Matthieu Joseph Miossec

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Eduardo Castro-NallarUniversidad de TalcaZweryfikowany adres z utalca.cl
Claudio MenesesFac. de Agronomía Sist. Naturales/ Fac. de Cs. Biológicas/ Pontificia Universidad Católica de ChileZweryfikowany adres z uc.cl
Sandro ValenzuelaUniversity of HelsinkiZweryfikowany adres z helsinki.fi
Katterinne N. MendezJohannes Gutenberg University MainzZweryfikowany adres z uni-mainz.de
Ignacio Poblete-CastroDepartment of Chemical and Bioprocess Engineering, Universidad de Santiago de ChileZweryfikowany adres z usach.cl
Fernando Danilo Gonzalez Nilo, PhDDirector Center for Bioinformatics and Integrative Biology, Universidad Andres Bello, SantiagoZweryfikowany adres z unab.cl
Yorley DuarteAssociate Professor, Universidad Andrés Bello, Santiago-ChileZweryfikowany adres z unab.cl
Valeria Marquez MirandaUniversidad Andrés BelloZweryfikowany adres z unab.cl
Nicolás PachecoPhD in Biotechnology , Universidad Andrés BelloZweryfikowany adres z uandresbello.edu
Andrés Marcoleta (ORCiD 0000-0003-...Assistant Professor, Department of Biology, Faculty of Science, University of ChileZweryfikowany adres z uchile.cl
Matias Orellana-SaezTesista de Doctorado, Universidad Andrés BelloZweryfikowany adres z uandresbello.edu
Helen LockstoneZweryfikowany adres z well.ox.ac.uk
Giacomo G. RossettiMaître Assistant, University of GenevaZweryfikowany adres z unige.ch
Andreas PanagopoulosPostdoctoral Researcher, University of Zürich, SwitzerlandZweryfikowany adres z dmmd.uzh.ch
Andrew N. BlackfordAssociate Professor, University of OxfordZweryfikowany adres z imm.ox.ac.uk
Michalis PetropoulosPostdoctoral Researcher, University of Geneva, SwitzerlandZweryfikowany adres z unige.ch
Vasilis S. DionellisPostdoctoral Researcher, University of GenevaZweryfikowany adres z unige.ch
Matthias AltmeyerUniversity of ZurichZweryfikowany adres z uzh.ch
Birbal PrasadSanofiZweryfikowany adres z sanofi.com
Fena OchsAssociate Professor BRIC CopenhagenZweryfikowany adres z bric.ku.dk

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Matthieu Joseph Miossec

Head of Computational Genomics SRF, Centre for Human Genetics, University of Oxford

Zweryfikowany adres z well.ox.ac.uk - Strona główna

WES WGS bulk RNA-Seq single-cell spatial transcriptomics


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
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	188	2019
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	65	2019
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	49	2019
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	37	2022
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	25	2020
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	7	2023
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	7	2017
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	2	2018
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	1	2019
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	1	2018
Spatial analysis of rhesus macaque lung tissue shows a key role for vaccination or previous SARS-CoV-2 challenge in immune pulmonary status C Gartlan, FJ Salguero, AR Cross, P Todd, M Bradbury, M Miossec, ... EUROPEAN JOURNAL OF IMMUNOLOGY 54, 1424-1424, 2024		2024
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

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