Tingfeng Qin - Publications

Anisometropia at Age 7 After Bilateral Secondary Intraocular Lens Implantation at 2 to Younger than 6 Years for Pediatric Aphakia: The CCPMOH Report.

Journal: Ophthalmology science

Published: March 16, 2026

Two-year outcomes after goniotomy with or without secondary intraocular lens implantation in pediatric glaucoma following cataract surgery: a prospective cohort study.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: October 17, 2025

Visual Acuity and Complications at Age 7 Years Following Bilateral Secondary Intraocular Lens Implantation at 2 to Younger Than 6 Years for Pediatric Aphakia.

Journal: JAMA ophthalmology

Published: May 15, 2025

Phenotype-genotype correlation of patients with congenital cataracts and hair anomalies.

Journal: Molecular vision

Published: December 24, 2024

Surgical approach to and morphology of visually significant persistent pupillary membranes.

Journal: Journal of cataract and refractive surgery

Published: August 16, 2023

Early Diagnosis of Syndromic Congenital Cataracts in a Large Cohort of Congenital Cataracts.

Journal: American journal of ophthalmology

Published: May 25, 2023

Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patients.

Journal: BMC medical genomics

Published: May 19, 2023

Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome.

Journal: Genes

Published: November 07, 2022

Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases.

Journal: Genes

Published: July 08, 2022

Broadening the genotypic and phenotypic spectrum of MAF in three Chinese Han congenital cataracts families.

Journal: American journal of medical genetics. Part A

Published: February 21, 2022

Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation.

Journal: Orphanet journal of rare diseases

Published: August 06, 2021

DOCK4 stimulates MUC2 production through its effect on goblet cell differentiation.

Journal: Journal of cellular physiology

Published: November 18, 2020