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Lisätietoja molekyylilääketieteen julkaisuihin

Julkaistu 16.11.2005

Lisätietoja julkaisuihin


Additional information to publications


Indicative oligodendrocyte dysfunction in spinal cords of human fetuses suffering from a lethal motoneuron disease
J Neurobiol. 65(3): 269-281 (2005)

Search for cognitive trait components of schizophrenia reveals a locus for
verbal learning and memory on 4q and for visual working memory on
2q

Human Molecular Genetics 13(16):1693-702 (2004)


Familial combined hyperlipidemia is associated with upstream transcription
factor 1 (USF1)

Nature Genetics 36(4):371-6 (2004)


The interval of linkage disequilibrium (LD) detected with microsatellite and
SNP markers in chromosomes of Finnish populations with different
histories

Human Molecular Genetics 12(1):1-9 (2003)


The SLC6A14 Gene Shows Evidence of Association with Obesity

The Journal of Clinical Investigation 112 (11):1762-1772 (2003)


A genomewide screen for autism-spectrum disorders: evidence for a major
susceptibility locus on chromosome 3q25-27.

The American Journal of Human Genetics 71(4):777-90 (2002)


QTL analysis of body mass index and stature by combined analysis of five
Finnish genome scans

The American Journal of Human Genetics 69(1):117-23 (2001)


Chromosome 1 loci in Finnish schizophrenia families

Human Molecular Genetics 15:1611-1617 (2001)


A system for specific, high-throughput genotyping by allele-specific primer
extension on microarrays

Genome Research 10:1031-1042 (2000)


Linkage disequilibrium in isolated populations: Finland and a young
sub-population of Kuusamo

European Journal of Human Genetics 8(8): 604-12 (2000)


Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome
Xq24

Journal of Clinical Endocrinology & Metabolism 85(9):3183-3190 (2000)


Genome-wide scan for schizophrenia in the Finnish population: evidence for a
locus on chromosome 7q22

Human Molecular Genetics 9:1049-1057 (2000)


A genomewide screen for schizophrenia genes in an isolated Finnish
subpopulation, suggesting multiple susceptibility loci.

The American Journal of Human Genetics 65(4):1114-24 (1999)


Genome Scan for Predisposing Loci of Distal Interphalangeal Joint
Osteoarthritis: Evidence for a Locus on 2q

The American Journal of Human Genetics 65(4):1060-7 (1999)


Linkage of familial combined hyperlipidemia to chromosome 1q21-q23

Nature Genetics 18:369-373 (1998)


Evidence for Involvement of the Angiotensin Receptor Type 1 Locus in Essential Hypertension

Hypertension 33(3):844-9 (1999)


Array-based multiplex analysis of candidate genes reveals two independent and
additive genetic risk factors for myocardial infarction in the Finnish population

Human Molecular Genetics 7(9):1453-1462 (1998)


Genome-wide scan of MS in finnish multiplex families

The American Journal of Human Genetics 61:1379-1387 (1997)




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