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Details

Role Clinical Geneticist
Group Clinical Services

Top Publications

  • Wilson, GR, Sunley, J, Smith, KR, Pope, K, Bromhead, CJ, Fitzpatrick, E, Di Rocco, M, van Steensel, M, Coman, DJ, Leventer, RJ, et al. Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. European Journal of Human Genetics 22(6) : 741 -747 2014
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  • Stark, Z, Delatycki, MB. Parentage determination: a medical responsibility?. Journal of Medical Ethics 40(6) : 387 2014
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  • Delatycki, MB, Tai, G, Corben, L, Yiu, EM, Evansā€Galea, MV, Stephenson, SEM, Gurrin, L, Allen, KJ, Lynch, D, Lockhart, PJ. HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia. Movement Disorders 29(7) : 940 -943 2014
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  • Hocking, DR, Corben, LA, Fielding, J, Cremer, PD, Millist, L, White, OB, Delatycki, MB. Saccade reprogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement. Brain and Cognition 87: 161 -167 2014
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  • Zalesky, A, Akhlaghi, H, Corben, LA, Bradshaw, JL, Delatycki, MB, Storey, E, Georgiou-Karistianis, N, Egan, GF. Cerebello-cerebral connectivity deficits in Friedreich ataxia. Brain Structure and Function 219(3) : 969 -981 2014
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