Artikelen met mandaten voor openbare toegang - Augusto RendonMeer informatie
TotaalMRCNIHRWellcomeNIHBHFCancer Research UKEuropean CommissionDFGCIHRNHMRCGovernment of SpainFWOSNSFBBSRCCSOESRCFWFGenome CanadaEMBLINSERMSwedish Research CouncilEPSRCParkinson's UKHealth Data Research, UKARCNWOVersus Arthritis, UKANRDHFGovernment of ItalyUK Research & InnovationBrain Research, UKDOEVAHHMIFRQSNSERCHelmholtzBanking Foundation "la Caixa"Academy of FinlandHEAHRBSFITelethonAlzheimers's UKDiabetes UKDMTMotor Neurone Disease Association, UKZonMwState of CalifoniaBMBFSCLNKFICZI
Nergens beschikbaar: 3
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
Mandaten: UK Medical Research Council
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
LR Claus, C Chen, J Stallworth, JL Turner, GG Slaats, AL Hawks, ...
Kidney International 104 (5), 995-1007, 2023
Mandaten: Swiss National Science Foundation, Nederlandse Organisatie voor …
Developing Conformal Therapy Treatment Planning for Photodynamic Therapy
L Lilge, A Rendon
Biomedical Optics, BWB1, 2008
Mandaten: Canadian Institutes of Health Research
Ergens beschikbaar: 84
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
Mandaten: US National Institutes of Health, British Heart Foundation, Dunhill Medical …
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
Mandaten: US National Institutes of Health, Health Research Board, Ireland, UK Medical …
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
Mandaten: Swiss National Science Foundation, US National Institutes of Health …
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
Mandaten: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
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
Mandaten: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandaten: US National Institutes of Health, Austrian Science Fund, British Heart …
Whole-genome sequencing of patients with rare diseases in a national health system
E Turro, WJ Astle, K Megy, S Gräf, D Greene, O Shamardina, HL Allen, ...
Nature 583 (7814), 96-102, 2020
Mandaten: European Molecular Biology Laboratory, British Heart Foundation, Cancer …
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report
100,000 Genomes Project Pilot Investigators
New England Journal of Medicine 385 (20), 1868-1880, 2021
Mandaten: US National Institutes of Health, Versus Arthritis, UK, Cancer Research UK …
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
Mandaten: US National Institutes of Health
PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels
AR Martin, E Williams, RE Foulger, S Leigh, LC Daugherty, O Niblock, ...
Nature genetics 51 (11), 1560-1565, 2019
Mandaten: British Heart Foundation, UK Medical Research Council, National Institute …
Seventy-five genetic loci influencing the human red blood cell
P Van Der Harst, W Zhang, I Mateo Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369-375, 2012
Mandaten: US National Institutes of Health, Austrian Science Fund, British Heart …
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
Mandaten: British Heart Foundation
Genetic evidence of assortative mating in humans
MR Robinson, A Kleinman, M Graff, AAE Vinkhuyzen, D Couper, ...
Nature Human Behaviour 1 (1), 0016, 2017
Mandaten: US National Institutes of Health, Australian Research Council, National …
Transcriptional diversity during lineage commitment of human blood progenitors
L Chen, M Kostadima, JHA Martens, G Canu, SP Garcia, E Turro, ...
Science 345 (6204), 1251033, 2014
Mandaten: Fonds Wetenschappelijk Onderzoek (Vlaanderen), British Heart Foundation …
Lawson criterion for ignition exceeded in an inertial fusion experiment
H Abu-Shawareb, R Acree, P Adams, J Adams, B Addis, R Aden, P Adrian, ...
Physical review letters 129 (7), 075001, 2022
Mandaten: US Department of Energy, UK Engineering and Physical Sciences Research Council
A HaemAtlas: characterizing gene expression in differentiated human blood cells
NA Watkins, A Gusnanto, B De Bono, S De, D Miranda-Saavedra, ...
Blood, The Journal of the American Society of Hematology 113 (19), e1-e9, 2009
Mandaten: US National Institutes of Health
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), 4926, 2014
Mandaten: US National Institutes of Health, National Health and Medical Research …
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