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Genetic Determinants of Ototoxicity During and After Childhood Cancer Treatment: Protocol for the PanCareLIFE Study.
Clemens E, Meijer AJ, Broer L, Langer T, van der Kooi AL, Uitterlinden AG, de Vries A, Kuehni CE, Garrè ML, Kepak T, Kruseova J, Winther JF, Kremer LC, van Dulmen-den Broeder E, Tissing WJ, Rechnitzer C, Kenborg L, Hasle H, Grabow D, Parfitt R, Binder H, Carleton BC, Byrne J, Kaatsch P, Am Zehnhoff-Dinnesen A, Zolk O, van den Heuvel-Eibrink MM. Clemens E, et al. Among authors: uitterlinden ag. JMIR Res Protoc. 2019 Mar 19;8(3):e11868. doi: 10.2196/11868. JMIR Res Protoc. 2019. PMID: 30888333 Free PMC article.
Association of HSP70 and its co-chaperones with Alzheimer's disease.
Broer L, Ikram MA, Schuur M, DeStefano AL, Bis JC, Liu F, Rivadeneira F, Uitterlinden AG, Beiser AS, Longstreth WT, Hofman A, Aulchenko Y, Seshadri S, Fitzpatrick AL, Oostra BA, Breteler MM, van Duijn CM. Broer L, et al. Among authors: uitterlinden ag. J Alzheimers Dis. 2011;25(1):93-102. doi: 10.3233/JAD-2011-101560. J Alzheimers Dis. 2011. PMID: 21403392 Free PMC article.
A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology.
Gasten AC, Ramdas WD, Broer L, van Koolwijk LM, Ikram MK, de Jong PT, Aulchenko YS, Wolfs RC, Hofman A, Rivadeneira F, Uitterlinden AG, Oostra BA, Lemij HG, Klaver CC, Jansonius NM, Vingerling JR, van Duijn CM. Gasten AC, et al. Among authors: uitterlinden ag. Invest Ophthalmol Vis Sci. 2012 Mar 21;53(3):1485-91. doi: 10.1167/iovs.11-7384. Invest Ophthalmol Vis Sci. 2012. PMID: 22266513
Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma.
van Nistelrooij AM, van der Korput HA, Broer L, van Marion R, van Berge Henegouwen MI, van Noesel CJ, Biermann K, Spaander MC, Tilanus HW, van Lanschot JJ, Hofman A, Uitterlinden AG, Wijnhoven BP, Dinjens WN. van Nistelrooij AM, et al. Among authors: uitterlinden ag. J Carcinog. 2015 May 21;14:5. doi: 10.4103/1477-3163.157441. eCollection 2015. J Carcinog. 2015. PMID: 26085818 Free PMC article.
Burden of genetic risk variants in multiple sclerosis families in the Netherlands.
Mescheriakova JY, Broer L, Wahedi S, Uitterlinden AG, van Duijn CM, Hintzen RQ. Mescheriakova JY, et al. Among authors: uitterlinden ag. Mult Scler J Exp Transl Clin. 2016 May 6;2:2055217316648721. doi: 10.1177/2055217316648721. eCollection 2016 Jan-Dec. Mult Scler J Exp Transl Clin. 2016. PMID: 28607725 Free PMC article.
1,283 results