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Iiris Hovatta
Iiris Hovatta
Professor of Behavioral Genetics, University of Helsinki
Geverifieerd e-mailadres voor helsinki.fi - Homepage
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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia
CM Lewis, DF Levinson, LH Wise, LE DeLisi, RE Straub, I Hovatta, ...
The American Journal of Human Genetics 73 (1), 34-48, 2003
14662003
Identification of seven loci affecting mean telomere length and their association with disease
V Codd, CP Nelson, E Albrecht, M Mangino, J Deelen, JL Buxton, ...
Nature genetics 45 (4), 422-427, 2013
9662013
FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
7372023
The transcriptional landscape of age in human peripheral blood
MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ...
Nature communications 6 (1), 1-14, 2015
5912015
Glyoxalase 1 and glutathione reductase 1 regulate anxiety in mice
I Hovatta, RS Tennant, R Helton, RA Marr, O Singer, JM Redwine, ...
Nature 438 (7068), 662-666, 2005
5632005
Chromosome 1 loci in Finnish schizophrenia families
J Ekelund, I Hovatta, A Parker, T Paunio, T Varilo, R Martin, J Suhonen, ...
Human molecular genetics 10 (15), 1611-1617, 2001
3852001
Oxidative stress in anxiety and comorbid disorders
I Hovatta, J Juhila, J Donner
Neuroscience research 68 (4), 261-275, 2010
3792010
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
MedRxiv, 2022.03. 03.22271360, 2022
3482022
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
I Hovatta, T Varilo, J Suvisaari, JD Terwilliger, V Ollikainen, R Arajärvi, ...
The American Journal of Human Genetics 65 (4), 1114-1124, 1999
3461999
Mitochondrial myopathy induces a starvation-like response
H Tyynismaa, CJ Carroll, N Raimundo, S Ahola-Erkkilä, T Wenz, ...
Human molecular genetics 19 (20), 3948-3958, 2010
3302010
Childhood adversities are associated with shorter telomere length at adult age both in individuals with an anxiety disorder and controls
L Kananen, I Surakka, S Pirkola, J Suvisaari, J Lönnqvist, L Peltonen, ...
PloS one 5 (5), e10826, 2010
3282010
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22
J Ekelund, D Lichtermann, I Hovatta, P Ellonen, J Suvisaari, JD Terwilliger, ...
Human Molecular Genetics 9 (7), 1049-1057, 2000
2442000
Exercise prevents sleep deprivation-associated anxiety-like behavior in rats: potential role of oxidative stress mechanisms
C Vollert, M Zagaar, I Hovatta, M Taneja, A Vu, A Dao, A Levine, K Alkadhi, ...
Behavioural brain research 224 (2), 233-240, 2011
2362011
Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 are associated with panic disorder and regulate several anxiety candidate genes and related pathways
M Muiños-Gimeno, Y Espinosa-Parrilla, M Guidi, B Kagerbauer, T Sipilä, ...
Biological psychiatry 69 (6), 526-533, 2011
2352011
A susceptibility locus for migraine with aura, on chromosome 4q24
M Wessman, M Kallela, MA Kaunisto, P Marttila, E Sobel, J Hartiala, ...
The American Journal of Human Genetics 70 (3), 652-662, 2002
2302002
The semaphorin 3A receptor may directly regulate the activity of small GTPases
B Rohm, B Rahim, B Kleiber, I Hovatta, AW Püschel
FEBS letters 486 (1), 68-72, 2000
2182000
Antagonistic effects of Rnd1 and RhoD GTPases regulate receptor activity in Semaphorin 3A-induced cytoskeletal collapse
SM Zanata, I Hovatta, B Rohm, AW Püschel
Journal of Neuroscience 22 (2), 471-477, 2002
2072002
Adult mouse brain gene expression patterns bear an embryologic imprint
MA Zapala, I Hovatta, JA Ellison, L Wodicka, JA Del Rio, R Tennant, ...
Proceedings of the National Academy of Sciences 102 (29), 10357-10362, 2005
2052005
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q
T Paunio, J Ekelund, T Varilo, A Parker, I Hovatta, JA Turunen, K Rinard, ...
Human molecular genetics 10 (26), 3037-3048, 2001
1962001
Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts
A Polvi, T Linnankivi, T Kivelä, R Herva, JP Keating, O Mäkitie, ...
The American Journal of Human Genetics 90 (3), 540-549, 2012
1722012
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Artikelen 1–20