Mike Gerards (M.)

Gerards, M (2014) “Leigh syndrome: the heterogeneity story continues” Brain 137(Pt 11): 2872-2873 IF: 10.226

Gospodaryov D. V., O. V. Lushchak, B. M. Rovenko, N. V. Perkhulyn, M. Gerards, T. Tuomela and H. T. Jacobs (2014) “Ciona intestinalis NADH dehydrogenase NDX confers stress-resistance and extended lifespan on Drosophila.” BBA Bioenergetics 12;1837(11):1861-1869 IF: 4.829

Fukuoh, A., G. Cannino, M. Gerards, S. Buckley, S. Kazancioglu, F. Scialo, E. Lihavainen, A. Ribeiro, E. Dufour and H. T. Jacobs (2014) "Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthase." Mol Syst Biol 10(6): 734. IF: 11.34

Gerards, M., R. de Coo and H. Smeets (2014) "Reply: Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease." Brain. IF: 9.490

Gerards, M., R. Kamps, J. van Oevelen, I. Boesten, E. Jongen, B. de Koning, H. R. Scholte, I. de Angst, K. Schoonderwoerd, A. Sefiani, I. Ratbi, W. Coppieters, L. Karim, R. de Coo, B. van den Bosch and H. Smeets (2013) "Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome." Brain 136(Pt 3): 882-890. IF: 9.457

van den Bosch, B. J*., M. Gerards*, W. Sluiter, A. P. Stegmann, E. L. Jongen, D. M. Hellebrekers, R. Oegema, E. H. Lambrichs, H. Prokisch, K. Danhauser, K. Schoonderwoerd, I. F. de Coo and H. J. Smeets (2012) "Defective NDUFA9 as a novel cause of neonatally fatal complex I disease." J Med Genet 49(1): 10-15. (*joint authorship) IF: 7.037

Bonneux, S., E. Fransen, E. Van Eyken, L. Van Laer, J. Huyghe, P. Van de Heyning, A. Voets, M. Gerards, A. P. Stassen, A. T. Hendrickx, H. J. Smeets and G. Van Camp (2011) "Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population." Mitochondrion 11(5): 729-734. IF: 4.145

Gerards, M*., B. J. van den Bosch*, K. Danhauser, V. Serre, M. van Weeghel, R. J. Wanders, G. A. Nicolaes, W. Sluiter, K. Schoonderwoerd, H. R. Scholte, H. Prokisch, A. Rotig, I. F. de Coo and H. J. Smeets (2011) "Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene." Brain 134(Pt 1): 210-219. (*joint authorship) IF: 9.490

Gerards, M., B. van den Bosch, C. Calis, K. Schoonderwoerd, K. van Engelen, M. Tijssen, R. de Coo, A. van der Kooi and H. Smeets (2010) "Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy." Mitochondrion 10(5): 510-515. IF: 4.145

Gerards, M., W. Sluiter, B. J. van den Bosch, L. E. de Wit, C. M. Calis, M. Frentzen, H. Akbari, K. Schoonderwoerd, H. R. Scholte, R. J. Jongbloed, A. T. Hendrickx, I. F. de Coo and H. J. Smeets (2010) "Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome." J Med Genet 47(8): 507-512. IF: 5.751

Hudson, G., V. Carelli, L. Spruijt, M. Gerards, C. Mowbray, A. Achilli, A. Pyle, J. Elson, N. Howell, C. La Morgia, M. L. Valentino, K. Huoponen, M. L. Savontaus, E. Nikoskelainen, A. A. Sadun, S. R. Salomao, R. Belfort, Jr., P. Griffiths, P. Y. Man, R. F. de Coo, R. Horvath, M. Zeviani, H. J. Smeets, A. Torroni and P. F. Chinnery (2007). "Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background." Am J Hum Genet 81(2): 228-233. IF: 12.303

Jacobs, L., M. Gerards, P. Chinnery, J. Dumoulin, I. de Coo, J. Geraedts and H. Smeets (2007). "mtDNA point mutations are present at various levels of heteroplasmy in human oocytes." Mol Hum Reprod 13(3): 149-154. IF: 3.005

van Eijsden, R. G.*, M. Gerards*, L. M. Eijssen, A. T. Hendrickx, R. J. Jongbloed, J. H. Wokke, R. Q. Hintzen, M. E. Rubio-Gozalbo, I. F. De Coo, E. Briem, V. Tiranti and H. J. Smeets (2006). "Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients." Genet Med 8(10): 620-627. (*joint authorship) IF: 3.922