Author

Yue Huang

University of California, Los AngelesORCID 0000-0002-6088-9273Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Yue Huang2 papers · Capital Medical University

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:Drosophila· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Julián A. Martínez-AgostoiD· 2 shared Alden Yen-Wen Huang· 1 shared Alina KurolapiD· 1 shared Amy Siemon· 1 shared Annelise Yoo Mah-SomiD· 1 shared Annick Raas‐RothschildiD· 1 shared Ashita Dave‐Wala· 1 shared Boris KereniD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetics

Julián A. Martínez-AgostoORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintFeb 6, 2024

Loss of function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

Yue Huang, Kristy L. Jay, Alden Yen-Wen Huang…·Julián A. Martínez-Agosto

The paper identifies de novo RBBP5 variants in individuals with neurodevelopmental disorders and shows they cause loss of function through structural and Drosophila model analyses.

2 citations

Drosophilaexperimental assay

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Genetic & Genomic MedicineScience AdvancesPeer-reviewedMay 12, 2021

Pathogenic variants in SMARCA5, a chromatin remodeler, cause a range of syndromic neurodevelopmental features

Dong Li, Qin Wang, Naihua Natalie Gong…·Hakon H. Hakonarson

The paper identifies pathogenic variants in SMARCA5 as a cause of a neurodevelopmental syndrome with mild facial dysmorphia and developmental delay.

30 citations

humanDrosophila

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