Evolutionary Diversity of the Mitochondrial Calcium UniporterBICK, Alexander G; CALVO, Sarah E; MOOTHAT, Vamsi K et al.Science (Washington, D.C.). 2012, Vol 336, Num 6083, issn 0036-8075, p. 886Article

MPVI7 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsGARONE, Caterina; RUBIO, Juan Carlos; CALVO, Sarah E et al.Archives of neurology (Chicago). 2012, Vol 69, Num 12, pp 1648-1651, issn 0003-9942, 4 p.Article

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiencyCALVO, Sarah E; TUCKER, Elena J; REDMAN, Michelle C et al.Nature genetics. 2010, Vol 42, Num 10, pp 851-858, issn 1061-4036, 8 p.Article

The genome sequence of the filamentous fungus Neurospora crassaGALAGAN, James E; CALVO, Sarah E; REHMAN, Bushra et al.Nature (London). 2003, Vol 422, Num 6934, pp 859-868, issn 0028-0836, 10 p.Article

Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzaeGALAGAN, James E; CALVO, Sarah E; KAPITONOV, Vladimir et al.Nature (London). 2005, Vol 438, Num 7071, pp 1105-1115, issn 0028-0836, 11 p.Article

Targeted exome sequencing of suspected mitochondrial disordersLIEBER, Daniel S; CALVO, Sarah E; SCHMAHMANN, Jeremy D et al.Neurology. 2013, Vol 80, Num 19, pp 1762-1770, issn 0028-3878, 9 p.Article

Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletionsRONCHI, Dario; GARONE, Caterina; CORTI, Stefania et al.Brain. 2012, Vol 135, pp 3404-3415, issn 0006-8950, 12 p., 11Article

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathyFASSONE, Elisa; DUNCAN, Andrew J; BITNER-GLINDZICZ, Maria et al.Human molecular genetics (Print). 2010, Vol 19, Num 24, pp 4837-4847, issn 0964-6906, 11 p.Article