Lahermo P - Search Results

1

A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.

Koillinen H, Lahermo P, Rautio J, Hukki J, Peyrard-Janvid M, Kere J. Koillinen H, et al. Among authors: lahermo p. J Med Genet. 2005 Feb;42(2):177-84. doi: 10.1136/jmg.2004.019646. J Med Genet. 2005. PMID: 15689458 Free PMC article. No abstract available.

2

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Koillinen H, et al. Among authors: lahermo p. Eur J Hum Genet. 2001 Oct;9(10):747-52. doi: 10.1038/sj.ejhg.5200713. Eur J Hum Genet. 2001. PMID: 11781685

3

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.

Kaminen N, Hannula-Jouppi K, Kestilä M, Lahermo P, Muller K, Kaaranen M, Myllyluoma B, Voutilainen A, Lyytinen H, Nopola-Hemmi J, Kere J. Kaminen N, et al. Among authors: lahermo p. J Med Genet. 2003 May;40(5):340-5. doi: 10.1136/jmg.40.5.340. J Med Genet. 2003. PMID: 12746395 Free PMC article.

4

Linkage mapping of systemic lupus erythematosus (SLE) in Finnish families multiply affected by SLE.

Koskenmies S, Lahermo P, Julkunen H, Ollikainen V, Kere J, Widén E. Koskenmies S, et al. Among authors: lahermo p. J Med Genet. 2004 Jan;41(1):e2-5. doi: 10.1136/jmg.2003.009977. J Med Genet. 2004. PMID: 14729842 Free PMC article. No abstract available.

5

Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.

Salmela E, Taskinen O, Seppänen JK, Sistonen P, Daly MJ, Lahermo P, Savontaus ML, Kere J. Salmela E, et al. Among authors: lahermo p. J Med Genet. 2006 Jul;43(7):590-7. doi: 10.1136/jmg.2005.038414. Epub 2006 Jan 27. J Med Genet. 2006. PMID: 16443857 Free PMC article.

6

Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.

Laivuori H, Lahermo P, Ollikainen V, Widen E, Häivä-Mällinen L, Sundström H, Laitinen T, Kaaja R, Ylikorkala O, Kere J. Laivuori H, et al. Among authors: lahermo p. Am J Hum Genet. 2003 Jan;72(1):168-77. doi: 10.1086/345311. Epub 2002 Dec 9. Am J Hum Genet. 2003. PMID: 12474145 Free PMC article.

7

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.

Peyrard-Janvid M, Anthoni H, Onkamo P, Lahermo P, Zucchelli M, Kaminen N, Hannula-Jouppi K, Nopola-Hemmi J, Voutilainen A, Lyytinen H, Kere J. Peyrard-Janvid M, et al. Among authors: lahermo p. Hum Genet. 2004 Apr;114(5):510-6. doi: 10.1007/s00439-004-1103-0. Epub 2004 Mar 6. Hum Genet. 2004. PMID: 15007729

8

Psoriasis susceptibility locus on 18p revealed by genome scan in Finnish families not associated with PSORS1.

Asumalahti K, Laitinen T, Lahermo P, Suomela S, Itkonen-Vatjus R, Jansen C, Karvonen J, Karvonen SL, Reunala T, Snellman E, Uurasmaa T, Saarialho-Kere U, Kere J. Asumalahti K, et al. Among authors: lahermo p. J Invest Dermatol. 2003 Oct;121(4):735-40. doi: 10.1046/j.1523-1747.2003.12483.x. J Invest Dermatol. 2003. PMID: 14632189 Free article.

9

ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.

Hodgson U, Pulkkinen V, Dixon M, Peyrard-Janvid M, Rehn M, Lahermo P, Ollikainen V, Salmenkivi K, Kinnula V, Kere J, Tukiainen P, Laitinen T. Hodgson U, et al. Among authors: lahermo p. Am J Hum Genet. 2006 Jul;79(1):149-54. doi: 10.1086/504639. Epub 2006 May 9. Am J Hum Genet. 2006. PMID: 16773575 Free PMC article.

10

Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs.

Hannelius U, Salmela E, Lappalainen T, Guillot G, Lindgren CM, von Döbeln U, Lahermo P, Kere J. Hannelius U, et al. Among authors: lahermo p. BMC Genet. 2008 Aug 19;9:54. doi: 10.1186/1471-2156-9-54. BMC Genet. 2008. PMID: 18713460 Free PMC article.

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