Syvänen AC - Search Results

1

Experimental validation of data mined single nucleotide polymorphisms from several databases and consecutive dbSNP builds.

Edvardsen H, Irene Grenaker Alnaes G, Tsalenko A, Mulcahy T, Yuryev A, Lindersson M, Lien S, Omholt S, Syvänen AC, Børresen-Dale AL, Kristensen VN. Edvardsen H, et al. Among authors: syvanen ac. Pharmacogenet Genomics. 2006 Mar;16(3):207-17. doi: 10.1097/01.fpc.0000194422.12770.fb. Pharmacogenet Genomics. 2006. PMID: 16495780

2

Genetic variation in putative regulatory loci controlling gene expression in breast cancer.

Kristensen VN, Edvardsen H, Tsalenko A, Nordgard SH, Sørlie T, Sharan R, Vailaya A, Ben-Dor A, Lønning PE, Lien S, Omholt S, Syvänen AC, Yakhini Z, Børresen-Dale AL. Kristensen VN, et al. Among authors: syvanen ac. Proc Natl Acad Sci U S A. 2006 May 16;103(20):7735-40. doi: 10.1073/pnas.0601893103. Epub 2006 May 9. Proc Natl Acad Sci U S A. 2006. PMID: 16684880 Free PMC article.

3

A microarray minisequencing system for pharmacogenetic profiling of antihypertensive drug response.

Liljedahl U, Karlsson J, Melhus H, Kurland L, Lindersson M, Kahan T, Nyström F, Lind L, Syvänen AC. Liljedahl U, et al. Among authors: syvanen ac. Pharmacogenetics. 2003 Jan;13(1):7-17. doi: 10.1097/00008571-200301000-00003. Pharmacogenetics. 2003. PMID: 12544508 Clinical Trial.

4

Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients.

Nordgard SH, Johansen FE, Alnaes GI, Bucher E, Syvänen AC, Naume B, Børresen-Dale AL, Kristensen VN. Nordgard SH, et al. Among authors: syvanen ac. Genes Chromosomes Cancer. 2008 Aug;47(8):680-96. doi: 10.1002/gcc.20569. Genes Chromosomes Cancer. 2008. PMID: 18398821

5

SNP in TXNRD2 associated with radiation-induced fibrosis: a study of genetic variation in reactive oxygen species metabolism and signaling.

Edvardsen H, Landmark-Høyvik H, Reinertsen KV, Zhao X, Grenaker-Alnæs GI, Nebdal D, Syvänen AC, Rødningen O, Alsner J, Overgaard J, Borresen-Dale AL, Fosså SD, Kristensen VN. Edvardsen H, et al. Among authors: syvanen ac. Int J Radiat Oncol Biol Phys. 2013 Jul 15;86(4):791-9. doi: 10.1016/j.ijrobp.2013.02.025. Epub 2013 Apr 16. Int J Radiat Oncol Biol Phys. 2013. PMID: 23597419 Free article.

6

Genetic variations in sex steroid-related genes as predictors of serum estrogen levels in men.

Eriksson AL, Lorentzon M, Vandenput L, Labrie F, Lindersson M, Syvänen AC, Orwoll ES, Cummings SR, Zmuda JM, Ljunggren O, Karlsson MK, Mellström D, Ohlsson C. Eriksson AL, et al. Among authors: syvanen ac. J Clin Endocrinol Metab. 2009 Mar;94(3):1033-41. doi: 10.1210/jc.2008-1283. Epub 2008 Dec 30. J Clin Endocrinol Metab. 2009. PMID: 19116238 Free PMC article.

7

Discovery, scoring and utilization of human single nucleotide polymorphisms: a multidisciplinary problem.

Isaksson A, Landegren U, Syvänen AC, Bork P, Stein C, Ortigao F, Brookes AJ. Isaksson A, et al. Among authors: syvanen ac. Eur J Hum Genet. 2000 Feb;8(2):154-6. doi: 10.1038/sj.ejhg.5200424. Eur J Hum Genet. 2000. PMID: 10757651

8

A quality assessment survey of SNP genotyping laboratories.

Lahermo P, Liljedahl U, Alnaes G, Axelsson T, Brookes AJ, Ellonen P, Groop PH, Halldén C, Holmberg D, Holmberg K, Keinänen M, Kepp K, Kere J, Kiviluoma P, Kristensen V, Lindgren C, Odeberg J, Osterman P, Parkkonen M, Saarela J, Sterner M, Strömqvist L, Talas U, Wessman M, Palotie A, Syvänen AC. Lahermo P, et al. Among authors: syvanen ac. Hum Mutat. 2006 Jul;27(7):711-4. doi: 10.1002/humu.20346. Hum Mutat. 2006. PMID: 16786507

9

Ethnic differences in catechol O-methyltransferase pharmacogenetics: frequency of the codon 108/158 low activity allele is lower in Kenyan than Caucasian or South-west Asian individuals.

McLeod HL, Syvänen AC, Githang'a J, Indalo A, Ismail D, Dewar K, Ulmanen I, Sludden J. McLeod HL, et al. Among authors: syvanen ac. Pharmacogenetics. 1998 Jun;8(3):195-9. Pharmacogenetics. 1998. PMID: 9682265

10

Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland.

Syvänen AC, Ikonen E, Manninen T, Bengtström M, Söderlund H, Aula P, Peltonen L. Syvänen AC, et al. Genomics. 1992 Mar;12(3):590-5. doi: 10.1016/0888-7543(92)90452-x. Genomics. 1992. PMID: 1559710

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