検索結果 - Behrang Mahjani

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  1. 1
    Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank

    Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank 著者: Rebecca Birnbaum, Behrang Mahjani, Ruth J. F. Loos, Andrew J. Sharp

    出版事項 2022
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  2. 2
    Comorbidities in autism spectrum disorder and their etiologies

    Comorbidities in autism spectrum disorder and their etiologies 著者: Vahe Khachadourian, Behrang Mahjani, Sven Sandin, Alexander Kolevzon, Joseph D. Buxbaum, Abraham Reichenberg, Magdalena Janecka

    出版事項 2023
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    Artigo
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  3. 3
    Association Between Mental Health and Reproductive System Disorders in Women

    Association Between Mental Health and Reproductive System Disorders in Women 著者: Nina Zaks, Anita Batuure, Emma Lin, Anna‐Sophie Rommel, Abraham Reichenberg, Dorothy E. Grice, Veerle Bergink, Nathan S. Fox, Behrang Mahjani, Magdalena Janecka

    出版事項 2023
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  4. 4
    Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

    Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden 著者: Benjamin Hon Kei Yip, Dan Bai, Behrang Mahjani, Lambertus Klei, Yudi Pawitan, Christina M. Hultman, Dorothy E. Grice, Kathryn Roeder, Joseph D. Buxbaum, Bernie Devlin, Abraham Reichenberg, Sven Sandin

    出版事項 2017
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    Artigo
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  5. 5
    How rare and common risk variation jointly affect liability for autism spectrum disorder

    How rare and common risk variation jointly affect liability for autism spectrum disorder 著者: Lambertus Klei, Lora McClain, Behrang Mahjani, Klea Panayidou, Silvia De Rubeis, Anna-Carin Säll Grahnat, Gun Karlsson, Yangyi Lu, Nadine Melhem, Xinyi Xu, Abraham Reichenberg, Sven Sandin, Christina M. Hultman, Joseph D. Buxbaum, Kathryn Roeder, Bernie Devlin

    出版事項 2021
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    Artigo
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  6. 6
    Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort

    Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort 著者: Dan Bai, Benjamin Hon Kei Yip, Gayle C. Windham, André Sourander, Richard W. Francis, Rinat Yoffe, Emma J. Glasson, Behrang Mahjani, Auli Suominen, Helen Leonard, Mika Gissler, Joseph D. Buxbaum, Kingsley Wong, Diana Schendel, Arad Kodesh, Michaeline Breshnahan, Stephen Z. Levine, Erik Thorlund Parner, Stefan Nygaard Hansen, Christina M. Hultman, Abraham Reichenberg, Sven Sandin

    出版事項 2019
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    Artigo
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  7. 7
    Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

    Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations 著者: Marina Natividad Avila, Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura Sloofman, Lambertus Klei, Thariana Pichardo, Christine Stevens, Caroline Cusick, Jennifer Ames, Gabriele da Silva Campos, Hilda J Cerros, Roberto Chaskel, Claudia Ismania Samogy Costa, Michael L. Cuccaro, Andrea López, Magdalena Fernández, Eugenio Ferro, Liliana Galeano, Ana Cristina De Sanctis Girardi, Anthony J. Griswold, Luis C. Hernandez, Naila Cristina Vilaça Lourenço, Yunin Ludeña, Diana Núñez, Ryan K. Oyama, Katherine Peña, Isaac N. Pessah, Rebecca J. Schmidt, Holly Morsbach Sweeney, Lizbeth Tolentino, Jaqueline Y. T. Wang, Lilia Albores‐Gallo, Lisa Croen, Carlos Cruz-Fuentes, Irva Hertz‐Picciotto, Alexander Kolevzon, María Claudia Lattig, Liliana Mayo, Maria Rita Passos-Bueno, Margaret A. Pericak‐Vance, Paige M. Siper, Flora Tassone, M. Pilar Trelles, Michael E. Talkowski, Mark J. Daly, Behrang Mahjani, Silvia De Rubeis, Edwin H. Cook, Kathryn Roeder, Catalina Betancur, Bernie Devlin, Joseph D. Buxbaum

    出版事項 2025
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  8. 8
    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism 著者: Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Lambertus Klei, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Alfredo Brusco, Brian Hon‐Yin Chung, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina Girard, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Evelise Riberi, Rebecca J. Schmidt, Moyra Smith, Claudia I.C. Souza, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski

    出版事項 2021
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  9. 9
    Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism 著者: F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An, Minshi Peng, Ryan L. Collins, Jakob Grove, Lambertus Klei, Christine Stevens, Jennifer Reichert, Maureen Mulhern, Mykyta Artomov, Sherif Gerges, Brooke Sheppard, Xinyi Xu, Aparna Bhaduri, Utku Norman, Harrison Brand, Grace Schwartz, Rachel Nguyen, Elizabeth E. Guerrero, Caroline Dias, Catalina Betancur, Edwin H. Cook, Louise Gallagher, Michael Gill, James S. Sutcliffe, Audrey Thurm, Michael E. Zwick, Anders D. Børglum, Matthew W. State, A. Ercüment Çiçek, Michael E. Talkowski, David J. Cutler, Bernie Devlin, Stephan Sanders, Kathryn Roeder, Mark J. Daly, Joseph D. Buxbaum, Branko Aleksić, Richard Anney, Mafalda Barbosa, Somer Bishop, Alfredo Brusco, Jonas Bybjerg‐Grauholm, Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montserrat Fernández Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, Alexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew

    出版事項 2020
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  10. 10
    Genome-wide association study identifies new locus associated with OCD

    Genome-wide association study identifies new locus associated with OCD 著者: Nora I. Strom, Dongmei Yu, Zachary F. Gerring, Matthew Halvorsen, Abdel Abdellaoui, Cristina Rodríguez-Fontenla, Julia Sealock, Tim B. Bigdeli, Jonathan R. I. Coleman, Behrang Mahjani, Jackson G. Thorp, Katharina Bey, Christie L. Burton, Jurjen J. Luykx, Gwyneth Zai, Kathleen D. Askland, Cristina Barlassina, Judith Becker Nissen, Laura Bellodi, O. Joseph Bienvenu, Donald W. Black, Michael H. Bloch, Julia Boberg, Rosa Bosch, Michael S. Breen, Brian P. Brennan, Helena Brentani, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Enda M. Byrne, Beatríz Camarena, Adrian Camarena, Carolina Cappi, Ángel Carracedo, Miguel Casas, Maria Cristina Cavallini, Valentina Ciullo, Edwin H. Cook, Vladimir Coric, Bernadette Cullen, Elles de Schipper, Bernie Devlin, Srdjan Djurovic, Jason A. Elias, Lauren Erdman, Xavier Estivil, Martha J. Falkenstein, Bengt T. Fundín, Maiken E. Gabrielsen, Fernando S. Goes, Marco A. Grados, Jakob Grove, Wei Guo, Jan Haavik, Kristen Hagen, Alexandra Havdahl, Ana Gabriela Hounie, Donald Hucks, Christina M. Hultman, Magdalena Janecka, Michael A. Jenike, Elinor K. Karlsson, Julia Klawohn, Lambertus Klei, Janice Krasnow, Kristi Krebs, Jason W. Krompinger, Nuria Lanzagorta, Fabìo Macciardi, Brion S. Maher, Evonne McArthur, Nathaniel W. McGregor, Nicole McLaughlin, Sandra Meier, Eurípedes C. Miguel, Maureen Mulhern, Paul S. Nestadt, Erika L. Nurmi, Kevin S. O’Connell, Lisa Osiecki, Teemu Palviainen, Fabrizio Piras, Federica Piras, Ann E. Pulver, Raquel Rabionet, Alfredo Ramı́rez, Scott L. Rauch, Abraham Reichenberg, Jennifer Reichert, Mark A. Riddle, Stephan Ripke, Aline S. Sampaio, Miriam A. Schiele, Laura Sloofman, Jan Smit, Janet L. Sobell, María Soler Artigas, Laurent F. Thomas, Homero Vallada, Jeremy Veenstra‐VanderWeele

    出版事項 2021
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  11. 11
    Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci

    Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci 著者: Nora I. Strom, Zachary F. Gerring, Marco Galimberti, Dongmei Yu, Matthew Halvorsen, Abdel Abdellaoui, Cristina Rodríguez-Fontenla, Julia Sealock, Tim B. Bigdeli, Jonathan R. I. Coleman, Behrang Mahjani, Jackson G. Thorp, Katharina Bey, Christie L. Burton, Jurjen J. Luykx, Gwyneth Zai, Silvia Alemany, Christine André, Kathleen D. Askland, Nerisa Banaj, Cristina Barlassina, Judith Becker Nissen, O. Joseph Bienvenu, Donald W. Black, Michael H. Bloch, Julia Boberg, Sigrid Børte, Rosa Bosch, Michael S. Breen, Brian P. Brennan, Helena Brentani, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Enda M. Byrne, Judit Cabana‐Domínguez, Beatríz Camarena, Adrian Camarena, Carolina Cappi, Ángel Carracedo, Miguel Casas, Maria Cristina Cavallini, Valentina Ciullo, Edwin H. Cook, Jesse M. Crosby, Bernadette Cullen, Elles de Schipper, Richard Delorme, Srdjan Djurovic, Jason A. Elias, Xavier Estivill, Martha J. Falkenstein, Bengt T. Fundín, Lauryn E. Garner, Chris German, Christina Gironda, Fernando S. Goes, Marco A. Grados, Jakob Grove, Wei Guo, Jan Haavik, Kristen Hagen, Kelly Harrington, Alexandra Havdahl, Kira Höffler, Ana Gabriela Hounie, Donald Hucks, Christina M. Hultman, Magdalena Janecka, Eric Jenike, Elinor K. Karlsson, Kara N. Kelley, Julia Klawohn, Janice Krasnow, Kristi Krebs, Christoph Lange, Nuria Lanzagorta, Daniel F. Levey, Kerstin Lindblad‐Toh, Fabìo Macciardi, Brion S. Maher, Brittany M. Mathes, Evonne McArthur, Nathaniel W. McGregor, Nicole McLaughlin, Sandra Meier, Eurípedes C. Miguel, Maureen Mulhern, Paul S. Nestadt, Erika L. Nurmi, Kevin S. O’Connell, Lisa Osiecki, Olga Therese Ousdal, Teemu Palviainen, Nancy L. Pedersen, Fabrizio Piras, Federica Piras, Sriramya Potluri, Raquel Rabionet, Alfredo Ramı́rez, Scott L. Rauch

    出版事項 2024
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  12. 12
    Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder

    Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder 著者: Nora I. Strom, Zachary F. Gerring, Marco Galimberti, Dongmei Yu, Matthew Halvorsen, Abdel Abdellaoui, Cristina Rodríguez-Fontenla, Julia Sealock, Tim B. Bigdeli, Jonathan R. I. Coleman, Behrang Mahjani, Jackson G. Thorp, Katharina Bey, Christie L. Burton, Jurjen J. Luykx, Gwyneth Zai, Silvia Alemany, Christine André, Kathleen D. Askland, Julia Boberg, Nerisa Banaj, Cristina Barlassina, Judith Becker Nissen, O. Joseph Bienvenu, Donald W. Black, Michael H. Bloch, Sigrid Børte, Rosa Bosch, Michael S. Breen, Brian P. Brennan, Helena Brentani, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Enda M. Byrne, Judit Cabana‐Domínguez, Beatríz Camarena, Adrian Camarena, Carolina Cappi, Ángel Carracedo, Miguel Casas, Maria Cristina Cavallini, Valentina Ciullo, Edwin H. Cook, Jesse M. Crosby, Bernadette Cullen, Elles de Schipper, Richard Delorme, Srdjan Djurovic, Jason A. Elias, Xavier Estivill, Martha J. Falkenstein, Bengt T. Fundín, Lauryn E. Garner, Christina Gironda, Fernando S. Goes, Marco A. Grados, Jakob Grove, Wei Guo, Jan Haavik, Kristen Hagen, Kelly Harrington, Alexandra Havdahl, Kira Höffler, Ana Gabriela Hounie, Donald Hucks, Christina M. Hultman, Magdalena Janecka, Eric Jenike, Elinor K. Karlsson, Kara N. Kelley, Julia Klawohn, Janice Krasnow, Kristi Krebs, Christoph Lange, Nuria Lanzagorta, Daniel F. Levey, Kerstin Lindblad‐Toh, Fabìo Macciardi, Brion S. Maher, Brittany M. Mathes, Evonne McArthur, Nathaniel W. McGregor, Nicole McLaughlin, Sandra Meier, Eurípedes C. Miguel, Maureen Mulhern, Paul S. Nestadt, Erika L. Nurmi, Kevin S. O’Connell, Lisa Osiecki, Olga Therese Ousdal, Teemu Palviainen, Nancy L. Pedersen, Fabrizio Piras, Federica Piras, Sriramya Potluri, Raquel Rabionet, Alfredo Ramı́rez, Scott L. Rauch, Abraham Reichenberg

    出版事項 2025
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  13. 13
    Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

    Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk 著者: F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An, Minshi Peng, Ryan L. Collins, Jakob Grove, Lambertus Klei, Christine Stevens, Jennifer Reichert, Maureen Mulhern, Mykyta Artomov, Sherif Gerges, Brooke Sheppard, Xinyi Xu, Aparna Bhaduri, Utku Norman, Harrison Brand, Grace Schwartz, Rachel Nguyen, Elizabeth E. Guerrero, Caroline Dias, Branko Aleksić, Richard Anney, Mafalda Barbosa, Somer Bishop, Alfredo Brusco, Jonas Bybjerg‐Grauholm, Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montserrat Fernández Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, Alexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Montenegro M. de Souza, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura

    出版事項 2018
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  14. 14
    Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

    Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism 著者: F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An, Minshi Peng, Ryan L. Collins, Jakob Grove, Lambertus Klei, Christine Stevens, Jennifer Reichert, Maureen Mulhern, Mykyta Artomov, Sherif Gerges, Brooke Sheppard, Xinyi Xu, Aparna Bhaduri, Utku Norman, Harrison Brand, Grace Schwartz, Rachel Nguyen, Elizabeth E. Guerrero, Caroline Dias, Branko Aleksić, Richard Anney, Mafalda Barbosa, Somer Bishop, Alfredo Brusco, Jonas Bybjerg‐Grauholm, Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montserrat Fernández Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, Alexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Montenegro M. de Souza, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura

    出版事項 2018
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  15. 15
    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism 著者: Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montserrat Fernández Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt

    出版事項 2022
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