Результати пошуку - Mathieu Bourgey

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  1. 1
    Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia

    Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia за авторством Jasmine Healy, Chantal Richer, Mathieu Bourgey, Ekaterini A. Kritikou, Daniel Sinnett

    Опубліковано 2010
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  2. 2
    HLA related genetic risk for coeliac disease

    HLA related genetic risk for coeliac disease за авторством Mathieu Bourgey, Giuseppe Calcagno, Nadia Tinto, D. Gennarelli, Patricia Margaritte‐Jeannin, Laura Greco, M.G. Limongelli, O. Esposito, C Marano, R Troncone, A. Spampanato, Françoise Clerget‐Darpoux, Lucia Sacchetti

    Опубліковано 2007
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  3. 3
    Cell-free DNA tissues of origin by methylation profiling reveals significant cell, tissue, and organ-specific injury related to COVID-19 severity

    Cell-free DNA tissues of origin by methylation profiling reveals significant cell, tissue, and organ-specific injury related to COVID-19 severity за авторством Alexandre Pellan Cheng, Matthew P. Cheng, Wei Gu, Joan Sesing Lenz, Elaine Hsu, Erwin Schurr, Guillaume Bourque, Mathieu Bourgey, Jerome Ritz, Francisco M. Marty, Charles Y. Chiu, Donald C. Vinh, Iwijn De Vlaminck

    Опубліковано 2021
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  4. 4
    Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy

    Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy за авторством Charles P. Couturier, Shamini Ayyadhury, Phuong Uyen Le, Javad Nadaf, Jean Monlong, Gabriele Riva, Redouane Allache, Salma Baig, Xiaohua Yan, Mathieu Bourgey, Changseok Lee, Yu Chang David Wang, V. Wee Yong, Marie‐Christine Guiot, Hamed S. Najafabadi, Bratislav Mišić, Jack P. Antel, Guillaume Bourque, Jiannis Ragoussis, Kevin Petrecca

    Опубліковано 2020
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  5. 5
    A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome

    A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome за авторством Claude Bhérer, Robert Eveleigh, Katerina Trajanoska, Janick St-Cyr, Antoine Paccard, Praveen Nadukkalam Ravindran, Elizabeth Caron, Nimara Bader Asbah, Peyton McClelland, Clare Wei, Iris Baumgärtner, Marc Schindewolf, Yvonne Döring, Danielle Perley, François Lefebvre, Patricia Lepage, Mathieu Bourgey, Guillaume Bourque, Jiannis Ragoussis, Vincent Mooser, Daniel Taliun

    Опубліковано 2024
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  6. 6
    GenPipes: an open-source framework for distributed and scalable genomic analyses

    GenPipes: an open-source framework for distributed and scalable genomic analyses за авторством Mathieu Bourgey, Rola Dali, Robert Eveleigh, Kuang Chung Chen, Louis Létourneau, Joël Fillon, Marc Michaud, Maxime Caron, Johanna Sandoval, François Lefebvre, Gary Leveque, Eloi Mercier, David Bujold, Pascale Marquis, Patrick Tran Van, David Anderson de Lima Morais, Julien Tremblay, Xiaojian Shao, Édouard Henrion, Emmanuel González, Pierre-Olivier Quirion, B. Caron, Guillaume Bourque

    Опубліковано 2019
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  7. 7
    K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

    K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas за авторством Dong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos, Xiao-Yang Liu, Adam M. Fontebasso, Éric Bouffet, Ute Bartels, Steffen Albrecht, Jeremy Schwartzentruber, Louis Létourneau, Mathieu Bourgey, Guillaume Bourque, Alexandre Montpetit, Geneviève Bourret, Pierre Lepage, Adam Fleming, Peter Lichter, Marcel Kool, Andreas von Deimling, Dominik Sturm, Andrey Korshunov, Damien Faury, David Jones, Jacek Majewski, Stefan M. Pfister, Nada Jabado, Cynthia Hawkins

    Опубліковано 2012
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  8. 8
    Evolution of chromosome-arm aberrations in breast cancer through genetic network rewiring

    Evolution of chromosome-arm aberrations in breast cancer through genetic network rewiring за авторством Elena Kuzmin, Toby M. Baker, Tom Lesluyes, Jean Monlong, Kento T. Abe, Paula P. Coelho, Michael Schwartz, Joseph Del Corpo, Dongmei Zou, Geneviève Morin, Alain Pacis, Yang Yang, Constanza Martínez, Jarrett J. Barber, Hellen Kuasne, Rui Li, Mathieu Bourgey, Anne-Marie Fortier, Peter Davison, Atilla Ömeroğlu, Marie‐Christine Guiot, Quaid Morris, Claudia L. Kleinman, Sidong Huang, Anne‐Claude Gingras, Jiannis Ragoussis, Guillaume Bourque, Peter Van Loo, Morag Park

    Опубліковано 2024
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  9. 9
    Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot за авторством Donna J. Page, Matthieu J. Miossec, Simon G. Williams, Richard M. Monaghan, Elisavet Fotiou, Heather J. Cordell, Louise Sutcliffe, Ana Töpf, Mathieu Bourgey, Guillaume Bourque, Robert Eveleigh, Sally L. Dunwoodie, David S. Winlaw, Shoumo Bhattacharya, Jeroen Breckpot, Koenraad Devriendt, Marc Gewillig, J. David Brook, Kerry Setchfield, Frances Bu’Lock, John O’Sullivan, Graham Stuart, Connie R. Bezzina, Barbara J.M. Mulder, Alex V. Postma, James R. Bentham, Martín Baron, Sanjeev S. Bhaskar, Graeme Black, William G. Newman, Kathryn E. Hentges, G.M. Lathrop, Mauro Santibanez‐Koref, Bernard Keavney

    Опубліковано 2019
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  10. 10
    Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria

    Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria за авторством Rui Yang, Federico Mele, Lisa Worley, David Langlais, Jérémie Rosain, Ibithal Benhsaien, Houda Elarabi, Carys A. Croft, Jean‐Marc Doisne, Peng Zhang, Marc Weißhaar, David Jarrossay, Daniela Latorre, Yichao Shen, Jing Han, Masato Ogishi, Conor Gruber, Janet Markle, Fatima Al Ali, Mahbuba Rahman, Taushif Khan, Yoann Seeleuthner, Gaspard Kerner, Lucas Husquin, Julia L. Maclsaac, Mohamed Jeljeli, Abderrahmane Errami, Fatima Ailal, Michael S. Kobor, Carmen Oleaga‐Quintas, Manon Roynard, Mathieu Bourgey, Jamila El Baghdadi, Stéphanie Boisson‐Dupuis, Anne Puel, Frédéric Batteux, Flore Rozenberg, Nico Marr, Qiang Pan‐Hammarström, Dusan Bogunovic, Lluís Quintana‐Murci, Thomas Carroll, S. Cindy, Laurent Abel, Aziz Bousfiha, James P. Di Santo, Laurie H. Glimcher, Philippe Gros, Stuart G. Tangye, Federica Sallusto, Jacinta Bustamante, Jean‐Laurent Casanova

    Опубліковано 2020
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  11. 11
    Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations

    Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations за авторством Pawel Buczkowicz, Christine M. Hoeman, Patricia Rakopoulos, Sanja Pajovic, Louis Létourneau, Misko Dzamba, Andrew Morrison, Peter W. Lewis, Éric Bouffet, Ute Bartels, Jennifer Zuccaro, Sameer Agnihotri, Scott Ryall, Mark Barszczyk, Yevgen Chornenkyy, Mathieu Bourgey, Guillaume Bourque, Alexandre Montpetit, Francisco J. Cordero, Pedro Castelo‐Branco, Joshua Mangerel, Uri Tabori, King Ching Ho, Annie Huang, Kathryn R. Taylor, Alan Mackay, Anne Bendel, Javad Nazarian, Jason Fangusaro, Matthias A. Karajannis, David Zagzag, Nicholas K. Foreman, Andrew M. Donson, Julia Hegert, Amy Smith, Jennifer A. Chan, Lucy Lafay-Cousin, Sandra E. Dunn, Juliette Hukin, Christopher Dunham, Katrin Scheinemann, Jean Michaud, Shayna Zelcer, David A. Ramsay, Jason E. Cain, Cameron Brennan, Mark M. Souweidane, Chris Jones, C. David Allis, Michael Brudno, Oren J. Becher, Cynthia Hawkins

    Опубліковано 2014
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  12. 12
    Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19

    Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 за авторством Gundula Povysil, Guillaume Butler‐Laporte, Ning Shang, Chen Wang, Atlas Khan, Manal Alaamery, Tomoko Nakanishi, Sirui Zhou, Vincenzo Forgetta, Robert Eveleigh, Mathieu Bourgey, Naveed Aziz, Steven J.M. Jones, Bartha Maria Knoppers, Stephen W. Scherer, Lisa J. Strug, Pierre Lepage, Jiannis Ragoussis, Guillaume Bourque, Jahad Alghamdi, Nora Aljawini, Nour Albes, Hani Al-Afghani, Bader Alghamdi, Mansour Almutairi, Ebrahim Mahmoud, Leen Abu‐Safieh, Hadeel El Bardisy, Fawz S. Al Harthi, Abdulraheem Alshareef, Bandar A. Suliman, Saleh A. Alqahtani, Abdulaziz Almalik, May Alrashed, Salam Massadeh, Vincent Mooser, Mark Lathrop, Fawzy Mohamed, Yaseen M. Arabi, Hamdi Mbarek, Chadi Saad, Wadha Al‐Muftah, Junghyun Jung, Serghei Mangul, Radja Badji, Asma Al Thani, Said I. Ismail, Ali G. Gharavi, Malak Abedalthagafi, J. Brent Richards, David B. Goldstein, Krzysztof Kiryluk

    Опубліковано 2021
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  13. 13
    Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child

    Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child за авторством Masato Ogishi, Rui Yang, Caner Aytekin, David Langlais, Mathieu Bourgey, Taushif Khan, Fatima Al Ali, Mahbuba Rahman, Ottavia M. Delmonte, Maya Chrabieh, Peng Zhang, Conor Gruber, Simon J. Pelham, András N. Spaan, Jérémie Rosain, Wei‐Te Lei, Scott Drutman, Matthew D. Hellmann, Margaret K. Callahan, Matthew Adamow, Phillip Wong, Jedd D. Wolchok, Geetha Rao, S. Cindy, Yuka Nakajima, Tomonori Yaguchi, Kenji Chamoto, Samuel C. Williams, Jean‐François Emile, Flore Rozenberg, Michael S. Glickman, Franck Rapaport, Gaspard Kerner, Garrett Allington, İlhan Tezcan, Deniz Çağdaş, Ferda Özbay Hoşnut, Figen Doğu, Aydan İkincioğulları, V. Koneti Rao, Leena Kainulainen, Vivien Béziat, Jacinta Bustamante, Sílvia Vilarinho, Richard P. Lifton, Bertrand Boisson, Laurent Abel, Dusan Bogunovic, Nico Marr, Luigi D. Notarangelo, Stuart G. Tangye, Tasuku Honjo, Philippe Gros, Stéphanie Boisson‐Dupuis, Jean‐Laurent Casanova

    Опубліковано 2021
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  14. 14
    Variation in genomic landscape of clear cell renal cell carcinoma across Europe

    Variation in genomic landscape of clear cell renal cell carcinoma across Europe за авторством Ghislaine Scélo, Yasser Riazalhosseini, Liliana Greger, Louis Létourneau, Mar González-Porta, Magdalena B. Wozniak, Mathieu Bourgey, Patricia Harnden, Lars Egevad, Sharon M. Jackson, Mehran Karimzadeh, Madeleine Arseneault, Pierre Lepage, Alexandre How‐Kit, Antoine Daunay, Victor Renault, Hélène Blanché, Emmanuel Tubacher, Jeremy Sehmoun, Juris Vīksna, Edgars Celms, Mārtiņš Opmanis, Andris Zarins, Naveen Vasudev, Morag Seywright, Behnoush Abedi‐Ardekani, Christine Carreira, Peter J. Selby, Jon Cartledge, Graham Byrnes, Jiří Zavadil, Jing Su, Ivana Holcátová, A. Brisuda, Давид Заридзе, Anush Moukeria, Lenka Foretová, Marie Navrátilová, Dana Mateș, Viorel Jinga, Artem V. Artemov, Artem Nedoluzhko, Alexander M. Mazur, Sergey Rastorguev, Eugenia Boulygina, Simon Heath, Marta Gut, Marie‐Thérèse Bihoreau, Doris Lechner, Mario Foglio, Marta Gut, K. G. Skryabin, Egor Prokhortchouk, Anne Cambon‐Thomsen, Johan Rung, Guillaume Bourque, Paul Brennan, Jörg Tost, Rosamonde E. Banks, Alvis Brāzma, G.M. Lathrop

    Опубліковано 2014
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  15. 15
    Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI

    Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI за авторством Yunju Yang, Maria J. Knol, Ruiqi Wang, Aniket Mishra, Dan Liu, Michelle Luciano, Alexander Teumer, Nicola J. Armstrong, Joshua C. Bis, Min A. Jhun, Shuo Li, Hieab H.H. Adams, N. Ahmad Aziz, Mark E. Bastin, Mathieu Bourgey, Jennifer A. Brody, Stefan Frenzel, Rebecca F. Gottesman, Norbert Hosten, Lifang Hou, Sharon L. R. Kardia, Valerie Lohner, Pascale Marquis, Susana Muñoz Maniega, Claudia L. Satizábal, Farzaneh A. Sorond, Maria C. Valdés Hernández, Cornelia M. van Duijn, Meike W. Vernooij, Katharina Wittfeld, Qiong Yang, Wei Zhao, Eric Boerwinkle, Daniel Levy, Ian J. Deary, Jiyang Jiang, Karen A. Mather, Thomas H. Mosley, Bruce M. Psaty, Perminder S. Sachdev, Jennifer A. Smith, Nona Sotoodehnia, Charles DeCarli, Monique M.B. Breteler, M. Arfan Ikram, Hans J. Grabe, Joanna M. Wardlaw, W. T. Longstreth, Lenore J. Launer, Sudha Seshadri, Stéphanie Debette, Myriam Fornage

    Опубліковано 2022
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  16. 16
    Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

    Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy за авторством Vivien Béziat, Franck Rapaport, Jiafen Hu, Matthias Titeux, Mathilde Bonnet des Claustres, Mathieu Bourgey, Heather Griffin, Élise Bandet, S. Cindy, Roya Sherkat, Hassan Rokni‐Zadeh, David M. Louis, Majid Changi‐Ashtiani, Ottavia M. Delmonte, Toshiaki Fukushima, Tanwir Habib, Andrea Guennoun, Taushif Khan, Noemi Bender, Mahbuba Rahman, Frédégonde About, Rui Yang, Geetha Rao, Claire Rouzaud, Jingwei Li, Debra A. Shearer, Karla K. Balogh, Fatima Al Ali, Manar Ata, Soroosh Dabiri, Mana Momenilandi, Justine Nammour, Marie-Alexandra Alyanakian, Marianne Leruez‐Ville, David Guenat, Marie Materna, Léa Marcot, Natasha Vladikine, Christine Soret, Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Jouni Uitto, Émilie Catherinot, Shadi Sadat Navabi, Mohammed Zarhrate, David T. Woodley, Mohamed Jeljeli, Thomas Abraham, Serkan Belkaya, Lazaro Lorenzo, Jérémie Rosain, Mousa Bayat, Fanny Lanternier, Olivier Lortholary, Faramarz Zakavi, Philippe Gros, Gérard Orth, Laurent Abel, Jean‐Luc Prétet, Sylvie Fraitag, Emmanuelle Jouanguy, Mark M. Davis, Stuart G. Tangye, Luigi D. Notarangelo, Nico Marr, Tim Waterboer, David Langlais, John Doorbar, Alain Hovnanian, Neil D. Christensen, Xavier Bossuyt, Mohammad Shahrooei, Jean‐Laurent Casanova

    Опубліковано 2021
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  17. 17
    precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions

    precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions за авторством Nathan D. Olson, Justin Wagner, Jennifer McDaniel, Sarah H. Stephens, Samuel T. Westreich, Anish G. Prasanna, Elaine Johanson, Emily S. Boja, Ezekiel J. Maier, Omar Serang, David Jáspez, José M. Lorenzo-Salazar, Adrián Muñoz‐Barrera, Luis A. Rubio‐Rodríguez, Carlos Flores, Konstantinos Kyriakidis, Andigoni Malousi, Kishwar Shafin, Trevor Pesout, Miten Jain, Benedict Paten, Pi-Chuan Chang, Alexey Kolesnikov, Maria Nattestad, Gunjan Baid, Sidharth Goel, Howard H. Yang, Andrew Carroll, Robert Eveleigh, Mathieu Bourgey, Guillaume Bourque, Gen Li, MA ChouXian, LinQi Tang, DU YuanPing, Shaowei Zhang, Jordi Morata, Raúl Tonda, Genı́s Parra, Jean-Rémi Trotta, Christian Brueffer, Sinem Demirkaya-Budak, Duygu Kabakci-Zorlu, Deniz Turgut, Özem Kalay, Güngör Budak, Kübra Narcı, Elif Acar Arslan, Matthew A. Brown, Ivan J. Johnson, Alexey Dolgoborodov, Vladimir Semenyuk, Amit Jain, H. Serhat Tetikol, Varun Jain, Mike Ruehle, Bryan R. Lajoie, Cooper Roddey, Severine Catreux, Rami Mehio, Mian Umair Ahsan, Qian Liu, Kai Wang, Sayed Mohammad Ebrahim Sahraeian, Li Tai Fang, Marghoob Mohiyuddin, Calvin Hung, Chirag Jain, Hanying Feng, Zhipan Li, Luoqi Chen, Fritz J. Sedlazeck, Justin M. Zook

    Опубліковано 2020
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  18. 18
    PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions

    PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions за авторством Nathan D. Olson, Justin Wagner, Jennifer McDaniel, Sarah H. Stephens, Samuel T. Westreich, Anish G. Prasanna, Elaine Johanson, Emily S. Boja, Ezekiel J. Maier, Omar Serang, David Jáspez, José M. Lorenzo-Salazar, Adrián Muñoz‐Barrera, Luis A. Rubio‐Rodríguez, Carlos Flores, Konstantinos Kyriakidis, Andigoni Malousi, Kishwar Shafin, Trevor Pesout, Miten Jain, Benedict Paten, Pi-Chuan Chang, Alexey Kolesnikov, Maria Nattestad, Gunjan Baid, Sidharth Goel, Howard H. Yang, Andrew Carroll, Robert Eveleigh, Mathieu Bourgey, Guillaume Bourque, Gen Li, Chouxian Ma, LinQi Tang, Yuanping Du, Shaowei Zhang, Jordi Morata, Raúl Tonda, Genı́s Parra, Jean-Rémi Trotta, Christian Brueffer, Sinem Demirkaya-Budak, Duygu Kabakci-Zorlu, Deniz Turgut, Özem Kalay, Güngör Budak, Kübra Narcı, Elif Acar Arslan, Matthew A. Brown, Ivan J. Johnson, Alexey Dolgoborodov, Vladimir Semenyuk, Amit Jain, H. Serhat Tetikol, Varun Jain, Mike Ruehle, Bryan R. Lajoie, Cooper Roddey, Severine Catreux, Rami Mehio, Mian Umair Ahsan, Qian Liu, Kai Wang, Sayed Mohammad Ebrahim Sahraeian, Li Tai Fang, Marghoob Mohiyuddin, Calvin Hung, Chirag Jain, Hanying Feng, Zhipan Li, Luoqi Chen, Fritz J. Sedlazeck, Justin M. Zook

    Опубліковано 2022
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  19. 19
    Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

    Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria за авторством Jérémie Rosain, Anna‐Lena Neehus, Jérémy Manry, Rui Yang, Jérémie Le Pen, Wassim Daher, Zhiyong Liu, Yi‐Hao Chan, Natalia Tahuil, Özden Türel, Mathieu Bourgey, Masato Ogishi, Jean‐Marc Doisne, Helena M. Izquierdo, Takayoshi Shirasaki, Tom Le Voyer, Antoine Guérin, Paul Bastard, Marcela Moncada‐Vélez, Ji Eun Han, Taushif Khan, Franck Rapaport, Seon-Hui Hong, Andrew Cheung, Kathrin Haake, Barbara C. Mindt, Laura Pérez, Quentin Philippot, Danyel Lee, Peng Zhang, Darawan Rinchai, Fatima Al Ali, Manar Ata, Mahbuba Rahman, Jessica N. Peel, Søren Heissel, Henrik Molina, Yasemin Kendir Demirkol, Rasheed Bailey, Shuxiang Zhao, Jonathan Bohlen, Mathieu Mancini, Yoann Seeleuthner, Marie Roelens, Lazaro Lorenzo, Camille Soudée, María Elvira Josefina Paz, María Laura González, Mohamed Jeljeli, Jean Soulier, Serge Romana, Anne-Sophie L’Honneur, Marie Materna, Rubén Martínez‐Barricarte, Mathieu Pochon, Carmen Oleaga‐Quintas, Alexandre Michev, Mélanie Migaud, Romain Lévy, Marie‐Alexandra Alyanakian, Flore Rozenberg, Carys A. Croft, Guillaume Vogt, Jean‐François Emile, Laurent Kremer, S. Cindy, Jörg H. Fritz, Stanley M. Lemon, András N. Spaan, Nicolas Manel, Laurent Abel, Margaret R. MacDonald, Stéphanie Boisson‐Dupuis, Nico Marr, Stuart G. Tangye, James P. Di Santo, Qian Zhang, Shen‐Ying Zhang, Charles M. Rice, Vivien Béziat, Nico Lachmann, David Langlais, Jean‐Laurent Casanova, Philippe Gros, Jacinta Bustamante

    Опубліковано 2023
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  20. 20
    Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

    Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease за авторством Marie‐Gabrielle Duperron, Maria J. Knol, Quentin Le Grand, Tavia E. Evans, Aniket Mishra, Ami Tsuchida, Gennady V. Roshchupkin, Takahiro Konuma, David‐Alexandre Trégouët, José R. Romero, Stefan Frenzel, Michelle Luciano, Edith Hofer, Mathieu Bourgey, Nicole Dueker, Pilar Delgado, Saima Hilal, Rick M. Tankard, Florian Dubost, Jean Shin, Yasaman Saba, Nicola J. Armstrong, Constance Bordes, Mark E. Bastin, Alexa Beiser, Henry Brodaty, Robin Bülow, Caty Carrera, Christopher Chen, Ching‐Yu Cheng, Ian J. Deary, Piyush Gampawar, Jayandra J. Himali, Jiyang Jiang, Takahisa Kawaguchi, Shuo Li, Mélissa Macalli, Pascale Marquis, Zoë Morris, Susana Muñoz Maniega, Susumu Miyamoto, Masakazu Okawa, Matthew Paradise, Pedram Parva, Tatjana Rundek, Muralidharan Sargurupremraj, Sabrina Schilling, Kazuya Setoh, Omar Soukarieh, Yasuharu Tabara, Alexander Teumer, Anbupalam Thalamuthu, Julian N. Trollor, Maria C. Valdés Hernández, Meike W. Vernooij, Uwe Völker, Katharina Wittfeld, Tien Yin Wong, Margaret J. Wright, Junyi Zhang, Wanting Zhao, Yi‐Cheng Zhu, Helena Schmidt, Perminder S. Sachdev, Wei Wen, Kazumichi Yoshida, Anne Joutel, Claudia L. Satizábal, Ralph L. Sacco, Guillaume Bourque, Quentin Le Grand, Mark Lathrop, Tomáš Paus, Israel Fernández‐Cadenas, Qiong Yang, Bernard Mazoyer, Philippe Boutinaud, Yukinori Okada, Hans J. Grabe, Karen A. Mather, Reinhold Schmidt, Marc Joliot, M. Arfan Ikram, Fumihiko Matsuda, Christophe Tzourio, Joanna M. Wardlaw, Sudha Seshadri, Hieab H.H. Adams, Stéphanie Debette

    Опубліковано 2023
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