Liyang Liang
No. 107 Yanjiang West Road
Guangzhou, 510120, China
Guangzhou, 510120, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 45 publications
Estrogen deficiency and risk of hearing loss in pediatric Turner syndrome.
Journal: The Journal of clinical investigation
Published: October 08, 2025
Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.
Journal: Human genetics
Published: September 17, 2025
Sox11 deficiency induces paravertebral muscle injury and scoliosis via Mlxipl upregulation.
Journal: Genes & diseases
Published: May 19, 2025
Case Report: Observation of early-onset high myopia with fundus tessellation changes in Coffin-Siris syndrome 9 (CSS9) and literature review.
Journal: Frontiers in pediatrics
Published: April 01, 2025
Predicting the diagnostic efficacy of trio-based whole exome sequencing in children with low-function autism spectrum disorders: a multicenter study.
Journal: Frontiers in neurology
Published: March 21, 2025
Five-year safety and growth response of long-acting PEGylated recombinant human growth hormone in children with growth hormone deficiency-data from CGLS database.
Journal: European journal of pediatrics
Published: March 04, 2025
Establishment and validation of a phenotype-driven predictive model for the diagnostic efficacy of trio-based whole exome sequencing (trio-WES) in children with genetic neurodevelopmental disorders (g-NDDs).
Journal: Frontiers in neurology
Published: February 11, 2025
Eustachian Tube Characteristics in Patients With Turner Syndrome: A CT-Based Radiological Analysis.
Journal: The Laryngoscope
Published: December 12, 2024
Extending curve matching with flexible hyperparameter selection to predict response to long-acting PEGylated growth hormone treatment in growth hormone deficiency children: method development and validation.
Journal: Journal of endocrinological investigation
Published: November 14, 2024
TCL1A in naïve B cells as a therapeutic target for type 1 diabetes.
Journal: EBioMedicine
Published: September 11, 2024
Novel ANKRD17 variants implicate synaptic and mitochondrial disruptions in intellectual disability and autism spectrum disorder.
Journal: Journal of neurodevelopmental disorders
Published: August 14, 2024
A Novel Y-Shaped Pegylated Recombinant Human Growth Hormone for Children With Growth Hormone Deficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 11, 2024
Last Updated: 09/26/2026