Browsing by Author Estivill, Xavier, 1955-
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| Issue Date | Title | Author(s) |
|---|---|---|
| 26-Apr-2019 | eDiVA - Classification and prioritization of pathogenic variants for clinical diagnostics | Bosio, Mattia; Drechsel, Oliver; Rahman, Rubayte; Muyas, Francesc; Rabionet Janssen, Raquel; Bezdan, Daniela; Domenech Salgado, Laura; Hor, Hyun G.; Schott, Jean-Jacques; Munell Casadesús, Francina; Colobran, Roger; Macaya Ruiz, Alfons; Estivill, Xavier, 1955-; Ossowski, Stephan |
| 19-Feb-2021 | Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation | Susak, Hana; Serra-Saurina, Laura; Demidov, German; Rabionet Janssen, Raquel; Domènech, Laura; Bosio, Mattia; Muyas, Francesc; Estivill, Xavier, 1955-; Escaramís Babiano, Geòrgia; Ossowski, Stephan |
| 4-Oct-2019 | Epigenetic modification of the pentose phosphate pathway and the IGF-axis in women with gestational diabetes mellitus | Steyn, Angela; Crowther, Nigel J.; Norris, Shane A.; Rabionet Janssen, Raquel; Estivill, Xavier, 1955-; Ramsay, Michèle |
| 2000 | Errors congènits del metabolisme (ECM). | Pàmpols i Ros, Teresa; Arranz, J. A.; Artuch Iriberri, Rafael; Baiget Bastús, Montserrat; Borja, F.; Briones, P.; Casals, T.; Chabás, A.; Coll, M. J.; Rio, E. del; Domínguez, C.; Estivill, Xavier, 1955-; Gallano, Pia; Giròs, Marisa; Martínez, M.; Maya, A.; Milà i Recasens, Montserrat; Margarit, E.; Nunes Martínez, Virginia; Oriola Ambrós, Josep |
| 25-Feb-2000 | Estudi clinicopatòlogic i genètic del melanoma maligne i de la síndrome del nevus displàstic. | Puig i Sardà, Susana |
| 29-Mar-2016 | Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia | Costas, Javier; Carrera, Noa; Alonso, Pino; Gurriarán, X.; Segalàs Cosi, Cinto; Real, Eva; López Solà, Clara; Mas Herrero, Sergi; Gassó Astorga, Patricia; Domènech, Lluis; Morell, Marta; Quintela, Inés; Lázaro García, Luisa; Menchón Magriñá, José Manuel; Estivill, Xavier, 1955-; Carracedo, Arkaitz |
| 15-Jul-1993 | Expression cloning of a human renal cDNA that induces high affinity transport of L-cystine shared with dibasic amino acids in Xenopus oocytes | Bertran, Joan; Werner, Andreas; Chillarón Chaves, José Julio; Nunes Martínez, Virginia; Biber, Jürg; Testar, Xavier; Zorzano Olarte, Antonio; Estivill, Xavier, 1955-; Murer, Heini; Palacín Prieto, Manuel |
| 27-Jun-2012 | Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa | Müller, Timo D.; Greene, Brandon H.; Bellodi, Laura; Cavallini, Maria C.; Cellini, Elena; Bella, Daniela Di; Ehrlich, Stefan; Erzegovesi, Stefano; Estivill, Xavier, 1955-; Fernández Aranda, Fernando; Fichter, Manfred M.; Fleischhaker, Christian; Scherag, Susan; Gratacòs, Mònica; Grallert, Harald; Herpertz Dahlmann, Beate; Herzog, Wolfgang; Illig, Thomas; Lehmkuhl, Ulrike; Nacmias, Benedetta; Ribasés Haro, Marta; Ricca, Valdo; Schäfer, Helmut; Scherag, André; Sorbi, Sandro; Wichmann, H.-Erich; Hebebrand, Johannes; Hinney, Anke |
| 11-Jan-2008 | Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility | Solé Acha, Xavier; Hernández, Pilar; López de Heredia, Miguel; Armengol, Lluís; Rodríguez Santiago, Benjamín; Gómez, Laia; Maxwell, Christopher A.; Aguiló Lúcia, Fernando; Condom i Mundó, Enric; Abril, Jesús; Pérez Jurado, Luis; Estivill, Xavier, 1955-; Nunes Martínez, Virginia; Capellá, G. (Gabriel); Gruber, Stephen B.; Moreno Aguado, Víctor; Pujana Genestar, M. Ángel |
| 7-Dec-2016 | Genetic architecture distinguishes systemic juvenile idiopathic arthritis from otherforms of juvenile idiopathic arthritis: clinical and therapeutic implications | Ombrello, Michael J.; Arthur, Victoria L.; Remmers, Elaine F.; Hinks, Anne; Tachmazidou, Ioanna; Grom, Alexei A.; Foell, Dirk; Martini, Alberto; Gattorno, Marco; Ozen, Seza; Prahalad, Sampath; Zeft, Andrew S.; Bohnsack, John F.; Ilowite, Norman T.; Mellins, Elizabeth D.; Russo, Ricardo; Len, Claudio A.; Odete e Hilario, Maria; Oliveira, Sheila; Yeung, Rae S. M.; Rosenberg, Alan M.; Wedderburn, Lucy R.; Antón López, Jordi; Haas, Johannes-Peter; Rosen-Wolff, Angela; Minden, Kirsten; Tenbrock, Klaus; Demirkaya, Erkan; Cobb, Joanna; Baskin, Elizabeth; Signa, Sara; Shuldiner, Emily; Duerr, Richard H.; Achkar, Jean-Paul; Kamboh, M. Ilyas; Kaufman, Kenneth M.; Kottyan, Leah C.; Pinto, Dalila; Scherer, Stephen W.; Alarcón Riquelme, Marta; Docampo, Elisa; Estivill, Xavier, 1955-; Gül, Ahmet; British Society of Pediatric and Adolescent Rheumatology (BSPAR) Study Group; Inception Cohort of Newly Diagnosed Patients with Juvenile Idiopathic Arthritis (ICON-JIA) Study Group; Childhood Arthritis Prospective Study (CAPS) Group; Randomized Placebo Phase Study of Rilonacept in sJIA (RAPPORT) Investigators; Sparks-Childhood Arthritis Response to Medication Study (CHARMS) Group; Biologically Based Outcome Predictors in JIA (BBOP) Group Carl D Langefeld; Thompson, Susan; Zeggini, Eleftheria; Kastner, Daniel L.; Woo, Patricia; Thomson, Wendy |
| 23-Feb-2011 | Genetic variants of the FADS gene cluster and ELOVL gene family, colostrums LC-PUFA levels, breastfeeding, and child cognition | Morales, Eva; Bustamante Pineda, Mariona; González, Juan R.; Guxens, Mònica; Torrent, Maties; Méndez, Michelle; García-Esteban, Raquel; Julvez, Jordi; Forns, Joan; Vrijheid, Martine; Moltó-Puigmartí, Carolina; López Sabater, María del Carmen; Estivill, Xavier, 1955-; Sunyer Deu, Jordi |
| Jun-2014 | Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system | Docampo Martínez, Elisa; Escaramís Babiano, Geòrgia; Gratacòs, Mònica; Villatoro, Sergi; Puig, Anna; Kogevinas, Manolis; Collado, Antonio; Carbonell, Jordi; Rivera, Javier; Vidal, Javier; Alegre, Jose; Estivill, Xavier, 1955-; Rabionet Janssen, Raquel |
| 1-Aug-2019 | Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa | Watson, Hunna J.; Yilmaz, Zeynep; Thorntont, Laura M.; Hubel, Christopher; Coleman, Jonathan R. I.; Gaspar, Helena A.; Bryois, Julien; Hinney, Anke; Leppa, Virpi M.; Mattheisen, Manuel; Medland, Sarah E.; Jiménez-Murcia, Susana; Forzan, Monica; Zeggini, Eleftheria; Bulik, Cynthia M.; Herpertz-Dahlmann, Beate; Gorwood, Philip; Raevuori, Anu; Keski-Rahkonen, Anna; Helder, Sietske G.; Boden, Joseph M.; Wade, Tracey D.; Sorbi, Sandro; Estivill, Xavier, 1955-; Lin, Bochao Danae; Huckins, Laura M.; Tsitsika, Artemis; Navratilova, Marie; Kennedy, Martin; Favaro, Angela; Pedersen, Nancy L.; Grove, Jakob; Breen, Gerome; Ntalla, Ioanna; Kiezebrink, Kirsty; Seitz, Jochen; Schork, Nicholas J.; Fischer, Krista; Crowley, James J.; Crawford, Steven; Franklin, Christopher S.; Werge, Thomas; Tziouvas, Konstantinos; Giegling, Ina; Gonidakis, Fragiskos; Ehrlich, Stefan; Sullivan, Patrick F.; Klump, Kelly L.; Kaye, Walter H.; Larsen, Janne T.; Dikeos, Dimitris; Dina, Christian; Schosser, Alexandra; Slachtova, Lenka; Palotie, Aarno; Gallinger, Steven; Scherer, Stephen W.; Perica, Vesna Boraska; Kirk, Katherine M.; Birgegård, Andreas; Widen, Elisabeth; Wagner, Gudrun; Rujescu, Dan; Hudson, James I.; Martin, Nicholas G.; Treasure, Janet; Hakonarson, Hakon; Gordon, Scott; Maj, Mario; Monteleone, Palmiero; Dick, Danielle M.; Adan, Roger A. H.; Pantel, Jacques; Reichborn-Kjennerud, Ted; Cichon, Sven; Szatkiewicz, Jin P.; Jordan, Jennifer; Schmidt, Ulrike; Fernández Aranda, Fernando; Egberts, Karin; Esko, Tõnu; Hatzikotoulas, Konstantinos; Pinto, Dalila; Norring, Claes; Giusti-Rodriguez, Paola; Escaramís Babiano, Geòrgia; Degortes, Daniela; Petersen, Liselotte; Walton, Esther; Halmi, Katherine A.; Olsen, Catherine M.; Kas, Martien J. H.; Klareskog, Lars; Tachmazidou, Ioanna; Tozzi, Federica; Johnson, Craig; Egberts, Karin; Karwautz, Andreas; Via, Maria C. La; Meulenbelt, Ingrid; Farmer, Anne; Magistretti, Pierre J.; Papezova, Hana; Mitchell, James; Andreassen, Ole A.; McGuffin, Peter; Woodside, D. Blake; Li, Dong; Hebebrand, Johannes; Cassina, Matteo; Ramoz, Nicolas; Herzog, Wolfgang; Forstner, Andreas J.; Hauser, Joanna; Fichter, Manfred M.; Purves, Kirstin L.; Kaprio, Jaakko; Kennedy, James L.; Davis, Oliver S. P.; Ritschel, Franziska; Tortorella, Alfonso; Herms, Stefan; Mannik, Katrin; Scherag, André; Nacmias, Benedetta; Marsal, Sara; Föcker, Manuel; Baker, Jessica H.; Montgomery, Grant W.; Docampo, Elisa; Rybakowski, Filip; Slof-Op ‘t Landt, Margarita C. T.; Boehm, Ilka; Kaplan, Allan S.; Foretova, Lenka; Roberts, Marion; Monteleone, Alessio Maria; Ripke, Stephan; Ando, Tetsuya; Brandt, Harry; Lilenfeld, Lisa; Lissowska, Jolanta; Dedoussis, George; Hellard, Stephanie Le; Juréus, Anders; Tenconi, Elena; Metspalu, Andres; Pearson, John F.; Knudsen, Gun Peggy S.; Ophoff, Roel A.; Bergen, Andrew W.; Parker, Richard; Mortensen, Preben Bo; Gratacòs, Mònica; Kim, Youl-Ri; Buehren, Katharina; Boni, Claudette; Berrettini, Wade H.; Henders, Anjali K.; Burghardt, Roland; Rotondo, Alessandro; Luykx, Jurjen; Dmitrzak-Weglarz, Monika; Rabionet Janssen, Raquel; Imgart, Hartmut; Zwaan, Martina de; van Furth, Eric F.; Janout, Vladimir; Yao, Shuyang; Tyszkiewicz-Nwafor, Marta; Zipfel, Stephan; Karhunen, Leila; Landén, Mikael; Courtet, Philippe; Padyukov, Leonid; Świątkowska, Beata; Crow, Scott; Strober, Michael; Kaminská, Deborah; Julià, Antonio; Cone, Roger D.; Inoko, Hidetoshi; Mitchell, Karen; Ricca, Valdo; DeSocio, Janiece E.; Danner, Unna N.; Giuranna, Johanna; Slagboom, P. Eline; Horwood, L. John; Lichtenstein, Paul; Slopien, Agnieszka; Alfredsson, Lars; McDevitt, Sara; Guo, Yiran; Ripatti, Samuli; Kalsi, Gursharan; O’Toole, Julie K.; Zerwas, Stephanie; Levitan, Robert D.; Hanscombe, Ken B.; Marshall, Christian R.; Stuber, Garret D.; van Elburg, Annemarie A.; Clementi, Maurizio; Duncan, Laramie E.; Santonastaso, Paolo; Micali, Nadia; Mattingsdal, Morten; Munn-Chernoff, Melissa A.; Guillaume, Sébastien; Whiteman, David C. |
| 3-Jan-2018 | Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics | Beaumont, Robin N.; Warrington, Nicole M.; Cavadino, Alana; Tyrrell, Jessica; Nodzenski, Michael; Horikoshi, Momoko; Geller, Frank; Myhre, Ronny; Richmond, Rebecca C.; Paternoster, Lavinia; Bradfield, Jonathan P.; Kreiner-Moller, Eskil; Huikari, Ville; Metrustry, Sarah; Lunetta, Kathryn L.; Painter, Jodie N.; Hottenga, Jouke-Jan; Allard, Catherine; Barton, Sheila J.; Espinosa Cardiel, Ana; Marsh, Julie A.; Potter, Catherine; Zhang, Ge; Ang, Wei; Berry, Diane J.; Bouchard, Luigi; Das, Shikta; Early Growth Genetics (EGG) Consortium; Hakonarson, Hakon; Heikkinen, Jani; Helgeland, Øyvind; Hocher, Berthold; Hofman, Albert; Inskip, Hazel M.; Jones, Samuel E.; Kogevinas, Manolis; Lind, Penelope A.; Marullo, Letizia; Medland, Sarah E.; Murray, Anna; Murray, Jeffrey C.; Njolstad, Pal R.; Nohr, Ellen Aagard; Reichetzeder, Christoph; Ring, Susan M.; Ruth, Katherine S.; Santa Marina, Loreto; Scholtens, Denise M.; Sebert, Sylvain; Sengpiel, Verena; Tuke, Marcus A.; Vaudel, Marc; Weedon, Michael N.; Willemsen, Gonneke; Wood, Andrew R.; Yaghootkar, Hanieh; Muglia, Louis J.; Bartels, Meike; Relton, Caroline L.; Pennell, Craig E.; Chatzi, Leda; Estivill, Xavier, 1955-; Holloway, John W.; Boomsma, Dorret I.; Montgomery, Grant W.; Murabito, Joanne M.; Spector, Tim D.; Power, Christine; Järvelin, Marjo-Ritta; Bisgaard, Hans; Grant, Struan F.; Sorensen, Thorkild I. A.; Jaddoe, Vincent W.; Jacobsson, Bo; Melbye, Mads; McCarthy, Mark I.; Hattersley, Andrew T.; Hayes, M. Geoffrey; Frayling, Timothy M.; Hivert, Marie-France; Felix, Janine F.; Hyppönen, Elina; Lowe, William L.; Evans, David M.; Lawlor, Debbie A.; Feenstra, Bjarke; Freathy, Rachel M. |
| 12-Dec-2001 | Identificació de nous gens a la regió cromosòmica 21q22. Caracterització molecular de KCNE2 i KCNE3. | Domenech Gimeno, Anna |
| Jul-2016 | Identification of gene mutations and fusion genes in patients with Sézary Syndrome | Prasad, Aparna; Rabionet Janssen, Raquel; Espinet Solà, Blanca; Zapata, Luis; Puiggros Metje, Anna M.; Melero, Carme; Puig, Anna; Sarria Trujillo, Yaris; Ossowski, Stephan; Garcia-Muret, Maria P.; Estrach Panella, Ma. Teresa (María Teresa); Servitje Bedate, Octavio; Lopez Lerma, Ingrid; Gallardo, Fernando; Pujol, Ramon M.; Estivill, Xavier, 1955- |
| 16-Apr-2013 | Identification of genetic susceptibility factors for fibromyalgia | Docampo Martínez, Elisa |
| 19-Aug-2020 | In utero and childhood exposure to tobacco smoke and multi-layer molecular signatures in children | Vives, Marta; Hernández Ferrer, Carles; Maitre, Léa; Ruiz Arenas, Carlos; Andrusaityte, Sandra; Borràs, Eva; Carracedo Álvarez, Ángel; Casas, Maribel; Chatzi, Leda; Coen, Muireann; Estivill, Xavier, 1955-; González, Juan R.; Grazuleviciene, Regina; Gutzkow, Kristine B.; Keun, Hector C.; Lau, Chung-Ho E.; Cadiou, Solène; Lepeule, Johanna; Mason, Dan; Quintela, Inés; Robinson, Oliver; Sabidó Aguadé, Eduard; Santorelli, Gillian; Schwarze, Per E.; Siskos, Alexandros P.; Slama, Rémy; Vafeiadi, Marina; Martí Puig, Eulàlia; Vrijheid, Martine; Bustamante, Mariona |
| 11-Apr-1991 | Mspl restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene. | Bosch, A.; Kruyer, H.; Nunes Martínez, Virginia; Estivill, Xavier, 1955- |
| 5-Jul-1990 | Mutation analysis in cystic fibrosis | Gasparini, Paolo; Pignatti, P. F.; Novelli, Giuseppe; Dallapiccola, B.; Nunes Martínez, Virginia; Casals, T.; Estivill, Xavier, 1955-; Fernández Muñoz, Esteve; Balassopoulou, A.; Loukopoulos, D.; Lavinha, J.; Simova, L.; Komel, R. |