Two TaqI dimorphic sites at the human beta-hydroxylase locus.

Por D'Amato, T, Leboyer, M, Malafosse, A, Samolyk, D, Lamouroux, A, Junien, C, Mallet, J
Publicado em 1989

Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene

Por Perroud, N, Salzmann, A, Prada, P, Nicastro, R, Hoeppli, M-E, Furrer, S, Ardu, S, Krejci, I, Karege, F, Malafosse, A
Publicado em 2013

Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1).

Por Lalioti, M D, Mirotsou, M, Buresi, C, Peitsch, M C, Rossier, C, Ouazzani, R, Baldy-Moulinier, M, Bottani, A, Malafosse, A, Antonarakis, S E
Publicado em 1997

Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma

Por Perroud, N, Paoloni-Giacobino, A, Prada, P, Olié, E, Salzmann, A, Nicastro, R, Guillaume, S, Mouthon, D, Stouder, C, Dieben, K, Huguelet, P, Courtet, P, Malafosse, A
Publicado em 2011

A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset.

Por Lalioti, M D, Scott, H S, Genton, P, Grid, D, Ouazzani, R, M'Rabet, A, Ibrahim, S, Gouider, R, Dravet, C, Chkili, T, Bottani, A, Buresi, C, Malafosse, A, Antonarakis, S E
Publicado em 1998

Association of the connexin36 gene with juvenile myoclonic epilepsy

Por Mas, C, Taske, N, Deutsch, S, Guipponi, M, Thomas, P, Covanis, A, Friis, M, Kjeldsen, M, Pizzolato, G, Villemure, J, Buresi, C, Rees, M, Malafosse, A, Gardiner, M, Antonarakis, S, Meda, P
Publicado em 2004