Hemminki K - Search Results

1

Influence of genetic variants in type I interferon genes on melanoma survival and therapy.

Lenci RE, Bevier M, Brandt A, Bermejo JL, Sucker A, Moll I, Planelles D, Requena C, Nagore E, Hemminki K, Schadendorf D, Kumar R. Lenci RE, et al. Among authors: hemminki k. PLoS One. 2012;7(11):e50692. doi: 10.1371/journal.pone.0050692. Epub 2012 Nov 27. PLoS One. 2012. PMID: 23209811 Free PMC article.

2

Separation of 7-methyl- and 7-(2-hydroxyethyl)-guanine adducts in human DNA samples using a combination of TLC and HPLC.

Kumar R, Hemminki K. Kumar R, et al. Among authors: hemminki k. Carcinogenesis. 1996 Mar;17(3):485-92. doi: 10.1093/carcin/17.3.485. Carcinogenesis. 1996. PMID: 8631134

3

Mutations in the CDKN2A (p16INK4a) gene in microdissected sporadic primary melanomas.

Kumar R, Lundh Rozell B, Louhelainen J, Hemminki K. Kumar R, et al. Among authors: hemminki k. Int J Cancer. 1998 Jan 19;75(2):193-8. doi: 10.1002/(sici)1097-0215(19980119)75:2<193::aid-ijc5>3.0.co;2-p. Int J Cancer. 1998. PMID: 9462707

4

Loss of heterozygosity at chromosome 9p21 (INK4-p14ARF locus): homozygous deletions and mutations in the p16 and p14ARF genes in sporadic primary melanomas.

Kumar R, Smeds J, Lundh Rozell B, Hemminki K. Kumar R, et al. Among authors: hemminki k. Melanoma Res. 1999 Apr;9(2):138-47. doi: 10.1097/00008390-199904000-00005. Melanoma Res. 1999. PMID: 10380936

5

Increased frequency of LOH on chromosome 9 in sporadic primary melanomas is associated with increased patient age at diagnosis.

Smeds J, Kumar R, Rozell BL, Hemminki K. Smeds J, et al. Among authors: hemminki k. Mutagenesis. 2000 May;15(3):257-60. doi: 10.1093/mutage/15.3.257. Mutagenesis. 2000. PMID: 10792020

6

Single nucleotide polymorphism analyses of the human proliferating cell nuclear antigen (pCNA) and flap endonuclease (FEN1) genes.

Ma X, Jin Q, Försti A, Hemminki K, Kumar R. Ma X, et al. Among authors: hemminki k. Int J Cancer. 2000 Dec 15;88(6):938-42. doi: 10.1002/1097-0215(20001215)88:6<938::aid-ijc16>3.0.co;2-g. Int J Cancer. 2000. PMID: 11093818

7

Polymorphic insertion of additional repeat within an area of direct 8 bp tandem repeats in the 5'-untranslated region of the p53R2 gene and cancer risk.

Smeds J, Kumar R, Hemminki K. Smeds J, et al. Among authors: hemminki k. Mutagenesis. 2001 Nov;16(6):547-50. doi: 10.1093/mutage/16.6.547. Mutagenesis. 2001. PMID: 11682647

8

Significant impact of promoter hypermethylation and the 540 C>T polymorphism of CDKN2A in cutaneous melanoma of the vertical growth phase.

Straume O, Smeds J, Kumar R, Hemminki K, Akslen LA. Straume O, et al. Among authors: hemminki k. Am J Pathol. 2002 Jul;161(1):229-37. doi: 10.1016/S0002-9440(10)64174-0. Am J Pathol. 2002. PMID: 12107107 Free PMC article.

9

Single nucleotide polymorphisms in the XPG gene: determination of role in DNA repair and breast cancer risk.

Kumar R, Höglund L, Zhao C, Försti A, Snellman E, Hemminki K. Kumar R, et al. Among authors: hemminki k. Int J Cancer. 2003 Feb 20;103(5):671-5. doi: 10.1002/ijc.10870. Int J Cancer. 2003. PMID: 12494477

10

Correspondence re: Zheng et al, Haplotype of two variants in p16 (CDKN2/MTS-1/INK4a) exon 3 and risk of squamous cell carcinoma of the head and neck: a case-control study. 11: 640-645, 2002.

Kumar R, Hemminki K. Kumar R, et al. Among authors: hemminki k. Cancer Epidemiol Biomarkers Prev. 2003 Jan;12(1):71; author reply 72. Cancer Epidemiol Biomarkers Prev. 2003. PMID: 12540508 No abstract available.

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