Yi Ding - Publications

Serum FAM132A/Adipolin correlates with endothelial dysfunction in children with obesity.

Journal: Pediatric research

Published: December 08, 2025

Obesity impairs male reproductive development in prepubertal boys via local adipose tissue inflammation and the STAT3/CYP19A1 pathway.

Journal: Journal of endocrinological investigation

Published: October 22, 2025

Circulating spexin and adiponectin as early biomarkers of insulin resistance in pediatric obesity.

Journal: BMC endocrine disorders

Published: September 26, 2025

Methodological considerations in evaluating the association between combined oral contraceptives and gastroparesis.

Journal: Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver

Published: May 13, 2025

Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: September 28, 2024

Treatment and genetic analysis of multiple supernumerary and impacted teeth in an adolescent patient.

Journal: BMC oral health

Published: March 28, 2024

Anti-inflammatory response-based risk assessment in acute type A aortic dissection: A national multicenter cohort study.

Journal: International journal of cardiology. Heart & vasculature

Published: November 16, 2023

Conjugation of dual-natural milk-derived proteins with fucoidan to prepare controllable glycosylation products via dielectric barrier discharge cold plasma.

Journal: International journal of biological macromolecules

Published: September 01, 2023

Whole-exome sequencing identifies ECPAS as a novel potentially pathogenic gene in multiple hereditary families with nonsyndromic orofacial cleft.

Journal: Protein & cell

Published: July 30, 2023

Identification of rare loss-of-function variants in FAM3B associated with non-syndromic orofacial clefts.

Journal: Genomics

Published: March 02, 2023

Rare loss-of-function variants in FLNB cause non-syndromic orofacial clefts.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: December 21, 2022

A392V and R945X mutations cause orofacial clefts via impairing PTCH1 function.

Journal: Genomics

Published: April 14, 2022