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 | 1467 | 2003 |
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 | 966 | 2013 |
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 | 787 | 2023 |
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 | 591 | 2015 |
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 | 563 | 2005 |
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 | 386 | 2001 |
Oxidative stress in anxiety and comorbid disorders I Hovatta, J Juhila, J Donner Neuroscience research 68 (4), 261-275, 2010 | 379 | 2010 |
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 | 354 | 2022 |
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 | 346 | 1999 |
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 | 330 | 2010 |
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 | 328 | 2010 |
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 | 244 | 2000 |
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 | 237 | 2011 |
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 | 235 | 2011 |
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 | 230 | 2002 |
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 | 218 | 2000 |
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 | 207 | 2002 |
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 | 205 | 2005 |
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 | 196 | 2001 |
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 | 172 | 2012 |