Результаты поиска - Marianthi Georgitsi

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  1. 1
    The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

    The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery по Marianthi Georgitsi, A. Jeremy Willsey, Carol A. Mathews, Matthew W. State, Jeremiah M. Scharf, Peristera Paschou

    Опубликовано 2016
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    Artigo
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  2. 2
    Mice with Inactivation of Aryl Hydrocarbon Receptor-Interacting Protein (Aip) Display Complete Penetrance of Pituitary Adenomas with Aberrant ARNT Expression

    Mice with Inactivation of Aryl Hydrocarbon Receptor-Interacting Protein (Aip) Display Complete Penetrance of Pituitary Adenomas with Aberrant ARNT Expression по Anniina Raitila, Heli Lehtonen, Johanna Arola, Elina Heliövaara, Manuel Ahlsten, Marianthi Georgitsi, Anu Jalanko, Anders Paetau, Lauri A. Aaltonen, Auli Karhu

    Опубликовано 2010
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    Artigo
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  3. 3
    Large Genomic Deletions in<i>AIP</i>in Pituitary Adenoma Predisposition

    Large Genomic Deletions in<i>AIP</i>in Pituitary Adenoma Predisposition по Marianthi Georgitsi, Elina Heliövaara, Ralf Paschke, Ajith Kumar, Marc Tischkowitz, Outi Vierimaa, Pasi Salmela, Timo Sane, Ernesto De Menis, Salvatore Cannavò, Sadi Gündoğdu, Anneke Lucassen, Louise Izatt, Simon Aylwin, Gul Bano, Shirley Hodgson, Christian A. Koch, Auli Karhu, Lauri A. Aaltonen

    Опубликовано 2008
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    Artigo
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  4. 4
    Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations

    Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations по Marianthi Georgitsi, Anniina Raitila, Auli Karhu, Karoliina Tuppurainen, Markus J. Mäkinen, Outi Vierimaa, Ralf Paschke, Wolfgang Saeger, Rob B. van der Luijt, Timo Sane, Mercedes Robledo, Ernesto De Menis, Robert J. Weil, A. Wasik, Grzegorz Zieliński, Olga Lucewicz, Jan Lubiński, Virpi Launonen, Pia Vahteristo, Lauri A. Aaltonen

    Опубликовано 2007
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    Artigo
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  5. 5
    Germline CDKN1B/p27Kip1 Mutation in Multiple Endocrine Neoplasia

    Germline CDKN1B/p27Kip1 Mutation in Multiple Endocrine Neoplasia по Marianthi Georgitsi, Anniina Raitila, Auli Karhu, Rob B. van der Luijt, Cora M. Aalfs, Timo Sane, Outi Vierimaa, Markus J. Mäkinen, Karoliina Tuppurainen, R Paschke, Oliver Gimm, Christian A. Koch, Sadi Gündoğdu, Anneke Lucassen, Marc Tischkowitz, Louise Izatt, Simon Aylwin, Gul Bano, Shirley Hodgson, Ernesto De Menis, Virpi Launonen, Pia Vahteristo, Lauri A. Aaltonen

    Опубликовано 2007
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    Artigo
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  6. 6
    Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

    Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin по Joseph Borg, Petros Papadopoulos, Marianthi Georgitsi, Laura Gutiérrez, Godfrey Grech, Pavlos Fanis, Marios Phylactides, Annemieke J.M.H. Verkerk, Peter J. van der Spek, Christian Scerri, Wilhelmina Cassar, Ruth Galdies, Wilfred F. J. van IJcken, Zeliha Özgür, Nynke Gillemans, Jun Hou, Marisa Bugeja, Frank Grosveld, Marieke von Lindern, Alex E. Felice, George P. Patrinos, Sjaak Philipsen

    Опубликовано 2010
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    Artigo
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  7. 7
    European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents

    European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents по Anette Schrag, Davide Martino, Alan Apter, Juliane Ball, Erika Bartolini, Noa Benaroya-Milshtein, Maura Buttiglione, Francesco Cardona, Roberta Creti, Androulla Efstratiou, Maria Gariup, Marianthi Georgitsi, Tammy Hedderly, Isobel Heyman, Immaculada Margarit, Pablo Mir, Natalie Moll, Ástrid Morer, Norbert Müller, Kirsten Müller‐Vahl, Alexander Münchau, Graziella Orefici, Kerstin Jessica Plessen, Cesare Porcelli, Peristera Paschou, Renata Rizzo, Veit Roessner, Markus Schwarz, Tamar Steinberg, Friederike Tagwerker Gloor, Zsanett Tárnok, Susanne Walitza, Andrea Dietrich, Pieter J. Hoekstra

    Опубликовано 2018
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    Artigo
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  8. 8
    Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

    Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach по Belinda Giardine, Joseph Borg, Douglas R. Higgs, Kenneth R. Peterson, Sjaak Philipsen, Donna Maglott, Belinda K. Singleton, David J. Anstee, A. Nazlı Başak, Barnaby Clark, Flavia C Costa, Paula Faustino, Halyna Fedosyuk, Alex E. Felice, Alain Francina, Renzo Galanello, Monica V.E. Gallivan, Marianthi Georgitsi, Richard J. Gibbons, Piero C. Giordano, Cornelis L. Harteveld, James D. Hoyer, Martin Jarvis, Philippe Joly, Emmanuel Kanavakis, Panagoula Κollia, Stephan Menzel, Webb Miller, Kamran Moradkhani, John Old, Adamantia Papachatzopoulou, Manoussos N. Papadakis, Petros Papadopoulos, Sonja Pavlović, Lucia Perseu, Milena Radmilovic, Cathy Riemer, Stefania Satta, Iris Schrijver, Maja Stojiljković, Swee Lay Thein, Joanne Traeger‐Synodinos, Ray Tully, Takahito Wada, John S. Waye, Claudia Wiemann, Branka Zukić, David H.K. Chui, Henri Wajcman, Ross C. Hardison, George P. Patrinos

    Опубликовано 2011
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    Artigo
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  9. 9
    Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line<i>AIP</i>Mutations and Pituitary Adenomas: An International Collaborative Study

    Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line<i>AIP</i>Mutations and Pituitary Adenomas: An International Collaborative Study по Adrian Daly, María A. Tichomirowa, Patrick Pétrossians, Elina Heliövaara, Marie‐Lise Jaffrain‐Rea, Anne Barlier, Luciana Ansaneli Naves, Tapani Ebeling, Auli Karhu, Antti Raappana, Laure Cazabat, Ernesto De Menis, Carmen Fajardo, Gérald Raverot, Robert J. Weil, Timo Sane, Dominique Maiter, Sebastian Neggers, Maria Yaneva, Antoine Tabarin, Elisa Verrua, Eija Eloranta, Arnaud Murat, Outi Vierimaa, Pasi Salmela, Philippe Émy, Rodrigo A. Toledo, Maria Sabaté, Chiara Villa, Marc Popelier, Roberto Salvatori, Juliet Jennings, A Ferrández Longás, José Ignacio Labarta Aizpún, Marianthi Georgitsi, Ralf Paschke, Cristina L. Ronchi, Matti Välimäki, Carola Saloranta, Wouter W. de Herder, Renato Cozzi, Mirtha Guitelman, Flavia Magri, Maria Stefania Lagonigro, Georges Halaby, Vinciane Corman, Marie-Thérèse Hagelstein, Jean-François Vanbellinghen, Gustavo Barcelos Barra, Anne‐Paule Gimenez‐Roqueplo, Fergus Cameron, Françoise Borson‐Chazot, I. M. Holdaway, S. P. A. Toledo, Günter K. Stalla, Anna Spada, Sabina Zacharieva, Jérôme Bertherat, Thierry Brue, Vincent Bours, Philippe Chanson, Lauri A. Aaltonen, Albert Beckers

    Опубликовано 2010
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    Artigo
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  10. 10
    Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

    Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome по Pritesh Jain, Tyne W. Miller‐Fleming, Apostolia Topaloudi, Dongmei Yu, Petros Drineas, Marianthi Georgitsi, Zhiyu Yang, Renata Rizzo, Kirsten Müller‐Vahl, Zeynep Tümer, Nanette Mol Debes, Andreas Hartmann, Christel Depienne, Yulia Worbe, Pablo Mir, Daniëlle C. Cath, Dorret I. Boomsma, Veit Roessner, Tomasz Wolańczyk, Piotr Janik, Natalia Szejko, Cezary Żekanowski, Csaba Barta, Zsófia Nemoda, Zsanett Tárnok, Joseph D. Buxbaum, Dorothy E. Grice, Jeffrey Glennon, Hreinn Stefánsson, Bastian Hengerer, Noa Benaroya-Milshtein, Francesco Cardona, Tammy Hedderly, Isobel Heyman, Chaim Huyser, Ástrid Morer, Norbert Mueller, Alexander Münchau, Kerstin Jessica Plessen, Cesare Porcelli, Susanne Walitza, Anette Schrag, Davide Martino, Thomas D. Als, H.N. Aschauer, Gil Atzmon, Matie Bækvad-Hansen, Csaba Barta, Cathy L. Barr, Nir Barzilai, James R. Batterson, Robert Batterson, Fortu Benarroch, Cheston M. Berlin, Julia Boberg, Benjamin Bodmer, Julia Bohnenpoll, Anders D. Børglum, Lawrence W. Brown, Ruth D. Bruun, Cathy L. Budman, Randy L. Buckner, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Daniëlle C. Cath, Keun‐Ah Cheon, Sylvain Chouinard, Barbara Coffey, Giovanni Coppola, James J. Crowley, Niklas Dahl, Lea K. Davis, Sabrina M. Darrow, Mark J. Daly, Christel Depienne, Silvia De Rubeis, Andrea Dietrich, Yves Dion, Diana R. Djurfeldt, Laura Domenech-Salgado, Valsamma Eapen, Lonneke Elzerman, Thomas Fernandez, Nelson B. Freimer Carolin Fremer, Blanca García-Delgar, Marcos Madruga Garrido, Donald L. Gilbert, Paola Giusti‐Rodríguez, Marco A. Grados, Erica Greenberg, Jakob Grove, Dorothy E. Grice, Julie Hagstrøm, Matthew Halvorsen, Andreas Hartmann, Bjarne Hansen, Jan Haavik, Johannes Hebebrand, Gary A. Heiman, Luis Diego Herrera

    Опубликовано 2023
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    Revisão
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