Jenice Brown

Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy

H. Cui, Renkui Bai, Taosheng Huang, 2020, Human mutation.

Heteroplasmy variability in individuals with biparentally inherited mitochondrial DNA

Y. Chien, W. Hwu, L. Wong, 2020, bioRxiv.

Biparental Inheritance of Mitochondrial DNA in Humans

Y. Chien, W. Hwu, L. Wong, 2018, Proceedings of the National Academy of Sciences.

Misleading results from saliva samples of patients post-BMT in exome analyses.

Kejian Zhang, C. A. Valencia, A. Mathur, 2014, Blood.

Clinical utility of whole genome sequencing for the detection of mitochondrial genome mutations.

Ammar Husami, C. A. Valencia, Taosheng Huang, 2020, Journal of genetics and genomics = Yi chuan xue bao.

Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments

Y. Chien, W. Hwu, L. Wong, 2019, Proceedings of the National Academy of Sciences.