List of works - Xiaolin Zhu

A Genome-Wide Association Study Confirms Previously Reported Loci for Type 2 Diabetes in Han Chinese ⬇️

scientific article published on July 22, 2011

A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations

scientific article published on 29 November 2017

A gradient-boosting approach for filtering de novo mutations in parent-offspring trios

scientific article

Advanced research on risk factors of type 2 diabetes.

scientific article published on December 2012

An evaluation of copy number variation detection tools from whole-exome sequencing data

scientific article

Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies

scientific article

De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.

scientific article

De-novo mutations in patients with chronic ultra-refractory epilepsy with onset after age five years

scientific article published on 31 January 2019

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

scientific article published on 20 April 2016

Impaired lung function is associated with increased carotid intima-media thickness in middle-aged and elderly Chinese

scientific article published on 15 February 2013

Joint detection of copy number variations in parent-offspring trios

scientific article published on 07 December 2015

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

scientific article published on 15 September 2017

One gene, many neuropsychiatric disorders: lessons from Mendelian diseases.

scientific article published on 27 May 2014

Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease

scientific article

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study

scientific article published on 31 January 2019

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

scientific article published on 15 January 2015

List of works by Xiaolin Zhu

A Genome-Wide Association Study Confirms Previously Reported Loci for Type 2 Diabetes in Han Chinese ⬇️

A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations

A gradient-boosting approach for filtering de novo mutations in parent-offspring trios

Advanced research on risk factors of type 2 diabetes.

An evaluation of copy number variation detection tools from whole-exome sequencing data

Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies

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 years

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

Impaired lung function is associated with increased carotid intima-media thickness in middle-aged and elderly Chinese

Joint detection of copy number variations in parent-offspring trios

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

One gene, many neuropsychiatric disorders: lessons from Mendelian diseases.

Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios