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Alison Meynert
Alison Meynert
Fulcrum Genomics
Verified email at fulcrumgenomics.com
Title
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Year
A promoter-level mammalian expression atlas
Nature 507 (7493), 462-470, 2014
17322014
Genetic mechanisms of critical illness in COVID-19
E Pairo-Castineira, S Clohisey, L Klaric, AD Bretherick, K Rawlik, D Pasko, ...
Nature 591 (7848), 92-98, 2021
13582021
A small-cell lung cancer genome with complex signatures of tobacco exposure
ED Pleasance, PJ Stephens, S O’Meara, DJ McBride, A Meynert, D Jones, ...
Nature 463 (7278), 184-190, 2010
12972010
SARS-CoV-2 Omicron-B. 1.1. 529 leads to widespread escape from neutralizing antibody responses
W Dejnirattisai, J Huo, D Zhou, J Zahradník, P Supasa, C Liu, ...
Cell 185 (3), 467-484. e15, 2022
9322022
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
7512021
Co-infections, secondary infections, and antimicrobial use in patients hospitalised with COVID-19 during the first pandemic wave from the ISARIC WHO CCP-UK study: a multicentre …
CD Russell, CJ Fairfield, TM Drake, L Turtle, RA Seaton, DG Wootton, ...
The Lancet Microbe 2 (8), e354-e365, 2021
3022021
Variant detection sensitivity and biases in whole genome and exome sequencing
AM Meynert, M Ansari, DR FitzPatrick, MS Taylor
BMC bioinformatics 15, 1-11, 2014
2642014
Small Latin squares, quasigroups, and loops
BD McKay, A Meynert, W Myrvold
Journal of Combinatorial Designs 15 (2), 98-119, 2007
2352007
Development and validation of the ISARIC 4C Deterioration model for adults hospitalised with COVID-19: a prospective cohort study
RK Gupta, EM Harrison, A Ho, AB Docherty, SR Knight, M van Smeden, ...
The Lancet Respiratory Medicine 9 (4), 349-359, 2021
2242021
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
M Ansari, G Poke, Q Ferry, K Williamson, R Aldridge, AM Meynert, ...
Journal of medical genetics 51 (10), 659-668, 2014
1812014
Risk of adverse outcomes in patients with underlying respiratory conditions admitted to hospital with COVID-19: a national, multicentre prospective cohort study using the …
CI Bloom, TM Drake, AB Docherty, BJ Lipworth, SL Johnston, ...
The Lancet Respiratory Medicine 9 (7), 699-711, 2021
1712021
A prenylated dsRNA sensor protects against severe COVID-19
A Wickenhagen, E Sugrue, S Lytras, S Kuchi, M Noerenberg, ML Turnbull, ...
Science 374 (6567), eabj3624, 2021
1532021
Characterisation of in-hospital complications associated with COVID-19 using the ISARIC WHO Clinical Characterisation Protocol UK: a prospective, multicentre cohort study
TM Drake, AM Riad, CJ Fairfield, C Egan, SR Knight, R Pius, ...
The Lancet 398 (10296), 223-237, 2021
1512021
Differential roles of epigenetic changes and Foxp3 expression in regulatory T cell-specific transcriptional regulation
H Morikawa, N Ohkura, A Vandenbon, M Itoh, S Nagao-Sato, H Kawaji, ...
Proceedings of the National Academy of Sciences 111 (14), 5289-5294, 2014
1432014
CAG-encoded polyglutamine length polymorphism in the human genome
SL Butland, RS Devon, Y Huang, CL Mead, AM Meynert, SJ Neal, SS Lee, ...
BMC genomics 8, 1-18, 2007
1122007
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects
KA Williamson, J Rainger, JAB Floyd, M Ansari, A Meynert, KV Aldridge, ...
The American Journal of Human Genetics 94 (2), 295-302, 2014
1052014
Heterochromatin delays CRISPR-Cas9 mutagenesis but does not influence the outcome of mutagenic DNA repair
EM Kallimasioti-Pazi, K Thelakkad Chathoth, GC Taylor, A Meynert, ...
PLoS Biology 16 (12), e2005595, 2018
1012018
Changes in in-hospital mortality in the first wave of COVID-19: a multicentre prospective observational cohort study using the WHO Clinical Characterisation Protocol UK
AB Docherty, RH Mulholland, NI Lone, CP Cheyne, D De Angelis, ...
The Lancet Respiratory Medicine 9 (7), 773-785, 2021
1002021
Quantifying single nucleotide variant detection sensitivity in exome sequencing
AM Meynert, LS Bicknell, ME Hurles, AP Jackson, MS Taylor
BMC bioinformatics 14, 1-10, 2013
982013
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations
J Rainger, D Pehlivan, S Johansson, H Bengani, L Sanchez-Pulido, ...
The American Journal of Human Genetics 94 (6), 915-923, 2014
932014
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