Risultati della ricerca - Jaqueline Y. T. Wang

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  1. 1
    MHC Variants Associated With Symptomatic Versus Asymptomatic SARS-CoV-2 Infection in Highly Exposed Individuals

    MHC Variants Associated With Symptomatic Versus Asymptomatic SARS-CoV-2 Infection in Highly Exposed Individuals di Erick C. Castelli, Mateus Vidigal de Castro, Michel Satya Naslavsky, Marília O. Scliar, Nayane S. B. Silva, Heloisa S. Andrade, Andréia S. Souza, Raphaela Neto Pereira, Camila Ferreira Bannwart Castro, Celso Teixeira Mendes‐Junior, Diogo Meyer, Kelly Nunes, Larissa R. B. Matos, Monize V. R. Silva, Jaqueline Y. T. Wang, Joyce Esposito, Vivian R. Cória, Raul Hernandes Bortolin, Mário Hiroyuki Hirata, Jhosiene Y. Magawa, Edécio Cunha‐Neto, Verônica Coelho, Keity Souza Santos, Maria Lúcia Carnevale Marin, Jorge Kalil, Miguel Mitne‐Neto, Rui M. B. Maciel, Maria Rita Passos‐Bueno, Mayana Zatz

    Pubblicazione 2021
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  2. 2
    “Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2”

    “Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2” di Mateus Vidigal de Castro, Keity Souza Santos, Juliana de Souza Apostólico, Edgar Ruz Fernandes, Rafael Ribeiro Almeida, Gabriel Levin, Jhosiene Y. Magawa, João Paulo Silva Nunes, Miriam Bruni, Márcio Yamamoto, Ariane C. Lima, Monize V. R. Silva, Larissa R. B. Matos, Vivian R. Cória, Erick C. Castelli, Marília O. Scliar, Andréia Kuramoto, Fernanda R. Bruno, Lucas Cauê Jacintho, Kelly Nunes, Jaqueline Y. T. Wang, Verônica Coelho, Miguel Mitne‐Neto, Rui M. B. Maciel, Michel Satya Naslavsky, Maria Rita Passos‐Bueno, Silvia Beatriz Boscardin, Daniela Santoro Rosa, Jorge Kalil, Mayana Zatz, Edécio Cunha‐Neto

    Pubblicazione 2021
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  3. 3
    Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair

    Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair di Mateus Vidigal de Castro, Keity Souza Santos, Juliana de Souza Apostólico, Edgar Ruz Fernandes, Rafael Ribeiro Almeida, Gabriel Levin, Jhosiene Y. Magawa, João Paulo Silva Nunes, Mirian Bruni, Márcio Yamamoto, Ariane C. Lima, Monize V. R. Silva, Larissa R. B. Matos, Vivian R. Cória, Erick C. Castelli, Marília O. Scliar, Andréia Kuramoto, Fernanda R. Bruno, Lucas Cauê Jacintho, Kelly Nunes, Jaqueline Y. T. Wang, Verônica Coelho, Miguel Mitne‐Neto, Rui M. B. Maciel, Michel Satya Naslavsky, Maria Rita Passos‐Bueno, Silvia Beatriz Boscardin, Daniela Santoro Rosa, Jorge Kalil, Mayana Zatz, Edécio Cunha‐Neto

    Pubblicazione 2022
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  4. 4
    MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil

    MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil di Erick C. Castelli, Mateus Vidigal de Castro, Michel Satya Naslavsky, Marília O. Scliar, Nayane S. B. Silva, Raphaela Neto Pereira, Viviane A. O. Ciriaco, Camila Ferreira Bannwart Castro, Celso Teixeira Mendes‐Junior, Etiele de S. Silveira, Iuri Marques de Oliveira, Eduardo Antonio, Gustavo Fioravanti Vieira, Diogo Meyer, Kelly Nunes, Larissa R. B. Matos, Monize V. R. Silva, Jaqueline Y. T. Wang, Joyce Esposito, Vivian R. Cória, Jhosiene Y. Magawa, Keity Souza Santos, Edécio Cunha‐Neto, Jorge Kalil, Raul Hernandes Bortolin, Mário Hiroyuki Hirata, Luiz P. Dell’Aquila, Álvaro Razuk-Filho, Pedro B. Batista-Júnior, Amaro Nunes Duarte‐Neto, Marisa Dolhnikoff, Paulo Hilário Nascimento Saldiva, Maria Rita Passos‐Bueno, Mayana Zatz

    Pubblicazione 2022
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  5. 5
    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 di 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

    Pubblicazione 2025
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  6. 6
    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 di 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

    Pubblicazione 2021
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  7. 7
    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 di 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

    Pubblicazione 2022
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