Suchergebnisse - Sergi Villatoro
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1
Human inversions and their functional consequences von Marta Puig, Sònia Casillas, Sergi Villatoro, Mario Cáceres
Veröffentlicht 2015Revisão -
2
Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system von Elisa Docampo, Geòrgia Escaramís, Mónica Gratacòs, Sergi Villatoro, Anna Puig, Manolis Kogevinas, Antonio Collado, Jordi Carbonell, Javier Rivera, Javier Vidal, José Alegre, Xavier Estivill, Raquel Rabionet
Veröffentlicht 2014Artigo -
3
Evolutionary and functional impact of common polymorphic inversions in the human genome von Carla Giner-Delgado, Sergi Villatoro, Jon Lerga-Jaso, Magdalena Gayà‐Vidal, Meritxell Oliva, David Castellano, Lorena Pantano, Bárbara Domingues Bitarello, David Izquierdo, Isaac Noguera, Íñigo Olalde, Alejandra Delprat, Antoine Blancher, Carles Lalueza‐Fox, Tõnu Esko, Paul F. O’Reilly, Aida M. Andrés, Luca Ferretti, Marta Puig, Mario Cáceres
Veröffentlicht 2019Artigo -
4
Prospective detection of mutations in cerebrospinal fluid, pleural effusion, and ascites of advanced cancer patients to guide treatment decisions von Sergi Villatoro, Clara Mayo‐de‐las‐Casas, Núria Jordana‐Ariza, Santiago Viteri, Mónica Garzón‐Ibáñez, Irene Moya‐Horno, Beatriz García‐Peláez, María González‐Cao, Umberto Malapelle, Ariadna Balada‐Bel, Alejandro Martínez‐Bueno, Raquel Munhoz da Silveira Campos, Noemı́ Reguart, Margarita Majem, Remei Blanco, Ana Blasco, María José Catalán, Xavier González, Giancarlo Troncone, Niki Karachaliou, Rafael Rosell, Miguel Ángel Molina‐Vila
Veröffentlicht 2019Artigo -
5
Liquid Biopsy in Non-Small Cell Lung Cancer von Miguel Ángel Molina‐Vila, Clara Mayo‐de‐las‐Casas, Ana Giménez‐Capitán, Núria Jordana‐Ariza, Mónica Garzón, Ariadna Balada, Sergi Villatoro, Cristina Teixidó, Beatriz García‐Peláez, Cristina Aguado, María José Catalán, Raquel Munhoz da Silveira Campos, Ana Pérez-Rosado, Jordi Bertran‐Alamillo, Alejandro Martínez‐Bueno, María-de-los-Llanos Gil, María González‐Cao, Xavier González, Daniela Morales-Espinosa, Santiago Viteri, Niki Karachaliou, Rafael Rosell
Veröffentlicht 2016Revisão -
6
Large scale, prospective screening of EGFR mutations in the blood of advanced NSCLC patients to guide treatment decisions von Clara Mayo‐de‐las‐Casas, Núria Jordana‐Ariza, Mónica Garzón‐Ibáñez, Ariadna Balada‐Bel, Jordi Bertran‐Alamillo, Santiago Viteri, Noemı́ Reguart, M. A. Muñoz-Quintana, Pilar Lianes-Barragán, Carlos Camps, Eloísa Jantus‐Lewintre, J. Remon-Massip, Silvia Calabuig‐Fariñas, David Aguiar, M.L. Vilardell Gil, Núria Viñolas, A.K. Santos-Rodríguez, Margarita Majem, Beatriz García‐Peláez, Sergi Villatoro, Ana Pérez-Rosado, J.C. Monasterio, E. Ovalle, M.J. Catalán, Raquel Munhoz da Silveira Campos, Daniela Morales-Espinosa, Alejandro Martínez‐Bueno, María González‐Cao, Xavier González, Irene Moya‐Horno, Aaron E. Sosa, Niki Karachaliou, Rafael Rosell, Miguel Ángel Molina‐Vila
Veröffentlicht 2017Artigo -
7
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus von Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D. Beckmann, Guðmar Þorleifsson, Marco Belfiore, Sonia Bouquillon, Dominique Campion, Nicole de Leeuw, Bert B.A. de Vries, Tõnu Esko, Bridget A. Fernandez, Fernando Fernández‐Aranda, José Manuel Fernández‐Real, Mónica Gratacòs, Audrey Guilmatre, Juliane Hoyer, Marjo‐Riitta Järvelin, R. Frank Kooy, Ants Kurg, Cédric Le Caignec, Katrin Männik, Orah S. Platt, Damien Sanlaville, Mieke M. van Haelst, Sergi Villatoro, Faida Walha, Bai-Lin Wu, Yongguo Yu, Azzedine Aboura, Marie‐Claude Addor, Yves Alembik, Stylianos E. Antonarakis, Benoı̂t Arveiler, Magalie Barth, Nathalie Bednarek, Frédérique Béna, Sven Bergmann, Mylène Béri, Laura Bernardini, Bettina Blaumeiser, Dominique Bonneau, Armand Bottani, Odile Boute, Han G. Brunner, Dorothée Cailley, Patrick Callier, Jean Chiésa, Jacqueline Chrast, Lachlan Coin, Charles Coutton, Jean‐Marie Cuisset, J. Cuvellier, Albert David, Bénédicte de Fréminville, Bruno Delobel, Marie‐Ange Delrue, Bénédicte Demeer, Dominique Descamps, Gérard Didelot, Klaus Dieterich, Vittoria Disciglio, Martine Doco‐Fenzy, Séverine Drunat, Bénédicte Duban‐Bedu, Christèle Dubourg, Julia S. El-Sayed Moustafa, Paul Elliott, Brigitte H. W. Faas, Laurence Faivre, Anne Faudet, Florence Fellmann, Alessandra Ferrarini, Richard Fisher, Elisabeth Flori, Lukas Forer, Dominique Gaillard, Marion Gérard, Christian Gieger, Stefania Gimelli, Giorgio Gimelli, Hans J. Grabe, Agnès Guichet, Olivier Guillin, Anna‐Liisa Hartikainen, Delphine Héron, Loyse Hippolyte, Muriel Holder, Georg Homuth, Bertrand Isidor, Sylvie Jaillard, Zdenek Jaros, Susana Jiménez‐Múrcia, Géraldine Joly Helas
Veröffentlicht 2011Artigo
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Gene
Genetics
Medicine
Internal medicine
Cancer
Computational biology
Genome
Lung cancer
Neuroscience
Pathology
Adaptation (eye)
Biopsy
Evolutionary biology
Genotype
Human genome
Liquid biopsy
Oncology
Phenotype
Psychiatry
Single-nucleotide polymorphism
Anorexia nervosa
Ascites
Body mass index
Cancer research
Central nervous system
Cerebrospinal fluid
Chromosomal inversion
Chromosome
Copy-number variation