On the public citation graph
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
0 signed · 371 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ijc.22074openalex-snapshot
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
inferredcites →https://doi.org/10.1016/j.jdermsci.2005.08.001openalex-snapshot
Association study of the g.8818A > G polymorphism of the human agouti gene with melanoma risk and pigmentary characteristics in a French population
inferredcites →https://doi.org/10.1016/j.peptides.2004.11.021openalex-snapshot
The relation between melanocortin 1 receptor (MC1R) variation and the generation of phenotypic diversity in the cutaneous response to ultraviolet radiation
inferredcites →https://doi.org/10.1016/j.tig.2004.06.010openalex-snapshot
Eye colour: portals into pigmentation genes and ancestry
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/s0190-9622(08)81509-5openalex-snapshot
Nonmelanoma skin cancer in the United States: Incidence
inferredcites →https://doi.org/10.1034/j.1600-0749.2002.00039.xopenalex-snapshot
Agouti: from Mouse to Man, from Skin to Fat
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.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/ng1732openalex-snapshot
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2064openalex-snapshot
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer
inferredcites →https://doi.org/10.1046/j.0022-202x.2001.01421.xopenalex-snapshot
Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color
inferredcites →https://doi.org/10.1046/j.1523-1747.2001.01224.xopenalex-snapshot
Melanocortin-1 Receptor Genotype is a Risk Factor for Basal and Squamous Cell Carcinoma
inferredcites →https://doi.org/10.1086/302711openalex-snapshot
Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype?
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/10.1086/339076openalex-snapshot
A Polymorphism in the Agouti Signaling Protein Gene Is Associated with Human Pigmentation
inferredcites →https://doi.org/10.1086/510885openalex-snapshot
A Three–Single-Nucleotide Polymorphism Haplotype in Intron 1 of OCA2 Explains Most Human Eye-Color Variation
inferredcites →https://doi.org/10.1093/genetics/165.4.2071openalex-snapshot
Sequences Associated With Human Iris Pigmentation
inferredcites →https://doi.org/10.1093/hmg/5.10.1663openalex-snapshot
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
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/jnci/dji176openalex-snapshot
MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population
inferredcites →https://doi.org/10.1093/nar/gkl679openalex-snapshot
A novel endonuclease IV post-PCR genotyping system
inferredcites →https://doi.org/10.1111/1523-1747.ep12292572openalex-snapshot
Agouti Signaling Protein Inhibits Melanogenesis and the Response of Human Melanocytes to α-Melanotropin
inferredcites →https://doi.org/10.1111/j.1365-2133.2006.07229.xopenalex-snapshot
Genetics and risk factors for basal cell carcinoma
inferredcites →https://doi.org/10.1136/adc.2005.086918openalex-snapshot
Sun exposure and risk of melanoma
inferredcites →https://doi.org/10.1172/jci115064openalex-snapshot
Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4611303openalex-extracted
Title Epidemiology of Facial Skin Cancers Managed in a French Ambulatory Surgical Center
inferred← citeshttps://doi.org/10.1002/9780470015902.a0005180.pub2openalex-snapshot
de CODE and Iceland: A Critique
inferred← citeshttps://doi.org/10.1002/cncr.24994openalex-snapshot
Does MC1R genotype convey information about melanoma risk beyond risk phenotypes?
inferred← citeshttps://doi.org/10.1002/cncr.25562openalex-snapshot
Characteristics of the coexistence of melanoma and renal cell carcinoma
inferred← citeshttps://doi.org/10.1002/gcc.20931openalex-snapshot
Genome‐wide linkage analysis of Swedish families to identify putative susceptibility loci for cutaneous malignant melanoma
inferred← citeshttps://doi.org/10.1002/gcc.21952openalex-snapshot
MC1R, ASIP, TYR, and TYRP1 gene variants in a population‐based series of multiple primary melanomas
inferred← citeshttps://doi.org/10.1002/gcc.22363openalex-snapshot
The role of germline alterations in the DNA damage response genes BRIP1 and BRCA2 in melanoma susceptibility
inferred← citeshttps://doi.org/10.1002/gcc.22528openalex-snapshot
Truncating mutations of TP53AIP1 gene predispose to cutaneous melanoma
inferred← citeshttps://doi.org/10.1002/humu.20971openalex-snapshot
Identification and functional analysis of novel variants of the human melanocortin 1 receptor found in melanoma patients
inferred← citeshttps://doi.org/10.1002/ijc.24327openalex-snapshot
Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians
inferred← citeshttps://doi.org/10.1002/ijc.24548openalex-snapshot
Melanocortin receptor 1 variants and melanoma risk: A study of 2 European populations
inferred← citeshttps://doi.org/10.1002/ijc.24622openalex-snapshot
Identification of modifier genes for cutaneous malignant melanoma in melanoma‐prone families with and without CDKN2A mutations
inferred← citeshttps://doi.org/10.1002/ijc.25243openalex-snapshot
Estimating the attributable fraction for melanoma: A meta‐analysis of pigmentary characteristics and freckling
inferred← citeshttps://doi.org/10.1002/ijc.25804openalex-snapshot
Melanocortin 1 receptor and risk of cutaneous melanoma: A meta‐analysis and estimates of population burden
inferred← citeshttps://doi.org/10.1002/ijc.25912openalex-snapshot
The association between Parkinson's disease and melanoma
inferred← citeshttps://doi.org/10.1002/ijc.27648openalex-snapshot
Variants at chromosome 20 (ASIP locus) and melanoma risk
inferred← citeshttps://doi.org/10.1002/ijc.29257openalex-snapshot
Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predisposition
inferred← citeshttps://doi.org/10.1002/ijc.29317openalex-snapshot
Inherited variation at MC1R and ASIP and association with melanoma‐specific survival
inferred← citeshttps://doi.org/10.1002/mnfr.201500822openalex-snapshot
Molecular mechanisms of flavonoids in melanin synthesis and the potential for the prevention and treatment of melanoma
inferred← citeshttps://doi.org/10.1007/978-1-4419-6694-0_3openalex-snapshot
Hereditary Factors and Pre-invasive Disease
inferred← citeshttps://doi.org/10.1007/978-1-4614-7357-2_2openalex-snapshot
Epidemiology and Prevention of Cutaneous Tumors
inferred← citeshttps://doi.org/10.1007/978-1-4939-3554-3_5openalex-snapshot
Inherited Gene Mutations in Melanoma
inferred← citeshttps://doi.org/10.1007/978-1-60761-171-4_19openalex-snapshot
Genodermatoses: Inherited Diseases of the Skin
inferred← citeshttps://doi.org/10.1007/978-3-030-05070-2_48openalex-snapshot
Molecular Epidemiology of Melanoma
inferred← citeshttps://doi.org/10.1007/978-3-030-05070-2_8openalex-snapshot
Acquired Precursor Lesions and Phenotypic Markers of Increased Risk for Cutaneous Melanoma
inferred← citeshttps://doi.org/10.1007/978-3-030-26887-9_1openalex-snapshot
Epidemiology and Risk Factors of Basal Cell Carcinoma
inferred← citeshttps://doi.org/10.1007/978-3-032-18222-7_8openalex-snapshot
Germline Mutations Associated Melanocytic Lesions
inferred← citeshttps://doi.org/10.1007/978-3-319-41088-3openalex-snapshot
Personalized, Evolutionary, and Ecological Dermatology
inferred← citeshttps://doi.org/10.1007/978-3-319-41319-8_4openalex-snapshot
Melanoma Genetics and Genomics
inferred← citeshttps://doi.org/10.1007/978-3-319-43102-4_8openalex-snapshot
UV and Skin: Photocarcinogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-46029-1_48-1openalex-snapshot
Molecular Epidemiology of Melanoma
inferred← citeshttps://doi.org/10.1007/978-3-319-46029-1_8-1openalex-snapshot
Acquired Precursor Lesions and Phenotypic Markers of Increased Risk for Cutaneous Melanoma
inferred← citeshttps://doi.org/10.1007/978-3-642-27814-3_171-1openalex-snapshot
The Genetics of Skin Aging
inferred← citeshttps://doi.org/10.1007/978-3-662-47081-7_3openalex-snapshot
Genomics of SCC: Tumor Formation, Progression, and Future Therapeutic Implications for High-Risk Cutaneous Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.1007/978-3-662-47398-6_171openalex-snapshot
The Genetics of Skin Aging
inferred← citeshttps://doi.org/10.1007/978-3-7091-0371-5_4openalex-snapshot
Melanoma Genetics and Genomics
inferred← citeshttps://doi.org/10.1007/978-94-007-7192-5_16openalex-snapshot
Molecular Pathology and Diagnostics of Cutaneous Malignancy
inferred← citeshttps://doi.org/10.1007/978-981-99-2196-6_14-1openalex-snapshot
Skin Cancer: An Overview
inferred← citeshttps://doi.org/10.1007/978-981-99-6263-1_14openalex-snapshot
Skin Cancer: An Overview
inferred← citeshttps://doi.org/10.1007/s00438-020-01681-xopenalex-snapshot
Heat-shock-induced tyrosinase gene ablation with CRISPR in zebrafish
inferred← citeshttps://doi.org/10.1007/s00439-009-0715-9openalex-snapshot
Genetic risk factors for melanoma
inferred← citeshttps://doi.org/10.1007/s00726-013-1509-xopenalex-snapshot
Metazoan innovation: from aromatic amino acids to extracellular signaling
inferred← citeshttps://doi.org/10.1007/s10552-010-9633-3openalex-snapshot
MC1R genotype may modify the effect of sun exposure on melanoma risk in the GEM study
inferred← citeshttps://doi.org/10.1007/s10552-010-9724-1openalex-snapshot
ASIP genetic variants and the number of non-melanoma skin cancers
inferred← citeshttps://doi.org/10.1016/b978-0-12-384978-6.00081-9openalex-snapshot
The Epidemiology of Melanoma of the Skin
inferred← citeshttps://doi.org/10.1016/b978-0-12-812531-1.00014-2openalex-snapshot
The Genetics of Skin Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-443-45863-7.00076-7openalex-snapshot
The epidemiology of melanoma of the skin
inferred← citeshttps://doi.org/10.1016/b978-0-7020-6275-9.00065-9openalex-snapshot
10.1016/b978-0-7020-6275-9.00065-9
inferred← citeshttps://doi.org/10.1016/b978-1-4377-1788-4.00003-4openalex-snapshot
The Biology of the Melanocyte
inferred← citeshttps://doi.org/10.1016/j.abb.2014.04.007openalex-snapshot
Updates of reactive oxygen species in melanoma etiology and progression
inferred← citeshttps://doi.org/10.1016/j.abd.2019.09.023openalex-snapshot
Albinism: epidemiology, genetics, cutaneous characterization, psychosocial factors
inferred← citeshttps://doi.org/10.1016/j.abdp.2019.09.001openalex-snapshot
10.1016/j.abdp.2019.09.001
inferred← citeshttps://doi.org/10.1016/j.ajhg.2010.05.017openalex-snapshot
IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma
inferred← citeshttps://doi.org/10.1016/j.ajhg.2021.07.002openalex-snapshot
A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR
inferred← citeshttps://doi.org/10.1016/j.ajhg.2025.04.015openalex-snapshot
Mapping chromatin interactions at melanoma susceptibility loci uncovers distant cis-regulatory gene targets
inferred← citeshttps://doi.org/10.1016/j.aopr.2024.04.001openalex-snapshot
A UV-related risk analysis in ophthalmic malignancies: Increased UV exposure may cause ocular malignancies
inferred← citeshttps://doi.org/10.1016/j.cancergen.2014.02.007openalex-snapshot
Investigation of a putative melanoma susceptibility locus at chromosome 3q29
inferred← citeshttps://doi.org/10.1016/j.canep.2019.101582openalex-snapshot
High SLC7A11 expression in normal skin of melanoma patients
inferred← citeshttps://doi.org/10.1016/j.ctarc.2024.100837openalex-snapshot
Unveiling the genetic landscape of hereditary melanoma: From susceptibility to surveillance
inferred← citeshttps://doi.org/10.1016/j.currproblcancer.2011.07.001openalex-snapshot
Hereditary Melanoma
inferred← citeshttps://doi.org/10.1016/j.det.2008.12.002openalex-snapshot
Melanoma Epidemiology and Public Health
inferred← citeshttps://doi.org/10.1016/j.ejca.2009.02.001openalex-snapshot
MC1R variant alleles and malignant melanoma risk in Israel
inferred← citeshttps://doi.org/10.1016/j.ejca.2009.04.034openalex-snapshot
Variants of the xeroderma pigmentosum variant gene (POLH) are associated with melanoma risk
inferred← citeshttps://doi.org/10.1016/j.ejca.2009.06.011openalex-snapshot
Vitamin D receptor gene polymorphisms, serum 25-hydroxyvitamin D levels, and melanoma: UK case–control comparisons and a meta-analysis of published VDR data
inferred← citeshttps://doi.org/10.1016/j.ejca.2010.04.024openalex-snapshot
High-ceiling diuretics are associated with an increased risk of basal cell carcinoma in a population-based follow-up study
inferred← citeshttps://doi.org/10.1016/j.ejca.2010.10.008openalex-snapshot
Relationship between sun exposure and melanoma risk for tumours in different body sites in a large case-control study in a temperate climate
inferred← citeshttps://doi.org/10.1016/j.ejca.2011.09.017openalex-snapshot
Do discordant cancers share familial susceptibility?
inferred← citeshttps://doi.org/10.1016/j.ejca.2012.03.006openalex-snapshot
MC1R, SLC45A2 and TYR genetic variants involved in melanoma susceptibility in Southern European populations: Results from a Meta-analysis
inferred← citeshttps://doi.org/10.1016/j.ejca.2012.05.017openalex-snapshot
Perceptions of genetic research and testing among members of families with an increased risk of malignant melanoma
inferred← citeshttps://doi.org/10.1016/j.ejca.2013.03.010openalex-snapshot
Risk of subsequent cutaneous malignancy in patients with prior keratinocyte carcinoma: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.fsigen.2014.06.017openalex-snapshot
Development of a forensic skin colour predictive test
inferred← citeshttps://doi.org/10.1016/j.fsigen.2019.07.012openalex-snapshot
DNA-based predictive models for the presence of freckles
inferred← citeshttps://doi.org/10.1016/j.gde.2010.03.013openalex-snapshot
Genetic dissection of intermediate phenotypes as a way to discover novel cancer susceptibility alleles
inferred← citeshttps://doi.org/10.1016/j.gim.2021.09.003openalex-snapshot
Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma
inferred← citeshttps://doi.org/10.1016/j.hoc.2009.03.005openalex-snapshot
Applications of Genomics in Melanoma Oncogene Discovery
inferred← citeshttps://doi.org/10.1016/j.hoc.2010.06.003openalex-snapshot
Hereditary Genodermatoses with Cancer Predisposition
inferred← citeshttps://doi.org/10.1016/j.hoc.2010.06.009openalex-snapshot
Genome-wide Association Studies of Cancer Predisposition
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.148504openalex-snapshot
Analysis of the mechanism of lncRNA_89636 in the regulation of asip by targeting miR-200a in koi carp skin color differentiation
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103107openalex-snapshot
caAtlas: An immunopeptidome atlas of human cancer
inferred← citeshttps://doi.org/10.1016/j.jaad.2008.08.011openalex-snapshot
Immunosuppression may be present within condyloma acuminata
inferred← citeshttps://doi.org/10.1016/j.jaad.2012.02.042openalex-snapshot
Germline melanoma susceptibility and prognostic genes: A review of the literature
inferred← citeshttps://doi.org/10.1016/j.jdermsci.2011.07.003openalex-snapshot
Assessment of tyrosinase variants and skin cancer risk in a large cohort of French subjects
inferred← citeshttps://doi.org/10.1016/j.jdermsci.2012.02.017openalex-snapshot
Genome-wide association study of skin complex diseases
inferred← citeshttps://doi.org/10.1016/j.jdermsci.2012.09.016openalex-snapshot
Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree
inferred← citeshttps://doi.org/10.1016/j.jgg.2011.05.005openalex-snapshot
Recent progress in the genetics of generalized vitiligo
inferred← citeshttps://doi.org/10.1016/j.jid.2016.01.013openalex-snapshot
Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.1016/j.jid.2016.03.047openalex-snapshot
The Molecular Revolution in Cutaneous Biology: The Era of Genome-Wide Association Studies and Statistical, Big Data, and Computational Topics
inferred← citeshttps://doi.org/10.1016/j.jid.2018.03.1511openalex-snapshot
Inverse Relationship between Vitiligo-Related Genes and Skin Cancer Risk
inferred← citeshttps://doi.org/10.1016/j.jid.2018.04.025openalex-snapshot
Inherited Genetic Variants Associated with Melanoma BRAF/NRAS Subtypes
inferred← citeshttps://doi.org/10.1016/j.jid.2021.07.135openalex-snapshot
Cells to Surgery Quiz: September 2021
inferred← citeshttps://doi.org/10.1016/j.jss.2008.11.834openalex-snapshot
New Concepts for Basal Cell Carcinoma. Demographic, Clinical, Histological Risk Factors, and Biomarkers. A Systematic Review of Evidence Regarding Risk for Tumor Development, Susceptibility for Second Primary and Recurrence
inferred← citeshttps://doi.org/10.1016/j.mehy.2008.10.011openalex-snapshot
Pigmentation genes link Parkinson’s disease to melanoma, opening a window on both etiologies
inferred← citeshttps://doi.org/10.1016/j.mehy.2010.10.044openalex-snapshot
Synthetic aromatic compounds interfering with melanogenesis are responsible of the rising trend of malignant melanoma incidence
inferred← citeshttps://doi.org/10.1016/j.mgene.2018.08.003openalex-snapshot
Association of the 16q24.3 region gene variants rs1805007 and rs4785763 with heightened risk of melanoma in Latvian population
inferred← citeshttps://doi.org/10.1016/j.molonc.2011.01.006openalex-snapshot
Tyrosinase related protein 1 (TYRP1/gp75) in human cutaneous melanoma
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2010.06.011openalex-snapshot
Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma
inferred← citeshttps://doi.org/10.1016/j.mrrev.2010.06.002openalex-snapshot
Genetics of pigmentation in skin cancer — A review
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2013.12.020openalex-snapshot
Susceptibility loci for pigmentation and melanoma in relation to Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.piel.2010.09.020openalex-snapshot
Evolución de la pigmentación en la especie humana
inferred← citeshttps://doi.org/10.1016/j.sder.2010.06.002openalex-snapshot
Genetic Determinants of Cutaneous Melanoma Predisposition
inferred← citeshttps://doi.org/10.1016/j.semcdb.2008.11.016openalex-snapshot
Specification and loss of melanocyte stem cells
inferred← citeshttps://doi.org/10.1016/j.semcdb.2013.03.013openalex-snapshot
Colorful DNA polymorphisms in humans
inferred← citeshttps://doi.org/10.1016/j.suc.2014.07.013openalex-snapshot
Epidemiology, Risk Factors, Prevention, and Early Detection of Melanoma
inferred← citeshttps://doi.org/10.1016/j.xgen.2026.101322openalex-snapshot
Polygenic risk scores and plasma proteomics identify cancer-related proteins and trans-regulated protein networks
inferred← citeshttps://doi.org/10.1016/j.xjidi.2023.100217openalex-snapshot
Mendelian Randomization Analysis reveals Inverse Genetic Risks between Skin Cancers and Vitiligo
inferred← citeshttps://doi.org/10.1016/j.xjidi.2024.100322openalex-snapshot
Identification of Associations with Dermatologic Diseases through a Focused GWAS of the UK Biobank
inferred← citeshttps://doi.org/10.1016/j.xjidi.2025.100374openalex-snapshot
Evaluation of Actinic Keratosis as a Risk Factor for Subsequent Nonskin Cancer Risk
inferred← citeshttps://doi.org/10.1016/s0140-6736(09)61196-xopenalex-snapshot
Non-melanoma skin cancer
inferred← citeshttps://doi.org/10.1016/s0151-9638(09)73382-4openalex-snapshot
Quoi de neuf en recherche dermatologique ?
inferred← citeshttps://doi.org/10.1016/s1877-1173(09)88004-6openalex-snapshot
Chapter 4 The Melanocortin‐1 Receptor Gene Polymorphism and Association with Human Skin Cancer
inferred← citeshttps://doi.org/10.1017/cbo9781139046947.003openalex-snapshot
Genome-wide association studies of cancer predisposition
inferred← citeshttps://doi.org/10.1017/cbo9781139046947.063openalex-snapshot
Molecular oncology of basal cell carcinomas
inferred← citeshttps://doi.org/10.1021/bi300723fopenalex-snapshot
An Unusual Conformation of γ-Melanocyte-Stimulating Hormone Analogues Leads to a Selective Human Melanocortin 1 Receptor Antagonist for Targeting Melanoma Cells
inferred← citeshttps://doi.org/10.1038/cti.2013.5openalex-snapshot
The delicate balance of melanoma immunotherapy
inferred← citeshttps://doi.org/10.1038/ejhg.2009.7openalex-snapshot
Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power
inferred← citeshttps://doi.org/10.1038/jid.2009.258openalex-snapshot
Multiple Pigmentation Gene Polymorphisms Account for a Substantial Proportion of Risk of Cutaneous Malignant Melanoma
inferred← citeshttps://doi.org/10.1038/jid.2011.303openalex-snapshot
CHEK2*1100delC and Risk of Malignant Melanoma: Danish and German Studies and Meta-Analysis
inferred← citeshttps://doi.org/10.1038/jid.2011.321openalex-snapshot
Six Decades of Vitiligo Genetics: Genome-Wide Studies Provide Insights into Autoimmune Pathogenesis
inferred← citeshttps://doi.org/10.1038/jid.2011.402openalex-snapshot
Host Phenotype Characteristics and MC1R in Relation to Early-Onset Basal Cell Carcinoma
inferred← citeshttps://doi.org/10.1038/jid.2012.4openalex-snapshot
A Community-Based Study of Nucleotide Excision Repair Polymorphisms in Relation to the Risk of Non-Melanoma Skin Cancer
inferred← citeshttps://doi.org/10.1038/jid.2012.75openalex-snapshot
Melanoma Genetics: Recent Findings Take Us Beyond Well-Traveled Pathways
inferred← citeshttps://doi.org/10.1038/nature10630openalex-snapshot
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
inferred← citeshttps://doi.org/10.1038/nbt.2282openalex-snapshot
Full-length mRNA-Seq from single-cell levels of RNA and individual circulating tumor cells
inferred← citeshttps://doi.org/10.1038/nbt.2749openalex-snapshot
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
inferred← citeshttps://doi.org/10.1038/ncomms12048openalex-snapshot
Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma
inferred← citeshttps://doi.org/10.1038/ncomms7825openalex-snapshot
New basal cell carcinoma susceptibility loci
inferred← citeshttps://doi.org/10.1038/ncomms8033openalex-snapshot
Genetic similarity between cancers and comorbid Mendelian diseases identifies candidate driver genes
inferred← citeshttps://doi.org/10.1038/ng.234openalex-snapshot
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits
inferred← citeshttps://doi.org/10.1038/ng.2571openalex-snapshot
A variant in FTO shows association with melanoma risk not due to BMI
inferred← citeshttps://doi.org/10.1038/ng.296openalex-snapshot
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types
inferred← citeshttps://doi.org/10.1038/ng.323openalex-snapshot
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
inferred← citeshttps://doi.org/10.1038/ng.3373openalex-snapshot
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
inferred← citeshttps://doi.org/10.1038/ng.411openalex-snapshot
Genome-wide association study identifies three loci associated with melanoma risk
inferred← citeshttps://doi.org/10.1038/ng.412openalex-snapshot
New common variants affecting susceptibility to basal cell carcinoma
inferred← citeshttps://doi.org/10.1038/ng.424openalex-snapshot
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
inferred← citeshttps://doi.org/10.1038/ng.926openalex-snapshot
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
inferred← citeshttps://doi.org/10.1038/ng.958openalex-snapshot
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
inferred← citeshttps://doi.org/10.1038/ng.959openalex-snapshot
Genome-wide association study identifies three new melanoma susceptibility loci
inferred← citeshttps://doi.org/10.1038/nrc.2017.82openalex-snapshot
Genome-wide association studies of cancer: current insights and future perspectives
inferred← citeshttps://doi.org/10.1038/nrc2503openalex-snapshot
Basal cell carcinomas: attack of the hedgehog
inferred← citeshttps://doi.org/10.1038/nrc2840openalex-snapshot
Architecture of inherited susceptibility to common cancer
inferred← citeshttps://doi.org/10.1038/s41416-022-01923-2openalex-snapshot
Associations between circulating proteins and risk of breast cancer by intrinsic subtypes: a Mendelian randomisation analysis
inferred← citeshttps://doi.org/10.1038/s41467-020-16067-1openalex-snapshot
Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors
inferred← citeshttps://doi.org/10.1038/s41467-020-16590-1openalex-snapshot
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma
inferred← citeshttps://doi.org/10.1038/s41531-024-00638-wopenalex-snapshot
Discovering genetic mechanisms underlying the co-occurrence of Parkinson’s disease and non-motor traits
inferred← citeshttps://doi.org/10.1038/s41588-024-01841-4openalex-snapshot
A sequence of SVA retrotransposon insertions in ASIP shaped human pigmentation
inferred← citeshttps://doi.org/10.1038/s41588-024-01849-wopenalex-snapshot
Mobile element insertions affect human pigmentation and skin cancer risk
inferred← citeshttps://doi.org/10.1039/c0pp90044copenalex-snapshot
The human health effects of ozone depletion and interactions with climate change
inferred← citeshttps://doi.org/10.1051/medsci/2011272153openalex-snapshot
La biogenèse des mélanosomes
inferred← citeshttps://doi.org/10.1053/j.seminoncol.2012.01.011openalex-snapshot
Advances in the Treatment of Basal Cell Carcinoma: Hedgehog Inhibitors
inferred← citeshttps://doi.org/10.1053/j.seminoncol.2016.08.003openalex-snapshot
Genetic predisposition to melanoma
inferred← citeshttps://doi.org/10.1056/jd200806060000001openalex-snapshot
Genotypes for Pigmentation and Skin Cancer
inferred← citeshttps://doi.org/10.1056/nejmoa0908547openalex-snapshot
Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
inferred← citeshttps://doi.org/10.1073/pnas.0806753106openalex-snapshot
Microarray analysis sheds light on the dedifferentiating role of agouti signal protein in murine melanocytes via the Mc1r
inferred← citeshttps://doi.org/10.1073/pnas.2525288123openalex-snapshot
Scalable and accurate rare-variant association tests for whole genome sequencing time-to-event analysis in large biobanks
inferred← citeshttps://doi.org/10.1089/thy.2010.1643openalex-snapshot
Shared Genetic Relationships Underlying Generalized Vitiligo and Autoimmune Thyroid Disease
inferred← citeshttps://doi.org/10.1093/annonc/mdp252openalex-snapshot
Epidemiology of invasive cutaneous melanoma
inferred← citeshttps://doi.org/10.1093/annonc/mdz247.134openalex-snapshot
Investigation on gastric cancer susceptibility genes in Chinese early-onset diffuse gastric cancer
inferred← citeshttps://doi.org/10.1093/bib/bbaf564openalex-snapshot
Genetic imputation of transcriptome and proteome illuminates novel therapeutic targets of cutaneous melanoma
inferred← citeshttps://doi.org/10.1093/biomet/asy064openalex-snapshot
Counting process-based dimension reduction methods for censored outcomes
inferred← citeshttps://doi.org/10.1093/bmb/ldq038openalex-snapshot
Genome-wide association studies for detecting cancer susceptibility
inferred← citeshttps://doi.org/10.1093/carcin/bgu140openalex-snapshot
Identification of a melanoma susceptibility locus and somatic mutation inTET2
inferred← citeshttps://doi.org/10.1093/carcin/bgz173openalex-snapshot
Functional annotation of melanoma risk loci identifies novel susceptibility genes
inferred← citeshttps://doi.org/10.1093/cei/uxab002openalex-snapshot
Patho-immunological mechanisms of vitiligo: the role of the innate and adaptive immunities and environmental stress factors
inferred← citeshttps://doi.org/10.1093/genetics/iyaf204openalex-snapshot
Mutation ages and population origins inferred from genomes in structured populations
inferred← citeshttps://doi.org/10.1093/hmg/ddn287openalex-snapshot
Genome-wide association studies in cancer
inferred← citeshttps://doi.org/10.1093/hmg/ddp003openalex-snapshot
Molecular genetics of human pigmentation diversity
inferred← citeshttps://doi.org/10.1093/hmg/ddr287openalex-snapshot
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
inferred← citeshttps://doi.org/10.1093/hmg/ddr415openalex-snapshot
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma†
inferred← citeshttps://doi.org/10.1093/hmg/dds381openalex-snapshot
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
inferred← citeshttps://doi.org/10.1093/hmg/ddt671openalex-snapshot
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma
inferred← citeshttps://doi.org/10.1093/hmg/ddv076openalex-snapshot
IRF4, MC1R and TYR genes are risk factors for actinic keratosis independent of skin color
inferred← citeshttps://doi.org/10.1093/jnci/djn437openalex-snapshot
A Field Synopsis on Low-Penetrance Variants in DNA Repair Genes and Cancer Susceptibility
inferred← citeshttps://doi.org/10.1093/jnci/djr219openalex-snapshot
Comprehensive Field Synopsis and Systematic Meta-analyses of Genetic Association Studies in Cutaneous Melanoma
inferred← citeshttps://doi.org/10.1093/jnci/djw004openalex-snapshot
Association of Interferon Regulatory Factor-4 Polymorphism rs12203592 With Divergent Melanoma Pathways
inferred← citeshttps://doi.org/10.1093/med/9780198746690.003.0563openalex-snapshot
Tumours of the skin
inferred← citeshttps://doi.org/10.1097/cmr.0b013e328336b000openalex-snapshot
Melanoma susceptibility genes
inferred← citeshttps://doi.org/10.1097/cmr.0b013e32833b159dopenalex-snapshot
Influence of loss of function MC1R variants in genetic susceptibility of familial melanoma in Spain
inferred← citeshttps://doi.org/10.1097/gim.0b013e3181993175openalex-snapshot
Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families
inferred← citeshttps://doi.org/10.1097/scs.0000000000010597openalex-snapshot
Mapping the Research on Periocular Basal Cell Carcinoma in the Past 20 Years: A Bibliometric Network Analysis
inferred← citeshttps://doi.org/10.1101/2020.08.25.20181610openalex-snapshot
Recommendations for Primary Prevention of Skin Melanoma
inferred← citeshttps://doi.org/10.1101/2024.09.16.613289openalex-snapshot
Proof of concept study deploying CRISPR inhibition and activation opens new avenues for systematic biological exploration in zebrafish
inferred← citeshttps://doi.org/10.1101/2024.11.14.24317204openalex-snapshot
Mapping chromatin interactions at melanoma susceptibility loci and cell-type specific dataset integration uncovers distant gene targets of cis -regulation
inferred← citeshttps://doi.org/10.1101/2025.02.09.25321567openalex-snapshot
DeepSpot: Leveraging Spatial Context for Enhanced Spatial Transcriptomics Prediction from H&E Images
inferred← citeshttps://doi.org/10.1101/231423openalex-snapshot
Cell-type specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes
showing the first 200 of 341 · page through all 341
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.