Devriendt K - Search Results

1

Association of CDH11 with non-syndromic ASD.

Crepel A, De Wolf V, Brison N, Ceulemans B, Walleghem D, Peuteman G, Lambrechts D, Steyaert J, Noens I, Devriendt K, Peeters H. Crepel A, et al. Among authors: devriendt k. Am J Med Genet B Neuropsychiatr Genet. 2014 Jul;165B(5):391-8. doi: 10.1002/ajmg.b.32243. Epub 2014 May 19. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24839052

2

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

Castermans D, Wilquet V, Steyaert J, Van de Ven W, Fryns JP, Devriendt K. Castermans D, et al. Among authors: devriendt k. Autism. 2004 Jun;8(2):141-61. doi: 10.1177/1362361304042719. Autism. 2004. PMID: 15165431 Review.

3

Human laterality disorders.

Peeters H, Devriendt K. Peeters H, et al. Among authors: devriendt k. Eur J Med Genet. 2006 Sep-Oct;49(5):349-62. doi: 10.1016/j.ejmg.2005.12.003. Epub 2006 Jan 3. Eur J Med Genet. 2006. PMID: 16461029 Review.

4

Focal preauricular dermal dysplasia: distinctive congenital lesions with a bilateral and symmetric distribution.

Prescott T, Devriendt K, Hamel B, Pasch MC, Peeters H, Vander Poorten V, Tallerås O. Prescott T, et al. Among authors: devriendt k. Eur J Med Genet. 2006 Mar-Apr;49(2):135-9. doi: 10.1016/j.ejmg.2005.06.005. Epub 2005 Aug 11. Eur J Med Genet. 2006. PMID: 16530710 Review.

5

Two female siblings with congenital heart disease, postaxial polydactyly, ectopic neuropituitary gland, hair anomalies and characteristic facial features: a new syndrome?

Goossens L, Janssens S, Meersschaut V, Peeters H, Devlieger H, Devriendt K. Goossens L, et al. Among authors: devriendt k. Clin Dysmorphol. 2006 Apr;15(2):71-4. doi: 10.1097/01.mcd.0000194409.30794.66. Clin Dysmorphol. 2006. PMID: 16531731

6

Sesn1 is a novel gene for left-right asymmetry and mediating nodal signaling.

Peeters H, Voz ML, Verschueren K, De Cat B, Pendeville H, Thienpont B, Schellens A, Belmont JW, David G, Van De Ven WJ, Fryns JP, Gewillig M, Huylebroeck D, Peers B, Devriendt K. Peeters H, et al. Among authors: devriendt k. Hum Mol Genet. 2006 Nov 15;15(22):3369-77. doi: 10.1093/hmg/ddl413. Epub 2006 Oct 12. Hum Mol Genet. 2006. PMID: 17038485 Free article.

7

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Castermans D, Vermeesch JR, Fryns JP, Steyaert JG, Van de Ven WJ, Creemers JW, Devriendt K. Castermans D, et al. Among authors: devriendt k. Eur J Hum Genet. 2007 Apr;15(4):422-31. doi: 10.1038/sj.ejhg.5201785. Epub 2007 Feb 7. Eur J Hum Genet. 2007. PMID: 17290275

8

Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autism.

Castermans D, Thienpont B, Volders K, Crepel A, Vermeesch JR, Schrander-Stumpel CT, Van de Ven WJ, Steyaert JG, Creemers JW, Devriendt K. Castermans D, et al. Among authors: devriendt k. Eur J Hum Genet. 2008 Oct;16(10):1187-92. doi: 10.1038/ejhg.2008.71. Epub 2008 Apr 16. Eur J Hum Genet. 2008. PMID: 18414512

9

Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4.

Backx L, Ceulemans B, Vermeesch JR, Devriendt K, Van Esch H. Backx L, et al. Among authors: devriendt k. Eur J Hum Genet. 2009 Mar;17(3):378-82. doi: 10.1038/ejhg.2008.180. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854870 Free PMC article.

10

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

Castermans D, Volders K, Crepel A, Backx L, De Vos R, Freson K, Meulemans S, Vermeesch JR, Schrander-Stumpel CT, De Rijk P, Del-Favero J, Van Geet C, Van De Ven WJ, Steyaert JG, Devriendt K, Creemers JW. Castermans D, et al. Among authors: devriendt k. Hum Mol Genet. 2010 Apr 1;19(7):1368-78. doi: 10.1093/hmg/ddq013. Epub 2010 Jan 12. Hum Mol Genet. 2010. PMID: 20071347

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