Min‐xin Guan - Genetic Mutations

Author Information

Dr. Min-xin Guan is a prominent researcher affiliated with the Division of Medical Genetics and Genomics at the Children's Hospital, Zhejiang University School of Medicine, located in Hangzhou, Zhejiang, China. Dr. Guan's research primarily focuses on mitochondrial genetics, with significant contributions to understanding mitochondrial dysfunction and its impact on human health.

Research Contributions

Dr. Min-xin Guan has made substantial contributions to the field of genetics, particularly in mitochondrial research. His work includes investigating the mechanisms of mitochondrial ADP/ATP transporters, exploring genetic mutations linked to mitochondrial dysfunction, and developing non-invasive methods for detecting mitochondrial mutations. Dr. Guan's research has implications for various health conditions, including hearing impairment, Leber's Hereditary Optic Neuropathy, and other mitochondrial-related diseases. His studies often utilize advanced techniques such as molecular dynamics simulations, genetic correction in induced pluripotent stem cells (iPSCs), and animal models to unravel the complexities of mitochondrial function and pathology.

Aliases

Min Guan, M.-x. Guan, Min-xin Guan, Minxin Guan, M X Guan, Min-xin Guan

Publication and Citation Metrics

Metric Value
Citation Count 8008
H-index 49
Paper Count 274

Publications:

DOI: 10.12122/j.issn.1673-4254.2021.01.23

Year: 2021

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