A. Rengmark

发表

Parkinson's disease correlates with promoter methylation in the α‐synuclein gene

M. Toft, L. Pihlstrøm, V. Berge, 2015, Movement disorders : official journal of the Movement Disorder Society.

Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene

N. Blau, J. Koht, C. Tallaksen, 2014, Acta neurologica Scandinavica. Supplementum.

Genomic structure of the Nile tilapia (Oreochromis niloticus) transferrin gene and a haplotype associated with saltwater tolerance

F. Lingaas, A. Rengmark, 2007 .

Identification and mapping of genes associated with salt tolerance in tilapia

F. Lingaas, A. Slettan, Ø. Lie, 2007 .

Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease

M. Toft, L. Pihlstrøm, K. A. Bjørnarå, 2014, Annals of human genetics.

Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

Zafar Iqbal, Lasse Pihlstrøm, Mathias Toft, 2017, PloS one.

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease

D. Rujescu, H. Hakonarson, U. Lindenberger, 2015, Alzheimer's & Dementia.

A study of inherited short tail and taillessness in Pembroke Welsh corgi.

F. Lingaas, A. Indrebø, M. Langeland, 2008, The Journal of small animal practice.

Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease

E. Dietrichs, L. Forsgren, M. Toft, 2015, Journal of Human Genetics.

Genetic variability in wild and farmed Atlantic salmon (Salmo salar) strains estimated by SNP and microsatellites

Ø. Skaala, F. Lingaas, A. Slettan, 2006 .

Low frequency of GCH1 and TH mutations in Parkinson's disease.

L. Forsgren, M. Toft, J. Linder, 2016, Parkinsonism & related disorders.

Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene

T. Selberg, A. Rengmark, Kari Anne Bjørnarå, 2014, Acta neurologica Scandinavica. Supplementum.