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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Märker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R. Arts HH, et al. Among authors: farin fm. Nat Genet. 2007 Jul;39(7):882-8. doi: 10.1038/ng2069. Epub 2007 Jun 10. Nat Genet. 2007. PMID: 17558407
Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease.
Ahmed I, Lee PC, Lill CM, Searles Nielsen S, Artaud F, Gallagher LG, Loriot MA, Mulot C, Nacfer M, Liu T, Biernacka JM, Armasu S, Anderson K, Farin FM, Lassen CF, Hansen J, Olsen JH, Bertram L, Maraganore DM, Checkoway H, Ritz B, Elbaz A. Ahmed I, et al. Among authors: farin fm. PLoS Genet. 2014 Nov 20;10(11):e1004788. doi: 10.1371/journal.pgen.1004788. eCollection 2014 Nov. PLoS Genet. 2014. PMID: 25412286 Free PMC article. No abstract available.
Genotype and age at Parkinson disease diagnosis.
Searles Nielsen S, Bammler TK, Gallagher LG, Farin FM, Longstreth W Jr, Franklin GM, Swanson PD, Checkoway H. Searles Nielsen S, et al. Among authors: farin fm. Int J Mol Epidemiol Genet. 2013;4(1):61-9. Epub 2013 Mar 18. Int J Mol Epidemiol Genet. 2013. PMID: 23565323 Free PMC article.
LINE-1 DNA methylation, smoking and risk of Parkinson's disease.
Searles Nielsen S, Checkoway H, Butler RA, Nelson HH, Farin FM, Longstreth WT Jr, Franklin GM, Swanson PD, Kelsey KT. Searles Nielsen S, et al. Among authors: farin fm. J Parkinsons Dis. 2012;2(4):303-8. doi: 10.3233/JPD-012129. J Parkinsons Dis. 2012. PMID: 23938260 Free PMC article.
Genetic polymorphisms in Parkinson's disease.
Checkoway H, Farin FM, Costa-Mallen P, Kirchner SC, Costa LG. Checkoway H, et al. Among authors: farin fm. Neurotoxicology. 1998 Aug-Oct;19(4-5):635-43. Neurotoxicology. 1998. PMID: 9745923 Review.
Glutathione S-transferase M1, T1, and P1 polymorphisms and Parkinson's disease.
Kelada SN, Stapleton PL, Farin FM, Bammler TK, Eaton DL, Smith-Weller T, Franklin GM, Swanson PD, Longstreth WT Jr, Checkoway H. Kelada SN, et al. Among authors: farin fm. Neurosci Lett. 2003 Jan 30;337(1):5-8. doi: 10.1016/s0304-3940(02)01286-7. Neurosci Lett. 2003. PMID: 12524158
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.
Mata IF, Checkoway H, Hutter CM, Samii A, Roberts JW, Kim HM, Agarwal P, Alvarez V, Ribacoba R, Pastor P, Lorenzo-Betancor O, Infante J, Sierra M, Gómez-Garre P, Mir P, Ritz B, Rhodes SL, Colcher A, Van Deerlin V, Chung KA, Quinn JF, Yearout D, Martinez E, Farin FM, Wan JY, Edwards KL, Zabetian CP. Mata IF, et al. Among authors: farin fm. Mov Disord. 2012 Dec;27(14):1822-5. doi: 10.1002/mds.25226. Epub 2012 Oct 31. Mov Disord. 2012. PMID: 23115130 Free PMC article.
Association mapping of the PARK10 region for Parkinson's disease susceptibility genes.
Wan JY, Edwards KL, Hutter CM, Mata IF, Samii A, Roberts JW, Agarwal P, Checkoway H, Farin FM, Yearout D, Zabetian CP. Wan JY, et al. Among authors: farin fm. Parkinsonism Relat Disord. 2014 Jan;20(1):93-8. doi: 10.1016/j.parkreldis.2013.10.001. Epub 2013 Oct 11. Parkinsonism Relat Disord. 2014. PMID: 24156912 Free PMC article.
Parental smoking and risk of childhood brain tumors by functional polymorphisms in polycyclic aromatic hydrocarbon metabolism genes.
Barrington-Trimis JL, Searles Nielsen S, Preston-Martin S, Gauderman WJ, Holly EA, Farin FM, Mueller BA, McKean-Cowdin R. Barrington-Trimis JL, et al. Among authors: farin fm. PLoS One. 2013 Nov 18;8(11):e79110. doi: 10.1371/journal.pone.0079110. eCollection 2013. PLoS One. 2013. PMID: 24260161 Free PMC article. Clinical Trial.
130 results