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Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Melanocortin 1 receptor variants and skin cancer risk
inferredcites →https://doi.org/10.1002/ijc.23257openalex-snapshot
MC1R variants associated susceptibility to basal cell carcinoma of skin: Interaction with host factors and XRCC3 polymorphism
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GrinchGEF—A novel Rho-specific guanine nucleotide exchange factor
inferredcites →https://doi.org/10.1016/j.biocel.2006.03.008openalex-snapshot
Citrullination: A posttranslational modification in health and disease
inferredcites →https://doi.org/10.1016/j.jdermsci.2006.07.004openalex-snapshot
Peptidylarginine deiminases and deimination in biology and pathology: Relevance to skin homeostasis
inferredcites →https://doi.org/10.1016/j.mce.2007.05.005openalex-snapshot
Peptidylarginine deiminase (PAD) 6 is essential for oocyte cytoskeletal sheet formation and female fertility
inferredcites →https://doi.org/10.1016/s0025-6196(11)61033-1openalex-snapshot
Malignant Melanoma in the 21st Century, Part 1: Epidemiology, Risk Factors, Screening, Prevention, and Diagnosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81268-4openalex-snapshot
Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome
inferredcites →https://doi.org/10.1016/s1534-5807(03)00205-3openalex-snapshot
The Mammalian Passenger Protein TD-60 Is an RCC1 Family Member with an Essential Role in Prometaphase to Metaphase Progression
inferredcites →https://doi.org/10.1038/nature06758openalex-snapshot
Genetics of gene expression and its effect on disease
inferredcites →https://doi.org/10.1038/ng.160openalex-snapshot
Two newly identified genetic determinants of pigmentation in Europeans
inferredcites →https://doi.org/10.1038/ng.161openalex-snapshot
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
inferredcites →https://doi.org/10.1038/ng.192openalex-snapshot
Pathological responses to oncogenic Hedgehog signaling in skin are dependent on canonical Wnt/β-catenin signaling
inferredcites →https://doi.org/10.1038/ng.2007.13openalex-snapshot
Genetic determinants of hair, eye and skin pigmentation in Europeans
inferredcites →https://doi.org/10.1038/ng1245openalex-snapshot
The gene encoding phosphodiesterase 4D confers risk of ischemic stroke
inferredcites →https://doi.org/10.1038/ng1801openalex-snapshot
Evaluating coverage of genome-wide association studies
inferredcites →https://doi.org/10.1086/319500openalex-snapshot
Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red Hair
inferredcites →https://doi.org/10.1093/ije/dyl197openalex-snapshot
Risk factors for skin cancers: a nested case–control study within the Nurses’ Health Study
inferredcites →https://doi.org/10.1093/nar/gkl679openalex-snapshot
A novel endonuclease IV post-PCR genotyping system
inferredcites →https://doi.org/10.1101/gad.894301openalex-snapshot
Wrch-1, a novel member of the Rho gene family that is regulated by Wnt-1
inferredcites →https://doi.org/10.1111/j.0006-341x.1999.00997.xopenalex-snapshot
Genomic Control for Association Studies
inferredcites →https://doi.org/10.1111/j.1365-2133.2007.08273.xopenalex-snapshot
Epidemiology and aetiology of basal cell carcinoma
inferredcites →https://doi.org/10.1111/j.1365-2230.2004.01669.xopenalex-snapshot
Basal cell carcinoma: from host response and polymorphic variants to tumour suppressor genes
inferredcites →https://doi.org/10.1111/j.1365-4632.2006.02999.xopenalex-snapshot
Predictive value of phenotypic variables for skin cancer: Risk assessment beyond skin typing
inferredcites →https://doi.org/10.1126/science.272.5268.1668openalex-snapshot
Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
inferredcites →https://doi.org/10.1186/1476-4598-5-74openalex-snapshot
Investigation of the molecular profile of basal cell carcinoma using whole genome microarrays.
inferredcites →https://doi.org/10.1196/annals.1422.034openalex-snapshot
Citrullination by Peptidylarginine Deiminase in Rheumatoid Arthritis
inferredcites →https://doi.org/10.2741/1802openalex-snapshot
Histone arginine methylation and its dynamic regulation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Title Epidemiology of Facial Skin Cancers Managed in a French Ambulatory Surgical Center
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Deimination in Skin and Regulation of Peptidylarginine Deiminase Expression in Keratinocytes
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Epidemiology and Risk Factors of Basal Cell Carcinoma
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Association between TERT-CLPTM1L rs401681[C] allele and NMSC cancer risk: a meta-analysis including 45,184 subjects
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A prospective study of cigarette smoking and basal cell carcinoma
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Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma
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Gene expression profiling assigns CHEK2 1100delC breast cancers to the luminal intrinsic subtypes
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Interactions between breast cancer susceptibility loci and menopausal hormone therapy in relationship to breast cancer in the Breast and Prostate Cancer Cohort Consortium
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The association between smoking and risk of skin cancer: a meta-analysis of cohort studies
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RETRACTED ARTICLE: RCC2 contributes to tumor invasion and chemoresistance to cisplatin in hepatocellular carcinoma
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Skin Cancer
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Discovery and Characterization of Cancer Genetic Susceptibility Alleles
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RCC2 promotes proliferation and radio-resistance in glioblastoma via activating transcription of DNMT1
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A genetic variant at KIF1B predicts clinical outcome of HBV-related hepatocellular carcinoma in Chinese
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Family history of skin cancer is associated with early-onset basal cell carcinoma independent of MC1R genotype
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High-ceiling diuretics are associated with an increased risk of basal cell carcinoma in a population-based follow-up study
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Risk of subsequent cutaneous malignancy in patients with prior keratinocyte carcinoma: A systematic review and meta-analysis
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Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service
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Genome-wide Association Studies of Cancer Predisposition
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Delineation of clinical and biological factors associated with cutaneous squamous cell carcinoma among patients with chronic lymphocytic leukemia
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Genome-wide association study of skin complex diseases
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Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma
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The Molecular Revolution in Cutaneous Biology: The Era of Genome-Wide Association Studies and Statistical, Big Data, and Computational Topics
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Sex-Stratified Polygenic Risk Score Identifies Individuals at Increased Risk of Basal Cell Carcinoma
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Epidemiology of facial skin cancers managed in a French ambulatory surgical center
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Genetics of pigmentation in skin cancer — A review
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Cutaneous keratinocyte cancers of the head and neck: Epidemiology, risk factors and clinical, dermoscopic and reflectance confocal microscopic features
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Genome-wide association studies of cancer predisposition
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Molecular oncology of basal cell carcinomas
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PTEN regulates RPA1 and protects DNA replication forks
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Common variants modify the age of onset for basal cell carcinomas in Gorlin syndrome
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Worldwide genetic structure in 37 genes important in telomere biology
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DNA variations in human and medical genetics: 25 years of my experience
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A Community-Based Study of Nucleotide Excision Repair Polymorphisms in Relation to the Risk of Non-Melanoma Skin Cancer
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Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma
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New basal cell carcinoma susceptibility loci
inferred← citeshttps://doi.org/10.1038/ng.296openalex-snapshot
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types
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New common variants affecting susceptibility to basal cell carcinoma
inferred← citeshttps://doi.org/10.1038/ng.638openalex-snapshot
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers
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A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
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2009 Nobel Prize in Physiology or Medicine: telomeres and telomerase
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A novel tumor suppressor encoded by a 1p36.3 lncRNA functions as a phosphoinositide-binding protein repressing AKT phosphorylation/activation and promoting autophagy
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A systematic review of skin ageing genes: gene pleiotropy and genes on the chromosomal band 16q24.3 may drive skin ageing
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Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma
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The consequences for human health of stratospheric ozone depletion in association with other environmental factors
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ARHGEF10L expression regulates cell proliferation and migration in gastric tumorigenesis
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Genome-wide association studies for detecting cancer susceptibility
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Identification of a melanoma susceptibility locus and somatic mutation inTET2
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A genome-wide analysis of gene–caffeine consumption interaction on basal cell carcinoma
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Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
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Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans
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Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma
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Common genetic polymorphisms contribute to the association between chronic lymphocytic leukaemia and non-melanoma skin cancer
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A Compendium of Genome-Wide Associations for Cancer: Critical Synopsis and Reappraisal
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scVMAP: a comprehensive platform for integrating single-cell chromatin accessibility regions with causal variants
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Basal cell carcinoma genetic susceptibility increases the rate of skin ageing: a Mendelian randomization study
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Biochemical Pathways in Cancer
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Potential Role of Peptidylarginine Deiminase Enzymes and Protein Citrullination in Cancer Pathogenesis
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ARHGEF10L Promotes Cervical Tumorigenesis via RhoA-Mediated Signaling
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Data from Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk
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A Germline Variant in the Interferon Regulatory Factor 4 Gene as a Novel Skin Cancer Risk Locus
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Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk
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Overexpression of RCC2 Enhances Cell Motility and Promotes Tumor Metastasis in Lung Adenocarcinoma by Inducing Epithelial–Mesenchymal Transition
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Search for Cancer Risk Factors with Microarray-Based Genome-Wide Association Studies
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PADI4 and tumourigenesis
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Melanoma risk loci as determinants of melanoma recurrence and survival
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RCC2 over-expression in tumor cells alters apoptosis and drug sensitivity by regulating Rac1 activation
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Functional Analysis of RHOU and PADI6 Genes in Basal Cell Carcinoma: Insights from Genome-Wide Association Studies
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Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus
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Pathway Analysis for Genome-Wide Association Study of Basal Cell Carcinoma of the Skin
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Role of Single Nucleotide Polymorphisms of KIF1B Gene in HBV-Associated Viral Hepatitis
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Functional Assessment of Human Coding Mutations Affecting Skin Pigmentation Using Zebrafish
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Genome-Wide Association Studies of Multiple Keratinocyte Cancers
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Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility
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A Comprehensive Genetic Approach for Improving Prediction of Skin Cancer Risk in Humans
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Recent progress in genetic variants associated with cancer and their implications in diagnostics development
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Epidemiologia do carcinoma basocelular
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Molecular signatures of thyroid follicular neoplasia
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Update of the European guidelines for basal cell carcinoma management
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Pathway analysis of expression-related SNPs on genome-wide association study of basal cell carcinoma
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An Analysis of Genome-Wide Association Studies to Produce Evidence Useful in Guiding Their Reporting and Synthesis
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Genetic factors underlying basal cell carcinoma risk: a narrative review
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Basal Cell Carcinoma of the Skin (Part 1): Epidemiology, Pathology and Genetic Syndromes
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The Study for Diagnostic Value of β-Catenin Immunohistochemistry Marker in Distinction of Aggressive and Non-Aggressive Basal Cell Carcinoma
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Data-independent acquisition mass spectrometry quantitative proteomic analysis reveals that skin aging-related proteins differ between men and women
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Regulator of Chromosome Condensation 2 Modulates Cell Cycle Progression, Tumorigenesis, and Therapeutic Resistance
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Review of the Molecular Genetics of Basal Cell Carcinoma; Inherited Susceptibility, Somatic Mutations, and Targeted Therapeutics
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Risk Factors and Clinicopathological Features for Developing a Subsequent Primary Cutaneous Squamous and Basal Cell Carcinomas
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Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
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A Pilot Study on Peptidylarginine Deiminases and Protein Deimination in Animal Cancers across Vertebrate Species
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Molecular signatures of basal cell carcinoma susceptibility and pathogenesis: A genomic approach
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HBV Genotyping and Phylogenetic Analysis through Multiplex PCR Using Type Specific Primer Pairs in Pakistani Population
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Molecular Mechanisms in Formation and Progression of Malignant Melanoma
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Environmental, Phenotypic and Genetic Risk Factors for Basal Cell Carcinoma of the Skin Arising at Different Body Sites
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Leveraging statistical genetics approaches to explore skin cancer risk, prediction, causation and survival
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FIGURE 7 in A new genus and two new species of congrid eels (Teleostei: Anguilliformes: Congridae) from the IndoWest Pacific, with a redescription and osteology of Chiloconger dentatus
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Investigating the Pathogenic Role of PADI4 in Oesophageal Cancer
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RCC2 promotes breast cancer progression through regulation of Wnt signaling and inducing EMT
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Exploratory Investigation of Genetic Associations with Basal Cell Carcinoma Risk: Genome-Wide Association Study in Jeju Island, Korea
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