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Characterization of a cyclooxygenase-2-765G→C promoter polymorphism in human neural cellsCUI, Jian-Guo; SALEHI-RAD, Shabnam; ROGAEVA, Ekaterina et al.Neuroreport (Oxford). 2005, Vol 16, Num 6, pp 575-579, issn 0959-4965, 5 p.Article

SORCS1 Alters Amyloid Precursor Protein Processing and Variants May Increase Alzheimer's Disease RiskREITZ, Christiane; TOKUHIRO, Shinya; VARDARAJAN, Badri et al.Annals of neurology. 2011, Vol 69, Num 1, pp 47-64, issn 0364-5134, 18 p.Article

Distinct biochemical signatures characterize peripherin isoform expression in both traumatic neuronal injury and motor neuron diseaseMCLEAN, Jesse; LIU, Hsueh-Ning; MILETIC, Denise et al.Journal of neurochemistry. 2010, Vol 114, Num 4, pp 1177-1192, issn 0022-3042, 16 p.Article

T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson diseaseCHISHTI, Muhammad A; BOHLEGA, Saeed; AHMED, Maqbool et al.Archives of neurology (Chicago). 2006, Vol 63, Num 10, pp 1483-1485, issn 0003-9942, 3 p.Article

Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's diseaseSHIBATA, Nobuto; KAWARAI, Toshitaka; ROGAEVA, Ekaterina et al.Neuroscience letters. 2005, Vol 391, Num 3, pp 142-146, issn 0304-3940, 5 p.Article

Analysis of the glucocerebrosidase gene in Parkinson's diseaseSATO, Christine; MORGAN, Angharad; LANG, Anthony E et al.Movement disorders. 2004, Vol 20, Num 3, pp 367-370, issn 0885-3185, 4 p.Article

Brain levels of CDK5 activator p25 are not increased in Alzheimer's or other neurodegenerative diseases with neurofibrillary tanglesTANDON, Anurag; HAUNG YU; FRASER, Paul E et al.Journal of neurochemistry. 2003, Vol 86, Num 3, pp 572-581, issn 0022-3042, 10 p.Article

Clinical findings in a large family with a parkin Ex3Δ40 mutationMUNHOZ, Renato P; SA, Daniel S; ROGAEVA, Ekaterina et al.Archives of neurology (Chicago). 2004, Vol 61, Num 5, pp 701-704, issn 0003-9942, 4 p.Article

Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin geneORLACCHIO, Antonio; KAWARAI, Toshitaka; POLIDORO, Mario et al.Neuroscience letters. 2004, Vol 363, Num 1, pp 49-53, issn 0304-3940, 5 p.Article

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseNAJ, Adam C; JUN, Gyungah; LARSON, Eric B et al.Nature genetics. 2011, Vol 43, Num 5, pp 436-441, issn 1061-4036, 6 p.Article

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APPGUERREIRO, Rita Joao; BAQUERO, Miquel; GOMEZ-ISLA, Teresa et al.Neurobiology of aging. 2010, Vol 31, Num 5, pp 725-731, issn 0197-4580, 7 p.Article

LRRK2 and Parkin mutations in a family with parkinsonism—Lack of genotype-phenotype correlationMARRAS, Connie; KLEIN, Christine; BI, Andrew et al.Neurobiology of aging. 2010, Vol 31, Num 4, pp 721-722, issn 0197-4580, 2 p.Article

Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer diseaseLEE, Joseph H; RONG CHENG; GEORGE-HYSLOP, Peter St et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 2, pp 127-138, issn 1364-6745, 12 p.Article

TMP21 is a presenilin complex component that modulates γ-secretase but not ε-secretase activityFUSHENG CHEN; HASEGAWA, Hiroshi; WAKUTANI, Yosuke et al.Nature (London). 2006, Vol 440, Num 7088, pp 1208-1212, issn 0028-0836, 5 p.Article

Benign hereditary chorea: Clinical, genetic, and pathological findingsKLEINER-FISMAN, Galit; ROGAEVA, Ekaterina; HALLIDAY, William et al.Annals of neurology. 2003, Vol 54, Num 2, pp 244-247, issn 0364-5134, 4 p.Article

Global investigation and meta-analysis of the C9orf72 (G₄C₂)_n repeat in Parkinson diseaseTHEUNS, Jessie; VERSTRAETEN, Aline; KRÜGER, Rejko et al.Neurology. 2014, Vol 83, Num 21, pp 1906-1913, issn 0028-3878, 8 p.Article

Large-scale replication and heterogeneity in Parkinson disease genetic lociSHARMA, Manu; IOANNIDIS, John P. A; FACHERIS, Maurizio et al.Neurology. 2012, Vol 79, Num 7, pp 659-667, issn 0028-3878, 9 p.Article

Identification of Novel Loci for Alzheimer Disease and Replication of CLU, PICALM, and BIN1 in Caribbean Hispanic IndividualsLEE, Joseph H; RONG CHENG; BARRAL, Sandra et al.Archives of neurology (Chicago). 2011, Vol 68, Num 3, pp 320-328, issn 0003-9942, 9 p.Article

The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort. CommentaryROSENBERG, Roger N; LEE, Joseph H; GEORGE-HYSLOP, Peter St et al.Archives of neurology (Chicago). 2007, Vol 64, Num 4, issn 0003-9942, 479-480,501-506 [8 p.]Article

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer diseaseROGAEVA, Ekaterina; YAN MENG; FUSHENG CHEN et al.Nature genetics. 2007, Vol 39, Num 2, pp 168-177, issn 1061-4036, 10 p.Article

Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus)MUNHOZ, Renato P; KAWARAI, Toshitaka; TEIVE, Helio A et al.Movement disorders. 2006, Vol 21, Num 2, pp 279-281, issn 0885-3185, 3 p.Article

Novel SPG6 mutation p.A100T in a japanese family with autosomal dominant form of hereditary spastic paraplegiaKANEKO, Satoshi; KAWARAI, Toshitaka; ST GEORGE-HYSLOP, Peter et al.Movement disorders. 2006, Vol 21, Num 9, pp 1531-1533, issn 0885-3185, 3 p.Article

Conversion to dementia among two groups with cognitive impairment: A preliminary reportLUIS, Cheryl A; BARKER, Warren W; LOEWENSTEIN, David A et al.Dementia and geriatric cognitive disorders. 2004, Vol 18, Num 3-4, pp 307-313, issn 1420-8008, 7 p.Article

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutationHAGUE, Stephen; ROGAEVA, Ekaterina; GWINN-HARDY, Katrina et al.Annals of neurology. 2003, Vol 54, Num 2, pp 271-274, issn 0364-5134, 4 p.Article