Qiong Xu-Qiong

Shanghai, 200032, China

Last Updated: 09/26/2026

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Found 11 publications

Aberrant Emotion-Cognition Integration in FMR1 Premutation Carriers: a fNIRS Study.

Aberrant Emotion-Cognition Integration in FMR1 Premutation Carriers: a fNIRS Study.

Journal: eNeuro
Published: January 31, 2026

ADNP missense variant p.C687R disrupts chromatin regulation and GABAergic differentiation in Helsmoortel-Van der Aa syndrome.

ADNP missense variant p.C687R disrupts chromatin regulation and GABAergic differentiation in Helsmoortel-Van der Aa syndrome.

Journal: Molecular autism
Published: December 14, 2025

Enhanced accuracy and sensitivity in detecting FMR1 CGG repeats: a multicenter evaluation of a novel PCR-capillary electrophoresis assay.

Enhanced accuracy and sensitivity in detecting FMR1 CGG repeats: a multicenter evaluation of a novel PCR-capillary electrophoresis assay.

Journal: World journal of pediatrics : WJP
Published: August 03, 2025

Age-varying distinct neuroanatomy in young children with autism spectrum disorder and fragile X syndrome.

Age-varying distinct neuroanatomy in young children with autism spectrum disorder and fragile X syndrome.

Journal: Molecular psychiatry
Published: July 08, 2025

Effects of Metformin on children with Fragile X Syndrome: a randomized, double-blind, placebo-controlled trial.

Effects of Metformin on children with Fragile X Syndrome: a randomized, double-blind, placebo-controlled trial.

Journal: Molecular autism
Published: June 14, 2025

Molecular genetic testing and cohort analysis of 32 twin pairs with neurodevelopmental disorders-Reporting a novel de novo variant of TET3.

Molecular genetic testing and cohort analysis of 32 twin pairs with neurodevelopmental disorders-Reporting a novel de novo variant of TET3.

Journal: Human genomics
Published: October 20, 2024

Distinct and shared intrinsic resting-state functional networks in children with idiopathic autism spectrum disorder and fragile X syndrome.

Distinct and shared intrinsic resting-state functional networks in children with idiopathic autism spectrum disorder and fragile X syndrome.

Journal: Molecular psychiatry
Published: October 08, 2024

Facial characteristics description and classification based on 3D images of Fragile X syndrome in a retrospective cohort of young Chinese males.

Facial characteristics description and classification based on 3D images of Fragile X syndrome in a retrospective cohort of young Chinese males.

Journal: Computers in biology and medicine
Published: May 24, 2024

Generation of a human induced pluripotent stem cell line (FDIBSi001-A) from a patient with ADNP syndrome carrying ADNP mutation (c. 2059 T>C).

Generation of a human induced pluripotent stem cell line (FDIBSi001-A) from a patient with ADNP syndrome carrying ADNP mutation (c. 2059 T>C).

Journal: Stem cell research
Published: April 05, 2024

Clinical impact and in vitro characterization of ADNP variants in pediatric patients.

Clinical impact and in vitro characterization of ADNP variants in pediatric patients.

Journal: Molecular autism
Published: October 27, 2023

Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line.

Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line.

Journal: Stem cell research
Published: February 13, 2021
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Last Updated: 09/26/2026