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Your search keyword '"Isohanni, Matti"' showing total 496 results
Start Over Author "Isohanni, Matti" Publication Type Academic Journals
496 results on '"Isohanni, Matti"'

6. Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

Author

Stoll, Georg, Pietiläinen, Olli PH, Linder, Bastian, Suvisaari, Jaana, Brosi, Cornelia, Hennah, William, Leppä, Virpi, Torniainen, Minna, Ripatti, Samuli, Ala-Mello, Sirpa, Plöttner, Oliver, Rehnström, Karola, Tuulio-Henriksson, Annamari, Varilo, Teppo, Tallila, Jonna, Kristiansson, Kati, Isohanni, Matti, Kaprio, Jaakko, Eriksson, Johan G, Raitakari, Olli T, Lehtimäki, Terho, Jarvelin, Marjo-Riitta, Salomaa, Veikko, Hurles, Matthew, Stefansson, Hreinn, Peltonen, Leena, Sullivan, Patrick F, Paunio, Tiina, Lönnqvist, Jouko, Daly, Mark J, Fischer, Utz, Freimer, Nelson B, and Palotie, Aarno

Subjects
Neurosciences, Schizophrenia, Intellectual and Developmental Disabilities (IDD), Mental Health, Genetics, Fragile X Syndrome, Rare Diseases, Brain Disorders, Aetiology, 2.1 Biological and endogenous factors, Mental health, Abnormalities, Multiple, Adolescent, Adult, Aged, Chromosome Deletion, Chromosomes, Human, Pair 22, Cognition Disorders, Cohort Studies, DNA Topoisomerases, Type I, DiGeorge Syndrome, Family Health, Female, Finland, Fragile X Mental Retardation Protein, Gene Expression Profiling, Genetic Association Studies, Genotype, HEK293 Cells, Health Surveys, Humans, Male, Middle Aged, Models, Molecular, Proteins, Ribonucleoproteins, Sequence Deletion, Young Adult, Psychology, Cognitive Sciences, Neurology & Neurosurgery
Abstract

Implicating particular genes in the generation of complex brain and behavior phenotypes requires multiple lines of evidence. The rarity of most high-impact genetic variants typically precludes the possibility of accruing statistical evidence that they are associated with a given trait. We found that the enrichment of a rare chromosome 22q11.22 deletion in a recently expanded Northern Finnish sub-isolate enabled the detection of association between TOP3B and both schizophrenia and cognitive impairment. Biochemical analysis of TOP3β revealed that this topoisomerase was a component of cytosolic messenger ribonucleoproteins (mRNPs) and was catalytically active on RNA. The recruitment of TOP3β to mRNPs was independent of RNA cis-elements and was coupled to the co-recruitment of FMRP, the disease gene product in fragile X mental retardation syndrome. Our results indicate a previously unknown role for TOP3β in mRNA metabolism and suggest that it is involved in neurodevelopmental disorders.

Published
2013

19. MAINTENANCE OF GENETIC VARIATION IN HUMAN PERSONALITY: TESTING EVOLUTIONARY MODELS BY ESTIMATING HERITABILITY DUE TO COMMON CAUSAL VARIANTS AND INVESTIGATING THE EFFECT OF DISTANT INBREEDING

Author

Verweij, Karin J.H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Råback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kähönen, Mika, Viikari, Jorma, Räikkönen, Katri, Eriksson, Johan G, Keltikangas-Järvinen, Liisa, Lehtimäki, Terho, Martin, Nicholas G., Järvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C., and Zietsch, Brendan P.

Published
2012

21. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Author

Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivières, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stéphane, Cavalcanti-Proença, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna, Edenberg, Howard J., Esk, Tõnu, Fernández-Medarde, Alberto, Foroud, Tatiana, Freimer, Nelson B., Girault, Jean-Antoine, Grobbee, Diederick E., Guarrera, Simonetta, Gudbjartsson, Daniel F., Hartikainen, Anna-Liisa, Heath, Andrew C., Hesselbrock, Victor, Hofman, Albert, Hottenga, Jouke-Jan, Isohanni, Matti K., Kaprio, Jaakko, Khaw, Kay-Tee, Kuehnel, Brigitte, Laitinen, Jaana, Lobbens, Stéphane, Luan, Jian'an, Mangino, Massimo, Maroteaux, Matthieu, Matullo, Giuseppe, McCarthy, Mark I., Mueller, Christian, Navis, Gerjan, Numans, Mattijs E., Núñez, Alejandro, Nyholt, Dale R., Onland-Moret, Charlotte N., Oostra, Ben A., O'Reilly, Paul F., Palkovits, Miklos, Penninx, Brenda W., Polidoro, Silvia, Pouta, Anneli, Prokopenko, Inga, Ricceri, Fulvio, Santos, Eugenio, Smit, Johannes H., Soranzo, Nicole, Song, Kijoung, Sovio, Ulla, Stumvoll, Michael, Surakk, Ida, Thorgeirsson, Thorgeir E., Thorsteinsdottir, Unnur, Troakes, Claire, Tyrfingsson, Thorarinn, Tönjes, Anke, Uiterwaal, Cuno S., Uitterlinden, Andre G., van der Harst, Pim, van der Schouw, Yvonne T., Staehlin, Oliver, Vogelzangs, Nicole, Vollenweider, Peter, Waeber, Gerard, Wareham, Nicholas J., Waterworth, Dawn M., Whitfield, John B., Wichmann, Erich H., Willemsen, Gonneke, Witteman, Jacqueline C., Yuan, Xin, Zhai, Guangju, Zhao, Jing H., Zhang, Weihua, Martin, Nicholas G., Metspalu, Andres, Doering, Angela, Scott, James, Spector, Tim D., Loos, Ruth J., Boomsma, Dorret I., Mooser, Vincent, Peltonen, Leena, Stefansson, Kari, van Duijn, Cornelia M., Vineis, Paolo, Sommer, Wolfgang H., Kooner, Jaspal S., Spanagel, Rainer, Heberlein, Ulrike A., Jarvelin, Marjo-Riitta, Elliott, Paul, and Singer, Burton H.

Published
2011

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