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Publications by Kun Xia

PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior

Cell Reports
BiochemistryGeneticsMolecular Biology
2018English

Genes With De Novo Mutations Are Shared by Four Neuropsychiatric Disorders Discovered From NPdenovo Database

Molecular Psychiatry
PsychiatryMolecular NeuroscienceMental HealthMolecular BiologyCellular
2015English

Mutations of P4HA2 Encoding Prolyl 4-Hydroxylase 2 Are Associated With Nonsyndromic High Myopia

Genetics in Medicine
MedicineGenetics
2015English

AKAP2identified as a Novel Gene Mutated in a Chinese Family With Adolescent Idiopathic Scoliosis

Journal of Medical Genetics
Genetics
2016English

A Novel Locus for Congenital Simple Microphthalmia Family Mapping to 17p12-Q12

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2011English

Hmgb1 Inhibits Klotho Expression and Malignant Phenotype in Melanoma Cells by Activating NF-κB

Oncotarget
Oncology
2016English

Identification of a Potential Exosomal Biomarker in Spinocerebellar Ataxia Type 3/Machado–Joseph Disease

Epigenomics
Cancer ResearchGenetics
2019English

Identification of a De Novo DYNC1H1 Mutation via WES According to Published Guidelines

Scientific Reports
Multidisciplinary
2016English

Elevated Mitochondrial DNA Copy Number in Peripheral Blood Cells Is Associated With Childhood Autism

BMC Psychiatry
PsychiatryMental Health
2015English

Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective

PLoS ONE
Multidisciplinary
2015English

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