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Items: 1 to 20 of 30

1.

Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds.

Schaefer RJ, Schubert M, Bailey E, Bannasch DL, Barrey E, Bar-Gal GK, Brem G, Brooks SA, Distl O, Fries R, Finno CJ, Gerber V, Haase B, Jagannathan V, Kalbfleisch T, Leeb T, Lindgren G, Lopes MS, Mach N, da Câmara Machado A, MacLeod JN, McCoy A, Metzger J, Penedo C, Polani S, Rieder S, Tammen I, Tetens J, Thaller G, Verini-Supplizi A, Wade CM, Wallner B, Orlando L, Mickelson JR, McCue ME.

BMC Genomics. 2017 Jul 27;18(1):565. doi: 10.1186/s12864-017-3943-8.

2.

Maternal and child cytokine relationship in early life is not altered by cytokine gene polymorphisms.

Djuardi Y, Supali T, Wibowo H, Heijmans BT, Deelen J, Slagboom EP, Houwing-Duistermaat JJ, Sartono E, Yazdanbakhsh M.

Genes Immun. 2016 Dec;17(7):380-385. doi: 10.1038/gene.2016.35. Epub 2016 Sep 1.

3.

Influence of ATP-binding cassette polymorphisms on neurological outcome after traumatic brain injury.

Cousar JL, Conley YP, Willyerd FA, Sarnaik AA, Puccio AM, Empey PE, Kochanek PM, Bell MJ, Okonkwo DO, Clark RS.

Neurocrit Care. 2013 Oct;19(2):192-8. doi: 10.1007/s12028-013-9881-7.

4.

Impact of genetic polymorphisms of SLC2A2, SLC2A5, and KHK on metabolic phenotypes in hypertensive individuals.

Le MT, Lobmeyer MT, Campbell M, Cheng J, Wang Z, Turner ST, Chapman AB, Boerwinkle E, Gums JG, Gong Y, Johnson RJ, Johnson JA.

PLoS One. 2013;8(1):e52062. doi: 10.1371/journal.pone.0052062. Epub 2013 Jan 14.

5.

Prevalence and prognostic effect of sarcopenia in breast cancer survivors: the HEAL Study.

Villaseñor A, Ballard-Barbash R, Baumgartner K, Baumgartner R, Bernstein L, McTiernan A, Neuhouser ML.

J Cancer Surviv. 2012 Dec;6(4):398-406. doi: 10.1007/s11764-012-0234-x. Epub 2012 Oct 4.

6.

California Very Preterm Birth Study: design and characteristics of the population- and biospecimen bank-based nested case-control study.

Kharrazi M, Pearl M, Yang J, DeLorenze GN, Bean CJ, Callaghan WM, Grant A, Lackritz E, Romero R, Satten GA, Simhan H, Torres AR, Westover JB, Yolken R, Williamson DM.

Paediatr Perinat Epidemiol. 2012 May;26(3):250-63. doi: 10.1111/j.1365-3016.2011.01252.x. Epub 2012 Jan 31.

7.

Effects of genetic variation in H3K79 methylation regulatory genes on clinical blood pressure and blood pressure response to hydrochlorothiazide.

Duarte JD, Zineh I, Burkley B, Gong Y, Langaee TY, Turner ST, Chapman AB, Boerwinkle E, Gums JG, Cooper-Dehoff RM, Beitelshees AL, Bailey KR, Fillingim RB, Kone BC, Johnson JA.

J Transl Med. 2012 Mar 22;10:56. doi: 10.1186/1479-5876-10-56.

8.

Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine.

Arav-Boger R, Wojcik GL, Duggal P, Ingersoll RG, Beaty T, Pass RF, Yolken RH.

BMC Res Notes. 2012 Mar 13;5:140. doi: 10.1186/1756-0500-5-140.

9.

Genetic polymorphisms in carnitine palmitoyltransferase 1A gene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos.

Lemas DJ, Wiener HW, O'Brien DM, Hopkins S, Stanhope KL, Havel PJ, Allison DB, Fernandez JR, Tiwari HK, Boyer BB.

J Lipid Res. 2012 Jan;53(1):175-84. doi: 10.1194/jlr.P018952. Epub 2011 Nov 1.

10.

Case-control study of vitamin D, dickkopf homolog 1 (DKK1) gene methylation, VDR gene polymorphism and the risk of colon adenoma in African Americans.

Ashktorab H, Nguza B, Fatemi M, Nouraie M, Smoot DT, Schäffer AA, Kupfer SS, Camargo CA Jr, Brim H.

PLoS One. 2011;6(10):e25314. doi: 10.1371/journal.pone.0025314. Epub 2011 Oct 13.

11.

Downregulated kynurenine 3-monooxygenase gene expression and enzyme activity in schizophrenia and genetic association with schizophrenia endophenotypes.

Wonodi I, Stine OC, Sathyasaikumar KV, Roberts RC, Mitchell BD, Hong LE, Kajii Y, Thaker GK, Schwarcz R.

Arch Gen Psychiatry. 2011 Jul;68(7):665-74. doi: 10.1001/archgenpsychiatry.2011.71.

12.

Serotonin transporter gene polymorphisms and brain function during emotional distraction from cognitive processing in posttraumatic stress disorder.

Morey RA, Hariri AR, Gold AL, Hauser MA, Munger HJ, Dolcos F, McCarthy G.

BMC Psychiatry. 2011 May 5;11:76. doi: 10.1186/1471-244X-11-76.

13.

SNPPicker: high quality tag SNP selection across multiple populations.

Sicotte H, Rider DN, Poland GA, Dhiman N, Kocher JP.

BMC Bioinformatics. 2011 May 2;12:129. doi: 10.1186/1471-2105-12-129.

14.

VKORC1 common variation and bone mineral density in the Third National Health and Nutrition Examination Survey.

Crawford DC, Brown-Gentry K, Rieder MJ.

PLoS One. 2010 Dec 13;5(12):e15088. doi: 10.1371/journal.pone.0015088.

15.

Tight junction defects in patients with atopic dermatitis.

De Benedetto A, Rafaels NM, McGirt LY, Ivanov AI, Georas SN, Cheadle C, Berger AE, Zhang K, Vidyasagar S, Yoshida T, Boguniewicz M, Hata T, Schneider LC, Hanifin JM, Gallo RL, Novak N, Weidinger S, Beaty TH, Leung DY, Barnes KC, Beck LA.

J Allergy Clin Immunol. 2011 Mar;127(3):773-86.e1-7. doi: 10.1016/j.jaci.2010.10.018. Epub 2010 Dec 15.

16.

Combined influence of LDLR and HMGCR sequence variation on lipid-lowering response to simvastatin.

Mangravite LM, Medina MW, Cui J, Pressman S, Smith JD, Rieder MJ, Guo X, Nickerson DA, Rotter JI, Krauss RM.

Arterioscler Thromb Vasc Biol. 2010 Jul;30(7):1485-92. doi: 10.1161/ATVBAHA.110.203273. Epub 2010 Apr 22.

17.

FastTagger: an efficient algorithm for genome-wide tag SNP selection using multi-marker linkage disequilibrium.

Liu G, Wang Y, Wong L.

BMC Bioinformatics. 2010 Jan 29;11:66. doi: 10.1186/1471-2105-11-66.

18.

Efficient genome-wide TagSNP selection across populations via the linkage disequilibrium criterion.

Liu L, Wu Y, Lonardi S, Jiang T.

J Comput Biol. 2010 Jan;17(1):21-37. doi: 10.1089/cmb.2007.0228.

19.

Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome.

Heike CL, Starr JR, Rieder MJ, Cunningham ML, Edwards KL, Stanaway IB, Crawford DC.

Birth Defects Res A Clin Mol Teratol. 2010 Jan;88(1):54-63. doi: 10.1002/bdra.20604.

20.

The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study.

Franceschini N, North KE, Arnett D, Pankow JS, Chung JH, Baird L, Leppert MF, Eckfeldt JH, Boerwinkle E, Gu CC, Lewis CE, Myers RH, Turner ST, Weder A, Kao WH, Mosley TH, Chakravarti A, Kramer H, Zhang J, Hunt SC.

Am J Hypertens. 2009 May;22(5):552-8. doi: 10.1038/ajh.2009.41. Epub 2009 Mar 5.

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