Browsing by Subject Genètica humana

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Showing results 122 to 141 of 146 < previous   next >
Issue DateTitleAuthor(s)
Nov-2013Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studiesCarreño, Oriel; Corominas Castiñeira, Roser; Serra, Selma Angèlica; Sintas Vives, Cèlia; Fernàndez Castillo, Noèlia; Vila Pueyo, Marta; Toma, Claudio; González Gené, Gemma; Pons, Roser; Llaneza, Miguel; Sobrido, María Jesús; Grinberg Vaisman, Daniel Raúl; Valverde, Miguel Ángel; Fernández-Fernández, José Manuel; Macaya Ruiz, Alfons; Cormand Rifà, Bru
24-Nov-2006Selecció d'embrionsBueno i Torrens, David, 1965-
9-Nov-2015Sequence information gain based motif analysisMaynou, J.; Pairó, E.; Marco Colás, Santiago; Perera Lluna, Alexandre
Feb-2019Serum magnesium and calcium levels in relation to ischemic stroke Mendelian randomization studyLarsson, Susanna C.; Traylor, Matthew; Burgess, Stephen; Boncoraglio, Giorgio B.; Jern, Christina; Michaëlsson, Karl; Markus, Hugh Stephen; MEGASTROKE project of the International Stroke Genetics Consortium; Rabionet Janssen, Raquel
12-Apr-2023Sibling Differences in Genetic Propensity for Education: How Do Parents React?Sanz-de-Galdeano, Anna; Terskaya, Anastasia
9-Sep-2010Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish populationFernández-Rozadilla, Ceres; Castro, Luisa de; Clofent, Juan; Brea-Fernández, Alejandro; Bessa i Caserras, Xavier; Abulí, Anna; Andreu, Montserrat; Jover, Rodrigo; Xicola, Rosa; Llor, Xavier; Castells Garangou, Antoni; Castellví Bel, Sergi; Carracedo Álvarez, Ángel; Ruiz-Ponte, Clara; Gastrointestinal Oncology Group of the Spanish Gas
24-Oct-2022Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pWeiner, Daniel J.; Ling, Emi; Erdin, Serkan; Tai, Derek J.C.; Yadav, Rachita; Grove, Jakob; Fu, Jack M.; Nadig, Ajay; Carey, Caitlin E.; Baya, Nikolas; Bybjerg Grauholm, Jonas; iPSYCH Consortium; PGC ASD; PGC ADHD; Berretta, Sabina; Macosko, Evan Z.; Sebat, Jonathan; O'Connor, Luke J.; Hougaard, David M.; Børglum, Anders D.; Talkowski, Michael E.; McCarroll, Steven A.; Robinson, Elise B.
28-Jan-2022Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosisAl Khleifat, Ahmad; Iacoangeli, Alfredo; Vugt, Joke J. F. A. van; Bowles, Harry; Moisse, Matthieu; Zwamborn, Ramona A. J.; Spek, Rick A. A. van der; Shatunov, Aleksey; Cooper-Knock, Johnathan; Topp, Simon; Byrne, Ross; Gellera, Cinzia; López, Victoria; Jones, Ashley R.; Opie-Martin, Sarah; Vural, Atay; Campos, Yolanda; Rheenen, Wouter van; Kenna, Brendan; Eijk, Kristel R. van; Kenna, Kevin; Weber, Markus; Smith, Bradley; Fogh, Isabella; Silani, Vincenzo; Morrison, Karen E.; Dobson, Richard; Es, Michael A. van; Mclaughlin, Russell L.; Vourc’h, Patrick; Chio, Adriano; Corcia, Philippe; Carvalho, Mamede de; Gotkine, Marc; Panades, Monica P.; Mora, Jesus S.; Shaw, Pamela J.; Landers, John E.; Glass, Jonathan D.; Shaw, Christopher E.; Basak, Nazli; Hardiman, Orla; Robberecht, Wim; Damme, Philip van; Berg, Leonard H. van der; Veldink, Jan H.; Al Chalabi, Ammar
15-Jul-2020Study of complex chromosomal rearrangements in cancer. The role of extrachromosomal circular DNA as a genome remodeler in neuroblastomaRodriguez Fos, Elias
14-Jul-2020Study of the components that determine the applicability of pathogenicity predictors in the clinical settingAguirre Gómez, Josu
17-Apr-2013Telomere length and genetic anticipation in lynch syndromeSeguí Gracia, Nuria; Pineda Riu, Marta; Guinó, Elisabet; Borràs Flores, Ester; Navarro, Matilde; Bellido Molías, Fernando; Moreno Aguado, Víctor; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Valle Velasco, Laura
10-Jun-2018The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring-Opitz syndromeUrreizti, Roser; Gürsoy, Semra; Castilla-Vallmanya, Laura; Cunill, Guillem; Rabionet Janssen, Raquel; Erçal, Derya; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana
3-Oct-2012The clinical significance of MiR-148a as a predictive biomarker in patients with advanced colorectal cancerTakahashi, Masanobu; Cuatrecasas Freixas, Miriam; Balaguer Prunés, Francesc; Hur, Keun; Toiyama, Yuji; Castells Garangou, Antoni; Boland, C. Richard; Goel, Ajay
2012The complex organization of human cognitive domains and their heritability: a systematic reviewGoldberg, Ximena; Lemos Giráldez, Serafín; Fañanás Saura, Lourdes
12-Dec-2022The impact of adaptor selection on genotyping in 2b-RAD studiesGalià Camps, Carles; Carreras Huergo, Carlos; Turon, Xavier; Pascual Berniola, Marta
28-Jun-2022The impact of rare germline variants on human somatic mutation processesVali-Pour, Mischan; Park, Solip; Espinosa-Carrasco, José; Ortiz Martínez, Daniel; Lehner, Ben; Supek, Fran
14-Feb-2020The role of schizotypal traits and the OXTR gene in theory of mind in schizophrenia: A family-based studyGiralt-López, M.; Miret, Salvador; Soler, Jordi; Campanera, Silvia; Parellada, Mara; Fañanás Saura, Lourdes; Fatjó-Vilas Mestre, Mar
17-Jul-2017Transancestral mapping and genetic load in systemic lupus erythematosusLangefeld, Carl D.; Ainsworth, Hannah C.; Graham, Deborah S. Cunninghame; Kelly, Jennifer A.; Comeau, Mary E.; Marion, Miranda C.; Howard, Timothy D.; Ramos, Paula S.; Croker, Jennifer A.; Morris, David L.; Sandling, Johanna K.; Almlöf, Jonas Carlsson; Acevedo-Vásquez, Eduardo M.; Alarcón, Graciela; Babini, Alejandra M.; Baca, Vicente; Bengtsson, Anders A.; Berbotto, Guillermo A.; Bijl, Marc; Brown, Elizabeth E.; Brunner, Hermine I.; Cardiel, Mario H.; Catoggio, Luis; Cervera i Segura, Ricard, 1960-; Cucho-Venegas, Jorge M.; Dahlqvist, Solbritt Rantapää; D'Alfonso, Sandra; Da Silva, Berta Martins; de la Rúa Figueroa, Iñigo; Doria, Andrea; Edberg, Jeffrey C.; Endreffy, Emóke; Esquivel-Valerio, Jorge A.; Fortin, Paul R.; Freedman, Barry I.; Frostegård, Johan; García, Mercedes A.; de la Torre, Ignacio García; Gilkeson, Gary S.; Gladman, Dafna D.
2-Feb-2011Triem els amicsBueno i Torrens, David, 1965-
17-Jun-2022Unraveling potential disease modifiers of myotonic dystrophy type 1Koehorst, Emma Agathe