Fryns JP - Search Results

1

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

2

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: fryns jp. 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

3

Psychiatric genetics: the case of single gene disorders.

Steyaert J, Fryns JP. Steyaert J, et al. Among authors: fryns jp. 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.

4

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse.

Peeters H, Debeer P, Bairoch A, Wilquet V, Huysmans C, Parthoens E, Fryns JP, Gewillig M, Nakamura Y, Niikawa N, Van de Ven W, Devriendt K. Peeters H, et al. Among authors: fryns jp. Hum Genet. 2003 May;112(5-6):573-80. doi: 10.1007/s00439-003-0917-5. Epub 2003 Feb 27. Hum Genet. 2003. PMID: 12607115

5

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.

Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K. Lukusa T, et al. Among authors: fryns jp. Genet Couns. 2004;15(3):293-301. Genet Couns. 2004. PMID: 15517821

6

Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutation.

Debeer P, Huysmans C, Van de Ven WJ, Fryns JP, Devriendt K. Debeer P, et al. Among authors: fryns jp. Am J Med Genet A. 2005 Apr 30;134(3):318-20. doi: 10.1002/ajmg.a.30645. Am J Med Genet A. 2005. PMID: 15736221

7

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: fryns jp. 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.

8

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.

Thienpont B, Mertens L, de Ravel T, Eyskens B, Boshoff D, Maas N, Fryns JP, Gewillig M, Vermeesch JR, Devriendt K. Thienpont B, et al. Among authors: fryns jp. Eur Heart J. 2007 Nov;28(22):2778-84. doi: 10.1093/eurheartj/ehl560. Epub 2007 Mar 23. Eur Heart J. 2007. PMID: 17384091

9

Glypican 1 gene: good candidate for brachydactyly type E.

Syrrou M, Keymolen K, Devriendt K, Holvoet M, Thoelen R, Verhofstadt K, Fryns JP. Syrrou M, et al. Among authors: fryns jp. Am J Med Genet. 2002 Apr 1;108(4):310-4. doi: 10.1002/ajmg.10266. Am J Med Genet. 2002. PMID: 11920836

10

Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasia.

Groenen PM, Garcia E, Thoelen R, Aly M, Schoenmakers EF, Devriendt K, Fryns JP, Van de Ven WJ. Groenen PM, et al. Among authors: fryns jp. Cytogenet Cell Genet. 1996;75(4):210-5. doi: 10.1159/000134485. Cytogenet Cell Genet. 1996. PMID: 9067426

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