Baoheng Gui
Department of Genetics and Metabolism
Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region
BAOHENG GUI, PhD, is a postdoctoral researcher at Shenzhen Research Institute, The Chinese University of Hong Kong, and is an associate researcher in the Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region. Dr. Gui received his bachelor and doctorate degree on genetics at the State Key Laboratory of Medical Genetics of China, Central South University in 2010 and 2015, respectively. He has been at the Human Genetics Division, Cincinnati Children's Hospital Medical Center (USA) for one year as a visiting scholar. His research interests focus on molecular genetics and cytogenetics, preimplantation genetic testing (PGT), next-generation sequencing (NGS), chromosome microarray (CMA), embryo assessment and selection in assisted reproductive technologies (ART), especially in embryo mosaicism. He has obtained several funding including National Natural Science Foundation of China, China Postdoctoral Science Foundation, National Major Research Plan, and Major Research Plan of the Provincial Science and Technology Foundation of Guangxi, etc. He has more than 20 research articles published in related fields.
Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
Clinica chimica acta; international journal of clinical chemistry Nov, 2016 | Pubmed ID: 27637299
Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants.
Clinica chimica acta; international journal of clinical chemistry Nov, 2017 | Pubmed ID: 28969986
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
Human molecular genetics 12, 2017 | Pubmed ID: 29040572
Perspective: Is Random Monoallelic Expression a Contributor to Phenotypic Variability of Autosomal Dominant Disorders?
Frontiers in genetics , 2017 | Pubmed ID: 29250101
Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome.
Gene May, 2018 | Pubmed ID: 29462647
Biparental Inheritance of Mitochondrial DNA in Humans.
Proceedings of the National Academy of Sciences of the United States of America 12, 2018 | Pubmed ID: 30478036
Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments.
Proceedings of the National Academy of Sciences of the United States of America 02, 2019 | Pubmed ID: 30674682
New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype-phenotype profiling of in 190 Chinese patients.
Journal of medical genetics Jun, 2019 | Pubmed ID: 31186340
A prospective study of non-invasive preimplantation genetic testing for aneuploidies (NiPGT-A) using next-generation sequencing (NGS) on spent culture media (SCM).
Journal of assisted reproduction and genetics Jul, 2019 | Pubmed ID: 31292818
Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.
Genetics in medicine : official journal of the American College of Medical Genetics Aug, 2019 | Pubmed ID: 31447483
Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy
Baoheng Gui*,1,2,3,
Yingxin Zhang*,4,
Bo Liang5,
Yvonne Ka Yin Kwok4,
Wai Ting Lui4,
Queenie Sum Yee Yeung4,
Lingyin Kong6,
Liming Xuan6,
Jacqueline Pui Wah Chung4,
Kwong Wai Choy3,4
1Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region,
2, Birth Defects Prevention and Control Institute of Guangxi Zhuang Autonomous Region,
3Shenzhen Research Institute, The Chinese University of Hong Kong,
4Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong,
5State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University,
6, Basecare Medical Device Co., Ltd
A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
Huilin Wang*,1,
Xiaofan Zhu*,2,3,
Baoheng Gui*,3,4,
Wan Chee Cheung2,
Mengmeng Shi2,3,
Zhenjun Yang2,3,
Ka Yin Kwok2,
Ricky Lim5,
Sanna Pietilä5,
Yuanfang Zhu6,7,
Kwong Wai Choy2,3
1Central Laboratory, Bao'an Maternity and Child Health Hospital, Jinan University,
2Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong,
3Shenzhen Research Institute, The Chinese University of Hong Kong,
4Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region,
5, PerkinElmer Diagnostics,
6Department of Obstetrics and Gynecology, Bao'an Maternity and Child Health Hospital, Jinan University,
7Maternal-Fetal Medicine Institute, Bao'an Maternity and Child Health Hospital, Jinan University
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