Liang-liang Q. Fan

Changsha, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 101 publications

A novel mutation in SETD1A is associated with early-onset epilepsy-a rare case report.

A novel mutation in SETD1A is associated with early-onset epilepsy-a rare case report.

Journal: Frontiers in neuroscience

Published: April 25, 2026

Whole exome sequencing identified a novel compound heterozygous mutation of nephrocystin 4 in a child with nephronophthisis-a rare case report.

Whole exome sequencing identified a novel compound heterozygous mutation of nephrocystin 4 in a child with nephronophthisis-a rare case report.

Journal: Frontiers in pediatrics

Published: April 25, 2026

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Journal: DNA and cell biology

Published: April 06, 2026

Clinical and immunological features of a patient exhibiting delayed puberty, microcephaly, scoliosis and epilepsy caused by a novel mutation in IGSF10.

Clinical and immunological features of a patient exhibiting delayed puberty, microcephaly, scoliosis and epilepsy caused by a novel mutation in IGSF10.

Journal: Frontiers in cell and developmental biology

Published: February 25, 2026

A rare mutation (p.Ala264Thr) of GATA4 is responsible for atrial septal defect and pulmonary valve stenosis.

A rare mutation (p.Ala264Thr) of GATA4 is responsible for atrial septal defect and pulmonary valve stenosis.

Journal: Scientific reports

Published: January 10, 2026

Associations of metabolic memory burden with chronic complication in type 1 diabetes: a baseline study of the PS-LT1D cohort

Associations of metabolic memory burden with chronic complication in type 1 diabetes: a baseline study of the PS-LT1D cohort

Journal: Zhonghua nei ke za zhi

Published: January 08, 2026

Whole exome sequencing identified two novel mutations of ACD in Chinese patients with idiopathic pulmonary fibrosis.

Whole exome sequencing identified two novel mutations of ACD in Chinese patients with idiopathic pulmonary fibrosis.

Journal: Frontiers in cell and developmental biology

Published: December 11, 2025

Pain and Kidney Disease Risk in Older Adults: CHARLS Longitudinal Study.

Pain and Kidney Disease Risk in Older Adults: CHARLS Longitudinal Study.

Journal: Pain management nursing : official journal of the American Society of Pain Management Nurses

Published: November 27, 2025

A Rare TERT Mutation Associated with Idiopathic Pulmonary Fibrosis and COPD in a Chinese Family.

A Rare TERT Mutation Associated with Idiopathic Pulmonary Fibrosis and COPD in a Chinese Family.

Journal: Balkan medical journal

Published: September 01, 2025

A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.

A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.

Journal: Medicine

Published: June 09, 2025

Whole exome sequencing identified three novel mutations of RTEL1 in Chinese patients with idiopathic pulmonary fibrosis.

Whole exome sequencing identified three novel mutations of RTEL1 in Chinese patients with idiopathic pulmonary fibrosis.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: March 07, 2025

Lipin3 deficiency promotes hepatocyte ferroptosis and pyroptosis via activating JAK1-STAT3 pathway during acetaminophen induced acute liver injury.

Lipin3 deficiency promotes hepatocyte ferroptosis and pyroptosis via activating JAK1-STAT3 pathway during acetaminophen induced acute liver injury.

Journal: Molecular biomedicine

Published: March 03, 2025

Showing 1-12 of 101

Last Updated: 09/26/2026