Xilin Xu

Evaluation of phenotype-driven gene prioritization methods for Mendelian diseases

P. Zhang, Wenbo Mu, Q. Gong, 2022, Briefings Bioinform..

The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility

G. Lin, F. Gong, Yong Gao, 2021, Journal of Assisted Reproduction and Genetics.

Gene-Focused Networks Underlying Phenotypic Convergence in a Systematically Phenotyped Cohort With Heterogeneous Intellectual Disability

X. Yang, Yan Wang, Zhi-Chun Feng, 2020, Frontiers in Bioengineering and Biotechnology.

MetaDP: a comprehensive web server for disease prediction of 16S rRNA metagenomic datasets

Aiping Wu, Taijiao Jiang, T. Jiang, 2016, Biophysics reports.

Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella

G. Lin, L. Fan, Y. Tan, 2023, Frontiers in Cell and Developmental Biology.

Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.

G. Lin, Yueqiu Tan, Weili Wang, 2022, Molecular human reproduction.

Increases in computationally predicted deleterious variants of unknown significance and sperm mtDNA copy numbers may be associated with semen quality.

Liang Hu, Shuoping Zhang, G. Lin, 2023, Andrology.