Genetics of melanoma predisposition (Q34203435)

31 July 2017

title

Genetics of melanoma predisposition. (English)

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31 July 2017

Nicholas K Hayward

1

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31 July 2017

publication date

1 May 2003

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31 July 2017

language of work or name

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31 July 2017

volume

22

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31 July 2017

issue

20

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31 July 2017

page(s)

3053-3062

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publication type of scholarly work

31 July 2017

review article

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Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Familial cutaneous malignant melanoma and tumors of the nervous system. A hereditary cancer syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Geographical variation in the penetrance of CDKN2A mutations for melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Glutathione S-transferase M1 and T1 polymorphisms: susceptibility to colon cancer and age of onset

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Human CYP2D6 gene polymorphism in Slovene cancer patients and healthy controls

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Genotype-Phenotype Relationships in U.S. Melanoma-Prone Families With CDKN2A and CDK4 Mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Evidence for variable selective pressures at MC1R

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Glutathione S-transferase GSTM1 phenotypes and protection against cutaneous tumours

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

A polymorphism in the agouti signaling protein gene is associated with human pigmentation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

A familial syndrome with cutaneous malignant melanoma and cerebral astrocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Loss of p16Ink4a confers susceptibility to metastatic melanoma in mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Phenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma. MMM group. Multidisciplinary Malignant Melanoma Group

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Patients with both pancreatic adenocarcinoma and melanoma may harbor germline CDKN2A mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Isozyme variation in Larrea ameghinoi and Larrea nitida (Zygophyllaceae): genetic diversity and its bearing on their relationship

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

CDKN2A Germline Mutations in U.K. Patients with Familial Melanoma and Multiple Primary Melanomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

CDKN2AMutations in Multiple Primary Melanomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

G2 phase cell cycle arrest in human skin following UV irradiation.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

CDKN2A germline splicing mutation affecting both p16ink4 and p14arf RNA processing in a melanoma/neurofibroma kindred

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

A melanoma-associated germline mutation in exon 1beta inactivates p14ARF.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Analysis of G1/S checkpoint regulators in metastatic melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Glutathione S-transferase GSTM1 null genotype is not overrepresented in Australian patients with nevoid basal cell carcinoma syndrome or sporadic melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Human pigmentation genetics: the difference is only skin deep

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

A Familial Syndrome of Pancreatic Cancer and Melanoma with a Mutation in theCDKN2Tumor-Suppressor Gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Germline CDKN2A Mutations in Childhood Melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Relationship between the debrisoquine hydroxylase polymorphism and cancer susceptibility.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Familial tumor syndrome associated with a germline nonfunctional p16INK4a allele

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1206445

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Dimensions publication ID

31 July 2017

1044380080

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