Profil bibliographique

Yuyang Chen

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

12Publications signalées

235Citations signalées

4Affiliations récentes

Institutions déclarées

Centre for Human Genetics Open Data Institute University of Oxford Oxford BioMedica (United Kingdom)

Domaines associés

RNA Research and SplicingRNA regulation and diseaseRNA modifications and cancerRNA and protein synthesis mechanismsGenomics and Rare Diseases

Publications récentes

Accès ouvert 2026 erratumOpenAlex

Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

Rocío Rius, Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe et autres

0 citationsNature Genetics

Accès ouvert 2026 preprintOpenAlex

A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discovery

Anthony McGuigan, Alistair T. Pagnamenta, Laura Covill, Jacob Sampson et autres

0 citationsmedRxiv

Accès ouvert 2026 articleOpenAlex

Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji, Elsa Leitão et autres

4 citationsNature

Accès ouvert 2026 articleOpenAlex

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

Rocío Rius, Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe et autres

7 citationsNature Genetics

Accès ouvert 2025 preprintOpenAlex

Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

Rocío Rius, Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe et autres

5 citationsmedRxiv

Accès ouvert 2025 articleOpenAlex

Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption

Caroline Nava, Benjamin Cogné, Elsa Leitão, François Lecoquierre et autres

49 citationsNature Genetics

Accès ouvert 2025 preprintOpenAlex

Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji, Elsa Leitão et autres

13 citationsmedRxiv

Accès ouvert 2024 articleOpenAlex

Identification and analysis of drought-responsive F-box genes in upland rice and involvement of OsFBX148 in ABA response and ROS accumulation

Yifan Wang, Fang Chen, Yuyang Chen, Kaiwen Ren et autres

13 citationsBMC Plant Biology

Accès ouvert 2024 preprintOpenAlex

Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption

Caroline Nava, Benjamin Cogné, Elsa Leitão, François Lecoquierre et autres

3 citationsmedRxiv

Accès ouvert 2024 preprintOpenAlex

Identification and analysis of drought-responsive F-box genes in upland rice and involvement of OsFBX148 in ABA response and ROS accumulation

Yifan Wang, Fang Chen, Yuyang Chen, Kaiwen Ren et autres

0 citationsResearch Square

Accès ouvert 2024 articleOpenAlex

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome

Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Alicia Ljungdahl et autres

131 citationsNature

Accès ouvert 2024 preprintOpenAlex

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton et autres

10 citationsmedRxiv

Profil ORCID Notice OpenAlex

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