Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.

Por Szepetowski, P, Rochette, J, Berquin, P, Piussan, C, Lathrop, G M, Monaco, A P
Publicado em 1997

Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.

Por Thein, S. L., Sampietro, M., Rohde, K., Rochette, J., Weatherall, D. J., Lathrop, G. M., Demenais, F.
Publicado em 1994

Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

Por Cadet, E, Capron, D, Gallet, M, Omanga-Leke, M, Boutignon, H, Julier, C, Robson, K, Rochette, J
Publicado em 2005

Recent advances in understanding haemochromatosis: a transition state

Por Robson, K, Merryweather-Clar..., A, Cadet, E, Viprakasit, V, Zaahl, M, Pointon, J, Weatherall, D, Rochette, J
Publicado em 2004

The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading

Por Livesey, K, Wimhurst, V, Carter, K, Worwood, M, Cadet, E, Rochette, J, Roberts, A, Pointon, J, Merryweather-Clar..., A, Bassett, M, Jouanolle, A, Mosser, A, David, V, Poulton, J, Robson, K
Publicado em 2004

Multicentric origin of hemochromatosis gene (HFE) mutations.

Por Rochette, J, Pointon, J J, Fisher, C A, Perera, G, Arambepola, M, Arichchi, D S, De Silva, S, Vandwalle, J L, Monti, J P, Old, J M, Merryweather-Clarke, A T, Weatherall, D J, Robson, K J
Publicado em 1999