Haiwei M. Wang

Fujian Provincial Key Laboratory Of Prenatal Diagnosisand Birth Defects
Fuzhou, 350122, China

Last Updated: 09/26/2026

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Found 38 publications

Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.

Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.

Journal: Scientific reports

Published: January 03, 2026

Retraction Note: Synergy between arsenic trioxide and JQ1 on autophagy in pancreatic cancer.

Retraction Note: Synergy between arsenic trioxide and JQ1 on autophagy in pancreatic cancer.

Journal: Oncogene

Published: November 25, 2025

Expression patterns of bone morphogenetic protein 7 (BMP7) and its prognostic roles in neuroblastoma: An integrated bioinformatics analysis.

Expression patterns of bone morphogenetic protein 7 (BMP7) and its prognostic roles in neuroblastoma: An integrated bioinformatics analysis.

Journal: PloS one

Published: September 10, 2025

Identification of chromosomal abnormalities in miscarriages using single-nucleotide polymorphism arrays.

Identification of chromosomal abnormalities in miscarriages using single-nucleotide polymorphism arrays.

Journal: Archives of gynecology and obstetrics

Published: April 25, 2025

A phenome-wide Mendelian randomization analysis reveals the genetical associations of myocardial infarction, angina pectoris and Alzheimer's disease with lung cancer.

A phenome-wide Mendelian randomization analysis reveals the genetical associations of myocardial infarction, angina pectoris and Alzheimer's disease with lung cancer.

Journal: Scientific reports

Published: September 19, 2024

Transforming growth factor-induced gene TGFBI is correlated with the prognosis and immune infiltrations of breast cancer.

Transforming growth factor-induced gene TGFBI is correlated with the prognosis and immune infiltrations of breast cancer.

Journal: World journal of surgical oncology

Published: September 18, 2023

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.

Journal: International journal of pediatric otorhinolaryngology

Published: July 25, 2023

AEP-cleaved DDX3X induces alternative RNA splicing events to mediate cancer cell adaptation in harsh microenvironments.

AEP-cleaved DDX3X induces alternative RNA splicing events to mediate cancer cell adaptation in harsh microenvironments.

Journal: The Journal of clinical investigation

Published: June 27, 2023

RARRES2 is Downregulated in Isocitrate Dehydrogenase 1 Mutant Glioma Patients and Served as an Unfavorable Prognostic Factor of Glioma.

RARRES2 is Downregulated in Isocitrate Dehydrogenase 1 Mutant Glioma Patients and Served as an Unfavorable Prognostic Factor of Glioma.

Journal: World neurosurgery

Published: May 25, 2023

Chromosome 1p36 candidate gene ZNF436 predicts the prognosis of neuroblastoma: a bioinformatic analysis.

Chromosome 1p36 candidate gene ZNF436 predicts the prognosis of neuroblastoma: a bioinformatic analysis.

Journal: Italian journal of pediatrics

Published: April 25, 2023

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression.

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression.

Journal: PloS one

Published: April 18, 2023

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family.

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family.

Journal: Clinical genetics

Published: October 11, 2022

Showing 1-12 of 38

Last Updated: 09/26/2026