Lin Han

Changsha, 421001, China

Last Updated: 09/26/2026

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Found 9 publications

Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesis.

Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesis.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: October 18, 2021

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Journal: Nature communications

Published: October 22, 2020

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Journal: Nature communications

Published: April 09, 2020

Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.

Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.

Journal: Clinical genetics

Published: August 01, 2019

POGZ de novo missense variants in neuropsychiatric disorders.

POGZ de novo missense variants in neuropsychiatric disorders.

Journal: Molecular genetics & genomic medicine

Published: April 02, 2019

Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.

Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.

Journal: Science advances

Published: March 08, 2019

Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.

Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.

Journal: Molecular genetics & genomic medicine

Published: February 22, 2019

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.

Journal: Molecular autism

Published: July 27, 2018

Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development.

Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: July 20, 2018

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Last Updated: 09/26/2026