LRRTM1-deficient mice show a rare phenotype of avoiding small enclosures—A tentative mouse model for claustrophobia-like behaviour

Por Voikar, V., Kulesskaya, N., Laakso, T., Lauren, J., Strittmatter, S.M., Airaksinen, M.S.
Publicado em 2012

Barriers to medication counselling for people with mental health disorders: a six country study

Por Aaltonen SE, Laine NP, Volmer D, Gharat MS, Ruta Muceniece R, Vitola A, Foulon V, Desplenter FA, Airaksinen MS, Chen TF, Bell JS
Publicado em 2010-06-01

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Por Francks, C, Maegawa, S, Laurén, J, Abrahams, BS, Velayos-Baeza, A, Medland, SE, Colella, S, Groszer, M, McAuley, EZ, Caffrey, TM, Timmusk, T, Pruunsild, P, Koppel, I, Lind, PA, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, AJ, Riley, BP, Martin, NG, Strittmatter, SM, Möller, H-J, Rujescu, D, St Clair, D, Muglia, P, Roos, JL, Fisher, SE, Wade-Martins, R, Rouleau, GA, Stein, JF, Karayiorgou, M, Geschwind, DH, Ragoussis, J, Kendler, KS, Airaksinen, MS, Oshimura, M, DeLisi, LE, Monaco, AP
Publicado em 2007