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Results 1-10 of 11 (Search time: 0.016 seconds).
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Issue DateTitleAuthor(s)
18-Mar-2021GASVeM: A New Machine Learning Methodology for Multi-SNP Analysis of GWAS Data Based on Genetic Algorithms and Support Vector MachinesDíez Díaz, Fidel; Sánchez Lasheras, Fernando; Moreno Aguado, Víctor; Moratalla Navarro, Ferran; Molina de la Torre, Antonio José; Martín Sánchez, Vicente
16-Sep-2021The Genetic Basis of Moyamoya DiseaseMertens, Robert; Graupera i Garcia-Milà, Mariona; Gerhardt, Holger; Bersano, Anna; Tournier-lasserve, Elisabeth; Mensah, Martin A.; Mundlos, Stefan; Vajkoczy, Peter
1-May-2021Asymptomatic carotid atherosclerosis cardiovascular risk factors and common hypertriglyceridemia genetic variants in patients with systemic erythematosus lupusFanlo Maresma, Marta; Candás Estébanez, Beatriz; Esteve Luque, Virginia; Padró i Miquel, Ariadna; Escrihuela Vidal, Francesc; Carratini-Moraes, Monica; Corbella, Emili; Corbella, Xavier; Pintó Sala, Xavier
2-Nov-2021The apolipoprotein receptor LRP3 compromises APP levelsCuchillo Ibañez, Inmaculada; Lennol, Matthew P.; Escamilla, Sergio; Mata Balaguer, Trinidad; Valverde Vozmediano, Lucía; Lopez Font, Inmaculada; Ferrer, Isidro (Ferrer Abizanda); Sáez Valero, Javier
17-Oct-2021A Clinical-Genetic Score for Predicting Weight Loss after Bariatric Surgery: The OBEGEN StudyCiudin, Andrea; Fidilio, Enzamaria; Gutiérrez Carrasquilla, Liliana; Caixàs i Pedragós, Assumpta; Vilarrasa, Nuria; Pellitero, Silvia; Simó Servat, Andreu; Vilallonga, Ramon; Ruiz, Amador; Fuente, Maricruz de la; Luna, Alexis; Sánchez, Enric; Rigla, Mercedes; Hernández Munain, Cristina; Salas, Eduardo; Simó, Rafael; Lecube, Albert
17-Feb-2021A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersPujana Genestar, M. Ángel; Teulé-Vega, Àlex; GEMO Study Collaborators; EMBRACE Collaborators; KConFab Investigators; HEBON Investigators; ABCTB Investigators
27-May-2021Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancerFernández Rozadilla, C.; Álvarez Barona, M.; Quintana, Isabel; López Novo, Anael; Amigo, J.; Cameselle Teijeiro, J. M.; Roman, E.; González, D.; Llor, Xavier; Bujanda, Luis; Bessa, X.; Jover, R.; Balaguer, F.; Castells Garangou, Antoni; Castellví Bel, Sergi; Capellá, G. (Gabriel); Carracedo Álvarez, Ángel; Valle, Laura; Ruiz Ponte, Clara
20-Apr-2021Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannomaEvans, D. Gareth; Messiaen, Ludwine M.; Foulkes, William D.; Irving, Rachel E. A.; Murray, Alexandra J.; Perez-becerril, Cristina; Rivera, Barbara; McDonald McGinn, Donna M.; Stevenson, David A.; Smith, Miriam J.
25-Feb-2021Genetic architectures of proximal and distal colorectal cancer are partly distinctHuyghe, Jeroen R.; Harrison, Tabitha A.; Bien, Stephanie A.; Hampel, Heather; Figueiredo, Jane C.; Schmit, Stephanie L.; Conti, David V.; Chen, Sai; Qu, Conghui; Lin, Yi; Barfield, Richard; De La Chapelle, Albert; Rennert, Hedy S.; Hudson, Thomas J.; Moreno, Lorena; Easton, Douglas F.; English, Dallas R.; Giles, Graham G.; Feskens, Edith J. M.; Su, Yu-ru; Kooperberg, Charles; Ogino, Shuji; Goodman, Phyllis J.; Grady, William M.; Pharoah, Paul D. P.; Grove, John S.; Cross, Amanda J.; Li, Christopher I.; Hampe, Jochen; Hoffmeister, Michael; Rennert, Gad; Hopper, John L.; Perduca, Vittorio; Platz, Elizabeth A.; Jenab, Mazda; Jenkins, Mark A.; Song, Mingyang; Joshi, Amit D.; Riboli, Elio; Kühn, Tilman; Küry, Sébastien; Ulrich, Cornelia M.; Le Marchand, Loic; Tangen, Catherine M.; Li, Li; Lieb, Wolfgang; Weigl, Korbinian; Lindblom, Annika; Männistö, Satu; Markowitz, Sanford D.; Wu, Anna H.; Milne, Roger L.; Murphy, Neil; Nassir, Rami; Kundaje, Anshul; Offit, Kenneth; Panico, Salvatore; Parfrey, Patrick S.; Potter, John D.; Pearlman, Rachel; Van Guelpen, Bethany; Visvanathan, Kala; Moreno Aguado, Víctor; Prentice, Ross L.; Qi, Lihong; Baron, John A.; Raskin, Leon; Arndt, Volker; Weinstein, Stephanie J.; Schafmayer, Clemens; Schoen, Robert E.; Levine, David M.; Seminara, Daniela; Gallinger, Steven; Diergaarde, Brenda; Thibodeau, Stephen N.; Thomas, Duncan C.; Van Duijnhoven, Fränzel J. B.; Trichopoulou, Antonia; Pérez Cornago, Aurora; Vodicka, Pavel; Vodickova, Ludmila; Arnau Collell, Coral; Vymetalkova, Veronika; Agudo, Antonio; White, Emily; Wolk, Alicja; Bishop, D. Timothy; Woods, Michael O.; Abecasis, Gonçalo R.; Nickerson, Deborah A.; Brezina, Stefanie; Scacheri, Peter C.; Casey, Graham; Gruber, Stephen B.; Campbell, Peter T.; Hsu, Li; Hayes, Richard B.; Newcomb, Polly A.; Duggan, David; Peters, Ulrike; Gunter, Marc J.; Banbury, Barbara L.; Chan, Andrew T.; Harlid, Sophia; Imaz, Liher; Sakoda, Lori C.; Kang, Hyun Min; Huang, Wen-yi; Boehm, Juergen; Schumacher, Fredrick R.; Slattery, Martha L.; Gala, Manish; Toland, Amanda E.; Phipps, Amanda I.; Buch, Stephan; Albanes, Demetrius; Alonso Aguado, Maria Henar; Gsur, Andrea; Anderson, Kristin; Gauderman, W. James; Bassik, Michael C.; Berndt, Sonja I.; Hsu, Wan-ling; Bézieau, Stéphane; Haile, Robert W.; Boeing, Heiner; Boutron Ruault, Marie Christine; Keku, Temitope O.; Brenner, Hermann; Buchanan, Daniel D.; Burnett Hartman, Andrea; Lejbkowicz, Flavio; Caan, Bette J.; Carr, Prudence R.; Castells Garangou, Antoni; Lindor, Noralane M.; Castellví Bel, Sergi; Chang Claude, Jenny; Chanock, Stephen J.; Curtis, Keith R.
15-Feb-2021Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized ApproachJordà Burgos, Paloma; Toro, Rocío; Diez, Carles; Salazar Mendiguchía, Joel; Fernández Falgueras, Anna; Pérez Serra, Alexandra; Coll, Mònica; Puigmulé, Marta; Arbelo, Elena; García Álvarez, Ana; Sarquella Brugada, Georgia; Cesar, Sergi; Tiron, Coloma; Iglesias, Anna; Brugada Terradellas, Josep, 1958-; Brugada, Ramon; Campuzano, Òscar