Lingqian Wu

15PUBLICATIONS
27CO-AUTHORS
Neurology and neuromuscular diseasesOptical technologyFoetal development and medicineMedical molecular engineering of nucleic acids and proteinsDevelopmental genetics (incl. sex determination)
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Publications (15)

|Jun 30, 2026
Disruption of dynactin complex function in intellectual disability.

|Apr 26, 2025
The Spectra of Pathogenic Variants and Phenotypes in a Chinese Cohort of 298 Families with Osteogenesis Imperfecta.

Siji Zhou, Xiuzhi Ren, Yixuan Cao

|Feb 04, 2025
A rare viable delivery of a 45,X/46,XY mosaicism female with complete gonadal dysgenesis after receiving oocyte donation and overcoming multiple pregnancy complications.

Yingliu Luo, Xi Liao, Juan Wen

|Nov 20, 2023
Chinese experts' consensus guideline on preimplantation genetic testing of monogenic disorders.

Liying Yan, Yunxia Cao, Zi-Jiang Chen

|May 04, 2021
Molecular diagnosis for 55 fetuses with skeletal dysplasias by whole-exome sequencing: A retrospective cohort study.

Li Zhang, Lijuan Pan, Yanling Teng

|Oct 03, 2020
Novel GZF1 pathogenic variants identified in two Chinese patients with Larsen syndrome.

Lanlan Zeng, Zhibin Li, Lijuan Pan

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Frequent Collaborators

5 joint publications

Zhuo Li

2 joint publications

Desheng Liang

1 joint publications

Hua Wang

1 joint publications

Yingdi Liu