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Research
  1. Queen Mary University of London
  2. Research
  3. Publications

Publications: Mrs Eva Wozniak

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Higham JP, Bhebhe CN, Gupta RA, Tranter MM, Barakat FM, Dogra H, Bab N, Wozniak E et al. ( 2024 ) . Transcriptomic profiling reveals a pronociceptive role for angiotensin II in inflammatory bowel disease . Pain
Batty P, Watson D, Wozniak E, Mein C, Barnes M ( 2023 ) . Transcriptomic Profiling to Understand Inhibitor Development in Previously Untreated Patients with Severe Hemophilia a . Blood vol. 142 , ( Supplement 1 )
Laycock K, Cabrera C, Wozniak E, Mein C, Azizan E, Wu X, Argentesi G, Goodchild E et al. ( 2023 ) . FRI144 Using Single Cell Technology To Predict The Cell Of Origin Of Aldosterone-producing Adrenal Adenomas . Journal of the Endocrine Society vol. 7 , ( Supplement_1 )
Thomas BR, Tan XL, Van Duijvenboden S, Hogan SC, Hughes AJ, Tawfik SS, Dhoat S, Atkar R et al. ( 2023 ) . Deep palmar phenotyping in atopic eczema: patterns associated with filaggrin variants, disease severity and barrier function in a South Asian population . British Journal of Dermatology vol. 188 , ( 6 ) 785 - 792 .
Ponnusamy V, Ip RTH, Mohamed MAEK, Clarke P, Wozniak E, Mein C, Schwendimann L, Barlas A et al. ( 2021 ) . Neuronal let-7b-5p acts through the Hippo-YAP pathway in neonatal encephalopathy . Communications Biology vol. 4 , ( 1 )
( 2021 ) . Correction: BS18 Profiling endothelial gene expression in coronary atherosclerotic plaques in a human-like D374Y-PCSK9 hyperlipidaemic porcine model . Heart vol. 107 , ( 19 ) e10 - e10 .
Zhou J, Azizan EAB, Cabrera CP, Fernandes-Rosa FL, Boulkroun S, Argentesi G, Cottrell E, Amar L et al. ( 2021 ) . Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause . Nature Genetics
Argentesi G, Azizan E, Zhou J, Cabrera C, O’Toole S, Wu X, Goodchild E, Cottrell E et al. ( 2021 ) . Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause . Nature Genetics
Naser J, Mein CA, Wozniak E, Carassiti D, Mahomed AS, Krams R, de Silva R ( 2021 ) . BS18 Profiling endothelial gene expression in coronary atherosclerotic plaques in a human-like D374Y-PCSK9 hyperlipidaemic porcine model . Heart . Conference: Heart vol. 107 , a166 - a167 .
Acton R, Yuan W, Gao F, Xia Y, Bourne E, Wozniak E, Bell J, Lillycrop K et al. ( 2021 ) . The Genomic Loci of Specific Human tRNA Genes Exhibit Ageing-Related DNA Hypermethylation . Nature Communications
Zhou J, Boulkroun S, Cabrera CP, Azizan EAB, Fernandes-Rosa F, Cottrell E, Argentesi G, Wu X et al. ( 2021 ) . CTNNB1-Mutant Aldosterone-Producing Adenomas With Somatic Mutations of GNA11/GNAQ Have Distinct Phenotype and Genotype . Journal of the Endocrine Society vol. 5 , ( Suppl 1 ) a65 - a66 .
Azizan EAB, Zhou J, Cabrera CP, Fernandes-Rosa FL, Boulkroun S, Argentesi G, Cottrell E, Amar L et al. ( 2021 ) . Somatic Mutations of GNA11 and GNAQ in CTNNB1-Mutant Aldosterone-Producing Adenomas Increases Aldosterone and Aldosterone Synthase (CYP11B2) . Journal of the Endocrine Society vol. 5 , ( Supplement_1 ) a72 - a72 .
Argentesi G, Zhou J, Azizan E, Cabrera CP, Cottrell E, Wu X, Goodchild E, Foo R et al. ( 2021 ) . Aldosterone-producing adenomas with dual mutations of GNA11/Q and CTNNB1 lead to hypertension in puberty, pregnancy or menopause, and complete cure by adrenalectomy . JOURNAL OF HUMAN HYPERTENSION . vol. 35 , 5 - 5 .
Wu X, Garg S, Cabrera CP, Azizan E, Zhou J, Mein C, Wozniak E, Zhao W et al. ( 2020 ) . OR34-02 Somatic Transmembrane Domain Mutations of a Cell Adhesion Molecule, CADM1, Cause Primary Aldosteronism by Preventing Gap Junction Communication Between Adrenocortical Cells . Journal of the Endocrine Society vol. 4 , ( Supplement_1 ) or34 - or02 .
Lone NM, Riaz S, Eusaph AZ, Mein CA, Wozniak EL, Xenakis T, Wu Z, Younis S et al. ( 2020 ) . Genotype-independent association between vitamin D deficiency and polycystic ovarian syndrome in Lahore, Pakistan . Scientific Reports vol. 10 , ( 1 )
Acton R, Yuan W, Gao F, Xia Y, Bourne E, Wozniak E, Bell J, Lillycrop K et al. ( 2019 ) . The Genomic Loci of Specific Human tRNA Genes Exhibit Ageing-Related DNA Hypermethylation .
Wu X, Garg S, Cabrera C, Azizan E, Zhou J, Mein C, Takaoka Y, Wozniak E et al. ( 2019 ) . Somatic transmembrane domain mutations of a cell adhesion molecule, CADM1, cause primary aldosteronism by preventing gap junction communication between adrenocortical cells . Endocrine Abstracts
Biserni M, Mesnage R, Ferro R, Wozniak E, Xenakis T, Mein CA, Antoniou MN ( 2019 ) . Quizalofop-p-Ethyl Induces Adipogenesis in 3T3-L1 Adipocytes . Toxicological Sciences vol. 170 , ( 2 ) 452 - 461 .
Mesnage R, Biserni M, Wozniak E, Xenakis T, Mein CA, Antoniou MN ( 2018 ) . Comparison of transcriptome responses to glyphosate, isoxaflutole, quizalofop-p-ethyl and mesotrione in the HepaRG cell line . Toxicology Reports vol. 5 , 819 - 826 .
Mesnage R, Biserni M, Balu S, Frainay C, Poupin N, Jourdan F, Wozniak E, Xenakis T et al. ( 2018 ) . Integrated transcriptomics and metabolomics reveal signatures of lipid metabolism dysregulation in HepaRG liver cells exposed to PCB 126 . Archives of Toxicology vol. 92 , ( 8 ) 2533 - 2547 .
Carbajosa G, Malki K, Lawless N, Wang H, Ryder JW, Wozniak E, Wood K, Mein CA et al. ( 2018 ) . Loss of Trem2 in microglia leads to widespread disruption of cell coexpression networks in mouse brain . Neurobiology of Aging vol. 69 , 151 - 166 .
Clark LV, Buckland M, Murphy G, Taylor N, Vleck V, Mein C, Wozniak E, Smuk M et al. ( 2017 ) . Cytokine responses to exercise and activity in patients with chronic fatigue syndrome: case–control study . Clinical & Experimental Immunology vol. 190 , ( 3 ) 360 - 371 .
Brugha R, Lowe R, Henderson AJ, Holloway JW, Rakyan V, Wozniak E, Mahmud N, Seymour K et al. ( 2017 ) . DNA methylation profiles between airway epithelium and proxy tissues in children . Acta Paediatrica
Bolton KL, Tyrer J, Song H, Ramus SJ, Notaridou M, Jones C, Sher T, Gentry-Maharaj A et al. ( 2016 ) . Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer . Nature Genetics vol. 48 , ( 1 ) 101 - 101 .
Salas-Alanis JC, Wozniak E, Mein CA, Mckinster CCD, Ocampo-Candiani J, Kelsell DP, Hua R, Garza-Rodriguez ML et al. ( 2015 ) . Mutations in EDA and EDAR Genes in a Large Mexican Hispanic Cohort with Hypohidrotic Ectodermal Dysplasia . Annals of Dermatology vol. 27 , ( 4 ) 474 - 477 .
Tawana K, Wang J, Renneville A, Bödör C, Hills R, Loveday C, Savic A, Van Delft FW et al. ( 2015 ) . Disease evolution and outcomes in familial AML with germline CEBPA mutations . Blood vol. 126 , ( 10 ) 1214 - 1223 .
Torrance HD, Brohi K, Pearse RM, Mein CA, Wozniak E, Prowle JR, Hinds CJ, O'Dwyer MJ ( 2015 ) . Association Between Gene Expression Biomarkers of Immunosuppression and Blood Transfusion in Severely Injured Polytrauma Patients . Annals of Surgery vol. 261 , ( 4 ) 751 - 759 .
Torrance HD, Brohi K, Pearse RM, Mein CA, Wozniak E, Prowle JR, Hinds CJ, O'Dwyer MJ ( 2015 ) . Association between gene expression biomarkers of immunosuppression and blood transfusion in severely injured polytrauma patients . Annals of Surgery vol. 261 , ( 4 ) 751 - 759 .
Batty P, Mein C, Wozniak E, Hart D ( 2015 ) . Reliable RNA retrieval from low-volume paxgene tubes in simulated "real world" next generation sequencing (RNA-SEQ): Gena-05 substudy pilot . JOURNAL OF THROMBOSIS AND HAEMOSTASIS . vol. 13 , 365 - 365 .
Torrance HD, Brohi K, Pearse RM, Mein CA, Wozniak E, Prowle JR, Hinds CJ, O’Dwyer MJ ( 2014 ) . Association between gene expression biomarkers of immunosuppression and blood transfusion in severely injured polytrauma patients . Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine . vol. 22 ,
Hunt KA, Mistry V, Bockett NA, Ahmad T, Ban M, Barker JN, Barrett JC, Blackburn H et al. ( 2013 ) . Negligible impact of rare autoimmune-locus coding-region variants on missing heritability . Nature vol. 498 , ( 7453 ) 232 - 235 .
Hunt KA, Mistry V, Bockett NA, Ahmad T, Ban M, Barker JN, Barrett JC, Blackburn H et al. ( 2013 ) . Negligible impact of rare autoimmune-locus coding-region variants on missing heritability . Nature vol. 498 , ( 7453 ) 232 - 235 .
Balogun N, Gentry-Maharaj A, Wozniak EL, Lim A, Ryan A, Ramus SJ, Ford J, Burnell M et al. ( 2010 ) . Recruitment of newly diagnosed ovarian cancer patients proved challenging in a multicentre biobanking study . Journal of Clinical Epidemiology vol. 64 , ( 5 ) 525 - 530 .
Bolton KL, Tyrer J, Song H, Ramus SJ, Notaridou M, Jones C, Sher T, Gentry-Maharaj A et al. ( 2010 ) . Common variants at 19p13 are associated with susceptibility to ovarian cancer . Nature Genetics vol. 42 , ( 10 ) 880 - 884 .
Song H, Koessler T, Ahmed S, Ramus SJ, Kjaer SK, DiCioccio RA, Wozniak E, Hogdall E et al. ( 2008 ) . Association Study of Prostate Cancer Susceptibility Variants with Risks of Invasive Ovarian, Breast, and Colorectal Cancer . Cancer Research vol. 68 , ( 21 ) 8837 - 8842 .
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