Search filters

List of works by Mathias Toft

A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease

scientific article published on 01 July 2018

A cumulative genetic risk score predicts progression in Parkinson's disease

scientific article published on 8 February 2016

A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease

scholarly article by Madeleine Kristiansen et al published February 2019 in Movement Disorders

Advances in genetic diagnosis of neurological disorders.

scientific article published on January 2014

Aggravated stuttering following subthalamic deep brain stimulation in Parkinson's disease--two cases

scientific article

Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

scientific article published on 17 October 2019

CHCHD2 and Parkinson's disease

scientific article published in July 2015

Clinical Heterogeneity of the LRRK2 G2019S Mutation

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

scientific article

Clinical features associated with sleep disturbances in Parkinson's disease

scientific article published on 27 June 2014

Clinical features of LRRK2-associated Parkinson's disease in central Norway

scientific article published in May 2005

Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD.

scientific article published in September 2005

Copy number variation in Parkinson's disease ⬇️

scientific article published on 06 September 2010

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

scientific article published on 12 October 2017

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

scientific article published on 01 July 2008

Cumulative genetic risk and age at onset in Parkinson's disease

scientific article published on 03 August 2015

ELAVL4, PARK10, and the Celts

article

Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease

scientific article

Exome Variant Mining in Familial Parkinson Disease: Will Replication Find the Gold?

scientific article

FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy

scientific article published in June 2005

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

scientific article

Fine-mapping and candidate gene investigation within the PARK10 locus

scientific article

Found in transcription: accurate Parkinson's disease classification in peripheral blood.

scientific article published in January 2013

GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

scientific article published on 07 May 2019

Genetic variability in SNCA and Parkinson's disease

scientific article published on 29 July 2011

Genomewide association, Parkinson disease, and PARK10

scientific article published on June 2006

Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population

scientific article published in February 2006

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

scientific article

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease

scientific article published on 20 December 2017

Integrative analysis identifies bHLH transcription factors as contributors to Parkinson's disease risk mechanisms

scientific article published on 10 February 2021

International consortium identifies new genetic risk factors for Parkinson's disease ⬇️

scientific article published on March 1, 2011

LRRK2 and Parkinson’s disease in Norway

scientific article published on 01 January 2007

LRRK2 mutations and Parkinsonism

scientific article published in The Lancet

LRRK2 mutations are not common in Alzheimer's disease

scientific article published in November 2005

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

scientific article

Levodopa-responsive parkinsonism in probable extrapontine myelinolysis of the mesencephalon

scientific article published in October 2011

Linkage disequilibrium and association of MAPT H1 in Parkinson disease

scientific article

Long-term efficacy and mortality in Parkinson's disease patients treated with subthalamic stimulation

scientific article published on 8 June 2011

Long-term follow-up of thalamic deep brain stimulation for essential tremor - patient satisfaction and mortality

scientific article

Longitudinal assessment of probable rapid eye movement sleep behaviour disorder in Parkinson's disease

scientific article published on 22 April 2015

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

scientific article published on 07 May 2016

Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions

scientific article published on 7 December 2006

Lrrk2 R1441 substitution and progressive supranuclear palsy

scientific article published on 01 February 2006

Lrrk2 and Lewy body disease

scientific article published in February 2006

MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's disease

scientific article published in May 2007

Malignant hyperthermia--a hereditary and potentially life-threatening condition

scientific article published in October 2005

Medication costs following subthalamic nucleus deep brain stimulation for Parkinson's disease

scientific article published on 21 May 2013

Missense mutations in DYT-TOR1A dystonia

scientific article published on 06 June 2019

Multiple Microelectrode Recordings in STN‐DBS Surgery for Parkinson's Disease: A Randomized Study.

scientific article published on 8 May 2018

Multiplealpha-synucleingene polymorphisms are associated with Parkinson’s disease in a Norwegian population

scientific article published on 15 May 2008

No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease

article

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

scientific article

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

scientific article published on 27 December 2014

Parkinson's disease: What remains of the "missing heritability"?

scientific article published on 02 August 2011

Parkinsonism, FXTAS, and FMR1 premutations

scientific article published in February 2005

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

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

Personality changes after deep brain stimulation in Parkinson's disease

scientific article published on 29 January 2015

Premutation alleles and fragile X-associated tremor/ataxia syndrome

scientific article published in January 2005

Progression and survival in Parkinson's disease with subthalamic nucleus stimulation

scientific article published on 4 February 2014

REM sleep behavior disorder in Parkinson's disease--is there a gender difference?

scientific article published on 20 June 2012

Rare variants in dementia genes and Parkinson's disease

scientific article published on 22 June 2016

Risk variants of the α-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study

scientific article published on 21 February 2018

Self-Reported Executive Functioning in Everyday Life in Parkinson's Disease after Three Months of Subthalamic Deep Brain Stimulation

scientific article published on 18 June 2015

Subthalamic deep brain stimulation improves sleep and excessive sweating in Parkinson's disease

scientific article published on 14 October 2020

Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease

scientific article published on 13 November 2012

Surgical site infections after deep brain stimulation surgery: frequency, characteristics and management in a 10-year period

scientific article

TMEM230 variants in Parkinson's disease.

scientific article published in March 2019

Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

scientific article

The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal

scientific article

The Wilson films — MS Tremor ⬇️

scientific article published on December 1, 2011

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

scientific article

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

scientific article published on 12 February 2007

[The genetics of Parkinson disease]

scientific article published on 01 April 2004

[Treatment of movement disorders with deep brain stimulation]

scientific article published on 01 September 2008

Paulina is supported by:

About Paulina

Help