Výsledky vyhledávání - Ashley Beecham

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  1. 1
    Properties of global‐ and local‐ancestry adjustments in genetic association tests in admixed populations

    Properties of global‐ and local‐ancestry adjustments in genetic association tests in admixed populations Autor Eden R. Martin, Ilker Tunc, Zhi Liu, Susan H. Slifer, Ashley Beecham, Gary W. Beecham

    Vydáno 2017
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  2. 2
    Association of the Sirtuin and Mitochondrial Uncoupling Protein Genes with Carotid Plaque

    Association of the Sirtuin and Mitochondrial Uncoupling Protein Genes with Carotid Plaque Autor Chuanhui Dong, David Della‐Morte, Liyong Wang, Digna Cabral, Ashley Beecham, Mark S. McClendon, Corneliu Luca, Susan H. Blanton, Ralph L. Sacco, Tatjana Rundek

    Vydáno 2011
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  3. 3
    GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis

    GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis Autor John P. Hussman, Ashley Beecham, Michael A. Schmidt, Eden R. Martin, Jacob L. McCauley, Jeffery M. Vance, Jonathan L. Haines, Margaret A. Pericak‐Vance

    Vydáno 2016
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  4. 4
    Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA–CLEC16A–SOCS1 gene complex

    Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA–CLEC16A–SOCS1 gene complex Autor Rebecca L. Zuvich, William S. Bush, Jacob L. McCauley, Ashley Beecham, Philip L. De Jager, Adrian J. Ivinson, Alastair Compston, David A. Hafler, Stephen L. Hauser, Stephen Sawcer, Margaret A. Pericak‐Vance, Lisa F. Barcellos, Douglas P. Mortlock, Jonathan L. Haines

    Vydáno 2011
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  5. 5
    An ImmunoChip study of multiple sclerosis risk in African Americans

    An ImmunoChip study of multiple sclerosis risk in African Americans Autor Noriko Isobe, Lohith Madireddy, Pouya Khankhanian, Takuya Matsushita, Stacy J. Caillier, Jayaji M. Moré, Pierre‐Antoine Gourraud, Jacob L. McCauley, Ashley Beecham, Laura Piccio, Joseph Herbert, Omar Khan, Jeffrey A. Cohen, Lael A. Stone, Adam Santaniello, Bruce Cree, Suna Önengüt-Gümüşcü, Stephen S. Rich, Stephen L. Hauser, Stephen Sawcer, Jorge R. Oksenberg

    Vydáno 2015
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  6. 6
    Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci

    Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci Autor Jacob L. McCauley, Rebecca L. Zuvich, Ashley Beecham, Philip L. De Jager, Ioanna Konidari, Patrice L. Whitehead, Cristin Aubin, Maria Ban, Susan Pobywajlo, Rebeccah Briskin, Susan Romano, Neelum T. Aggarwal, Laura Piccio, Wendy L. McArdle, David P. Strachan, Denis A. Evans, Anne H. Cross, Bruce Cree, John D. Rioux, Lisa F. Barcellos, Adrian J. Ivinson, Alastair Compston, David A. Hafler, Stephen L. Hauser, Jorge R. Oksenberg, Stephen Sawcer, Margaret A. Pericak‐Vance, Jonathan L. Haines

    Vydáno 2009
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  7. 7
    Class II HLA interactions modulate genetic risk for multiple sclerosis

    Class II HLA interactions modulate genetic risk for multiple sclerosis Autor Loukas Moutsianas, Luke Jostins-Dean, Ashley Beecham, Alexander Dilthey, Dionysia K Xifara, Maria Ban, Tejas Shah, Nikolaos A. Patsopoulos, Lars Alfredsson, Carl A. Anderson, Kathrine E. Attfield, Sergio E. Baranzini, Jeffrey C. Barrett, Thomas M.C. Binder, David R. Booth, Dorothea Buck, Elisabeth Gulowsen Celius, Chris Cotsapas, Sandra D’Alfonso, Calliope A. Dendrou, Peter Donnelly, Bénédicte Dubois, Bertrand Fontaine, Lars Fugger, An Goris, Pierre‐Antoine Gourraud, Christiane Graetz, Bernhard Hemmer, Jan Hillert, Ingrid Kockum, Stephen Leslie, Christina M. Lill, Filippo Martinelli Boneschi, Jorge R. Oksenberg, Tomas Olsson, Annette Oturai, Janna Saarela, Helle Bach Søndergaard, Anne Spurkland, Bruce Taylor, Juliane Winkelmann, Frauke Zipp, Jonathan L. Haines, Margaret A. Pericak‐Vance, Chris C. A. Spencer, Graeme J. Stewart, David A. Hafler, Adrian J. Ivinson, Hanne F. Harbo, Stephen L. Hauser, Philip L. De Jager, Alastair Compston, Jacob L. McCauley, Stephen Sawcer, Gil McVean

    Vydáno 2015
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  8. 8
    A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis

    A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis Autor Lohith Madireddy, Nikolaos A. Patsopoulos, Chris Cotsapas, Steffan D. Bos, Ashley Beecham, Jacob L. McCauley, Kicheol Kim, Xiaoming Jia, Adam Santaniello, Stacy J. Caillier, Till F. M. Andlauer, Lisa F. Barcellos, Tone Berge, Luisa Bernardinelli, Filippo Martinelli Boneschi, David R. Booth, Farren Briggs, Elisabeth Gulowsen Celius, Manuel Comabella, Giacomo P. Comi, Bruce Cree, Sandra D’Alfonso, Katrina Dedham, Pierre Duquette, Efthimios Dardiotis, Federica Esposito, Bertrand Fontaine, Christiane Gasperi, An Goris, Bénédicte Dubois, Pierre‐Antoine Gourraud, Georgios Hadjigeorgiou, Jonathan L. Haines, Clive Hawkins, Bernhard Hemmer, Rogier Hintzen, Dana Horáková, Noriko Isobe, Seema Kalra, Jun‐ichi Kira, Michael Khalil, Ingrid Kockum, Christina M. Lill, Matthew R. Lincoln, Felix Luessi, Roland Martinꝉ, Annette Oturai, Aarno Palotie, Margaret A. Pericak‐Vance, Roland G. Henry, Janna Saarela, Adrian J. Ivinson, Tomas Olsson, Bruce Taylor, Graeme J. Stewart, Hanne F. Harbo, Alastair Compston, Stephen L. Hauser, D Hafler, Frauke Zipp, Philip L. De Jager, Stephen Sawcer, Jorge R. Oksenberg, Sergio E. Baranzini

    Vydáno 2019
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  9. 9
    Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

    Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis Autor Ashley Beecham, Nikolaos A. Patsopoulos, Dionysia K. Xifara, Mary F. Davis, Anu Kemppinen, Chris Cotsapas, Tejas Shah, Chris C. A. Spencer, David J. Booth, An Goris, Annette Oturai, Janna Saarela, Bertrand Fontaine, Bernhard Hemmer, Claes Martin, Frauke Zipp, Sandra D’Alfonso, Filippo Martinelli Boneschi, Bruce Taylor, Hanne F. Harbo, Ingrid Kockum, Jan Hillert, Tomas Olsson, Maria Ban, Jorge R. Oksenberg, Rogier Hintzen, Lisa F. Barcellos, Cristina Agliardi, Lars Alfredsson, Mehdi Alizadeh, Carl A. Anderson, Robert Andrews, Helle Bach Søndergaard, Amie Baker, Gavin Band, Sergio E. Baranzini, Nadia Barizzone, Jeffrey C. Barrett, Céline Bellenguez, Laura Bergamaschi, Luisa Bernardinelli, Achim Berthele, Viola Biberacher, Thomas M.C. Binder, Hannah Blackburn, Izaura Lima Bomfim, Paola Brambilla, Simon Broadley, Bruno Brochet, Lou Brundin, Dorothea Buck, Helmut Butzkueven, Stacy J. Caillier, William Camu, Wassila Carpentier, Paola Cavalla, Elisabeth Gulowsen Celius, Irène Coman, Gıancarlo Comı, Lucia Corrado, Leentje Cosemans, Isabelle Cournu‐Rebeix, Bruce Cree, Daniele Cusi, Vincent Damotte, Gilles Defer, Silvia Delgado, Panos Deloukas, Alessia Di Sapio, Alexander Dilthey, Peter Donnelly, Bénédicte Dubois, Martin Duddy, Sarah Edkins, Irina Elovaara, Federica Esposito, Nikos Evangelou, Barnaby Fiddes, Judith Field, André Franke, Colin Freeman, Irene Y. Frohlich, Daniela Galimberti, Christian Gieger, Pierre‐Antoine Gourraud, Christiane Graetz, Andrew Graham, Verena Grummel, Clara Guaschino, Athena Hadjixenofontos, Hákon Hákonarson, Christopher Halfpenny, Gillian Hall, Per Hall, Anders Hamsten, James Harley, Timothy Harrower, Clive Hawkins, Garrett Hellenthal, Charles Hillier

    Vydáno 2013
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  10. 10
    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk Autor Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Beecham, Theresa Dankowski, An Goris, Bénédicte Dubois, Marie D’hooghe, Robin Lemmens, Philip Van Damme, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sorensen, Henrik Ullum, Lise Wegner Thørner, Thomas Werge, Janna Saarela, Isabelle Cournu‐Rebeix, Vincent Damotte, Bertrand Fontaine, Léna Guillot‐Noël, Mark Lathrop, Sandra Vukusik, Pierre‐Antoine Gourraud, Till F. M. Andlauer, Viola Pongratz, Dorothea Buck, Christiane Gasperi, Antonios Bayas, Christoph Heesen, Tania Kümpfel, Ralf A. Linker, Friedemann Paul, Martin Stangel, Björn Tackenberg, Florian Then Bergh, Clemens Warnke, Heinz Wiendl, Brigitte Wildemann, Uwe K. Zettl, Ulf Ziemann, Hayrettin Tumani, Ralf Gold, Verena Grummel, Bernhard Hemmer, Benjamin Knier, Christina M. Lill, Felix Luessi, Efthimios Dardiotis, Cristina Agliardi, Nadia Barizzone, Elisabetta Mascia, Luisa Bernardinelli, Giancarlo Comi, Daniele Cusi, Federica Esposito, Laura Ferrè, Cristoforo Comi, Daniela Galimberti, Maurizio Leone, Melissa Sorosina, Julia Mescheriakova, Rogier Hintzen, Cornelia M. van Duijn, Charlotte E. Teunissen, Steffan D. Bos, Kjell‐Morten Myhr, Elisabeth Gulowsen Celius, Benedicte A. Lie, Anne Spurkland, Manuel Comabella, Xavier Montalbán, Lars Alfredsson, Pernilla Stridh, Jan Hillert, Maja Jagodic, Fredrik Piehl, Ilijas Jelčić, Roland Martinꝉ, Mireia Sospedra, Maria Ban, Clive Hawkins, Pirro G. Hysi, Seema Kalra, Fredrik Karpe, Jyoti Khadake, Geneviève Lachance, Matthew Neville, Adam Santaniello, Stacy J. Caillier, Peter A. Calabresi, Bruce Cree, Anne H. Cross, Mary F. Davis, Jonathan L. Haines, Paul I. W. de Bakker, Silvia Delgado, Marieme Dembele, Keith R. Edwards, Kathryn C. Fitzgerald, Hákon Hákonarson

    Vydáno 2018
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  11. 11
    Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

    Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility Autor Nikolaos A. Patsopoulos, Sergio E. Baranzini, Adam Santaniello, Parisa Shoostari, Chris Cotsapas, Garrett Wong, Ashley Beecham, Tojo James, Joseph M. Replogle, Ioannis S. Vlachos, Cristin McCabe, Tune H. Pers, Aaron Brandes, Charles C. White, Brendan T Keenan, Maria Cimpean, Phoebe A. Winn, Ioannis-Pavlos Panteliadis, Allison Robbins, Till F. M. Andlauer, Onigiusz Zarzycki, Bénédicte Dubois, An Goris, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sorensen, Henrik Ullum, Lise Wegner Thørner, Janna Saarela, Isabelle Cournu‐Rebeix, Vincent Damotte, Bertrand Fontaine, Léna Guillot‐Noël, Mark Lathrop, Sandra Vukusic, Achim Berthele, Viola Pongratz, Dorothea Buck, Christiane Gasperi, Christiane Graetz, Verena Grummel, Bernhard Hemmer, Muni Hoshi, Benjamin Knier, Thomas Korn, Christina M. Lill, Felix Luessi, Mark Mühlau, Frauke Zipp, Efthimios Dardiotis, Cristina Agliardi, Antonio Amoroso, Nadia Barizzone, Maria Donata Benedetti, Luisa Bernardinelli, Paola Cavalla, Ferdinando Clarelli, Gıancarlo Comı, Daniele Cusi, Federica Esposito, Laura Ferrè, Daniela Galimberti, Clara Guaschino, Maurizio Leone, Vittorio Martinelli, Lucia Moiola, Marco Salvetti, Melissa Sorosina, Domizia Vecchio, Andrea Zauli, Silvia Santoro, Nicasio Mancini, Miriam Zuccalà, Julia Mescheriakova, Cornelia M. van Duijn, Steffan D. Bos, Elisabeth Gulowsen Celius, Anne Spurkland, Manuel Comabella, Xavier Montalbán, Lars Alfredsson, Izaura Lima Bomfim, David Gómez-Cabrero, Jan Hillert, Maja Jagodic, Magdalena Lindén, Fredrik Piehl, Ilijas Jelčić, Roland Martinꝉ, Mirela Sospedra, Amie Baker, Maria Ban, Clive Hawkins, Pirro G. Hysi, Seema Kalra, Fredrik Karpe, Jyoti Khadake, Geneviève Lachance, Paul Molyneux, Matthew Neville

    Vydáno 2019
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  12. 12
    Novel genetic loci associated with hippocampal volume

    Novel genetic loci associated with hippocampal volume Autor Derrek P. Hibar, Hieab H.H. Adams, Neda Jahanshad, Ganesh Chauhan, Jason L. Stein, Edith Hofer, Miguel E. Rentería, Joshua C. Bis, Alejandro Arias Vásquez, M. Kamran Ikram, Sylvane Desrivières, Meike W. Vernooij, Lucija Abramovic, Saud Alhusaini, Najaf Amin, Micael Andersson, Konstantinos Arfanakis, Benjamin S. Aribisala, Nicola J. Armstrong, Lavinia Athanasiu, Tomas Axelsson, Ashley Beecham, Alexa Beiser, Manon Bernard, Susan H. Blanton, Marc M. Bohlken, Marco P. Boks, Janita Bralten, Adam M. Brickman, Owen Carmichael, M. Mallar Chakravarty, Qiang Chen, Christopher R. K. Ching, Vincent Chouraki, Gabriel Cuéllar-Partida, Fabrice Crivello, Anouk den Braber, Nhat Trung Doan, Stefan Ehrlich, Sudheer Giddaluru, Aaron L. Goldman, Rebecca F. Gottesman, O. Grimm, Michael Griswold, Tulio Guadalupe, Boris A. Gutman, Johanna Haß, Unn K. Haukvik, David Hoehn, Avram J. Holmes, Martine Hoogman, Deborah Janowitz, Tianye Jia, Kjetil Nordbø Jørgensen, Nazanin Karbalai, Dalia Kasperavičiūtė, Sungeun Kim, Marieke Klein, Bernd Kraemer, Phil H. Lee, David C. Liewald, Lorna M. Lopez, Michelle Luciano, Christine Macare, André F. Marquand, Mar Matarín, Karen A. Mather, Manuel Mattheisen, David R. McKay, Yuri Milaneschi, Susana Muñoz Maniega, Kwangsik Nho, Allison C. Nugent, Paul Nyquist, Loes M. Olde Loohuis, Jaap Oosterlaan, Martina Papmeyer, Lukas Pirpamer, Benno Pütz, Adaikalavan Ramasamy, Jennifer S. Richards, Shannon L. Risacher, Roberto Roiz-Santiañez, Nanda Rommelse, Stefan Ropele, Emma Rose, Natalie A. Royle, Tatjana Rundek, Philipp G. Sämann, Arvin Saremi, Claudia L. Satizábal, Lianne Schmaal, Andrew J. Schork, Li Shen, Jean Shin, Elena Shumskaya, Albert V. Smith, Emma Sprooten, Lachlan T. Strike, Alexander Teumer

    Vydáno 2017
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  13. 13
    Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

    Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility Autor Aleksejs Sazonovs, Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu, Tariq Ahmad, Matthieu Allez, Ashwin N. Ananthakrishnan, Gil Atzmon, Aris Baras, Jeffrey C. Barrett, Nir Barzilai, Laurent Beaugerie, Ashley Beecham, Charles N. Bernstein, Alain Bitton, Bernd Bokemeyer, Andrew Chan, Daniel C. Chung, Isabelle Cleynen, Jacques Cosnes, David J. Cutler, Allan Daly, Oriana M. Damas, Lisa W. Datta, Noor Dawany, Marcella Devoto, Sheila Dodge, Eva Ellinghaus, Laura Fachal, Martti Färkkilâ, William A. Faubion, Manuel A. R. Ferreira, Denis Franchimont, Stacey Gabriel, Tian Ge, Michel Georges, Kyle Gettler, Mamta Giri, Benjamin Gläser, Siegfried Goerg, Philippe Goyette, Daniel B. Graham, Eija Hämäläinen, Talin Haritunians, Graham Heap, Mikko Hiltunen, Marc P. Hoeppner, Julie Horowitz, Peter M. Irving, Vivek Iyer, Chaim Jalas, Judith R. Kelsen, Hamed Khalili, Barbara S. Kirschner, Kimmo Kontula, Jukka Koskela, Subra Kugathasan, Juozas Kupčinskas, Christopher A Lamb, Matthias Laudes, Chloé Lévesque, Adam P. Levine, James D. Lewis, Claire Liefferinckx, Britt-Sabina Loescher, Édouard Louis, John Mansfield, Sandra May, Jacob L. McCauley, Emebet Mengesha, Myriam Mni, Paul Moayyedi, Christopher J. Moran, Rodney D. Newberry, Sirimon O’Charoen, David T. Okou, Bas Oldenburg, Harry Ostrer, Aarno Palotie, Jean Paquette, Joel Pekow, Inga Peter, Marieke Pierik, Cyriel Y. Ponsioen, Nikolas Pontikos, Natalie J. Prescott, Ann E. Pulver, Souad Rahmouni, Daniel L Rice, Päivi Saavalainen, Bruce E. Sands, R. Balfour Sartor, Elena Schiff, Stefan Schreiber, L. Philip Schumm, Anthony W. Segal, Philippe Seksik, Rasha Shawky

    Vydáno 2022
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  14. 14
    Locus for severity implicates CNS resilience in progression of multiple sclerosis

    Locus for severity implicates CNS resilience in progression of multiple sclerosis Autor Adil Harroud, Pernilla Stridh, Jacob L. McCauley, Janna Saarela, Aletta M.R. van den Bosch, Hendrik J. Engelenburg, Ashley Beecham, Lars Alfredsson, Katayoun Alikhani, Lilyana Amezcua, Till F. M. Andlauer, Maria Ban, Lisa F. Barcellos, Nadia Barizzone, Tone Berge, Achim Berthele, Stefan Bittner, Steffan D. Bos, Farren Briggs, Stacy J. Caillier, Peter A. Calabresi, Domenico Caputo, David X. Carmona-Burgos, Paola Cavalla, Elisabeth Gulowsen Celius, Gabriel Cerono, Ángel Chinea, Tanuja Chitnis, Ferdinando Clarelli, Manuel Comabella, Gıancarlo Comı, Chris Cotsapas, Bruce Cree, Sandra D’Alfonso, Efthimios Dardiotis, Philip L. De Jager, Silvia Delgado, Bénédicte Dubois, Sinah Engel, Federica Esposito, Marzena J. Fabis‐Pedrini, Massimo Filippi, Kathryn C. Fitzgerald, Christiane Gasperi, Lissette Gomez, Refujia Gomez, Georgios M. Hadjigeorgiou, Jörg Hamann, Friederike Held, Roland G. Henry, Jan Hillert, Jesse Huang, Inge Huitinga, Talat Islam, Noriko Isobe, Maja Jagodic, Allan G. Kermode, Michael Khalil, Trevor J. Kilpatrick, Ioanna Konidari, Karim L. Kreft, Jeannette Lechner‐Scott, Maurizio Leone, Felix Luessi, Sunny Malhotra, Ali Manouchehrinia, Clara P. Manrique, Filippo Martinelli Boneschi, Andrea C. Martinez, Viviana Martínez-Maldonado, Elisabetta Mascia, Luanne M. Metz, Luciana Midaglia, Xavier Montalbán, Jorge R. Oksenberg, Tomas Olsson, Annette Oturai, Kimmo Pääkkönen, Grant P. Parnell, Nikolaos A. Patsopoulos, Margaret A. Pericak‐Vance, Fredrik Piehl, Justin P. Rubio, Adam Santaniello, Silvia Santoro, Catherine Schaefer, Finn Sellebjerg, Hengameh Shams, Klementy Shchetynsky, Cláudia Silva, Vasileios Siokas, Helle Bach Søndergaard, Melissa Sorosina, Bruce Taylor, Marijne Vandebergh, Eleni S. Vasileiou, Domizia Vecchio, Margarete M. Voortman, Howard L. Weiner, Dennis Wever

    Vydáno 2023
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  15. 15
    Novel genetic loci underlying human intracranial volume identified through genome-wide association

    Novel genetic loci underlying human intracranial volume identified through genome-wide association Autor Hieab H.H. Adams, Derrek P. Hibar, Vincent Chouraki, Jason L. Stein, Paul Nyquist, Miguel E. Rentería, Stella Trompet, Alejandro Arias Vásquez, Sudha Seshadri, Sylvane Desrivières, Ashley Beecham, Neda Jahanshad, Katharina Wittfeld, Sven J. van der Lee, Lucija Abramovic, Saud Alhusaini, Najaf Amin, Micael Andersson, Konstantinos Arfanakis, Benjamin S. Aribisala, Nicola J. Armstrong, Lavinia Athanasiu, Tomas Axelsson, Alexa Beiser, Manon Bernard, Joshua C. Bis, Laura M. E. Blanken, Susan H. Blanton, Marc M. Bohlken, Marco P. Boks, Janita Bralten, Adam M. Brickman, Owen Carmichael, M. Mallar Chakravarty, Ganesh Chauhan, Qiang Chen, Christopher R. K. Ching, Gabriel Cuéllar-Partida, Anouk den Braber, Nhat Trung Doan, Stefan Ehrlich, Irina Filippi, Tian Ge, Sudheer Giddaluru, Aaron L. Goldman, Rebecca F. Gottesman, Corina U. Greven, O. Grimm, Michael Griswold, Tulio Guadalupe, Johanna Haß, Unn K. Haukvik, Saima Hilal, Edith Hofer, David Hoehn, Avram J. Holmes, Martine Hoogman, Deborah Janowitz, Tianye Jia, Dalia Kasperavičiūtė, Sung Eun Kim, Marieke Klein, Bernd Kraemer, Phil H. Lee, Jiemin Liao, David C. Liewald, Lorna M. Lopez, Michelle Luciano, Christine Macare, André F. Marquand, Mar Matarín, Karen A. Mather, Manuel Mattheisen, Bernard Mazoyer, David R. McKay, Rebekah McWhirter, Yuri Milaneschi, Nazanin Mirza‐Schreiber, Ryan L. Muetzel, Susana Muñoz Maniega, Kwangsik Nho, Allison C. Nugent, Loes M. Olde Loohuis, Jaap Oosterlaan, Martina Papmeyer, Irene Pappa, Lukas Pirpamer, Sara Pudas, Benno Pütz, Kumar B. Rajan, Adaikalavan Ramasamy, Jennifer S. Richards, Shannon L. Risacher, Roberto Roiz‐Santiáñez, Nanda Rommelse, Emma J. Rose, Natalie A. Royle, Tatjana Rundek, Philipp G. Sämann, Claudia L. Satizábal

    Vydáno 2016
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  16. 16
    Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

    Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting Autor Ganesh Chauhan, Hieab H.H. Adams, Claudia L. Satizábal, Joshua C. Bis, Alexander Teumer, Muralidharan Sargurupremraj, Edith Hofer, Stella Trompet, Saima Hilal, Albert V. Smith, Xueqiu Jian, Rainer Malik, Matthew Traylor, Sara L. Pulit, Philippe Amouyel, Bernard Mazoyer, Yi‐Cheng Zhu, Sara Kaffashian, Sabrina Schilling, Gary W. Beecham, Thomas J. Montine, Gerard D. Schellenberg, Ólafur Kjartansson, Vilmundur Guðnason, David S. Knopman, Michael Griswold, B. Gwen Windham, Rebecca F. Gottesman, Thomas H. Mosley, Reinhold Schmidt, Yasaman Saba, Helena Schmidt, Fumihiko Takeuchi, Shuhei Yamaguchi, Toru Nabika, Norihiro Kato, Kumar B. Rajan, Neelum T. Aggarwal, Philip L. De Jager, Denis A. Evans, Bruce M. Psaty, Jerome I. Rotter, Kenneth Rice, Oscar L. Lopez, Jiemin Liao, Christopher Chen, Ching‐Yu Cheng, Tien Yin Wong, M. Kamran Ikram, Sven J. van der Lee, Najaf Amin, Vincent Chouraki, Anita L. DeStefano, Hugo J. Aparicio, José R. Romero, Pauline Maillard, Charles DeCarli, Joanna M. Wardlaw, María del C. Valdés Hernández, Michelle Luciano, David C. Liewald, Ian J. Deary, John M. Starr, Mark E. Bastin, Susana Muñoz Maniega, P. Eline Slagboom, Marian Beekman, Joris Deelen, Hae‐Won Uh, Robin Lemmens, Henry Brodaty, Margaret J. Wright, David Ames, Giorgio B. Boncoraglio, Jemma C. Hopewell, Ashley Beecham, Susan H. Blanton, Clinton B. Wright, Ralph L. Sacco, Wei Wen, Anbupalam Thalamuthu, Nicola J. Armstrong, Elizabeth Chong, Peter R. Schofield, John B. Kwok, Jeroen van der Grond, David J. Stott, Ian Ford, J. Wouter Jukema, Meike W. Vernooij, Albert Hofman, André G. Uitterlinden, Aad van der Lugt, Katharina Wittfeld, Hans J. Grabe, Norbert Hosten, Bettina von Sarnowski, Uwe Völker, Christopher Levi, Jordi Jiménez-Conde

    Vydáno 2019
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  17. 17
    Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI

    Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI Autor Benjamin F.J. Verhaaren, Stéphanie Debette, Joshua C. Bis, Jennifer A. Smith, M. Kamran Ikram, Hieab H.H. Adams, Ashley Beecham, Kumar B. Rajan, Lorna M. Lopez, Sandra Barral, Mark A. van Buchem, Jeroen van der Grond, Albert V. Smith, Katrin Hegenscheid, Neelum T. Aggarwal, Mariza de Andrade, Elizabeth J. Atkinson, Marian Beekman, Alexa Beiser, Susan H. Blanton, Eric Boerwinkle, Adam M. Brickman, R. Nick Bryan, Ganesh Chauhan, Christopher Chen, Vincent Chouraki, Anton J. M. de Craen, Fabrice Crivello, Ian J. Deary, Joris Deelen, Philip L. De Jager, Carole Dufouil, Mitchell S.V. Elkind, Denis A. Evans, Paul Freudenberger, Rebecca F. Gottesman, Vilmundur Guðnason, Mohamad Habes, Susan R. Heckbert, Gerardo Heiss, Saima Hilal, Edith Hofer, Albert Hofman, Carla A. Ibrahim‐Verbaas, David S. Knopman, Cora E. Lewis, Jiemin Liao, David C. Liewald, Michelle Luciano, Aad van der Lugt, Oliver Martinez, Richard Mayeux, Bernard Mazoyer, Mike A. Nalls, Matthias Nauck, Wiro J. Niessen, Ben A. Oostra, Bruce M. Psaty, Kenneth Rice, Jerome I. Rotter, Bettina von Sarnowski, Helena Schmidt, Pamela J. Schreiner, Maaike Schuur, Stephen Sidney, Sigurður Sigurðsson, P. Eline Slagboom, David J.M. Stott, John C. van Swieten, Alexander Teumer, Anna Maria Töglhofer, Matthew Traylor, Stella Trompet, Stephen T. Turner, Christophe Tzourio, Hae‐Won Uh, André G. Uitterlinden, Meike W. Vernooij, Jing Jing Wang, Tien Yin Wong, Joanna M. Wardlaw, B. Gwen Windham, Katharina Wittfeld, Christiane Wolf, Clinton B. Wright, Qiong Yang, Wei Zhao, Alex Zijdenbos, J. Wouter Jukema, Ralph L. Sacco, Sharon L. R. Kardia, Philippe Amouyel, Thomas H. Mosley, W. T. Longstreth, Charles DeCarli, Cornelia M. van Duijn, Reinhold Schmidt, Lenore J. Launer, Hans J. Grabe, Sudha Seshadri

    Vydáno 2015
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