Výsledky vyhledávání - Diego Vozzi

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  1. 1
    Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss

    Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss Autor Giorgia Girotto, Khalid Abdulhadi, Annalisa Buniello, Diego Vozzi, Danilo Licastro, Angela D’Eustacchio, Dragana Vuckovic, Moza Khalifa Alkowari, Karen P. Steel, Ramin Badii, Paolo Gasparini

    Vydáno 2013
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  2. 2
    Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations

    Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations Autor Ilaria Gandin, Flavio Faletra, Francesca Faletra, Massimo Carella, Vanna Pecile, Giovanni Battista Ferrero, Elisa Biamino, Pietro Palumbo, Orazio Palumbo, Paolo Bosco, Corrado Romano, Chiara Belcaro, Diego Vozzi, Pio D’Adamo

    Vydáno 2014
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  3. 3
    Genome-wide association analysis on normal hearing function identifies<i>PCDH20</i>and<i>SLC28A3</i>as candidates for hearing function and loss

    Genome-wide association analysis on normal hearing function identifies<i>PCDH20</i>and<i>SLC28A3</i>as candidates for hearing function and loss Autor Dragana Vuckovic, Sally J. Dawson, Déborah Scheffer, Taina Rantanen, Anna Morgan, Mariateresa Di Stazio, Diego Vozzi, Teresa Nutile, Maria Pina Concas, Ginevra Biino, Lisa S. Nolan, Aileen Bahl, Anu Loukola, Anne Viljanen, Adrian Davis, Marina Ciullo, David P. Corey, Mario Pirastu, Paolo Gasparini, Giorgia Girotto

    Vydáno 2015
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  4. 4
    Type I interferon-mediated autoinflammation due to DNase II deficiency

    Type I interferon-mediated autoinflammation due to DNase II deficiency Autor Mathieu P. Rodero, Alessandra Tesser, Eva Bartok, Gillian Rice, Erika Della Mina, Marine Depp, Benoît Beitz, Vincent Bondet, Nicolas Cagnard, Darragh Duffy, Michaël Dussiot, Marie‐Louise Frémond, Marco Gattorno, Flavia Guillem, Naoki Kitabayashi, Fabrice Porcheray, Frédéric Rieux‐Laucat, Luís Seabra, Carolina Uggenti, Stefano Volpi, Leo Zeef, Marie-Alexandra Alyanakian, Jacques Beltrand, Anna Monica Bianco, Nathalie Boddaert, Chantal Brouzes, Sophie Candon, Roberta Caorsi, Marina Charbit, Monique Fabrè, Flavio Faletra, M Girard, Annie Harroche, Evelyn Hartmann, Dominique Lasne, Annalisa Marcuzzi, Bénédicte Neven, Patrick Nitschké, Tiffany Pascreau, Serena Pastore, Capucine Pïcard, Paolo Picco, Elisa Piscianz, Michel Polak, Pierre Quartier, Marion Rabant, Gabriele Stocco, Andrea Taddio, Florence Uettwiller, Erica Valencic, Diego Vozzi, Gunther Hartmann, Winfried Barchet, Olivier Hermine, Brigitte Bader‐Meunier, Alberto Tommasini, Yanick J. Crow

    Vydáno 2017
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  5. 5
    Genome Analyses of &gt;200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

    Genome Analyses of &gt;200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders Autor Symen Ligthart, Ahmad Vaez, Urmo Võsa, Maria G. Stathopoulou, Paul S. de Vries, Bram P. Prins, Peter J. van der Most, Toshiko Tanaka, Elnaz Naderi, Lynda M. Rose, Ying Wu, Robert Karlsson, Maja Barbalić, Honghuang Lin, René Pool, Gu Zhu, Aurélien Mace, Carlo Sidore, Stella Trompet, Massimo Mangino, Maria Sabater‐Lleal, John P. Kemp, Ali Abbasi, Tim Kacprowski, Niek Verweij, Albert V. Smith, Tao Huang, Carola Marzi, Mary F. Feitosa, Kurt K. Lohman, Marcus E. Kleber, Yuri Milaneschi, Christian Mueller, Mahmudul Huq, Efthymia Vlachopoulou, Leo-Pekka Lyytikäinen, Christopher Oldmeadow, Joris Deelen, Markus Perola, Jing Hua Zhao, Bjarke Feenstra, Marzyeh Amini, Jari Lahti, Katharina E. Schraut, Myriam Fornage, Bhoom Suktitipat, Wei-Min Chen, Xiaohui Li, Teresa Nutile, Giovanni Malerba, Jian’an Luan, Tom Bak, Nicholas J. Schork, Fabiola Del Greco M, Elisabeth Thiering, Anubha Mahajan, Riccardo E. Marioni, Evelin Mihailov, Joel Eriksson, Ayse Bilge Ozel, Weihua Zhang, Maria Nethander, Yu-Ching Cheng, Stella Aslibekyan, Wei Ang, Ilaria Gandin, Loïc Yengo, Laura Portas, Charles Kooperberg, Edith Hofer, Kumar B. Rajan, Claudia Schurmann, Wouter den Hollander, Tarunveer S. Ahluwalia, Jing Zhao, Harmen H. M. Draisma, Ian Ford, Nicholas J. Timpson, Alexander Teumer, Hongyan Huang, Simone Wahl, Yongmei Liu, Jie Huang, Hae‐Won Uh, Frank Geller, Peter K. Joshi, Lisa R. Yanek, Elisabetta Trabetti, Benjamin Lehne, Diego Vozzi, Marie Verbanck, Ginevra Biino, Yasaman Saba, Ingrid Meulenbelt, Jeff R. O’Connell, Markku Laakso, Franco Giulianini, Patrik K. E. Magnusson, Christie M. Ballantyne, J. J. Hottenga

    Vydáno 2018
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  6. 6
    Rare coding variants and X-linked loci associated with age at menarche

    Rare coding variants and X-linked loci associated with age at menarche Autor Kathryn L. Lunetta, Felix R. Day, Patrick Sulem, Katherine S. Ruth, Joyce Y. Tung, David A. Hinds, Tõnu Esko, Cathy E. Elks, Elisabeth Altmaier, Chunyan He, Jennifer E. Huffman, Evelin Mihailov, Eleonora Porcu, Antonietta Robino, Lynda M. Rose, Ursula M. Schick, Lisette Stolk, Alexander Teumer, Deborah J. Thompson, Michela Traglia, Carol A. Wang, Laura M. Yerges-Armstrong, Antonis C. Antoniou, Caterina Barbieri, Andrea D. Coviello, Francesco Cucca, Ellen W. Demerath, Alison M. Dunning, Ilaria Gandin, Megan L. Grove, Daníel F. Guðbjartsson, Lynne J. Hocking, Albert Hofman, Jinyan Huang, Rebecca D. Jackson, David Karasik, Jennifer Kriebel, Ethan M. Lange, Leslie A. Lange, Claudia Langenberg, Xin Li, Jian’an Luan, Reedik Mägi, Alanna C. Morrison, Sandosh Padmanabhan, Ailith Pirie, Ozren Polašek, David J. Porteous, Alex P. Reiner, Fernando Rivadeneira, Igor Rudan, Cinzia Sala, David Schlessinger, Robert A. Scott, Doris Stöckl, Jenny A. Visser, Uwe Völker, Diego Vozzi, James G. Wilson, Marek Zygmunt, Nita G. Forouhi, Nicola D. Kerrison, Stephen J. Sharp, Matt Sims, Inês Barroso, Panos Deloukas, Mark I. McCarthy, Larraitz Arriola, Beverley Balkau, Aurelio Barricarte, Heiner Boeing, Paul W. Franks, Carlos A. González, Sara Grioni, Rudolf Kaaks, Timothy J. Key, Carmen Navarro, Peter M. Nilsson, Kim Overvad, Domenico Palli, Salvatore Panico, J. Ramón Quirós, Olov Rolandsson, Carlotta Sacerdote, María‐José Sánchez, Nadia Slimani, Anne Tjønneland, ­Rosario ­Tumino, Daphne L. van der A, Yvonne T. van der Schouw, Elio Ríboli, Blair H. Smith, Archie Campbell, Ian J. Deary, Andrew M. McIntosh, Eric Boerwinkle, Julie E. Buring, Laura Crisponi, Douglas F. Easton, Caroline Hayward

    Vydáno 2015
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