Lissens W - Search Results

1

Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer.

Amfo K, Neyns B, Teugels E, Lissens W, Bourgain C, De Sutter P, Vandamme B, Vamos E, De Grève J. Amfo K, et al. Among authors: lissens w. Oncogene. 1995 Jul 20;11(2):351-8. Oncogene. 1995. PMID: 7624149

2

Expression of the jun family of genes in human ovarian cancer and normal ovarian surface epithelium.

Neyns B, Katesuwanasing, Vermeij J, Bourgain C, Vandamme B, Amfo K, Lissens W, DeSutter P, Hooghe-Peters E, DeGrève J. Neyns B, et al. Among authors: lissens w. Oncogene. 1996 Mar 21;12(6):1247-57. Oncogene. 1996. PMID: 8649827

3

Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factor.

Vandamme B, Lissens W, Amfo K, De Sutter P, Bourgain C, Vamos E, De Grève J. Vandamme B, et al. Among authors: lissens w. Cancer Res. 1992 Dec 1;52(23):6646-52. Cancer Res. 1992. PMID: 1423308

4

De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genes.

Teugels E, De Brakeleer S, Goelen G, Lissens W, Sermijn E, De Grève J. Teugels E, et al. Among authors: lissens w. Hum Mutat. 2005 Sep;26(3):284. doi: 10.1002/humu.9366. Hum Mutat. 2005. PMID: 16088935

5

Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunit.

De Meirleir L, Lissens W, Vamos E, Liebaers I. De Meirleir L, et al. Among authors: lissens w. Hum Genet. 1992 Mar;88(6):649-52. doi: 10.1007/BF02265291. Hum Genet. 1992. PMID: 1551669

6

Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunit.

de Meirleir LJ, Lissens W, Vamos E, Liebaers I. de Meirleir LJ, et al. Among authors: lissens w. J Inherit Metab Dis. 1991;14(3):301-4. doi: 10.1007/BF01811687. J Inherit Metab Dis. 1991. PMID: 1770778 No abstract available.

7

Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A.

De Vos A, Sermon K, Van de Velde H, Joris H, Vandervorst M, Lissens W, Mortier G, De Sutter P, Löfgren A, Van Broeckhoven C, Liebaers I, Van Steirteghem A. De Vos A, et al. Among authors: lissens w. Mol Hum Reprod. 1998 Oct;4(10):978-84. doi: 10.1093/molehr/4.10.978. Mol Hum Reprod. 1998. PMID: 9809680

8

Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families.

De Brakeleer S, De Grève J, Loris R, Janin N, Lissens W, Sermijn E, Teugels E. De Brakeleer S, et al. Among authors: lissens w. Hum Mutat. 2010 Mar;31(3):E1175-85. doi: 10.1002/humu.21200. Hum Mutat. 2010. PMID: 20077502

9

Systematic detection of pathogenic alu element insertions in NGS-based diagnostic screens: the BRCA1/BRCA2 example.

De Brakeleer S, De Grève J, Lissens W, Teugels E. De Brakeleer S, et al. Among authors: lissens w. Hum Mutat. 2013 May;34(5):785-91. doi: 10.1002/humu.22297. Epub 2013 Mar 11. Hum Mutat. 2013. PMID: 23420552

10

A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis.

Seneca S, Abramowicz M, Lissens W, Muller MF, Vamos E, de Meirleir L. Seneca S, et al. Among authors: lissens w. J Inherit Metab Dis. 1996;19(2):115-8. doi: 10.1007/BF01799407. J Inherit Metab Dis. 1996. PMID: 8739943 No abstract available.

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