Neurogenetics Department

Selected Publications

Christodoulou K, Kyriakides T, Hristova A.H., Georgiou D.M., Kalaydjieva L,Yshpekova B, Ivanova T, Weber JL, Middleton L.T. (1995). "Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p". Hum Mol Genet 4:1629-1632.

Christodoulou K, Tsingis M, Stavrou C, Eleftheriou A, Papapavlou P, Patsalis PC, Ioannou P, Pierides A, Constantinou Deltas C. (1998). "Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease". Hum Mol Genet 7:905-911.

Christodoulou K, Tsingis M, Deymeer F, Serdaroglu P, Ozdemir C, Al-Shehap A, Bairactaris C, Mavromatis I, Mylonas I, Evoli A, Kyriallis K, Middleton LT.(1997). " Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type la) gene to chromosome 17p with evidence of genetic homogeneity". Hum Mol Genet. 6:635-40.

Middleton LT, Ohno K, Christodoulou K, Brengman J, Milone M, Neocleous V, Serdaroglu P, Deymeer F, Ozdemir C, Mubaidin A, Horany K, Al-Shehab A, Mavromatis I, Mylonas I, Tsingis M, Zamba E, Pantzaris M, Kyriallis K, Engel AG. (1999). "Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor e-subunit gene". Neurology 53:1076-1082.

Bolino A, Muglia M, Conforti FL, LeGuern E, Salih MA, Georgiou DM, Christodoulou K, Hausmanowa-Petrusewicz I, Mandich P, Schenone A, Gambardella A, Bono F, Quattrone A, Devoto M, Monaco AP (2000). "Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2". Nature Genet 25:17-19.

Christodoulou K, Zamba E, Tsingis M, Mubaidin A, Horani K, Abu-Sheik S, El-Khateeb M, Kyriacou K, Kyriakides T, Al-Qudah AK, Middleton LT (2000). "Anovel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12". Ann Neurol 48:877-884.

Bently DR, Deloukas P, Dunham A, French L, Gregory SG, Humphray SJ, et al. (2001). "The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X". Nature 409:942-943.

Christodoulou K, Deymeer F, Serdaroglu P, Ozdemir C, Poda M, Georgiou DM, Ioannou P, Tsingis M, Zamba E, Middleton LT, (2001). "Mapping of the second Friedreich’s ataxia (FRDA2) locus to chromosome 9p23-pll: evidence for further locus heterogeneity". Neurogenetics 3:127-132.