Baoheng Gui

Baoheng Gui

Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region

Affiliated withMaternal and Child Health Hospital of Guangxi Zhuang Autonomous RegionBirth Defects Prevention and Control Institute of Guangxi Zhuang Autonomous RegionThe Chinese University of Hong Kong

Research Area

Biography

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.

JoVE Journal Publications

ArticleTotal : 2
Year
Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy
Publication title

Cited by 2

2019
2019

Other Publications

Article
Year
Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.

Clinica chimica acta; international journal of clinical chemistry| PubMed ID: 27637299

2016
Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants.

Clinica chimica acta; international journal of clinical chemistry| PubMed ID: 28969986

2017
2017
2017
2018
Biparental Inheritance of Mitochondrial DNA in Humans.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 30478036

2018
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| PubMed ID: 30674682

2019
2019
2019
Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.

Genetics in medicine : official journal of the American College of Medical Genetics| PubMed ID: 31447483

2019