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427 results

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Page 1
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, Follett J, Farrer MJ, Trinh J, Gasser T, Goldwurm S, Gustavsson E, Klein C, Lang AE, Langston JW, Latourelle J, Lynch T, Marder K, Marras C, Martin ER, McLean CY, Mejia-Santana H, Molho E, Myers RH, Nuytemans K, Ozelius L, Payami H, Raymond D, Rogaeva E, Rogers MP, Ross OA, Samii A, Saunders-Pullman R, Schüle B, Schulte C, Scott WK, Tanner C, Tolosa E, Tomkins JE, Vilas D, Trojanowski JQ; 23andMe Research Team; Uitti R, Vance JM, Visanji NP, Wszolek ZK, Zabetian CP, Mirelman A, Giladi N, Orr Urtreger A, Cannon P, Fiske B, Foroud T. Lai D, et al. Among authors: rogaeva e. Ann Neurol. 2021 Jul;90(1):76-88. doi: 10.1002/ana.26094. Epub 2021 May 17. Ann Neurol. 2021. PMID: 33938021 Free PMC article.
Homozygous inheritance of the Machado-Joseph disease gene.
Lang AE, Rogaeva EA, Tsuda T, Hutterer J, St George-Hyslop P. Lang AE, et al. Among authors: rogaeva ea. Ann Neurol. 1994 Sep;36(3):443-7. doi: 10.1002/ana.410360318. Ann Neurol. 1994. PMID: 8080254
Association between bleomycin hydrolase and Alzheimer's disease in caucasians.
Farrer LA, Abraham CR, Haines JL, Rogaeva EA, Song Y, McGraw WT, Brindle N, Premkumar S, Scott WK, Yamaoka LH, Saunders AM, Roses AD, Auerbach SA, Sorbi S, Duara R, Pericak-Vance MA, St George-Hyslop PH. Farrer LA, et al. Among authors: rogaeva ea. Ann Neurol. 1998 Nov;44(5):808-11. doi: 10.1002/ana.410440515. Ann Neurol. 1998. PMID: 9818937
Association between angiotensin-converting enzyme and Alzheimer disease.
Farrer LA, Sherbatich T, Keryanov SA, Korovaitseva GI, Rogaeva EA, Petruk S, Premkumar S, Moliaka Y, Song YQ, Pei Y, Sato C, Selezneva ND, Voskresenskaya S, Golimbet V, Sorbi S, Duara R, Gavrilova S, St George-Hyslop PH, Rogaev EI. Farrer LA, et al. Among authors: rogaeva ea. Arch Neurol. 2000 Feb;57(2):210-4. doi: 10.1001/archneur.57.2.210. Arch Neurol. 2000. PMID: 10681079 Clinical Trial.
Parkin-proven disease: common founders but divergent phenotypes.
Lincoln S, Wiley J, Lynch T, Langston JW, Chen R, Lang A, Rogaeva E, Sa DS, Munhoz RP, Harris J, Marder K, Klein C, Bisceglio G, Hussey J, West A, Hulihan M, Hardy J, Farrer M. Lincoln S, et al. Among authors: rogaeva e. Neurology. 2003 May 27;60(10):1605-10. doi: 10.1212/01.wnl.0000064289.49410.a9. Neurology. 2003. PMID: 12771249
Benign hereditary chorea: clinical, genetic, and pathological findings.
Kleiner-Fisman G, Rogaeva E, Halliday W, Houle S, Kawarai T, Sato C, Medeiros H, St George-Hyslop PH, Lang AE. Kleiner-Fisman G, et al. Among authors: rogaeva e. Ann Neurol. 2003 Aug;54(2):244-7. doi: 10.1002/ana.10637. Ann Neurol. 2003. PMID: 12891678
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Hague S, Rogaeva E, Hernandez D, Gulick C, Singleton A, Hanson M, Johnson J, Weiser R, Gallardo M, Ravina B, Gwinn-Hardy K, Crawley A, St George-Hyslop PH, Lang AE, Heutink P, Bonifati V, Hardy J, Singleton A. Hague S, et al. Among authors: rogaeva e. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685
Analysis of the glucocerebrosidase gene in Parkinson's disease.
Sato C, Morgan A, Lang AE, Salehi-Rad S, Kawarai T, Meng Y, Ray PN, Farrer LA, St George-Hyslop P, Rogaeva E. Sato C, et al. Among authors: rogaeva e. Mov Disord. 2005 Mar;20(3):367-70. doi: 10.1002/mds.20319. Mov Disord. 2005. PMID: 15517592
427 results