Nuytemans K - Search Results

1

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.

Nuytemans K, Rademakers R, Theuns J, Pals P, Engelborghs S, Pickut B, de Pooter T, Peeters K, Mattheijssens M, Van den Broeck M, Cras P, De Deyn PP, van Broeckhoven C. Nuytemans K, et al. Eur J Hum Genet. 2008 Apr;16(4):471-9. doi: 10.1038/sj.ejhg.5201986. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197194

2

Explainable machine learning aggregates polygenic risk scores and electronic health records for Alzheimer's disease prediction.

Gao XR, Chiariglione M, Qin K, Nuytemans K, Scharre DW, Li YJ, Martin ER. Gao XR, et al. Among authors: nuytemans k. Sci Rep. 2023 Jan 9;13(1):450. doi: 10.1038/s41598-023-27551-1. Sci Rep. 2023. PMID: 36624143 Free PMC article.

3

Celis K, Moreno MDMM, Rajabli F, Whitehead P, Hamilton-Nelson K, Dykxhoorn DM, Nuytemans K, Wang L, Flanagan M, Weintraub S, Geula C, Gearing M, Dalgard CL, Jin F, Bennett DA, Schuck T, Pericak-Vance MA, Griswold AJ, Young JI, Vance JM. Celis K, et al. Among authors: nuytemans k. Alzheimers Dement. 2023 Sep;19(9):3902-3915. doi: 10.1002/alz.13075. Epub 2023 Apr 10. Alzheimers Dement. 2023. PMID: 37037656 Free PMC article.

4

Identification of novel genes for age-at-onset of Alzheimer's disease by combining quantitative and survival trait analyses.

Li YJ, Nuytemans K, La JO, Jiang R, Slifer SH, Sun S, Naj A, Gao XR, Martin ER. Li YJ, et al. Among authors: nuytemans k. Alzheimers Dement. 2023 Jul;19(7):3148-3157. doi: 10.1002/alz.12927. Epub 2023 Feb 4. Alzheimers Dement. 2023. PMID: 36738287

5

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, Mattheijssens M, Peeters K, Sciot R, Martin JJ, Cras P, Santens P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, Sleegers K. Brouwers N, et al. Among authors: nuytemans k. Arch Neurol. 2007 Oct;64(10):1436-46. doi: 10.1001/archneur.64.10.1436. Arch Neurol. 2007. PMID: 17923627

6

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

Haugarvoll K, Rademakers R, Kachergus JM, Nuytemans K, Ross OA, Gibson JM, Tan EK, Gaig C, Tolosa E, Goldwurm S, Guidi M, Riboldazzi G, Brown L, Walter U, Benecke R, Berg D, Gasser T, Theuns J, Pals P, Cras P, De Deyn PP, Engelborghs S, Pickut B, Uitti RJ, Foroud T, Nichols WC, Hagenah J, Klein C, Samii A, Zabetian CP, Bonifati V, Van Broeckhoven C, Farrer MJ, Wszolek ZK. Haugarvoll K, et al. Among authors: nuytemans k. Neurology. 2008 Apr 15;70(16 Pt 2):1456-60. doi: 10.1212/01.wnl.0000304044.22253.03. Epub 2008 Mar 12. Neurology. 2008. PMID: 18337586 Free PMC article.

7

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.

Bogaerts V, Nuytemans K, Reumers J, Pals P, Engelborghs S, Pickut B, Corsmit E, Peeters K, Schymkowitz J, De Deyn PP, Cras P, Rousseau F, Theuns J, Van Broeckhoven C. Bogaerts V, et al. Among authors: nuytemans k. Hum Mutat. 2008 Jun;29(6):832-40. doi: 10.1002/humu.20713. Hum Mutat. 2008. PMID: 18401856

8

Progranulin variability has no major role in Parkinson disease genetic etiology.

Nuytemans K, Pals P, Sleegers K, Engelborghs S, Corsmit E, Peeters K, Pickut B, Mattheijssens M, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C. Nuytemans K, et al. Neurology. 2008 Oct 7;71(15):1147-51. doi: 10.1212/01.wnl.0000327563.10320.2b. Neurology. 2008. PMID: 18838661

9

GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population.

Meeus B, Nuytemans K, Crosiers D, Engelborghs S, Pals P, Pickut B, Peeters K, Mattheijssens M, Corsmit E, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C. Meeus B, et al. Among authors: nuytemans k. Neurobiol Aging. 2011 Feb;32(2):308-12. doi: 10.1016/j.neurobiolaging.2009.02.016. Epub 2009 Mar 24. Neurobiol Aging. 2011. PMID: 19321232

10

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

Nuytemans K, Meeus B, Crosiers D, Brouwers N, Goossens D, Engelborghs S, Pals P, Pickut B, Van den Broeck M, Corsmit E, Cras P, De Deyn PP, Del-Favero J, Van Broeckhoven C, Theuns J. Nuytemans K, et al. Hum Mutat. 2009 Jul;30(7):1054-61. doi: 10.1002/humu.21007. Hum Mutat. 2009. PMID: 19405094

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