Laatste update: 02/12/2016

Wetenschappelijke publicaties


Publicaties 2007

Limaye N, Revencu N, Van Regemorter N, Garzon M, Bonduelle M, Chung W, Daras MD, Fahey MC, Garrett C, Gillerot Y, Gillessen-Kaesbach G, Giménez-Arnau A, Guzzetta F, Battaglia D, Heimdal K, Lissens W, Taub E, Van Maldergem L, Van Paesschen W, Wieczorek D, Wood NW, Boon L, Vikkula M. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. Hum Genet. 2007 Dec;122(5):552. PubMed PMID: 18383597.

Goossens V, De Rycke M, De Vos A, Staessen C, Michiels A, Verpoest W, Van Steirteghem A, Bertrand C, Liebaers I, Devroey P, Sermon K. Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for pre-implantation genetic diagnosis. Hum Reprod. 2008 Mar;23(3):481-92. Epub 2007 Dec 22. PubMed PMID: 18156649.

Meulemans A, Gerlo E, Seneca S, Lissens W, Smet J, Van Coster R, De Meirleir L. The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disorders. Acta Neurol Belg. 2007 Sep;107(3):78-83. PubMed PMID: 18072335.

Mathys R, Deconinck H, Keymolen K, Jansen A, Van Esch H. Severe visual impairment and retinal changes in a boy with a deletion of the gene for Nance-Horan syndrome. Bull Soc Belge Ophtalmol. 2007;(305):49-53. PubMed PMID: 18018428.

Jansen AC, Cao H, Kaplan P, Silver K, Leonard G, De Meirleir L, Lissens W, Liebaers I, Veilleux M, Andermann F, Hegele RA, Andermann E. Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene. Arch Neurol. 2007 Nov;64(11):1629-34. PubMed PMID: 17998446.

Leunens L, Celestin-Westreich S, Bonduelle M, Liebaers I, Ponjaert-Kristoffersen I. Follow-up of cognitive and motor development of 10-year-old singleton children born after ICSI compared with spontaneously conceived children. Hum Reprod. 2008 Jan;23(1):105-11. Epub 2007 Nov 2. PubMed PMID: 17981820.

Scalais E, Nuttin C, Seneca S, Smet J, De Paepe B, Martin JJ, Stevens R, Pierart F, Battisti O, Lissens W, De Meirleir L, Van Coster R. Infantile presentation of the mitochondrial A8344G mutation. Eur J Neurol. 2007 Nov;14(11):e3-5. PubMed PMID: 17956438.

Sermon K, De Rycke M. Single cell polymerase chain reaction for pre-implantation genetic diagnosis: methods, strategies, and limitations. Methods Mol Med. 2007;132:31-42. PubMed PMID: 17876074.

Meulemans A, De Paepe B, De Bleecker J, Smet J, Lissens W, Van Coster R, De Meirleir L, Seneca S. Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy. Arch Neurol. 2007 Sep;64(9):1339-43. PubMed PMID: 17846276.

Mutesa L, Muganga N, Lissens W, Boemer F, Schoos R, Pierquin G, Bours V. Molecular analysis in two siblings African patients with severe form of Hunter Syndrome: identification of a novel (p.Y54X) nonsense mutation. J Trop Pediatr. 2007 Dec;53(6):434-7. Epub 2007 Jul 5. PubMed PMID: 17616540.

Kajosch H, Vanderbruggen N, Keymolen K, D'haenen H, de Baerdemaeker E. [Mild mental retardation and complex psychiatric symptoms are accompanied by submicroscopic sub-telomeric deletion of a long arm of chromosome 3. A case study]. Tijdschr Psychiatr. 2007;49(6):405-9. Review. Dutch. PubMed PMID: 17611941.

Lissens W, Arena A, Seneca S, Rafi M, Sorge G, Liebaers I, Wenger D, Fiumara A. A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) region. Hum Mutat. 2007 Jul;28(7):742. PubMed PMID: 17579360.

de Wert G, Liebaers I, Van de Velde H. The future (r)evolution of pre-implantation genetic diagnosis/human leukocyte antigen testing: ethical reflections. Stem Cells. 2007 Sep;25(9):2167-72. Epub 2007 May 24. PubMed PMID: 17525240.

Balikova I, Menten B, de Ravel T, Le Caignec C, Thienpont B, Urbina M, Doco-Fenzy M, de Rademaeker M, Mortier G, Kooy F, van den Ende J, Devriendt K, Fryns JP, Speleman F, Vermeesch JR. Subtelomeric imbalances in phenotypically normal individuals. Hum Mutat. 2007 Oct;28(10):958-67. PubMed PMID: 17492636.

Spits C, Le Caignec C, De Rycke M, Van Haute L, Van Steirteghem A, Liebaers I, Sermon K. Whole-genome multiple displacement amplification from single cells. Nat Protoc. 2006;1(4):1965-70. Epub 2006 Nov 30. PubMed PMID: 17487184.

Storm K, Moens E, Vits L, De Vlieger H, Delaere G, D'Hollander M, Wuyts W, Biervliet M, Van Schil L, Desager K, Nöthen MM. High incidence of the CFTR mutations 3272-26A-->G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A-->G, E588V, and 1671insTATCA). J Cyst Fibros. 2007 Nov 30;6(6):371-5. Epub 2007 May 3. Erratum in: J Cyst Fibros. 2008 Sep;7(5):461. PubMed PMID: 17481968.

Massaad D, Poppe K, Lissens W, Velkeniers B. A case of thyroid hormone resistance: Prospective follow-up during pregnancy and obstetric outcome. Eur J Intern Med. 2007 May;18(3):253-4. PubMed PMID: 17449404.

De Brakeleer S, Bogdani M, De Grève J, Decock J, Sermijn E, Bonduelle M, Goelen G, Teugels E. Loss of nuclear BRCA1 protein staining in normal tissue cells derived from BRCA1 and BRCA2 mutation carriers. Mutat Res. 2007 Jun 1;619(1-2):104-12. Epub 2007 Mar 12. PubMed PMID: 17445839.

Keymolen K, Goossens V, De Rycke M, Sermon K, Boelaert K, Bonduelle M, Van Steirteghem A, Liebaers I. Clinical outcome of pre-implantation genetic diagnosis for cystic fibrosis: the Brussels' experience. Eur J Hum Genet. 2007 Jul;15(7):752-8. Epub 2007 Apr 18. PubMed PMID: 17440499.

Morava E, Zeevaert R, Korsch E, Huijben K, Wopereis S, Matthijs G, Keymolen K, Lefeber DJ, De Meirleir L, Wevers RA. A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia. Eur J Hum Genet. 2007 Jun;15(6):638-45. Epub 2007 Mar 14. Erratum in: Eur J Hum Genet. 2007 Jul;15(7):819. PubMed PMID: 17356545.

Spits C, De Rycke M, Van Ranst N, Verpoest W, Lissens W, Van Steirteghem A, Liebaers I, Sermon K. Pre-implantation genetic diagnosis for cancer predisposition syndromes. Prenat Diagn. 2007 May;27(5):447-56. PubMed PMID: 17330926.

Geuns E, De Temmerman N, Hilven P, Van Steirteghem A, Liebaers I, De Rycke M. Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human. Eur J Hum Genet. 2007 Mar;15(3):352-61. Epub 2007 Jan 10. PubMed PMID: 17213841.

Donoso P, Verpoest W, Papanikolaou EG, Liebaers I, Fatemi HM, Sermon K, Staessen C, Van der Elst J, Devroey P. Single embryo transfer in pre-implantation genetic diagnosis cycles for women <36 years does not reduce delivery rate. Hum Reprod. 2007 Apr;22(4):1021-5. Epub 2007 Jan 4. PubMed PMID: 17204531.