Alison Meynert
Alison Meynert
MRC IGMM Human Genetics Unit, University of Edinburgh
Verified email at
Cited by
Cited by
A promoter-level mammalian expression atlas
Fantom Consortium
Nature 507 (7493), 462, 2014
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
Small Latin squares, quasigroups, and loops
BD McKay, A Meynert, W Myrvold
Journal of Combinatorial Designs 15 (2), 98-119, 2007
Variant detection sensitivity and biases in whole genome and exome sequencing
AM Meynert, M Ansari, DR FitzPatrick, MS Taylor
BMC bioinformatics 15 (1), 1-11, 2014
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
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
Genetic mechanisms of critical illness in Covid-19
E Pairo-Castineira, S Clohisey, L Klaric, AD Bretherick, K Rawlik, D Pasko, ...
Nature, 1-1, 2020
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), 1-18, 2007
Quantifying single nucleotide variant detection sensitivity in exome sequencing
AM Meynert, LS Bicknell, ME Hurles, AP Jackson, MS Taylor
BMC bioinformatics 14 (1), 1-10, 2013
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
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
Heterochromatin delays CRISPR-Cas9 mutagenesis but does not influence the outcome of mutagenic DNA repair
EM Kallimasioti-Pazi, KT Chathoth, GC Taylor, A Meynert, T Ballinger, ...
PLoS biology 16 (12), e2005595, 2018
DNA polymerase epsilon deficiency causes IMAGe syndrome with variable immunodeficiency
CV Logan, JE Murray, DA Parry, A Robertson, R Bellelli, Ž Tarnauskaitė, ...
The American Journal of Human Genetics 103 (6), 1038-1044, 2018
Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg …
MT Handley, A Mégarbané, AM Meynert, S Brown, E Freyer, MS Taylor, ...
Molecular genetics & genomic medicine 2 (4), 319-325, 2014
Picking pyknons out of the human genome
A Meynert, E Birney
Cell 125 (5), 836-838, 2006
Novel PEX11B mutations extend the peroxisome biogenesis disorder 14B phenotypic spectrum and underscore congenital cataract as an early feature
RL Taylor, MT Handley, S Waller, C Campbell, J Urquhart, AM Meynert, ...
Investigative ophthalmology & visual science 58 (1), 594-603, 2017
Dynamic epigenetic changes to VHL occur with sunitinib in metastatic clear cell renal cancer
GD Stewart, T Powles, C Van Neste, A Meynert, F O'Mahony, A Laird, ...
Oncotarget 7 (18), 25241, 2016
A small cell lung cancer genome reports complex tobacco exposure signatures
ED Pleasance, PJ Stephens, S O'Meara, DJ McBride, A Meynert, D Jones, ...
Nature 463 (7278), 184, 2010
Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations
RL Hollis, AM Meynert, M Churchman, T Rye, M Mackean, F Nussey, ...
BMC cancer 18 (1), 1-8, 2018
Clinical and molecular characterization of ovarian carcinoma displaying isolated lymph node relapse
RL Hollis, J Carmichael, AM Meynert, M Churchman, A Hallas-Potts, ...
American journal of obstetrics and gynecology 221 (3), 245. e1-245. e15, 2019
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