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List of works by Ignacio F Mata

A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.

scientific article published on 11 November 2011

APOE ε4 increases risk for dementia in pure synucleinopathies

scientific article published on February 2013

APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease

scientific article

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease

scientific article published on 28 July 2018

Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).

scientific article

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

scientific article

Association between the TNFalpha-308 A/G polymorphism and the onset-age of Alzheimer disease

scientific article

Association mapping of the PARK10 region for Parkinson's disease susceptibility genes

scientific article

C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex

scientific article published on June 2013

Chemokines (RANTES and MCP-1) and chemokine-receptors (CCR2 and CCR5) gene polymorphisms in Alzheimer's and Parkinson's disease

scientific article published in November 2004

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

Cognitive profile of LRRK2-related Parkinson's disease

scientific article

Common variation in the LRRK2 gene is a risk factor for Parkinson's disease

scientific article

Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson's disease

scientific article published on 09 April 2020

Digenic parkinsonism: investigation of the synergistic effects of PRKN and LRRK2.

scientific article published on December 2006

GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology

scientific article

GCH1 in early-onset Parkinson's disease.

scientific article

Genetics of restless legs syndrome

scientific article

Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients

scientific article published on 05 November 2020

Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.

scientific article

Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders

scientific article

Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism

scientific article published on 8 February 2005

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

scientific article

LRRK2 R1441G in Spanish patients with Parkinson's disease.

scientific article

LRRK2 in Parkinson's disease: protein domains and functional insights

scientific article (publication date: May 2006)

LRRK2 mutations and Parkinsonism

scientific article published in The Lancet

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease

scientific article

LRRK2 mutations are a common cause of Parkinson's disease in Spain

article

LRRK2 mutations in Parkinson disease

scientific article published on 01 September 2005

LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay

scientific article published on 05 November 2008

LRRK2: a common pathway for parkinsonism, pathogenesis and prevention?

scientific article

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

scientific article published on 7 December 2006

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

scientific article

Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America

scientific article

Lrrk2 pathogenic substitutions in Parkinson's disease

scientific article published on 17 September 2005

Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

article

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

scientific article

Multivariate prediction of dementia in Parkinson's disease

scientific article published on 25 August 2020

Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease.

scientific article

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

scientific article

Parkin genetics: one model for Parkinson's disease

scientific article

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

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

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

scientific article (publication date: July 2008)

RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts

scientific article published in 2022

Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.

scientific article

Risk prediction for complex diseases: application to Parkinson disease.

scientific article

SNCA variant associated with Parkinson disease and plasma alpha-synuclein level

scientific article

Sex differences in progression to mild cognitive impairment and dementia in Parkinson's disease

scientific article published on 9 February 2018

Single-nucleotide polymorphisms in the promoter region of the PARKIN gene and Parkinson's disease

scientific article published on 01 August 2002

The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population

scientific article

The genetics of Parkinson disease

scientific article

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