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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