Lifei Gong
Beijing, 100026, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Population-based newborn screening for inherited metabolic diseases in Beijing, China: findings from 404,990 infants.
Journal: Molecular genetics and metabolism
Published: June 25, 2026
Dried blood spot quality in newborn inherited metabolic disease screening in Beijing, 2020-2024: a retrospective analysis of incidence, causes, and improvement strategies.
Journal: BMC pediatrics
Published: April 12, 2026
Retraction Note: Circular RNA circCTNNA1 promotes colorectal cancer progression by sponging miR-149-5p and regulating FOXM1 expression.
Journal: Cell death & disease
Published: February 04, 2026
MassARRAY-based targeted detection of SLC22A5 mutations: A feasibility study for secondary screening of primary carnitine deficiency in newborns.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 15, 2025
Impact of maternal anemia during pregnancy on neonatal metabolic profiles: evidence from the Beijing Birth Cohort Study.
Journal: BMC pregnancy and childbirth
Published: January 21, 2025
Six Chinese patients with propionic acidemia: from asymptomatic to death in the neonatal period.
Journal: Orphanet journal of rare diseases
Published: September 26, 2024
Four novel variants identified in the ACADVL gene causing very-long-chain acyl-coenzyme A dehydrogenase deficiency in four unrelated Chinese families.
Journal: Frontiers in genetics
Published: May 15, 2024
Identification of gene mutations in six Chinese patients with maple syrup urine disease.
Journal: Frontiers in genetics
Published: December 27, 2022
Clinical characteristics and genetics analysis for the ITD of congenital hypothyroidism.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: January 28, 2022
Showing 1-11 of 11
Last Updated: 09/26/2026