Publications:
Charles
Mein
Research
Queen Mary University of London
Research
Publications
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Coca Membribes S, Xu W, Suárez C, Patel PM, Larkin J, Valderrama BP, Mein C, Ackermann C et al.
2026
KIM-1 in Advanced Papillary and Clear Cell Renal Cell Carcinoma
European Urology
10.1016/j.eururo.2026.03.005
Jacobs BM, Schalk L, Tregaskis-Daniels E, Scalfari A, Nandoskar A, Dunne A, Gran B, Mein CA et al.
2026
Genetic Determinants of Multiple Sclerosis Susceptibility in People From Diverse Ancestral Backgrounds
Neurology
vol.
106
10.1212/wnl.0000000000214708
Turner DC, Raastad T, Ullrich M, Christiansen SF, Sutherland H, Boot J, Wozniak E, Mein C et al.
2026
Repeated Disuse Atrophy Imprints a Molecular Memory in Skeletal Muscle: Transcriptional Resilience in Young Adults and Susceptibility in Aged Muscle
Advanced Science
10.1002/advs.202522726
Millner TO, Panday P, Xiao Y, Nicholson J, Boot JR, Arpe Z, Stevens P, Rahman N et al.
2025
P09.02.A DISRUPTION OF DNA METHYLATION UNDERPINS THE NEUROINFLAMMATION INDUCED BY TARGETED CNS RADIOTHERAPY
Neuro-Oncology
vol.
27
Supplement_3
iii89
iii89
10.1093/neuonc/noaf193.293
Morgan OB, Singleton S, Florea R, Hestehave S, Sarter T, Wozniak E, Mein CA, Hausch F et al.
2025
Stress, epigenetic remodeling and FKBP51: Pathways to chronic pain vulnerability
Brain Behavior and Immunity
vol.
130
10.1016/j.bbi.2025.106119
Aminuddin A, Rahman ANA, Latif FA, Cabrera CP, Stevens P, Laycock K, Ng E, Goodchild E et al.
2025
THE MUTATIONAL LANDSCAPE OF ADRENAL GLANDS WITH ALDOSTERONE-PRODUCING LESIONS AT SINGLE-CELL RESOLUTION
Journal of Hypertension
vol.
43
Suppl 1
10.1097/01.hjh.0001115772.97800.31
Millner TO, Panday P, Xiao Y, Nicholson JG, Boot JR, Arpe Z, Stevens PA, Rahman NN et al.
2025
Disruption of DNA methylation underpins the neuroinflammation induced by targeted CNS radiotherapy
Brain
vol.
148
3137
3152
10.1093/brain/awaf163
Kowala A, Boot J, Meng J, Mein CA, Pourquié O, Connelly JT, Morgan JE, Lin Y-Y
2025
Engineered human myogenic cells in hydrogels generate innervated vascularized myofibers within dystrophic mouse muscle on long-term engraftment
Cell Reports Medicine
vol.
10.1016/j.xcrm.2025.102019
Goodchild E, Wu X, Senanayake R, MacFarlane J, Argentesi G, Laycock K, Bashari WA, Cabrera CP et al.
2025
Molecular Imaging Versus Adrenal Vein Sampling for the Detection of Surgically Curable Primary Aldosteronism : A Prospective Within-Patient Trial
Annals of Internal Medicine
vol.
178
336
347
10.7326/annals-24-00761
Vinel C, Boot J, Jin W, Pomella N, Hadaway A, Mein C, Zabet NR, Marino S
2025
Mapping chromatin remodelling in glioblastoma identifies epigenetic regulation of key molecular pathways and novel druggable targets
BMC Biology
vol.
23
10.1186/s12915-025-02127-9
Laycock K, Cabrera C, Wozniak E, Ng E, Wu X, Goodchild E, Azizan EAB, Boot J et al.
2024
8310 CACNA1D- and KCNJ5-Mutant Aldosterone-Producing Adenomas (APAs) Have Opposite 2-Year Clinical Outcomes from Adrenalectomy: Prospective Trial Findings Explained By Different Cells-Of-Origin
Journal of the Endocrine Society
vol.
Supplement_1
10.1210/jendso/bvae163.560
Vadgama A, Boot J, Dark N, Allan HE, Mein CA, Armstrong PC, Warner TD
2024
Multiparameter phenotyping of platelets and characterization of the effects of agonists using machine learning
Research and Practice in Thrombosis and Haemostasis
vol.
10.1016/j.rpth.2024.102523
Tan XL, Chan J, Thomas B, Van Duijvenboden S, Hogan S, Hughes A, Tawfik S, Dhoat S et al.
2024
O11 Associations between hyperlinearity of the sole and filaggrin variants in atopic eczema in a South Asian population: a cross-sectional study
British Journal of Dermatology
vol.
191
Supplement_1
i6
i7
10.1093/bjd/ljae090.011
Humphreys DT, Lewis A, Pan‐Castillo B, Berti G, Mein C, Wozniak E, Gordon H, Gadhok R et al.
2024
Single cell sequencing data identify distinct B cell and fibroblast populations in stricturing Crohn's disease
Journal of Cellular and Molecular Medicine
vol.
28
10.1111/jcmm.18344
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
vol.
165
1592
1604
10.1097/j.pain.0000000000003159
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
10.1182/blood-2023-181845
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.
Supplement_1
10.1210/jendso/bvad114.656
Wu X, Goodchild E, Senanayake R, Bashari W, Salsbury J, Cabrera CP, Argentesi G, O’Toole SM et al.
2023
OR02-02 Pre-operative Blood Pressure Response To Aldosterone Antagonists And Urinary Hybrid Steroid Ratios Predict Clinical Outcomes In Unilateral Primary Aldosteronism For At Least 2 Years Post-adrenalectomy
Journal of the Endocrine Society
vol.
Supplement_1
10.1210/jendso/bvad114.573
Maiarù M, Acton RJ, Woźniak EL, Mein CA, Bell CG, Géranton SM
2023
A DNA methylation signature in the stress driver gene Fkbp5 indicates a neuropathic component in chronic pain
Clinical Epigenetics
vol.
15
10.1186/s13148-023-01569-8
Wu X, Azizan EAB, Goodchild E, Garg S, Hagiyama M, Cabrera CP, Fernandes-Rosa FL, Boulkroun S et al.
2023
Somatic mutations of CADM1 in aldosterone-producing adenomas and gap junction-dependent regulation of aldosterone production
Nature Genetics
vol.
55
1009
1021
10.1038/s41588-023-01403-0
Jacobs BM, Schalk L, Dunne A, Scalfari A, Nandoskar A, Gran B, Mein CA, Sellers C et al.
2023
ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UK
BMJ Open
vol.
13
10.1136/bmjopen-2023-071656
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
785
792
10.1093/bjd/ljad036
Wu X, Senanayake R, Goodchild E, Bashari WA, Salsbury J, Cabrera CP, Argentesi G, O’Toole SM et al.
2023
[11C]metomidate PET-CT versus adrenal vein sampling for diagnosing surgically curable primary aldosteronism: a prospective, within-patient trial
Nature Medicine
vol.
29
190
202
10.1038/s41591-022-02114-5
Mesnage R, Panzacchi S, Bourne E, Mein CA, Perry MJ, Hu J, Chen J, Mandrioli D et al.
2022
Glyphosate and its formulations Roundup Bioflow and RangerPro alter bacterial and fungal community composition in the rat caecum microbiome
Frontiers in Microbiology
vol.
13
10.3389/fmicb.2022.888853
Mesnage R, Panzacchi S, Bourne E, Mein C, Perry M, Hu J, Chen J, Mandrioli D et al.
2022
SOC-IV-10 Glyphosate and its formulations Roundup Bioflow and RangerPro alter bacterial and fungal community composition in the rat caecum microbiome
Toxicology Letters
vol.
368
10.1016/j.toxlet.2022.07.167
Mesnage R, Ibragim M, Mandrioli D, Falcioni L, Tibaldi E, Belpoggi F, Brandsma I, Bourne E et al.
2021
Comparative Toxicogenomics of Glyphosate and Roundup Herbicides by Mammalian Stem Cell-Based Genotoxicity Assays and Molecular Profiling in Sprague-Dawley Rats
Toxicological Sciences
vol.
186
83
101
10.1093/toxsci/kfab143
Mesnage R, Mahmud N, Mein CA, Antoniou MN
2021
Alterations in small RNA profiles in liver following a subchronic exposure to a low-dose pesticide mixture in Sprague-Dawley rats
Toxicology Letters
vol.
353
20
26
10.1016/j.toxlet.2021.10.001
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.
10.1038/s42003-021-02672-3
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
10.1136/heartjnl-2021-bcs.216corr1
Cardosa SR, Ogunkolade BW, Lowe R, Savage E, Mein CA, Boucher BJ, Hitman GA
2021
Areca catechu-(Betel-nut)-induced whole transcriptome changes in a human monocyte cell line that may have relevance to diabetes and obesity; a pilot study
BMC Endocrine Disorders
vol.
21
10.1186/s12902-021-00827-1
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
vol.
53
1360
1372
10.1038/s41588-021-00906-y
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:
Basic science
vol.
107
a166
a167
10.1136/heartjnl-2021-bcs.216
Acton RJ, 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
vol.
12
10.1038/s41467-021-22639-6
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.
Supplement_1
a65
a66
10.1210/jendso/bvab048.133
Mesnage R, Teixeira M, Mandrioli D, Falcioni L, Ibragim M, Ducarmon QR, Zwittink RD, Amiel C et al.
2021
Multi-omics phenotyping of the gut-liver axis reveals metabolic perturbations from a low-dose pesticide mixture in rats
Communications Biology
vol.
10.1038/s42003-021-01990-w
Thomas BR, Tan XL, Javadzadeh S, Robinson EJ, McDonald BS, Dhoat S, Krupiczojc MA, Rahman SR et al.
2021
Phenotype association with filaggrin loss-of-function variants in 349 individuals with eczema from the Tower Hamlets Eczema Assessment (THEA)
BRITISH JOURNAL OF DERMATOLOGY
vol.
185
131
132
Crescente M, Armstrong PC, Kirkby NS, Edin ML, Chan MV, Lih FB, Jiao J, Maffucci T et al.
2020
Profiling the eicosanoid networks that underlie the anti‐ and pro‐thrombotic effects of aspirin
The FASEB Journal
vol.
34
10027
10040
10.1096/fj.202000312r
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
10.1038/s41598-020-59228-4
Thomas AM, Cabrera CP, Finlay M, Lall K, Nobles M, Schilling RJ, Wood K, Mein CA et al.
2019
Differentially expressed genes for atrial fibrillation identified by RNA sequencing from paired human left and right atrial appendages
Physiological Genomics
vol.
51
323
332
10.1152/physiolgenomics.00012.2019
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
452
461
10.1093/toxsci/kfz097
Seaborne RA, Strauss J, Cocks M, Shepherd S, O’Brien TD, Someren KAV, Bell PG, Murgatroyd C et al.
2018
Methylome of human skeletal muscle after acute & chronic resistance exercise training, detraining & retraining
Scientific Data
vol.
10.1038/sdata.2018.213
Jolliffe DA, Greiller CL, Mein CA, Hoti M, Bakhsoliani E, Telcian AG, Simpson A, Barnes NC et al.
2018
Vitamin D receptor genotype influences risk of upper respiratory infection
British Journal Of Nutrition
vol.
120
891
900
10.1017/s000711451800209x
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.
819
826
10.1016/j.toxrep.2018.08.005
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
2533
2547
10.1007/s00204-018-2235-7
Soulsbury CD, Lipponen A, Wood K, Mein CA, Hoffman JI, Lebigre C
2018
Age‐ and quality‐dependent DNA methylation correlate with melanin‐based coloration in a wild bird
Ecology and Evolution
vol.
13
6547
6557
10.1002/ece3.4132
Pigors M, Common JEA, Wong XFCC, Malik S, Scott CA, Tabarra N, Liany H, Liu J et al.
2018
Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes
Journal of Investigative Dermatology
vol.
138
12
2674
2677
10.1016/j.jid.2018.05.013
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
10.1016/j.neurobiolaging.2018.04.019
Gilbert RM, Zhang X, Sampson RD, Ehrenstein MR, Nguyen DX, Chaudhry M, Mein C, Mahmud N et al.
2018
Clinical Remission of Sight-Threatening Non-Infectious Uveitis Is Characterized by an Upregulation of Peripheral T-Regulatory Cell Polarized Towards T-bet and TIGIT
Frontiers in Immunology
vol.
10.3389/fimmu.2018.00907
Munroe PB, Addison S, Abrams DJ, Sebire NJ, Cartwright J, Donaldson I, Cohen MM, Mein C et al.
2018
Postmortem Genetic Testing for Cardiac Ion Channelopathies in Stillbirths
Circulation Genomic and Precision Medicine
vol.
11
10.1161/circgen.117.001817
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
360
371
10.1111/cei.13023
Das A, Rouault-Pierre K, Kamdar S, Gomez-Tourino I, Wood K, Donaldson I, Mein CA, Bonnet D et al.
2017
Adaptive from Innate: Human IFN-γ+CD4+ T Cells Can Arise Directly from CXCL8-Producing Recent Thymic Emigrants in Babies and Adults
The Journal of Immunology
vol.
199
1696
1705
10.4049/jimmunol.1700551
Turner R, Bourne E, Mein C, Birring S, Shaheen S, Bothamley G
2016
M12 TRPV1 polymorphism in chronic cough: no evidence for an effect on objective measurements of cough
Thorax
vol.
71
10.1136/thoraxjnl-2016-209333.454
Kitchen M, Bryan R, Emes R, Glossop J, Luscombe C, Cheng K, Zeegers M, James N et al.
2016
936 Quantitative genome-wide methylation analysis of high-grade non-muscle invasive bladder cancer
European Urology Open Science
vol.
15
10.1016/s1569-9056(16)60938-7
Kitchen MO, Bryan RT, Emes RD, Glossop JR, Luscombe C, Cheng KK, Zeegers MP, James ND et al.
2016
Quantitative genome-wide methylation analysis of high-grade non-muscle invasive bladder cancer
Epigenetics
vol.
11
237
246
10.1080/15592294.2016.1154246
Kokkinopoulos I, Ishida H, Saba R, Ruchaya P, Cabrera C, Struebig M, Barnes M, Terry A et al.
2015
Single-Cell Expression Profiling Reveals a Dynamic State of Cardiac Precursor Cells in the Early Mouse Embryo
PLOS ONE
vol.
10
10
10.1371/journal.pone.0140831
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
474
477
10.5021/ad.2015.27.4.474
Yousaf N, Low WY, Onipinla A, Mein C, Caulfield M, Munroe PB, Chernajovsky Y
2015
Differences between disease-associated endoplasmic reticulum aminopeptidase 1 (ERAP1) isoforms in cellular expression, interactions with tumour necrosis factor receptor 1 (TNF-R1) and regulation by cytokines
Clinical & Experimental Immunology
vol.
180
289
304
10.1111/cei.12575
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
751
759
10.1097/sla.0000000000000653
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
751
759
10.1097/SLA.0000000000000653
Bulmer DC, Botha CA, Wheeldon A, Grey K, Mein CA, Lee K, Knowles CH, Winchester WJ et al.
2015
Evidence of a role for GTP cyclohydrolase‐1 in visceral pain
Neurogastroenterology & Motility
vol.
27
656
662
10.1111/nmo.12538
Martineau AR, MacLaughlin BD, Hooper RL, Barnes NC, Jolliffe DA, Greiller CL, Kilpin K, McLaughlin D et al.
2015
Double-blind randomised placebo-controlled trial of bolus-dose vitamin D3 supplementation in adults with asthma (ViDiAs)
Thorax
vol.
70
10.1136/thoraxjnl-2014-206449
Rautanen A, Mills TC, Gordon AC, Hutton P, Steffens M, Nuamah R, Chiche J-D, Parks T et al.
2014
Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study
The Lancet Respiratory Medicine
vol.
53
60
10.1016/s2213-2600(14)70290-5
Haworth KE, Farrell WE, Emes RD, Ismail KM, Carroll WD, Hubball E, Rooney A, Yates AM et al.
2014
Methylation of the FGFR2 gene is associated with high birth weight centile in humans
Epigenomics
vol.
477
491
10.2217/epi.14.40
Jolliffe D, Martineau A, James W, Islam K, Mein C, Timms P, Walton R, Griffiths C
2014
M145 Prevalence And Determinants Of Vitamin D Deficiency In Patients With Chronic Obstructive Pulmonary Disease
Thorax
vol.
69
a215
a216
10.1136/thoraxjnl-2014-206260.440
Jolliffe D, Martineau A, Maclaughlin B, Kiplin K, Timms P, Mein C, Walton R, Griffiths C
2014
P48 Prevalence And Determinants Of Vitamin D Deficiency In Asthma Patients
Thorax
vol.
69
a94
a95
10.1136/thoraxjnl-2014-206260.189
Fryer AA, Emes RD, Ismail KMK, Haworth KE, Mein C, Carroll WD, Farrell WE
2014
Quantitative, high-resolution epigenetic profiling of CpG loci identifies associations with cord blood plasma homocysteine and birth weight in humans
Epigenetics
vol.
86
94
10.4161/epi.6.1.13392
Carter JA, Górecki DC, Mein CA, Ljungberg B, Hafizi S
2014
CpG dinucleotide-specific hypermethylation of the TNS3 gene promoter in human renal cell carcinoma
Epigenetics
vol.
739
747
10.4161/epi.25075
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
10.1186/1757-7241-22-s1-o7
Addison S, Munroe P, Mein C, Cohen M, Fowler D, Sebire N, Peebles D, Taylor A et al.
2014
8.2 Cardiac Ion Channelopathies in Unexplained Stillbirths
Archives of Disease in Childhood Fetal & Neonatal
vol.
99
Suppl 1
10.1136/archdischild-2014-306576.31
Hill MJ, Donocik JG, Nuamah RA, Mein CA, Sainz-Fuertes R, Bray NJ
2014
Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells
Schizophrenia Research
vol.
153
1-3
225
230
10.1016/j.schres.2014.01.034
Riebler A, Menigatti M, Song JZ, Statham AL, Stirzaker C, Mahmud N, Mein CA, Clark SJ et al.
2014
BayMeth: improved DNA methylation quantification for affinity capture sequencing data using a flexible Bayesian approach
Genome Biology
vol.
15
10.1186/gb-2014-15-2-r35
Torrance HDT, 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
Suppl 1
O7
O7
10.1186/1757-7241-22-s1-o7
Okosun J, Bödör C, Wang J, Araf S, Yang CY, Pan C, Boller S, Cittaro D et al.
2014
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma
Nature Genetics
vol.
46
176
181
10.1038/ng.2856
Okosun J, Bödör C, Wang J, Araf S, Yang C-Y, Pan C, Boller S, Cittaro D et al.
2013
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma
Nature Genetics
vol.
46
176
181
10.1038/ng.2856
Riebler A, Menigatti M, Song JZ, Statham AL, Stirzaker C, Mahmud N, Mein CA, Clark SJ et al.
2013
BayMeth: Improved DNA methylation quantification for affinity capture sequencing data using a flexible Bayesian approach
10.48550/arxiv.1312.3115
Pryce G, Visintin C, Ramagopalan SV, Al‐Izki S, De Faveri LE, Nuamah RA, Mein CA, Montpetit A et al.
2013
Control of spasticity in a multiple sclerosis model using central nervous system‐excluded CB1 cannabinoid receptor agonists
The FASEB Journal
vol.
28
117
130
10.1096/fj.13-239442
Coussens AK, Wilkinson RJ, Nikolayevskyy V, Elkington PT, Hanifa Y, Islam K, Timms PM, Bothamley GH et al.
2013
Ethnic Variation in Inflammatory Profile in Tuberculosis
PLOS Pathogens
vol.
10.1371/journal.ppat.1003468
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
10.1038/nature12170
Coussens AK, Wilkinson RJ, Nikolayevskyy V, Elkington PT, Hanifa Y, Islam K, Timms PM, Bothamley GH et al.
2013
Ethnic variation in inflammatory profile in tuberculosis
PLoS Pathog
vol.
10.1371/journal.ppat.1003468
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
10.1038/nature12170
Martineau A, Coussens A, Nikolayevskyy V, Elkington P, Bothamley G, Packe G, Darmalingam M, Drobniewski F et al.
2012
S2 Ethnic Variation in Inflammatory Profile in Tuberculosis
Thorax
vol.
67
10.1136/thoraxjnl-2012-202678.008
Gueorguiev M, Lecoeur C, Meyre D, Benzinou M, Mein CA, Hinney A, Vatin V, Weill J et al.
2012
Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity
Obesity
vol.
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Inflammatory Transcriptome Profiling of Human Monocytes Exposed Acutely to Cigarette Smoke
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Blood Pressure Loci Identified with a Gene-Centric Array
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Retinoic Acid–Induced Pancreatic Stellate Cell Quiescence Reduces Paracrine Wnt–β-Catenin Signaling to Slow Tumor Progression
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Harlequin Ichthyosis: A Review of Clinical and Molecular Findings in 45 Cases
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Blood
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Maeda E, Fleischmann C, Mein CA, Shelton JC, Bader DL, Lee DA
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Functional analysis of tenocytes gene expression in tendon fascicles subjected to cyclic tensile strain
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Homozygous Mutations in the 5′ Region of the JUP Gene Result in Cutaneous Disease but Normal Heart Development in Children
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WWOX tumour suppressor gene polymorphisms and ovarian cancer pathology and prognosis
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A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure
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Integrated Functional, Gene Expression and Genomic Analysis for the Identification of Cancer Targets
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Gueorguiev M, Lecoeur C, Benzinou M, Mein CA, Meyre D, Vatin V, Weill J, Heude B et al.
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A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature
Annals of Human Genetics
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Successful amplification of degraded DNA for use with high‐throughput SNP genotyping platforms
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Distinctive Patterns of MicroRNA Expression Associated with Karyotype in Acute Myeloid Leukaemia
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Dobson RJB, Munroe PB, Mein CA, Caulfield MJ, Saqi MAS
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Combining Protein-Protein Interaction (PPI) Network and Sequence Attributes for Predicting Hypertension Related Proteins
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Methylation profiling in 158 cases of previously untreated follicular lymphoma (FL)
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A new variation in the promoter region, the −604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance
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Association of MicroRNA Expression Profiles with Karyotype in Acute Myeloid Leukaemias Revealed by Real-Time PCR and In Situ Hybridisation
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Examining the Candidacy of Ghrelin as a Gene Responsible for Variation in Adult Stature in a United Kingdom Population with Type 2 Diabetes
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Identifying Mutations in Single Gene Disorders
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Sinclair C, O'Toole EA, Paige D, Mein CA, Kelsell DP
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A comprehensive survey of 28 candidate genes for atopic dermatitis using a hapTAG approach in a unique Bangladeshi population of East London
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The South African “Bathing Suit Ichthyosis” Is a Form of Lamellar Ichthyosis Caused by a Homozygous Missense Mutation, p.R315L, in Transglutaminase 1
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A Molecular Genetic and Statistical Approach for the Diagnosis of Dual-Site Cancers
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NO ASSOCIATION OF THE WNK1 GENE WITH ESSENTIAL HYPERTENSION IN THE MRC BRIGHT STUDY
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Haplotype Structure, LD Blocks, and Uneven Recombination Within the LRP5 Gene
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Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes
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Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome
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Adiponectin gene is associated with obesity and obesity correlated traits in childhood
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10.21203/rs.3.rs-1179128/v1
Cardoso S, Ogunkolade BW, Lowe R, Savage E, Mein CA, Boucher BJ, Hitman GA
Areca catechu-(Betel-nut)-induced whole transcriptome changes associated with diabetes, obesity and metabolic syndrome in a human monocyte cell line
10.1101/2020.08.03.233932
Mesnage R, Ibragim M, Mandrioli D, Falcioni L, Tibaldi E, Belpoggi F, Brandsma I, Bourne E et al.
Comparative toxicogenomics of glyphosate and Roundup herbicides by mammalian stem cell-based genotoxicity assays and molecular profiling in Sprague-Dawley rats
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Jacobs BM, Schalk L, Tregaskis-Daniels E, Scalfari A, Nandoskar A, Dunne A, Gran B, Mein CA et al.
Genetic determinants of Multiple Sclerosis susceptibility in diverse ancestral backgrounds
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Mesnage R, Panzacchi S, Bourne E, Mein CA, Perry MJ, Hu J, Chen J, Mandrioli D et al.
Glyphosate and its formulations Roundup Bioflow and RangerPro alter bacterial and fungal community composition in the rat caecum microbiome
10.1101/2021.11.19.468976
Gisby JS, Purcell R, Withnell I, Cabrera CP, Watson DS, Masarone S, Hernández Mir G, Savage E et al.
Human-porcine transcriptomics reveals resuscitation-responsive pathways in trauma shock
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Integrated transcriptomics and metabolomics reveal signatures of lipid metabolism dysregulation in HepaRG liver cells exposed to PCB 126
10.1101/259093
Farinha J, Clausi M, Pardo FOC, Sanchez-Perea N, Boot J, Mein CA, Yip P, Paredes UM
Intergenerational transmission of parental rejection effects on survival, behaviour, and miRNA expression in owl monkeys
10.1101/2024.12.20.629709
Carbajosa G, Malki K, Lawless N, Wang H, Ryder JW, Wozniak E, Wood K, Mein CA et al.
Loss of Trem2 in microglia leads to widespread disruption of cell co-expression networks in mouse brain
10.1101/248757
Vinel C, Boot J, Jin W, Pomella N, Mein C, Zabet NR, Marino S
Mapping chromatin remodelling in glioblastoma identifies epigenetic regulation of key molecular pathways and novel druggable targets
10.1101/2024.02.24.581853
Farinha J, Clausi-Marroquin M, Pardo FOC, Sánchez-Perea N, Mein CA, Yip P, Paredes UM
Maternal rejecting of newborns is epigenetic, intergenerationally transmitted and associated with altered miRNAs expression in owl monkeys
10.1101/2025.07.01.662553
Mesnage R, Teixeira M, Mandrioli D, Falcioni L, Ducarmon QR, Zwittink RD, Amiel C, Panoff J-M et al.
Multi-omics phenotyping of the gut-liver axis allows health risk predictability from in vivo subchronic toxicity tests of a low-dose pesticide mixture
10.1101/2020.08.25.266528
Vadgama A, Boot J, Allan HE, Mein CA, Armstrong PC, Warner TD
Multi-parameter phenotyping of platelets and characterisation of the effects of agonists using machine learning
10.1101/2023.12.08.570628
Ponnusamy V, Ip R, Mohamed M, Clarke P, Wozniak E, Mein C, Schwendimann L, Barlas A et al.
Novel mechanism of action for neuronal let-7b-5p in neonatal encephalopathy through the Hippo pathway
10.21203/rs.3.rs-337473/v1
Turner DC, Raastad T, Ullrich M, Christiansen SF, Sutherland H, Boot J, Wozniak E, Mein C et al.
Repeated disuse atrophy imprints a molecular memory in skeletal muscle: transcriptional resilience in young adults and susceptibility in aged muscle
10.1101/2025.10.16.681134
Humphreys DT, Lewis A, Pan-Castillo B, Berti G, Mein C, Wozniak E, Gordon H, Gadhok R et al.
Single cell sequencing data identify distinct B cell and fibroblast populations in stricturing Crohn’s disease
10.1101/2023.09.04.556163
Morgan OB, Singleton S, Hestehave S, Sarter T, Wozniak E, Mein CA, Hausch F, Bell CG et al.
Stress, Epigenetic Remodeling and FKBP51: Pathways to Chronic Pain Vulnerability
10.1101/2025.01.07.631709
Carbajosa G, Malki K, Lawless N, Wang H, Ryder JW, Wozniak E, Wood K, Mein CA et al.
TREM2 impacts brain microglia, oligodendrocytes and endothelial co-expression modules revealing genes and pathways important in Alzheimer’s disease
10.1101/2021.07.16.452732
Acton RJ, Yuan W, Gao F, Xia Y, Bourne E, Wozniak E, Bell J, Lillycrop K et al.
The Genomic Loci of Specific Human tRNA Genes Exhibit Ageing-Related DNA Hypermethylation
10.1101/870352
Millner T, Panday P, Xiao Y, Boot, Nicholson J, Arpe Z, Stevens P, Rahman N et al.
The inflammatory micro-environment induced by targeted CNS radiotherapy is underpinned by disruption of DNA methylation
10.1101/2024.03.04.581366
Higham JP, Bhebhe CN, Gupta RA, Tranter M, Barakat FM, Dogra H, Bab N, Wozniak E et al.
Transcriptomic profiling reveals a pro-nociceptive role for Angiotensin II in inflammatory bowel disease
10.1101/2023.06.16.545265
Maiarù M, Acton RJ, Woźniak EL, Mein CA, Bell CG, Géranton SM
Using the DNA methylation profile of the stress driver gene FKBP5 for chronic pain diagnosis
10.1101/2022.12.22.521573
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