applications to kindreds with Li-Fraumeni syndrome.

Shete S, Amos CI, Hwang SJ, Strong LC. Shete S, et al. Am J Hum Genet. 2002 Mar;70(3):813-7. doi: 10.1086/339370. Epub 2002 Jan 30. Am J Hum Genet. 2002. PMID: 11822026 Free PMC article.

7

Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting.

Shete S, Amos CI. Shete S, et al. Am J Hum Genet. 2002 Mar;70(3):751-7. doi: 10.1086/338931. Epub 2002 Feb 8. Am J Hum Genet. 2002. PMID: 11836650 Free PMC article.

8

Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes.

Qiao Y, Spitz MR, Shen H, Guo Z, Shete S, Hedayati M, Grossman L, Mohrenweiser H, Wei Q. Qiao Y, et al. Carcinogenesis. 2002 Feb;23(2):295-9. doi: 10.1093/carcin/23.2.295. Carcinogenesis. 2002. PMID: 11872635

9

p53 Genotypes and Haplotypes Associated With Lung Cancer Susceptibility and Ethnicity.

Wu X, Zhao H, Amos CI, Shete S, Makan N, Hong WK, Kadlubar FF, Spitz MR. Wu X, et al. J Natl Cancer Inst. 2002 May 1;94(9):681-90. doi: 10.1093/jnci/94.9.681. J Natl Cancer Inst. 2002. PMID: 11983757

10

Improving the power of sib pair quantitative trait loci detection by phenotype winsorization.

Fernández JR, Etzel C, Beasley TM, Shete S, Amos CI, Allison DB. Fernández JR, et al. Hum Hered. 2002;53(2):59-67. doi: 10.1159/000057984. Hum Hered. 2002. PMID: 12037405

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