Search Results - Céline Bellenguez

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  1. 1
    Genetics of Alzheimer’s disease: where we are, and where we are going

    Genetics of Alzheimer’s disease: where we are, and where we are going by Céline Bellenguez, Benjamin Grenier‐Boley, Jean‐Charles Lambert

    Published 2019
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  2. 2
    Step by step: towards a better understanding of the genetic architecture of Alzheimer’s disease

    Step by step: towards a better understanding of the genetic architecture of Alzheimer’s disease by Jean‐Charles Lambert, Alfredo Ramı́rez, Benjamin Grenier‐Boley, Céline Bellenguez

    Published 2023
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  3. 3
    A robust clustering algorithm for identifying problematic samples in genome-wide association studies

    A robust clustering algorithm for identifying problematic samples in genome-wide association studies by Céline Bellenguez, Amy Strange, Colin Freeman, Peter Donnelly, Chris C. A. Spencer

    Published 2011
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  4. 4
    PLD3 and sporadic Alzheimer's disease risk

    PLD3 and sporadic Alzheimer's disease risk by Jean‐Charles Lambert, Benjamin Grenier‐Boley, Céline Bellenguez, Florence Pasquier, Dominique Campion, Jean‐François Dartigues, Claudine Berr, Christophe Tzourio, Philippe Amouyel

    Published 2015
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  5. 5
    Genome-wide association interaction analysis for Alzheimer's disease

    Genome-wide association interaction analysis for Alzheimer's disease by Elena S. Gusareva, Minerva M. Carrasquillo, Céline Bellenguez, Elise Cuyvers, Samuel Colon, Neill R. Graff‐Radford, Ronald C. Petersen, Dennis W. Dickson, Jestinah Mahachie John, Kyrylo Bessonov, Christine Van Broeckhoven, Denise Harold, Julie Williams, Philippe Amouyel, Kristel Sleegers, Nilüfer Ertekin‐Taner, Jean‐Charles Lambert, Kristel Van Steen

    Published 2014
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  6. 6
    Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology

    Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology by Pierre Dourlen, Francisco-José Fernández-Gómez, Clément Dupont, Benjamin Grenier‐Boley, Céline Bellenguez, Hélène Obriot, Raphaëlle Caillierez, Yoann Sottejeau, Julien Chapuis, Alexis Bretteville, Farida Abdelfettah, C. Delay, Nicolas Malmanche, Hilkka Soininen, Mikko Hiltunen, Marie‐Christine Galas, Philippe Amouyel, Nicolas Sergeant, Luc Buée, Jean‐Charles Lambert, Bart Dermaut

    Published 2016
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  7. 7
    Genome‐wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways

    Genome‐wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways by Richard Sherva, Alden L. Gross, Shubhabrata Mukherjee, Ryan Koesterer, Philippe Amouyel, Céline Bellenguez, Carole Dufouil, David Bennett, Lori B. Chibnik, Carlos Cruchaga, Jorge L. Del-Águila, Lindsay A. Farrer, Richard Mayeux, Leanne Munsie, Ashley R. Winslow, Stephen Newhouse, Andrew J. Saykin, John S.K. Kauwe, Paul K. Crane, Robert C. Green

    Published 2020
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  8. 8
    Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

    Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies by 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

    Published 2016
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  9. 9
    Risk Variants Associated With Normal Pressure Hydrocephalus

    Risk Variants Associated With Normal Pressure Hydrocephalus by Joel Räsänen, Sami Heikkinen, Kiira Mäklin, Anssi Lipponen, Teemu Kuulasmaa, Juha Mehtonen, Ville E. Korhonen, Antti Junkkari, Benjamin Grenier‐Boley, Céline Bellenguez, Minna Oinas, Cecilia Avellan, Janek Frantzén, Anna Kotkansalo, Jaakko Rinne, Antti Ronkainen, Mikko Kauppinen, Mikael von und zu Fraunberg, Kimmo Lönnrot, Jarno Satopää, Markus Perola, Anne M. Koivisto, Valtteri Julkunen, Anne M. Portaankorva, Graham J. Mann, Hilkka Soininen, Seppo Helisalmi, Juha E. Jääskeläinen, Jean‐Charles Lambert, Per Kristian Eide, Aarno Palotie, Mitja Kurki, Mikko Hiltunen, Ville Leinonen

    Published 2024
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  10. 10
    Association of variants in<i>HTRA1</i>and<i>NOTCH3</i>with MRI-defined extremes of cerebral small vessel disease in older subjects

    Association of variants in<i>HTRA1</i>and<i>NOTCH3</i>with MRI-defined extremes of cerebral small vessel disease in older subjects by Aniket Mishra, Ganesh Chauhan, Marie-Helene Violleau, Dina Vojinović, Xueqiu Jian, Joshua C. Bis, Shuo Li, Yasaman Saba, Benjamin Grenier‐Boley, Qiong Yang, Traci M. Bartz, Edith Hofer, Aïcha Soumaré, Fen Peng, Marie-Gabrielle Duperron, Mario Foglio, Thomas H. Mosley, Reinhold Schmidt, Bruce M. Psaty, Lenore J. Launer, Eric Boerwinkle, Yi‐Cheng Zhu, Bernard Mazoyer, Mark Lathrop, Céline Bellenguez, Cornelia M. van Duijn, M. Arfan Ikram, Helena Schmidt, W.T. Longstreth, Myriam Fornage, Sudha Seshadri, Anne Joutel, Christophe Tzourio, Stéphanie Debette

    Published 2019
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  11. 11
    SUCLG2 identified as both a determinator of CSF Aβ1–42 levels and an attenuator of cognitive decline in Alzheimer's disease

    SUCLG2 identified as both a determinator of CSF Aβ1–42 levels and an attenuator of cognitive decline in Alzheimer's disease by Alfredo Ramı́rez, Wiesje M. van der Flier, Christine Herold, David Ramonet, Stefanie Heilmann‐Heimbach, Piotr Lewczuk, Julius Popp, André Lacour, Dmitriy Drichel, Eva Louwersheimer, Markus P. Kummer, Carlos Cruchaga, Per Hoffmann, Charlotte E. Teunissen, Henne Holstege, Johannes Kornhuber, Oliver Peters, Adam C. Naj, Vincent Chouraki, Céline Bellenguez, Amy Gerrish, Reiner Heun, Lutz Frölich, Michael Hüll, Lara Buscemi, Stefan Herms, Heike Kölsch, Philip Scheltens, Monique M.B. Breteler, Eckart Rüther, Jens Wiltfang, Alison Goate, Frank Jessen, Wolfgang Maier, Michael T. Heneka, Tim Becker, Markus M. Nöthen

    Published 2014
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  12. 12
    Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer’s Disease

    Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer’s Disease by Vincent Chouraki, Christiane Reitz, Fleur Maury, Joshua C. Bis, Céline Bellenguez, Lei Yu, Jóhanna Jakobsdóttir, Shubhabrata Mukherjee, Hieab H.H. Adams, Seung Hoan Choi, Eric B. Larson, Annette L. Fitzpatrick, André G. Uitterlinden, Philip L. De Jager, Albert Hofman, Vilmundur Guðnason, Badri N. Vardarajan, Carla A. Ibrahim‐Verbaas, Sven J. van der Lee, Lorna M. Lopez, Jean‐François Dartigues, Claudine Berr, Philippe Amouyel, David A. Bennett, Cornelia M. van Duijn, Anita L. DeStefano, Lenore J. Launer, M. Arfan Ikram, Paul K. Crane, Jean‐Charles Lambert, Richard Mayeux, Sudha Seshadri

    Published 2016
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  13. 13
    Missense variant in TREML2 protects against Alzheimer's disease

    Missense variant in TREML2 protects against Alzheimer's disease by Bruno A. Benítez, Sheng Chih Jin, Rita Guerreiro, Rob Graham, Jenny Lord, Denise Harold, Rebecca Sims, Jean‐Charles Lambert, J. Raphael Gibbs, José Brás, Celeste Sassi, Oscar Harari, Sarah Bertelsen, Michelle K. Lupton, John Powell, Céline Bellenguez, Kristelle Brown, Christopher Medway, Patrick C. G. Haddick, Marcel P. van der Brug, Tushar Bhangale, Ward Ortmann, Tim Behrens, Richard Mayeux, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Gerard D. Schellenberg, Jonathan L. Haines, James Turton, Anne Braae, Imelda Barber, Anne M. Fagan, David M. Holtzman, John C. Morris, Julie Williams, John S.K. Kauwe, Philippe Amouyel, Kevin Morgan, Andy Singleton, John Hardy, Alison Goate, Carlos Cruchaga

    Published 2013
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  14. 14
    Follow-up of loci from the International Genomics of Alzheimer’s Disease Project identifies TRIP4 as a novel susceptibility gene

    Follow-up of loci from the International Genomics of Alzheimer’s Disease Project identifies TRIP4 as a novel susceptibility gene by Agustı́n Ruiz, Stefanie Heilmann‐Heimbach, Tim Becker, Isabel Hernández, Holger Wagner, M. Thelen, Ana Mauleón, Maiteé Rosende‐Roca, Céline Bellenguez, Joshua C. Bis, Denise Harold, Amy Gerrish, Rebecca Sims, Óscar Sotolongo‐Grau, Ana Espinosa, Montserrat Alegret, J. López Arrieta, André Lacour, Markus Leber, Jessica Becker, A. Lafuente, Susana Ruiz, Liliana Vargas, Octavio Rodríguez, Gemma Ortega, M-A Dominguez, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Gerard D. Schellenberg, Vincent Chouraki, Lenore J. Launer, Cornelia M. van Duijn, Sudha Seshadri, Carmen Antúnez, Monique M.B. Breteler, Manuel Serrano‐Ríos, Frank Jessen, Lluís Tárraga, Markus M. Nöthen, W. Maier, Merçé Boada, Alfredo Ramı́rez

    Published 2014
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  15. 15
    Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

    Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology by Julien Chapuis, Franck Hansmannel, Marc Gistelinck, A Mounier, Caroline Van Cauwenberghe, Kristof Van Kolen, Frank Geller, Yoann Sottejeau, Denise Harold, Pierre Dourlen, Benjamin Grenier‐Boley, Yoichiro Kamatani, B. Delepine, Florie Demiautte, Diana Zélénika, Nadège Zommer, Malika Hamdane, Céline Bellenguez, Dartigues Jf, J J Hauw, Florent Letronne, A-M Ayral, Kristel Sleegers, Ann Schellens, Lies Vanden Broeck, Sebastiaan Engelborghs, Peter Paul De Deyn, Rik Vandenberghe, Michael O’Donovan, Michael J. Owen, Jacques Epelbaum, Marc Mercken, Eric Karran, Marcus Bantscheff, Gerard Drewes, Gérard Joberty, Dominique Campion, J-N Octave, Claudine Berr, Mark Lathrop, Patrick Callaerts, David M. A. Mann, Julie Williams, Luc Buée, Ilse Dewachter, Christine Van Broeckhoven, Philippe Amouyel, Dieder Moechars, Bart Dermaut, Jean‐Charles Lambert

    Published 2013
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  16. 16
    Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

    Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis by Michaela Fakiola, Amy Strange, Heather J. Cordell, E. Nancy Miller, Matti Pirinen, Zhan Su, Anshuman Mishra, Sanjana Mehrotra, Glória R. Monteiro, Gavin Band, Céline Bellenguez, Serge Dronov, Sarah Edkins, Colin Freeman, Eleni Giannoulatou, Emma Gray, Sarah Hunt, Hênio Godeiro Lacerda, Cordelia Langford, Richard D. Pearson, Núbia N. Pontes, Madhukar Rai, Shri Prakash Singh, L. J. Smith, Olívia Maria Santos Sousa, Damjan Vukcevic, Elvira Bramon, Matthew A. Brown, Juan P. Casas, Aiden Corvin, Audrey Duncanson, Janusz Jankowski, Hugh S. Markus, Christopher G. Mathew, Colin N. A. Palmer, Robert Plomin, Anna Rautanen, Stephen Sawcer, Richard C. Trembath, Ananth C. Viswanathan, Nicholas Wood, Mary E. Wilson, Panos Deloukas, Leena Peltonen, Frank Christiansen, Campbell S. Witt, Selma M. B. Jerônimo, Shyam Sundar, Chris C. A. Spencer, Jenefer M. Blackwell, Peter Donnelly

    Published 2013
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  17. 17
    Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

    Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21 by Chris C. A. Spencer, Vincent Plagnol, A. Strange, Michelle Gardner, Coro Paisán‐Ruíz, Guido P. H. Band, Roger A. Barker, Céline Bellenguez, Kailash P. Bhatia, H. Blackburn, J. M. Blackwell, Elvira Bramon, Matthew A. Brown, Matthew A. Brown, David J. Burn, Juan P. Casas, Patrick F. Chinnery, Carl E Clarke, Aiden Corvin, Nick Craddock, Panos Deloukas, Sarah Edkins, Jonathan Evans, Colin L. Freeman, Emma Gray, John Hardy, Gavin Hudson, Sarah Hunt, Janusz Jankowski, C. Langford, Andrew Lees, Hugh S. Markus, Christopher G. Mathew, Mark I. McCarthy, Karen Morrison, Colin N. A. Palmer, Justin Pearson, L. Peltonen, Matti Pirinen, Robert Plomin, Simon Potter, Anna Rautanen, Stephen Sawcer, Zhan Su, Richard C. Trembath, A. C. Viswanathan, Namor Williams, Huw R. Morris, Peter Donnelly, Nicholas Wood

    Published 2010
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  18. 18
    Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

    Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes by Kaixin Zhou, Céline Bellenguez, Chris C A Spencer, Amanda J. Bennett, Ruth L. Coleman, Roger Tavendale, Simon A. Hawley, Louise A. Donnelly, Chris Schofield, Christopher J. Groves, Lindsay Burch, Fiona Carr, Amy Strange, Colin Freeman, Jenefer M Blackwell, Elvira Bramon, Matthew A. Brown, Juan Pablo Casas, Aiden Corvin, Nicholas Craddock, Panos Deloukas, Serge Dronov, Audrey Duncanson, Sarah Edkins, Emma Gray, Sarah Hunt, Janusz Jankowski, Cordelia Langford, Hugh S Markus, Christopher G. Mathew, Robert Plomin, Anna Rautanen, Stephen J Sawcer, Nilesh J. Samani, Richard C. Trembath, Ananth C Viswanathan, Nicholas Wood, Lorna W. Harries, Andrew T. Hattersley, Alex S. F. Doney, Helen M. Colhoun, Andrew D. Morris, Calum Sutherland, D. Grahame Hardie, Leena Peltonen, Mark I. McCarthy, Rury R. Holman, Colin N. A. Palmer, Peter Donnelly, Ewan R. Pearson

    Published 2010
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  19. 19
    Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease

    Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease by Carolina Dalmasso, Luis Ignacio Brusco, Natividad Olivar, Carolina Muchnik, Claudia Hanses, Esther Milz, Julian Becker, Stefanie Heilmann‐Heimbach, Per Hoffmann, Federico Ariel Prestia, Pablo Galeano, Mariana Soledad Sanchez Avalos, Luis Eduardo Martínez, Mariana Estela Carulla, Pablo Javier Azurmendi, Cynthia Liberczuk, Cristina Fezza, Marcelo Sampaño, Maria Fierens, Guillermo Jemar, Patricia Solís, Nancy Medel, Julieta Lisso, Zulma Sevillano, Paolo Bosco, Paola Bossù, Gianfranco Spalletta, Daniela Galimberti, Michelangelo Mancuso, Benedetta Nacmias, Sandro Sorbi, Patrizia Mecocci, Alberto Pilotto, Paolo Caffarra, Francesco Panza, María J. Bullido, Jordi Clarimón, Pascual Sánchez‐Juan, Eliécer Coto, Florentino Sánchez-García, Caroline Graff, Martin Ingelsson, Céline Bellenguez, Eduardo M. Castaño, Claudia Kairiyama, Daniel Gustavo Politis, Silvia Kochen, Horacio Scaro, Wolfgang Maier, Frank Jessen, Carlos A. Mangone, Jean‐Charles Lambert, Laura Morelli, Alfredo Ramı́rez

    Published 2019
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  20. 20
    Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy

    Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy by Estelle Colin, Jens Daniel, Alban Ziegler, Jamal Wakim, Aurora Scrivo, Tobias B. Haack, Salim Khiati, Anne‐Sophie Denommé‐Pichon, Patrizia Amati‐Bonneau, Majida Charif, Vincent Procaccio, Pascal Reynier, Kyrieckos A. Aleck, Lorenzo D. Botto, Claudia Lena Herper, Charlotte Sophia Kaiser, Rima Nabbout, Sylvie N’Guyen, José Antonio Mora-Lorca, Birgit Assmann, Stine Christ, Thomas Meitinger, Tim M. Strom, Holger Prokisch, Antonio Miranda‐Vizuete, Georg F. Hoffmann, Guy Lenaers, Pascale Bomont, Eva Liebau, Dominique Bonneau, Emmanuelle Génin, Dominique Campion, Jean‐François Dartigues, Jean‐François Deleuze, Jean‐Charles Lambert, Richard Redon, Thomas Ludwig, Benjamin Grenier‐Boley, Sébastien Letort, Pierre Lindenbaum, Vincent Meyer, Olivier Quenez, Christian Dina, Céline Bellenguez, Camille Charbonnier -Le Clézio, Joanna Giemza, Stéphanie Chatel, Claude Férec, Hervé Le Marec, Luc Letenneur, Gaël Nicolas, Karen Rouault, Delphine Bacq, Anne Boland, Doris Lechner

    Published 2016
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