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Jack M. Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao and 107 more
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Fu, J. M., Satterstrom, F. K., Peng, M., Brand, H., Collins, R. L., Dong, S., Wamsley, B., Klei, L., Wang, L., Hao, S. P., Stevens, C. R., Cusick, C. M., Babadi, M., Banks, E., Collins, B. L., Dodge, S., Gabriel, S., Gauthier, L. D., Lee, S. K., … Talkowski, M. E. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54(9), 1320–1331. https://doi.org/10.1038/s41588-022-01104-0
Fu, Jack M., et al. "Rare coding variation provides insight into the genetic architecture and phenotypic context of autism." Nature Genetics, vol. 54, no. 9, 2022, pp. 1320–1331, https://doi.org/10.1038/s41588-022-01104-0.
Fu, Jack M., F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, et al. "Rare coding variation provides insight into the genetic architecture and phenotypic context of autism." Nature Genetics 54, no. 9 (2022): 1320–1331. https://doi.org/10.1038/s41588-022-01104-0.
Fu J. M., Satterstrom F. K., Peng M. [и др.] Rare coding variation provides insight into the genetic architecture and phenotypic context of autism // Nature Genetics. — 2022. — Vol. 54, № 9. — P. 1320–1331. — URL: https://doi.org/10.1038/s41588-022-01104-0
@article{fu2022rare,
title = {{Rare coding variation provides insight into the genetic architecture and phenotypic context of autism}},
author = {Jack M. Fu and F. Kyle Satterstrom and Minshi Peng and Harrison Brand and Ryan L. Collins and Shan Dong and Brie Wamsley and Lambertus Klei and Lily Wang and Stephanie P. Hao and Christine R. Stevens and Caroline M. Cusick and Mehrtash Babadi and Eric Banks and Brett L. Collins and Sheila Dodge and Stacey Gabriel and Laura Doyle Gauthier and Samuel K. Lee and Lindsay Liang and Alicia Ljungdahl and Behrang Mahjani and Laura Gail Sloofman and Andrey N. Smirnov and Mafalda Barbosa and Catalina Betancur and Alfredo Brusco and Brian Hon‐Yin Chung and Edwin H. Cook and Michael L. Cuccaro and Enrico Domenici and Giovanni Battista Ferrero and J. Jay Gargus and Gail E. Herman and Irva Hertz‐Picciotto and Patrı́cia Maciel and Dara S. Manoach and Maria Rita Passos‐Bueno and Antonio Maria Persico and Alessandra Renieri and James S. Sutcliffe and Flora Tassone and Elisabetta Trabetti and Gabriele da Silva Campos and Simona Cardaropoli and Diana Carli and Marcus C.Y. Chan and Chiara Fallerini and Elisa Giorgio and Ana Cristina De Sanctis Girardi and Emily Hansen‐Kiss and So Lun Lee and Carla Lintas and Yunin Ludeña and Rachel L. Nguyen and Lisa Pavinato and Margaret Ann Pericak‐Vance and Isaac N. Pessah and Rebecca J. Schmidt and Moyra Smith and Claudia Ismania Samogy Costa and Slavica Trajkova and Jaqueline Yu Ting Wang and Mullin H.C. Yu and Branko Aleksić and Mykyta Artomov and Elisa Benetti and Monica Biscaldi-Schafer and Anders Dupont Børglum and Ãngel Carracedo and Andreas G. Chiocchetti and Hilary H Coon and Ryan N. Doan and Montse Fernández‐Prieto and Christine Margarete Freitag and Sherif Gerges and Stephen J. Guter and DAVID MICHAEL HOUGAARD and Christina M. Hultman and Suma Jacob and Miia Kaartinen and Alexander Kolevzon and Itaru Kushima and Terho J. Lehtimäki and Caterina Lo Rizzo and Nell Maltman and Marianna Manara and Gal Meiri and Idan Menashe and Judith Miller and Nancy J. Minshew and Matthew W. Mosconi and Norio Ozaki and Aarno V. Palotie and Mara Parellada and Kaija Puura and Abraham Reichenberg and Sven Sandin and Stephen W. Scherer and Sabine Schlitt and Lauren Schmitt and Katja Schneider-Momm and Paige M. Siper and Pål Surén and John A. Sweeney and Karoline Teufel and Maria del Pilar Trelles and Lauren A. Weiss and Ryan K. C. Yuen and David J. Cutler and Silvia De Rubeis and Joseph D. Buxbaum and Mark J. Daly and Bernie Devlin and Kathryn Roeder and Stephan Sanders and Michael E. Talkowski},
journal = {Nature Genetics},
year = {2022},
volume = {54},
number = {9},
pages = {1320--1331},
doi = {10.1038/s41588-022-01104-0},
url = {https://doi.org/10.1038/s41588-022-01104-0}
}TY - JOUR AU - Fu, Jack M. AU - Satterstrom, F. Kyle AU - Peng, Minshi AU - Brand, Harrison AU - Collins, Ryan L. AU - Dong, Shan AU - Wamsley, Brie AU - Klei, Lambertus AU - Wang, Lily AU - Hao, Stephanie P. AU - Stevens, Christine R. AU - Cusick, Caroline M. AU - Babadi, Mehrtash AU - Banks, Eric AU - Collins, Brett L. AU - Dodge, Sheila AU - Gabriel, Stacey AU - Gauthier, Laura Doyle AU - Lee, Samuel K. AU - Liang, Lindsay AU - Ljungdahl, Alicia AU - Mahjani, Behrang AU - Sloofman, Laura Gail AU - Smirnov, Andrey N. AU - Barbosa, Mafalda AU - Betancur, Catalina AU - Brusco, Alfredo AU - Chung, Brian Hon‐Yin AU - Cook, Edwin H. AU - Cuccaro, Michael L. AU - Domenici, Enrico AU - Ferrero, Giovanni Battista AU - Gargus, J. Jay AU - Herman, Gail E. AU - Hertz‐Picciotto, Irva AU - Maciel, Patrı́cia AU - Manoach, Dara S. AU - Passos‐Bueno, Maria Rita AU - Persico, Antonio Maria AU - Renieri, Alessandra AU - Sutcliffe, James S. AU - Tassone, Flora AU - Trabetti, Elisabetta AU - Campos, Gabriele da Silva AU - Cardaropoli, Simona AU - Carli, Diana AU - Chan, Marcus C.Y. AU - Fallerini, Chiara AU - Giorgio, Elisa AU - Girardi, Ana Cristina De Sanctis AU - Hansen‐Kiss, Emily AU - Lee, So Lun AU - Lintas, Carla AU - Ludeña, Yunin AU - Nguyen, Rachel L. AU - Pavinato, Lisa AU - Pericak‐Vance, Margaret Ann AU - Pessah, Isaac N. AU - Schmidt, Rebecca J. AU - Smith, Moyra AU - Costa, Claudia Ismania Samogy AU - Trajkova, Slavica AU - Wang, Jaqueline Yu Ting AU - Yu, Mullin H.C. AU - Aleksić, Branko AU - Artomov, Mykyta AU - Benetti, Elisa AU - Biscaldi-Schafer, Monica AU - Børglum, Anders Dupont AU - Carracedo, Ãngel AU - Chiocchetti, Andreas G. AU - Coon, Hilary H AU - Doan, Ryan N. AU - Fernández‐Prieto, Montse AU - Freitag, Christine Margarete AU - Gerges, Sherif AU - Guter, Stephen J. AU - HOUGAARD, DAVID MICHAEL AU - Hultman, Christina M. AU - Jacob, Suma AU - Kaartinen, Miia AU - Kolevzon, A lexander AU - Kushima, Itaru AU - Lehtimäki, Terho J. AU - Rizzo, Caterina Lo AU - Maltman, Nell AU - Manara, Marianna AU - Meiri, Gal AU - Menashe, Idan AU - Miller, Judith AU - Minshew, Nancy J. AU - Mosconi, Matthew W. AU - Ozaki, Norio AU - Palotie, Aarno V. AU - Parellada, Mara AU - Puura, Kaija AU - Reichenberg, Abraham AU - Sandin, Sven AU - Scherer, Stephen W. AU - Schlitt, Sabine AU - Schmitt, Lauren AU - Schneider-Momm, Katja AU - Siper, Paige M. AU - Surén, Pål AU - Sweeney, John A. AU - Teufel, Karoline AU - Trelles, Maria del Pilar AU - Weiss, Lauren A. AU - Yuen, Ryan K. C. AU - Cutler, David J. AU - Rubeis, Silvia De AU - Buxbaum, Joseph D. AU - Daly, Mark J. AU - Devlin, Bernie AU - Roeder, Kathryn AU - Sanders, Stephan AU - Talkowski, Michael E. TI - Rare coding variation provides insight into the genetic architecture and phenotypic context of autism JO - Nature Genetics VL - 54 IS - 9 SP - 1320 EP - 1331 PY - 2022 DA - 2022/08/18 DO - 10.1038/s41588-022-01104-0 UR - https://doi.org/10.1038/s41588-022-01104-0 ER -
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