نتائج بحث المؤلف

1

Genetics of VEGF Serum Variation in Human Isolated Populations of Cilento: Importance of VEGF Polymorphisms حسب Daniela Ruggiero, Cyril Dalmasso, Teresa Nutile, Rossella Sorice, Laura Dionisi, Mario Aversano, Philippe Broët, Anne‐Louise Leutenegger, Catherine Bourgain, Marina Ciullo

منشور في 2011

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Artigo

2

Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways حسب Giorgia Girotto, Nicola Pirastu, Rossella Sorice, Ginevra Biino, Harry Campbell, Pio D’Adamo, N D Hastie, Teresa Nutile, Ozren Polašek, Laura Portas, Igor Rudan, Sheila Ulivi, Tatijana Zemunik, Alan F. Wright, Marina Ciullo, Caroline Hayward, Mario Pirastu, Paolo Gasparini

منشور في 2011

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Revisão

3

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

منشور في 2015

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Revisão

4

Age- And Sex-Related Variations in Platelet Count in Italy: A Proposal of Reference Ranges Based on 40987 Subjects' Data حسب Ginevra Biino, Iolanda Santimone, Cosetta Minelli, Rossella Sorice, Bruno Frongia, Michela Traglia, Sheila Ulivi, Augusto Di Castelnuovo, Martin Gögele, Teresa Nutile, Marcella Francavilla, Cinzia Sala, Nicola Pirastu, Chiara Cerletti, Licia Iacoviello, Paolo Gasparini, Daniela Toniolo, Marina Ciullo, Peter P. Pramstaller, Mario Pirastu, Giovanni de Gaetano, Carlo L. Balduini

منشور في 2013

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Artigo

5

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies حسب Seung Hoan Choi, Daniela Ruggiero, Rossella Sorice, Ci Song, Teresa Nutile, Albert V. Smith, Maria Pina Concas, Michela Traglia, Caterina Barbieri, Ndeye Coumba Ndiaye, Maria G. Stathopoulou, Vasiliki Lagou, Giovanni Battista Maestrale, Cinzia Sala, Stéphanie Debette, Péter Kovács, Lars Lind, John Lamont, Peter Fitzgerald, Anke Tönjes, Vilmundur Guðnason, Daniela Toniolo, Mario Pirastu, Céline Bellenguez, Ramachandran S. Vasan, Erik Ingelsson, Anne‐Louise Leutenegger, Andrew D. Johnson, Anita L. DeStefano, Sophie Visvikis‐Siest, Sudha Seshadri, Marina Ciullo

منشور في 2016

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Revisão

6

Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels حسب Adrienne Tin, Yong Li, Jennifer A. Brody, Teresa Nutile, Audrey Y. Chu, Jennifer E. Huffman, Qiong Yang, Ming‐Huei Chen, Cassianne Robinson‐Cohen, Aurélien Macé, Jun Liu, Ayşe Demirkan, Rossella Sorice, Sanaz Sedaghat, Melody Swen, Bing Yu, Sahar Ghasemi, Alexander Teumer, Péter Vollenweider, Marina Ciullo, Meng Li, André G. Uitterlinden, Robert Kraaij, Najaf Amin, Jeroen van Rooij, Zoltán Kutalik, Abbas Dehghan, Barbara McKnight, Cornelia M. van Duijn, Alanna C. Morrison, Bruce M. Psaty, Eric Boerwinkle, Caroline S. Fox, Owen M. Woodward, Anna Köttgen

منشور في 2018

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Artigo

7

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking حسب Antonio Terracciano, Tõnu Esko, Angelina R. Sutin, Marleen H. M. de Moor, Osorio Meirelles, Gu Zhu, Toshiko Tanaka, Ina Giegling, Teresa Nutile, Anu Realo, Jüri Allïk, Narelle K. Hansell, Margaret J. Wright, Grant W. Montgomery, Gonneke Willemsen, J-J Hottenga, M. Friedl, Daniela Ruggiero, Rossella Sorice, Serena Sanna, Alessandra Cannas, Katri Räikkönen, Elisabeth Widén, Aarno Palotie, Johan G. Eriksson, Francesco Cucca, Robert F. Krueger, Jari Lahti, Michelle Luciano, Jordan W. Smoller, Cornelia M. van Duijn, Gonçalo R. Abecasis, Dorret I. Boomsma, Marina Ciullo, Paul T. Costa, Luigi Ferrucci, Nicholas G. Martin, Andres Metspalu, Dan Rujescu, David Schlessinger, Manuela Uda

منشور في 2011

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Revisão

8

Meta-analysis of genome-wide association studies for personality حسب Marleen H. M. de Moor, Paul T. Costa, Antonio Terracciano, R F Krueger, Eco J. C. de Geus, Toshiko Tanaka, B W J H Penninx, Tõnu Esko, Pamela A. F. Madden, Jaime Derringer, Najaf Amin, Gonneke Willemsen, J-J Hottenga, Marijn A. Distel, Manuela Uda, Serena Sanna, Philip Spinhoven, C A Hartman, Patrick F. Sullivan, Anu Realo, Jüri Allïk, Andrew C. Heath, Michele L. Pergadia, A Agrawal, Ping Lin, Richard A. Grucza, Teresa Nutile, Marina Ciullo, D Rujescu, I Giegling, Bettina Konte, Elisabeth Widén, D L Cousminer, Johan G. Eriksson, Aarno Palotie, L. Peltonen, Michelle Luciano, Albert Tenesa, G Davies, Lorna M. Lopez, Narelle K. Hansell, Sarah E. Medland, Luigi Ferrucci, David Schlessinger, Grant W. Montgomery, Margaret J. Wright, Yurii S. Aulchenko, A. Cecile J.W. Janssens, B A Oostra, Andres Metspalu, Gonçalo R. Abecasis, Ian J. Deary, Katri Räikkönen, L J Bierut, Nicholas G. Martin, Cornelia M. van Duijn, D.I. Boomsma

منشور في 2010

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Revisão

9

Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans حسب 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

منشور في 2015

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Revisão

10

Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory حسب Stéphanie M. van den Berg, Marleen H. M. de Moor, Matt McGue, Erik Pettersson, Antonio Terracciano, Karin J. H. Verweij, Najaf Amin, Jaime Derringer, Tõnu Esko, Gerard van Grootheest, Narelle K. Hansell, Jennifer E. Huffman, Bettina Konte, Jari Lahti, Michelle Luciano, Lindsay Matteson, Alexander Viktorin, Jasper Wouda, Arpana Agrawal, Jüri Allïk, Laura J. Bierut, Ulla Broms, Harry Campbell, George Davey Smith, Johan G. Eriksson, Luigi Ferrucci, Barbara Franke, Jean‐Paul Fox, Eco J. C. de Geus, Ina Giegling, Alan J. Gow, Richard A. Grucza, Annette M. Hartmann, Andrew C. Heath, Kauko Heikkilä, William G. Iacono, Joost Janzing, Markus Jokela, Lambertus A. Kiemeney, Terho Lehtimäki, Pamela A. F. Madden, Patrik K. E. Magnusson, Kate Northstone, Teresa Nutile, Klaasjan G. Ouwens, Aarno Palotie, Alison Pattie, Anu‐Katriina Pesonen, Ozren Polašek, Lea Pulkkinen, Laura Pulkki-Råbäck, Olli T. Raitakari, Anu Realo, Richard J. Rose, Daniela Ruggiero, Ilkka Seppälä, Wendy S. Slutske, David C. Smyth, Rossella Sorice, John M. Starr, Angelina R. Sutin, Toshiko Tanaka, Josine Verhagen, Sita H. Vermeulen, Eero Vuoksimaa, Elisabeth Widén, Gonneke Willemsen, Margaret J. Wright, Lina Zgaga, Dan Rujescu, Andres Metspalu, James F. Wilson, Marina Ciullo, Caroline Hayward, Igor Rudan, Ian J. Deary, Katri Räikkönen, Alejandro Arias Vásquez, Paul T. Costa, Liisa Keltikangas–Järvinen, Cornelia M. van Duijn, Brenda W.J.H. Penninx, Robert F. Krueger, David M. Evans, Jaakko Kaprio, Nancy L. Pedersen, Nicholas G. Martin, Dorret I. Boomsma

منشور في 2014

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Artigo

11

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder حسب Marleen H. M. de Moor, Stéphanie M. van den Berg, Karin J. H. Verweij, Robert F. Krueger, Michelle Luciano, Alejandro Arias Vásquez, Lindsay Matteson, Jaime Derringer, Tõnu Esko, Najaf Amin, Scott D. Gordon, Narelle K. Hansell, Amy Hart, Ilkka Seppälä, Jennifer E. Huffman, Bettina Konte, Jari Lahti, Minyoung Lee, Mike Miller, Teresa Nutile, Toshiko Tanaka, Alexander Teumer, Alexander Viktorin, Juho Wedenoja, Gonçalo R. Abecasis, Daniel E. Adkins, Arpana Agrawal, Jüri Allïk, Katja Appel, T. Bernard Bigdeli, Fabio Busonero, Harry Campbell, Paul T. Costa, George Davey Smith, Gail Davies, Harriet de Wit, Jun Ding, Barbara E. Engelhardt, Johan G. Eriksson, Iryna O. Fedko, Luigi Ferrucci, Barbara Franke, Ina Giegling, Richard A. Grucza, Annette M. Hartmann, Andrew C. Heath, Kati Heinonen, Anjali K. Henders, Georg Homuth, Jouke‐Jan Hottenga, William G. Iacono, Joost Janzing, Markus Jokela, Robert Karlsson, John P. Kemp, Matthew G. Kirkpatrick, Antti Latvala, Terho Lehtimäki, David C. Liewald, Pamela A. F. Madden, Chiara Magri, Patrik K. E. Magnusson, Jonathan Marten, Andrea Maschio, Sarah E. Medland, Evelin Mihailov, Yuri Milaneschi, Grant W. Montgomery, Matthias Nauck, Klaasjan G. Ouwens, Aarno Palotie, Erik Pettersson, Ozren Polašek, Yong Qian, Laura Pulkki-Råbäck, Olli T. Raitakari, Anu Realo, Richard J. Rose, Daniela Ruggiero, Carsten Oliver Schmidt, Wendy S. Slutske, Rossella Sorice, John M. Starr, Beaté St Pourcain, Angelina R. Sutin, Nicholas J. Timpson, Holly Trochet, Sita H. Vermeulen, Eero Vuoksimaa, Elisabeth Widén, Jasper Wouda, Margaret J. Wright, Lina Zgaga, David J. Porteous, Alessandra Minelli, Abraham A. Palmer, Dan Rujescu, Marina Ciullo, Caroline Hayward, Igor Rudan

منشور في 2015

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Revisão

12

Directional dominance on stature and cognition in diverse human populations حسب Peter K. Joshi, Tõnu Esko, Hannele Mattsson, Niina Eklund, Ilaria Gandin, Teresa Nutile, Anne Jackson, Claudia Schurmann, Albert V. Smith, Weihua Zhang, Yukinori Okada, Alena Stančáková, Jessica D. Faul, Wei Zhao, Traci M. Bartz, Maria Pina Concas, Nora Franceschini, Stefan Enroth, Véronique Vitart, Stella Trompet, Xiuqing Guo, Daniel I. Chasman, Jeffrey R. O’Connel, Tanguy Corre, Suraj S. Nongmaithem, Yuning Chen, Massimo Mangino, Daniela Ruggiero, Michela Traglia, Aliki‐Eleni Farmaki, Tim Kacprowski, Andrew Bjonnes, Ashley van der Spek, Ying Wu, Anil K. Giri, Lisa R. Yanek, Lihua Wang, Edith Hofer, Cornelius A. Rietveld, Olga McLeod, Marilyn C. Cornelis, Cristian Pattaro, Niek Verweij, Clemens Baumbach, Abdel Abdellaoui, Helen R. Warren, Dragana Vuckovic, Hao Mei, Claude Bouchard, John R. B. Perry, Stefania Cappellani, Saira Saeed Mirza, Miles C. Benton, Ulrich Broeckel, Sarah E. Medland, Penelope A. Lind, Giovanni Malerba, Alexander Drong, Loïc Yengo, Lawrence F. Bielak, Degui Zhi, Peter J. van der Most, Daniel Shriner, Reedik Mägi, Gibran Hemani, Tugce Karaderi, Thomas J. Wang, Tian Liu, Ilja Demuth, Jing Hua Zhao, Weihua Meng, Lazaros Lataniotis, Sander W. van der Laan, Jonathan P. Bradfield, Andrew R. Wood, Amélie Bonnefond, Tarunveer S. Ahluwalia, Leanne M. Hall, Erika Salvi, Seyhan Yazar, Lisbeth Carstensen, Hugoline G. de Haan, Mark Abney, Uzma Afzal, Matthew Allison, Najaf Amin, Folkert W. Asselbergs, Stephan J. L. Bakker, R. Graham Barr, Sebastian E. Baumeister, Daniel J. Benjamin, Sven Bergmann, Eric Boerwinkle, Erwin P. Böttinger, Archie Campbell, Aravinda Chakravarti, Yingleong Chan, Stephen J. Chanock, Constance Chen, Y.-D. Ida Chen

منشور في 2015

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13

52 Genetic Loci Influencing Myocardial Mass حسب Pim van der Harst, Jessica van Setten, Niek Verweij, Georg Vogler, Lude Franke, Matthew T. Maurano, Xinchen Wang, Irene Mateo Leach, Mark Eijgelsheim, Nona Sotoodehnia, Caroline Hayward, Rossella Sorice, Osorio Meirelles, Leo‐Pekka Lyytikäinen, Ozren Polašek, Toshiko Tanaka, Dan E. Arking, Sheila Ulivi, Stella Trompet, Martina Müller‐Nurasyid, Albert V. Smith, Marcus Dörr, Kathleen F. Kerr, Jared W. Magnani, Fabiola Del Greco M, Weihua Zhang, Ilja M. Nolte, Claudia Silva, Sandosh Padmanabhan, Vinicius Tragante, Tõnu Esko, Gonçalo R. Abecasis, Michiel Adriaens, Karl Andersen, Phil Barnett, Joshua C. Bis, Rolf Bodmer, Brendan M. Buckley, Harry Campbell, Megan V. Cannon, Aravinda Chakravarti, Lin Y. Chen, Alessandro Delitala, Richard B. Devereux, Pieter A. Doevendans, Anna F. Dominiczak, Luigi Ferrucci, Ian Ford, Christian Gieger, Tamara B. Harris, Eric Haugen, Matthias Heinig, Dena Hernandez, Hans L. Hillege, Joel N. Hirschhorn, Albert Hofman, Norbert Hübner, Shih-Jen Hwang, Alfonso Iorio, Mika Kähönen, Manolis Kellis, Ivana Kolčić, Ishminder K. Kooner, Jaspal S. Kooner, Jan A. Kors, Edward G. Lakatta, Kasper Lage, Lenore J. Launer, Daniel Levy, Alicia Lundby, Peter W. Macfarlane, Dalit May, Thomas Meitinger, Andres Metspalu, Stefania Nappo, Silvia Naitza, Shane Neph, Alex S. Nord, Teresa Nutile, Peter M. Okin, Jesper V. Olsen, Ben A. Oostra, Josef Penninger, L Pennacchio, Tune H. Pers, Siegfried Perz, Annette Peters, Yigal M. Pinto, Arne Pfeufer, Maria Grazia Pilia, Peter P. Pramstaller, Bram P. Prins, Olli T. Raitakari, Soumya Raychaudhuri, Kenneth Rice, Elizabeth J. Rossin, Jerome I. Rotter, Sebastian Schäfer, David Schlessinger, Carsten Oliver Schmidt

منشور في 2016

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Artigo

14

Genome-wide analysis identifies 12 loci influencing human reproductive behavior حسب Nicola Barban, Rick Jansen, Ronald de Vlaming, Ahmad Vaez, Jornt J. Mandemakers, Felix C. Tropf, Xia Shen, James F. Wilson, Daniel I. Chasman, Ilja M. Nolte, Vinicius Tragante, Sander W. van der Laan, John R. B. Perry, Augustine Kong, Tarunveer S. Ahluwalia, Eva Albrecht, Laura M. Yerges-Armstrong, Gil Atzmon, Kirsi Auro, Kristin L. Ayers, Andrew Bakshi, Danny Ben‐Avraham, Kenneth I. Berger, Aviv Bergman, Lars Bertram, Lawrence F. Bielak, Gyða Björnsdóttir, Marc Jan Bonder, Linda Broer, Minh Bui, Caterina Barbieri, Alana Cavadino, Jorge E. Chavarro, Constance Turman, Maria Pina Concas, Heather J. Cordell, Gail Davies, Peter Eibich, Nicholas Eriksson, Tõnu Esko, Joel Eriksson, Fahimeh Falahi, Janine F. Felix, Mark Alan Fontana, Lude Franke, Ilaria Gandin, Audrey J. Gaskins, Christian Gieger, Erica P. Gunderson, Xiuqing Guo, Caroline Hayward, Chunyan He, Edith Hofer, Hongyan Huang, Peter K. Joshi, Stavroula Kanoni, Robert Karlsson, Stefan Kiechl, Annette Kifley, Alexander Kluttig, Peter Kraft, Vasiliki Lagou, Cécile Lecœur, Jari Lahti, Ruifang Li‐Gao, Penelope A. Lind, Tian Liu, Enes Makalic, Crysovalanto Mamasoula, Lindsay Matteson, Hamdi Mbarek, Patrick F. McArdle, George McMahon, S. Fleur W. Meddens, Evelin Mihailov, Mike Miller, Stacey A. Missmer, Claire Monnereau, Peter J. van der Most, Ronny Myhre, Mike A. Nalls, Teresa Nutile, Ioanna Panagiota Kalafati, Eleonora Porcu, Inga Prokopenko, Kumar B. Rajan, Janet W. Rich‐Edwards, Cornelius A. Rietveld, Antonietta Robino, Lynda M. Rose, Rico Rueedi, Kathleen A. Ryan, Yasaman Saba, Daniel Schmidt, Jennifer A. Smith, Lisette Stolk, Elizabeth A. Streeten, Anke Tönjes, Guðmar Þorleifsson, Sheila Ulivi

منشور في 2016

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Artigo

15

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function حسب Philipp S. Wild, Janine F. Felix, Arne Schillert, Alexander Teumer, Ming‐Huei Chen, Maarten J.G. Leening, Uwe Völker, Vera Großmann, Jennifer A. Brody, Marguerite R. Irvin, Sanjiv J. Shah, Setia Pramana, Wolfgang Lieb, Reinhold Schmidt, Alice Stanton, Dörthe Malzahn, Albert V. Smith, Johan Sundström, Cosetta Minelli, Daniela Ruggiero, Leo‐Pekka Lyytikäinen, Daniel Tiller, J. G. Smith, Claire Monnereau, Marco R. Di Tullio, Solomon K. Musani, Alanna C. Morrison, Tune H. Pers, Michael P. Morley, Marcus E. Kleber, Jayashri Aragam, Emelia J. Benjamin, Joshua C. Bis, Egbert Bisping, Ulrich Broeckel, Susan Cheng, Jaap W. Deckers, Fabiola Del Greco M, Frank Edelmann, Myriam Fornage, Lude Franke, Nele Friedrich, Tamara B. Harris, Edith Hofer, Albert Hofman, Jie Huang, Alun D. Hughes, Mika Kähönen, KNHI investigators, Jochen Kruppa, Karl J. Lackner, Lars Lannfelt, Rafael Laskowski, Lenore J. Launer, Margrét Leósdóttir, Honghuang Lin, Cecilia M. Lindgren, Christina Loley, Calum A. MacRae, Deborah Mascalzoni, Jamil Mayet, Daniel Medenwald, Andrew P. Morris, Christian Müller, Martina Müller‐Nurasyid, Stefania Nappo, Peter M. Nilsson, Sebastian Nuding, Teresa Nutile, Annette Peters, Arne Pfeufer, Diana Pietzner, Peter P. Pramstaller, Olli T. Raitakari, Kenneth Rice, Fernando Rivadeneira, Jerome I. Rotter, Saku Ruohonen, Ralph L. Sacco, Tandaw E. Samdarshi, Helena Schmidt, Andrew Sharp, Denis C. Shields, Rossella Sorice, Nona Sotoodehnia, Bruno H. Stricker, Praveen Surendran, Simon Thom, Anna Maria Töglhofer, André G. Uitterlinden, Rolf Wachter, Henry Völzke, Andreas Ziegler, Thomas Münzel, Winfried März, Thomas P. Cappola, Joel N. Hirschhorn, Gary F. Mitchell, Nicholas L. Smith, Ervin R. Fox

منشور في 2017

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Artigo

16

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

منشور في 2018

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Revisão

17

A catalog of genetic loci associated with kidney function from analyses of a million individuals حسب Matthias Wuttke, Yong Li, Man Li, Karsten B. Sieber, Mary F. Feitosa, Mathias Gorski, Adrienne Tin, Lihua Wang, Audrey Y. Chu, Anselm Hoppmann, Holger Kirsten, Ayush Giri, Jin Fang Chai, Garðar Sveinbjörnsson, Bamidele O. Tayo, Teresa Nutile, Christian Fuchsberger, Jonathan Marten, Massimiliano Cocca, Sahar Ghasemi, Yizhe Xu, Katrin Horn, Damia Noce, Peter J. van der Most, Sanaz Sedaghat, Zhi Yu, Masato Akiyama, Saima Afaq, Tarunveer S. Ahluwalia, Peter Almgren, Najaf Amin, Johan Ärnlöv, Stephan J. L. Bakker, Nisha Bansal, Daniela Baptista, Sven Bergmann, Mary L. Biggs, Ginevra Biino, Michael Boehnke, Eric Boerwinkle, Mathilde Boissel, Erwin P. Böttinger, Thibaud Boutin, Hermann Brenner, Marco Brumat, Ralph Burkhardt, Adam S. Butterworth, Eric Campana, Archie Campbell, Harry Campbell, Mickaël Canouil, Robert J. Carroll, Eulalia Catamo, John C. Chambers, Miao-Ling Chee, Miao-Li Chee, Xu Chen, Ching‐Yu Cheng, Yurong Cheng, Kaare Christensen, Renata Cífková, Marina Ciullo, Maria Pina Concas, James P. Cook, Josef Coresh, Tanguy Corre, Cinzia Sala, Daniele Cusi, John Danesh, E. Warwick Daw, Martin H. de Borst, Alessandro De Grandi, Renée de Mutsert, Aiko P. J. de Vries, Frauke Degenhardt, Graciela Delgado, Ayşe Demirkan, Emanuele Di Angelantonio, Katalin Dittrich, Jasmin Divers, Rajkumar Dorajoo, Kai‐Uwe Eckardt, Georg Ehret, Paul Elliott, Karlhans Endlich, Michele K. Evans, Janine F. Felix, Valencia Hui Xian Foo, Oscar H. Franco, André Franke, Barry I. Freedman, Sandra Freitag‐Wolf, Yechiel Friedlander, Philippe Froguel, Ron T. Gansevoort, He Gao, Paolo Gasparini, J. Michael Gaziano, Vilmantas Giedraitis, Christian Gieger

منشور في 2019

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Revisão

18

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels حسب Adrienne Tin, Jonathan Marten, Victoria L. Halperin Kuhns, Yong Li, Matthias Wuttke, Holger Kirsten, Karsten B. Sieber, Chengxiang Qiu, Mathias Gorski, Zhi Yu, Ayush Giri, Garðar Sveinbjörnsson, Man Li, Audrey Y. Chu, Anselm Hoppmann, Luke J. O’Connor, Bram P. Prins, Teresa Nutile, Damia Noce, Masato Akiyama, Massimiliano Cocca, Sahar Ghasemi, Peter J. van der Most, Katrin Horn, Yizhe Xu, Christian Fuchsberger, Sanaz Sedaghat, Saima Afaq, Najaf Amin, Johan Ärnlöv, Stephan J. L. Bakker, Nisha Bansal, Daniela Baptista, Sven Bergmann, Mary L. Biggs, Ginevra Biino, Eric Boerwinkle, Erwin P. Böttinger, Thibaud Boutin, Marco Brumat, Ralph Burkhardt, Eric Campana, Archie Campbell, Harry Campbell, Robert J. Carroll, Eulalia Catamo, John C. Chambers, Marina Ciullo, Maria Pina Concas, Josef Coresh, Tanguy Corre, Daniele Cusi, Cinzia Sala, Martin H. de Borst, Alessandro De Grandi, Renée de Mutsert, Aiko P. J. de Vries, Graciela Delgado, Ayşe Demirkan, Olivier Devuyst, Katalin Dittrich, Kai‐Uwe Eckardt, Georg Ehret, Karlhans Endlich, Michele K. Evans, Ron T. Gansevoort, Paolo Gasparini, Vilmantas Giedraitis, Christian Gieger, Giorgia Girotto, Martin Gögele, Scott D. Gordon, Daníel F. Guðbjartsson, Vilmundur Guðnason, Toomas Haller, Pavel Hamet, Tamara B. Harris, Caroline Hayward, Andrew A. Hicks, Edith Hofer, Hilma Hólm, Wei Huang, Nina Hutri‐Kähönen, Shih‐Jen Hwang, M. Arfan Ikram, Raychel M. Lewis, Erik Ingelsson, Jóhanna Jakobsdóttir, Ingileif Jónsdóttir, Helgi Jónsson, Peter K. Joshi, Navya Shilpa Josyula, Bettina Jung, Mika Kähönen, Yoichiro Kamatani, Masahiro Kanai, Shona M. Kerr, Wieland Kieß, Marcus E. Kleber, Wolfgang Köenig

منشور في 2019

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Artigo

19

Identification of sixteen novel candidate genes for late onset Parkinson’s disease حسب Alessandro Gialluisi, Mafalda Giovanna Reccia, Nicola Modugno, Teresa Nutile, Alessia Lombardi, Luca Giovanni Di Giovannantonio, Sara Pietracupa, Daniela Ruggiero, Simona Scala, Stefano Gambardella, Alastair Noyce, Rauan Kaiyrzhanov, Ben Middlehurst, Demis A. Kia, Manuela Tan, Henry Houlden, Huw R. Morris, Hélène Plun‐Favreau, Peter Holmans, John Hardy, Daniah Trabzuni, John P. Quinn, Vivien J. Bubb, Kin Y. Mok, Kerri J. Kinghorn, Kimberley J. Billingsley, Nicholas Wood, Patrick A. Lewis, Sebastian R. Schreglmann, Ruth C. Lovering, Lea R’Bibo, Claudia Manzoni, Mie Rizig, Mina Ryten, Sebastian Guelfi, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, Nigel Williams, Karen Morrison, Carl E Clarke, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Mark Cookson, Sara Bandrés‐Ciga, Cornelis Blauwendraat, David W. Craig, Derek P. Narendra, Faraz Faghri, J. Raphael Gibbs, Dena Hernández, Kendall Van Keuren‐Jensen, Joshua Shulman, Hirotaka Iwaki, Hampton L. Leonard, Mike A. Nalls, Laurie Robak, José Brás, Rita Guerreiro, Steven Lubbe, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Andrew Singleton, Sonja W. Scholz, Xylena Reed, Roy N. Alcalay, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohn, Lynne Krohn, Jacobus J. van Hilten, Johan Marinus, Astrid Adarmes‐Gómez, Miquel Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Marta Blázquez Estrada, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, Dolores Buiza‐Rueda, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Jordi Clarimón, Yaroslau Compta

منشور في 2021

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Artigo

20

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by andro... حسب Markus Scholz, Katrin Horn, Janne Pott, Matthias Wuttke, Andreas Kühnapfel, M. Kamal Nasr, Holger Kirsten, Yong Li, Anselm Hoppmann, Mathias Gorski, Sahar Ghasemi, Man Li, Adrienne Tin, Jin Fang Chai, Massimiliano Cocca, Luyu Wang, Teresa Nutile, Masato Akiyama, Bjørn Olav Åsvold, Nisha Bansal, Mary L. Biggs, Thibaud Boutin, Hermann Brenner, Ben Brumpton, Ralph Burkhardt, Jianwen Cai, Archie Campbell, Harry Campbell, John Chalmers, Daniel I. Chasman, Miao Ling Chee, Miao Li Chee, Xu Chen, Ching‐Yu Cheng, Renata Cífková, Martha L. Daviglus, Graciela Delgado, Katalin Dittrich, Todd L. Edwards, Karlhans Endlich, J. Michael Gaziano, Ayush Giri, Franco Giulianini, Scott D. Gordon, Daníel F. Guðbjartsson, Stein Hallan, Pavel Hamet, Catharina A. Hartman, Caroline Hayward, Iris M. Heid, Jacklyn N. Hellwege, Bernd Holleczek, Hilma Hólm, Nina Hutri‐Kähönen, Kristian Hveem, Berend Isermann, Jost B. Jonas, Peter K. Joshi, Yoichiro Kamatani, Masahiro Kanai, Mika Kastarinen, Chiea Chuen Khor, Wieland Kieß, Marcus E. Kleber, Antje Körner, Péter Kovács, Alena Krajčoviechová, Holly Kramer, Bernhard K. Krämer, Mikko Kuokkanen, Mika Kähönen, Leslie A. Lange, James P. Lash, Terho Lehtimäki, Hengtong Li, Bridget M. Lin, Jianjun Liu, Markus Loeffler, Leo‐Pekka Lyytikäinen, Patrik K. E. Magnusson, Nicholas G. Martin, Koichi Matsuda, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Grant W. Montgomery, Dennis O. Mook‐Kanamori, Josyf C. Mychaleckyj, Winfried März, Matthias Nauck, Kjell Nikus, Ilja M. Nolte, Raymond Noordam, Yukinori Okada, Ísleifur Ólafsson, Albertine J. Oldehinkel, Brenda W.J.H. Penninx, Markus Perola, Nicola Pirastu, Ozren Polašek

منشور في 2024

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Revisão

نتائج البحث - Teresa Nutile

Genetics of VEGF Serum Variation in Human Isolated Populations of Cilento: Importance of VEGF Polymorphisms حسب Daniela Ruggiero, Cyril Dalmasso, Teresa Nutile, Rossella Sorice, Laura Dionisi, Mario Aversano, Philippe Broët, Anne‐Louise Leutenegger, Catherine Bourgain, Marina Ciullo

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