Dheedene A - Search Results

1

A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome.

Meerschaut I, Vergult S, Dheedene A, Menten B, De Groote K, De Wilde H, Muiño Mosquera L, Panzer J, Vandekerckhove K, Coucke PJ, De Wolf D, Callewaert B. Meerschaut I, et al. Among authors: dheedene a. Genes (Basel). 2021 Jul 8;12(7):1048. doi: 10.3390/genes12071048. Genes (Basel). 2021. PMID: 34356064 Free PMC article.

2

Expanding the Phenotype of B3GALNT2-Related Disorders.

D'haenens E, Vergult S, Menten B, Dheedene A, Kooy RF, Callewaert B. D'haenens E, et al. Among authors: dheedene a. Genes (Basel). 2022 Apr 14;13(4):694. doi: 10.3390/genes13040694. Genes (Basel). 2022. PMID: 35456500 Free PMC article.

3

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.

Raman L, Dheedene A, De Smet M, Van Dorpe J, Menten B. Raman L, et al. Among authors: dheedene a. Nucleic Acids Res. 2019 Feb 28;47(4):1605-1614. doi: 10.1093/nar/gky1263. Nucleic Acids Res. 2019. PMID: 30566647 Free PMC article.

4

Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability.

Vergult S, Dheedene A, Meurs A, Faes F, Isidor B, Janssens S, Gautier A, Le Caignec C, Menten B. Vergult S, et al. Among authors: dheedene a. Eur J Hum Genet. 2015 May;23(5):628-32. doi: 10.1038/ejhg.2014.141. Epub 2014 Jul 30. Eur J Hum Genet. 2015. PMID: 25074461 Free PMC article.

5

Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method.

Deleye L, De Coninck D, Christodoulou C, Sante T, Dheedene A, Heindryckx B, Van den Abbeel E, De Sutter P, Menten B, Deforce D, Van Nieuwerburgh F. Deleye L, et al. Among authors: dheedene a. Sci Rep. 2015 Jun 30;5:11711. doi: 10.1038/srep11711. Sci Rep. 2015. PMID: 26122179 Free PMC article.

6

Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.

Dheedene A, Sante T, De Smet M, Vanbellinghen JF, Grisart B, Vergult S, Janssens S, Menten B. Dheedene A, et al. Prenat Diagn. 2016 Aug;36(8):699-707. doi: 10.1002/pd.4841. Epub 2016 Jul 1. Prenat Diagn. 2016. PMID: 27176606 Free PMC article.

7

Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing.

Deleye L, De Coninck D, Dheedene A, De Sutter P, Menten B, Deforce D, Van Nieuwerburgh F. Deleye L, et al. Among authors: dheedene a. Sci Rep. 2016 Aug 22;6:31825. doi: 10.1038/srep31825. Sci Rep. 2016. PMID: 27546482 Free PMC article.

8

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF, Bartell T, Bernstein JA, Beyer E, Blumenthal I, Bongers EM, Brilstra EH, Brown CW, Brüggenwirth HT, Callewaert B, Chiang C, Corning K, Cox H, Cuppen E, Currall BB, Cushing T, David D, Deardorff MA, Dheedene A, D'Hooghe M, de Vries BB, Earl DL, Ferguson HL, Fisher H, FitzPatrick DR, Gerrol P, Giachino D, Glessner JT, Gliem T, Grady M, Graham BH, Griffis C, Gripp KW, Gropman AL, Hanson-Kahn A, Harris DJ, Hayden MA, Hill R, Hochstenbach R, Hoffman JD, Hopkin RJ, Hubshman MW, Innes AM, Irons M, Irving M, Jacobsen JC, Janssens S, Jewett T, Johnson JP, Jongmans MC, Kahler SG, Koolen DA, Korzelius J, Kroisel PM, Lacassie Y, Lawless W, Lemyre E, Leppig K, Levin AV, Li H, Li H, Liao EC, Lim C, Lose EJ, Lucente D, Macera MJ, Manavalan P, Mandrile G, Marcelis CL, Margolin L, Mason T, Masser-Frye D, McClellan MW, Mendoza CJ, Menten B, Middelkamp S, Mikami LR, Moe E, Mohammed S, Mononen T, Mortenson ME, Moya G, Nieuwint AW, Ordulu Z, Parkash S, Pauker SP, … See abstract for full author list ➔ Redin C, et al. Among authors: dheedene a. Nat Genet. 2017 Jan;49(1):36-45. doi: 10.1038/ng.3720. Epub 2016 Nov 14. Nat Genet. 2017. PMID: 27841880 Free PMC article.

9

Shallow Whole Genome Sequencing on Circulating Cell-Free DNA Allows Reliable Noninvasive Copy-Number Profiling in Neuroblastoma Patients.

Van Roy N, Van Der Linden M, Menten B, Dheedene A, Vandeputte C, Van Dorpe J, Laureys G, Renard M, Sante T, Lammens T, De Wilde B, Speleman F, De Preter K. Van Roy N, et al. Among authors: dheedene a. Clin Cancer Res. 2017 Oct 15;23(20):6305-6314. doi: 10.1158/1078-0432.CCR-17-0675. Epub 2017 Jul 14. Clin Cancer Res. 2017. PMID: 28710315

10

Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability.

Van Paemel R, De Bruyne P, van der Straaten S, D'hondt M, Fränkel U, Dheedene A, Menten B, Callewaert B. Van Paemel R, et al. Among authors: dheedene a. Am J Med Genet A. 2017 Nov;173(11):3104-3108. doi: 10.1002/ajmg.a.38407. Epub 2017 Sep 8. Am J Med Genet A. 2017. PMID: 28884947

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