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Publications by Yuqian Zheng

Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2017English

Augmented BMPRIA-Mediated BMP Signaling in Cranial Neural Crest Lineage Leads to Cleft Palate Formation and Delayed Tooth Differentiation

PLoS ONE
Multidisciplinary
2013English

Related publications

Whole Exome Sequencing Identified Novel CRB1 Mutations in Chinese and Indian Populations With Autosomal Recessive Retinitis Pigmentosa

Scientific Reports
Multidisciplinary
2016English

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

Archives of Ophthalmology
2007English

Whole Exome Sequencing Identified Sixty-Five Coding Mutations in Four Neuroblastoma Tumors

Scientific Reports
Multidisciplinary
2017English

Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations

PLoS ONE
Multidisciplinary
2016English

CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa With Incomplete Penetrance

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2012English

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

PLoS ONE
Multidisciplinary
2013English

Prevalence of Mutations Causing Retinitis Pigmentosa and Other Inherited Retinopathies

Human Mutation
Genetics
2000English

NMNAT1 Mutation Causing Retinitis Pigmentosa

Acta Ophthalmologica
MedicineOphthalmology
2018English

Identification of Novel EXT Mutations in Patients With Hereditary Multiple Exostoses Using Whole-Exome Sequencing

Orthopaedic surgery
SurgeryOrthopedicsSports Medicine
2020English

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