Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's diseaseMARX, Frank P; HOLZMANN, Carsten; ENGELENDER, Simone et al.Human molecular genetics (Print). 2003, Vol 12, Num 11, pp 1223-1231, issn 0964-6906, 9 p.Article

LRRK2 Variation and Parkinson's Disease in African AmericansROSS, Owen A; WILHOITE, Greggory J; MESCHIA, James F et al.Movement disorders. 2010, Vol 25, Num 12, pp 1973-1976, issn 0885-3185, 4 p.Article

Comparison of kindreds with Parkinsonism and α-synuclein genomic multiplicationsFARRER, Matt; KACHERGUS, Jennifer; LANGSTON, J. William et al.Annals of neurology. 2004, Vol 55, Num 2, pp 174-179, issn 0364-5134, 6 p.Article

Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonismLOCKHART, Paul J; BOUNDS, Rebecca; HULIHAN, Mary et al.Movement disorders. 2004, Vol 19, Num 9, pp 1065-1069, issn 0885-3185, 5 p.Article

Translation Initiator EIF4G1 Mutations in Familial Parkinson DiseaseCHARTIER-HARLIN, Marie-Christine; DACHSEL, Justus C; LE RHUN, Emilie et al.American journal of human genetics. 2011, Vol 89, Num 3, pp 398-406, issn 0002-9297, 9 p.Article

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's diseaseTOFT, Mathias; MATA, Ignacio F; WHITE, Linda R et al.Movement disorders. 2007, Vol 22, Num 3, pp 389-392, issn 0885-3185, 4 p.Article

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism : Evidence of a common founder across European populationsKACHERGUS, Jennifer; MATA, Ignacio F; PAYAMI, Haydeh et al.American journal of human genetics. 2005, Vol 76, Num 4, pp 672-680, issn 0002-9297, 9 p.Article

Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with Parkin mutationsWILEY, Joseph; LYNCH, Timothy; LINCOLN, Sarah et al.Movement disorders. 2004, Vol 19, Num 6, pp 677-681, issn 0885-3185, 5 p.Article

Comprehensive Sequencing of the LRRK2 Gene in Patients with Familial Parkinson's Disease from North AfricaJASINSKA-MYGA, Barbara; KACHERGUS, Jennifer; SAMIA BEN YAHMED et al.Movement disorders. 2010, Vol 25, Num 13, pp 2052-2058, issn 0885-3185, 7 p.Article

Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson diseaseDACHSEL, Justus C; NISHIOKA, Kenya; DICKSON, Dennis W et al.Mechanisms of ageing and development. 2010, Vol 131, Num 3, pp 210-214, issn 0047-6374, 5 p.Article

The PARK8 locus in autosomal dominant Parkinsonism: Confirmation of linkage and further delineation of the disease-containing intervalZIMPRICH, Alexander; MÜLLER-MYHSOK, Bertram; STOESSL, Jon et al.American journal of human genetics. 2004, Vol 74, Num 1, pp 11-19, issn 0002-9297, 9 p.Article

α-synuclein locus duplication as a cause of familial Parkinson's disease. CommentaryCHARTIER-HARLIN, Marie-Christine; KACHERGUS, Jennifer; WAUCQUIER, Nawal et al.Lancet (British edition). 2004, Vol 364, Num 9440, pp 1105-1107, issn 0140-6736, 6 p.Article

LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseVILARINO-GÜELL, Carles; WIDER, Christian; TESTA, Claudia M et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 4, pp 401-408, issn 1364-6745, 8 p.Article

Genomic Investigation of α-Synuclein Multiplication and ParkinsonismROSS, Owen A; BRAITHWAITE, Adam T; ADLER, Charles H et al.Annals of neurology. 2008, Vol 63, Num 6, pp 743-750, issn 0364-5134, 8 p.Article

Clinical features of LRRK2- associated Parkinson's disease in central NorwayAASLY, Jan O; TOFT, Mathias; FERNANDEZ-MATA, Ignacio et al.Annals of neurology. 2005, Vol 57, Num 5, pp 762-765, issn 0364-5134, 4 p.Article

LRRK2 R1441G in Spanish patients with Parkinson's diseaseMATA, Ignacio F; TAYLOR, Julie P; MARTINEZ, Carmen et al.Neuroscience letters. 2005, Vol 382, Num 3, pp 309-311, issn 0304-3940, 3 p.Article

α-Synuclein missense and multiplication mutations in autosomal dominant Parkinson's diseaseHOPE, Andrew D; MYHRE, Ronny; KACHERGUS, Jennifer et al.Neuroscience letters. 2004, Vol 367, Num 1, pp 97-100, issn 0304-3940, 4 p.Article

Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North AfricaNISHIOKA, Kenya; VILARINO-GÜELL, Carles; COBB, Stephanie A et al.Neuroscience letters. 2010, Vol 477, Num 2, pp 57-60, issn 0304-3940, 4 p.Article

Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonismMATA, Ignacio F; ALVAREZ, Victoria; COTO, Eliecer et al.Neuroscience letters. 2005, Vol 380, Num 3, pp 257-259, issn 0304-3940, 3 p.Article

Leucine-rich repeat kinase 1 : a paralog of LRRK2 and a candidate gene for Parkinson's diseaseTAYLOR, Julie P; HULIHAN, Mary M; GASSER, Thomas et al.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 2, pp 95-102, issn 1364-6745, 8 p.Article

Expanding the Clinical Phenotype of SNCA Duplication CarriersNISHIOKA, Kenya; ROSS, Owen A; IMAI, Hisamasa et al.Movement disorders. 2009, Vol 24, Num 12, pp 1811-1819, issn 0885-3185, 9 p.Article

Lrrk2 mutations in South America : A study of Chilean Parkinson's diseasePEREZ-PASTENE, Carolina; COBB, Stephanie A; FARRER, Matthew J et al.Neuroscience letters. 2007, Vol 422, Num 3, pp 193-197, issn 0304-3940, 5 p.Article

Lrrk2 pathogenic substitutions in Parkinson's diseaseMATA, Ignacio F; KACHERGUS, Jennifer M; LAHOZ, Carlos et al.Neurogenetics (Oxford. Print). 2005, Vol 6, Num 4, pp 171-177, issn 1364-6745, 7 p.Article

Novel Pathogenic LRRK2 p.Asn1437His Substitution in Familial Parkinson's DiseaseAASLY, Jan O; VILARINO-GÜELL, Carles; KACHERGUS, Jennifer M et al.Movement disorders. 2010, Vol 25, Num 13, pp 2156-2163, issn 0885-3185, 8 p.Article

Fine-mapping and candidate gene investigation within the PARK10 locusHAUGARVOLL, Kristoffer; TOFT, Mathias; WHITE, Linda R et al.European journal of human genetics. 2009, Vol 17, Num 3, pp 336-343, issn 1018-4813, 8 p.Article