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Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population.
Axenovich T, Zorkoltseva I, Belonogova N, van Koolwijk LM, Borodin P, Kirichenko A, Babenko V, Ramdas WD, Amin N, Despriet DD, Vingerling JR, Lemij HG, Oostra BA, Klaver CC, Aulchenko Y, van Duijn CM. Axenovich T, et al. Among authors: van koolwijk lm, van duijn cm. J Med Genet. 2011 Dec;48(12):802-9. doi: 10.1136/jmedgenet-2011-100436. Epub 2011 Nov 5. J Med Genet. 2011. PMID: 22058429
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.
Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P. Rizzu P, et al. Among authors: van duijn cm, van swieten jc. Am J Hum Genet. 1999 Feb;64(2):414-21. doi: 10.1086/302256. Am J Hum Genet. 1999. PMID: 9973279 Free PMC article.
CYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.
Harhangi BS, Oostra BA, Heutink P, van Duijn CM, Hofman A, Breteler MM. Harhangi BS, et al. Among authors: van duijn cm. Mov Disord. 2001 Mar;16(2):290-3. doi: 10.1002/mds.1041. Mov Disord. 2001. PMID: 11295783 Clinical Trial.
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.
Njajou OT, Vaessen N, Joosse M, Berghuis B, van Dongen JW, Breuning MH, Snijders PJ, Rutten WP, Sandkuijl LA, Oostra BA, van Duijn CM, Heutink P. Njajou OT, et al. Among authors: van duijn cm, van dongen jw. Nat Genet. 2001 Jul;28(3):213-4. doi: 10.1038/90038. Nat Genet. 2001. PMID: 11431687
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.
van Duijn CM, Dekker MC, Bonifati V, Galjaard RJ, Houwing-Duistermaat JJ, Snijders PJ, Testers L, Breedveld GJ, Horstink M, Sandkuijl LA, van Swieten JC, Oostra BA, Heutink P. van Duijn CM, et al. Among authors: van swieten jc. Am J Hum Genet. 2001 Sep;69(3):629-34. doi: 10.1086/322996. Epub 2001 Jul 2. Am J Hum Genet. 2001. PMID: 11462174 Free PMC article.
1,197 results