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Nele Bockaert

Explore the profile of Nele Bockaert including associated specialties, affiliations and a list of published articles. Areas
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Articles 4
Citations 116
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Recent Articles
1.
Meerschaut I, Rochefort D, Revencu N, Petre J, Corsello C, Rouleau G, et al.
J Med Genet . 2017 Jul; 54(9):613-623. PMID: 28735298
Background: Mutations in forkhead box protein P1 () cause intellectual disability (ID) and specific language impairment (SLI), with or without autistic features (MIM: 613670). Despite multiple case reports no specific...
2.
Adegbola A, Musante L, Callewaert B, Maciel P, Hu H, Isidor B, et al.
Eur J Hum Genet . 2015 Mar; 23(10):1308-17. PMID: 25758992
Congenital cardiac and neurodevelopmental deficits have been recently linked to the mediator complex subunit 13-like protein MED13L, a subunit of the CDK8-associated mediator complex that functions in transcriptional regulation through...
3.
De Rocker N, Vergult S, Koolen D, Jacobs E, Hoischen A, Zeesman S, et al.
Genet Med . 2014 Sep; 17(6):460-6. PMID: 25232846
Purpose: Submicroscopic deletions of chromosome band 2p25.3 are associated with intellectual disability and/or central obesity. Although MYT1L is believed to be a critical gene responsible for intellectual disability, so far...
4.
Tlili A, Hoischen A, Ripoll C, Benabou E, Badel A, Ronan A, et al.
Mol Neurobiol . 2012 Jun; 46(2):297-303. PMID: 22669612
Down syndrome or trisomy 21 is the most common genetic disorder leading to mental retardation. One feature is impaired short- and long-term spatial memory, which has been linked to altered...