George Stavrides
Wellcome Sanger Institute(GB)
Publications by Year
Research Areas
Genomics and Chromatin Dynamics, Genetic Associations and Epidemiology, Chromosomal and Genetic Variations, Epilepsy research and treatment, DNA Repair Mechanisms
Most-Cited Works
- → The DNA sequence and comparative analysis of human chromosome 20(2001)374 cited
- → Genetic Variation Near the Hepatocyte Nuclear Factor-4α Gene Predicts Susceptibility to Type 2 Diabetes(2004)268 cited
- → X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 Gene(1999)260 cited
- → The impact of SNP density on fine-scale patterns of linkage disequilibrium(2004)197 cited
- → Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes(2000)162 cited
- → Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y‐chromosome instability(2005)86 cited
- → Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy(2006)8 cited
- → The influence of vascular pressure and different primes on the fluid balance of, and oxygen supply to, the patient during CABG(1995)4 cited
- Sex differences and their impact on clinical outcome after percutaneous or surgical revascularisation: a report from the Arterial Revascularisation Therapies Study (ARTS).(2006)
- Positional cloning of the gene for CHED 1: A YAC/PAC and transcript map spanning the locus on 20p11.2.(2000)