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Filtros : "Fu, Jack M." Limpar

Filtros

Indexado em
Collaboration
Normalized affiliation
Non normalized affiliation
- center for genomic medicine, massachusetts general hospital, boston, ma, usa (1)
- department of biomedical informatics, harvard medical school, boston, ma, usa (1)
- department of genetics, harvard medical school, boston, ma, usa (1)
- department of statistics and data science, carnegie mellon university, pittsburgh, pa (1)
- program in medical and population genetics, broad institute of mit and harvard, cambridge, ma (1)

Artigo de periodico
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p (2022)
Weiner, Daniel J. ; Ling, Emi ; Erdin, Serkan ; Tai, Derek J. C.; Yadav, Rachita; Grove, Jakob ; Fu, Jack M. ; Nadig, Ajay; Rovaris, Diego Luiz
Source: Nature Genetics. Unidade: ICB
Assunto: FISIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WEINER, Daniel J. et al. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics, v. 54, p. 1630–1639, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01203-y. Acesso em: 29 abr. 2026.
APA
Weiner, D. J., Ling, E., Erdin, S., Tai, D. J. C., Yadav, R., Grove, J., et al. (2022). Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics, 54, 1630–1639. doi:10.1038/s41588-022-01203-y
NLM
Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Rovaris DL. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p [Internet]. Nature Genetics. 2022 ; 54 1630–1639.[citado 2026 abr. 29 ] Available from: https://doi.org/10.1038/s41588-022-01203-y
Vancouver
Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Rovaris DL. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p [Internet]. Nature Genetics. 2022 ; 54 1630–1639.[citado 2026 abr. 29 ] Available from: https://doi.org/10.1038/s41588-022-01203-y
Artigo de periodico
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism (2022)
Fu, Jack M. ; Satterstrom, F. Kyle; Peng, Minshi; Passos-Bueno, Maria Rita
Source: Nature Genetics. Unidade: IB
Subjects: TRANSTORNO AUTÍSTICO, DOENÇAS GENÉTICAS, DOENÇAS DO SISTEMA NERVOSO, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FU, Jack M. et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, v. 54, p. 1320–1331, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01104-0. Acesso em: 29 abr. 2026.
APA
Fu, J. M., Satterstrom, F. K., Peng, M., & Passos-Bueno, M. R. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54, 1320–1331. doi:10.1038/s41588-022-01104-0
NLM
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2026 abr. 29 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Vancouver
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2026 abr. 29 ] Available from: https://doi.org/10.1038/s41588-022-01104-0

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