van Duijn CM - Search Results

1

A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions.

Janssens AC, Gwinn M, Bradley LA, Oostra BA, van Duijn CM, Khoury MJ. Janssens AC, et al. Among authors: van duijn cm. Am J Hum Genet. 2008 Mar;82(3):593-9. doi: 10.1016/j.ajhg.2007.12.020. Am J Hum Genet. 2008. PMID: 18319070 Free PMC article.

2

A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.

van Duijn CM, Hendriks L, Farrer LA, Backhovens H, Cruts M, Wehnert A, Hofman A, Van Broeckhoven C. van Duijn CM, et al. Among authors: van broeckhoven c. Am J Hum Genet. 1994 Oct;55(4):714-27. Am J Hum Genet. 1994. PMID: 7942850 Free PMC article.

3

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC. Heutink P, et al. Among authors: van duijn cm, van swieten jc. Ann Neurol. 1997 Feb;41(2):150-9. doi: 10.1002/ana.410410205. Ann Neurol. 1997. PMID: 9029063

4

Apolipoprotein E gene and sporadic frontal lobe dementia.

Stevens M, van Duijn CM, de Knijff P, van Broeckhoven C, Heutink P, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: van duijn cm, van swieten jc, van broeckhoven c. Neurology. 1997 Jun;48(6):1526-9. doi: 10.1212/wnl.48.6.1526. Neurology. 1997. PMID: 9191760

5

Familial aggregation in frontotemporal dementia.

Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, Scheltens P, Ravid R, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: van duijn cm, van swieten jc, van gool wa. Neurology. 1998 Jun;50(6):1541-5. doi: 10.1212/wnl.50.6.1541. Neurology. 1998. PMID: 9633692

6

Genetic association of apolipoprotein E with age-related macular degeneration.

Klaver CC, Kliffen M, van Duijn CM, Hofman A, Cruts M, Grobbee DE, van Broeckhoven C, de Jong PT. Klaver CC, et al. Among authors: van duijn cm, van broeckhoven c. Am J Hum Genet. 1998 Jul;63(1):200-6. doi: 10.1086/301901. Am J Hum Genet. 1998. PMID: 9634502 Free PMC article.

7

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.

8

N-acetyltransferase-2 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. J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):518-20. doi: 10.1136/jnnp.67.4.518. J Neurol Neurosurg Psychiatry. 1999. PMID: 10486401 Free PMC article.

9

Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample.

van Duijn CM, Cruts M, Theuns J, Van Gassen G, Backhovens H, van den Broeck M, Wehnert A, Serneels S, Hofman A, Van Broeckhoven C. van Duijn CM, et al. Among authors: van den broeck m, van gassen g, van broeckhoven c. Eur J Hum Genet. 1999 Oct-Nov;7(7):801-6. doi: 10.1038/sj.ejhg.5200373. Eur J Hum Genet. 1999. PMID: 10573013

10

A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction.

Vaessen N, Heutink P, Janssen JA, Witteman JC, Testers L, Hofman A, Lamberts SW, Oostra BA, Pols HA, van Duijn CM. Vaessen N, et al. Among authors: van duijn cm. Diabetes. 2001 Mar;50(3):637-42. doi: 10.2337/diabetes.50.3.637. Diabetes. 2001. PMID: 11246885 Free article.

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