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Alison M. Meynert, PhD - Publications

Affiliations: 
University of Edinburgh, Edinburgh, Scotland, United Kingdom 
 European Bioinformatics Institute University of Cambridge, Cambridge, England, United Kingdom 
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24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Hall HN, Parry D, Halachev M, Williamson KA, Donnelly K, Campos Parada J, Bhatia S, Joseph J, Holden S, Prescott TE, Bitoun P, Kirk EP, Newbury-Ecob R, Lachlan K, Bernar J, ... ... Meynert A, et al. Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. Journal of Medical Genetics. PMID 38050128 DOI: 10.1136/jmg-2023-109181  0.307
2022 Hernandez-Moran BA, Papanastasiou AS, Parry D, Meynert A, Gautier P, Grimes G, Adams IR, Trejo-Reveles V, Bengani H, Keighren M, Jackson IJ, Adams DJ, FitzPatrick DR, Rainger J. Robust Genetic Analysis of the X-Linked Anophthalmic () Mouse. Genes. 13. PMID 36292683 DOI: 10.3390/genes13101797  0.373
2022 Younger NT, Wilson ML, Martinez Lyons A, Jarman EJ, Meynert AM, Grimes GR, Gournopanos K, Waddell SH, Tennant PA, Wilson DH, Guest RV, Wigmore SJ, Acosta JC, Kendall TJ, Taylor MS, et al. In vivo modeling of patient genetic heterogeneity identifies new ways to target cholangiocarcinoma. Cancer Research. PMID 35074757 DOI: 10.1158/0008-5472.CAN-21-2556  0.46
2020 Hollis RL, Thomson JP, Stanley B, Churchman M, Meynert AM, Rye T, Bartos C, Iida Y, Croy I, Mackean M, Nussey F, Okamoto A, Semple CA, Gourley C, Herrington CS. Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome. Nature Communications. 11: 4995. PMID 33020491 DOI: 10.1038/s41467-020-18819-5  0.347
2020 Hollis RL, Thomson J, Stanley B, Meynert AM, Churchman M, Rye T, Herrington CS, Gourley C. Abstract 4161: Integrated analysis of whole exome sequencing and hormone receptor expression data in endometrioid ovarian cancer Cancer Research. 80: 4161-4161. DOI: 10.1158/1538-7445.Am2020-4161  0.388
2019 Halachev M, Meynert A, Taylor MS, Vitart V, Kerr SM, Klaric L, Aitman TJ, Haley CS, Prendergast JG, Pugh C, Hume DA, Harris SE, Liewald DC, Deary IJ, et al. Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. Plos Genetics. 15: e1008480. PMID 31765389 DOI: 10.1371/Journal.Pgen.1008480  0.506
2019 Kerr SM, Klaric L, Halachev M, Hayward C, Boutin TS, Meynert AM, Semple CA, Tuiskula AM, Swan H, Santoyo-Lopez J, Vitart V, Haley C, Dean J, Miedzybrodzka Z, Aitman TJ, et al. An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. Scientific Reports. 9: 10964. PMID 31358886 DOI: 10.1038/S41598-019-47436-6  0.434
2019 Handley MT, Reddy K, Wills J, Rosser E, Kamath A, Halachev M, Falkous G, Williams D, Cox P, Meynert A, Raymond ES, Morrison H, Brown S, Allan E, Aligianis I, et al. ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy. Plos Genetics. 15: e1007605. PMID 30856165 DOI: 10.1371/Journal.Pgen.1007605  0.419
2018 Kallimasioti-Pazi EM, Thelakkad Chathoth K, Taylor GC, Meynert A, Ballinger T, Kelder MJE, Lalevée S, Sanli I, Feil R, Wood AJ. Heterochromatin delays CRISPR-Cas9 mutagenesis but does not influence the outcome of mutagenic DNA repair. Plos Biology. 16: e2005595. PMID 30540740 DOI: 10.1371/Journal.Pbio.2005595  0.397
2018 Hollis RL, Meynert AM, Churchman M, Rye T, Mackean M, Nussey F, Arends MJ, Sims AH, Semple CA, Herrington CS, Gourley C. Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations. Bmc Cancer. 18: 16. PMID 29298688 DOI: 10.1186/S12885-017-3981-2  0.335
2017 Taylor RL, Handley MT, Waller S, Campbell C, Urquhart J, Meynert AM, Ellingford JM, Donnelly D, Wilcox G, Lloyd IC, Mundy H, FitzPatrick DR, Deshpande C, Clayton-Smith J, Black GC. Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. Investigative Ophthalmology & Visual Science. 58: 594-603. PMID 28129423 DOI: 10.1167/Iovs.16-21026  0.403
2016 Stewart GD, Powles T, Van Neste C, Meynert A, O'Mahony F, Laird A, Deforce D, Van Nieuwerburgh F, Trooskens G, Van Criekinge W, De Meyer T, Harrison DJ. Dynamic epigenetic changes to VHL occur with sunitinib in metastatic clear cell renal cancer. Oncotarget. PMID 27029034 DOI: 10.18632/Oncotarget.8308  0.357
2015 Stewart G, Neste CV, Meynert A, Semple C, O'Mahony F, Laird A, Mackay A, Trooskens G, Criekinge WV, Meyer TD, Powles T, Harrison DJ. Effect of sunitinib treatment on mutations and methylation in metastatic renal cancer. Journal of Clinical Oncology. 33: 492-492. DOI: 10.1200/Jco.2015.33.7_Suppl.492  0.379
2015 Stewart G, Neste CV, Meynert A, Semple C, O'Mahony F, Laird A, Mackay A, Trooskens G, Criekinge WV, Meyer TD, Powles T, Harrison D. 779 Effect of sunitinib therapy on intratumoural heterogeneity and differential expression of genetic mutations and DNA methylation in metastatic renal cell cancer European Urology Supplements. 14. DOI: 10.1016/S1569-9056(15)60769-2  0.359
2014 Ansari M, Poke G, Ferry Q, Williamson K, Aldridge R, Meynert AM, Bengani H, Chan CY, Kayserili H, Avci S, Hennekam RC, Lampe AK, Redeker E, Homfray T, Ross A, et al. Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. Journal of Medical Genetics. 51: 659-68. PMID 25125236 DOI: 10.1136/Jmedgenet-2014-102573  0.556
2014 Handley MT, Mégarbané A, Meynert AM, Brown S, Freyer E, Taylor MS, Jackson IJ, Aligianis IA. Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. Molecular Genetics & Genomic Medicine. 2: 319-25. PMID 25077174 DOI: 10.1002/Mgg3.70  0.532
2014 Meynert AM, Ansari M, FitzPatrick DR, Taylor MS. Variant detection sensitivity and biases in whole genome and exome sequencing. Bmc Bioinformatics. 15: 247. PMID 25038816 DOI: 10.1186/1471-2105-15-247  0.527
2014 Rainger J, Pehlivan D, Johansson S, Bengani H, Sanchez-Pulido L, Williamson KA, Ture M, Barker H, Rosendahl K, Spranger J, Horn D, Meynert A, Floyd JA, Prescott T, Anderson CA, et al. Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations. American Journal of Human Genetics. 94: 915-23. PMID 24906020 DOI: 10.1016/J.Ajhg.2014.05.005  0.502
2014 Forrest AR, Kawaji H, Rehli M, Baillie JK, de Hoon MJ, Haberle V, Lassmann T, Kulakovskiy IV, Lizio M, Itoh M, Andersson R, Mungall CJ, Meehan TF, Schmeier S, ... ... Meynert A, et al. A promoter-level mammalian expression atlas. Nature. 507: 462-70. PMID 24670764 DOI: 10.1038/Nature13182  0.567
2014 Williamson KA, Rainger J, Floyd JA, Ansari M, Meynert A, Aldridge KV, Rainger JK, Anderson CA, Moore AT, Hurles ME, Clarke A, van Heyningen V, Verloes A, Taylor MS, Wilkie AO, et al. Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. American Journal of Human Genetics. 94: 295-302. PMID 24462371 DOI: 10.1016/J.Ajhg.2014.01.001  0.528
2013 Meynert AM, Bicknell LS, Hurles ME, Jackson AP, Taylor MS. Quantifying single nucleotide variant detection sensitivity in exome sequencing. Bmc Bioinformatics. 14: 195. PMID 23773188 DOI: 10.1186/1471-2105-14-195  0.486
2010 Pleasance ED, Stephens PJ, O'Meara S, McBride DJ, Meynert A, Jones D, Lin ML, Beare D, Lau KW, Greenman C, Varela I, Nik-Zainal S, Davies HR, Ordoñez GR, Mudie LJ, et al. A small-cell lung cancer genome with complex signatures of tobacco exposure. Nature. 463: 184-90. PMID 20016488 DOI: 10.1038/Nature08629  0.514
2007 Butland SL, Devon RS, Huang Y, Mead CL, Meynert AM, Neal SJ, Lee SS, Wilkinson A, Yang GS, Yuen MM, Hayden MR, Holt RA, Leavitt BR, Ouellette BF. CAG-encoded polyglutamine length polymorphism in the human genome. Bmc Genomics. 8: 126. PMID 17519034 DOI: 10.1186/1471-2164-8-126  0.358
2006 Meynert A, Birney E. Picking Pyknons out of the Human Genome Cell. 125: 836-838. PMID 16751093 DOI: 10.1016/J.Cell.2006.05.019  0.464
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