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Ellen Mary McDonagh
Ellen Mary McDonagh
Genomics England / Queen Mary University London
Verified email at genomicsengland.co.uk
Title
Cited by
Cited by
Year
Pharmacogenomics knowledge for personalized medicine
M Whirl‐Carrillo, EM McDonagh, JM Hebert, L Gong, K Sangkuhl, ...
Clinical Pharmacology & Therapeutics 92 (4), 414-417, 2012
20352012
Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process
K E Caudle, T E Klein, J M Hoffman, D J Muller, M Whirl-Carrillo, L Gong, ...
Current drug metabolism 15 (2), 209-217, 2014
4312014
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
4092018
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
3652021
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
3262019
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics
M Ghoussaini, E Mountjoy, M Carmona, G Peat, EM Schmidt, A Hercules, ...
Nucleic acids research 49 (D1), D1311-D1320, 2021
3202021
Open Targets Platform: supporting systematic drug–target identification and prioritisation
D Ochoa, A Hercules, M Carmona, D Suveges, A Gonzalez-Uriarte, ...
Nucleic acids research 49 (D1), D1302-D1310, 2021
2952021
From pharmacogenomic knowledge acquisition to clinical applications: the PharmGKB as a clinical pharmacogenomic biomarker resource
EM McDonagh, M Whirl-Carrillo, Y Garten, RB Altman, TE Klein
Biomarkers in medicine 5 (6), 795-806, 2011
2062011
The chemokine receptor CXCR3 is degraded following internalization and is replenished at the cell surface by de novo synthesis of receptor
A Meiser, A Mueller, EL Wise, EM McDonagh, SJ Petit, N Saran, PC Clark, ...
The Journal of Immunology 180 (10), 6713-6724, 2008
1522008
Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for human leukocyte antigen B (HLA‐B) genotype and allopurinol dosing: 2015 update
Y Saito, LK Stamp, KE Caudle, MS Hershfield, EM McDonagh, ...
Clinical Pharmacology & Therapeutics 99 (1), 36-37, 2016
1462016
PharmGKB summary: very important pharmacogene information for: N:-acetyltransferase 2
EM McDonagh, S Boukouvala, E Aklillu, DW Hein, RB Altman, TE Klein
Pharmacogenetics and genomics 24 (8), 409-425, 2014
1462014
PharmGKB summary: caffeine pathway
CF Thorn, E Aklillu, EM McDonagh, TE Klein, RB Altman
Pharmacogenetics and genomics 22 (5), 389-395, 2012
1452012
Nomenclature for alleles of the thiopurine methyltransferase gene
ML Appell, J Berg, J Duley, WE Evans, MA Kennedy, L Lennard, ...
Pharmacogenetics and genomics 23 (4), 242-248, 2013
1402013
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for Rasburicase Therapy in the Context of G6PD Deficiency Genotype
MV Relling, EM McDonagh, T Chang, KE Caudle, HL McLeod, CE Haidar, ...
Clinical Pharmacology & Therapeutics 96 (2), 169-174, 2014
1392014
CXCL4-induced migration of activated T lymphocytes is mediated by the chemokine receptor CXCR3
A Mueller, A Meiser, EM McDonagh, JM Fox, SJ Petit, G Xanthou, ...
Journal of Leucocyte Biology 83 (4), 875-882, 2008
1322008
The next-generation Open Targets Platform: reimagined, redesigned, rebuilt
D Ochoa, A Hercules, M Carmona, D Suveges, J Baker, C Malangone, ...
Nucleic acids research 51 (D1), D1353-D1359, 2023
1102023
Human genetics evidence supports two-thirds of the 2021 FDA-approved drugs
D Ochoa, M Karim, M Ghoussaini, DG Hulcoop, EM McDonagh, I Dunham
Nat Rev Drug Discov 21 (8), 551, 2022
922022
Opportunities and challenges for molecular understanding of ciliopathies–the 100,000 genomes project
G Wheway, Genomics England Research Consortium, HM Mitchison
Frontiers in genetics 10, 127, 2019
902019
Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
K Ibañez, J Polke, RT Hagelstrom, E Dolzhenko, D Pasko, ERA Thomas, ...
The Lancet Neurology 21 (3), 234-245, 2022
892022
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for Ivacaftor Therapy in the Context of CFTR Genotype
JP Clancy, SG Johnson, SW Yee, EM McDonagh, KE Caudle, TE Klein, ...
Clinical Pharmacology & Therapeutics 95 (6), 592-597, 2014
742014
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