Nele Bockaert
Overview
Explore the profile of Nele Bockaert including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
4
Citations
116
Followers
0
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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...