Marta Bleda

Marta Bleda

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Marta Bleda

Marta Bleda

Publications by authors named "Marta Bleda"

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21Publications

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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.

Authors:
Christopher J Rhodes Ken Batai Marta Bleda Matthias Haimel Laura Southgate Marine Germain Michael W Pauciulo Charaka Hadinnapola Jurjan Aman Barbara Girerd Amit Arora Jo Knight Ken B Hanscombe Jason H Karnes Marika Kaakinen Henning Gall Anna Ulrich Lars Harbaum Inês Cebola Jorge Ferrer Katie Lutz Emilia M Swietlik Ferhaan Ahmad Philippe Amouyel Stephen L Archer Rahul Argula Eric D Austin David Badesch Sahil Bakshi Christopher Barnett Raymond Benza Nitin Bhatt Harm J Bogaard Charles D Burger Murali Chakinala Colin Church John G Coghlan Robin Condliffe Paul A Corris Cesare Danesino Stéphanie Debette C Gregory Elliott Jean Elwing Melanie Eyries Terry Fortin Andre Franke Robert P Frantz Adaani Frost Joe G N Garcia Stefano Ghio Hossein-Ardeschir Ghofrani J Simon R Gibbs John Harley Hua He Nicholas S Hill Russel Hirsch Arjan C Houweling Luke S Howard Dunbar Ivy David G Kiely James Klinger Gabor Kovacs Tim Lahm Matthias Laudes Rajiv D Machado Robert V MacKenzie Ross Keith Marsolo Lisa J Martin Shahin Moledina David Montani Steven D Nathan Michael Newnham Andrea Olschewski Horst Olschewski Ronald J Oudiz Willem H Ouwehand Andrew J Peacock Joanna Pepke-Zaba Zia Rehman Ivan Robbins Dan M Roden Erika B Rosenzweig Ghulam Saydain Laura Scelsi Robert Schilz Werner Seeger Christian M Shaffer Robert W Simms Marc Simon Olivier Sitbon Jay Suntharalingam Haiyang Tang Alexander Y Tchourbanov Thenappan Thenappan Fernando Torres Mark R Toshner Carmen M Treacy Anton Vonk Noordegraaf Quinten Waisfisz Anna K Walsworth Robert E Walter John Wharton R James White Jeffrey Wilt Stephen J Wort Delphine Yung Allan Lawrie Marc Humbert Florent Soubrier David-Alexandre Trégouët Inga Prokopenko Richard Kittles Stefan Gräf William C Nichols Richard C Trembath Ankit A Desai Nicholas W Morrell Martin R Wilkins

Lancet Respir Med 2019 Mar 5;7(3):227-238. Epub 2018 Dec 5.

Department of Medicine, Imperial College London, London, UK. Electronic address:

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http://dx.doi.org/10.1016/S2213-2600(18)30409-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391516PMC
March 2019

Plasma Metabolomics Implicates Modified Transfer RNAs and Altered Bioenergetics in the Outcomes of Pulmonary Arterial Hypertension.

Circulation 2017 01 21;135(5):460-475. Epub 2016 Nov 21.

From the Department of Medicine, Imperial College London, Hammersmith Campus, United Kingdom (C.J.R., P.G., J.W., K.C.R.-A., G.W., M.R.W.); Department of Medicine, University of Cambridge School of Clinical Medicine, United Kingdom (C.H., M.B., M.H., M.R.T., S.G., N.W.M.); Cardiology Department, Royal Free Hospital, London, United Kingdom (G.C.); Institute of Cellular Medicine, Newcastle University and the Newcastle Upon Tyne Hospitals NHS Foundation Trust, United Kingdom (P.A.C.); National Pulmonary Hypertension Service, Imperial College Healthcare NHS Trust, Hammersmith Hospital, London, United Kingdom (L.S.H., J.S.R.G.); National Heart and Lung Institute, Imperial College London, Hammersmith Campus, United Kingdom (L.S.H., J.S.R.G.); Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, United Kingdom (D.G.K.); Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, United Kingdom (D.G.K., A.L.); Scottish Pulmonary Vascular Unit, Golden Jubilee National Hospital, Glasgow, United Kingdom (A.J.P.); Pulmonary Vascular Disease Unit, Papworth Hospital, Cambridge, United Kingdom (J.P.Z., M.R.T.); Pulmonary Hypertension Service, Royal Brompton Hospital, London, United Kingdom (S.J.W.); and Department of Haematology, University of Cambridge, United Kingdom (S.G.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.116.024602DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287439PMC
January 2017

The pan-cancer pathological regulatory landscape.

Sci Rep 2016 12 21;6:39709. Epub 2016 Dec 21.

Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), Valencia, 46012, Spain.

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http://dx.doi.org/10.1038/srep39709DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5175166PMC
December 2016

Web-based network analysis and visualization using CellMaps.

Bioinformatics 2016 10 13;32(19):3041-3. Epub 2016 Jun 13.

Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain Bioinformatics of Rare Diseases (BIER), CIBER de Enfermedades Raras (CIBERER), Valencia, Spain Functional Genomics Node, (INB, PRB2, ISCIII) at CIPF, Valencia 46012, Spain.

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http://dx.doi.org/10.1093/bioinformatics/btw332DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039919PMC
October 2016

267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation.

Mol Biol Evol 2016 05 13;33(5):1205-18. Epub 2016 Jan 13.

Medical Genome Project, Genomics and Bioinformatics Platform of Andalusia (GBPA), Sevilla, Spain Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/Consejo Superior de Investigaciones Científicas/University of Seville, Sevilla, Spain Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Sevilla, Spain

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http://dx.doi.org/10.1093/molbev/msw005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839216PMC
May 2016

Identification of epistatic interactions through genome-wide association studies in sporadic medullary and juvenile papillary thyroid carcinomas.

BMC Med Genomics 2015 Dec 21;8:83. Epub 2015 Dec 21.

Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.

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http://dx.doi.org/10.1186/s12920-015-0160-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685628PMC
December 2015

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.

Sci Rep 2015 Nov 12;5:16473. Epub 2015 Nov 12.

Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.

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http://dx.doi.org/10.1038/srep16473DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642299PMC
November 2015

Babelomics 5.0: functional interpretation for new generations of genomic data.

Nucleic Acids Res 2015 Jul 20;43(W1):W117-21. Epub 2015 Apr 20.

Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), Valencia, 46012, Spain Computational Genomics Chair, Bull-CIPF, Valencia, 46012, Spain Bioinformatics of Rare Diseases (BIER), CIBER de Enfermedades Raras (CIBERER), Valencia, 46012, Spain Functional Genomics Node, (INB) at CIPF, Valencia, 46012, Spain

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http://dx.doi.org/10.1093/nar/gkv384DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489263PMC
July 2015

Pathways systematically associated to Hirschsprung's disease.

Orphanet J Rare Dis 2013 Dec 2;8:187. Epub 2013 Dec 2.

Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Av, Manuel Siurot s/n, Seville, 41013, Spain.

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http://dx.doi.org/10.1186/1750-1172-8-187DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879038PMC
December 2013

Genome Maps, a new generation genome browser.

Nucleic Acids Res 2013 Jul 8;41(Web Server issue):W41-6. Epub 2013 Jun 8.

Department of Computational Genomics, Centro de Investigación Príncipe Felipe, Valencia 46012, Spain.

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http://dx.doi.org/10.1093/nar/gkt530DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692043PMC
July 2013

Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease.

Orphanet J Rare Dis 2012 Dec 28;7:103. Epub 2012 Dec 28.

Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS, University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.

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http://dx.doi.org/10.1186/1750-1172-7-103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575329PMC
December 2012

Inferring the regulatory network behind a gene expression experiment.

Nucleic Acids Res 2012 Jul 11;40(Web Server issue):W168-72. Epub 2012 Jun 11.

Department of Bioinformatics and Genomics, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain.

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http://dx.doi.org/10.1093/nar/gks573DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394273PMC
July 2012

VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing.

Nucleic Acids Res 2012 Jul 11;40(Web Server issue):W54-8. Epub 2012 Jun 11.

Department of Bioinformatics and Genomics, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain.

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http://dx.doi.org/10.1093/nar/gks572DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394276PMC
July 2012

CellBase, a comprehensive collection of RESTful web services for retrieving relevant biological information from heterogeneous sources.

Nucleic Acids Res 2012 Jul 12;40(Web Server issue):W609-14. Epub 2012 Jun 12.

Department of Bioinformatics and Genomics, Centro de Investigación Príncipe Felipe (CIPF), 46012 Valencia, Spain.

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http://dx.doi.org/10.1093/nar/gks575DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394301PMC
July 2012