Helisalmi S - Search Results

1

The C9ORF72 expansion sizes in patients with psychosis: a population-based study on the Northern Finland Birth Cohort 1966.

Solje E, Miettunen J, Marttila R, Helisalmi S, Laitinen M, Koivumaa-Honkanen H, Isohanni M, Hiltunen M, Jääskeläinen E, Remes AM. Solje E, et al. Among authors: helisalmi s. Psychiatr Genet. 2016 Apr;26(2):92-4. doi: 10.1097/YPG.0000000000000118. Psychiatr Genet. 2016. PMID: 26862832

2

Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patients.

Hiltunen M, Mannermaa A, Helisalmi S, Koivisto A, Lehtovirta M, Ryynänen M, Riekkinen P Sr, Soininen H. Hiltunen M, et al. Among authors: helisalmi s. Neurosci Lett. 1998 Jun 26;250(1):69-71. doi: 10.1016/s0304-3940(98)00453-4. Neurosci Lett. 1998. PMID: 9696068

3

Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients.

Hiltunen M, Mannermaa A, Koivisto AM, Lehtovirta M, Helisalmi S, Ryynänen M, Riekkinen P Sr, Soininen H. Hiltunen M, et al. Among authors: helisalmi s. Eur J Hum Genet. 1999 Sep;7(6):652-8. doi: 10.1038/sj.ejhg.5200342. Eur J Hum Genet. 1999. PMID: 10482953

4

Is the presenilin-1 E318G missense mutation a risk factor for Alzheimer's disease?

Helisalmi S, Hiltunen M, Mannermaa A, Koivisto AM, Lehtovirta M, Alafuzoff I, Ryynänen M, Soininen H. Helisalmi S, et al. Neurosci Lett. 2000 Jan 7;278(1-2):65-8. doi: 10.1016/s0304-3940(99)00891-5. Neurosci Lett. 2000. PMID: 10643802

5

The leucine (7)-to-proline (7) polymorphism in the signal peptide of neuropeptide Y is not associated with Alzheimer's disease or the link apolipoprotein E.

Helisalmi S, Valve R, Karvonen MK, Hiltunen M, Pirskanen M, Mannermaa A, Koulu M, Pesonen U, Uusitupa M, Soininen H. Helisalmi S, et al. Neurosci Lett. 2000 Jun 16;287(1):25-8. doi: 10.1016/s0304-3940(00)01126-5. Neurosci Lett. 2000. PMID: 10841982

6

Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?

Hiltunen M, Helisalmi S, Mannermaa A, Alafuzoff I, Koivisto AM, Lehtovirta M, Pirskanen M, Sulkava R, Verkkoniemi A, Soininen H. Hiltunen M, et al. Among authors: helisalmi s. Eur J Hum Genet. 2000 Apr;8(4):259-66. doi: 10.1038/sj.ejhg.5200423. Eur J Hum Genet. 2000. PMID: 10854108

7

Apolipoprotein E alleles in women with intrahepatic cholestasis of pregnancy.

Eloranta ML, Heiskanen J, Hiltunen M, Helisalmi S, Mannermaa A, Heinonen S. Eloranta ML, et al. Among authors: helisalmi s. Scand J Gastroenterol. 2000 Sep;35(9):966-8. doi: 10.1080/003655200750023048. Scand J Gastroenterol. 2000. PMID: 11063158

8

Apolipoprotein E alleles in women with pre-eclampsia.

Makkonen N, Heinonen S, Hiltunen M, Helisalmi S, Mannermaa A, Kirkinen P. Makkonen N, et al. Among authors: helisalmi s. J Clin Pathol. 2001 Aug;54(8):652-4. doi: 10.1136/jcp.54.8.652. J Clin Pathol. 2001. PMID: 11477126 Free PMC article.

9

Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in Finland.

Hiltunen M, Mannermaa A, Thompson D, Easton D, Pirskanen M, Helisalmi S, Koivisto AM, Lehtovirta M, Ryynänen M, Soininen H. Hiltunen M, et al. Among authors: helisalmi s. Neurology. 2001 Nov 13;57(9):1663-8. doi: 10.1212/wnl.57.9.1663. Neurology. 2001. PMID: 11706108

10

Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.

Laasanen J, Romppanen EL, Hiltunen M, Helisalmi S, Mannermaa A, Punnonen K, Heinonen S. Laasanen J, et al. Among authors: helisalmi s. Eur J Hum Genet. 2002 Sep;10(9):569-73. doi: 10.1038/sj.ejhg.5200849. Eur J Hum Genet. 2002. PMID: 12173035

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