Kun Xia - Genetic Mutations

Author Information

Kun Xia is affiliated with the Center for Medical Genetics at the School of Life Sciences, Central South University, located in Changsha, China. This institution is known for its significant contributions to genetic research, and Kun Xia plays an essential role in advancing the understanding of genetic diseases and disorders through his work at this center.

Research Contributions

Kun Xia has made substantial contributions to the field of genetics, particularly in understanding the genetic basis of various disorders. Some of his recent research includes exploring mitochondrial dysfunction in autism spectrum disorder, investigating GLRA2 gene mutations linked to high myopia, and analyzing the function and pathogenicity of non-coding variants. His work often involves cutting-edge methodologies such as single-cell analysis and targeted sequencing, with a focus on neurodevelopmental disorders, autism, and Alzheimer's disease. His research not only expands the current knowledge in genetics but also has practical implications for diagnosis and treatment.

Aliases

Kun Xia is also known by other variants of his name, including K Xia and K. Xia. These aliases are commonly used in academic publications to refer to the same individual.

Publication and Citation Metrics

Metric	Value
Total Citation Count	12,202
h-index	54
Total Paper Count	541

Publications:

Odor identification impairment in autism spectrum disorder might be associated with mitochondrial dysfunction.

DOI: 10.1016/j.ajp.2022.103072

Year: 2022

GLRA2 gene mutations cause high myopia in humans and mice

DOI: 10.1136/jmedgenet-2022-108425

Year: 2022

Performance comparison of computational methods for the prediction of the function and pathogenicity of non-coding variants.

DOI: 10.1016/j.gpb.2022.02.002

Year: 2022

Single‐cell analysis of nonhuman primate preimplantation development in comparison to humans and mice

DOI: 10.1002/dvdy.295

Year: 2021

GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases

DOI: 10.1016/j.csbj.2021.03.011

Year: 2021

Anesthesia, sex and miscarriage history may influence the association between cesarean delivery and autism spectrum disorder

DOI: 10.1186/s12887-021-02518-1

Year: 2021

Inhibition of miR-331-3p and miR-9-5p ameliorates Alzheimer's disease by enhancing autophagy

DOI: 10.7150/thno.47408

Year: 2021

Anxiety and depression in spinocerebellar ataxia patients during the COVID-19 pandemic in China: A cross-sectional study

DOI: 10.1016/j.jocn.2021.03.004

Year: 2021

Targeted sequencing and integrative analysis of 3195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes.

DOI: 10.1016/J.JGG.2021.03.002

Year: 2021

Rare NRXN1 missense variants identified in autism interfered protein degradation and Drosophila sleeping.

DOI: 10.1016/j.jpsychires.2021.09.013

Year: 2021

What Are Chromosomal Mutations?

How Do Genetic Mutations Cause Developmental Disorders?

Why are Non-Coding Regions Important?

How are Inherited Mutations Detected?

Is Autism Spectrum Disorder Genetic?

Are Synonymous Mutations Considered in Genetic Research?

How Does Hydroxyurea Affect Genetic Mutations?

Are All Environmental Mutations Harmful?

What are the Latest Diagnostic Tools?

What are Driver Mutations and Passenger Mutations?

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