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Matthieu Joseph Miossec
Matthieu Joseph Miossec
Head of Computational Genomics Group, Centre for Human Genetics, University of Oxford
在 well.ox.ac.uk 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Whole exome sequencing reveals the major genetic contributors to nonsyndromic tetralogy of Fallot
DJ Page, MJ Miossec, SG Williams, RM Monaghan, E Fotiou, HJ Cordell, ...
Circulation research 124 (4), 553-563, 2019
1632019
Integration of target discovery, drug discovery and drug delivery: a review on computational strategies
Y Duarte, V Márquez‐Miranda, MJ Miossec, F González‐Nilo
Wiley Interdisciplinary Reviews: Nanomedicine and Nanobiotechnology 11 (4 …, 2019
502019
In-Depth Genomic and Phenotypic Characterization of the Antarctic Psychrotolerant Strain Pseudomonas sp. MPC6 Reveals Unique Metabolic Features, Plasticity …
M Orellana-Saez, N Pacheco, JI Costa, KN Mendez, MJ Miossec, ...
Frontiers in microbiology 10, 1154, 2019
462019
Mitotic DNA synthesis is caused by transcription-replication conflicts in BRCA2-deficient cells
FJ Groelly, RA Dagg, M Petropoulos, GG Rossetti, B Prasad, ...
Molecular Cell 82 (18), 3382-3397. e7, 2022
272022
Evaluation of computational methods for human microbiome analysis using simulated data
MJ Miossec, SL Valenzuela, M Pérez-Losada, WE Johnson, KA Crandall, ...
PeerJ 8, e9688, 2020
232020
Computational methods for human microbiome analysis
MJ Miossec, SL Valenzuela, KN Mendez, E Castro‐Nallar
Current Protocols in Microbiology 47 (1), 1E. 14.1-1E. 14.17, 2017
62017
Identification of grapevine clones via high-throughput amplicon sequencing: a proof-of-concept study
C Urra, D Sanhueza, C Pavez, P Tapia, G Núñez-Lillo, A Minio, ...
G3: Genes, Genomes, Genetics 13 (9), jkad145, 2023
52023
Deleterious genetic variants in NOTCH1 are a major contributor to the incidence of non-syndromic Tetralogy of Fallot
DJ Page, MJ Miossec, SG Williams, E Fotiou, RM Monaghan, HJ Cordell, ...
BioRxiv, 300905, 2018
22018
Scientific business abstracts of the 113th annual meeting of the Association of Physicians of Great Britain and Ireland
TM Cacciottolo, A Perikari, A van der Klaauw, E Henning, LKJ Stadler, ...
QJM: An International Journal of Medicine 112 (9), 724-729, 2019
12019
Genome sequence of two members of the chloroaromatic-degrading MT community: Pseudomonas reinekei MT1 and Achromobacter xylosoxidans MT3
I Gutierrez-Urrutia, MJ Miossec, SL Valenzuela, C Meneses, ...
Journal of biotechnology 275, 13-16, 2018
12018
GeneFEAST: the pivotal, gene-centric step in functional enrichment analysis interpretation
A Taylor, VM Macaulay, AK Maurya, MJ Miossec, FM Buffa
arXiv preprint arXiv:2309.00061, 2023
2023
Cardiomyocyte tetrahydrobiopterin synthesis regulates fatty acid metabolism and susceptibility to ischaemia–reperfusion injury
SM Chu, LC Heather, S Chuaiphichai, T Nicol, B Wright, M Miossec, ...
Experimental Physiology, 2023
2023
Cardiomyocyte Tetrahydrobiopterin Synthesis Regulates Fatty Acid Metabolism and Susceptibility to Ischemia Reperfusion Injury
SM Chu, LC Heather, S Chuaiphichai, T Nicol, B Wright, M Miossec, ...
Available at SSRN 4151379, 2022
2022
Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland: Whole exome sequencing reveals the major genetic …
D Page, M Miossec, S Williams, R Monaghan, E Fotiou, ...
QJM: an international journal of medicine 112 (9), 728-729, 2019
2019
C Identification of the major genetic contributors to tetralogy of fallot
DJ Page, MJ Miossec, SG Williams, RM Monaghan, E Fotiou, HJ Cordell, ...
Heart 105 (Suppl 6), A182-A183, 2019
2019
Brugada syndrome caused by a 3p22.2 deletion including SCN5A and SCN10A defined using medium coverage whole exome sequencing
R Jewell, S Clasper, SP Page, CM Watson, O Claber, C Hayes, ...
Genomics and Molecular Cardiology, 2019
2019
Whole-Exome Capture and Next-Generation Sequencing to discover rare variants predisposing to congenital heart disease
MJ Miossec
Newcastle University, 2016
2016
Analysis of rare variants and CNVs in non-syndromic tetralogy of Fallot
J Goodship, M Miossec, D Brown, I Wilson, L Sutcliffe, A Topf, K Devriendt, ...
American Society of Human Genetics Annual Meeting (ASHG), 2015
2015
Investigating the cause of transposition of great arteries; exome sequencing analysis
WU Bada, MJ Miossec, R Hussain, T Rahman, A Topf, D Hall, ...
European Heart Journal 35, 581-581, 2014
2014
P328 Investigating the cause of transposition of great arteries.
WU Bada, MJ Miossec, R Hussain, J Goodship, B Keavney
Cardiovascular Research 103, 2014
2014
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