Haili Hu

Hefei, 230001, China

Last Updated: 09/26/2026

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Found 17 publications

Newborn Screening for Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency and Analysis of SLC25A13 Gene Mutations in Hefei, China.

Newborn Screening for Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency and Analysis of SLC25A13 Gene Mutations in Hefei, China.

Journal: International journal of neonatal screening

Published: May 08, 2026

Prenatal exposure to PM2.5 specific constituents and child neurodevelopmental delay: The role of maternal metabolites and mediterranean diet.

Prenatal exposure to PM2.5 specific constituents and child neurodevelopmental delay: The role of maternal metabolites and mediterranean diet.

Journal: Ecotoxicology and environmental safety

Published: March 16, 2026

The relationship between low-fat diets and telomere length among USA adults: nationwide cross-sectional study.

The relationship between low-fat diets and telomere length among USA adults: nationwide cross-sectional study.

Journal: The British journal of nutrition

Published: December 17, 2025

Newborn screening for methylmalonic acidemia: insights from a retrospective analysis in Hefei, China.

Newborn screening for methylmalonic acidemia: insights from a retrospective analysis in Hefei, China.

Journal: Orphanet journal of rare diseases

Published: September 11, 2025

Prevalence and Mutation Analysis of Medium-Chain Acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening in Hefei, China.

Prevalence and Mutation Analysis of Medium-Chain Acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening in Hefei, China.

Journal: International journal of neonatal screening

Published: June 23, 2025

Prevalence and Mutation Analysis of Short-Chain acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening in Hefei, China.

Prevalence and Mutation Analysis of Short-Chain acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening in Hefei, China.

Journal: International journal of neonatal screening

Published: July 12, 2024

Newborn screening of primary carnitine deficiency: clinical and molecular genetic characteristics.

Newborn screening of primary carnitine deficiency: clinical and molecular genetic characteristics.

Journal: Italian journal of pediatrics

Published: June 29, 2024

Clinical outcomes of patients with mut-type methylmalonic acidemia identified through expanded newborn screening in China.

Clinical outcomes of patients with mut-type methylmalonic acidemia identified through expanded newborn screening in China.

Journal: Human genomics

Published: November 20, 2023

Analysis of chromosomal aberrations in early pregnancy loss using high-throughput ligation-dependent probe amplification and single tandem repeats.

Analysis of chromosomal aberrations in early pregnancy loss using high-throughput ligation-dependent probe amplification and single tandem repeats.

Journal: Molecular cytogenetics

Published: November 19, 2023

Evaluation of the clinical, biochemical, genotype and prognosis of mut-type methylmalonic acidemia in 365 Chinese cases.

Evaluation of the clinical, biochemical, genotype and prognosis of mut-type methylmalonic acidemia in 365 Chinese cases.

Journal: Journal of medical genetics

Published: May 06, 2022

The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening.

The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening.

Journal: Frontiers in genetics

Published: October 30, 2021

Associations of Maternal Adverse Childhood Experiences with Behavioral Problems in Preschool Children.

Associations of Maternal Adverse Childhood Experiences with Behavioral Problems in Preschool Children.

Journal: Journal of interpersonal violence

Published: October 15, 2021

Showing 1-12 of 17

Last Updated: 09/26/2026