Y. Cheng - CFFT Lab, Cystic Fibrosis Foundation

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论文共 36 篇作者统计合作学者相似作者

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Clinical and genetic characteristics of PLA2G6-parkinsonism in southwest China and a review of heterogeneity of phenotype and genotype between Asian and Caucasian patients

Y. Cheng, H. Shang

Parkinsonism & Related Disorders (2024)

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Education level and the clinical characteristics and disease progression in Huntington’s disease: An Observational and Mendelian Randomization Study

S. Zhang,Y. Cheng, H. Shang

Parkinsonism & Related Disorders (2024)

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Epigenome-wide DNA methylation signatures of excessive daytime sleepiness in Parkinson's Disease: Analysis of the PPMI Cohort

T. Yang,Y. Cheng, C. Li, Q. Wei, H. Shang

Parkinsonism & Related Disorders (2024)

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Baseline lipid traits and the clinical characteristics and disease progression in Huntington’s disease

S. Zhang,Y. Cheng, H. Shang

Parkinsonism & Related Disorders (2024)

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273 Screening the Calibr ReFRAME drug-repurposing library for efficient functional restoration of native CFTR nonsense variants

F. Liang, H. Shang,Y. Cheng, S. Cantu,L. Wang, J. Shepard, K. Coote,H. Bihler,M. Mense

Journal of Cystic Fibrosis (2023): S138-S138

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305 Comparing functional responses of nonsense CFTR variants to modulators in human primary enteric monolayer, human bronchial epithelial, and 16hBEge cell cultures

J. Chin, M. Mulligan, D. Patel, K. Arnold, P. Bhatt, J. Harrington,Y. Cheng,H. Bihler,M. Mense, K. Coote

Journal of Cystic Fibrosis (2023): S153-S154

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Epigenome-wide meta-analysis of sex-differential DNA methylation in Parkinson's disease

T. Yang, C. Li, Q. Wei, R. Ou,Y. Cheng, K. Liu, J. Lin, Y. Xiao, H. Shang

MOVEMENT DISORDERS (2023): S465-S465

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257 Evaluating genetic components to move toward a highly effective CFTR super exon

K. Yan, A. Bell, C. Macadino, J. Conte, M. Armstrong,Y. Cheng, K. Coote, N. Allaire,A. Sivachenko,M. Mense, C. Cotton, H. Valley

Journal of Cystic Fibrosis (2023): S130-S130

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663 Modulation of cystic fibrosis transmembrane conductance regulator intron 22 alternative polyadenylation use may have therapeutic potential for the treatment of certain 3′ cystic fibrosis transmembrane conductance regulator premature termination codon variants

N. Allaire, J. Yoon, M. Armstrong, H. Valley, C. Macadino,A. Sivachenko, J. Conte, B. Tabak, H. Bihler,Y. Cheng, K. Coote,C. Cotton,

Journal of Cystic Fibrosis (2022): S363-S363

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634 Generation of a cystic fibrosis transmembrane conductance regulator R1162X “TAG” model and comparison of readthrough to the naturally occurring R1162X “TGA”

K. Bukis,Y. Cheng, M. Armstrong, J. Conte, K. Coote, N. Allaire,A. Sivachenko, M. Mense,C. Cotton, H. Valley

Journal of Cystic Fibrosis (2022)

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