檢索結果 - Elisabetta Trabetti

  • Showing 1 - 18 results of 18
Refine Results
  1. 1
    The bone microenvironment: new insights into the role of stem cells and cell communication in bone regeneration

    The bone microenvironment: new insights into the role of stem cells and cell communication in bone regeneration 由 Luca Dalle Carbonare, Mattia Cominacini, Elisabetta Trabetti, Cristina Bombieri, João Pessoa, Maria Romanelli, Maria Teresa Valenti

    出版 2025
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  2. 2
    Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids

    Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids 由 Cristina Bombieri, Andrea Corsi, Elisabetta Trabetti, Alessandra Ruggiero, Giulia Marchetto, Gaetano Vattemi, Maria Teresa Valenti, Donato Zipeto, Maria Grazia Romanelli

    出版 2024
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  3. 3
    Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery disease

    Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery disease 由 Ugo Cavallari, Elisabetta Trabetti, Giovanni Malerba, Michele Biscuola, Domenico Girelli, Oliviero Olivieri, Nicola Martinelli, Dominick J. Angiolillo, Roberto Corrocher, Pier Franco Pignatti

    出版 2007
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  4. 4
    Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries

    Reconstruction and functional analysis of altered molecular pathways in human atherosclerotic arteries 由 Stefano Cagnin, Michele Biscuola, Cristina Patuzzo, Elisabetta Trabetti, Alessandra Pasquali, Paolo Laveder, Giuseppe Faggian, Mauro Iafrancesco, Alessandro Mazzucco, Pier Franco Pignatti, Gerolamo Lanfranchi

    出版 2009
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  5. 5
    FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease

    FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease 由 Nicola Martinelli, Domenico Girelli, Giovanni Malerba, Patrizia Guarini, Thomas Illig, Elisabetta Trabetti, Marco Sandri, Simonetta Friso, Francesca Pizzolo, Linda Schaeffer, Joachim Heinrich, Pier Franco Pignatti, Roberto Corrocher, Oliviero Olivieri

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    Contribution of Gene Sequence Variations of the Hepatic Cytochrome P450 3A4 Enzyme to Variability in Individual Responsiveness to Clopidogrel

    Contribution of Gene Sequence Variations of the Hepatic Cytochrome P450 3A4 Enzyme to Variability in Individual Responsiveness to Clopidogrel 由 Dominick J. Angiolillo, Antonio Fernández-Ortı́z, Esther Bernardo, Celia Ramírez, Ugo Cavallari, Elisabetta Trabetti, Manel Sabaté, Rosana Hernández, Raúl Moreno, Javier Escaned, Fernándo Alfonso, Camino Bañuelos, Marco A. Costa, Theodore A. Bass, Pier Franco Pignatti, Carlos Macaya

    出版 2006
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  7. 7
    Impact of Insulin Receptor Substrate-1 Genotypes on Platelet Reactivity and Cardiovascular Outcomes in Patients With Type 2 Diabetes Mellitus and Coronary Artery Disease

    Impact of Insulin Receptor Substrate-1 Genotypes on Platelet Reactivity and Cardiovascular Outcomes in Patients With Type 2 Diabetes Mellitus and Coronary Artery Disease 由 Dominick J. Angiolillo, Esther Bernardo, Martina Zanoni, David Vivas, Piera Capranzano, Giovanni Malerba, Davide Capodanno, Paola Prandini, Alessandra Pasquali, Elisabetta Trabetti, Manel Sabaté, Pilar Jiménez‐Quevedo, José Luis Ferreiro, Masafumi Ueno, Theodore A. Bass, Pier Franco Pignatti, Antonio Fernández-Ortı́z, Carlos Macaya

    出版 2011
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  8. 8
    The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project

    The Gene-Environment Interactions in Respiratory Diseases (GEIRD) Project 由 Roberto de Marco, Simone Accordini, Leonardo Antonicelli, Vincenzo Bellia, M.D. Bettin, Cristina Bombieri, F. Bonifazi, Massimiliano Bugiani, Aurelia Carosso, L Casali, Lucia Cazzoletti, Isa Cerveri, Angelo Guido Corsico, Marcello Ferrari, Alessandro G. Fois, Vincenzo Lo Cascio, Alessandro Marcon, Alessandra Marinoni, Mario Olivieri, Luigi Perbellini, П. Ф. Пигнатти, Pietro Pirina, Albino Poli, Giovanni Rolla, Elisabetta Trabetti, Giovanna Verlato, Simona Villani, Maria Elisabetta Zanolin

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  9. 9
    IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma

    IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma 由 Lenuta Balaci, Maria Cristina Spada, Nazario Olla, Gabriella Sole, Laura Loddo, Francesca Anedda, Silvia Naitza, Maria Antonietta Zuncheddu, Andrea Maschio, Daniele Altea, Manuela Uda, Sabrina Pilia, Serena Sanna, Marco Masala, Laura Crisponi, Matilde Fattori, Marcella Devoto, Silvia Doratiotto, Stefania Rassu, S Mereu, Enrico Giua, Natalina Graziella Cadeddu, Roberto Atzeni, Umberto Pelosi, A Corrias, Roberto Perra, Pier Luigi Torrazza, Pietro Pirina, Francesco Ginesu, Silvano Marcias, Maria Grazia Schintu, Del Giacco Gs, Paolo Emilio Manconi, Giovanni Malerba, Andrea Bisognin, Elisabetta Trabetti, Attilio Boner, Lydia Pescollderungg, Pier Franco Pignatti, David Schlessinger, Antonio Cao, Giuseppe Pilia

    出版 2007
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism 由 Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Lambertus Klei, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Alfredo Brusco, Brian Hon‐Yin Chung, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina Girard, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Evelise Riberi, Rebecca J. Schmidt, Moyra Smith, Claudia I.C. Souza, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski

    出版 2021
    獲取全文 獲取全文
    Pré-impressão
    加到收藏夾
    Saved in:
  11. 11
    Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

    Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans 由 Jennifer E. Huffman, Eva Albrecht, Alexander Teumer, Massimo Mangino, Karen Kapur, Toby Johnson, Zoltán Kutalik, Nicola Pirastu, Giorgio Pistis, Lorna M. Lopez, Toomas Haller, Perttu Salo, Anuj Goel, Man Li, Toshiko Tanaka, Abbas Dehghan, Daniela Ruggiero, Giovanni Malerba, Albert V. Smith, Ilja M. Nolte, Laura Portas, Amanda Phipps‐Green, Lora Boteva, Pau Navarro, Åsa Johansson, Andrew A. Hicks, Ozren Polašek, Tõnu Esko, John F. Peden, Sarah E. Harris, Federico Murgia, Sarah H. Wild, Albert Tenesa, Adrienne Tin, Evelin Mihailov, Anne Grotevendt, Gauti Kjartan Gíslason, Josef Coresh, Pio D’Adamo, Sheila Ulivi, Péter Vollenweider, Gérard Waeber, Susan Campbell, Ivana Kolčić, Krista Fisher, Margus Viigimaa, Jeffrey Metter, Corrado Masciullo, Elisabetta Trabetti, Cristina Bombieri, Rossella Sorice, Angela Döring, Eva Reischl, Konstantin Strauch, Albert Hofman, André G. Uitterlinden, Mélanie Waldenberger, H‐Erich Wichmann, Gail Davies, Alan J. Gow, Nicola Dalbeth, Lisa K. Stamp, Johannes H. Smit, Mirna Kirin, Ramaiah Nagaraja, Matthias Nauck, Claudia Schurmann, Kathrin Budde, Susan M. Farrington, Evropi Τheodoratou, Antti Jula, Veikko Salomaa, Cinzia Sala, Christian Hengstenberg, Michel Burnier, Reedik Mägi, Norman Klopp, Stefan Kloiber, Sabine Schipf, Samuli Ripatti, Stefano Cabras, Nicole Soranzo, Georg Homuth, Teresa Nutile, Patricia B. Munroe, Nicholas D. Hastie, Harry Campbell, Igor Rudan, Claudia Cabrera, Chris Haley, Oscar H. Franco, Tony R. Merriman, Vilmundur Guðnason, Mario Pirastu, Brenda W.J.H. Penninx, Harold Snieder, Andres Metspalu, Marina Ciullo, Peter P. Pramstaller, Cornelia M. van Duijn

    出版 2015
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  12. 12
    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel 由 Jie Huang, Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min, Petr Danecek, Giovanni Malerba, Elisabetta Trabetti, Hou‐Feng Zheng, Saeed Al Turki, Antoinette Amuzu, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Bala, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Marianne Benn, Jamie Bentham, Shoumo Bhattacharya, Ewan Birney, Douglas Blackwood, Martin Bobrow, Elena G. Bochukova, Patrick Bolton, Rebecca Bounds, Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Juan P. Casas, John C. Chambers, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Cocca, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Ian N.M. Day, Aaron Day-Williams, George Dedoussis, Thomas A. Down, Yuanping Du, Cornelia M. van Duijn, Ian Dunham, Sarah Edkins, Rosemary Ekong, Peter Ellis, David M. Evans, I. Sadaf Farooqi, David Fitzpatrick, Paul Flicek, James Floyd, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Paolo Gasparini, Tom R. Gaunt, Matthias Geihs, Daniel H. Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xiaosen Guo, Xueqin Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Jie Huang, Tim Hubbard, Steve E. Humphries, Matthew E. Hurles, Pirro G. Hysi, Valentina Iotchkova, Aaron Isaacs, David K. Jackson, Yalda Jamshidi, Jon Johnson, Christopher Joyce, Konrad J. Karczewski, Jane Kaye, Thomas Keane, John P. Kemp

    出版 2015
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  13. 13
    Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies

    Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies 由 Themistocles L. Assimes, Hilma Hólm, Sekar Kathiresan, Muredach P. Reilly, Guðmar Þorleifsson, Benjamin F. Voight, Jeanette Erdmann, Christina Willenborg, Dhananjay Vaidya, Changchun Xie, C. C. Patterson, Thomas M. Morgan, Mary Susan Burnett, Mingyao Li, Mark A. Hlatky, Joshua W. Knowles, John R. Thompson, Devin Absher, Carlos Iribarren, Alan S. Go, Stephen P. Fortmann, Stephen Sidney, Neil Risch, Hua Tang, Richard M. Myers, Kenneth I. Berger, Monika Stoll, Svati H. Shah, Guðmundur Þorgeirsson, Karl Andersen, Aki S. Havulinna, J. Enrique Herrera, Nauder Faraday, Yoonhee Kim, Brian G. Kral, Rasika A. Mathias, Ingo Ruczinski, Bhoom Suktitipat, Alexander F. Wilson, Lisa R. Yanek, Lewis C. Becker, Patrick Linsel‐Nitschke, Wolfgang Lieb, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Wibke Reinhard, Janina Winogradow, Martina Grassl, Anika Großhennig, Michael Preuß, Stefan Schreiber, H-Erich Wichmann, Christa Meisinger, Jean Yee, Yechiel Friedlander, Ron Do, James B. Meigs, Gordon H. Williams, David M. Nathan, Calum A. MacRae, Liming Qu, Robert L. Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Augusto D. Pichard, Kenneth M. Kent, Lowell F. Satler, Joseph Lindsay, Ron Waksman, Christopher W. Knouff, Dawn Waterworth, Max Walker, Vincent Mooser, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, Nicola Martinelli, Oliviero Olivieri, Elisabetta Trabetti, Giovanni Malerba, Pier Franco Pignatti, Candace Guiducci, Daniel B. Mirel, Melissa Parkin, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Yan V. Sun, Mark J. Daly, Shaun Purcell, Sandra Eifert, Peter S. Braund, Benjamin J. Wright, Anthony J. Balmforth, Stephen G. Ball

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  14. 14
    Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

    Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm 由 Sólveig Grétarsdóttir, Annette F. Baas, Guðmar Þorleifsson, Hilma Hólm, Martin den Heijer, Jean-Paul P.M. de Vries, Steef Kranendonk, Clark J. Zeebregts, S.M. van Sterkenburg, Robert H. Geelkerken, André M. van Rij, Michael Williams, A.P.M. Boll, Jelena P. Kostic, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, G. Bragi Walters, Gísli Másson, Patrick Sulem, Jona Saemundsdottir, Magali Mouy, Kristinn P. Magnússon, Gerard Tromp, James R. Elmore, Natzi Sakalihasan, Raymond Limet, Jean-Olivier Defraigne, Robert E. Ferrell, Antti Ronkainen, Ynte M. Ruigrok, Cisca Wijmenga, Diederick E. Grobbee, Svati H. Shah, Christopher B. Granger, Arshed A. Quyyumi, Viola Vaccarino, Riyaz S. Patel, A. Maziar Zafari, Allan I. Levey, Harland Austin, Domenico Girelli, Pier Franco Pignatti, Oliviero Olivieri, Nicola Martinelli, Giovanni Malerba, Elisabetta Trabetti, Lewis C. Becker, Diane M. Becker, Muredach P. Reilly, Daniel J. Rader, Thomas Mueller, Benjamin Dieplinger, Meinhard Haltmayer, Sigitas Urbonavičius, Bengt Lindblad, Anders Gottsäter, Eleonora Gaetani, Roberto Pola, Philip Wells, Marc Rodger, Melissa Forgie, Nicole Langlois, Javier Corral, Vicente Vicente, J. Fontcuberta, Francisco España, Niels Grarup, Torben Jørgensen, Daniel R. Witte, Torben Hansen, Oluf Pedersen, Katja K.H. Aben, Jacqueline de Graaf, Suzanne Holewijn, Lasse Folkersen, Anders Franco‐Cereceda, Per Eriksson, David Collier, Hreinn Stefánsson, Valgerður Steinthórsdóttir, Þórunn Rafnar, Einar Már Valdimarsson, Hulda B. Magnadottir, Sigurlaug Sveinbjörnsdóttir, Ísleifur Ólafsson, Magnús K. Magnússon, Róbert Pálmason, Vilhelmína Haraldsdóttir, Karl Andersen, Páll T. Önundarson, Guðmundur Þorgeirsson, Lambertus A. Kiemeney, Janet T. Powell, David J. Carey, Helena Kuivaniemi, Jes S. Lindholt, Gregory T. Jones, Augustine Kong, Jan D. Blankensteijn, Stefán E. Matthíasson

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  15. 15
    Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

    Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension 由 Praveen Surendran, Fotios Drenos, Robin Young, Helen R. Warren, James P. Cook, Alisa K. Manning, Niels Grarup, Xueling Sim, Daniel R. Barnes, Kate Witkowska, James R Staley, Vinicius Tragante, Taru Tukiainen, Hanieh Yaghootkar, Nicholas G. D. Masca, Daniel F. Freitag, Teresa Ferreira, Olga Giannakopoulou, Andrew Tinker, Magdaléna Harakaľová, Evelin Mihailov, Chunyu Liu, Aldi T. Kraja, Yan V. Sun, Asif Rasheed, Maria Samuel, Wei Zhao, Lori L. Bonnycastle, Anne Jackson, Narisu Narisu, Amy J. Swift, Lorraine Southam, Jonathan Marten, Jeroen R. Huyghe, Alena Stančáková, Cristiano Fava, Therese Ohlsson, Angela Matchan, Kathleen Stirrups, Jette Bork‐Jensen, Anette P. Gjesing, Jukka Kontto, Markus Perola, Susan Shaw-Hawkins, Aki S. Havulinna, He Zhang, Louise A. Donnelly, Christopher J. Groves, Nigel W. Rayner, Matt J. Neville, Neil R. Robertson, Andrianos M. Yiorkas, Karl‐Heinz Herzig, Eero Kajantie, Weihua Zhang, Sara M. Willems, Lars Lannfelt, Giovanni Malerba, Nicole Soranzo, Elisabetta Trabetti, Niek Verweij, Εvangelos Εvangelou, Alireza Moayyeri, Anne‐Claire Vergnaud, Christopher P. Nelson, Alaitz Poveda, Tibor V. Varga, Muriel Caslake, Anton J. M. de Craen, Stella Trompet, Jian’an Luan, Robert A. Scott, Sarah E. Harris, David C. Liewald, Riccardo E. Marioni, Cristina Menni, Aliki-Eleni Farmaki, Göran Hallmans, Frida Renström, Jennifer E. Huffman, Maija Hassinen, Stephen Burgess, Ramachandran S. Vasan, Janine F. Felix, Maria Uria-Nickelsen, Anders Mälarstig, Dermot F. Reilly, Maarten Hoek, Thomas Vogt, Honghuang Lin, Wolfgang Lieb, Matthew Traylor, Hugh S. Markus, Heather M. Highland, Anne E. Justice, Eirini Marouli, Jaana Lindström, Matti Uusitupa, Pirjo Komulainen, Timo A. Lakka

    出版 2016
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  16. 16
    Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

    Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 由 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

    出版 2018
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  17. 17
    Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

    Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders 由 Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe, Madelyn A. Gillentine, Amy B. Wilfert, Luis A. Pérez‐Jurado, Malin Kvarnung, Yoeri Sleyp, Rachel K. Earl, Jill A. Rosenfeld, Madeleine R. Geisheker, Lin Han, Bing Du, Chris Barnett, E. A. Thompson, Marie Shaw, Renée Carroll, Kathryn Friend, Rachael Catford, Elizabeth E. Palmer, Xiaobing Zou, Jianjun Ou, Honghui Li, Hui Guo, Jennifer Gerdts, Emanuela Avola, Giuseppe Calabrese, Maurizio Elia, Donatella Greco, Anna Lindstrand, Ann Nordgren, Britt‐Marie Anderlid, Geert Vandeweyer, Anke Van Dijck, Nathalie Van der Aa, Brooke G. McKenna, Miroslava Hančárová, Šárka Bendová, Markéta Havlovicová, Giovanni Malerba, Bernardo Dalla Bernardina, Pierandrea Muglia, Arie van Haeringen, Mariëtte J.V. Hoffer, Barbara Franke, Gerarda Cappuccio, Martin B. Delatycki, Paul J. Lockhart, Melanie A. Manning, Pengfei Liu, Ingrid E. Scheffer, Nicola Brunetti‐Pierri, Nanda Rommelse, David G. Amaral, Gijs W.E. Santen, Elisabetta Trabetti, Zdeněk Sedláček, Jacob J. Michaelson, Karen Pierce, Eric Courchesne, R. Frank Kooy, John Acampado, J. Andrea, Alpha Amatya, Irina Astrovskaya, Asif Bashar, Elizabeth Brooks, Martin E. Butler, Lindsey A. Cartner, Wubin Chin, Wendy K. Chung, Amy M. Daniels, Pamela Feliciano, Chris Fleisch, Swami Ganesan, William B. Jensen, Alex E. Lash, Richard P. Marini, Vincent J. Myers, Eirene O’Connor, Chris Rigby, B. E. Robertson, Neelay Shah, Swapnil Shah, Emily Singer, LeeAnne Green Snyder, Alexandra N. Stephens, Jennifer Tjernagel, Brianna M. Vernoia, Natalia Volfovsky, L. Casey White, Alexander Hsieh, Yufeng Shen, Xueya Zhou, Tychele N. Turner, Ethan Bahl, Taylor R. Thomas

    出版 2020
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  18. 18
    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism 由 Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montserrat Fernández Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt

    出版 2022
    獲取全文
    Revisão
    加到收藏夾
    Saved in:

檢索工具: