Laatste update: 02/12/2016

Wetenschappelijke publicaties


Publicaties 2010

Diedrich K, Fauser BC, Devroey P; Evian Annual Reproduction (EVAR) Workshop Group 2009. Cancer and fertility: strategies to preserve fertility. Reprod Biomed Online. 2011 Mar;22(3):232-48. doi: 10.1016/j.rbmo.2010.11.001. Epub 2010 Nov 13. Review. PubMed PMID: 21269884.

Leyder M, Laubach M, Breugelmans M, Keymolen K, De Greve J, Foulon W. Specific congenital malformations after exposure to cyclophosphamide, epirubicin and 5-fluorouracil during the first trimester of pregnancy. Gynecol Obstet Invest. 2011;71(2):141-4. doi: 10.1159/000317264. Epub 2010 Dec 14. PubMed PMID: 21160143.

Van Landuyt L, Verpoest W, Verheyen G, De Vos A, Van de Velde H, Liebaers I, Devroey P, Van den Abbeel E. Closed blastocyst vitrification of biopsied embryos: evaluation of 100 consecutive warming cycles. Hum Reprod. 2011 Feb;26(2):316-22. doi: 10.1093/humrep/deq338. Epub 2010 Dec 7. PubMed PMID: 21138906.

Belva F, Bonduelle M, Schiettecatte J, Tournaye H, Painter RC, Devroey P, De Schepper J. Salivary testosterone concentrations in pubertal ICSI boys compared with spontaneously conceived boys. Hum Reprod. 2011 Feb;26(2):438-41. doi: 10.1093/humrep/deq345. Epub 2010 Dec 7. PubMed PMID: 21138905.

Stouffs K, Vandermaelen D, Tournaye H, Liebaers I, Lissens W. Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages. Reprod Biomed Online. 2011 Jan;22(1):65-71. doi: 10.1016/j.rbmo.2010.08.004. Epub 2010 Aug 31. PubMed PMID: 21126912.

Denayer E, Chmara M, Brems H, Kievit AM, van Bever Y, Van den Ouweland AM, Van Minkelen R, de Goede-Bolder A, Oostenbrink R, Lakeman P, Beert E, Ishizaki T, Mori T, Keymolen K, Van den Ende J, Mangold E, Peltonen S, Brice G, Rankin J, Van Spaendonck-Zwarts KY, Yoshimura A, Legius E. Legius syndrome in fourteen families. Hum Mutat. 2011 Jan;32(1):E1985-98. doi: 10.1002/humu.21404. PubMed PMID: 21089071; PubMed Central PMCID: PMC3038325.

Fiumara A, Barone R, Arena A, Filocamo M, Lissens W, Pavone L, Sorge G. Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation. Clin Genet. 2011 Nov;80(5):452-8. doi: 10.1111/j.1399-0004.2010.01572.x. Epub 2010 Nov 11. PubMed PMID: 21070211.

Robberecht K, Decock C, Stevens A, Seneca S, De Bleecker J, Leroy BP. Ptosis as an associated finding in maternally inherited diabetes and deafness. Ophthalmic Genet. 2010 Dec;31(4):240-3. doi: 10.3109/13816810.2010.520297. PubMed PMID: 21067488.

Harton GL, De Rycke M, Fiorentino F, Moutou C, SenGupta S, Traeger-Synodinos J, Harper JC; European Society for Human Reproduction and Embryology (ESHRE) PGD Consortium. ESHRE PGD consortium best practice guidelines for amplification-based PGD. Hum Reprod. 2011 Jan;26(1):33-40. doi: 10.1093/humrep/deq231. Epub 2010 Oct 21. PubMed PMID: 20966462.

Stouffs K, Lissens W, Tournaye H, Haentjens P. What about gr/gr deletions and male infertility? Systematic review and meta-analysis. Hum Reprod Update. 2011 Mar-Apr;17(2):197-209. doi: 10.1093/humupd/dmq046. Epub 2010 Oct 19. Review. PubMed PMID: 20959348.

Buysse K, Vergult S, Mussche S, Ceuterick-de Groote C, Speleman F, Menten B, Lissens W, Van Coster R. Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene. Am J Med Genet A. 2010 Nov;152A(11):2802-4. doi:10.1002/ajmg.a.33508. PubMed PMID: 20949505.

De Rycke M. Singling out genetic disorders and disease. Genome Med. 2010 Oct 6;2(10):74. doi: 10.1186/gm195. PubMed PMID: 20925967; PubMed Central PMCID: PMC2988447.

Belva F, Bonduelle M, Painter RC, Schiettecatte J, Devroey P, De Schepper J. Serum inhibin B concentrations in pubertal boys conceived by ICSI: first results. Hum Reprod. 2010 Nov;25(11):2811-4. doi: 10.1093/humrep/deq249. Epub 2010 Sep 16. PubMed PMID: 20847184.

Hannan FM, Nesbit MA, Christie PT, Lissens W, Van der Schueren B, Bex M, Bouillon R, Thakker RV. A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia. Clin Endocrinol (Oxf). 2010 Dec;73(6):715-22. doi: 10.1111/j.1365-2265.2010.03870.x.
PubMed PMID: 20846291.

Harper JC, Coonen E, De Rycke M, Harton G, Moutou C, Pehlivan T, Traeger-Synodinos J, Van Rij MC, Goossens V. ESHRE PGD Consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008. Hum Reprod. 2010 Nov;25(11):2685-707. doi: 10.1093/humrep/deq228. Epub 2010 Sep 2. PubMed PMID: 20813804.

Spits C, Seneca S, Hilven P, Liebaers I, Sermon K. Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the disease. J Med Genet. 2010 Oct;47(10):700-3.doi: 10.1136/jmg.2009.074211. Epub 2010 Jul 19. PubMed PMID: 20644219.

Kyrou D, Verpoest W, Staessen C, De Vos A, Haentjens P, Liebaers I, Devroey P. No relationship between the type of pituitary suppression for IVF and chromosomal abnormality rates of blastomeres: an observational study. Fertil Steril. 2011 Feb;95(2):563-7. doi: 10.1016/j.fertnstert.2010.05.020. Epub 2010 Jun 23. PubMed PMID: 20576261.

Donoso P, Staessen C, Collins J, Verpoest W, Fatemi HM, Papanikolaou EG, Devroey P. Prognostic factors for delivery in patients undergoing repeated pre-implantation genetic aneuploidy screening. Fertil Steril. 2010 Nov;94(6):2362-4. doi: 10.1016/j.fertnstert.2010.04.004. Epub 2010 Jun 1. PubMed PMID: 20522325.

Morán M, Marín-Buera L, Gil-Borlado MC, Rivera H, Blázquez A, Seneca S, Vázquez-López M, Arenas J, Martín MA, Ugalde C. Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency. Hum Mutat. 2010 Aug;31(8):930-41. doi: 10.1002/humu.21294. PubMed PMID: 20518024.

Bonduelle M, Oberyé J, Mannaerts B, Devroey P. Large prospective, pregnancy and infant follow-up trial assures the health of 1000 fetuses conceived after treatment with the GnRH antagonist ganirelix during controlled ovarian stimulation. Hum Reprod. 2010 Jun;25(6):1433-40. doi: 10.1093/humrep/deq072. Epub 2010 Apr 8. PubMed PMID: 20378616.

D'haene B, Hellemans J, Craen M, De Schepper J, Devriendt K, Fryns JP,
Keymolen K, Debals E, de Klein A, de Jong EM, Segers K, De Paepe A, Mortier G, Vandesompele J, De Baere E. Improved molecular diagnostics of idiopathic short stature and allied disorders: quantitative polymerase chain reaction-based copy number profiling of SHOX and pseudoautosomal region 1. J Clin Endocrinol Metab. 2010 Jun;95(6):3010-8. doi: 10.1210/jc.2009-2218. Epub 2010 Apr 7. PubMed PMID: 20375215.

Mateizel I, Spits C, De Rycke M, Liebaers I, Sermon K. Derivation, culture, and characterization of VUB hESC lines. In Vitro Cell Dev Biol Anim. 2010 Apr;46(3-4):300-8. doi: 10.1007/s11626-010-9284-4. Epub 2010 Mar 12. PubMed PMID:20224973.

Verpoest W, Seneca S, De Rademaeker M, Sermon K, De Rycke M, De Vos M, Haentjens P, Devroey P, Liebaers I. The reproductive outcome of female patients with myotonic dystrophy type 1 (DM1) undergoing PGD is not affected by the size of the expanded CTG repeat tract. J Assist Reprod Genet. 2010 Jun;27(6):327-33. doi: 10.1007/s10815-010-9392-9. Epub 2010 Mar 11. PubMed PMID: 20221684; PubMed Central PMCID: PMC2914592.

Perdu B, de Freitas F, Frints SG, Schouten M, Schrander-Stumpel C, Barbosa M, Pinto-Basto J, Reis-Lima M, de Vernejoul MC, Becker K, Freckmann ML, Keymolen K, Haan E, Savarirayan R, Koenig R, Zabel B, Vanhoenacker FM, Van Hul W. Osteopathia striata with cranial sclerosis owing to WTX gene defect. J Bone Miner Res. 2010 Jan;25(1):82-90. doi: 10.1359/jbmr.090707. PubMed PMID: 20209645.

Sequeiros J, Seneca S, Martindale J. Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias. Eur J Hum Genet. 2010 Nov;18(11):1188-95. doi: 10.1038/ejhg.2010.10. Epub 2010 Feb 24. PubMed PMID: 20179748; PubMed Central PMCID: PMC2987480.

Hoornaert KP, Vereecke I, Dewinter C, Rosenberg T, Beemer FA, Leroy JG, Bendix L, Björck E, Bonduelle M, Boute O, Cormier-Daire V, De Die-Smulders C, Dieux-Coeslier A, Dollfus H, Elting M, Green A, Guerci VI, Hennekam RC, Hilhorts-Hofstee Y, Holder M, Hoyng C, Jones KJ, Josifova D, Kaitila I, Kjaergaard S, Kroes YH, Lagerstedt K, Lees M, Lemerrer M, Magnani C, Marcelis C, Martorell L, Mathieu M, McEntagart M, Mendicino A, Morton J, Orazio G, Paquis V, Reish O, Simola KO, Smithson SF, Temple KI, Van Aken E, Van Bever Y, van den Ende J, Van Hagen JM, Zelante L, Zordania R, De Paepe A, Leroy BP, De Buyzere M, Coucke PJ, Mortier GR. Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients. Eur J Hum Genet. 2010 Aug;18(8):872-80. doi: 10.1038/ejhg.2010.23. Epub 2010 Feb 24. Erratum in: Eur J Hum Genet. 2010 Aug;18(8):881. PubMed PMID: 20179744; PubMed Central PMCID: PMC2987380.

Sequeiros J, Martindale J, Seneca S, Giunti P, Kämäräinen O, Volpini V, Weirich H, Christodoulou K, Bazak N, Sinke R, Sulek-Piatkowska A, Garcia-Planells J, Davis M, Frontali M, Hämäläinen P, Wieczorek S, Zühlke C, Saraiva-Pereira ML, Warner J, Leguern E, Thonney F, Quintáns Castro B, Jonasson J, Storm K, Andersson A, Ravani A, Correia L, Silveira I, Alonso I, Martins C, Pinto Basto J, Coutinho P, Perdigão A, Barton D, Davis M; European Molecular Quality Genetics Network. EMQN Best Practice Guidelines for molecular genetic testing of SCAs. Eur J Hum Genet. 2010 Nov;18(11):1173-6. doi: 10.1038/ejhg.2010.8. Epub 2010 Feb 24.
Erratum in: Eur J Hum Genet. 2010 Nov;18(11):1176-7. multiple author names added. PubMed PMID: 20179742; PubMed Central PMCID: PMC2987475.

Harper J, Coonen E, De Rycke M, Fiorentino F, Geraedts J, Goossens V, Harton G, Moutou C, Pehlivan Budak T, Renwick P, Sengupta S, Traeger-Synodinos J, Vesela K. What next for pre-implantation genetic screening (PGS)? A position statement
from the ESHRE PGD Consortium Steering Committee. Hum Reprod. 2010
Apr;25(4):821-3. doi: 10.1093/humrep/dep476. Epub 2010 Feb 2. PubMed PMID:
20124394.

De Brakeleer S, De Grève J, Loris R, Janin N, Lissens W, Sermijn E, Teugels E. Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families. Hum Mutat. 2010 Mar;31(3):E1175-85. doi: 10.1002/humu.21200. PubMed PMID: 20077502.

Bellavia M, Von Der Weid N, Peddes C, Jacquemont S, Liebaers I, Hohlfeld P, Wunder-Galié D, de Ziegler D. Pre-implantation genetic diagnosis (PGD) for HLA typing: bases for setting up an open international collaboration when PGD is not available. Fertil Steril. 2010 Aug;94(3):1129-31. doi: 10.1016/j.fertnstert.2009.11.007. Epub 2010 Jan 13. PubMed PMID: 20074727. Dey M, Morgan M, Bonduelle M. Filshie clip migration and retention. J Fam Plann Reprod Health Care. 2010 Jan;36(1):44-5. doi: 10.1783/147118910790291118. PubMed PMID: 20067673.

Dermaut B, Seneca S, Dom L, Smets K, Ceulemans L, Smet J, De Paepe B, Tousseyn S, Weckhuysen S, Gewillig M, Pals P, Parizel P, De Bleecker JL, Boon P, De Meirleir L, De Jonghe P, Van Coster R, Van Paesschen W, Santens P. Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C. J Neurol Neurosurg Psychiatry. 2010 Jan;81(1):90-3. doi: 10.1136/jnnp.2008.157354. PubMed PMID: 20019223.

Hendrickx JJ, Keymolen K, Desprechins B, Casselman J, Gordts F. Floating-Harbor syndrome associated with middle ear abnormalities. Am J Med Genet A. 2010 Jan;152A(1):161-4. doi: 10.1002/ajmg.a.33033. PubMed PMID: 20014123.