Cruts M - Search Results

1

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.

Philtjens S, Van Mossevelde S, van der Zee J, Wauters E, Dillen L, Vandenbulcke M, Vandenberghe R, Ivanoiu A, Sieben A, Willems C, Benussi L, Ghidoni R, Binetti G, Borroni B, Padovani A, Pastor P, Diez-Fairen M, Aguilar M, de Mendonça A, Miltenberger-Miltényi G, Hernández I, Boada M, Ruiz A, Nacmias B, Sorbi S, Almeida MR, Santana I, Clarimón J, Lleó A, Frisoni GB, Sanchez-Valle R, Lladó A, Gómez-Tortosa E, Gelpi E, Van den Broeck M, Peeters K, Cras P, De Deyn PP, Engelborghs S, Cruts M, Van Broeckhoven C; BELNEU Consortium; EU EOD Consortium. Philtjens S, et al. Among authors: cruts m. Neurobiol Aging. 2018 Jun;66:181.e3-181.e10. doi: 10.1016/j.neurobiolaging.2018.02.011. Epub 2018 Feb 17. Neurobiol Aging. 2018. PMID: 29555433 Free article.

2

Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3.

Van Broeckhoven C, Backhovens H, Cruts M, De Winter G, Bruyland M, Cras P, Martin JJ. Van Broeckhoven C, et al. Among authors: cruts m. Nat Genet. 1992 Dec;2(4):335-9. doi: 10.1038/ng1292-335. Nat Genet. 1992. PMID: 1303290

3

Dinucleotide repeat polymorphism at the D21S258 locus.

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

4

Dinucleotide repeat polymorphism at the D21S145 locus.

Cruts M, Backhovens H, Van Broeckhoven C. Cruts M, et al. Nucleic Acids Res. 1992 Mar 11;20(5):1159. Nucleic Acids Res. 1992. PMID: 1549494 Free PMC article.

5

Dinucleotide repeat polymorphism at the D21S16 [correction of D1S16] locus.

Cruts M, Backhovens H, Van Broeckhoven C. Cruts M, et al. Nucleic Acids Res. 1992 Mar 11;20(5):1159. Nucleic Acids Res. 1992. PMID: 1549495 Free PMC article.

6

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: cruts m. Genomics. 1992 Jan;12(1):158-60. doi: 10.1016/0888-7543(92)90420-w. Genomics. 1992. PMID: 1733854

7

Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3.

Cruts M, Backhovens H, Theuns J, Clark RF, Le Paslier D, Weissenbach J, Goate AM, Martin JJ, Van Broeckhoven C. Cruts M, et al. Hum Mol Genet. 1995 Aug;4(8):1355-64. doi: 10.1093/hmg/4.8.1355. Hum Mol Genet. 1995. PMID: 7581374

8

Genetic analysis of the cellular oncogene fos in patients with chromosome 14 encoded Alzheimer's disease.

Cruts M, Backhovens H, Martin JJ, van Broeckhoven C. Cruts M, et al. Neurosci Lett. 1994 Jun 6;174(1):97-100. doi: 10.1016/0304-3940(94)90128-7. Neurosci Lett. 1994. PMID: 7970166

9

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. Hum Mol Genet. 1998 Jan;7(1):43-51. doi: 10.1093/hmg/7.1.43. Hum Mol Genet. 1998. PMID: 9384602

10

Presenilin mutations in Alzheimer's disease.

Cruts M, Van Broeckhoven C. Cruts M, et al. Hum Mutat. 1998;11(3):183-90. doi: 10.1002/(SICI)1098-1004(1998)11:3<183::AID-HUMU1>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9521418 Review.

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