B. Fontaine

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families

B. Fontaine, J. Vale-Santos, K Jurkat-Rott et al. · Nature Genetics · 1994 · 234 citations

Health Sciences, Cytogenetics, European Families +8

ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence

Christian Kubisch, Thomas Schmidt‐Rose, B. Fontaine et al. · Human Molecular Genetics · 1998 · 122 citations

CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

Cyril Goizet, A. Boukhris, A. Dürr et al. · Brain · 2009 · 109 citations

HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis

Isabelle Cournu‐Rebeix, Emmanuelle Génin, Emmanuelle Leray et al. · Genes and Immunity · 2008 · 27 citations

Autoimmune Disease, Neurological Disorder, Later Course +6

Genetic mapping across autoimmune diseases reveals shared associations and mechanisms

Matthew R. Lincoln, Noah Connally, Pierre‐Paul Axisa et al. · Nature Genetics · 2024 · 27 citations · Full text

Immunogenetics, Autoimmune Disease, Autoantibody Production +10