Lahermo P - Search Results

1

Genetic background of ataxia in children younger than 5 years in Finland.

Ignatius E, Isohanni P, Pohjanpelto M, Lahermo P, Ojanen S, Brilhante V, Palin E, Suomalainen A, Lönnqvist T, Carroll CJ. Ignatius E, et al. Among authors: lahermo p. Neurol Genet. 2020 Jun 5;6(4):e444. doi: 10.1212/NXG.0000000000000444. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32637629 Free PMC article.

2

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.

3

Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene.

Hackman P, Rusanen SM, Johari M, Vihola A, Jonson PH, Sarparanta J, Donner K, Lahermo P, Koivunen S, Luque H, Soininen M, Mahjneh I, Auranen M, Arumilli M, Savarese M, Udd B. Hackman P, et al. Among authors: lahermo p. Neurol Genet. 2021 Oct 27;7(6):e632. doi: 10.1212/NXG.0000000000000632. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34722876 Free PMC article.

4

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.

5

Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.

Salmela E, Lappalainen T, Liu J, Sistonen P, Andersen PM, Schreiber S, Savontaus ML, Czene K, Lahermo P, Hall P, Kere J. Salmela E, et al. Among authors: lahermo p. PLoS One. 2011 Feb 9;6(2):e16747. doi: 10.1371/journal.pone.0016747. PLoS One. 2011. PMID: 21347369 Free PMC article.

6

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.

Lammi L, Arte S, Somer M, Jarvinen H, Lahermo P, Thesleff I, Pirinen S, Nieminen P. Lammi L, et al. Among authors: lahermo p. Am J Hum Genet. 2004 May;74(5):1043-50. doi: 10.1086/386293. Epub 2004 Mar 23. Am J Hum Genet. 2004. PMID: 15042511 Free PMC article.

7

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.

Salmela E, Lappalainen T, Fransson I, Andersen PM, Dahlman-Wright K, Fiebig A, Sistonen P, Savontaus ML, Schreiber S, Kere J, Lahermo P. Salmela E, et al. Among authors: lahermo p. PLoS One. 2008;3(10):e3519. doi: 10.1371/journal.pone.0003519. Epub 2008 Oct 24. PLoS One. 2008. PMID: 18949038 Free PMC article.

8

High prevalence of four long QT syndrome founder mutations in the Finnish population.

Marjamaa A, Salomaa V, Newton-Cheh C, Porthan K, Reunanen A, Karanko H, Jula A, Lahermo P, Väänänen H, Toivonen L, Swan H, Viitasalo M, Nieminen MS, Peltonen L, Oikarinen L, Palotie A, Kontula K. Marjamaa A, et al. Among authors: lahermo p. Ann Med. 2009;41(3):234-40. doi: 10.1080/07853890802668530. Ann Med. 2009. PMID: 19160088 Free PMC article.

9

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results.

Siggberg L, Ala-Mello S, Linnankivi T, Avela K, Scheinin I, Kristiansson K, Lahermo P, Hietala M, Metsähonkala L, Kuusinen E, Laaksonen M, Saarela J, Khuutila S. Siggberg L, et al. Among authors: lahermo p. BMC Med Genet. 2012 Sep 17;13:84. doi: 10.1186/1471-2350-13-84. BMC Med Genet. 2012. PMID: 22984989 Free PMC article.

10

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

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