J. Symmons

发表

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

K. Brown, J. Trent, D. Bishop, 2011, Nature.

POT1 loss-of-function variants predispose to familial melanoma

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

Nevi, family history, and fair skin increase the risk of second primary melanoma.

N. Martin, J. Aitken, N. Hayward, 2011, The Journal of investigative dermatology.

Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers

N. Hayward, P. Johansson, A. Pritchard, 2018, PloS one.

From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes

E. Gillanders, J. Aitken, K. Dutton-Regester, 2012, Hereditary Cancer in Clinical Practice.

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.

Prevalence of Germline BAP1, CDKN2A, and CDK4 Mutations in an Australian Population-Based Sample of Cutaneous Melanoma Cases

N. Martin, G. Montgomery, N. Hayward, 2015, Twin Research and Human Genetics.

Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4

N. Hayward, P. Johansson, C. Ingvar, 2015, Oncotarget.

Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide

Ivana K. Kim, S. Puig, N. Hayward, 2018, Journal of the National Cancer Institute.

miR-514a regulates the tumour suppressor NF1 and modulates BRAFi sensitivity in melanoma

P. Pollock, N. Hayward, M. Stark, 2015, Oncotarget.

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

N. Martin, G. Montgomery, N. Hayward, 2016, Familial Cancer.

POLE mutations in families predisposed to cutaneous melanoma

Nicholas G. Martin, Ian Tomlinson, Grant W. Montgomery, 2015, Familial Cancer.

Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma.

K. Brown, G. Mann, N. Hayward, 2019, Melanoma research.

Multiplex melanoma families are enriched for polygenic risk

M. Iles, D. Duffy, N. Martin, 2020, Human molecular genetics.

Assessment of PALB2 as a Candidate Melanoma Susceptibility Gene

K. Brown, J. Trent, N. Martin, 2014, PloS one.

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

K. Brown, J. Trent, D. Bishop, 2011, Nature.

PUBLISHED VERSION

J. Trent, D. Bishop, D. Duffy, 2018 .

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

G. Montgomery, N. Hayward, J. Palmer, 2016, Familial Cancer.

POT1 loss-of-function variants predispose to familial melanoma

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