H. Snowden

发表

Developing a local shared care protocol for managing people with psychotic illness in primary care

S. Marriott, H. Snowden, 2003 .

POT1 loss-of-function variants predispose to familial melanoma

Thomas M. Keane, K. Brown, D. Bishop, 2014, Nature Genetics.

Genome-wide association study identifies three new melanoma susceptibility loci

Jeffrey E. Lee, J. Malvehy, S. Puig, 2011, Nature Genetics.

Next-generation sequencing identifies germline MRE11A variants as markers of radiotherapy outcomes in muscle-invasive bladder cancer

T. Ørntoft, J. Barrett, A. Kiltie, 2014, Annals of oncology : official journal of the European Society for Medical Oncology.

Reduced type II interleukin-4 receptor signalling drives initiation, but not progression, of colorectal carcinogenesis: evidence from transgenic mouse models and human case–control epidemiological observations

D. Bishop, H. Snowden, N. Scott, 2013, Carcinogenesis.

The determinants of serum vitamin D levels in participants in a melanoma case–control study living in a temperate climate

J. Barrett, D. Bishop, M. Harland, 2011, Cancer Causes & Control.

High-Resolution Copy Number Patterns From Clinically Relevant FFPE Material

C. Taylor, D. Bishop, M. Harland, 2019, Scientific Reports.

Next-generation sequencing identi ﬁ es germline MRE11A variants as markers of radiotherapy outcomes in muscle-invasive bladder cancer

T. Ørntoft, J. Barrett, A. Kiltie, 2014 .

Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.

Thomas M. Keane, K. Brown, J. Trent, 2015, Journal of the National Cancer Institute.

Alstrom syndrome in four sibs from northern Jordan

H. Snowden, K. Ajlouni, H. Hamamy, 2006, Annals of Saudi medicine.

MGMT promoter methylation is associated with temozolomide response and prolonged progression‐free survival in disseminated cutaneous melanoma

J. J. van den Oord, J. Hansson, H. Johansson, 2015, International journal of cancer.

A variant in FTO shows association with melanoma risk not due to BMI

Marko Hočevar, Florence Demenais, Kari Stefansson, 2013, Nature Genetics.

High-Resolution Copy Number Patterns From Clinically Relevant FFPE Material

C. Taylor, D. Bishop, M. Harland, 2019, Scientific Reports.

AKT1 mutations in bladder cancer: identification of a novel oncogenic mutation that can co-operate with E17K

H Snowden, M. Knowles, F. Platt, 2010, Oncogene.

A complex population of RNAs exists in human ejaculate spermatozoa: implications for understanding molecular aspects of spermiogenesis.

S. Rollinson, R. Lilford, H. Snowden, 1999, Gene.

Inherited variation in the PARP1 gene and survival from melanoma

Dirk Schadendorf, Susana Puig, Johan Hansson, 2014, International journal of cancer.

Next-generation sequencing identifies germline MRE11A variants as markers of radiotherapy outcomes in muscle-invasive bladder cancer.

T. Ørntoft, J. Barrett, A. Kiltie, 2014 .

POT1 loss-of-function variants predispose to familial melanoma

V. Quesada, C. López-Otín, K. Pooley, 2014, Nature Genetics.