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Items: 1 to 20 of 21

1.

Germline genetic profiling in prostate cancer: latest developments and potential clinical applications.

Ahmed M, Eeles R.

Future Sci OA. 2015 Dec 18;2(1):FSO87. doi: 10.4155/fso.15.87. eCollection 2016 Mar. Review.

2.

Cloud computing-based TagSNP selection algorithm for human genome data.

Hung CL, Chen WP, Hua GJ, Zheng H, Tsai SJ, Lin YL.

Int J Mol Sci. 2015 Jan 5;16(1):1096-110. doi: 10.3390/ijms16011096.

3.

Variation in human β-defensin genes: new insights from a multi-population study.

Mehlotra RK, Zimmerman PA, Weinberg A, Jurevic RJ.

Int J Immunogenet. 2013 Aug;40(4):261-9. doi: 10.1111/iji.12021. Epub 2012 Nov 29.

4.

Worldwide variation in human drug-metabolism enzyme genes CYP2B6 and UGT2B7: implications for HIV/AIDS treatment.

Li J, Menard V, Benish RL, Jurevic RJ, Guillemette C, Stoneking M, Zimmerman PA, Mehlotra RK.

Pharmacogenomics. 2012 Apr;13(5):555-70. doi: 10.2217/pgs.11.160.

5.

Polymorphisms and a haplotype in heparanase gene associations with the progression and prognosis of gastric cancer in a northern Chinese population.

Li AL, Song YX, Wang ZN, Gao P, Miao Y, Zhu JL, Yue ZY, Xu HM.

PLoS One. 2012;7(1):e30277. doi: 10.1371/journal.pone.0030277. Epub 2012 Jan 20.

6.

Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome.

Yang Q, Li L, Yang R, Shen GQ, Chen Q, Foldvary-Schaefer N, Ondo WG, Wang QK.

Mov Disord. 2011 Feb 15;26(3):516-9. doi: 10.1002/mds.23459. Epub 2011 Jan 24.

7.

Rare BRCA1 haplotypes including 3'UTR SNPs associated with breast cancer risk.

Pelletier C, Speed WC, Paranjape T, Keane K, Blitzblau R, Hollestelle A, Safavi K, van den Ouweland A, Zelterman D, Slack FJ, Kidd KK, Weidhaas JB.

Cell Cycle. 2011 Jan 1;10(1):90-9. Epub 2011 Jan 1.

8.

Linkage disequilibrium reveals different demographic history in egg laying chickens.

Qanbari S, Hansen M, Weigend S, Preisinger R, Simianer H.

BMC Genet. 2010 Nov 15;11:103. doi: 10.1186/1471-2156-11-103.

9.

Genome-wide association studies in cancer--current and future directions.

Chung CC, Magalhaes WC, Gonzalez-Bosquet J, Chanock SJ.

Carcinogenesis. 2010 Jan;31(1):111-20. doi: 10.1093/carcin/bgp273. Epub 2009 Nov 11.

10.

Comparative description of haplotype structure and genetic diversity of MDR1 (ABCB1) in HIV-positive and HIV-negative populations.

Benish RL, Rodriguez B, Zimmerman PA, Mehlotra RK.

Infect Genet Evol. 2010 Jan;10(1):60-7. doi: 10.1016/j.meegid.2009.09.018. Epub 2009 Oct 9.

11.

Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited.

Koshiol J, Hildesheim A, Gonzalez P, Bratti MC, Porras C, Schiffman M, Herrero R, Rodriguez AC, Wacholder S, Yeager M, Chanock SJ, Burk RD, Wang SS.

Cancer Epidemiol Biomarkers Prev. 2009 May;18(5):1631-7. doi: 10.1158/1055-9965.EPI-08-0830.

12.
13.

Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.

Pezzolesi MG, Li Y, Zhou XP, Pilarski R, Shen L, Eng C.

Am J Hum Genet. 2006 Nov;79(5):923-34. Epub 2006 Sep 29.

14.

The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer.

Stredrick DL, Garcia-Closas M, Pineda MA, Bhatti P, Alexander BH, Doody MM, Lissowska J, Peplonska B, Brinton LA, Chanock SJ, Struewing JP, Sigurdson AJ.

Hum Mutat. 2006 Jun;27(6):538-44.

15.

Haplotype diversity in 11 candidate genes across four populations.

Beaty TH, Fallin MD, Hetmanski JB, McIntosh I, Chong SS, Ingersoll R, Sheng X, Chakraborty R, Scott AF.

Genetics. 2005 Sep;171(1):259-67. Epub 2005 Jun 18.

16.

Classification of BRCA1 missense variants of unknown clinical significance.

Phelan CM, Dapic V, Tice B, Favis R, Kwan E, Barany F, Manoukian S, Radice P, van der Luijt RB, van Nesselrooij BP, Chenevix-Trench G, kConFab, Caldes T, de la Hoya M, Lindquist S, Tavtigian SV, Goldgar D, Borg A, Narod SA, Monteiro AN.

J Med Genet. 2005 Feb;42(2):138-46.

17.

Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes.

Long JR, Zhao LJ, Liu PY, Lu Y, Dvornyk V, Shen H, Liu YJ, Zhang YY, Xiong DH, Xiao P, Deng HW.

BMC Genet. 2004 May 24;5:11.

18.

Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11.

Olivier M, Wang X, Cole R, Gau B, Kim J, Rubin EM, Pennacchio LA.

Genomics. 2004 May;83(5):912-23.

19.

Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations.

Crawford DC, Carlson CS, Rieder MJ, Carrington DP, Yi Q, Smith JD, Eberle MA, Kruglyak L, Nickerson DA.

Am J Hum Genet. 2004 Apr;74(4):610-22. Epub 2004 Mar 10.

20.

SNPs in cancer research and treatment.

Erichsen HC, Chanock SJ.

Br J Cancer. 2004 Feb 23;90(4):747-51. Review.

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