CUBN Is a Gene Locus for AlbuminuriaBÖGER, Carsten A; CHEN, Ming-Huei; LIU, Ching-Ti et al.Journal of the American Society of Nephrology. 2011, Vol 22, Num 3, pp 555-570, issn 1046-6673, 16 p.Article

A Common Variation in Deiodinase 1 Gene DIO1 Is Associated with the Relative Levels of Free Thyroxine and TriiodothyroninePANICKER, Vijay; CLUETT, Christie; DURANT, Claire et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 8, pp 3075-3081, issn 0021-972X, 7 p.Article

Neurofibrillary tau Pathology Modulated by Genetic Variation of α-SynucleinPEURALINNA, Terhi; OINAS, Minna; TIENARI, Pentti J et al.Annals of neurology. 2008, Vol 64, Num 3, pp 348-352, issn 0364-5134, 5 p.Article

Lewy bodies and Parkinsonism in families with Parkin mutationsFARRER, Matt; PIU CHAN; SINGLETON, Andrew et al.Annals of neurology. 2001, Vol 50, Num 3, pp 293-300, issn 0364-5134Article

A candidate gene for autoimmune myasthenia gravisLANDOURE, Guida; KNIGHT, Melanie A; RINALDI, Carlo et al.Neurology. 2012, Vol 79, Num 4, pp 342-347, issn 0028-3878, 6 p.Article

Characterization of PLA2G6 as a Locus for Dystonia-ParkinsonismPAISAN-RUIZ, Coro; BHATIA, Kailash P; LI, Abi et al.Annals of neurology. 2009, Vol 65, Num 1, pp 19-23, issn 0364-5134, 5 p.Article

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11HOULDEN, Henry; JOHNSON, Janel; DAVIS, Mary B et al.Nature genetics. 2007, Vol 39, Num 12, pp 1434-1436, issn 1061-4036, 3 p.Article

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and CaucasiansSUBRAMONY, S. H; HERNANDEZ, Dena; SINGLETON, Andrew et al.Movement disorders. 2002, Vol 17, Num 5, pp 1068-1071, issn 0885-3185Article

Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesSAILER, Anna; SCHOLZ, Sonja W; HARDY, John et al.Neurology. 2012, Vol 79, Num 2, pp 127-131, issn 0028-3878, 5 p.Article

A duplication at chromosome 11q12,2-11q12-3 is associated with spinocerebellar ataxia type 20KNIGHT, Melanie A; HERNANDEZ, Dena; TAPSCOTT, Stephen J et al.Human molecular genetics (Print). 2008, Vol 17, Num 24, pp 3847-3853, issn 0964-6906, 7 p.Article

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individualsSIMON-SANCHEZ, Javier; SCHOLZ, Sonja; CRAWLEY, Anthony et al.Human molecular genetics (Print). 2007, Vol 16, Num 1, pp 1-14, issn 0964-6906, 14 p.Article

Linkage and association analyses of type 2 diabetes/impaired glucose metabolism and adiponectin serum levels in Japanese Americans from HawaiiKOVAC, Ilija P; HAVLIK, Richard J; MASAKI, Kamal et al.Diabetes (New York, NY). 2007, Vol 56, Num 2, pp 537-540, issn 0012-1797, 4 p.Article

Analysis of SCA-2 and SCA-3 repeats in parkinsonism : Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's diseaseSIMON-SANCHEZ, Javier; HANSON, Melissa; SINGLETON, Andrew B et al.Neuroscience letters. 2005, Vol 382, Num 1-2, pp 191-194, issn 0304-3940, 4 p.Article

Advancing age is associated with gene expression changes resembling mTOR inhibition: Evidence from two human populationsHARRIES, Lorna W; FEHOWS, Alexander D; PILLING, Luke C et al.Mechanisms of ageing and development. 2012, Vol 133, Num 8, pp 556-562, issn 0047-6374, 7 p.Article

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisCHIO, Adriano; SCHYMICK, Jennifer C; RAPHAEL GIBBS, J et al.Human molecular genetics (Print). 2009, Vol 18, Num 8, pp 1524-1532, issn 0964-6906, 9 p.Article

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

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

ApoE ε3-haplotype modulates Alzheimer beta-amyloid deposition in the brainMYLLYKANGAS, Liisa; POLVIKOSKI, Tuomo; HARDY, John et al.American journal of medical genetics. 2002, Vol 114, Num 3, pp 288-291, issn 0148-7299Article

X-linked dystonia (Lubag) presenting predominantly with parkinsonism: A more benign phenotype?EVIDENTE, Virgilio Gerald H; GWINN-HARDY, Katrina; HARDY, John et al.Movement disorders. 2002, Vol 17, Num 1, pp 200-202, issn 0885-3185Article

Normal localization of ΔF323-Y328 mutant torsinA in transfected human cellsO'FARRELL, Casey; HERNANDEZ, Dena G; EVEY, Crystal et al.Neuroscience letters. 2002, Vol 327, Num 2, pp 75-78, issn 0304-3940Article

Survival and plasticity of basal forebrain cholinergic systems in mice transgenic for presenilin- I and amyloid precursor protein mutant genesHERNANDEZ, Dena; SUGAYA, Kiminobu; TINGYU QU et al.Neuroreport (Oxford). 2001, Vol 12, Num 7, pp 1377-1384, issn 0959-4965Article

Are Myocardial Infarction-Associated Single-Nucleotide Polymorphisms Associated With Ischemic Stroke?CHENG, Yu-Ching; ANDERSON, Christopher D; BARLERA, Simona et al.Stroke (1970). 2012, Vol 43, Num 4, pp 980-986, issn 0039-2499, 7 p.Article

Siblings With Ischemic Stroke Study: Results of a Genome-Wide Scan for Stroke LociMESCHIA, James F; NALLS, Michael; FERRUCCI, Luigi et al.Stroke (1970). 2011, Vol 42, Num 10, pp 2726-2732, issn 0039-2499, 7 p.Article

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24GOODE, Ellen L; CHENEVIX-TRENCH, Georgia; BIRRER, Michael J et al.Nature genetics. 2010, Vol 42, Num 10, pp 874-879, issn 1061-4036, 6 p.Article

Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human PlasmaCARRASQUILLO, Minerva M; NICHOLSON, Alexandra M; SINGLETON, Andrew et al.American journal of human genetics. 2010, Vol 87, Num 6, pp 890-897, issn 0002-9297, 8 p.Article