Details
Role
Clinical Geneticist
Group
Clinical Services
Top Publications
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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, Evans‐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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