An interstitial deletion within 9p21.3 and extending beyondCDKN2Apredisposes to melanoma, neural system tumours and possible haematological malignancies

A large de novo9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

(2014) Simona Frigerio et al.   BMC Medical Genetics

POT1 loss-of-function variants predispose to familial melanoma

(2014) Carla Daniela Robles-Espinoza et al.   NATURE GENETICS

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

(2014) Jianxin Shi et al.   NATURE GENETICS

Copy Number Loss of the Interferon Gene Cluster in Melanomas Is Linked to Reduced T Cell Infiltrate and Poor Patient Prognosis

(2014) Peter S. Linsley et al.   PLoS One

Functional Network Pipeline Reveals Genetic Determinants Associated with in Situ Lymphocyte Proliferation and Survival of Cancer Patients

(2014) B. Mlecnik et al.   Science Translational Medicine

Multiple neurofibromas as the presenting feature of familial atypical multiple malignant melanoma (FAMMM) syndrome

(2013) Rachel Vanneste et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

TERT Promoter Mutations in Familial and Sporadic Melanoma

(2013) S. Horn et al.   SCIENCE

Influence of Genetic Variants in Type I Interferon Genes on Melanoma Survival and Therapy

(2012) Romina Elizabeth Lenci et al.   PLoS One

Germline mutations in BAP1 predispose to melanocytic tumors

(2011) Thomas Wiesner et al.   NATURE GENETICS

Sunbed use during adolescence and early adulthood is associated with increased risk of early-onset melanoma

(2010) Anne E. Cust et al.   INTERNATIONAL JOURNAL OF CANCER

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

(2010) Michael S. Cunnington et al.   PLoS Genetics

Familial Melanoma

(2008) Johan Hansson   SURGICAL CLINICS OF NORTH AMERICA