Wuhen Xu

Spectrum of RB1 Germline Mutations and Clinical Features in Unrelated Chinese Patients With Retinoblastoma

Xiaoping Lan, Wuhen Xu, Xiaojun Tang et al. · Frontiers in Genetics · 2020 · 36 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Diagnostic Utility of Trio–Exome Sequencing for Children With Neurodevelopmental Disorders

Xiaoping Lan, Xiaojun Tang, Wenhao Weng et al. · JAMA Network Open · 2025 · 16 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Segawa syndrome caused by TH gene mutation and its mechanism

Yilin Wang, Chunmei Wang, Meiyan Liu et al. · Frontiers in Genetics · 2022 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

De novo variants in <i>WDR45</i> underlie beta‐propeller protein‐associated neurodegeneration in five independent families

Xiaojun Tang, Xiaoping Lan, Xiaozhen Song et al. · Molecular Genetics & Genomic Medicine · 2020 · 13 citations · Full text

Medicine, Genetics, Neurology +17

Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiency

Xiaojun Tang, Wuhen Xu, Xiaozhen Song et al. · Genes & Genomics · 2022 · 11 citations

Life Sciences, Genetics, Molecular Genetics +11