Hemminki K - Search Results

1

Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood.

Prasad RB, Hosking FJ, Vijayakrishnan J, Papaemmanuil E, Koehler R, Greaves M, Sheridan E, Gast A, Kinsey SE, Lightfoot T, Roman E, Taylor M, Pritchard-Jones K, Stanulla M, Schrappe M, Bartram CR, Houlston RS, Kumar R, Hemminki K. Prasad RB, et al. Among authors: hemminki k. Blood. 2010 Mar 4;115(9):1765-7. doi: 10.1182/blood-2009-09-241513. Epub 2009 Dec 30. Blood. 2010. PMID: 20042726 Free 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

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

4

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.

5

Simultaneous detection of the exon 10 polymorphism and a novel intronic single base insertion polymorphism in the XPD gene using single strand conformation polymorphism.

Kumar R, Angelini S, Hemminki K. Kumar R, et al. Among authors: hemminki k. Mutagenesis. 2003 Mar;18(2):207-9. doi: 10.1093/mutage/18.2.207. Mutagenesis. 2003. PMID: 12621078

6

Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.

Kumar R, Angelini S, Hemminki K. Kumar R, et al. Among authors: hemminki k. Oncogene. 2003 Dec 18;22(58):9217-24. doi: 10.1038/sj.onc.1206909. Oncogene. 2003. PMID: 14681681

7

BRAF mutations are common somatic events in melanocytic nevi.

Kumar R, Angelini S, Snellman E, Hemminki K. Kumar R, et al. Among authors: hemminki k. J Invest Dermatol. 2004 Feb;122(2):342-8. doi: 10.1046/j.0022-202X.2004.22225.x. J Invest Dermatol. 2004. PMID: 15009715 Free article.

8

Single nucleotide polymorphisms in breast cancer.

Försti A, Angelini S, Festa F, Sanyal S, Zhang Z, Grzybowska E, Pamula J, Pekala W, Zientek H, Hemminki K, Kumar R. Försti A, et al. Among authors: hemminki k. Oncol Rep. 2004 Apr;11(4):917-22. Oncol Rep. 2004. PMID: 15010895

9

Familial risk of lymphoproliferative tumors in families of patients with chronic lymphocytic leukemia: results from the Swedish Family-Cancer Database.

Goldin LR, Pfeiffer RM, Li X, Hemminki K. Goldin LR, et al. Among authors: hemminki k. Blood. 2004 Sep 15;104(6):1850-4. doi: 10.1182/blood-2004-01-0341. Epub 2004 May 25. Blood. 2004. PMID: 15161669 Free article.

10

B-RAF mutations in tumors from melanoma-breast cancer families.

Gast A, Försti A, Söderberg M, Hemminki K, Kumar R. Gast A, et al. Among authors: hemminki k. Int J Cancer. 2005 Jan 10;113(2):336-7. doi: 10.1002/ijc.20560. Int J Cancer. 2005. PMID: 15386414 No abstract available.

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