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132 results

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Page 1
Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes.
McCarthy JJ, Parker A, Salem R, Moliterno DJ, Wang Q, Plow EF, Rao S, Shen G, Rogers WJ, Newby LK, Cannata R, Glatt K, Topol EJ; GeneQuest Investigators. McCarthy JJ, et al. J Med Genet. 2004 May;41(5):334-41. doi: 10.1136/jmg.2003.016584. J Med Genet. 2004. PMID: 15121769 Free PMC article.
Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism.
Rao F, Wessel J, Wen G, Zhang L, Rana BK, Kennedy BP, Greenwood TA, Salem RM, Chen Y, Khandrika S, Hamilton BA, Smith DW, Holstein-Rathlou NH, Ziegler MG, Schork NJ, O'Connor DT. Rao F, et al. Among authors: salem rm. Hypertension. 2007 May;49(5):1015-31. doi: 10.1161/HYPERTENSIONAHA.106.081679. Epub 2007 Mar 12. Hypertension. 2007. PMID: 17353515
Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension.
Rao F, Wen G, Gayen JR, Das M, Vaingankar SM, Rana BK, Mahata M, Kennedy BP, Salem RM, Stridsberg M, Abel K, Smith DW, Eskin E, Schork NJ, Hamilton BA, Ziegler MG, Mahata SK, O'Connor DT. Rao F, et al. Among authors: salem rm. Circulation. 2007 May 1;115(17):2271-81. doi: 10.1161/CIRCULATIONAHA.106.628859. Epub 2007 Apr 16. Circulation. 2007. PMID: 17438154
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo.
Rao F, Zhang L, Wessel J, Zhang K, Wen G, Kennedy BP, Rana BK, Das M, Rodriguez-Flores JL, Smith DW, Cadman PE, Salem RM, Mahata SK, Schork NJ, Taupenot L, Ziegler MG, O'Connor DT. Rao F, et al. Among authors: salem rm. Circulation. 2007 Aug 28;116(9):993-1006. doi: 10.1161/CIRCULATIONAHA.106.682302. Epub 2007 Aug 13. Circulation. 2007. PMID: 17698732
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk.
Zhang L, Rao F, Zhang K, Khandrika S, Das M, Vaingankar SM, Bao X, Rana BK, Smith DW, Wessel J, Salem RM, Rodriguez-Flores JL, Mahata SK, Schork NJ, Ziegler MG, O'Connor DT. Zhang L, et al. Among authors: salem rm. J Clin Invest. 2007 Sep;117(9):2658-71. doi: 10.1172/JCI31093. J Clin Invest. 2007. PMID: 17717598 Free PMC article.
Angiotensin-converting enzyme gene polymorphism predicts the time-course of blood pressure response to angiotensin converting enzyme inhibition in the AASK trial.
Bhatnagar V, O'Connor DT, Schork NJ, Salem RM, Nievergelt CM, Rana BK, Smith DW, Bakris GL, Middleton JP, Norris KC, Wright JT, Cheek D, Hiremath L, Contreras G, Appel LJ, Lipkowitz MS. Bhatnagar V, et al. Among authors: salem rm. J Hypertens. 2007 Oct;25(10):2082-92. doi: 10.1097/HJH.0b013e3282b9720e. J Hypertens. 2007. PMID: 17885551 Free PMC article. Clinical Trial.
Chromogranin A polymorphisms are associated with hypertensive renal disease.
Salem RM, Cadman PE, Chen Y, Rao F, Wen G, Hamilton BA, Rana BK, Smith DW, Stridsberg M, Ward HJ, Mahata M, Mahata SK, Bowden DW, Hicks PJ, Freedman BI, Schork NJ, O'Connor DT. Salem RM, et al. J Am Soc Nephrol. 2008 Mar;19(3):600-14. doi: 10.1681/ASN.2007070754. Epub 2008 Jan 30. J Am Soc Nephrol. 2008. PMID: 18235090 Free PMC article.
132 results