Ola Sandgren

Identification of the gene responsible for Best macular dystrophy

Konstantin Petrukhin, Markus J. Koisti, Benjamin Bakall et al. · Nature Genetics · 1998 · 679 citations

Ocular Disease, Ophthalmology, Genetics +2

Familial Amyloidotic Polyneuropathy in Sweden: Geographical Distribution, Age of Onset, and Prevalence

Alda Sousa, Rune Andersson, Ulf Drugge et al. · Human Heredity · 1993 · 146 citations

Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26.

Marie Burstedt, Ola Sandgren, Gösta Holmgren et al. · PubMed · 1999 · 130 citations

The mutation spectrum of the bestrophin protein - functional implications

Benjamin Bakall, Towa Marknell, Sofie Ingvast et al. · Human Genetics · 1999 · 106 citations

Protein Function, Medicine, Genetics +7

A Gene for Autosomal Dominant Progressive Cone Dystrophy (CORD5) Maps to Chromosome 17p12–p13

Jorune Balciuniene, Kent Johansson, Ola Sandgren et al. · Genomics · 1995 · 78 citations

Mendelian Disorder, Genetic Disorder, Genetics +7