Céline Bellenguez
Active 2009–2025
- 59
- Papers
- 27,257
- Citations
- 51
- h-index
- 57
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.1%
- University College London0.9%
- Broad Institute0.7%
- King's College London0.6%
- Inserm0.6%
- Massachusetts General Hospital0.6%
- Other95.5%
Fields
- Medicine42.3%
- Biochemistry, Genetics and Molecular Biology31.6%
- Neuroscience14.3%
- Immunology and Microbiology6.5%
- Computer Science1%
- Environmental Science0.9%
- Other3.4%
Topics
- Alzheimer's disease research and treatments9.4%
- Genetic Associations and Epidemiology5.9%
- Neuroinflammation and Neurodegeneration Mechanisms5.4%
- Dementia and Cognitive Impairment Research2.9%
- Bioinformatics and Genomic Networks2.9%
- Epigenetics and DNA Methylation1.8%
- Other71.7%
Coauthors
- Benjamin Grenier‐Boley30
- Joshua C. Bis20
- Rebecca Sims14
- Adam C. Naj11
- Itziar de Rojas11
- Sven J. van der Lee11
- Anne Boland10
- Jean‐Charles Lambert10
- Philippe Amouyel10
- Vincent Chouraki10
- Anita L. DeStefano9
- Amy Strange8
- Badri N. Vardarajan8
- Brian W. Kunkle8
- Chris C. A. Spencer8
- Fahri Küçükali8
- M. Arfan Ikram8
- Matti Pirinen8
- Zhan Su8
- Albert V. Smith7
- Denise Harold7
- Gavin Band7
- Iris E. Jansen7
- Sonia Moreno–Grau7
All papers
- New insights into the genetic etiology of Alzheimer’s disease and related dementias
Authors: Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Luca Kleineidam, Sonia Moreno–Grau, Najaf Amin, Adam C. Naj, Rafael Campos-Martín, Benjamin Grenier‐Boley, Víctor Andrade, Peter Holmans, Anne Boland, Vincent Damotte, Sven J. van der Lee, Marcos R. Costa, Teemu Kuulasmaa, Qiong Yang, Itziar de Rojas, Joshua C. Bis, Amber Yaqub, Ivana Nedeljković, Julien Chapuis, Shahzad Ahmad, Vilmantas Giedraitis, Dag Aarsland, Pablo García‐González, Carla Abdelnour, Emilio Alarcón‐Martín, Daniel Alcolea, Montserrat Alegret, Ignacio Álvarez, Victoria Álvarez, Nicola J. Armstrong, Anthoula Tsolaki, Carmen Antúnez, Ildebrando Appollonio, Marina Arcaro, Silvana Archetti, Alfonso Arias Pastor, Beatrice Arosio, Lavinia Athanasiu, Henri Bailly, Nerisa Banaj, Miquel Baquero, Sandra Barral, Alexa Beiser, Ana Belén Pastor, Jennifer E. Below, Penelope Benchek, Luisa Benussi, Claudine Berr, Céline Besse, Valentina Bessi, Giuliano Binetti, Alessandra Bizarro, Rafael Blesa, Merçé Boada, Eric Boerwinkle, Barbara Borroni, Silvia Boschi, Paola Bossù, Geir Bråthen, Jan Bressler, Catherine Bresner, Henry Brodaty, Keeley J. Brookes, Luis Ignacio Brusco, Dolores Buiza‐Rueda, Katharina Bürger, Vanessa Burholt, William S. Bush, Miguel Calero, Laura B. Cantwell, Geneviève Chêne, Jaeyoon Chung, Michael L. Cuccaro, Ãngel Carracedo, Roberta Cecchetti, Laura Cervera‐Carles, Camille Charbonnier, Hung‐Hsin Chen, Caterina Chillotti, Simona Ciccone, Jurgen A.H.R. Claassen, Christopher Clark, Elisa Conti, Anaïs Corma‐Gómez, Emanuele Maria Costantini, Carlo Custodero, Delphine Daian, Carolina Dalmasso, Antonio Daniele, Efthimios Dardiotis, Jean‐François Dartigues, Peter Paul De Deyn, Kátia de Paiva Lopes, Lot D. de Witte, Stéphanie Debette, Jürgen Deckert, Teodoro del Ser and 1,166 more - Nature Genetics 2022 cited by 2,471
- Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Authors: Brian W. Kunkle, The European Alzheimer’s Disease Initiative (EADI),, Benjamin Grenier‐Boley, Rebecca Sims, Joshua C. Bis, Vincent Damotte, Adam C. Naj, Anne Boland, Maria Vronskaya, Sven J. van der Lee, Alexandre Amlie‐Wolf, Céline Bellenguez, Aura Frizatti, Vincent Chouraki, Eden R. Martin, Kristel Sleegers, Nandini Badarinarayan, Jóhanna Jakobsdóttir, Kara L. Hamilton‐Nelson, Sonia Moreno–Grau, Robert Olaso, Rachel Raybould, Yuning Chen, Amanda B Kuzma, Mikko Hiltunen, Taniesha Morgan, Shahzad Ahmad, Badri N. Vardarajan, Jacques Epelbaum, Per Hoffmann, Merçé Boada, Gary W. Beecham, Jean-Guillaume Garnier, Denise Harold, Annette L. Fitzpatrick, Otto Valladares, Marie-Laure Moutet, Amy Gerrish, Albert V. Smith, Liming Qu, Delphine Bacq, Nicola Denning, Xueqiu Jian, Yi Zhao, Maria Del Zompo, Nick C. Fox, Seung‐Hoan Choi, Ignacio Mateo, Joseph T. Hughes, Hieab H.H. Adams, John Malamon, Florentino Sánchez-García, Yogen Patel, Jennifer A. Brody, Beth A. Dombroski, María Cándida Déniz Naranjo, Makrina Daniilidou, Guðný Eiríksdóttir, Shubhabrata Mukherjee, David Wallon, James Uphill, Thor Aspelund, Laura B. Cantwell, Fabienne Garzia, Daniela Galimberti, Edith Hofer, Mariusz Butkiewicz, Bertrand Fin, Elio Scarpini, Chloé Sarnowski, William S. Bush, Stéphane Meslage, Johannes Kornhuber, Charles C. White, Yuenjoo Song, Robert C. Barber, Sebastiaan Engelborghs, Sabrina Sordon, Dina Voijnovic, Perrie M. Adams, Rik Vandenberghe, Manuel Mayhaus, L. Adrienne Cupples, Marilyn S. Albert, Peter Paul De Deyn, Wei Gu, J.J. Himali, Duane Beekly, Alessio Squassina, Annette M. Hartmann, Adelina Orellana, Deborah Blacker, Eloy Rodríguez‐Rodríguez, Simon Lovestone, Melissa E. Garcia, Rachelle S. Doody, Carmen Munoz-Fernadez, Rebecca Sussams, Honghuang Lin, Thomas Fairchild and 369 more - Nature Genetics 2019 cited by 3,204
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Authors: European Alzheimer's Disease Initiative (EADI), Jean‐Charles Lambert, Genetic and Environmental Risk in Alzheimer's Disease (GERAD), Carla A. Ibrahim‐Verbaas, Denise Harold, Adam C. Naj, Rebecca Sims, Céline Bellenguez, Gyungah Jun, Anita L. DeStefano, Joshua C Bis, Gary W. Beecham, Benjamin Grenier‐Boley, Giancarlo Russo, Tricia A. Thornton‐Wells, Nicola Jones, Albert V. Smith, Vincent Chouraki, Charlene Thomas, M. Arfan Ikram, Diana Zélénika, Badri N. Vardarajan, Yoichiro Kamatani, Chiao‐Feng Lin, Amy Gerrish, Helena Schmidt, Brian W. Kunkle, Melanie Dunstan, Agustı́n Ruiz, Marie‐Thérèse Bihoreau, Seung‐Hoan Choi, Christiane Reitz, Florence Pasquier, Paul Hollingworth, Alfredo Ramı́rez, Olivier Hanon, Annette L. Fitzpatrick, Joseph D. Buxbaum, Dominique Campion, Paul K. Crane, Clinton T. Baldwin, Tim Becker, Vilmundur Guðnason, Carlos Cruchaga, David Craig, Najaf Amin, Claudine Berr, Oscar L Lopez, Philip L. De Jager, Vincent Deramecourt, Janet Johnston, Denis A. Evans, Simon Lovestone, Luc Letenneur, Francisco Jesús Morón, David C. Rubinsztein, Gudny Eiriksdottir, Kristel Sleegers, Alison Goate, Nathalie Fiévet, Matthew J. Huentelman, Michael Gill, Kristelle Brown, M. Ilyas Kamboh, Lina Keller, Pascale Barberger‐Gateau, Bernadette McGuinness, Eric B. Larson, Robert C. Green, Amanda Myers, Carole Dufouil, Stephen Todd, David Wallon, Seth Love, Ekaterina Rogaeva, John Gallacher, Peter St George‐Hyslop, Jordi Clarimón, Alberto Lleó, Anthony Bayer, Debby W. Tsuang, Lei Yu, Magda Tsolaki, Paola Bossù, Gianfranco Spalletta, Petroula Proitsi, John Collinge, Sandro Sorbi, Florentino Sánchez-García, Nick C. Fox, John Hardy, María Cándida Déniz Naranjo, Paolo Bosco, Robert Clarke, Carol Brayne, Daniela Galimberti, Michelangelo Mancuso, Fiona E. Matthews, Susanne Moebus, Patrizia Mecocci and 84 more - Nature Genetics 2013 cited by 4,659
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Authors: Stephen Sawcer, Maria Ban, Anu Kemppinen, Alastair Compston, Sheila Skidmore, Amie Baker, Colin Freeman, Matti Pirinen, Gavin Band, Amy Strange, Gil McVean, Peter Donnelly, Zhan Su, Eleni Giannoulatou, Chris C. A. Spencer, Céline Bellenguez, Garrett Hellenthal, Anna Rautanen, Nikolaos A. Patsopoulos, Paul I. W. de Bakker, Philip L. De Jager, Cristin Aubin, Kristin Ardlie, Philip L. De Jager, David A. Hafler, Cristin Aubin, Loukas Moutsianas, Philip L. De Jager, Sarah E. Hunt, Susan Pobywajlo, Peter Donnelly, Loukas Moutsianas, Alexander Dilthey, Pamela Whittaker, Sara Widaa, Sarah Hunt, Matthew Waller, Rathi Ravindrarajah, Sarah Edkins, Simon Potter, Naomi Hammond, Suzannah J. Bumpstead, Emma Gray, Michelle Ricketts, Panos Deloukas, Cordelia Langford, Aarno Palotie, M. L. Perez, Matthew Gillman, Hannah Blackburn, Owen T McCann, Rhian Gwilliam, Jennifer Liddle, Serge Dronov, Paul A. Weston, Alagurevathi Jayakumar, Graeme J. Stewart, Rob N. Heard, David R. Booth, Rita Dobosi, Bénédicte Dubois, Katleen Clysters, An Goris, Annette Oturai, Per Soelberg Sørensen, Finn Sellebjerg, Helle Bach Søndergaard, Aarno Palotie, Bernhard Hemmer, Janna Saarela, Dorothea Buck, Bertrand Fontaine, Claire Fontenille, Isabelle Cournu‐Rebeix, Bernhard Hemmer, Muna Hoshi, Dorothea Buck, Sabine Cepok, Stanley Hawkins, Achim Berthele, Frauke Zipp, Frauke Zipp, Roland Martinꝉ, Sabine Roesner, Stephen Leslie, Stanley Hawkins, Hanne F. Harbo, Laura Bergamaschi, Gıancarlo Comı, Mariaemma Rodegher, Vittorio Martinelli, Federica Esposito, Filippo Martinelli Boneschi, Hanne F. Harbo, Ewa Tronczynska, Elisabeth Gulowsen Celius, C. Smestad, Åslaug Rudjord Lorentzen, Hanne F. Harbo, Anne Spurkland and 141 more - Nature 2011 cited by 2,758
- Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Authors: Rebecca Sims, GERAD/PERADES, CHARGE, ADGC, EADI, Sven J. van der Lee, Adam C. Naj, Céline Bellenguez, Nandini Badarinarayan, Jóhanna Jakobsdóttir, Brian W. Kunkle, Anne Boland, Rachel Raybould, Joshua C Bis, Eden R. Martin, Benjamin Grenier‐Boley, Stefanie Heilmann‐Heimbach, Vincent Chouraki, Amanda Kuzma, Kristel Sleegers, Maria Vronskaya, Agustı́n Ruiz, Robert Graham, Robert Olaso, Per Hoffmann, Megan L. Grove, Badri N. Vardarajan, Mikko Hiltunen, Markus M. Nöthen, Charles C. White, Kara L. Hamilton‐Nelson, Jacques Epelbaum, Wolfgang Maier, Seung-Hoan Choi, Gary W. Beecham, Cécile Dulary, Stefan Herms, Albert V. Smith, Cory C. Funk, Céline Derbois, Andreas J. Forstner, Shahzad Ahmad, Hong‐Dong Li, Delphine Bacq, Denise Harold, Claudia L. Satizábal, Otto Valladares, Alessio Squassina, Rhodri Thomas, Jennifer A. Brody, Liming Qu, Pascual Sánchez‐Juan, Taniesha Morgan, Frank J. Wolters, Yi Zhao, Florentino Sánchez-García, Nicola Denning, Myriam Fornage, John Malamon, María Cándida Déniz Naranjo, Elisa Majounie, Thomas H. Mosley, Beth A. Dombroski, David Wallon, Michelle K. Lupton, Josée Dupuis, Patrice L. Whitehead, Laura Fratiglioni, Christopher Medway, Xueqiu Jian, Shubhabrata Mukherjee, Lina Keller, Kristelle Brown, Honghuang Lin, Laura B. Cantwell, Francesco Panza, Bernadette McGuinness, Sonia Moreno–Grau, Jeremy D. Burgess, Vincenzo Solfrizzi, Petra Proitsi, Hieab H.H. Adams, Mariet Allen, Davide Seripa, Pau Pástor, L. Adrienne Cupples, Nathan D. Price, Didier Hannequin, Ana Frank, Daniel Levy, Paramita Chakrabarty, Paolo Caffarra, Ina Giegling, Alexa Beiser, Vilmantas Giedraitis, Harald Hampel, Melissa E. Garcia, Xue Wang, Lars Lannfelt, Patrizia Mecocci, Gudny Eiriksdottir, Paul K. Crane, Florence Pasquier and 350 more - Nature Genetics 2017 cited by 1,104
- Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
Authors: Itziar de Rojas, Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen, Nancy L. Pedersen, Najada Stringa, Anna Zettergren, Isabel Hernández, Laura Montrreal, Carmen Antúnez, Anna Antonell, Rick M. Tankard, Joshua C. Bis, Rebecca Sims, Céline Bellenguez, Inés Quintela, Antonio González-Pérez, Miguel Calero, Emilio Franco‐Macías, Juan Macı́as, Rafael Blesa, Laura Cervera‐Carles, Manuel Menéndez‐González, Ana Frank, José Luís Royo, Fermín Moreno, Raquel Huerto Vilas, Miquel Baquero, Mónica Díez-Fairén, Carmen Lage, Sebastián García‐Madrona, Pablo García‐González, Emilio Alarcón‐Martín, Sergi Valero, Óscar Sotolongo‐Grau, Abbe Ullgren, Adam C. Naj, Afina W. Lemstra, Alba Benaque, Alba Pérez‐Cordón, Alberto Benussi, Alberto Rábano, Alessandro Padovani, Alessio Squassina, Alexandre de Mendonça, Alfonso Arias Pastor, Almar A. L. Kok, Alun Meggy, Ana Belén Pastor, Ana Espinosa, Anaïs Corma‐Gómez, Ángel Martín Montes, Ángela Sanabria, Anita L. DeStefano, Anja Schneider, Annakaisa Haapasalo, Anne Kinhult Ståhlbom, Anne Tybjærg‐Hansen, Annette M. Hartmann, Annika Spottke, Arturo Corbatón Anchuelo, Arvid Rongve, Barbara Borroni, Beatrice Arosio, Benedetta Nacmias, Børge G. Nordestgaard, Brian W. Kunkle, Camille Charbonnier, Carla Abdelnour, Carlo Masullo, Carmen Martínez Rodríguez, Carmen Muñoz-Fernández, Carole Dufouil, Caroline Graff, Catarina B. Ferreira, Caterina Chillotti, Chandra A. Reynolds, Chiara Fenoglio, Christine Van Broeckhoven, Christopher Clark, Claudia Pisanu, Claudia L. Satizábal, Clive Holmes, Dolores Buiza‐Rueda, Dag Aarsland, Dan Rujescu, Daniel Alcolea, Daniela Galimberti, David Wallon, Davide Seripa, Edna Grünblatt, Efthimios Dardiotis, Emrah Düzel, Elio Scarpini, Elisa Conti, Elisa Rubino, Ellen Gelpí, Eloy Rodríguez‐Rodríguez and 472 more - Nature Communications 2021 cited by 338
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
Authors: Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, James Boocock, Eli A. Stahl, Jennifer M. Whitehead Pavlides, Niamh Mullins, Alexander W. Charney, Anil P. S. Ori, Loes M. Olde Loohuis, Enrico Domenici, Arianna Di Florio, Sergi Papiol, János Kálmán, Vassily Trubetskoy, Rolf Adolfsson, Ingrid Agartz, Esben Agerbo, Huda Akil, Diego Albani, Margot Albus, Martin Alda, Madeline Alexander, Ney Alliey‐Rodriguez, Thomas D. Als, Farooq Amin, Adebayo Anjorin, María J. Arranz, Swapnil Awasthi, Silviu‐Alin Bacanu, Judith A. Badner, Marie Bækvad‐Hansen, Steven C. Bakker, Gavin Band, Jack D. Barchas, Inês Barroso, Nicholas Bass, Michael Bauer, Bernhard T. Baune, Martin Begemann, Céline Bellenguez, Richard A. Belliveau, Frank Bellivier, Stephan Bender, Judit Bene, Sarah E. Bergen, Wade H. Berrettini, Elizabeth Bevilacqua, Joanna M. Biernacka, Tim B. Bigdeli, Donald W. Black, Hannah Blackburn, Jenefer M. Blackwell, Douglas Blackwood, Carsten Bøcker Pedersen, Michael Boehnke, Marco P. Boks, Anders D. Børglum, Elvira Bramon, Gerome Breen, Matthew A. Brown, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Monika Budde, Brendan Bulik‐Sullivan, Suzannah J. Bumpstead, William E. Bunney, Margit Burmeister, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Juan P. Casas, Miguel Casas, Stanley V. Catts, Pablo Cervantes, Kimberley D. Chambert, Raymond C. K. Chan, Eric Chen, Ronald Y.L. Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, Toni‐Kim Clarke, C. Robert Cloninger, David Cohen, Nadine Cohen, Jonathan R. I. Coleman, David Collier, Paul Cormican, William Coryell, Nicholas Craddock, David W. Craig and 440 more - Cell 2018 cited by 821
- Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Authors: Athena Hadjixenofontos, Ashley Beecham, Jacob L. McCauley, Clara P. Manrique, Margaret A Pericak‐Vance, Ioanna Konidari, Nikolaos A Patsopoulos, Philip L. De Jager, Michelle Lee, Irene Y. Frohlich, Nikolaos A. Patsopoulos, Chris Spencer, Gavin Band, Céline Bellenguez, Alexander T Dilthey, Céline Bellenguez, Colin Freeman, Alexander Dilthey, Dionysia K. Xifara, Gavin Band, Peter Donnelly, Chris C. A. Spencer, Loukas Moutsianas, Amy Strange, Matti Pirinen, Gil McVean, Mary F. Davis, Nathalie Schnetz‐Boutaud, Jonathan L. Haines, Alastair Compston, Barnaby Fiddes, Stephen Sawcer, Anu Kemppinen, Maria Ban, Amie Baker, Robert Andrews, Chris Cotsapas, Hannah Blackburn, Cristin McCabe, Chris Cotsapas, David A. Hafler, Chris Cotsapas, Carl A. Anderson, Jeffrey C. Barrett, Sarah Hunt, Sarah Edkins, Panos Deloukas, Tejas Shah, Hannah Blackburn, Cordelia Langford, Robert Andrews, David J. Booth, Steve Vucic, Graeme J. Stewart, Leentje Cosemans, An Goris, Bénédicte Dubois, Annette Oturai, Per Soelberg Sørensen, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Virpi Leppä, Isabelle Cournu‐Rebeix, Bertrand Fontaine, Vincent Damotte, Angela Jochim, Juliane Winkelmann, Muni Hoshi, Achim Berthele, Thomas Korn, Rebecca Selter, Viola Biberacher, Volker Siffrin, Verena Grummel, Helena Kronsbein, Dorothea Buck, Laura Bergamaschi, Lucia Corrado, Filippo Martinelli-Boneschi, Claes Martin, Volker Siffrin, Frauke Zipp, Felix Luessi, Giuseppe Liberatore, Christiane Graetz, Eva Zindler, Mariaemma Rodegher, Lucia Corrado, Sandra D’Alfonso, Elisabeth G Celius, Inger-Lise Mero, Lucia Corrado, Sandra D’Alfonso, Jan Hillert, Tomas Olsson, Melissa Sorosina, Paola Brambilla, Giuseppe Liberatore, Magdalena Lindén and 93 more - Nature Genetics 2013 cited by 1,442
- A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
Authors: Amy Strange, Gavin Band, Gavin Band, Matti Pirinen, Chris C. A. Spencer, Céline Bellenguez, Colin L. Freeman, Anna Rautanen, Zhan Su, Francesca Capon, Christopher G. Mathew, Michael E. Weale, Alexandros Onoufriadis, Richard C. Trembath, Michael H. Allen, Alexandros Onoufriadis, Jo Knight, Catherine Smith, Frank O. Nestlé, Richard C. Trembath, Jo Knight, Frank O. Nestlé, Anne Barton, Jane Worthington, Joost Schalkwijk, Patrick L.J.M. Zeeuwen, Judith G.M. Bergboer, Jenefer M. Blackwell, Elvira Bramon, Emma Gray, Suzannah J. Bumpstead, Sarah Hunt, Simon Potter, Sarah Edkins, Cordelia Langford, Leena Peltonen, Panos Deloukas, Juan P. Casas, Michael J. Cork, Rachid Tazi‐Ahnini, Aiden Corvin, Gilean McVean, Alexander Dilthey, Gil McVean, Loukas Moutsianas, Stephen Leslie, Audrey Duncanson, Xavier Estivill, Eva Riveira‐Muñoz, Brian Kirby, Oliver FitzGerald, Emiliano Giardina, Giuseppe Novelli, Wolfgang Weger, Angelika Hofer, Wolfgang Salmhofer, André Reis, Ulrike Hüffmeier, Alan D. Irvine, Janusz Jankowski, Jesús Lascorz, A. David Burden, Joyce Leman, Katarina Wolk, Lotus Mallbris, Mona Ståhle, Hugh S. Markus, W.H. Irwin McLean, Lena Samuelsson, Colin N A Palmer, Carlo Perricone, Robert Plomin, Rotraut Mößner, Åsa Torinsson Naluai, Lena Samuelsson, Heiko Traupe, Carlo Perricone, Robert Plomin, Ramón M. Pujol, Adrian Hayday, Stephen Sawcer, Juha Kere, Catherine Smith, Heiko Traupe - Nature Genetics 2010 cited by 1,058
- Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Authors: Milly S. Tedja, Robert Wojciechowski, Pirro G. Hysi, Nicholas Eriksson, Nicholas A. Furlotte, Virginie J. M. Verhoeven, Adriana I. Iglesias, Magda A. Meester‐Smoor, Stuart W. Tompson, Qiao Fan, Anthony P. Khawaja, Ching‐Yu Cheng, René Höhn, Kenji Yamashiro, Adam S Wenocur, Clare Grazal, Toomas Haller, Andres Metspalu, Juho Wedenoja, Jost B. Jonas, Ya Xing Wang, Jing Xie, Paul Mitchell, Paul J. Foster, Ronald Klein, Ronald Klein, Andrew D. Paterson, S. Mohsen Hosseini, Rupal Shah, Cathy Williams, Yik Ying Teo, Yih Chung Tham, Preeti Gupta, Wanting Zhao, Yuan Shi, Woei‐Yuh Saw, E Shyong Tai, Xueling Sim, Jennifer E. Huffman, Ozren Polašek, Caroline Hayward, Goran Benčić, Igor Rudan, James F. Wilson, Peter K. Joshi, Akitaka Tsujikawa, Fumihiko Matsuda, Kristina N. Whisenhunt, Tanja Zeller, Peter J. van der Spek, Roxanna Haak, Hanne Meijers-Heijboer, Elisabeth M. van Leeuwen, Sudha K. Iyengar, Jonathan H. Lass, Albert Hofman, Fernando Rivadeneira, André G. Uitterlinden, Johannes R. Vingerling, Terho Lehtimäki, Olli T. Raitakari, Ginevra Biino, Maria Pina Concas, Tae-Hwi Schwantes-An, Robert P. Igo, Gabriel Cuéllar-Partida, Nicholas G. Martin, Jamie E. Craig, Puya Gharahkhani, Katie Williams, Abhishek Nag, Jugnoo S. Rahi, Phillippa Cumberland, Cécile Delcourt, Céline Bellenguez, Janina S. Ried, Arthur A. Bergen, Thomas Meitinger, Christian Gieger, Tien Yin Wong, Alex W. Hewitt, David A. Mackey, Claire L. Simpson, Norbert Pfeiffer, Olavi Pärssinen, Paul N. Baird, Véronique Vitart, Najaf Amin, Cornelia M. van Duijn, Joan E. Bailey‐Wilson, Terri L. Young, Seang‐Mei Saw, Dwight Stambolian, Stuart MacGregor, Jeremy A. Guggenheim, Joyce Y. Tung, Christopher J. Hammond, Caroline C. W. Klaver - Nature Genetics 2018 cited by 378
- Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
Authors: Jiao Luo, Jesper Qvist Thomassen, Céline Bellenguez, Benjamin Grenier‐Boley, Itziar de Rojas, Atahualpa Castillo-Morales, Kayenat Parveen, Fahri Küçükali, Aude Nicolas, Oliver Peters, Anja Schneider, Martin Dichgans, Dan Rujescu, Norbert Scherbaum, Jürgen Deckert, Steffi G. Riedel‐Heller, Lucrezia Hausner, Laura Molina‐Porcel, Emrah Düzel, Timo Grimmer, Jens Wiltfang, Stefanie Heilmann‐Heimbach, Susanne Moebus, Thomas Tegos, Nikolaos Scarmeas, Jordi Clarimón, Fermín Moreno, Jordi Pérez‐Tur, María J. Bullido, Pau Pástor, Raquel Sánchez‐Valle, Victoria Álvarez, Merçé Boada, Pablo García‐González, Raquel Puerta, Pablo Mir, Luís Miguel Real, Gerard Piñol‐Ripoll, José María García‐Alberca, José Luís Royo, Eloy Rodríguez‐Rodríguez, Hilkka Soininen, Teemu Kuulasmaa, Alexandre de Mendonça, Shima Mehrabian, Jakub Hort, Martin Vyhnálek, Sven J. van der Lee, Caroline Graff, Goran Papenberg, Vilmantas Giedraitis, Anne Boland, Delphine Bacq‐Daian, Jean‐François Deleuze, Gaël Nicolas, Carole Dufouil, Florence Pasquier, Olivier Hanon, Stéphanie Debette, Edna Grünblatt, Julius Popp, Luisa Benussi, Daniela Galimberti, Beatrice Arosio, Patrizia Mecocci, Vincenzo Solfrizzi, Lucilla Parnetti, Alessio Squassina, Lucio Tremolizzo, Barbara Borroni, Benedetta Nacmias, Sandro Sorbi, Paolo Caffarra, Davide Seripa, Innocenzo Rainero, Antonio Daniele, Carlo Masullo, Gianfranco Spalletta, Julie Williams, Philippe Amouyel, Frank Jessen, Patrick G. Kehoe, Magda Tsolaki, Giacomina Rossi, Pascual Sánchez‐Juan, Kristel Sleegers, Martin Ingelsson, Ole A. Andreassen, Mikko Hiltunen, Cornelia M. van Duijn, Rebecca Sims, Wiesje M. van der Flier, Agustı́n Ruiz, Alfredo Ramı́rez, Jean‐Charles Lambert, Ruth Frikke‐Schmidt - JAMA Network Open 2023 cited by 93
- A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease
Authors: The International Genomics of Alzheimer's Project, Kuan-lin Huang, The Alzheimer's Disease Neuroimaging Initiative, Edoardo Marcora, Anna A. Pimenova, Antonio Fabio Di Narzo, Manav Kapoor, Sheng Chih Jin, Oscar Harari, Sarah Bertelsen, Benjamin P. Fairfax, Jake Czajkowski, Vincent Chouraki, Benjamin Grenier‐Boley, Céline Bellenguez, Yuetiva Deming, Andrew McKenzie, Towfique Raj, Alan E. Renton, John Budde, Albert V. Smith, Annette L. Fitzpatrick, Joshua C Bis, Anita L. DeStefano, Hieab H.H. Adams, M. Arfan Ikram, Sven J. van der Lee, Jorge L. Del‐Aguila, María Victoria Fernández, Laura Ibáñez, Rebecca Sims, Valentina Escott‐Price, Richard Mayeux, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Jean‐Charles Lambert, Cornelia M. van Duijn, Lenore J. Launer, Sudha Seshadri, Julie Williams, Philippe Amouyel, Gerard D. Schellenberg, Bin Zhang, Ingrid B. Borecki, John S.K. Kauwe, Carlos Cruchaga, Ke Hao, Alison Goate - Nature Neuroscience 2017 cited by 471
- Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
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- Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
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Authors: Yann Le Guen, Guo Luo, Aditya Ambati, Vincent Damotte, Iris E. Jansen, Eric Yu, Aude Nicolas, Itziar de Rojas, Thiago Peixoto Leal, Akinori Miyashita, Céline Bellenguez, Michelle Mulan Lian, Kayenat Parveen, Takashi Morizono, Hyeonseul Park, Benjamin Grenier‐Boley, Tatsuhiko Naito, Fahri Küçükali, Seth D. Talyansky, Selina Yogeshwar, Vicente Peris Sempere, Wataru Satake, Victoria Álvarez, Beatrice Arosio, Michaël E. Belloy, Luisa Benussi, Anne Boland, Barbara Borroni, María J. Bullido, Paolo Caffarra, Jordi Clarimón, Antonio Daniele, D.H. Darling, Stéphanie Debette, Jean‐François Deleuze, Martin Dichgans, Carole Dufouil, Emmanuel During, Emrah Düzel, Daniela Galimberti, Guillermo García‐Ribas, José María García‐Alberca, Pablo García-González, Vilmantas Giedraitis, Oliver Goldhardt, Caroline Graff, Edna Grünblatt, Olivier Hanon, Lucrezia Hausner, Stefanie Heilmann‐Heimbach, Henne Holstege, Jakub Hort, Yoo Jin Jung, Jürgen Deckert, Silke Kern, Teemu Kuulasmaa, Kun Ho Lee, Ling Lin, Carlo Masullo, Patrizia Mecocci, Shima Mehrabian, Alexandre de Mendonça, Merçé Boada, Pablo Mir, Susanne Moebus, Fermín Moreno, Benedetta Nacmias, Gaël Nicolas, Shumpei Niida, Børge G. Nordestgaard, Goran Papenberg, Janne M. Papma, Lucilla Parnetti, Florence Pasquier, Pau Pástor, Oliver Peters, Yolande A.L. Pijnenburg, Gerard Piñol‐Ripoll, Julius Popp, Laura Molina‐Porcel, Raquel Puerta, Jordi Pérez‐Tur, Innocenzo Rainero, Inez H.G.B. Ramakers, Luís Miguel Real, Steffi G. Riedel‐Heller, Eloy Rodríguez‐Rodríguez, Owen A. Ross, José Luís Royo, Dan Rujescu, Nikolaos Scarmeas, Philip Scheltens, Norbert Scherbaum, Anja Schneider, Davide Seripa, Ingmar Skoog, Vincenzo Solfrizzi, Gianfranco Spalletta, Alessio Squassina, John C. van Swieten and 835 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2023 cited by 51
- Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
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- Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
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