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Items: 1 to 20 of 24

1.

Targeting Anti-Cancer Active Compounds: Affinity-Based Chromatographic Assays.

de Moraes MC, Cardoso CL, Seidl C, Moaddel R, Cass QB.

Curr Pharm Des. 2016;22(39):5976-5987. Review.

2.

Genetic polymorphisms in the androgen metabolism pathway and risk of prostate cancer in low incidence Malaysian ethnic groups.

Poniah P, Mohamed Z, Apalasamy YD, Mohd Zain S, Kuppusamy S, Razack AH.

Int J Clin Exp Med. 2015 Oct 15;8(10):19232-40. eCollection 2015.

3.

New approaches to establish genetic causality.

McNally EM, George AL Jr.

Trends Cardiovasc Med. 2015 Oct;25(7):646-52. doi: 10.1016/j.tcm.2015.02.013. Epub 2015 Mar 4. Review.

4.

Characterization of schizophrenia adverse drug interactions through a network approach and drug classification.

Sun J, Zhao M, Fanous AH, Zhao Z.

Biomed Res Int. 2013;2013:458989. doi: 10.1155/2013/458989. Epub 2013 Sep 9.

5.

Progress toward personalized medicine for glaucoma.

Moroi SE, Raoof DA, Reed DM, Zöllner S, Qin Z, Richards JE.

Expert Rev Ophthalmol. 2009 Apr;4(2):145-161.

6.

Relevant Networks involving the p53 Signalling Pathway in Renal Cell Carcinoma.

Villaamil VM, Gallego GA, Caínzos IS, Ruvira LV, Valladares-Ayerbes M, Aparicio LM.

Int J Biomed Sci. 2011 Dec;7(4):273-82.

7.

A novel generalized ridge regression method for quantitative genetics.

Shen X, Alam M, Fikse F, Rönnegård L.

Genetics. 2013 Apr;193(4):1255-68. doi: 10.1534/genetics.112.146720. Epub 2013 Jan 18.

8.

Large-scale association analysis identifies new risk loci for coronary artery disease.

CARDIoGRAMplusC4D Consortium, Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D, Erdmann J, Goldstein BA, Stirrups K, König IR, Cazier JB, Johansson A, Hall AS, Lee JY, Willer CJ, Chambers JC, Esko T, Folkersen L, Goel A, Grundberg E, Havulinna AS, Ho WK, Hopewell JC, Eriksson N, Kleber ME, Kristiansson K, Lundmark P, Lyytikäinen LP, Rafelt S, Shungin D, Strawbridge RJ, Thorleifsson G, Tikkanen E, Van Zuydam N, Voight BF, Waite LL, Zhang W, Ziegler A, Absher D, Altshuler D, Balmforth AJ, Barroso I, Braund PS, Burgdorf C, Claudi-Boehm S, Cox D, Dimitriou M, Do R; DIAGRAM Consortium; CARDIOGENICS Consortium, Doney AS, El Mokhtari N, Eriksson P, Fischer K, Fontanillas P, Franco-Cereceda A, Gigante B, Groop L, Gustafsson S, Hager J, Hallmans G, Han BG, Hunt SE, Kang HM, Illig T, Kessler T, Knowles JW, Kolovou G, Kuusisto J, Langenberg C, Langford C, Leander K, Lokki ML, Lundmark A, McCarthy MI, Meisinger C, Melander O, Mihailov E, Maouche S, Morris AD, Müller-Nurasyid M; MuTHER Consortium, Nikus K, Peden JF, Rayner NW, Rasheed A, Rosinger S, Rubin D, Rumpf MP, Schäfer A, Sivananthan M, Song C, Stewart AF, Tan ST, Thorgeirsson G, van der Schoot CE, Wagner PJ; Wellcome Trust Case Control Consortium, Wells GA, Wild PS, Yang TP, Amouyel P, Arveiler D, Basart H, Boehnke M, Boerwinkle E, Brambilla P, Cambien F, Cupples AL, de Faire U, Dehghan A, Diemert P, Epstein SE, Evans A, Ferrario MM, Ferrières J, Gauguier D, Go AS, Goodall AH, Gudnason V, Hazen SL, Holm H, Iribarren C, Jang Y, Kähönen M, Kee F, Kim HS, Klopp N, Koenig W, Kratzer W, Kuulasmaa K, Laakso M, Laaksonen R, Lee JY, Lind L, Ouwehand WH, Parish S, Park JE, Pedersen NL, Peters A, Quertermous T, Rader DJ, Salomaa V, Schadt E, Shah SH, Sinisalo J, Stark K, Stefansson K, Trégouët DA, Virtamo J, Wallentin L, Wareham N, Zimmermann ME, Nieminen MS, Hengstenberg C, Sandhu MS, Pastinen T, Syvänen AC, Hovingh GK, Dedoussis G, Franks PW, Lehtimäki T, Metspalu A, Zalloua PA, Siegbahn A, Schreiber S, Ripatti S, Blankenberg SS, Perola M, Clarke R, Boehm BO, O'Donnell C, Reilly MP, März W, Collins R, Kathiresan S, Hamsten A, Kooner JS, Thorsteinsdottir U, Danesh J, Palmer CN, Roberts R, Watkins H, Schunkert H, Samani NJ.

Nat Genet. 2013 Jan;45(1):25-33. doi: 10.1038/ng.2480. Epub 2012 Dec 2.

9.

Genetics of schizophrenia from a clinicial perspective.

Kukshal P, Thelma BK, Nimgaonkar VL, Deshpande SN.

Int Rev Psychiatry. 2012 Oct;24(5):393-404. doi: 10.3109/09540261.2012.709178. Review.

10.

Next-generation community genetics for low- and middle-income countries.

Kingsmore SF, Lantos JD, Dinwiddie DL, Miller NA, Soden SE, Farrow EG, Saunders CJ.

Genome Med. 2012 Mar 29;4(3):25. doi: 10.1186/gm324. eCollection 2012.

11.

Genetic evidence supporting the association of protease and protease inhibitor genes with inflammatory bowel disease: a systematic review.

Cleynen I, Jüni P, Bekkering GE, Nüesch E, Mendes CT, Schmied S, Wyder S, Kellen E, Villiger PM, Rutgeerts P, Vermeire S, Lottaz D.

PLoS One. 2011;6(9):e24106. doi: 10.1371/journal.pone.0024106. Epub 2011 Sep 8. Review.

12.

Systems genetics for drug target discovery.

Penrod NM, Cowper-Sal-lari R, Moore JH.

Trends Pharmacol Sci. 2011 Oct;32(10):623-30. doi: 10.1016/j.tips.2011.07.002. Epub 2011 Aug 19. Review.

13.

Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines.

Eng L, Ibrahim-zada I, Jarjanazi H, Savas S, Meschian M, Pritchard KI, Ozcelik H.

BMC Med Genomics. 2011 Feb 11;4:18. doi: 10.1186/1755-8794-4-18.

14.

In silico genotyping of the maize nested association mapping population.

Guo B, Beavis WD.

Mol Breed. 2011 Jan;27(1):107-113. Epub 2010 Sep 26.

15.

The impact of phenocopy on the genetic analysis of complex traits.

Lescai F, Franceschi C.

PLoS One. 2010 Jul 29;5(7):e11876. doi: 10.1371/journal.pone.0011876.

16.

Ascertainment biases in SNP chips affect measures of population divergence.

Albrechtsen A, Nielsen FC, Nielsen R.

Mol Biol Evol. 2010 Nov;27(11):2534-47. doi: 10.1093/molbev/msq148. Epub 2010 Jun 17.

17.

Determinants of renal disease variability in ADPKD.

Harris PC, Rossetti S.

Adv Chronic Kidney Dis. 2010 Mar;17(2):131-9. doi: 10.1053/j.ackd.2009.12.004. Review.

18.

Sequence variant on 3q28 and urinary bladder cancer risk: findings from the Los Angeles-Shanghai bladder case-control study.

Stern MC, Van Den Berg D, Yuan JM, Conti DV, Gago-Dominguez M, Pike MC, Xiang YB, Gao YT, Cortessis VK.

Cancer Epidemiol Biomarkers Prev. 2009 Nov;18(11):3057-61. doi: 10.1158/1055-9965.EPI-09-0492. Epub 2009 Oct 20.

19.

Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese population.

Nakano M, Ikeda Y, Taniguchi T, Yagi T, Fuwa M, Omi N, Tokuda Y, Tanaka M, Yoshii K, Kageyama M, Naruse S, Matsuda A, Mori K, Kinoshita S, Tashiro K.

Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12838-42. doi: 10.1073/pnas.0906397106. Epub 2009 Jul 22.

20.

Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases.

Khoury MJ, Bertram L, Boffetta P, Butterworth AS, Chanock SJ, Dolan SM, Fortier I, Garcia-Closas M, Gwinn M, Higgins JP, Janssens AC, Ostell J, Owen RP, Pagon RA, Rebbeck TR, Rothman N, Bernstein JL, Burton PR, Campbell H, Chockalingam A, Furberg H, Little J, O'Brien TR, Seminara D, Vineis P, Winn DM, Yu W, Ioannidis JP.

Am J Epidemiol. 2009 Aug 1;170(3):269-79. doi: 10.1093/aje/kwp119. Epub 2009 Jun 4.

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