Michael T Ryan

FunRich: An open access standalone functional enrichment and interaction network analysis tool

Ching-Seng Ang, Nicholas A Williamson, Agus Salim, 2015, Proteomics.

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

Katrien Stouffs, Melanie Bahlo, Holger Prokisch, 2016, American journal of human genetics.

Mitochondrial-nuclear communications.

Michael T Ryan, M. Ryan, Nicholas J Hoogenraad, 2007, Annual review of biochemistry.

Analysis of ER–mitochondria contacts using correlative fluorescence microscopy and soft X-ray tomography of mammalian cells

Michael T Ryan, Carolyn A Larabell, Elizabeth A. Smith, 2015, Journal of Cell Science.

Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy

Michael T Ryan, Joseph J Smolich, Michael Lazarou, 2012, Proceedings of the National Academy of Sciences.

Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease

Dominic Thyagarajan, Michael T Ryan, A. Ohtake, 2003, Annals of neurology.