Zhenjun Yang

Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics.

Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing.

Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay.

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.