Browsing by Subject Genètica humana

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Showing results 43 to 62 of 146 < previous   next >
Issue DateTitleAuthor(s)
2-Jan-2006Economia, colors i estigmesBueno i Torrens, David, 1965-
1-Oct-2008Els gens i el cervell socialBueno i Torrens, David, 1965-
16-Dec-2014Enhancing cognition before clinical symptoms of dementia.Franco Fernández, Rafael
1-Oct-2022Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT SyndromeGrassi, Simone; Campuzano, Òscar; Coll, Mònica; Cazzato, Francesca; Iglesias, Anna; Ausania, Francesco; Scarnicci, Francesca; Sarquella Brugada, Georgia; Brugada Terradellas, Josep, 1958-; Arena, Vicenzo; Oliva, Antonio; Brugada, Ramon
28-May-2007Espiritualitat genèticaBueno i Torrens, David, 1965-
20-Dec-2011Estat d'ànim sota la crisi / Estado de ánimo bajo la crisisBueno i Torrens, David, 1965-; Bufill, Enric; Colom, Francesc, 1971-; Redolar Ripoll, Diego; Sánchez, Xaro; Vieta i Pascual, Eduard, 1963-
25-Feb-2000Estudi clinicopatòlogic i genètic del melanoma maligne i de la síndrome del nevus displàstic.Puig i Sardà, Susana
16-May-2016Estudi de les funcions de la topoisomerasa II a la cromatina de Saccharomyces cerevisiaeFernández Georges, Xavier
19-Nov-2004Estudi genètic de la progressió de la insuficiència renal: anàlisi de polimorfisme de gens implicats a la fibrogènesi.Coll Piera, Elisabeth
1983Estudio genético de la escoliosis idiopática en el hombreMestres i Naval, Francesc
29-Mar-2016Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophreniaCostas, 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
29-Jan-2020Exploring genetic variants in obsessive compulsive disorder severity: a GWAS approachAlemany-Navarro, María; Cruz, Raquel; Real, Eva; Segalàs Cosi, Cinto; Bertolín, Sara; Baenas, Isabel; Domènech, Laura; Rabionet Janssen, Raquel; Carracedo Álvarez, Ángel; Menchón Magriñá, José Manuel; Alonso Ortega, María del Pino
11-Jun-2018Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.Dadaev, Tokhir; Saunders, Edward J.; Mengual Brichs, Lourdes; PRACTICAL Consortium
23-Sep-2013Gastric inhibitory polypeptide receptor methylation in newly diagnosed, drug-naïve patients with type 2 diabetes: a case-control studyCanivell Fusté, Silvia; Ruano, Elena G.; Sisó Almirall, Antoni; Kostov, Belchin; González de Paz, Luis; Fernandez-Rebollo, Eduardo; Hanzu, Felicia A.; Párrizas, Marcelina; Novials, Anna; Gomis, Ramon, 1946-
14-Jul-2017Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity DisorderGarcía Martínez, Iris; Sánchez Mora, Cristina; Soler Artigas, María; Rovira, Paula; Pagerols Teixidó, Mireia; Corrales, Montserrat; Calvo Sánchez, Eva; Richarte, Vanesa; Bustamante Pineda, Mariona; Sunyer Deu, Jordi; Cormand Rifà, Bru; Casas, Miquel; Ramos Quiroga, Josep Antoni; Ribasés Haro, Marta
24-Jul-2017Genetic and functional characterization of disease associations explains comorbidityRubio Perez, Carlota; Guney, Emre; Aguilar, Daniel; Piñero, Janet; García García, Javier; Iadarola, Barbara; Sanz, Ferran; Fernandez Fuentes, Narcís; Furlong, Laura I.; Oliva Miguel, Baldomero
7-Dec-2016Genetic architecture distinguishes systemic juvenile idiopathic arthritis from otherforms of juvenile idiopathic arthritis: clinical and therapeutic implicationsOmbrello, 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
27-Oct-2011Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and CaucasiansKupfer, Sonia S.; Anderson, Jeffrey R.; Ludvik, Anton E.; Hooker, Stanley; Skol, Andrew D.; Kittles, Rick A.; Keku, Temitope O.; Sandler, Robert S.; Ruiz-Ponte, Clara; Castellví Bel, Sergi; Castells Garangou, Antoni; Carracedo Álvarez, Ángel; Ellis, Nathan A.
30-Apr-2013Genetic origin of the relationship between parental negativity and behavior problems from early childhood to adolescence: A longitudinal genetically sensitive study.Alemany Sierra, Silvia; Rijsdijk, Fruhling V.; Haworth, Claire Margaret Alison; Fañanás Saura, Lourdes; Plomin, Robert
11-Nov-2016Genetic predisposition to chronic lymphocytic leukemia is mediated by a BMF super-enhancer polymorphismKandaswamy, Radhika; Sava, Georgina P.; Speedy, Helen E.; Beà Bobet, Sílvia M.; Martín-Subero, José Ignacio; Studd, James B.; Migliorini, Gabriele; Law, Philip J.; Puente, Xose S.; Martín García, David; Salaverria Frigola, Itziar; Gutiérrez-Abril, Jesús; López-Otin, Carlos; Catovsky, Daniel; Allan, James M.; Campo Güerri, Elias; Houlston, Richard S.