Browsing by Subject Genètica humana

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Issue DateTitleAuthor(s)
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.
1-May-2014Genetic Risk Score of NOS Gene Variants Associated with Myocardial Infarction Correlates with Coronary Incidence across EuropeCarreras Torres, Robert; Kundu, Suman; Zanetti, Daniela; Esteban i Torné, Maria Esther; Via i García, Marc; Moral Castrillo, Pedro
14-Apr-2016Genetic Variants Associated with Colorectal Adenoma SusceptibilityAbulí, Anna; Castells Garangou, Antoni; Bujanda, Luis; Lozano Salvatella, Juan José; Bessa i Caserras, Xavier; Hernández-Munain, Cristina; Álvarez Urturi, Cristina; Pellisé Urquiza, Maria; Esteban-Jurado, Clara; Hijona, Elizabeth; Burón, Andrea; Macià, Francesc; Grau Cano, J. (Jaume); Guayta, Rafael (Guayta Escolies); Castellví Bel, Sergi; Andreu, Montserrat; Trilla García, Antoni; PROCOLON Research Group
23-Feb-2011Genetic variants of the FADS gene cluster and ELOVL gene family, colostrums LC-PUFA levels, breastfeeding, and child cognitionMorales, 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
14-Nov-2016Genome editing in human pluripotent stem cells: a systematic approach unrevealing pancreas development and diseaseGarreta, Elena; Marco, Andrés; Izpisúa Belmonte, Juan Carlos; Montserrat, Núria
15-Jun-2019Genome-wide association meta-analysis of cocaine dependence: shared genetics with comorbid conditionsCabana Domínguez, Judit; Shivalikanjli, Anu; Fernàndez Castillo, Noèlia; Cormand Rifà, Bru
27-Mar-2013Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskCouch, Fergus J.; Wang, Xianshu; McGuffog, Lesley; Lee, Andrew; Olswold, Curtis; Kuchenbaecker, Karoline B.; Soucy, Penny; Fredericksen, Zachary; Barrowdale, Daniel; Dennis, Joe; Gaudet, Mia M.; Dicks, Ed; Kosel, Matthew; Healey, Sue; Sinilnikova, Olga M.; Bacot, François; Vincent, Daniel; Hogervorst, Frans B. L.; Peock, Susan; Stoppa-Lyonnet, Dominique; Jakubowska, Anna; Radice, Paolo; Schmutzler, Rita Katharina; Domchek, Susan M.; Piedmonte, Marion; Singer, Christian F.; Friedman, Eitan; Thomassen, Mads; Hansen, Thomas V. O.; Neuhausen, Susan L.; Szabo, Csilla I.; Blanco Guillermo, Ignacio; Greene, Mark H.; Karlan, Beth Y.; Garber, Judy; Phelan, Catherine M.; Weitzel, Jeffrey N.; Montagna, Marco; Olah, Edith
Nov-2014Genomic complexity and IGHV mutational status are key predictors of outcome of chronic lymphocytic leukemia patients with TP53 disruption.Delgado, Julio (Delgado González); Salaverria Frigola, Itziar; Baumann, Tycho; Martínez Trillos, Alejandra; Lee, Eriong; Jiménez, Laura; Navarro López, Alba; Royo Moreno, Cristina; Santacruz, Rodrigo; López, Cristina; Payer, Ángel R.; Colado, Enrique; González, Marcos; Armengol, Lluís; Colomer Pujol, Dolors; Pinyol, Magda; Villamor i Casas, Neus; Aymerich Gregorio, Marta; Carrió, Ana; Costa, Dolors; Clot, Guillem; Giné Soca, Eva; López Guillermo, Armando; Campo Güerri, Elias; Beà Bobet, Sílvia M.
24-Dec-2016Genomic expression differences between cutaneous cells from red hair color individuals and black hair color individuals based on bioinformatic analysis.Puig Butillé, Joan Anton; Gimenez-Xavier, Pol; Visconti, Alessia; Nsengimana, Jérémie; Garcia-García, Francisco; Tell Martí, Gemma; Escamez, Maria José; Newton-Bishop, Julia A.; Bataille, Veronique; Río, Marcela del; Dopazo, Joaquín; Falchi, Mario; Puig i Sardà, Susana
1-Dec-2022Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohortHendricks, Linda A.J.; Hoogerbrugge, Nicoline; Venselaar, Hanka; Aretz, Stefan; Spier, Isabel; Legius, Eric; Brems, Hilde; De Putter, Robin; Claes, Kathleen B.M.; Evans, D. Gareth; Woodward, Emma R.; Genuardi, Maurizio; Brugnoletti, Fulvia; Van Ierland, Yvette; Dijke, Kim; Tham, Emma; Tesi, Bianca; Schuurs Hoeijmakers, Janneke H.M.; Branchaud, Maud; Salvador, Hector; Jahn, Arne; Schnaiter, Simon; Anastasiadou, Violetta Christophidou; Brunet, Joan; Oliveira, Carla; Roht, Laura; Blatnik, Ana; Irmejs, Arvids; Mensenkamp, Arjen R.; Vos, Janet R.; Duijkers, Floor; Giltay, Jacques C.; Van Hest, Liselotte P.; Kleefstra, Tjitske; Leter, Edward M.; Nielsen, Maartje; Nijmeijer, Sebastiaan W.R.; Olderode-berends, Maran J.W.
21-Feb-2013Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotypeLópez de Heredia, Miguel; Clèries Soler, Ramon; Nunes Martínez, Virginia
22-May-2004Gens, paraules i l'origen dels europeusBueno i Torrens, David, 1965-
7-Jan-2008Gens,humans i rockBueno i Torrens, David, 1965-
15-Mar-2008Herència feliçBueno i Torrens, David, 1965-