Xinnian Pan
Guangxi Zhuang Autonomous Region, 530003, China
Last Updated: 09/26/2026
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Found 14 publications
Prenatal Ozone Exposure and Reduced Brain Volume in Infants: A Nationwide Population-Based Study.
Journal: Environmental science & technology
Published: April 15, 2026
Non-invasive high frequency oscillatory ventilation for primary respiratory support in extremely preterm infants: multicentre randomised controlled trial.
Journal: BMJ (Clinical research ed.)
Published: October 06, 2025
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project.
Journal: Kidney international reports
Published: July 21, 2023
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project.
Journal: Human genetics
Published: July 13, 2023
The long-term outcomes of preterm infants receiving non-invasive high-frequency oscillatory ventilation.
Journal: Frontiers in pediatrics
Published: January 29, 2022
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project.
Journal: Journal of medical genetics
Published: November 25, 2021
Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome Project.
Journal: Archives of disease in childhood. Fetal and neonatal edition
Published: October 22, 2021
Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes Project.
Journal: Critical care medicine
Published: May 03, 2021
Non-invasive high-frequency oscillatory ventilation in preterm infants after extubation: a randomized, controlled trial.
Journal: The Journal of international medical research
Published: March 01, 2021
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.
Journal: Human mutation
Published: July 29, 2020
Clinical exome sequencing revealed that FLNC variants contribute to the early diagnosis of cardiomyopathies in infant patients.
Journal: Translational pediatrics
Published: March 11, 2020
Last Updated: 09/26/2026