Xiaowen Wang
Shanghai, 200092, China
Last Updated: 09/26/2026
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Found 19 publications
Associations of prenatal exposure to organophosphate flame retardants and organophosphorus pesticides with cardiac structure in 4-year-old children: Evidence from the Shanghai Birth Cohort.
Journal: Environmental pollution (Barking, Essex : 1987)
Published: May 31, 2026
Prenatal exposure to mixed toxic metals and childhood blood pressure: the mediating role of amino acid and carnitine metabolism.
Journal: Environmental pollution (Barking, Essex : 1987)
Published: March 25, 2026
The cochlear cell atlas of Gjb2-/- mice exhibits alterations accompanied by autophagy-related metabolic imbalances.
Journal: Free radical biology & medicine
Published: May 25, 2025
Association of Maternal Whole Blood Selenium with Cardiac Structure at 4 y of Age: A Prospective Birth Cohort Study.
Journal: The Journal of nutrition
Published: November 03, 2024
Molecular etiology study of hearing loss in 13 Chinese Han families.
Journal: Frontiers in neurology
Published: September 19, 2022
Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing.
Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing.
Journal: Frontiers in neurology
Published: August 24, 2022
Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing.
Journal: International journal of pediatric otorhinolaryngology
Published: March 05, 2019
Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.
Journal: Scientific reports
Published: November 11, 2016
NLRP3 Is Expressed in the Spiral Ganglion Neurons and Associated with Both Syndromic and Nonsyndromic Sensorineural Deafness.
Journal: Neural plasticity
Published: August 30, 2016
Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and type II Waardenburg Syndrome.
Journal: Scientific reports
Published: May 18, 2016
A 7666-bp genomic deletion is frequent in Chinese Han deaf patients with non-syndromic enlarged vestibular aqueduct but without bi-allelic SLC26A4 mutations.
Journal: International journal of pediatric otorhinolaryngology
Published: June 09, 2015
Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.
Journal: International journal of pediatric otorhinolaryngology
Published: March 30, 2015
Last Updated: 09/26/2026