Ala-Kokko L - Search Results

1

Association between sequence variations in genes encoding human zona pellucida glycoproteins and fertilization failure in IVF.

Männikkö M, Törmälä RM, Tuuri T, Haltia A, Martikainen H, Ala-Kokko L, Tapanainen JS, Lakkakorpi JT. Männikkö M, et al. Hum Reprod. 2005 Jun;20(6):1578-85. doi: 10.1093/humrep/deh837. Epub 2005 Apr 28. Hum Reprod. 2005. PMID: 15860499

2

Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis.

Noponen-Hietala N, Kyllönen E, Männikkö M, Ilkko E, Karppinen J, Ott J, Ala-Kokko L. Noponen-Hietala N, et al. Ann Rheum Dis. 2003 Dec;62(12):1208-14. doi: 10.1136/ard.2003.008334. Ann Rheum Dis. 2003. PMID: 14644861 Free PMC article.

3

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.

Melkoniemi M, Koillinen H, Männikkö M, Warman ML, Pihlajamaa T, Kääriäinen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L. Melkoniemi M, et al. Eur J Hum Genet. 2003 Mar;11(3):265-70. doi: 10.1038/sj.ejhg.5200950. Eur J Hum Genet. 2003. PMID: 12673280

4

Novel mutations in the small leucine-rich repeat protein/proteoglycan (SLRP) genes in high myopia.

Majava M, Bishop PN, Hägg P, Scott PG, Rice A, Inglehearn C, Hammond CJ, Spector TD, Ala-Kokko L, Männikkö M. Majava M, et al. Hum Mutat. 2007 Apr;28(4):336-44. doi: 10.1002/humu.20444. Hum Mutat. 2007. PMID: 17117407

5

Aggrecan core protein of a certain length is protective against hand osteoarthritis.

Kämäräinen OP, Solovieva S, Vehmas T, Luoma K, Leino-Arjas P, Riihimäki H, Ala-Kokko L, Männikkö M. Kämäräinen OP, et al. Osteoarthritis Cartilage. 2006 Oct;14(10):1075-80. doi: 10.1016/j.joca.2006.04.005. Epub 2006 May 19. Osteoarthritis Cartilage. 2006. PMID: 16713721 Free article.

6

Heterozygous mutations in the LDL receptor-related protein 5 (LRP5) gene are associated with primary osteoporosis in children.

Hartikka H, Mäkitie O, Männikkö M, Doria AS, Daneman A, Cole WG, Ala-Kokko L, Sochett EB. Hartikka H, et al. J Bone Miner Res. 2005 May;20(5):783-9. doi: 10.1359/JBMR.050101. Epub 2005 Jan 4. J Bone Miner Res. 2005. PMID: 15824851 Free article.

7

Putative susceptibility locus on chromosome 21q for lumbar disc disease (LDD) in the Finnish population.

Virtanen IM, Noponen N, Barral S, Karppinen J, Li H, Vuoristo M, Niinimäki J, Ott J, Ala-Kokko L, Männikkö M. Virtanen IM, et al. J Bone Miner Res. 2007 May;22(5):701-7. doi: 10.1359/jbmr.070123. J Bone Miner Res. 2007. PMID: 17266399 Free article. Clinical Trial.

8

Common interleukin-6 promoter variants associate with the more severe forms of distal interphalangeal osteoarthritis.

Kämäräinen OP, Solovieva S, Vehmas T, Luoma K, Riihimäki H, Ala-Kokko L, Männikkö M, Leino-Arjas P. Kämäräinen OP, et al. Arthritis Res Ther. 2008;10(1):R21. doi: 10.1186/ar2374. Epub 2008 Feb 8. Arthritis Res Ther. 2008. PMID: 18257935 Free PMC article.

9

Rare variations in WNT3A and DKK1 may predispose carriers to primary osteoporosis.

Korvala J, Löija M, Mäkitie O, Sochett E, Jüppner H, Schnabel D, Mora S, Cole WG, Ala-Kokko L, Männikkö M. Korvala J, et al. Among authors: ala kokko l. Eur J Med Genet. 2012 Oct;55(10):515-9. doi: 10.1016/j.ejmg.2012.06.011. Epub 2012 Jul 9. Eur J Med Genet. 2012. PMID: 22789636

10

Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis.

Taipale M, Jakkula E, Kämäräinen OP, Gao P, Skarp S, Barral S, Kiviranta I, Kröger H, Ott J, Wei GH, Ala-Kokko L, Männikkö M. Taipale M, et al. Among authors: ala kokko l. Osteoarthritis Cartilage. 2016 Apr;24(4):655-63. doi: 10.1016/j.joca.2015.10.019. Epub 2015 Nov 19. Osteoarthritis Cartilage. 2016. PMID: 26603474 Free article.

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