| Artigo em revista |
- "Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements
by genome sequencing.". Asian journal of andrology (2022): https://doi.org/10.4103/aja2021106.
10.4103/aja2021106
- "Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic
disease". Stroke and Vascular Neurology (2021): https://svn.bmj.com/content/early/2021/12/07/svn-2021-001157.
10.1136/svn-2021-001157.
- "SVInterpreter: A Comprehensive Topologically Associated Domain-Based Clinical Outcome Prediction Tool for Balanced and Unbalanced
Structural Variants.". Frontiers in genetics (2021): https://europepmc.org/articles/PMC8671832.
10.3389/fgene.2021.757170
- "Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.".
Frontiers in genetics (2021): https://europepmc.org/articles/PMC8488434.
10.3389/fgene.2021.742325
- "Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics.". Genetics
in medicine : official journal of the American College of Medical Genetics (2021): https://doi.org/10.1038/s41436-021-01128-7.
10.1038/s41436-021-01128-7
- Yunli Lai; Xiaofan Zhu; Sheng He; Zirui Dong; Yanqing Tang; Fuben Xu; Yun Chen; et al. "Performance of Cell-Free DNA Screening
for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region
in Mainland China". Genes (2021): https://doi.org/10.3390/genes12040478.
10.3390/genes12040478
- Zirui Dong; Matthew Hoi Kin Chau; Yanyan Zhang; Peng Dai; Xiaofan Zhu; Tak Yeung Leung; Xiangdong Kong; et al. "Deciphering
the complexity of simple chromosomal insertions by genome sequencing". Human Genetics (2021): https://doi.org/10.1007/s00439-020-02210-x.
10.1007/s00439-020-02210-x
- Dong, Zirui. "Low-pass genome sequencing: a validated method in clinical cytogenetics". Human Genetics (2020): http://dx.doi.org/10.1007/s00439-020-02185-9.
10.1007/s00439-020-02185-9
- Huilin Wang; Zirui Dong; Rui Zhang; Matthew Hoi Kin Chau; Zhenjun Yang; Kathy Yin Ching Tsang; Hoi Kin Wong; et al. "Low-pass
genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis". Genetics in Medicine
(2020): https://doi.org/10.1038/s41436-019-0634-7.
10.1038/s41436-019-0634-7
- Dong, Zirui; Yan, Junhao; Xu, Fengping; Yuan, Jianying; Jiang, Hui; Wang, Huilin; Chen, Haixiao; et al. "Genome Sequencing
Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage". The American Journal of Human Genetics
105 6 (2019): 1102-1111. http://dx.doi.org/10.1016/j.ajhg.2019.10.003.
10.1016/j.ajhg.2019.10.003
- Qi Zhen; Zhenjun Yang; Wenjun Wang; Bao Li; Mingzhou Bai; Jing Wu; Huiyao Ge; et al. "Genetic Study on Small Insertions and
Deletions in Psoriasis Reveals a Role in Complex Human Diseases". Journal of Investigative Dermatology (2019): https://doi.org/10.1016/j.jid.2019.03.1157.
10.1016/j.jid.2019.03.1157
- Dong, Zirui. "Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.". Frontiers
in Genetics (2019):
10.3389/fgene.2019.00761
- Dong, Zirui. "Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection
of various genomic variants in one single assay.". DNA research : an international journal for rapid publication of reports
on genes and genomes (2019): https://doi.org/10.1093/dnares/dsz011.
10.1093/dnares/dsz011
- Dong, Zirui. "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.". Genetics
in Medicine (2017):
- Dong, Zirui. "Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing.". Current Protocols in Human Genetics
(2017):
- Zirui Dong; Jun Zhang; Ping Hu; Haixiao Chen; Jinjin Xu; Qi Tian; Lu Meng; et al. "Low-pass whole-genome sequencing in clinical
cytogenetics: a validated approach". Genetics in Medicine 18 9 (2016): 940-948. https://doi.org/10.1038/gim.2015.199.
10.1038/gim.2015.199
- Dong, Zirui. "Comparison of RNA-seq and microarray-based models for clinical endpoint prediction". GENOME BIOLOGY (2015):
- Dong, Zirui. "An investigation of biomarkers derived from legacy microarray data for their utility in the RNA-seq era.". GENOME
BIOLOGY (2014):
- Dong, Zirui. "A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality
Control Consortium.". NATURE BIOTECHNOLOGY (2014):
- Dong, Zirui. "Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families
with chromosome reciprocal translocation". GENOMICS (2014):
- Dong, Zirui. "A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole-Genome Low-Coverage
Sequencing". HUMAN MUTATION (2014): http://www.ncbi.nlm.nih.gov/pubmed/24610732.
- Dong, Zirui. "Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptome". NATURE BIOTECHNOLOGY
(2012):
|
