Keqin Yan

501 Smyth Road
Ottawa, ON, Canada

Last Updated: 09/26/2026

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Found 18 publications

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Journal: Research square

Published: October 16, 2023

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Journal: Nature communications

Published: September 01, 2023

PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS.

PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS.

Journal: EMBO reports

Published: June 13, 2023

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.

Journal: Human molecular genetics

Published: January 24, 2023

VGF is required for recovery after focal stroke.

VGF is required for recovery after focal stroke.

Journal: Experimental neurology

Published: September 07, 2022

Generation of a mouse model of the neurodevelopmental disorder with dysmorphic facies and distal limb anomalies syndrome.

Generation of a mouse model of the neurodevelopmental disorder with dysmorphic facies and distal limb anomalies syndrome.

Journal: Human molecular genetics

Published: January 10, 2022

Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson-Forssman-Lehmann Syndrome.

Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson-Forssman-Lehmann Syndrome.

Journal: Human molecular genetics

Published: December 28, 2020

Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse Retina.

Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse Retina.

Journal: Neuroscience

Published: June 09, 2020

Correction to: C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum.

Correction to: C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum.

Journal: Journal of neuroinflammation

Published: January 25, 2020

C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum.

C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum.

Journal: Journal of neuroinflammation

Published: June 02, 2019

Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development.

Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development.

Journal: Frontiers in molecular neuroscience

Published: April 10, 2019

Recovery from impaired muscle growth arises from prolonged postnatal accretion of myonuclei in Atrx mutant mice.

Recovery from impaired muscle growth arises from prolonged postnatal accretion of myonuclei in Atrx mutant mice.

Journal: PloS one

Published: May 02, 2017

Showing 1-12 of 18

Last Updated: 09/26/2026