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List of works by Kristoffer Haugarvoll

-Synuclein and Parkinson disease susceptibility

scientific article published on 13 September 2007

A Novel Compound Heterozygous Tyrosine Hydroxylase Mutation (p.R441P) with Complex Phenotype ⬇️

scientific article published on January 1, 2011

Autonomic symptoms and dopaminergic treatment in de novo Parkinson's disease

scientific article published on 23 September 2012

Clinical features of LRRK2 parkinsonism

scientific article

Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations

scientific article published on 01 July 2008

Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease

scientific article

Differential effect of environmental risk factors on postural instability gait difficulties and tremor dominant Parkinson's disease

scientific article published on September 2010

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

scientific journal article

Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease

scientific article published on 22 August 2008

ELAVL4, PARK10, and the Celts

article

En kvinne i 70-årene med langvarige gangvansker

scientific article published on 20 October 2015

FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression

scientific article

Fine-mapping and candidate gene investigation within the PARK10 locus

scientific article

GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical Studies

scientific article

Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain

scientific article published on 05 May 2021

Genomewide association, Parkinson disease, and PARK10

scientific article published on June 2006

Glitazone use associated with reduced risk of Parkinson's disease

scientific article published in September 2017

Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred

scholarly article by David Gosal et al published 2007 in Movement Disorders

HTRA2 p.G399S in Parkinson disease, essential tremor, and tremulous cervical dystonia

scientific article published on 30 March 2015

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism

scientific article published on 26 October 2008

Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis

scientific article

In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins

scientific article

LRRK2 and Parkinson?s disease in Norway

scientific article published on 01 January 2007

LRRK2 gene and tremor-dominant parkinsonism

scientific article published in September 2006

Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease

scientific article

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

scientific article published on 10 January 2007

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

scientific article published on 12 March 2008

MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing

scientific article published on 3 January 2013

Mitochondrial DNA homeostasis is essential for nigrostriatal integrity

scientific article published on 12 March 2016

Myoclonus-dystonia and epilepsy in a family with a novel epsilon-sarcoglycan mutation.

scientific article published on 3 December 2013

Neuronal complex I deficiency occurs throughout the Parkinson's disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage

scientific article

Nigrostriatal denervation sine parkinsonism

scientific article published on 25 January 2016

No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson's disease

scientific article published on 24 January 2018

Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy

scientific article

Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease

scientific article

Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population

scientific article published on 29 August 2012

PARK8 LRRK2 parkinsonism

scientific article

Parkinson disease: associated disorders in the Norwegian population based incident ParkWest study

scientific article published on 26 July 2012

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

scholarly article by Mathias Toft et al published 2007 in Movement Disorders

Phactr2 and Parkinson's disease

scientific article published on 10 February 2009

Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.

scientific article published on 5 September 2018

Reported mutations inGIGYF2are not a common cause of Parkinson's disease

scholarly article by Carles Vilariño-Güell et al published 15 March 2009 in Movement Disorders

Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations

scientific article published on 26 April 2013

Simvastatin is associated with decreased risk of Parkinson disease

scientific article published on 26 December 2016

The genetics of frontotemporal dementia

scientific article published on August 2007

The influence of cerebrovascular risk factors on incident dementia in patients with Parkinson's disease

scientific article published in December 2005

The role of APOE alleles in incident Parkinson's disease. The Norwegian ParkWest Study

scientific article published in December 2010

Treatment in early Parkinson's disease: the Norwegian ParkWest study.

scientific article

Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease

scientific article published on 8 December 2017

Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway

scientific article published on 12 February 2007

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