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Items: 1 to 20 of 45


An antimicrobial prophylaxis protocol using rectal swab cultures for transrectal prostate biopsy.

Summers SJ, Patel DP, Hamilton BD, Presson AP, Fisher MA, Lowrance WT, Southwick AW.

World J Urol. 2015 Dec;33(12):2001-7. doi: 10.1007/s00345-015-1571-y. Epub 2015 May 3.


Use of a polytetrafluoroethylene (GORE-TEX) bolster to close the renal parenchymal defect during open partial nephrectomy.

Redshaw JD, West JM, Stephenson RA, Lowrance WT, Hamilton BD, Southwick AW, Dechet CB.

Urology. 2014 Sep;84(3):707-11. doi: 10.1016/j.urology.2014.06.004.


A refined palate: bacterial consumption of host glycans in the gut.

Marcobal A, Southwick AM, Earle KA, Sonnenburg JL.

Glycobiology. 2013 Sep;23(9):1038-46. doi: 10.1093/glycob/cwt040. Epub 2013 May 28. Review.


Contemporary practice patterns of endoscopic surgical management for benign prostatic hyperplasia among urologists in the United States.

Lowrance WT, Southwick A, Maschino AC, Sandhu JS.

J Urol. 2013 May;189(5):1811-6. doi: 10.1016/j.juro.2012.11.171. Epub 2012 Dec 3.


Three cases of penile calciphylaxis: diagnosis, treatment strategies, and the role of sodium thiosulfate.

O'Neil B, Southwick AW.

Urology. 2012 Jul;80(1):5-8. doi: 10.1016/j.urology.2012.04.012. No abstract available.


A genome-wide SNP genotyping array reveals patterns of global and repeated species-pair divergence in sticklebacks.

Jones FC, Chan YF, Schmutz J, Grimwood J, Brady SD, Southwick AM, Absher DM, Myers RM, Reimchen TE, Deagle BE, Schluter D, Kingsley DM.

Curr Biol. 2012 Jan 10;22(1):83-90. doi: 10.1016/j.cub.2011.11.045. Epub 2011 Dec 22.


York-Mason procedure for repair of recto-urinary fistulae: a 40-year experience.

Hadley DA, Southwick A, Middleton RG.

BJU Int. 2012 Apr;109(7):1095-8. doi: 10.1111/j.1464-410X.2011.10472.x. Epub 2011 Oct 28.


Association of DRD2 and DRD3 polymorphisms with Parkinson's disease in a multiethnic consortium.

McGuire V, Van Den Eeden SK, Tanner CM, Kamel F, Umbach DM, Marder K, Mayeux R, Ritz B, Ross GW, Petrovitch H, Topol B, Popat RA, Costello S, Manthripragada AD, Southwick A, Myers RM, Nelson LM.

J Neurol Sci. 2011 Aug 15;307(1-2):22-9. doi: 10.1016/j.jns.2011.05.031. Epub 2011 Jun 12.


Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson's disease.

Popat RA, Van Den Eeden SK, Tanner CM, Kamel F, Umbach DM, Marder K, Mayeux R, Ritz B, Ross GW, Petrovitch H, Topol B, McGuire V, Costello S, Manthripragada AD, Southwick A, Myers RM, Nelson LM.

Eur J Neurol. 2011 May;18(5):756-65. doi: 10.1111/j.1468-1331.2011.03353.x. Epub 2011 Jan 31.


Overprescription of postoperative narcotics: a look at postoperative pain medication delivery, consumption and disposal in urological practice.

Bates C, Laciak R, Southwick A, Bishoff J.

J Urol. 2011 Feb;185(2):551-5. doi: 10.1016/j.juro.2010.09.088. Epub 2010 Dec 18.


Characterizing the admixed African ancestry of African Americans.

Zakharia F, Basu A, Absher D, Assimes TL, Go AS, Hlatky MA, Iribarren C, Knowles JW, Li J, Narasimhan B, Sidney S, Southwick A, Myers RM, Quertermous T, Risch N, Tang H.

Genome Biol. 2009;10(12):R141. doi: 10.1186/gb-2009-10-12-r141. Epub 2009 Dec 22.


Peroxisome proliferator-activated receptor gamma polymorphisms and coronary heart disease.

Dallongeville J, Iribarren C, Ferrières J, Lyon L, Evans A, Go AS, Arveiler D, Fortmann SP, Ducimetière P, Hlatky MA, Amouyel P, Southwick A, Quertermous T, Meirhaeghe A.

PPAR Res. 2009;2009:543746. doi: 10.1155/2009/543746. Epub 2009 Dec 1.


Adaptive evolution of pelvic reduction in sticklebacks by recurrent deletion of a Pitx1 enhancer.

Chan YF, Marks ME, Jones FC, Villarreal G Jr, Shapiro MD, Brady SD, Southwick AM, Absher DM, Grimwood J, Schmutz J, Myers RM, Petrov D, Jónsson B, Schluter D, Bell MA, Kingsley DM.

Science. 2010 Jan 15;327(5963):302-5. doi: 10.1126/science.1182213. Epub 2009 Dec 10.


Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.

Scott LJ, Muglia P, Kong XQ, Guan W, Flickinger M, Upmanyu R, Tozzi F, Li JZ, Burmeister M, Absher D, Thompson RC, Francks C, Meng F, Antoniades A, Southwick AM, Schatzberg AF, Bunney WE, Barchas JD, Jones EG, Day R, Matthews K, McGuffin P, Strauss JS, Kennedy JL, Middleton L, Roses AD, Watson SJ, Vincent JB, Myers RM, Farmer AE, Akil H, Burns DK, Boehnke M.

Proc Natl Acad Sci U S A. 2009 May 5;106(18):7501-6. doi: 10.1073/pnas.0813386106. Epub 2009 Apr 28.


Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.

Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, Risch N, Quertermous T.

Hum Mol Genet. 2008 Aug 1;17(15):2320-8. doi: 10.1093/hmg/ddn132. Epub 2008 Apr 28.


Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.

Knowles JW, Assimes TL, Boerwinkle E, Fortmann SP, Go A, Grove ML, Hlatky M, Iribarren C, Li J, Myers R, Risch N, Sidney S, Southwick A, Volcik KA, Quertermous T.

BMC Med Genet. 2008 Apr 2;9:23. doi: 10.1186/1471-2350-9-23.


Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.

Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, Iribarren C, Boerwinkle E, Myers R, Risch N, Quertermous T.

Hum Genet. 2008 May;123(4):399-408. doi: 10.1007/s00439-008-0489-5. Epub 2008 Mar 28.


Worldwide human relationships inferred from genome-wide patterns of variation.

Li JZ, Absher DM, Tang H, Southwick AM, Casto AM, Ramachandran S, Cann HM, Barsh GS, Feldman M, Cavalli-Sforza LL, Myers RM.

Science. 2008 Feb 22;319(5866):1100-4. doi: 10.1126/science.1153717.


Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction.

Knowles JW, Wang H, Itakura H, Southwick A, Myers RM, Iribarren C, Fortmann SP, Go AS, Quertermous T, Hlatky MA.

Am Heart J. 2007 Dec;154(6):1052-8.


Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease.

Hlatky MA, Ashley E, Quertermous T, Boothroyd DB, Ridker P, Southwick A, Myers RM, Iribarren C, Fortmann SP, Go AS; Atherosclerotic Disease, Vascular Function and Genetic Epidemiology (ADVANCE) Study.

Am Heart J. 2007 Dec;154(6):1043-51.

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