Vermeesch JR - Search Results

1

Cell-free DNA methylome analysis for early preeclampsia prediction.

De Borre M, Che H, Yu Q, Lannoo L, De Ridder K, Vancoillie L, Dreesen P, Van Den Ackerveken M, Aerden M, Galle E, Breckpot J, Van Keirsbilck J, Gyselaers W, Devriendt K, Vermeesch JR, Van Calsteren K, Thienpont B. De Borre M, et al. Among authors: vermeesch jr. Nat Med. 2023 Sep;29(9):2206-2215. doi: 10.1038/s41591-023-02510-5. Epub 2023 Aug 28. Nat Med. 2023. PMID: 37640858

2

Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.

Petit P, Devriendt K, Vermeesch JR, De Cock P, Fryns JP. Petit P, et al. Among authors: vermeesch jr. Ann Genet. 1998;41(1):22-6. Ann Genet. 1998. PMID: 9599647

3

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).

Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Petit P, et al. Among authors: vermeesch jr. Genet Couns. 1998;9(3):215-21. Genet Couns. 1998. PMID: 9777345

4

Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences.

Vermeesch JR, Baten E, Fryns JP, Devriendt K. Vermeesch JR, et al. Clin Genet. 2002 Nov;62(5):415-7. doi: 10.1034/j.1399-0004.2002.620511.x. Clin Genet. 2002. PMID: 12431259

5

Partial monosomy 11q and trisomy 12q: variable expression in two siblings.

Lukusa T, Holvoet M, Vermeesch JR, Devriendt K, Fryns JP. Lukusa T, et al. Among authors: vermeesch jr. Genet Couns. 2003;14(2):155-64. Genet Couns. 2003. PMID: 12872809

6

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: vermeesch jr. Genet Couns. 2004;15(3):293-301. Genet Couns. 2004. PMID: 15517821

7

Chromosomal phenotypes and submicroscopic abnormalities.

Devriendt K, Vermeesch JR. Devriendt K, et al. Among authors: vermeesch jr. Hum Genomics. 2004 Jan;1(2):126-33. doi: 10.1186/1479-7364-1-2-126. Hum Genomics. 2004. PMID: 15601540 Free PMC article. Review.

8

Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.

Van Esch H, Hollanders K, Badisco L, Melotte C, Van Hummelen P, Vermeesch JR, Devriendt K, Fryns JP, Marynen P, Froyen G. Van Esch H, et al. Among authors: vermeesch jr. Hum Mol Genet. 2005 Jul 1;14(13):1795-803. doi: 10.1093/hmg/ddi186. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888481

9

25 Mb deletion of 13q13.3-->q21.31 in a patient without retinoblastoma.

Thienpont B, Vermeesch JR, Fryns JP. Thienpont B, et al. Among authors: vermeesch jr. Eur J Med Genet. 2005 Jul-Sep;48(3):363-6. doi: 10.1016/j.ejmg.2005.05.008. Eur J Med Genet. 2005. PMID: 16179234 No abstract available.

10

Single-cell chromosomal imbalances detection by array CGH.

Le Caignec C, Spits C, Sermon K, De Rycke M, Thienpont B, Debrock S, Staessen C, Moreau Y, Fryns JP, Van Steirteghem A, Liebaers I, Vermeesch JR. Le Caignec C, et al. Among authors: vermeesch jr. Nucleic Acids Res. 2006 May 12;34(9):e68. doi: 10.1093/nar/gkl336. Nucleic Acids Res. 2006. PMID: 16698960 Free PMC article.

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