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Author Details

Alison Meynert
Institute of Genetics and Cancer, University of Edinburgh
2006
29
15
PMIDPaper TitleJournal TitlePublished Year
37169775Distinct histopathological features are associated with molecular subtypes and outcome in low grade serous ovarian carcinoma.Sci Rep2023
37207500Whole exome sequencing of low grade serous ovarian carcinoma identifies genomic events associated with clinical outcome.Gynecol Oncol2023
35074757In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma.Cancer Res2022
35668402Gorham-Stout case report: a multi-omic analysis reveals recurrent fusions as new potential drivers of the disease.BMC Med Genomics2022
36351380Toll-like receptor 2 orchestrates a tumor suppressor response in non-small cell lung cancer.Cell Rep2022
36292683Robust Genetic Analysis of the X-Linked Anophthalmic (<i>Ie</i>) Mouse.Genes (Basel)2022
35131896Ancient DNA at the edge of the world: Continental immigration and the persistence of Neolithic male lineages in Bronze Age Orkney.Proc Natl Acad Sci U S A2022
33307546Genetic mechanisms of critical illness in COVID-19.Nature2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
34079052Integrated molecular characterisation of endometrioid ovarian carcinoma identifies opportunities for stratification.NPJ Precis Oncol2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
31055034Clinical and molecular characterization of ovarian carcinoma displaying isolated lymph node relapse.Am J Obstet Gynecol2019
31765389Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.PLoS Genet2019
31358886An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.Sci Rep2019
30856165ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.PLoS Genet2019
29298688Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations.BMC Cancer2018
30540740Heterochromatin delays CRISPR-Cas9 mutagenesis but does not influence the outcome of mutagenic DNA repair.PLoS Biol2018
28129423Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature.Invest Ophthalmol Vis Sci2017
27029034Dynamic epigenetic changes to VHL occur with sunitinib in metastatic clear cell renal cancer.Oncotarget2016
24462371Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.Am J Hum Genet2014
25038816Variant detection sensitivity and biases in whole genome and exome sequencing.BMC Bioinformatics2014
25077174Loss 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.Mol Genet Genomic Med2014
25125236Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.J Med Genet2014
24906020Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.Am J Hum Genet2014
24670764A promoter-level mammalian expression atlas.Nature2014
23773188Quantifying single nucleotide variant detection sensitivity in exome sequencing.BMC Bioinformatics2013
20016488A small-cell lung cancer genome with complex signatures of tobacco exposure.Nature2010
17519034CAG-encoded polyglutamine length polymorphism in the human genome.BMC Genomics2007
16751093Picking pyknons out of the human genome.Cell2006
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Collaborators

Martin S Taylor
Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 9
David R FitzPatrick
Institute of Genetics and Cancer, The University of Edinburgh MRC Human Genetics Unit
Co-authored papers 7
Colin A Semple
Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 6
James F Wilson
Co-authored papers 5
Graeme R Grimes
Co-authored papers 4
John Kenneth Baillie
Roslin Institute, University of Edinburgh
Co-authored papers 4
Matthew E Hurles
Wellcome Sanger Institute
Co-authored papers 3
John P Thomson
MRC Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 3
Veronique Vitart
Co-authored papers 3
Kathleen A Williamson
Institute of Genetics and Cancer, The University of Edinburgh MRC Human Genetics Unit
Co-authored papers 3
Morad Ansari
Western General Hospital
Co-authored papers 3
Dorota Pasko
Co-authored papers 3
Charu Deshpande
Guy's Hospital
Co-authored papers 2
Anurag Verma
Corporal Michael J Crescenz VA Medical Center Philadelphia
Co-authored papers 2
Guillaume Butler-Laporte
McGill University
Co-authored papers 2
Lukas Habegger
Co-authored papers 2
Krzysztof Kiryluk
Columbia University
Co-authored papers 2
Joseph B Leader
Co-authored papers 2
Anne E Justice
Co-authored papers 2
Erika Kvikstad
University of Oxford
Co-authored papers 2
Jack A Kosmicki
Regeneron Pharmaceuticals
Co-authored papers 2
James G D Prendergast
The Roslin Institute, The University of Edinburgh
Co-authored papers 2
Anthony Marcketta
Co-authored papers 2
Alan R Shuldiner
University of Maryland School of Medicine
Co-authored papers 2
David A Hume
Mater Research Institute-UQ, Translational Research Institute
Co-authored papers 2
Mark J Caulfield
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
Chris P Ponting
The University of Edinburgh
Co-authored papers 2
Aris Baras
Co-authored papers 2
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 2
Gundula Povysil
Institute for Genomic Medicine, Columbia University Medical Center
Co-authored papers 2
Release 1.2