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Sfoglia per ???browse.type.metadata.subjectErc2011???  LS2_9 - Genetic epidemiology

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1-gen-2015 The 12p13.33/RAD52 Locus and Genetic Susceptibility to Squamous Cell Cancers of Upper Aerodigestive Tract Delahaye Sourdeix, M; Oliver, J; Timofeeva, Mn; Gaborieau, V; Johansson, M; Chabrier, A; Wozniak, Mb; Brenner, Dr; Vallée, Mp; Anantharaman, D; Lagiou, P; Holcátová, I; Richiardi, L; Kjaerheim, K; Agudo, A; Castellsagué, X; Macfarlane, Tv; Barzan, L; Canova, C; Thakker, Ns; Conway, Di; Znaor, A; Healy, Cm; Ahrens, W; Zaridze, D; Szeszenia Dabrowska, N; Lissowska, J; Fabianova, E; Mates, In; Bencko, V; Foretova, L; Janout, V; Curado, Mp; Koifman, S; Menezes, A; Wünsch Filho, V; Eluf Neto, J; Boffetta, P; Garrote, Lf; Serraino, D; Lener, M; Jaworowska, E; Lubiński, J; Boccia, Stefania; Rajkumar, T; Samant, Ta; Mahimkar, Mb; Matsuo, K; Franceschi, S; Byrnes, G; Brennan, P; Mckay, Jd
1-gen-2015 The Effect of CYP, GST, and SULT Polymorphisms and Their Interaction with Smoking on the Risk of Hepatocellular Carcinoma Boccia, Stefania; Miele, Luca; Panic, N; Turati, F; Arzani, Dario; Cefalo, Consuelo; Amore, R; Bulajic, M; Pompili, Maurizio; Rapaccini, Gian Ludovico; Gasbarrini, Antonio; La Vecchia, C; Grieco, Antonio
1-gen-2012 The familiarity of idiopathic scoliosis: statistical analysis and clinical considerations Aulisa, Angelo Gabriele; Guzzanti, Vincenzo; Galli, Marco; Bottaro, G; Vitelli, O; Ferrara, Pietro; Logroscino, Giandomenico
1-gen-2011 The FRAXopathies: Definition, overview, and update Neri, Giovanni; Pirozzi, Filomena; Tabolacci, Elisabetta
1-gen-2014 The link between genetic variation and variability in vaccine responses: Systematic review and meta-analyses Posteraro, Brunella; Pastorino, Roberta; Di Giannantonio, Paolo; Ianuale, Carolina; Amore, Rosarita; Ricciardi, Walter; Boccia, Stefania
1-gen-2014 TNFRSF11B gene polymorphisms increased risk of peripheral arterial occlusive disease and critical limb ischemia in patients with type 2 diabetes Biscetti, Federico; Bertucci, Flavio; Straface, Giuseppe; Santoliquido, Angelo; Tondi, Paolo; Angelini, Flavia; Pitocco, Dario; Gasbarrini, Antonio; Landolfi, Raffaele; Flex, Andrea
1-gen-2012 Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant. Crotti, L; Hu, D; Barajas Martinez, H; De Ferrari, Gm; Oliva, Antonio; Insolia, R; Pollevick, G; Dagradi, F; Guerchicoff, A; Greco, F; Schwartz, Pj; Viskin, S; Antzelevitch, C.
1-gen-2012 Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair Ferrero, Gb; Picco, G; Baldassarre, G; Flex, E; Isella, C; Cantarella, D; Corà, D; Chiesa, N; Crescenzio, N; Timeus, F; Merla, G; Mazzanti, L; Zampino, Giuseppe; Rossi, C; Silengo, M; Tartaglia, Marco; Medico, E.
1-gen-2012 Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction? Majore, Silvia; Ricerca, Bianca Maria; Radio, Fc; Binni, Francesco; Cosentino, I; Gallusi, Giulia; De Bernardo, Carmelilia; Morrone, Aldo; Grammatico, Paola
1-gen-2010 Unexpected finding of paternal premutation of the fragile X FMR1 gene in a female fetus of a premutation carrier mother Pomponi, Maria Grazia; Pietrobono, Roberta; Neri, Caterina; Chiurazzi, Pietro; Neri, Giovanni
1-gen-2015 Unique genomic profile associated with pediatric uveal melanoma Blasi, Maria Antonietta; Orteschi, Daniela; Pagliara, Monica Maria; Coco, Giulia; Asaro, Alessia; Mule', Antonino; Petrone, Gianluigi; Zollino, Marcella
1-gen-2014 Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder Zollino, Marcella; Orteschi, Daniela; Ruiter, M; Pfundt, R; Steindl, K; Cafiero, Concetta; Ricciardi, Stefania; Contaldo, Ilaria; Chieffo, Daniela Pia Rosaria; Ranalli, Domiziana; Acquafondata, Celeste; Murdolo, Marina; Marangi, Giuseppe; Asaro, Alessia; Battaglia, Domenica Immacolata
1-gen-2014 Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder Zollino, Marcella; Orteschi, Daniela; Ruiter, M; Pfundt, R; Steindl, K; Cafiero, Concetta; Ricciardi, Stefania; Contaldo, Ilaria; Chieffo, Daniela Pia Rosaria; Ranalli, Domiziana; Acquafondata, Celeste; Murdolo, Marina; Marangi, Giuseppe; Asaro, Alessia; Battaglia, Domenica Immacolata
1-gen-2014 Using ancestry-informative markers to identify fine structure across 15 populations of European origin Gambaro, Giovanni; Wellcome Trust Case Control Consortium, 3
1-gen-2021 Using genetic variants to evaluate the causal effect of cholesterol lowering on head and neck cancer risk: A Mendelian randomization study Gormley, M.; Yarmolinsky, J.; Dudding, T.; Burrows, K.; Martin, R. M.; Thomas, S.; Tyrrell, J.; Brennan, P.; Pring, M.; Boccia, Stefania; Olshan, A. F.; Diergaarde, B.; Hung, R. J.; Liu, Guopeng; Legge, D.; Tajara, E. H.; Severino, P.; Lacko, M.; Ness, A. R.; Smith, G. D.; Vincent, E. E.; Richmond, R. C.
1-gen-2014 Utility and Challenges of Next Generation Sequencing in Pediatric Disorders Longoni, M.; Marangi, Giuseppe; Zollino, Marcella
Mostrati risultati da 124 a 139 di 139
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