Wehnert A - Search Results

1

Apolipoprotein E genotype, atherosclerosis, and cognitive decline: the Rotterdam Study.

Slooter AJ, van Duijn CM, Bots ML, Ott A, Breteler MB, De Voecht J, Wehnert A, de Knijff P, Havekes LM, Grobbee DE, Van Broeckhoven C, Hofman A. Slooter AJ, et al. Among authors: wehnert a. J Neural Transm Suppl. 1998;53:17-29. doi: 10.1007/978-3-7091-6467-9_3. J Neural Transm Suppl. 1998. PMID: 9700643 Clinical Trial.

2

The apolipoprotein E epsilon 2 allele is associated with an increased risk of early-onset Alzheimer's disease and a reduced survival.

van Duijn CM, de Knijff P, Wehnert A, De Voecht J, Bronzova JB, Havekes LM, Hofman A, Van Broeckhoven C. van Duijn CM, et al. Among authors: wehnert a. Ann Neurol. 1995 May;37(5):605-10. doi: 10.1002/ana.410370510. Ann Neurol. 1995. PMID: 7755355

3

Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's disease.

van Duijn CM, de Knijff P, Cruts M, Wehnert A, Havekes LM, Hofman A, Van Broeckhoven C. van Duijn CM, et al. Among authors: wehnert a. Nat Genet. 1994 May;7(1):74-8. doi: 10.1038/ng0594-74. Nat Genet. 1994. PMID: 8075646

4

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: wehnert a. Am J Hum Genet. 1994 Oct;55(4):714-27. Am J Hum Genet. 1994. PMID: 7942850 Free PMC article.

5

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: wehnert a. Eur J Hum Genet. 1999 Oct-Nov;7(7):801-6. doi: 10.1038/sj.ejhg.5200373. Eur J Hum Genet. 1999. PMID: 10573013

6

Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease.

Cruts M, van Duijn CM, Backhovens H, Van den Broeck M, Wehnert A, Serneels S, Sherrington R, Hutton M, Hardy J, St George-Hyslop PH, Hofman A, Van Broeckhoven C. Cruts M, et al. Among authors: wehnert a. Hum Mol Genet. 1998 Jan;7(1):43-51. doi: 10.1093/hmg/7.1.43. Hum Mol Genet. 1998. PMID: 9384602

7

Mutation analysis of the chromosome 14q24.3 dihydrolipoyl succinyltransferase (DLST) gene in patients with early-onset Alzheimer disease.

Cruts M, Backhovens H, Van Gassen G, Theuns J, Wang SY, Wehnert A, van Duijn CM, Karlsson T, Hofman A, Adolfsson R, et al. Cruts M, et al. Among authors: wehnert a. Neurosci Lett. 1995 Oct 13;199(1):73-7. doi: 10.1016/0304-3940(95)11982-3. Neurosci Lett. 1995. PMID: 8584231

8

Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21.

Van Camp G, Cruts M, Backhovens H, Wehnert A, Van Broeckhoven C. Van Camp G, et al. Among authors: wehnert a. Genomics. 1992 Jan;12(1):158-60. doi: 10.1016/0888-7543(92)90420-w. Genomics. 1992. PMID: 1733854

9

Dinucleotide repeat polymorphism at the D21S258 locus.

Wehnert A, Cruts M, Backhovens H, Delabar JM, Thomas G, Van Broeckhoven C. Wehnert A, et al. Hum Mol Genet. 1992 Sep;1(6):449. doi: 10.1093/hmg/1.6.449. Hum Mol Genet. 1992. PMID: 1339475 No abstract available.

10

Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch).

Van Broeckhoven C, Haan J, Bakker E, Hardy JA, Van Hul W, Wehnert A, Vegter-Van der Vlis M, Roos RA. Van Broeckhoven C, et al. Among authors: wehnert a. Science. 1990 Jun 1;248(4959):1120-2. doi: 10.1126/science.1971458. Science. 1990. PMID: 1971458

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