Sleegers K - Search Results

1

Multiomics profiling of human plasma and cerebrospinal fluid reveals ATN-derived networks and highlights causal links in Alzheimer's disease.

Shi L, Xu J, Green R, Wretlind A, Homann J, Buckley NJ, Tijms BM, Vos SJB, Lill CM, Kate MT, Engelborghs S, Sleegers K, Frisoni GB, Wallin A, Lleó A, Popp J, Martinez-Lage P, Streffer J, Barkhof F, Zetterberg H, Visser PJ, Lovestone S, Bertram L, Nevado-Holgado AJ, Proitsi P, Legido-Quigley C. Shi L, et al. Among authors: sleegers k. Alzheimers Dement. 2023 Aug;19(8):3350-3364. doi: 10.1002/alz.12961. Epub 2023 Feb 15. Alzheimers Dement. 2023. PMID: 36790009

2

The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years.

Brouwers N, Sleegers K, Engelborghs S, Bogaerts V, van Duijn CM, De Deyn PP, Van Broeckhoven C, Dermaut B. Brouwers N, et al. Among authors: sleegers k. Neurosci Lett. 2006 Jan 9;392(1-2):72-4. doi: 10.1016/j.neulet.2005.08.064. Epub 2005 Oct 6. Neurosci Lett. 2006. PMID: 16214290

3

Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease.

Theuns J, Brouwers N, Engelborghs S, Sleegers K, Bogaerts V, Corsmit E, De Pooter T, van Duijn CM, De Deyn PP, Van Broeckhoven C. Theuns J, et al. Among authors: sleegers k. Am J Hum Genet. 2006 Jun;78(6):936-46. doi: 10.1086/504044. Epub 2006 Apr 10. Am J Hum Genet. 2006. PMID: 16685645 Free PMC article.

4

DNMBP is genetically associated with Alzheimer dementia in the Belgian population.

Bettens K, Brouwers N, Engelborghs S, De Pooter T, De Deyn PP, Sleegers K, Van Broeckhoven C. Bettens K, et al. Among authors: sleegers k. Neurobiol Aging. 2009 Dec;30(12):2000-9. doi: 10.1016/j.neurobiolaging.2008.02.003. Epub 2008 Mar 24. Neurobiol Aging. 2009. PMID: 18359537

5

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population.

Bettens K, Brouwers N, Engelborghs S, De Deyn PP, Van Broeckhoven C, Sleegers K. Bettens K, et al. Among authors: sleegers k. Hum Mutat. 2008 May;29(5):769-70. doi: 10.1002/humu.20725. Hum Mutat. 2008. PMID: 18407551

6

The association between APOE genotype and memory dysfunction in subjects with mild cognitive impairment is related to age and Alzheimer pathology.

Ramakers IH, Visser PJ, Aalten P, Bekers O, Sleegers K, van Broeckhoven CL, Jolles J, Verhey FR. Ramakers IH, et al. Among authors: sleegers k. Dement Geriatr Cogn Disord. 2008;26(2):101-8. doi: 10.1159/000144072. Epub 2008 Jul 11. Dement Geriatr Cogn Disord. 2008. PMID: 18617739 Free article.

7

Common variation in GRB-associated Binding Protein 2 (GAB2) and increased risk for Alzheimer dementia.

Sleegers K, Bettens K, Brouwers N, Engelborghs S, van Miegroet H, De Deyn PP, Van Broeckhoven C. Sleegers K, et al. Hum Mutat. 2009 Feb;30(2):E338-44. doi: 10.1002/humu.20909. Hum Mutat. 2009. PMID: 18853460

8

No association between CALHM1 and risk for Alzheimer dementia in a Belgian population.

Sleegers K, Brouwers N, Bettens K, Engelborghs S, van Miegroet H, De Deyn PP, Van Broeckhoven C. Sleegers K, et al. Hum Mutat. 2009 Apr;30(4):E570-4. doi: 10.1002/humu.20990. Hum Mutat. 2009. PMID: 19191332

9

APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease.

Bettens K, Brouwers N, Engelborghs S, Van Miegroet H, De Deyn PP, Theuns J, Sleegers K, Van Broeckhoven C. Bettens K, et al. Among authors: sleegers k. Hum Mutat. 2009 Aug;30(8):1207-13. doi: 10.1002/humu.21027. Hum Mutat. 2009. PMID: 19462468

10

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.

Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, Heun R, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J. Harold D, et al. Among authors: sleegers k. Nat Genet. 2009 Oct;41(10):1088-93. doi: 10.1038/ng.440. Epub 2009 Sep 6. Nat Genet. 2009. PMID: 19734902 Free PMC article.

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