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1 Ergebnisse
1
Rare coding variation provides insight into the genetic arc..:
Fu, Jack M
;
Satterstrom, F Kyle
;
Peng, Minshi
...
qt04m356rr. , 2022
Link:
https://escholarship.org/uc/item/04m356rr
RT Journal T1
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt04m356rr&Exemplar=1&LAN=DE A1 Fu, Jack M A1 Satterstrom, F Kyle A1 Peng, Minshi A1 Brand, Harrison A1 Collins, Ryan L A1 Dong, Shan A1 Wamsley, Brie A1 Klei, Lambertus A1 Wang, Lily A1 Hao, Stephanie P A1 Stevens, Christine R A1 Cusick, Caroline A1 Babadi, Mehrtash A1 Banks, Eric A1 Collins, Brett A1 Dodge, Sheila A1 Gabriel, Stacey B A1 Gauthier, Laura A1 Lee, Samuel K A1 Liang, Lindsay A1 Ljungdahl, Alicia A1 Mahjani, Behrang A1 Sloofman, Laura A1 Smirnov, Andrey N A1 Barbosa, Mafalda A1 Betancur, Catalina A1 Brusco, Alfredo A1 Chung, Brian HY A1 Cook, Edwin H A1 Cuccaro, Michael L A1 Domenici, Enrico A1 Ferrero, Giovanni Battista A1 Gargus, J Jay A1 Herman, Gail E A1 Hertz-Picciotto, Irva A1 Maciel, Patricia A1 Manoach, Dara S A1 Passos-Bueno, Maria Rita A1 Persico, Antonio M A1 Renieri, Alessandra A1 Sutcliffe, James S A1 Tassone, Flora A1 Trabetti, Elisabetta A1 Campos, Gabriele A1 Cardaropoli, Simona A1 Carli, Diana A1 Chan, Marcus CY A1 Fallerini, Chiara A1 Giorgio, Elisa A1 Girardi, Ana Cristina A1 Hansen-Kiss, Emily A1 Lee, So Lun A1 Lintas, Carla A1 Ludena, Yunin A1 Nguyen, Rachel A1 Pavinato, Lisa A1 Pericak-Vance, Margaret A1 Pessah, Isaac N A1 Schmidt, Rebecca J A1 Smith, Moyra A1 Costa, Claudia IS A1 Trajkova, Slavica A1 Wang, Jaqueline YT A1 Yu, Mullin HC A1 Cutler, David J A1 De Rubeis, Silvia A1 Buxbaum, Joseph D A1 Daly, Mark J A1 Devlin, Bernie A1 Roeder, Kathryn A1 Sanders, Stephan J A1 Talkowski, Michael E PB eScholarship, University of California YR 2022 K1 Biological Sciences K1 Bioinformatics and Computational Biology K1 Genetics K1 Autism K1 Brain Disorders K1 Pediatric K1 Biotechnology K1 Intellectual and Developmental Disabilities (IDD) K1 Human Genome K1 Mental Health K1 Clinical Research K1 Aetiology K1 2.1 Biological and endogenous factors K1 Autism Spectrum Disorder K1 Autistic Disorder K1 DNA Copy Number Variations K1 Genetic Predisposition to Disease K1 Humans K1 Mutation K1 Autism Sequencing Consortium K1 Broad Institute Center for Common Disease Genomics K1 iPSYCH-BROAD Consortium K1 Medical and Health Sciences K1 Developmental Biology K1 Agricultural biotechnology JF qt04m356rr LK http://dx.doi.org/https://escholarship.org/uc/item/04m356rr DO https://escholarship.org/uc/item/04m356rr SF ELIB - SuUB Bremen
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