Chen Xue

<i>CEP78</i> is mutated in a distinct type of Usher syndrome

Qing Fu, Mingchu Xu, Chen Xue et al. · Journal of Medical Genetics · 2016 · 54 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth

Yu An, Linna Zhang, Wenwen Liu et al. · Human Genetics · 2020 · 46 citations

Life Sciences, Genetics, Molecular Genetics +12

Restructuring of contralateral gray matter volume associated with cognition in patients with unilateral temporal lobe glioma before and after surgery

Guanjie Hu, Xin‐Hua Hu, Kun Yang et al. · Human Brain Mapping · 2019 · 34 citations · Full text

Medicine, Neurological Surgery, Neuroscience +15

Targeted Next-generation Sequencing Reveals Novel EYS Mutations in Chinese Families with Autosomal Recessive Retinitis Pigmentosa

Chen Xue, Xiaoxing Liu, Xunlun Sheng et al. · Scientific Reports · 2015 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Spectral parameter imaging for detection of prognostically significant histologic features in uveal melanoma

Ronald H. Silverman, Robert Folberg, Mark J. Rondeau et al. · Ultrasound in Medicine & Biology · 2003 · 31 citations

Medicine, Oncology, Pathology +16