Gruis NA - Search Results

1

Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma.

Potjer TP, van der Grinten TWJ, Lakeman IMM, Bollen SH, Rodríguez-Girondo M, Iles MM, Barrett JH, Kiemeney LA, Gruis NA, van Asperen CJ, van der Stoep N. Potjer TP, et al. Among authors: gruis na. J Med Genet. 2021 Nov;58(11):760-766. doi: 10.1136/jmedgenet-2020-107251. Epub 2020 Sep 29. J Med Genet. 2021. PMID: 32994281 Free PMC article.

2

The Dutch FAMMM family material: clinical and genetic data.

Bergman W, Gruis NA, Frants RR. Bergman W, et al. Among authors: gruis na. Cytogenet Cell Genet. 1992;59(2-3):161-4. doi: 10.1159/000133232. Cytogenet Cell Genet. 1992. PMID: 1737487 No abstract available.

3

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds.

Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, Bergman W, Frants RR. Gruis NA, et al. Nat Genet. 1995 Jul;10(3):351-3. doi: 10.1038/ng0795-351. Nat Genet. 1995. PMID: 7670475

4

Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to 1994.

Hille ET, van Duijn E, Gruis NA, Rosendaal FR, Bergman W, Vandenbroucke JP. Hille ET, et al. Among authors: gruis na. J Invest Dermatol. 1998 May;110(5):788-92. doi: 10.1046/j.1523-1747.1998.00185.x. J Invest Dermatol. 1998. PMID: 9579547 Free article.

5

Familial melanoma; CDKN2A and beyond.

Gruis NA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. J Investig Dermatol Symp Proc. 1999 Sep;4(1):50-4. doi: 10.1038/sj.jidsp.5640181. J Investig Dermatol Symp Proc. 1999. PMID: 10537008 Free article. Review.

6

Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair.

Bastiaens MT, ter Huurne JA, Kielich C, Gruis NA, Westendorp RG, Vermeer BJ, Bavinck JN; Leiden Skin Cancer Study Team. Bastiaens MT, et al. Among authors: gruis na. Am J Hum Genet. 2001 Apr;68(4):884-94. doi: 10.1086/319500. Epub 2001 Mar 16. Am J Hum Genet. 2001. PMID: 11254446 Free PMC article.

7

The melanocortin-1-receptor gene is the major freckle gene.

Bastiaens M, ter Huurne J, Gruis N, Bergman W, Westendorp R, Vermeer BJ, Bouwes Bavinck JN. Bastiaens M, et al. Hum Mol Genet. 2001 Aug 1;10(16):1701-8. doi: 10.1093/hmg/10.16.1701. Hum Mol Genet. 2001. PMID: 11487574

8

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

van der Velden PA, Sandkuijl LA, Bergman W, Pavel S, van Mourik L, Frants RR, Gruis NA. van der Velden PA, et al. Among authors: gruis na. Am J Hum Genet. 2001 Oct;69(4):774-9. doi: 10.1086/323411. Epub 2001 Aug 7. Am J Hum Genet. 2001. PMID: 11500806 Free PMC article.

9

Localization of a novel melanoma susceptibility locus to 1p22.

Gillanders E, Juo SH, Holland EA, Jones M, Nancarrow D, Freas-Lutz D, Sood R, Park N, Faruque M, Markey C, Kefford RF, Palmer J, Bergman W, Bishop DT, Tucker MA, Bressac-de Paillerets B, Hansson J, Stark M, Gruis N, Bishop JN, Goldstein AM, Bailey-Wilson JE, Mann GJ, Hayward N, Trent J; Lund Melanoma Study Group; Melanoma Genetics Consortium. Gillanders E, et al. Am J Hum Genet. 2003 Aug;73(2):301-13. doi: 10.1086/377140. Epub 2003 Jul 3. Am J Hum Genet. 2003. PMID: 12844286 Free PMC article.

10

Familial melanoma: a complex disorder leading to controversy on DNA testing.

de Snoo FA, Bergman W, Gruis NA. de Snoo FA, et al. Among authors: gruis na. Fam Cancer. 2003;2(2):109-16. doi: 10.1023/a:1025758527675. Fam Cancer. 2003. PMID: 14574160 Review.

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