Xi Wu

Key Laboratory For The Genetics Of Developmental And Neuropsychiatric Disorders
Shanghai, 200030, China

Last Updated: 09/26/2026

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Found 33 publications

Genetically proxied inhibition of Phosphodiesterase-5 and cancer risks: A drug-target Mendelian randomization analysis.

Genetically proxied inhibition of Phosphodiesterase-5 and cancer risks: A drug-target Mendelian randomization analysis.

Journal: Scientific reports

Published: October 15, 2024

Accelerated phase development in a late-onset adolescent Chediak-Higashi syndrome patient caused by compound novel LYST mutations in the setting of SARS-CoV-2 infection.

Accelerated phase development in a late-onset adolescent Chediak-Higashi syndrome patient caused by compound novel LYST mutations in the setting of SARS-CoV-2 infection.

Journal: Blood cells, molecules & diseases

Published: March 15, 2024

TULP4, a novel E3 ligase gene, participates in neuronal migration as a candidate in schizophrenia.

TULP4, a novel E3 ligase gene, participates in neuronal migration as a candidate in schizophrenia.

Journal: CNS neuroscience & therapeutics

Published: March 07, 2023

Different roles of microbiota and genetics in the prediction of treatment response in major depressive disorder.

Different roles of microbiota and genetics in the prediction of treatment response in major depressive disorder.

Journal: Journal of psychiatric research

Published: November 14, 2022

Upregulation of DGCR8, a Candidate Predisposing to Schizophrenia in Han Chinese, Contributes to Phenotypic Deficits and Neuronal Migration Delay.

Upregulation of DGCR8, a Candidate Predisposing to Schizophrenia in Han Chinese, Contributes to Phenotypic Deficits and Neuronal Migration Delay.

Journal: Frontiers in psychiatry

Published: February 11, 2022

A novel heterozygous missense variant of the ARID4A gene identified in Han Chinese families with schizophrenia-diagnosed siblings that interferes with DNA-binding activity.

A novel heterozygous missense variant of the ARID4A gene identified in Han Chinese families with schizophrenia-diagnosed siblings that interferes with DNA-binding activity.

Journal: Molecular psychiatry

Published: September 01, 2021

Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios.

Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios.

Journal: iScience

Published: March 16, 2021

Sex-specific association of MC2R polymorphisms and the risk of major depressive disorder in Chinese Southern Han.

Sex-specific association of MC2R polymorphisms and the risk of major depressive disorder in Chinese Southern Han.

Journal: Psychiatric genetics

Published: January 04, 2021

Comorbid major depression in first-episode drug-naïve patients with schizophrenia: Analysis of the Depression in Schizophrenia in China (DISC) study.

Comorbid major depression in first-episode drug-naïve patients with schizophrenia: Analysis of the Depression in Schizophrenia in China (DISC) study.

Journal: Journal of affective disorders

Published: October 11, 2020

Association between ABC family polymorphisms and antidepressant response in Chinese Han population with major depressive disorder.

Association between ABC family polymorphisms and antidepressant response in Chinese Han population with major depressive disorder.

Journal: Psychiatry research

Published: September 30, 2019

Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients.

Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients.

Journal: Translational psychiatry

Published: August 26, 2019

Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement.

Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement.

Journal: Orphanet journal of rare diseases

Published: April 08, 2019

Showing 1-12 of 33

Last Updated: 09/26/2026