Toril Fagerheim

A new gene (DYX3) for dyslexia is located on chromosome 2.

Toril Fagerheim, Peter Raeymaekers, Finn Egil Tønnessen et al. · PubMed · 1999 · 195 citations · Full text

Family Members, Genetics, Molecular Genetics +19

Identification of p.A684V missense mutation in the <i>WFS1</i> gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

Nanna Dahl Rendtorff, Marianne Lodahl, Houda Boulahbel et al. · American Journal of Medical Genetics Part A · 2011 · 119 citations · Full text

Optic Atrophy-1 Gene, Mendelian Disorder, Genetic Disorder +13

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment

Nanna Dahl Rendtorff, Mei Zhu, Toril Fagerheim et al. · European Journal of Human Genetics · 2006 · 67 citations · Full text

Developmental Biology, Hereditary Hearing Impairment, Mendelian Disorder +10

Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family

Toril Fagerheim · Human Molecular Genetics · 1996 · 62 citations

PREDICTION OF TIME TRENDS IN RECOVERY OF COGNITIVE FUNCTION AFTER MILD HEAD INJURY

Kay Müller, Tor Ingebrigtsen, Tom Wilsgaard et al. · Neurosurgery · 2009 · 44 citations