I. Gray

发表

Bioinformatics for geneticists.

M. Barnes, I. Gray, 2003 .

Evolutionary transience of hypervariable minisatellites in man and the primates

A. Jeffreys, I. Gray, 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Single nucleotide polymorphisms as tools in human genetics.

I. Gray, N. Spurr, D. Campbell, 2000, Human molecular genetics.

Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland

Nigel K. Spurr, Ian C. Gray, Michael R. Barnes, 2001, Nature Genetics.

The expression profile for the tumour suppressor gene PTEN and associated polymorphic markers

J. A. Hamilton, I. Gray, D. Snary, 2000, British Journal of Cancer.

Germline BRCA2 mutations in men with breast cancer.

I. Gray, D. Bishop, N. Spurr, 1997, British Journal of Cancer.

Loss of the chromosomal region 10q23-25 in prostate cancer.

J. Weissenbach, I. Gray, J. Neoptolemos, 1995, Cancer research.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.

S. Rastan, E. Fisher, K. Davies, 2001, Human molecular genetics.

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

Steve D. M. Brown, Ian C. Gray, Zuzanna Tymowska-Lalanne, 2000, Nature Genetics.

Towards a mutant map of the mouse – new models of neurological, behavioural, deafness, bone, renal and blood disorders

Claire E. Thornton, S. Rastan, E. Fisher, 2004, Genetica.

Novel phenotypes identified by plasma biochemical screening in the mouse

Steve D. M. Brown, S. Rastan, E. Fisher, 2002, Mammalian Genome.

CCR2 and coronary artery disease: a woscops substudy

I. Gray, C. Packard, A. McMahon, 2010, BMC Research Notes.

Atypical CTSK Transcripts and ARNT Transcription Read-Through Into CTSK

I. Gray, P. Murdock, N. Spurr, 2005, Comparative and functional genomics.

Rearrangement of the long arm of chromosome 10 in the prostate adenocarcinoma cell line LNCaP.

I. Gray, N. Spurr, S. Ford, 1998, Cancer genetics and cytogenetics.

An integrated physical and genetic map spanning chromosome band 10q24.

E. Volpi, J. Fallowfield, I. Gray, 1997, Genomics.

Identification of the skeletal remains of a murder victim by DNA analysis

Ian C. Gray, E. Hagelberg, A. Jeffreys, 1991, Nature.

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Steve D. M. Brown, E. Fisher, K. Steel, 2003, Current Biology.

Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource

Steve D. M. Brown, Steve D.M. Brown, Mark Strivens, 2000, Mammalian Genome.

A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders

I. Gray, N. Spurr, A. Angius, 1998, Mammalian Genome.

Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN.

J. A. Hamilton, I. Gray, N. Spurr, 1998, British Journal of Cancer.

Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes.

E. Volpi, I. Gray, N. Spurr, 1997, Genomics.

Principles and Recent Advances in DNA Fingerprinting

A. Jeffreys, R. Neumann, I. Gray, 1991 .

Principles and recent advances in human DNA fingerprinting.

A. Jeffreys, R. Neumann, I. Gray, 1991, EXS.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

Steve D. M. Brown, S. Rastan, E. Fisher, 2000 .

Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse

Steve D. M. Brown, S. Rastan, E. Fisher, 2004, Comparative and functional genomics.

A gene-driven ENU-based approach to generating an allelic series in any gene

Steve D. M. Brown, Roger D. Cox, Andy Greenfield, 2004, Mammalian Genome.

A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24.

N K Spurr, I. Gray, N. Spurr, 1995, Genomics.

Concluding Remarks: Final Thoughts and Future Trends

M. Barnes, I. Gray, 2003 .

A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse

Steve D. M. Brown, K. Davies, P. Oliver, 2003, The Journal of Neuroscience.

Characterization of Common Genetic Variants in Cathepsin K and Testing for Association With Bone Mineral Density in a Large Cohort of Perimenopausal Women From Scotland

R. McGinnis, I. Gray, D. Reid, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.