Genetics of Parkinson’s disease in Brazil: a systematic review of monogenic forms

The genetic landscape of Parkinson's disease

(2018) A. Lunati et al.   REVUE NEUROLOGIQUE

MDSGene: Closing Data Gaps in Genotype-Phenotype Correlations of Monogenic Parkinson’s Disease

(2018) Christine Klein et al.   Journal of Parkinsons Disease

Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease

(2017) Camilla P. da Silva et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

ClinVar: improving access to variant interpretations and supporting evidence

(2017) Melissa J Landrum et al.   NUCLEIC ACIDS RESEARCH

D NAJC 6 Mutations Associated With Early-Onset Parkinson's Disease

(2016) Simone Olgiati et al.   ANNALS OF NEUROLOGY

Autosomal dominant Parkinson’s disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil

(2016) Gabriella de M. Abreu et al.   NEUROSCIENCE LETTERS

Meta-analysis of Brazilian genetic admixture and comparison with other Latin America countries

(2015) Ronald Rodrigues de Moura et al.   AMERICAN JOURNAL OF HUMAN BIOLOGY

Alpha-synuclein A53T mutation is not frequent on a sample of Brazilian Parkinson’s disease patients

(2015) Gabriela S. Longo et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Association of LRRK2 and GBA mutations in a Brazilian family with Parkinson's disease

(2015) Mariana Spitz et al.   PARKINSONISM & RELATED DISORDERS

Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation

(2015) Márcia M.G. Pimentel et al.   PARKINSONISM & RELATED DISORDERS

Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson’s disease

(2014) Hsin Fen Chien et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Exon Dosage Variations in Brazilian Patients with Parkinson’s Disease: Analysis ofSNCA,PARKIN,PINK1andDJ-1Genes

(2013) Karla Cristina Vasconcelos Moura et al.   DISEASE MARKERS

Genetic Analysis ofPARK2andPINK1Genes in Brazilian Patients with Early-Onset Parkinson's Disease

(2013) Karla Cristina Vasconcelos Moura et al.   DISEASE MARKERS

Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

(2013) Marialuisa Quadri et al.   HUMAN MUTATION

Systematic Review and UK-Based Study ofPARK2 (parkin), PINK1, PARK7 (DJ-1)andLRRK2in early-onset Parkinson's disease

(2012) Laura L. Kilarski et al.   MOVEMENT DISORDERS

Clinical and molecular neuroimaging characteristics of Brazilian patients with Parkinson's disease and mutations in PARK2 or PARK8 genes

(2010) Orlando G.P. Barsottini et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Genetic analysis of LRRK2 functional domains in Brazilian patients with Parkinson’s disease

(2010) C. B. Abdalla-Carvalho et al.   EUROPEAN JOURNAL OF NEUROLOGY

Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease

(2010) Adriana Vaz dos Santos et al.   NEUROSCIENCE LETTERS

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency ofSNCA,PRKN,PINK1, andLRRK2mutations

(2009) Sarah Teixeira Camargos et al.   MOVEMENT DISORDERS

PINK1 polymorphism IVS1−7 A→G, exposure to environmental risk factors and anticipation of disease onset in Brazilian patients with early-onset Parkinson's Disease

(2009) Clecio Godeiro et al.   NEUROSCIENCE LETTERS

Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: A systematic review

(2009) L. Correia Guedes et al.   PARKINSONISM & RELATED DISORDERS

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

(2008) Daniel G Healy et al.   LANCET NEUROLOGY

Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients

(2008) Patricia de Carvalho Aguiar et al.   MOVEMENT DISORDERS

A study of LRRK2 mutations and Parkinson's disease in Brazil

(2007) Márcia Mattos Gonçalves Pimentel et al.   NEUROSCIENCE LETTERS