Parkinson's disease: from monogenic forms to genetic susceptibility factors

α-Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism

(2009) Pablo Ibáñez   ARCHIVES OF NEUROLOGY

Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease

(2008) Corinne Lautier et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP Arrays

(2008) Seyedmehdi Shojaee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2008) Owen A. Ross et al.   ANNALS OF NEUROLOGY

Lrrk2 R1628P in non-Chinese Asian races

(2008) Eng-King Tan et al.   ANNALS OF NEUROLOGY

Genomic investigation of α-synuclein multiplication and parkinsonism

(2008) Owen A. Ross et al.   ANNALS OF NEUROLOGY

Patients Homozygous and Heterozygous for SNCA Duplication in a Family With Parkinsonism and Dementia

(2008) Takeshi Ikeuchi et al.   ARCHIVES OF NEUROLOGY

Glucocerebrosidase Gene Mutations

(2008) Ignacio F. Mata et al.   ARCHIVES OF NEUROLOGY

The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study

(2008) Jeanne C Latourelle et al.   BMC Medicine

The role of autophagy-lysosome pathway in neurodegeneration associated with Parkinson's disease

(2008) T. Pan et al.   BRAIN

The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson’s disease

(2008) J. C. Möller et al.   EUROPEAN JOURNAL OF NEUROLOGY

LRRK2 Gly2385Arg variant is a risk factor of Parkinson’s disease among Han-Chinese from mainland China

(2008) X.-K. An et al.   EUROPEAN JOURNAL OF NEUROLOGY

LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence

(2008) E. K. Tan et al.   HUMAN GENETICS

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

(2008) Nathan Pankratz et al.   HUMAN GENETICS

Lack of replication of association between GIGYF2 variants and Parkinson disease

(2008) J. Bras et al.   HUMAN MOLECULAR GENETICS

Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls

(2008) J. Simon-Sanchez et al.   HUMAN MOLECULAR GENETICS

Genetic variability in the mitochondrial serine proteaseHTRA2contributes to risk for Parkinson disease

(2008) Veerle Bogaerts et al.   HUMAN MUTATION

Comprehensive analysis ofLRRK2in publicly available Parkinson's disease cases and neurologically normal controls

(2008) Coro Paisán-Ruíz et al.   HUMAN MUTATION

LRRK2 mutation in familial Parkinson’s disease in a Taiwanese population: clinical, PET, and functional studies

(2008) Chin-Hsien Lin et al.   JOURNAL OF BIOMEDICAL SCIENCE

LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson’s disease compared to late-onset patients

(2008) Daniel Kam Yin Chan et al.   JOURNAL OF NEURAL TRANSMISSION

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population

(2008) Chin-Song Lu et al.   NEUROGENETICS

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease

(2008) Jung Mi Choi et al.   NEUROGENETICS

CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA

(2008) T. Obi et al.   NEUROLOGY

 -Synuclein, pesticides, and Parkinson disease: A case-control study

(2008) L. Brighina et al.   NEUROLOGY

PROMINENT PSYCHIATRIC SYMPTOMS AND GLUCOSE HYPOMETABOLISM IN A FAMILY WITH A SNCA DUPLICATION

(2008) T. Uchiyama et al.   NEUROLOGY

 -Synuclein gene duplication is present in sporadic Parkinson disease

(2008) A. R. Troiano et al.   NEUROLOGY

 -Synuclein gene duplication is present in sporadic Parkinson disease

(2008) N. Brueggemann et al.   NEUROLOGY

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

(2008) S. Lesage et al.   NEUROLOGY

Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

(2008) Z. Gan-Or et al.   NEUROLOGY

Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore

(2008) C. H. Lin et al.   NEUROLOGY

PARK9-LINKED PARKINSONISM IN EASTERN ASIA: MUTATION DETECTION IN ATP13A2 AND CLINICAL PHENOTYPE

(2008) Y. P. Ning et al.   NEUROLOGY

Neurodegeneration associated with genetic defects in phospholipase A2

(2008) A. Gregory et al.   NEUROLOGY

Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan

(2008) Chin-Song Lu et al.   PARKINSONISM & RELATED DISORDERS

Essential tremor and the common LRRK2 G2385R variant

(2008) Eng-King Tan et al.   PARKINSONISM & RELATED DISORDERS

Genetic variation of Omi/HtrA2 and Parkinson's disease

(2008) Owen A. Ross et al.   PARKINSONISM & RELATED DISORDERS

Beyond Parkinson Disease: Amyotrophic Lateral Sclerosis and the Axon Guidance Pathway

(2008) Timothy G. Lesnick et al.   PLoS One

Neither Replication nor Simulation Supports a Role for the Axon Guidance Pathway in the Genetics of Parkinson's Disease

(2008) Yonghong Li et al.   PLoS One

Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3

(2008) Njideka Okubadejo et al.   PLoS One

Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy

(2007) Elvira V. De Marco et al.   MOVEMENT DISORDERS

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease

(2007) L. Warren et al.   PARKINSONISM & RELATED DISORDERS

Association between Parkinson's disease and glucocerebrosidase mutations in Brazil

(2007) Mariana Spitz et al.   PARKINSONISM & RELATED DISORDERS