about
A genome-wide association study confirms previously reported loci for type 2 diabetes in Han ChineseCombined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studiesA gradient-boosting approach for filtering de novo mutations in parent-offspring triosAn evaluation of copy number variation detection tools from whole-exome sequencing data.Impaired lung function is associated with increased carotid intima-media thickness in middle-aged and elderly ChineseWhole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.Joint detection of copy number variations in parent-offspring trios.Advanced research on risk factors of type 2 diabetes.One gene, many neuropsychiatric disorders: lessons from Mendelian diseases.Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations.Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease.De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.De-novo mutations in patients with chronic ultra-refractory epilepsy with onset after age five yearsWhole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
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description
researcher ORCID ID = 0000-0002-3221-595X
@en
wetenschapper
@nl
name
Xiaolin Zhu
@ast
Xiaolin Zhu
@en
Xiaolin Zhu
@es
Xiaolin Zhu
@nl
type
label
Xiaolin Zhu
@ast
Xiaolin Zhu
@en
Xiaolin Zhu
@es
Xiaolin Zhu
@nl
prefLabel
Xiaolin Zhu
@ast
Xiaolin Zhu
@en
Xiaolin Zhu
@es
Xiaolin Zhu
@nl
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56184722300
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P496
0000-0002-3221-595X