List of works - Weichen Zhou

A robust benchmark for detection of germline large deletions and insertions

scientific article published on 15 June 2020

A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models

scientific article published on 25 January 2018

Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks

scientific article published on 01 July 2011

Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population

scientific article published on 01 January 2011

Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.

scientific article

Author Correction: A robust benchmark for detection of germline large deletions and insertions

scientific article published on 22 July 2020

CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis

scientific article

Cas9 targeted enrichment of mobile elements using nanopore sequencing

scientific article published on 11 June 2021

Characterization of nuclear mitochondrial insertions in the whole genomes of primates

scientific article published on 16 November 2020

Comprehensive identification of somatic nucleotide variants in human brain tissue

scientific article

Comprehensive identification of somatic nucleotide variants in human brain tissue

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome

scientific article

Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders

scientific article published on 14 March 2017

Genome architecture and its roles in human copy number variation.

scientific article

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

scientific article published on 28 January 2014

Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

scientific article published on 01 February 2020

Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms

scientific article published on 7 March 2013

Predictive model for inflammation grades of chronic hepatitis B: Large-scale analysis of clinical parameters and gene expressions.

scientific article published on 22 March 2017

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

scientific article

knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable

scientific article published on 22 November 2018

List of works by Weichen Zhou

A robust benchmark for detection of germline large deletions and insertions

A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models

Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks

Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population

Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.

Author Correction: A robust benchmark for detection of germline large deletions and insertions

CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis

Cas9 targeted enrichment of mobile elements using nanopore sequencing

Characterization of nuclear mitochondrial insertions in the whole genomes of primates

Comprehensive identification of somatic nucleotide variants in human brain tissue

Comprehensive identification of somatic nucleotide variants in human brain tissue

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome

Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders

Genome architecture and its roles in human copy number variation.

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms

Predictive model for inflammation grades of chronic hepatitis B: Large-scale analysis of clinical parameters and gene expressions.

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable