Augusto Rendon
Augusto Rendon
Department of Haematology, University of Cambridge
Verified email at - Homepage
Cited by
Cited by
Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies
N Sarwar, AS Butterworth, DF Freitag, J Gregson, P Willeit, DN Gorman, ...
The Lancet 379 (9822), 1205-1213, 2012
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
N Soranzo, TD Spector, M Mangino, B Kühnel, A Rendon, A Teumer, ...
Nature genetics 41 (11), 1182-1190, 2009
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
SI Berndt, S Gustafsson, R Mägi, A Ganna, E Wheeler, MF Feitosa, ...
Nature genetics 45 (5), 501-512, 2013
The distribution of the anticancer drug Doxorubicin in relation to blood vessels in solid tumors
AJ Primeau, A Rendon, D Hedley, L Lilge, IF Tannock
Clinical Cancer Research 11 (24), 8782-8788, 2005
New gene functions in megakaryopoiesis and platelet formation
C Gieger, A Radhakrishnan, A Cvejic, W Tang, E Porcu, G Pistis, ...
Nature 480 (7376), 201-208, 2011
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
SK Ganesh, NA Zakai, FJA Van Rooij, N Soranzo, AV Smith, MA Nalls, ...
Nature genetics 41 (11), 1191-1198, 2009
Seventy-five genetic loci influencing the human red blood cell
P Van Der Harst, W Zhang, IM Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369-375, 2012
Genetic drivers of epigenetic and transcriptional variation in human immune cells
L Chen, B Ge, FP Casale, L Vasquez, T Kwan, D Garrido-Martín, S Watt, ...
Cell 167 (5), 1398-1414. e24, 2016
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
CA Albers, A Cvejic, R Favier, EE Bouwmans, MC Alessi, P Bertone, ...
Nature genetics 43 (8), 735-737, 2011
A HaemAtlas: characterizing gene expression in differentiated human blood cells
NA Watkins, A Gusnanto, B De Bono, S De, D Miranda-Saavedra, ...
Blood 113 (19), e1-e9, 2009
Transcriptional diversity during lineage commitment of human blood progenitors
L Chen, M Kostadima, JHA Martens, G Canu, SP Garcia, E Turro, ...
Science 345 (6204), 2014
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
C Turnbull, RH Scott, E Thomas, L Jones, N Murugaesu, FB Pretty, ...
Bmj 361, 2018
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
I Simeoni, JC Stephens, F Hu, SVV Deevi, K Megy, TK Bariana, ...
Blood, The Journal of the American Society of Hematology 127 (23), 2791-2803, 2016
A novel variant on chromosome 7q22. 3 associated with mean platelet volume, counts, and function
N Soranzo, A Rendon, C Gieger, CI Jones, NA Watkins, S Menzel, ...
Blood, The Journal of the American Society of Hematology 113 (16), 3831-3837, 2009
Multiple loci are associated with white blood cell phenotypes
MA Nalls, DJ Couper, T Tanaka, FJA Van Rooij, MH Chen, AV Smith, ...
PLoS Genet 7 (6), e1002113, 2011
Genetic evidence of assortative mating in humans
MR Robinson, A Kleinman, M Graff, AAE Vinkhuyzen, D Couper, ...
Nature Human Behaviour 1 (1), 1-13, 2017
Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans
M Rotival, T Zeller, PS Wild, S Maouche, S Szymczak, A Schillert, ...
PLoS Genet 7 (12), e1002367, 2011
Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders
SK Westbury, E Turro, D Greene, C Lentaigne, AM Kelly, TK Bariana, ...
Genome medicine 7 (1), 1-15, 2015
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis
B Benyamin, T Esko, JS Ried, A Radhakrishnan, SH Vermeulen, ...
Nature communications 5 (1), 1-11, 2014
SMIM1 underlies the Vel blood group and influences red blood cell traits
A Cvejic, L Haer-Wigman, JC Stephens, M Kostadima, PA Smethurst, ...
Nature genetics 45 (5), 542-545, 2013
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