Genome-wide search for nevus density shows linkage to two melanoma loci on chromosome 9 and identifies a new QTL on 5q31 in an adult twin cohort
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Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutationsSimulants of Malignant MelanomaGenome-wide association studies of pigmentation and skin cancer: a review and meta-analysisGenetic determination and linkage mapping of Plasmodium falciparum malaria related traits in Senegal.Genome-wide association studies and genetic architecture of common human diseasesIRF4 variants have age-specific effects on nevus count and predispose to melanoma.The use of the twin model to investigate the genetics and epigenetics of skin diseases with genomic, transcriptomic and methylation data.Associations of cumulative sun exposure and phenotypic characteristics with histologic solar elastosis.Promoter polymorphisms in matrix metallopeptidase 1 and risk of cutaneous melanoma.Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous neviFine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsMelanoma epidemiology.Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.Moderate- to low-risk variant alleles of cutaneous malignancies and nevi: lessons from genome-wide association studies.Germline variation at CDKN2A and associations with nevus phenotypes among members of melanoma families.Genome-wide associations studies for melanoma and neviNevus count associations with pigmentary phenotype, histopathological melanoma characteristics and survival from melanomaEvaluation of PAX3 genetic variants and nevus number.Genome-wide association studies of cancer: current insights and future perspectives.Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing.A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions
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P2860
Genome-wide search for nevus density shows linkage to two melanoma loci on chromosome 9 and identifies a new QTL on 5q31 in an adult twin cohort
description
im August 2006 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2006
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name
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@en
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@nl
type
label
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@en
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@nl
prefLabel
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@en
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@nl
P2093
P2860
P356
P1476
Genome-wide search for nevus d ...... n 5q31 in an adult twin cohort
@en
P2093
Bernet S. Kato
Tim D. Spector
Ursula Perks
Veronique Bataille
P2860
P304
P356
10.1093/HMG/DDL227
P50
P577
2006-08-23T00:00:00Z