List of works - Xueya Zhou

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

scientific article published on 18 July 2016

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

scientific article published on 22 February 2012

A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population

scientific article published on 19 October 2011

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

scientific article published on 03 June 2016

Co-occurring protein phosphorylation are functionally associated

scientific article

Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population

scientific article

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

scientific article published on 10 December 2018

Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy

scientific article published on 23 May 2016

Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family

scientific article published on 17 September 2014

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

scientific article published on 23 August 2019

Fine mapping of the awn gene on chromosome 4 in rice by association and linkage analyses

article

Identification and characterization of human snoRNA core promoters

scientific article published on 29 March 2010

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

scientific article published on 02 January 2017

Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing

scientific article published on 20 February 2012

MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations

scientific article

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

scientific article

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

scientific article

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

scientific article published on 30 August 2010

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches.

scientific article

Short read mapping for exome sequencing

scientific article published on 01 January 2013

Systematic characterization and prediction of post-translational modification cross-talk.

scientific article

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

scientific article

List of works by Xueya Zhou

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

Co-occurring protein phosphorylation are functionally associated

Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy

Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Fine mapping of the awn gene on chromosome 4 in rice by association and linkage analyses

Identification and characterization of human snoRNA core promoters

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing

MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches.

Short read mapping for exome sequencing

Systematic characterization and prediction of post-translational modification cross-talk.

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation