Birgit Kjer

Dominant optic atrophy mapped to chromosome 3q region

Birgit Kjer, Hans Eiberg, P Kjer et al. · Acta Ophthalmologica Scandinavica · 1996 · 176 citations

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis

Hans Eiberg, Birgit Kjer, P Kjer et al. · Human Molecular Genetics · 1994 · 154 citations

Ocular Disease, Ophthalmology, Genetic Disorder +13

A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect

Dawn L. Thiselton, Christiane Alexander, Simon P. Brooks et al. · Human Genetics · 2001 · 75 citations

Opa1 Gene, Ocular Disease, Exon 28 +7

Axonal loss occurs early in dominant optic atrophy

Dan Miléa, Birgit Sander, Marianne Wegener et al. · Acta Ophthalmologica · 2009 · 57 citations · Full text

Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig

Aðalbjörg Jónasdóttir, Hans Eiberg, Birgit Kjer et al. · Human Genetics · 1996 · 35 citations

1.4-Cm Interval, Ophthalmology, Cytogenetics +7