Browsing by Subject Genètica humana
Showing results 132 to 146 of 146
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| Issue Date | Title | Author(s) |
|---|---|---|
| 17-Apr-2013 | Telomere length and genetic anticipation in lynch syndrome | Seguí 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-2018 | The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring-Opitz syndrome | Urreizti, Roser; Gürsoy, Semra; Castilla-Vallmanya, Laura; Cunill, Guillem; Rabionet Janssen, Raquel; Erçal, Derya; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |
| 3-Oct-2012 | The clinical significance of MiR-148a as a predictive biomarker in patients with advanced colorectal cancer | Takahashi, Masanobu; Cuatrecasas Freixas, Miriam; Balaguer Prunés, Francesc; Hur, Keun; Toiyama, Yuji; Castells Garangou, Antoni; Boland, C. Richard; Goel, Ajay |
| 2012 | The complex organization of human cognitive domains and their heritability: a systematic review | Goldberg, Ximena; Lemos Giráldez, Serafín; Fañanás Saura, Lourdes |
| 12-Dec-2022 | The impact of adaptor selection on genotyping in 2b-RAD studies | Galià Camps, Carles; Carreras Huergo, Carlos; Turon, Xavier; Pascual Berniola, Marta |
| 28-Jun-2022 | The impact of rare germline variants on human somatic mutation processes | Vali-Pour, Mischan; Park, Solip; Espinosa-Carrasco, José; Ortiz Martínez, Daniel; Lehner, Ben; Supek, Fran |
| 14-Feb-2020 | The role of schizotypal traits and the OXTR gene in theory of mind in schizophrenia: A family-based study | Giralt-López, M.; Miret, Salvador; Soler, Jordi; Campanera, Silvia; Parellada, Mara; Fañanás Saura, Lourdes; Fatjó-Vilas Mestre, Mar |
| 17-Jul-2017 | Transancestral mapping and genetic load in systemic lupus erythematosus | Langefeld, 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-2011 | Triem els amics | Bueno i Torrens, David, 1965- |
| 17-Jun-2022 | Unraveling potential disease modifiers of myotonic dystrophy type 1 | Koehorst, Emma Agathe |
| 30-May-2019 | Variants del número de còpia al càncer colorectal: predisposició germinal i perfils genòmics tumorals | Franch Expósito, Sebastià |
| 21-Jul-2022 | Variants genètiques de baixa penetrància en la predisposició germinal al càncer colorectal i la síndrome de poliposi serrada | Arnau Collell, Coral |
| 24-Nov-2020 | Variants of the aggression-related RBFOX1 gene in a population representative birth cohort study: aggressiveness, personality and alcohol use disorder | Vaht, Mariliis; Laas, Kariina; Fernàndez Castillo, Noèlia; Kurrikoff, Triin; Kanarik, Margus; Faraone, Stephen V.; Tooding, Liina-Mai; Veidebaum, Toomas; Franke, Barbara; Reif, Andreas; Cormand Rifà, Bru; Harro, Jaanus |
| 3-Jul-2022 | Very long time persistent hyperCKemia as the first manifestation of McLeod syndrome: a case report. | Torres, Viviana; Painous Martí, Cèlia; Santacruz, Pilar; Sánchez, Aurora; Sanz, Cristina; Grau Junyent, Josep M. (Josep Maria); Muñoz, Esteban |
| 6-Nov-2020 | β-cells cis-regulatory networks and type 1 diabetes | Ramos Rodríguez, Mireia |