Get started
Author

Dehua Cheng

Observed names: C Dehua, Cheng Dehua, D.- H. Cheng, DEHUA CHENG, De-Hua Cheng, De-hua CHENG, De-hua Cheng, DeHua Cheng, De‐Hua Cheng
ORCID: 0000-0002-1725-0255
Observed ORCID: 0000-0002-1725-0255
OpenAlex ID: A5080701415
Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts1
2013 · XuYang Yin, Ke Tan, et al. · Biology of Reproduction · 154
Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers
2013 · Y.- Q. Tan, K. Tan, et al. · Human Reproduction · 135
HLA-Matching Potential of an Established Human Embryonic Stem Cell Bank in China
2009 · Ge Lin, Yubin Xie, et al. · Cell stem cell · 97
PDF
Number of biopsied trophectoderm cells is likely to affect the implantation potential of blastocysts with poor trophectoderm quality
2016 · Shuoping Zhang, Keli Luo, et al. · Fertility and Sterility · 95
PDF
Tumor progression of culture‐adapted human embryonic stem cells during long‐term culture
2008 · Sheng Yang, Ge Lin, et al. · Genes Chromosomes and Cancer · 88
Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure
2009 · De-Hua Cheng, Yue-Qiu Tan, et al. · Fertility and Sterility · 79
PDF
Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD
2020 · Chaofeng Tu, Hongchuan Nie, et al. · Human Genetics · 76
Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos
2016 · Liang Hu, Dehua Cheng, et al. · EBioMedicine · 64
PDF
Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform
2020 · Liang Hu, Fan Liang, et al. · Frontiers in Genetics · 60
PDF
The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes
2014 · Fang Xu, Ya-Nan Zhang, et al. · Molecular Cytogenetics · 43
PDF
A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions
2022 · Pingyuan Xie, Xiao Hu, et al. · Human Reproduction · 33
Cytogenetic analysis of human embryos and embryonic stem cells derived from monopronuclear zygotes
2009 · Hongqing Liao, Shuoping Zhang, et al. · Journal of Assisted Reproduction and Genetics · 28
Prevalence and authenticity of de-novo segmental aneuploidy (>16 Mb) in human blastocysts as detected by next-generation sequencing
2018 · Shuang Zhou, Dehua Cheng, et al. · Reproductive BioMedicine Online · 25
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia
2023 · Weili Wang, Lilan Su, et al. · Human Reproduction · 24
PDF
Self-diploidization of human haploid parthenogenetic embryos through the Rho pathway regulates endomitosis and failed cytokinesis
2017 · Lizhi Leng, Qi Ouyang, et al. · Scientific Reports · 24
PDF
Reproductive outcomes after preimplantation genetic testing in mosaic Turner syndrome: a retrospective cohort study of 100 cycles
2021 · Jingnan Liao, Keli Luo, et al. · Journal of Assisted Reproduction and Genetics · 20
Segmental aneuploidies with 1 Mb resolution in human preimplantation blastocysts
2022 · Pingyuan Xie, Ping Liu, et al. · Genetics in Medicine · 19
Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature
2018 · Haiyu Li, Juan Du, et al. · Molecular Cytogenetics · 14
PDF
The dynamic changes of X chromosome inactivation during early culture of human embryonic stem cells
2016 · Pingyuan Xie, Qi Ouyang, et al. · Stem Cell Research · 14
PDF
Identification of paternal germline mosaicism by MicroSeq and targeted next‐generation sequencing
2020 · Congling Dai, Dehua Cheng, et al. · Molecular Genetics & Genomic Medicine · 13
PDF
Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement
2021 · Dehua Cheng, Liang Hu, et al. · Journal of Assisted Reproduction and Genetics · 12
PDF
Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies
2020 · Ya-Qi Tan, Yue-Qiu Tan, et al. · Molecular Cytogenetics · 12
PDF
Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings
2018 · Aixiang Luo, Dehua Cheng, et al. · Molecular Cytogenetics · 12
PDF
Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby
2012 · De-Hua Cheng, Fei Gong, et al. · Journal of Assisted Reproduction and Genetics · 12
PDF
Pronuclear removal of tripronuclear zygotes can establish heteroparental normal karyotypic human embryonic stem cells
2016 · Hong-Qing Liao, Qi OuYang, et al. · Journal of Assisted Reproduction and Genetics · 10
Works count: 63
Citation count: 1,273
H-index: 17
I10-index: 26
Year
Topic
Type