L. An

发表

Novel CRISPR/Cas12a-based genetic diagnostic approach for SLC26A4 mutation-related hereditary hearing loss.

Shasha Huang, P. Dai, Xiaohua Jin, 2021, European journal of medical genetics.

Compound heterozygous variants of the FBXO7 gene resulting in infantile‐onset Parkinsonian‐pyramidal syndrome in siblings of a Chinese family

Xu Ma, Qian Liu, Yousheng Yan, 2020, Journal of clinical laboratory analysis.

Single nucleotide polymorphisms near the inhibin beta B gene on 2q14 are associated with pre-eclampsia in Han Chinese women.

Q. Wang, X. Wang, Y. Yang, 2015, European journal of obstetrics, gynecology, and reproductive biology.

Association between CRP gene polymorphisms and the risk of preeclampsia in Han Chinese women.

Qidi Wang, Xingyu Wang, Xu Ma, 2014, Genetic testing and molecular biomarkers.

Progesterone production requires activation of caspase-3 in preovulatory granulosa cells in a serum starvation model

Wei Han, Xu Ma, Ying Hu, 2012, Steroids.

Arsenic induced progesterone production in a caspase‐3‐dependent manner and changed redox status in preovulatory granulosa cells

Xu Ma, Nan Yao, Baiqing Yang, 2012, Journal of cellular physiology.

Polycomb group proteins are essential for spinal cord development.

Xu Ma, Jian-Jun Zhao, Caisheng Lu, 2010, Frontiers in bioscience.

Identification of novel deep intronic PAH gene variants in patients diagnosed with phenylketonuria

C. Yin, Xu Ma, Linlin Zhang, 2021, Human mutation.

High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord Blood.

Ruikun Cai, Xuerui Tan, Qidi Wang, 2016, The Journal of pediatrics.

Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients

Zongfu Cao, Cuixia Chen, Xu Ma, 2020, Journal of clinical laboratory analysis.

Variant analysis of 92 Chinese Han families with hearing loss

Xu Ma, Shasha Huang, P. Dai, 2022, BMC medical genomics.

High throughput sequencing reveals the diversity of TRB-CDR3 repertoire in patients with psoriasis vulgaris.

Ruikun Cai, Qidi Wang, Xingyu Wang, 2016, International immunopharmacology.

Exome sequencing reveals novel IRXI mutation in congenital heart disease.

Qidi Wang, Xiaodong Cao, Xu Ma, 2017, Molecular medicine reports.

Deep targeted sequencing reveals the diversity of TRB-CDR3 repertoire in patients with preeclampsia.

Ruikun Cai, Xuerui Tan, Qidi Wang, 2019, Human immunology.

Contribution of TIMP3 polymorphisms to the development of preeclampsia in Han Chinese women

Qidi Wang, Xingyu Wang, Xu Ma, 2015, Journal of Assisted Reproduction and Genetics.

Engineering of near-PAMless adenine base editor with enhanced editing activity and reduced off-target

Xingxu Huang, Shisheng Huang, Guanglei Li, 2022, Molecular therapy. Nucleic acids.

Exome sequencing reveals novel IRXI mutation in congenital heart disease.

Qidi Wang, Xiaodong Cao, Xu Ma, 2017, Molecular Medicine Reports.