2012

van der Harst, P. et al. (2012) Seventy-five genetic loci influencing the human red blood cell. Nature, 492 (7429). pp. 369-375. ISSN 0028-0836 (doi:10.1038/nature11677)

Sanna-Cherchi, S. et al. (2012) Copy-number disorders are a common cause of congenital kidney malformations. American Journal of Human Genetics, 91 (6). pp. 987-997. ISSN 0002-9297 (doi:10.1016/j.ajhg.2012.10.007)

Lyons, P.A. et al. (2012) Genetically distinct subsets within ANCA-associated vasculitis. New England Journal of Medicine, 367 (3). pp. 214-223. ISSN 0028-4793 (doi:10.1056/NEJMoa1108735)

Saxena, R. et al. (2012) Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American Journal of Human Genetics, 90 (3). pp. 410-425. ISSN 0002-9297 (doi:10.1016/j.ajhg.2011.12.022)

Delles, C., and Padmanabhan, S. (2012) Genetics and hypertension: is it time to change my practice? Canadian Journal of Cardiology, 28 (3). pp. 296-304. ISSN 0828-282X (doi:10.1016/j.cjca.2012.02.004)

Jeemon, P. et al. (2012) Impact of comprehensive cardiovascular risk reduction programme on risk factor clustering associated with elevated blood pressure in an Indian industrial population. Indian Journal of Medical Research, 135 (4). pp. 485-493. ISSN 0971-5916

Padmanabhan, S., Newton-Cheh, C., and Dominiczak, A.F. (2012) Genetic basis of blood pressure and hypertension. Trends in Genetics, 28 (8). pp. 397-408. ISSN 0168-9525 (doi:10.1016/j.tig.2012.04.001)

Salvi, E. et al. (2012) Genomewide Association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase. Hypertension, 59 (2). pp. 248-255. ISSN 0194-911X (doi:10.1161/HYPERTENSIONAHA.111.181990)

2011

Johnson, T. et al. (2011) Blood pressure loci identified with a gene-centric array. American Journal of Human Genetics, 89 (6). pp. 688-700. ISSN 0002-9297 (doi:10.1016/j.ajhg.2011.10.013)

Freathy, R.M. et al. (2011) Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index. International Journal of Epidemiology, 40 (6). pp. 1617-28. ISSN 0300-5771

Lanktree, Matthew B et al. (2011) Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics, 88 (1). pp. 6-18. ISSN 0002-9297 (doi:10.1016/j.ajhg.2010.11.007 )

Grassi, G. et al. (2011) Association between ADRA1A gene and the metabolic syndrome: candidate genes and functional counterpart in the PAMELA population. Journal of Hypertension, 29 (6). pp. 1121-1127777777777. ISSN 0263-6352 (doi:10.1097/HJH.0b013e328346d72c)

Menni, C. et al. (2011) Evaluation of How Gene-Job Strain Interaction Affects Blood Pressure in the PAMELA Study. Psychosomatic Medicine, 73 (4). pp. 304-309. ISSN 0033-3174 (doi:10.1097/PSY.0b013e318212e0be)

Shah, S. et al. (2011) Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy. Circulation: Cardiovascular Genetics, 4 (6). pp. 626-635. ISSN 1942-325X (doi:10.1161/CIRCGENETICS.111.960203)

Stanescu, H.C. et al. (2011) Risk HLA-DQA1 and PLA2R1 alleles in idiopathic membranous nephropathy. New England Journal of Medicine, 364 (7). pp. 616-626. ISSN 0028-4793 (doi:10.1056/NEJMoa1009742)

2010

Delles, C., McBride, M.W., Graham, D., Padmanabhan, S., and Dominiczak, A.F. (2010) Genetics of hypertension: from experimental animals to humans. Biochimica et Biophysica Acta - Molecular Basis of Disease, 1802 (12). pp. 1299-1308. ISSN 0925-4439 (doi:10.1016/j.bbadis.2009.12.006)

Feehally, J. et al. (2010) HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis. Journal of the American Society of Nephrology, 21 (10). pp. 1791-1797. ISSN 1046-6673 (doi:10.1681/ASN.2010010076)

Hastie, C. et al. (2010) Obesity paradox in a cohort of 4880 consecutive patients undergoing percutaneous coronary intervention. European Heart Journal, 31 (2). pp. 222-226. ISSN 0195-668X (doi:10.1093/eurheartj/ehp317)

Lang, C.C., Gupta, S., Kalra, P., Keavney, B., Menown, I., Morley, C., and Padmanabhan, S. (2010) Elevated heart rate and cardiovascular outcomes in patients with coronary artery disease: Clinical evidence and pathophysiological mechanisms. Atherosclerosis, 212 (1). pp. 1-8. ISSN 0021-9150 (doi:10.1016/j.atherosclerosis.2010.01.029)

Padmanabhan, S. (2010) Antihypertensive pharmacogenetics: missed opportunity. Journal of Hypertension, 28 (10). pp. 2007-2009. ISSN 0263-6352 (doi:10.1097/HJH.0b013e32833f2f56)

Padmanabhan, S., Hastie, C., Prabhakaran, D., and Dominiczak, A.F. (2010) Genomic approaches to coronary artery disease. Indian Journal of Medical Research, 132 (5). pp. 567-78. ISSN 0971-5916

Padmanabhan, S. et al. (2010) Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. PLoS Genetics, 6 (10). e1001177. ISSN 1553-7390 (doi:10.1371/journal.pgen.1001177)

Padmanabhan, S. et al. (2010) The effects of sex and method of blood pressure measurement on genetic associations with blood pressure in the PAMELA study. Journal of Hypertension, 28 (3). pp. 465-477. ISSN 0263-6352 (doi:10.1097/HJH.0b013e32833594d7)

Paul, L., Hastie, C.E., Li, W., Harrow, C., Muir, S., Connell, J.M.C., Dominiczak, A.F., McInnes, G.T., and Padmanabhan, S. (2010) Resting Heart Rate Pattern During Follow-Up and Mortality in Hypertensive Patients. Hypertension, 55 (2). pp. 567-574. ISSN 0194-911X (doi:10.1161/HYPERTENSIONAHA.109.144808)

Sotoodehnia, N. et al. (2010) Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nature Genetics, 42 (12). pp. 1068-1076. ISSN 1061-4036 (doi:10.1038/ng.716)

Timpson, N. J. et al. (2010) Genetic variation at the SLC23A1 locus is associated with circulating concentrations of L-ascorbic acid (vitamin C): evidence from 5 independent studies with >15,000 participants. American Journal of Clinical Nutrition, 92 (2). pp. 375-382. ISSN 0002-9165 (doi:10.3945/ajcn.2010.29438)

2009

Talmud, PJ et al. (2009) Gene-centric association signals for lipids and apolipoproteins identified via the humanCVD BeadChip. American Journal of Human Genetics, 85 (5). pp. 628-642. ISSN 0002-9297 (doi:10.1016/j.ajhg.2009.10.014)

Alvarez-Madrazo, S. et al. (2009) Familial and Phenotypic Associations of the Aldosterone Renin Ratio. Journal of Clinical Endocrinology and Metabolism, 94 (11). pp. 4324-4333. ISSN 0021-972X

Dominiczak, A. F., Delles, C, and Padmanabhan, S (2009) Are isolated populations better for studying genes that predispose to hypertension? Journal of Hypertension, 27 (5). pp. 939-940.

Padmanabhan, S (2009) Genetic causation: the end of parsimony? Journal of Hypertension, 27 (8). pp. 1521-1523.

Padmanabhan, S, Menni, C, Prabhakaran, D, and Dominiczak, AF (2009) Discovering the genetic determinants of complex diseases. Current Science, 97 (3). pp. 385-391.

Stewart, L., McInnes, G.T., Murray, L., Sloan, B., Walters, M., Morton, R., Padmanabhan, S., Reid, J.L., and Morrison, D.S. (2009) Risks of socioeconomic deprivation on mortality in hypertensive patients. Journal of Hypertension, 27 (4). pp. 730-735. ISSN 0263-6352 (doi:10.1097/HJH.0b013e328324ed58)

2008

Delles, C., McBride, M.W., Padmanabhan, S., and Dominiczak, A.F. (2008) The genetics of cardiovascular disease. Trends in Endocrinology and Metabolism, 19 (9). pp. 309-316. ISSN 1043-2760 (doi:10.1016/j.tem.2008.07.010 )

Delles, C et al. (2008) Glutathione S-transferase variants and hypertension. Journal of Hypertension, 26 (7). pp. 1343-1352. ISSN 0263-6352 (doi:10.1097/HJH.0b013e3282fe1d67)

Hastie, C, Padmanabhan, S, Slack, R, Dominiczak, AF, and Pell, J (2008) Factors that predict survival following Percutaneous coronary intervention in patients with and without hypertension. Journal of Hypertension, 26 . S113-S113. ISSN 0263-6352

Hastie, C, Padmanabhan, S, Slack, R, Isles, C, and Pell, J (2008) A study of the 'obesity paradox' across the spectrum of cardiovascular risk. Journal of Human Hypertension, 22 (10). pp. 717-718. ISSN 0950-9240

Padmanabhan, S, Melander, O, Hastie, C, Menni, C, Delles, C, Connell, J, and Dominiczak, AF (2008) Hypertension and genome-wide association studies: combining high fidelity phenotyping and hypercontrols. Journal of Hypertension, 26 (7). pp. 1275-1281.

Padmanabhan, S, Menni, C, Lee, WK, Brambilla, P, Laing, S, Sega, R, Cesana, G, Mancia, G, and Dominiczak, AF (2008) Cardiovascular gene centric association study of metabolic syndrome and ambulatory blood pressure in the PAMELA study. Journal of Hypertension, 26 . S18-S18.

2007

Tomaszewski, M, Charchar, FJ, Lynch, MD, Padmanabhan, S, Wang, WY, Miller, WH, Grzeszczak, W, Maric, C, Zukowska-Szczechowska, E, and Dominiczak, AF (2007) Fibroblast growth factor 1 gene and hypertension: from the quantitative trait locus to positional analysis. Circulation, 116 (17). pp. 1915-1924.

Tomaszewski, M, Charchar, FJ, Lynch, MD, Padmanabhan, S, Wang, WYS, Miller, WH, Grzeszczak, W, Maric, C, Zukowska-Szczechowska, E, and Dominiczak, AF (2007) Fibroblast growth factor 1 gene and hypertension - From the quantitative trait locus to positional analysis. Circulation, 116 . pp. 1915-1924. (doi:10.1161/CIRCULATIONAHA.107.710293)

2006

Padmanabhan, S et al. (2006) Chromosome 2p shows significant linkage to antihypertensive response in the British genetics of hypertension study. Hypertension, 47 . pp. 603-608. (doi:10.1161/01.HYP.0000197947.62601.9d)

2005

Whiteley, L., Padmanabhan, S., Hole, D., and Isles, C. (2005) Should diabetes be considered a coronary heart disease risk equivalent?: results from 25 years of follow-up in the Renfrew and Paisley survey. Diabetes Care, 28 (7). pp. 1588-1593. ISSN 0149-5992

Hole, D, Isles, C, Padmanabhan, S, and Whiteley, L (2005) Should diabetes be considered a coronary heart disease risk equivalent? Results from 25 years of follow-up in the Renfrew and Paisley Survey. Diabetes Care, 28 . pp. 1588-1593.

2004

Charchar, F., Padmanabhan, S., Anderson, N.H., Tomaszewski, M., Upton, M.N., McConnachie, A., Connell, J.M., Watt, G.C.M., Dominiczak, A.F., and Charchar, F.J. (2004) Y chromsome variant is a predictor of cardiovascular mortality. Journal of Hypertension - Supplement, 22 (S1). S58-S59. ISSN 0952-1178

Padmanabhan, S., Connell, J.M.C., Dominiczak, A.F., Inglis, G., Macfarlane, P.W., and Watt, G. (2004) Heritability and genetic determinants of electrocardiographic measures of left ventricular mass - a two generation family study. Journal of Hypertension - Supplement, 22 (S1). S180-S181. ISSN 0952-1178

2003

Charchar, FJ, Dominiczak, A.F., Grzeszczak, W, Padmanabhan, S, Tomaszewski, M, and Zukowska-Szczechowska, E (2003) Cardiovascular diseases and G-protein beta 3 subunit gene (GNB3) in the era of genomewide scans. Journal of Human Hypertension, 17 (6). pp. 379-380.

Swan, L, Birnie, DH, Padmanabhan, S, Inglis, G, Connell, JMC, and Hillis, WS (2003) The genetic determination of left ventricular mass in healthy adults. European Heart Journal, 24 . 579-U9. (doi:10.1016/S0195-668X(02)00524-9)

2002

Charchar, F.J. et al. (2002) The Y chromosome effect on blood pressure in two European populations. Hypertension, 39 . pp. 353-356. ISSN 0194-911X

Stanton, T., Inglis, G.C., Padmanabhan, S., Dominiczak, A.F., Jardine, A.G., and Connell, J.M. (2002) Variation at the beta-1 adrenoceptor gene locus affects left ventricular mass in renal failure. Journal of Nephrology, 15 (5). pp. 512-518.