G. Stavrides

The impact of SNP density on fine-scale patterns of linkage disequilibrium.

P. Deloukas, A. Morris, S. Hunt, 2004, Human molecular genetics.

The influence of vascular pressure and different primes on the fluid balance of, and oxygen supply to, the patient during CABG

G. Stavrides, B. Glenville, S. Davis, 1995, Perfusion.

X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.

A. Poustka, T. Vulliamy, G. Lestringant, 1999, American journal of human genetics.

Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y‐chromosome instability

C. Sismani, K. McElreavey, P. Patsalis, 2005, American journal of medical genetics. Part A.

Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

T. L. Hood, P. Deloukas, D. Bentley, 2000, Oncogene.

The DNA sequence and comparative analysis of human chromosome 20

D R Bentley, J E Sulston, C Carder, 2004, Nature.

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

S. Hunt, F. Collins, M. Boehnke, 2004, Diabetes.

Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

P. Deloukas, P. Striano, R. Michelucci, 2006, Epilepsy Research.