Resultados globales: 2 registros encontrados en 2.56 segundos.
Artículos, Encontrados 2 registros
Artículos Encontrados 2 registros  
1.
11 p, 912.1 KB Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing / Corominas, Jordi (Radboud University Medical Center) ; Klein, Marieke (Radboud University Medical Center) ; Zayats, Tetyana (University of Bergen) ; Rivero, Olga (University of Würzburg) ; Ziegler, Georg C. (University of Würzburg) ; Pauper, Marc (Radboud University Medical Center) ; Neveling, Kornelia (Radboud University Medical Center) ; Poelmans, Geert (Radboud University Medical Center) ; Jansch, Charline (University of Würzburg) ; Svirin, Evgeniy (I.M. Sechenov First Moscow State Medical University) ; Geissler, Julia (University Hospital of Würzburg) ; Weber, Heike (University Hospital Frankfurt) ; Reif, Andreas (University Hospital Frankfurt) ; Arias Vasquez, Alejandro (Radboud University Medical Center) ; Galesloot, Tessel E. (Radboud University Medical Center) ; Kiemeney, Lambertus A. L. M. (Radboud University Medical Center) ; Buitelaar, Jan K. (Radboud University Medical Center) ; Ramos Quiroga, Josep Antoni (Universitat Autònoma de Barcelona. Departament de Psiquiatria i de Medicina Legal) ; Cormand, Bru (Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat) ; Ribasés, Marta (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Hveem, Kristian (Norwegian University of Science and Technology) ; Gabrielsen, Maiken Elvestad (Norwegian University of Science and Technology) ; Hoffmann, Per (University of Basel) ; Cichon, Sven (University Hospital Basel) ; Haavik, Jan (Haukeland University Hospital) ; Johansson, Stefan (University of Bergen) ; Jacob, Christian P. (University of Würzburg) ; Romanos, Marcel (University Hospital of Würzburg) ; Franke, Barbara (Radboud University Medical Center) ; Lesch, Klaus-Peter (Maastricht University)
Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder with a complex genetic background, hampering identification of underlying genetic risk factors. We hypothesized that combining linkage analysis and whole-exome sequencing (WES) in multi-generation pedigrees with multiple affected individuals can point toward novel ADHD genes. [...]
2018 - 10.1038/s41380-018-0210-6
Molecular Psychiatry, Vol. 25 (august 2018) , p. 2047-2057  
2.
7 p, 508.5 KB Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk / Figlioli, Gisella (University of Pisa. Department of Biology) ; Chen, Bowang (German Cancer Research Center (DKFZ). Molecular Genetic Epidemiology (Germany)) ; Elisei, Rossella (University of Pisa. Department of Endocrinology and Metabolism (Italy)) ; Romei, Cristina (University of Pisa. Department of Endocrinology and Metabolism (Italy)) ; Campo, Chiara (University of Pisa. Department of Biology (Italy)) ; Cipollini, Monica (University of Pisa. Department of Biology (Italy)) ; Cristaudo, Alfonso (University of Pisa. Department of Endocrinology and Metabolism (Italy)) ; Bambi, Franco (Blood Centre, Azienda Ospedaliero Universitaria A. Meyer (Italy)) ; Paolicchi, Elisa (University of Pisa. Department of Biology (Italy)) ; Hoffmann, Per (University of Basel. Department of Biomedicine (Switzerland)) ; Herms, Stefan (University of Basel. Department of Biomedicine (Switzerland)) ; Kalemba, Michał (Maria Sklodowska-Curie Memorial Cancer Center. Department of Nuclear Medicine and Endocrine Oncology (Poland)) ; Kula, Dorota (Maria Sklodowska-Curie Memorial Cancer Center. Department of Nuclear Medicine and Endocrine Oncology (Poland)) ; Pastor Benito, Susana (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Marcos Dauder, Ricardo (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Velázquez Henar, Antonia (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Jarząb, Barbara (Maria Sklodowska-Curie Memorial Cancer Center. Department of Nuclear Medicine and Endocrine Oncology (Poland)) ; Landi, Stefano (University of Pisa. Department of Biology (Italy)) ; Hemminki, Kari (Lund University. Center for Primary Health Care Research, Clinical Research Center (Sweden)) ; Gemignani, Federica (University of Pisa. Department of Biology (Italy)) ; Försti, Asta (Lund University. Center for Primary Health Care Research, Clinical Research Center (Sweden))
A genome-wide association study (GWAS) performed on a high-incidence Italian population followed by replications on low-incidence cohorts suggested a strong association of differentiated thyroid cancer (DTC) with single nucleotide polymorphisms (SNPs) at 9q22. [...]
2015 - 10.1038/srep08922
Scientific reports, Vol. 5 (March 2015) , art. 8922  

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2 Hoffmann, P.
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