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Human Genetics|September 9, 2021
Revealing modifier variations characterizations for elucidating the genetic basis of human phenotypic variationsHong Sun, Xiaoping Lan, Liangxiao Ma, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 13, 2018
Evaluation of retinal vasculature before and after treatment of children with obstructive sleep apnea-hypopnea syndrome by optical coherence tomography angiographyHaiyun Ye, Ce Zheng, Xiaoping Lan, et al.
Environmental Pollution (Barking, Essex : 1987)|May 5, 2022
Microplastic bioaccumulation in estuary-caught fishery resourceZhenling Li, Min Chao, Xiaokang He, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 6, 2019
[Mutation analysis of two pedigrees with suspected oculocutaneous albinism]Haiyun Ye, Xiaoping Lan, Tong Qiao, et al.
Molecular Genetics & Genomic Medicine|October 10, 2020
De novo variants in WDR45 underlie beta-propeller protein-associated neurodegeneration in five independent familiesXiaojun Tang, Xiaoping Lan, Xiaozhen Song, et al.
Medicine|December 22, 2019
Ocular findings and strabismus surgery outcomes in Chinese children with Angelman syndrome: Three case reportsHaiyun Ye, Xiaoping Lan, Qingyu Liu, et al.
Ecotoxicology and Environmental Safety|November 27, 2025
Overlooked environmental risks of type 2 diabetes: Evidence from a case-control study on the roles of dechlorane plus (DPs) and novel brominated flame retardants (NBFRs)Jianing Zheng, Yongkang Chen, Jie Sun, et al.
Frontiers in Genetics|February 24, 2026
Identification and functional analysis of a novel TRAPPC2 intronic variant in a four-generation Chinese pedigree with SEDTYongfen Lyu, Wuhen Xu, Bin Xu, et al.
Genes & Genomics|April 28, 2022
Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiencyXiaojun Tang, Wuhen Xu, Xiaozhen Song, et al.
Molecular Genetics & Genomic Medicine|June 8, 2023
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boyXiaoang Sun, Xiaona Luo, Longlong Lin, et al.
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