Jamïlé Hazan

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Jamïlé Hazan, Núria Fonknechten, Delphine Mavel et al. · Nature Genetics · 1999 · 626 citations

Frequent Form, Medicine, Genetics +7

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

Jamïlé Hazan, Catherine Lamy, Judith Melki et al. · Nature Genetics · 1993 · 164 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

An ESCRT–spastin interaction promotes fission of recycling tubules from the endosome

Rachel Allison, Jennifer H. Lumb, Coralie Fassier et al. · The Journal of Cell Biology · 2013 · 161 citations · Full text

Endosomal Degradation, Cargo Degradation, Cell Signaling +15

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

Jamïlé Hazan, Bertrand Fontaine, R.P.M. Bruyn et al. · Human Molecular Genetics · 1994 · 143 citations

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q

Pascale Vincent, Henri Plauchu, Jamïlé Hazan et al. · Human Molecular Genetics · 1995 · 134 citations