Works by Meynert, Alison

Results: 18

Divergent trajectories to structural diversity impact patient survival in high grade serous ovarian cancer.

Published in:

Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-60655-y

By:

Ewing, Ailith;
Meynert, Alison;
Silk, Ryan;
Aitken, Stuart;
Bendixsen, Devin P.;
Churchman, Michael;
Brown, Stuart L.;
Hamdan, Alhafidz;
Mattocks, Joanne;
Grimes, Graeme R.;
Ballinger, Tracy;
Hollis, Robert L.;
Simon Herrington, C.;
Thomson, John P.;
Sherwood, Kitty;
Parry, Thomas;
Esiri-Bloom, Edward;
Bartos, Clare;
Croy, Ian;
Ferguson, Michelle

Publication type:

Article

Regionally enriched rare deleterious exonic variants in the UK and Ireland.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51604-2

By:

Halachev, Mihail;
Gountouna, Viktoria-Eleni;
Meynert, Alison;
Tzoneva, Gannie;
Shuldiner, Alan R.;
Semple, Colin A.;
Wilson, James F.

Publication type:

Article

Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations.

Published in:

2018

By:

Hollis, Robert L.;
Meynert, Alison M.;
Churchman, Michael;
Rye, Tzyvia;
Mackean, Melanie;
Nussey, Fiona;
Arends, Mark J.;
Sims, Andrew H.;
Semple, Colin A.;
Herrington, C. Simon;
Gourley, Charlie

Publication type:

journal article

Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.

Published in:

PLoS Genetics, 2019, v. 15, n. 11, p. 1, doi. 10.1371/journal.pgen.1008480

By:

Halachev, Mihail;
Meynert, Alison;
Taylor, Martin S.;
Vitart, Veronique;
Kerr, Shona M.;
Klaric, Lucija;
Aitman, Timothy J.;
Haley, Chris S.;
Prendergast, James G.;
Pugh, Carys;
Hume, David A.;
Harris, Sarah E.;
Liewald, David C.;
Deary, Ian J.;
Semple, Colin A.;
Wilson, James F.

Publication type:

Article

ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.

Published in:

PLoS Genetics, 2019, v. 15, n. 3, p. 1, doi. 10.1371/journal.pgen.1007605

By:

Handley, Mark T.;
Reddy, Kaalak;
Wills, Jimi;
Rosser, Elisabeth;
Kamath, Archith;
Halachev, Mihail;
Falkous, Gavin;
Williams, Denise;
Cox, Phillip;
Meynert, Alison;
Raymond, Eleanor S.;
Morrison, Harris;
Brown, Stephen;
Allan, Emma;
Aligianis, Irene;
Jackson, Andrew P.;
Ramsahoye, Bernard H.;
von Kriegsheim, Alex;
Taylor, Robert W.;
Finch, Andrew J.

Publication type:

Article

Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia.

Published in:

Pediatric Pulmonology, 2024, v. 59, n. 12, p. 3322, doi. 10.1002/ppul.27200

By:

Black, Holly A.;
de Proce, Sophie Marion;
Campos, Jose L.;
Meynert, Alison;
Halachev, Mihail;
Marsh, Joseph A.;
Hirst, Robert A.;
O'Callaghan, Chris;
Shoemark, Amelia;
Toddie‐Moore, Daniel;
Santoyo‐Lopez, Javier;
Murray, Jennie;
Macleod, Kenneth;
Urquhart, Don S.;
Unger, Stefan;
Aitman, Timothy J.;
Mill, Pleasantine

Publication type:

Article

Distinct histopathological features are associated with molecular subtypes and outcome in low grade serous ovarian carcinoma.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-34627-5

By:

Hollis, Robert L.;
Thomson, John P.;
van Baal, Juliette;
Ilenkovan, Narthana;
Churchman, Michael;
van de Vijver, Koen;
Dijk, Frederike;
Meynert, Alison M.;
Bartos, Clare;
Rye, Tzyvia;
Croy, Ian;
Diana, Patricia;
van Gent, Mignon;
Creedon, Helen;
Nirsimloo, Rachel;
Lok, Christianne;
Gourley, Charlie;
Herrington, C. Simon

Publication type:

Article

Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse.

Published in:

Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101797

By:

Hernandez-Moran, Brianda A.;
Papanastasiou, Andrew S.;
Parry, David;
Meynert, Alison;
Gautier, Philippe;
Grimes, Graeme;
Adams, Ian R.;
Trejo-Reveles, Violeta;
Bengani, Hemant;
Keighren, Margaret;
Jackson, Ian J.;
Adams, David J.;
FitzPatrick, David R.;
Rainger, Joe

Publication type:

Article

Integrated molecular characterisation of endometrioid ovarian carcinoma identifies opportunities for stratification.

Published in:

NPJ Precision Oncology, 2021, v. 5, n. 1, p. 1, doi. 10.1038/s41698-021-00187-y

By:

Hollis, Robert L.;
Stanley, Barbara;
Thomson, John P.;
Churchman, Michael;
Croy, Ian;
Rye, Tzyvia;
Bartos, Clare;
Nussey, Fiona;
Mackean, Melanie;
Meynert, Alison M.;
Semple, Colin A.;
Gourley, Charlie;
Herrington, C. Simon

Publication type:

Article

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47436-6

By:

Kerr, Shona M.;
Klaric, Lucija;
Halachev, Mihail;
Hayward, Caroline;
Boutin, Thibaud S.;
Meynert, Alison M.;
Semple, Colin A.;
Tuiskula, Annukka M.;
Swan, Heikki;
Santoyo-Lopez, Javier;
Vitart, Veronique;
Haley, Chris;
Dean, John;
Miedzybrodzka, Zosia;
Aitman, Timothy J.;
Wilson, James F.

Publication type:

Article

Small latin squares, quasigroups, and loops.

Published in:

Journal of Combinatorial Designs, 2007, v. 15, n. 2, p. 98, doi. 10.1002/jcd.20105

By:

McKay, Brendan D.;
Meynert, Alison;
Myrvold, Wendy

Publication type:

Article

Variant detection sensitivity and biases in whole genome and exome sequencing.

Published in:

BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-247

By:

Meynert, Alison M.;
Ansari, Morad;
FitzPatrick, David R.;
Taylor, Martin S.

Publication type:

Article

Quantifying single nucleotide variant detection sensitivity in exome sequencing.

Published in:

BMC Bioinformatics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2105-14-195

By:

Meynert, Alison M.;
Bicknell, Louise S.;
Hurles, Matthew E.;
Jackson, Andrew P.;
Taylor, Martin S.

Publication type:

Article

Heterochromatin delays CRISPR-Cas9 mutagenesis but does not influence the outcome of mutagenic DNA repair.

Published in:

PLoS Biology, 2018, v. 16, n. 12, p. 1, doi. 10.1371/journal.pbio.2005595

By:

Kallimasioti-Pazi, Eirini M.;
Thelakkad Chathoth, Keerthi;
Taylor, Gillian C.;
Meynert, Alison;
Ballinger, Tracy;
Kelder, Martijn J. E.;
Lalevée, Sébastien;
Sanli, Ildem;
Feil, Robert;
Wood, Andrew J.

Publication type:

Article

Rapid evolution of colistin resistance in a bioreactor model of infection of Klebsiella pneumoniae.

Published in:

Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06378-0

By:

Jiménez-Castellanos, Juan-Carlos;
Waclaw, Bartlomiej;
Meynert, Alison;
McAteer, Sean P.;
Schneiders, Thamarai

Publication type:

Article

Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18819-5

By:

Hollis, Robert L.;
Thomson, John P.;
Stanley, Barbara;
Churchman, Michael;
Meynert, Alison M.;
Rye, Tzyvia;
Bartos, Clare;
Iida, Yasushi;
Croy, Ian;
Mackean, Melanie;
Nussey, Fiona;
Okamoto, Aikou;
Semple, Colin A.;
Gourley, Charlie;
Herrington, C. Simon

Publication type:

Article

Gorham-Stout case report: a multi-omic analysis reveals recurrent fusions as new potential drivers of the disease.

Published in:

BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01277-x

By:

Yébenes Mayordomo, Marcos;
Al Shboul, Sofian;
Gómez-Herranz, Maria;
Azfer, Asim;
Meynert, Alison;
Salter, Donald;
Hayward, Larry;
Oniscu, Anca;
Patton, James T.;
Hupp, Ted;
Arends, Mark J.;
Alfaro, Javier Antonio

Publication type:

Article

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.

Published in:

Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 4, p. 319, doi. 10.1002/mgg3.70

By:

Handley, Mark T.;
Mégarbané, André;
Meynert, Alison M.;
Brown, Stephen;
Freyer, Elisabeth;
Taylor, Martin S.;
Jackson, Ian J.;
Aligianis, Irene A.

Publication type:

Article