Steyaert JG - Search Results

1

Steyaert JG, De la Marche W. Steyaert JG, et al. Eur J Pediatr. 2008 Oct;167(10):1091-101. doi: 10.1007/s00431-008-0764-4. Epub 2008 Jul 3. Eur J Pediatr. 2008. PMID: 18597114 Review.

2

Psychiatric genetics: the case of single gene disorders.

Steyaert J, Fryns JP. Steyaert J, et al. Eur Child Adolesc Psychiatry. 2002 Oct;11(5):201-9. doi: 10.1007/s00787-002-0284-0. Eur Child Adolesc Psychiatry. 2002. PMID: 12469237 Review.

3

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. Autism. 2004 Jun;8(2):141-61. doi: 10.1177/1362361304042719. Autism. 2004. PMID: 15165431 Review.

4

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: steyaert jg. 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

5

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: steyaert jg. 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

6

DISC1 duplication in two brothers with autism and mild mental retardation.

Crepel A, Breckpot J, Fryns JP, De la Marche W, Steyaert J, Devriendt K, Peeters H. Crepel A, et al. Clin Genet. 2010 Apr;77(4):389-94. doi: 10.1111/j.1399-0004.2009.01318.x. Epub 2009 Dec 10. Clin Genet. 2010. PMID: 20002455

7

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: steyaert jg. 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

8

An 8.9 year old girl with autism and Gorlin syndrome.

Delbroek H, Steyaert J, Legius E. Delbroek H, et al. Eur J Paediatr Neurol. 2011 May;15(3):268-70. doi: 10.1016/j.ejpn.2010.12.001. Epub 2010 Dec 28. Eur J Paediatr Neurol. 2011. PMID: 21190878

9

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.

Crepel A, Steyaert J, De la Marche W, De Wolf V, Fryns JP, Noens I, Devriendt K, Peeters H. Crepel A, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):243-5. doi: 10.1002/ajmg.b.31163. Epub 2011 Jan 11. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302354 No abstract available.

10

Quantitative autism traits in first degree relatives: evidence for the broader autism phenotype in fathers, but not in mothers and siblings.

De la Marche W, Noens I, Luts J, Scholte E, Van Huffel S, Steyaert J. De la Marche W, et al. Autism. 2012 May;16(3):247-60. doi: 10.1177/1362361311421776. Epub 2011 Sep 26. Autism. 2012. PMID: 21949002

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