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Items where Author is "Harbo, Hanne F."

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Jump to: 2019 | 2010
Number of items: 2.

2019

Kaufmann, Tobias and van der Meer, Dennis and Doan, Nhat Trung and Schwarz, Emanuel and Lund, Martina J. and Agartz, Ingrid and Alnæs, Dag and Barch, Deanna M. and Baur-Streubel, Ramona and Bertolino, Alessandro and Bettella, Francesco and Beyer, Mona K. and Bøen, Erlend and Borgwardt, Stefan and Brandt, Christine L. and Buitelaar, Jan and Celius, Elisabeth G. and Cervenka, Simon and Conzelmann, Annette and Córdova-Palomera, Aldo and Dale, Anders M. and de Quervain, Dominique J. F. and Di Carlo, Pasquale and Djurovic, Srdjan and Dørum, Erlend S. and Eisenacher, Sarah and Elvsåshagen, Torbjørn and Espeseth, Thomas and Fatouros-Bergman, Helena and Flyckt, Lena and Franke, Barbara and Frei, Oleksandr and Haatveit, Beathe and Håberg, Asta K. and Harbo, Hanne F. and Hartman, Catharina A. and Heslenfeld, Dirk and Hoekstra, Pieter J. and Høgestøl, Einar A. and Jernigan, Terry L. and Jonassen, Rune and Jönsson, Erik G. and Karolinska Schizophrenia Project, and Kirsch, Peter and Kłoszewska, Iwona and Kolskår, Knut K. and Landrø, Nils Inge and Le Hellard, Stephanie and Lesch, Klaus-Peter and Lovestone, Simon and Lundervold, Arvid and Lundervold, Astri J. and Maglanoc, Luigi A. and Malt, Ulrik F. and Mecocci, Patrizia and Melle, Ingrid and Meyer-Lindenberg, Andreas and Moberget, Torgeir and Norbom, Linn B. and Nordvik, Jan Egil and Nyberg, Lars and Oosterlaan, Jaap and Papalino, Marco and Papassotiropoulos, Andreas and Pauli, Paul and Pergola, Giulio and Persson, Karin and Richard, Geneviève and Rokicki, Jaroslav and Sanders, Anne-Marthe and Selbæk, Geir and Shadrin, Alexey A. and Smeland, Olav B. and Soininen, Hilkka and Sowa, Piotr and Steen, Vidar M. and Tsolaki, Magda and Ulrichsen, Kristine M. and Vellas, Bruno and Wang, Lei and Westman, Eric and Ziegler, Georg C. and Zink, Mathias and Andreassen, Ole A. and Westlye, Lars T.. (2019) Common brain disorders are associated with heritable patterns of apparent aging of the brain. Nature Neuroscience, 22 (10). pp. 1617-1623.

2010

Jakkula, Eveliina and Leppä, Virpi and Sulonen, Anna-Maija and Varilo, Teppo and Kallio, Suvi and Kemppinen, Anu and Purcell, Shaun and Koivisto, Keijo and Tienari, Pentti and Sumelahti, Marja-Liisa and Elovaara, Irina and Pirttilä, Tuula and Reunanen, Mauri and Aromaa, Arpo and Oturai, Annette Bang and Søndergaard, Helle Bach and Harbo, Hanne F. and Mero, Inger-Lise and Gabriel, Stacey B. and Mirel, Daniel B. and Hauser, Stephen L. and Kappos, Ludwig and Polman, Chris and De Jager, Philip L. and Hafler, David A. and Daly, Mark J. and Palotie, Aarno and Saarela, Janna and Peltonen, Leena. (2010) Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. American journal of human genetics, Vol. 86, H. 2. pp. 285-291.

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