Browsing by Author González, Juan R.
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) |
|---|---|---|
| 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 |
| 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 |
| 2008 | Probe-specific mixed-model approach to detect copy number differences using multiplex ligation-dependent probe amplification (MLPA) | González, Juan R.; Carrasco Jordan, Josep Lluís; Armengol, Lluís; Villatoro, Sergi; Jover Armengol, Lluís de; Yasui, Yutaka; Estivill, Xavier, 1955- |
| May-2022 | Systematic collaborative reanalysis of genomic data improves diagnostic yield in neurologic rare diseases | Bullich, Gemma; Matalonga, Leslie; Pujadas, Montserrat; Papakonstantinou, Anastasios; Piscia, Davide; Tonda, Raúl; Artuch, Rafael; Gallano, Pia; Garrabou Tornos, Glòria; González, Juan R.; Grinberg Vaisman, Daniel Raúl; Guitart, Míriam; Laurie, Steven; Lázaro, Conxi; Luengo, Critina; Martí, Ramon; Milà, Montserrat; Ovelleiro, David; Parra, Genís; Pujol, Aurora; Tizzano, Eduardo; Macaya, Alfonso; Palau, Francesc; Ribes, Antonio; Pérez-Jurado, Luis A.; Beltran, Sergi; Undiagnosed Rare Disease Program of Catalonia (URD-Cat) Consortium.; Rabionet Janssen, Raquel; Balcells Comas, Susana |
