scholarly article | Q13442814 |
meta-analysis | Q815382 |
P50 | author | Ruth Pfeiffer | Q90909936 |
Stephen Chanock | Q27662321 | ||
Maria Teresa Landi | Q28606990 | ||
Evangelos Evangelou | Q30436575 | ||
Monica Rodolfo | Q37376562 | ||
Stuart Macgregor | Q42711014 | ||
Eduardo Nagore | Q51812182 | ||
Matthew H Law | Q56420235 | ||
Lorenza Pastorino | Q56435904 | ||
Anne E Cust | Q56923556 | ||
P2093 | author name string | Fangyi Gu | |
D Timothy Bishop | |||
Jianxin Shi | |||
Arcangela De Nicolo | |||
Xing Hua | |||
Susana Puig | |||
Alexander J Stratigos | |||
Kevin M Brown | |||
Ketty Peris | |||
Paola Ghiorzo | |||
Curt T DellaValle | |||
Donato Calista | |||
Cristina Pellegrini | |||
Maria Concetta Fargnoli | |||
Tongwu Zhang | |||
Chiara Menin | |||
Ting-Huei Chen | |||
Melanoma Meta-Analysis Consortium | |||
MelaNostrum Consortium | |||
Mark I Iles | |||
P2860 | cites work | Risk of cutaneous melanoma associated with a family history of the disease | Q58283406 |
Epidemiology, etiology, and control of melanoma | Q74302576 | ||
Development of an individual score for melanoma risk | Q83601587 | ||
POT1 loss-of-function variants predispose to familial melanoma | Q24563091 | ||
Germline mutations in BAP1 predispose to melanocytic tumors | Q24594891 | ||
Melanesian blond hair is caused by an amino acid change in TYRP1 | Q24623400 | ||
PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder | Q28250609 | ||
Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma | Q28270834 | ||
Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data | Q28917124 | ||
TERT promoter mutations in familial and sporadic melanoma | Q29614920 | ||
pROC: an open-source package for R and S+ to analyze and compare ROC curves | Q30050695 | ||
Development and validation of a melanoma risk score based on pooled data from 16 case-control studies | Q30899396 | ||
Individual risk of cutaneous melanoma in New Zealand: developing a clinical prediction aid | Q33685033 | ||
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma | Q33751971 | ||
Familial Risk and Heritability of Cancer Among Twins in Nordic Countries | Q33874409 | ||
IRF4 variants have age-specific effects on nevus count and predispose to melanoma | Q33960494 | ||
Causal effects in clinical and epidemiological studies via potential outcomes: concepts and analytical approaches | Q33960730 | ||
Power and predictive accuracy of polygenic risk scores. | Q34337027 | ||
A prognostic model for predicting 10-year survival in patients with primary melanoma. The Pigmented Lesion Group | Q34388378 | ||
Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control study | Q34581022 | ||
Testing calibration of risk models at extremes of disease risk | Q34678258 | ||
Most common 'sporadic' cancers have a significant germline genetic component | Q34736858 | ||
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi | Q34831505 | ||
Joint effect of multiple common SNPs predicts melanoma susceptibility | Q35083167 | ||
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma | Q35102528 | ||
Indoor tanning and the MC1R genotype: risk prediction for basal cell carcinoma risk in young people. | Q35652527 | ||
Identifying Persons at Highest Risk of Melanoma Using Self-Assessed Risk Factors | Q35655735 | ||
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma | Q35699278 | ||
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up | Q35829596 | ||
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma | Q36019187 | ||
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores | Q36133352 | ||
Incidence of basal cell and squamous cell carcinomas in a population younger than 40 years | Q36224045 | ||
Estimating the population attributable risk for multiple risk factors using case-control data | Q36499362 | ||
Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents | Q37004819 | ||
Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies | Q37059182 | ||
PARKIN Inactivation Links Parkinson's Disease to Melanoma | Q38810658 | ||
Personal risk-factor chart for cutaneous melanoma | Q39200858 | ||
Prediction of Melanoma Risk in a Southern European Population Based on a Weighted Genetic Risk Score | Q40833067 | ||
Independent validation of six melanoma risk prediction models | Q41639663 | ||
Development of a targeted risk-group model for skin cancer screening based on more than 100,000 total skin examinations | Q42484750 | ||
Predicting melanoma risk for the Australian population | Q44280187 | ||
Identifying individuals at high risk of melanoma: a practical predictor of absolute risk | Q44986625 | ||
Adjuvant Nivolumab versus Ipilimumab in Resected Stage III or IV Melanoma | Q47551890 | ||
Melanoma staging: Evidence-based changes in the American Joint Committee on Cancer eighth edition cancer staging manual | Q47803820 | ||
Adjuvant Dabrafenib plus Trametinib in Stage III BRAF-Mutated Melanoma. | Q47824495 | ||
Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma. | Q47826637 | ||
Identifying individuals at high risk of melanoma: a simple tool. | Q53708923 | ||
Risk Factors and Individual Probabilities of Melanoma for Whites | Q57749811 | ||
P433 | issue | 23 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 4145-4156 | |
P577 | publication date | 2018-12-01 | |
P1433 | published in | Human Molecular Genetics | Q2720965 |
P1476 | title | Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma | |
P478 | volume | 27 |
Q91584550 | Interleukin 1 receptor antagonist gene variable number of tandem repeats polymorphism and cutaneous melanoma | cites work | P2860 |
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