Browsing by Author Estivill, Xavier, 1955-
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| Issue Date | Title | Author(s) |
|---|---|---|
| 6-Jul-2013 | A Common 56-kilobase deletion in a primate-specific segmental duplication creates a novel Butyrophilin-Like protein | Aigner, Johanna; Villatoro, Sergi; Rabionet Janssen, Raquel; Roquer, Jaume; Jiménez Conde, Jordi; Martí Puig, Eulàlia; Estivill, Xavier, 1955- |
| 2013 | A highly expressed miR-101 isomiR is a functional silencing small RNA | Llorens Torres, Franc; Bañez-Coronel, Mónica; Pantano, Lorena; Río Fernández, José Antonio del; Ferrer, Isidro (Ferrer Abizanda); Estivill, Xavier, 1955-; Martí Puig, Eulàlia |
| 30-Jun-2010 | A myriad of miRNA variants in control and Huntington's disease brain regions detected by massively parallel sequencing | Martí Puig, Eulàlia; Pantano, Lorena; Bañez-Coronel, Mónica; Llorens Torres, Franc; Miñones Moyano, Elena; Porta, Sílvia; Sumoy, Lauro; Ferrer, Isidro (Ferrer Abizanda); Estivill, Xavier, 1955- |
| 23-Feb-2012 | A pathogenic mechanism in Huntington"s disease involves small CAG-repeated RNAs with neurotoxic activity | Bañez-Coronel, Mónica; Porta, Sílvia; Kagerbauer, Birgit; Mateu Huertas, Elisabet; Pantano, Lorena; Ferrer, Isidro (Ferrer Abizanda); Guzmán, Manuel; Estivill, Xavier, 1955-; Martí Puig, Eulàlia |
| 25-May-1990 | A polymorphic DNA probe from chromosome 7 (7q22) | Casals, T.; Nunes Martínez, Virginia; Estivill, Xavier, 1955- |
| 1-Jan-2001 | Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26 | Pujana Genestar, M. Ángel; Nadal, Marga; Gratacòs, Mònica; Peral, Belén; Csiszar, Katalin; González Sarmiento, Rogelio; Sumoy, Lauro; Estivill, Xavier, 1955- |
| 24-Oct-2018 | Allele balance bias identifies systematic genotyping errors and false disease associations | Muyas, Francesc; Bosio, Mattia; Puig, Anna; Susak, Hana; Domènech, Laura; Escaramís Babiano, Geòrgia; Zapata, Luis; Demidov, German; Estivill, Xavier, 1955-; Rabionet Janssen, Raquel; Ossowski, Stephan |
| 3-Nov-1988 | Anàlisi genètica i molecular de la síndrome de Down. Aïllament de gens a la regió cromosòmica 21q22.2-q22.3: identificació i caracterització del gen Minibrain (MNBH) | Guimerà i Vilaró, Jordi |
| 24-Nov-2004 | Anàlisi transcripcional de 15q24-q26: caracterització d'un nou gen expressat al sistema límbic, LRRN6A/LERN1 | Carim Todd, Laura |
| 3-Dec-2012 | Análisis de la herencia epigenética en trastornos neurológicos | Iraola Guzmán, Susana |
| 1-Jul-2012 | Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder | Alonso Ortega, María del Pino; Gratacòs, Mònica; Segalàs Cosi, Cinto; Escaramís Babiano, Geòrgia; Real, Eva; Bayés Colomer, Mònica; Labad, Javier; López Solà, Clara; Estivill, Xavier, 1955-; Menchón Magriñá, José Manuel |
| 1-Jan-2014 | Association Of Irisin With Fat Mass, Resting Energy Expenditure, And Daily Activity In Conditions Of Extreme Body Mass Index | Pardo, María; Crujeiras, Ana B.; Amil, María; Agüera, Zaida; Jiménez-Murcia, Susana; Baños Rivera, Rosa María; Botella Arbona, Cristina; Torre Fornell, Rafael de la; Estivill, Xavier, 1955-; Fagundo, Ana Beatriz; Fernández-Real Lemos, José Manuel; Fernández García, José C.; Fruhbeck, Gema; Gómez Ambrosi, Javier; Rodríguez, Roser; Tinahones, Francisco J.; Fernández Aranda, Fernando; Casanueva, Felipe F. |
| 1995 | Bases moleculars de la cistinúria | Palacín Prieto, Manuel; Mora, Conchi; Chillarón Chaves, José Julio; Calonge, María Julia; Estévez Povedano, Raúl; Torrents, D.; Testar, Xavier; Zorzano Olarte, Antonio; Nunes Martínez, Virginia; Purroy, J.; Nadal, M.; Volpini Bertrán, Víctor; Estivill, Xavier, 1955-; Rousaud, F.; Barceló, P. |
| 14-Mar-2019 | Biallelic loss-of-function LACC1/FAMIN mutations presenting as rheumatoid factor-negative polyarticular juvenile idiopathic arthritis | Rabionet Janssen, Raquel; Remesal, Agustín; Mensa-Vilaró, Anna; Murías, Sara; Alcobendas, Rosa; González-Roca, Eva; Ruiz Ortiz, Estíbaliz; Antón, Jordi; Iglesias Jiménez, Estíbaliz; Modesto, Consuelo; Comas, David; Puig, Anna; Drechsel, Oliver; Ossowski, Stephan; Yagüe, Jordi; Merino, Rosa; Estivill, Xavier, 1955-; Aróstegui Gorospe, Juan Ignacio |
| 1-Apr-2008 | Blood levels of brain-derived neurotrophic factor correlate with several psychopathological symptoms in anorexia nervosa patients | Mercader, Josep M.; Fernández Aranda, Fernando; Gratacòs, Mònica; Ribasés Haro, Marta; Badía, Anna; Villarejo, Cynthia; Solano, Raquel; González, Juan R.; Vallejo Ruiloba, Julio; Estivill, Xavier, 1955- |
| 27-Jan-2022 | Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder | Domènech, Laura; Willis, Jesse; Alemany-Navarro, María; Morey i Ramonell, Marta; Real, Eva; Escaramís Babiano, Geòrgia; Bertolín, Sara; Sánchez Chinchilla, Daniel; Balcells Comas, Susana; Segalàs Cosi, Cinto; Estivill, Xavier, 1955-; Menchón Magriñá, José Manuel; Gabaldón, Toni; Alonso Ortega, María del Pino; Rabionet Janssen, Raquel |
| 5-Mar-2018 | Circulating miRNAs, isomiRs and small RNA clusters in human plasma and breast milk | Rubio, Mercedes; Bustamante Pineda, Mariona; Hernández Ferrer, Carles; Fernández Orth, Dietmar; Pantano, Lorena; Sarria Trujillo, Yaris; Piqué Borras, Maria; Vellve, Kilian; Agramunt, Silvia; Carreras, Ramon; Estivill, Xavier, 1955-; González, Juan Ramón; Mayor Aparicio, Alfredo Gabriel |
| 1-Jan-1995 | Clinical, neuropathologic and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred: (CAG)n expansion and early premonitory signs and symptoms | Genís, David; Matilla-Dueñas, Antoni; Volpini Bertrán, Víctor; Rosell, J.; Dávalos, Antoni; Ferrer, Isidro (Ferrer Abizanda); Molins, Albert; Estivill, Xavier, 1955- |
| 1-Oct-2022 | Common Genetic Variation and Age of Onset of Anorexia Nervosa | Watson, Hunna J.; Thornton, Laura M.; Yilmaz, Zeynep; Baker, Jessica H.; Coleman, Jonathan R. I.; Adan, Roger A. H.; Alfredsson, Lars; Andreassen, Ole A.; Ask, Helga; Berrettini, Wade H.; Boehnke, Michael; Ramoz, Nicolas; Reichborn-Kjennerud, Ted; Ricca, Valdo; Ripatti, Samuli; Ripke, Stephan; Ritschel, Franziska; Roberts, Marion; Rotondo, Alessandro; Rujescu, D.; Boni, Claudette; Zwaan, Martina de; Rybakowski, Filip; Scherag, André; Scherer, Stephen W.; Schmidt, Ulrike; Scott, Laura J.; Seitz, Jochen; Silén, Yasmina; Slachtova, Lenka; Slagboom, P. Eline; Slof-Op't Landt, Margarita C. T.; Dedoussis, George; Buehren, Katharina; Slopien, Agnieszka; Sorbi, Sandro; Swiqtkowska, Beata; Tortorella, Alfonso; Tozzi, Federica; Treasure, Janet; Tsitsika, Artemis; Tyszkiewicz-Nwafor, Marta; Tziouvas, Konstantinos; DeSocio, Janiece E.; Elburg, Annemarie A. van; Bulant, Josef; Furth, Eric F. van; Walton, Esther; Widen, Elisabeth; Zerwas, Stephanie; Zipfel, Stephan; Bergen, Andrew W.; Boden, Joseph M.; Brandt, Harry; Dick, Danielle M.; Crawford, Steven; Halmi, Katherine A.; Burghardt, Roland; Horwood, L. John; Johnson, Craig; Kaplan, Allan S.; Kaye, Walter H.; Mitchell, James E.; Olsen, Catherine M.; Pearson, John F.; Dikeos, Dimitris; Pedersen, Nancy L.; Strober, Michael; Werge, Thomas; Chang, Xiao; Whiteman, David C.; Woodside, D. Blake; Gordon, Scott; Maguire, Sarah; Larsen, Janne T.; Parker, Richard; Dina, Christian; Petersen, Liselotte Vogdrup; Jordan, Jennifer; Kennedy, Martin; Wade, Tracey D.; Cichon, Sven; Birgegård, Andreas; Lichtenstein, Paul; Landén, Mikael; Martin, Nicholas G.; Mortensen, Preben Bo; Djurovic, Srdjan; Breen, Gerome; Bulik, Cynthia M.; Cone, Roger D.; Courtet, Philippe; Crow, Scott; Crowley, James J.; Danner, Unna N.; Dmitrzak-Weglarz, Monika; Docampo Martínez, Elisa; Duriez, Philibert; Monteleone, Palmiero; Egberts, Karin; Ehrlich, Stefan; Eriksson, Johan G.; Escaramís Babiano, Geòrgia; Esko, Tõnu; Estivill, Xavier, 1955-; Farmer, Anne; Fernández Aranda, Fernando; Fichter, Manfred M.; Föcker, Manuel; Myers, Richard; Foretova, Lenka; Forstner, Andreas J.; Frei, Oleksandr; Gallinger, Steven; Giegling, Ina; Giuranna, Johanna; Gonidakis, Fragiskos; Gorwood, Philip; Gratacòs, Mònica; Guillaume, Sébastien; Navratilova, Marie; Guo, Yiran; Hakonarson, Hakon; Hauser, Joanna; Havdahl, Alexandra; Hebebrand, Johannes; Helder, Sietske G.; Herms, Stefan; Herpertz-Dahlmann, Beate; Herzog, Wolfgang; Hinney, Anke; Ntalla, Ioanna; Hübel, Christopher; Hudson, James I.; Imgart, Hartmut; Jamain, Stephanie; Janout, Vladimir; Jiménez-Murcia, Susana; Jones, Ian R.; Julià, Antonio; Kalsi, Gursharan; Kaminská, Deborah; O'Toole, Julie K.; Kaprio, Jaakko; Karhunen, Leila; Kas, Martien J. H.; Keel, Pamela P.; Kennedy, James L.; Keski-Rahkonen, Anna; Kiezebrink, Kirsty; Klareskog, Lars; Klump, Kelly L.; Knudsen, Gun Peggy S.; Ophoff, Roel A.; Via, Maria C. La; Le Hellard, Stephanie; Leboyer, Marion; Li, Dong; Lilenfeld, Lisa; Lin, Bochao; Lissowska, Jolanta; Luykx, Jurjen; Magistretti, Pierre J.; Maj, Mario; Padyukov, Leonid; Marsal Barril, Sara; Marshall, Christian R.; Mattingsdal, Morten; Meulenbelt, Ingrid; Micali, Nadia; Mitchell, Karen S.; Monteleone, Alessio Maria; Pantel, Jacques; Papezova, Hana; Pinto, Dalila; Boehm, Ilka; Raevuori, Anu |
| 27-Feb-2003 | Contribució a l'estudi genètic de les malalties complexes: Asma i psoriasi a la població espanyola | Cid Ibeas, Rafael de |