Laatste update: 02/12/2016

Wetenschappelijke publicaties


Publicaties 2011

The International Stem Cell Initiative, Amps K, Andrews PW, Anyfantis G, Armstrong L, Avery S, Baharvand H, Baker J, Baker D, Munoz MB, Beil S, Benvenisty N, Ben-Yosef D, Biancotti JC, Bosman A, Brena RM, Brison D, Caisander G, Camarasa MV, Chen J, Chiao E, Choi YM, Choo AB, Collins D, Colman A, Crook JM, Daley GQ, Dalton A, De Sousa PA, Denning C, Downie J, Dvorak P, Montgomery KD, Feki A, Ford A, Fox V, Fraga AM, Frumkin T, Ge L, Gokhale PJ, Golan-Lev T, Gourabi H, Gropp M, Guangxiu L, Hampl A, Harron K, Healy L, Herath W, Holm F, Hovatta O, Hyllner J, Inamdar MS, Irwanto AK, Ishii T, Jaconi M, Jin Y, Kimber S, Kiselev S, Knowles BB, Kopper O, Kukharenko V, Kuliev A, Lagarkova MA, Laird PW, Lako M, Laslett AL, Lavon N, Lee DR, Lee JE, Li C, Lim LS, Ludwig TE, Ma Y, Maltby E, Mateizel I, Mayshar Y, Mileikovsky M, Minger SL, Miyazaki T, Moon SY, Moore H, Mummery C, Nagy A, Nakatsuji N, Narwani K, Oh SK, Oh SK, Olson C, Otonkoski T, Pan F, Park IH, Pells S, Pera MF, Pereira LV, Qi O, Raj GS, Reubinoff B, Robins A, Robson P, Rossant J, Salekdeh GH, Schulz TC, Sermon K, Mohamed JS, Shen H, Sherrer E, Sidhu K, Sivarajah S, Skottman H, Spits C, Stacey GN, Strehl R, Strelchenko N, Suemori H, Sun B, Suuronen R, Takahashi K, Tuuri T, Venu P, Verlinsky Y, Oostwaard DW, Weisenberger DJ, Wu Y, Yamanaka S, Young L, Zhou Q. Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage. Nat Biotechnol. 2011 Nov 27. doi: 10.1038/nbt.2051. [Epub ahead of print] PubMed PMID: 22119741.

Geraedts J, Montag M, Magli MC, Repping S, Handyside A, Staessen C, Harper J, Schmutzler A, Collins J, Goossens V, van der Ven H, Vesela K, Gianaroli L. Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results. Hum Reprod. 2011 Nov;26(11):3173-80. Epub 2011 Sep 9. PubMed PMID: 21908463; PubMed Central PMCID: PMC3196878.

Orlando C, Lissens W, Hasaerts D, Jochmans K. Identification of two de novo mutations responsible for type I antithrombin deficiency. Thromb Haemost. 2011 Nov 24;107(1). [Epub ahead of print] PubMed PMID: 22116592.

Belva F, Painter R, Bonduelle M, Roelants M, Devroey P, De Schepper J. Are ICSI adolescents at risk for increased adiposity? Hum Reprod. 2011 Nov 11. [Epub ahead of print] PubMed PMID: 22081314.

Van Rij MC, De Rademaeker M, Moutou C, Dreesen JC, De Rycke M, Liebaers I, Geraedts JP, De Die-Smulders CE, Viville S. Pre-implantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres. Eur J Hum Genet. 2011 Nov 9. doi: 10.1038/ejhg.2011.202. [Epub ahead of print] PubMed PMID: 22071896.

Keymolen K, Staessen C, Verpoest W, Liebaers I, Bonduelle M. Pre-implantation genetic diagnosis in female and male carriers of reciprocal translocations: clinical outcome until delivery of 312 cycles. Eur J Hum Genet. 2011 Nov 9. doi: 10.1038/ejhg.2011.208. [Epub ahead of print] PubMed PMID: 22071893.

Desmyttere S, De Rycke M, Staessen C, Liebaers I, De Schrijver F, Verpoest W, Haentjens P, Bonduelle M. Neonatal follow-up of 995 consecutively born children after embryo biopsy for PGD. Hum Reprod. 2011 Nov 2. [Epub ahead of print] PubMed PMID: 22048989.

Nekkebroeck J, Van den Broeck W, Desmyttere S, Ponjaert-Kristoffersen I, Bonduelle M. The mental, motor, socio-emotional and language development of 2-year-old twins born after PGD/PGS and parental well-being. Hum Reprod. 2011 Oct 24. [Epub ahead of print] PubMed PMID: 22025226.

Claes K, Dahan K, Tejpar S, De Paepe A, Bonduelle M, Abramowicz M, Verellen C, Franchimont D, Van Cutsem E, Kartheuser A. The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP). Acta Gastroenterol Belg. 2011 Sep;74(3):421-6. PubMed PMID: 22103048.

Renard M, Callewaert B, Baetens M, Campens L, Macdermot K, Fryns JP, Bonduelle M, Dietz HC, Gaspar IM, Cavaco D, Stattin EL, Schrander-Stumpel C, Coucke P, Loeys B, De Paepe A, De Backer J. Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFß signaling in FTAAD. Int J Cardiol. 2011 Sep 19. [Epub ahead of print] PubMed PMID: 21937134.

Bissay V, Keymolen K, Lissens W, Schmedding E, De Keyser J. A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperature. J Neurol Sci. 2011 Sep 15;308(1-2):162-4. Epub 2011 Jul 14. PubMed PMID: 21752396.

Keymolen K, Van Berkel K, Vorsselmans A, Staessen C, Liebaers I. Pregnancy outcome in carriers of Robertsonian translocations. Am J Med Genet A. 2011 Oct;155A(10):2381-5. doi: 10.1002/ajmg.a.33941. Epub 2011 Sep 9. PubMed PMID: 21910218.

Tort F, Del Toro M, Lissens W, Montoya J, Fernàndez-Burriel M, Font A, Buján N, Navarro-Sastre A, López-Gallardo E, Arranz JA, Riudor E, Briones P, Ribes A. Screening for nuclear genetic defects in the ATP synthase-associated genes TMEM70, ATP12 and ATP5E in patients with 3-methylglutaconic aciduria. Clin Genet. 2011 Sep;80(3):297-300. doi: 10.1111/j.1399-0004.2011.01650.x. PubMed PMID: 21815885.

Bissay V, Keymolen K, Lissens W, Laureys G, Schmedding E, Keyser JD. Late onset painful cold-aggravated myotonia: three families with SCN4A L1436P mutation. Neuromuscul Disord. 2011 Aug;21(8):590-3. doi: 10.1016/j.nmd.2011.05.006. Epub 2011 Jun 12. PubMed PMID: 21664816.

Belva F, De Schrijver F, Tournaye H, Liebaers I, Devroey P, Haentjens P, Bonduelle M. Neonatal outcome of 724 children born after ICSI using non-ejaculated sperm. Hum Reprod. 2011 Jul;26(7):1752-8. Epub 2011 Apr 21. PubMed PMID: 21511713.

Smet J, De Paepe B, Seneca S, Lissens W, Kotarsky H, De Meirleir L, Fellman V, Van Coster R. Complex III staining in blue native polyacrylamide gels. J Inherit Metab Dis. 2011 Jun;34(3):741-7. Epub 2011 Apr 12. PubMed PMID: 21484424.

Berghmans LV, de Mendonça RH, Coppieters F, de Oliveira Maia O Jr, Takahashi WY, Lissens W, de Baere E, Leroy BP. Discordance for retinitis pigmentosa in two monozygotic twin pairs. Retina. 2011 Jun;31(6):1164-9. PubMed PMID: 21283054.

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. Epub 2010 Nov 13. Review. PubMed PMID: 21269884.

Jansen AC, Oostra A, Desprechins B, De Vlaeminck Y, Verhelst H, Régal L, Verloo P, Bockaert N, Keymolen K, Seneca S, De Meirleir L, Lissens W. TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria. Neurology. 2011 Mar 15;76(11):988-92. PubMed PMID: 21403111.

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. Epub 2010 Oct 19. PubMed PMID: 20959348.

Vanneste E, Melotte C, Voet T, Robberecht C, Debrock S, Pexsters A, Staessen C, Tomassetti C, Legius E, D'Hooghe T, Vermeesch JR. PGD for a complex chromosomal rearrangement by array comparative genomic hybridization. Hum Reprod. 2011 Feb 2. [Epub ahead of print] PubMed PMID: 21292638.

Kiliç M, Sivri HS, Dursun A, Tokatli A, De Meirleir L, Seneca S, Akçören Z, Yigit S, Topaloglu H, Coskun T. A novel mutation in the DGUOK gene in a Turkish newborn with mitochondrial depletion syndrome. Turk J Pediatr. 2011 Jan-Feb;53(1):79-82. PubMed PMID: 21534344

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. Epub 2010 Dec 7. PubMed PMID: 21138905.

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. Epub 2010 Jun 23. PubMed PMID: 20576261.

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. Epub 2010 Dec 7. PubMed PMID: 21138906.

Geens M, Sermon KD, Van de Velde H, Tournaye H. Sertoli cell-conditioned medium induces germ cell differentiation in human embryonic stem cells. J Assist Reprod Genet. 2011 Feb 12. [Epub ahead of print] PubMed PMID: 21318592.

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. Epub 2010 Oct 21. PubMed PMID: 20966462.

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. 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. PubMed PMID: 21089071; PubMed Central PMCID: PMC3038325.

Berghmans LV, de Mendonça RH, Coppieters F, de Oliveira Maia Júnior O, Takahashi WY, Lissens W, de Baere E, Leroy BP. DISCORDANCE FOR RETINITIS PIGMENTOSA IN TWO MONOZYGOTIC TWIN PAIRS. Retina. 2011 Jan 28. [Epub ahead of print] PubMed PMID: 21283054.

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. Epub 2010 Aug 31. PubMed PMID: 21126912.

Mummery C, Westgren M, Sermon K. Current controversies in prenatal diagnosis 1: is stem cell therapy ready for human fetuses? Prenat Diagn. 2011 Jan 3. [Epub ahead of print] PubMed PMID: 21197677.

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. Epub 2010 Oct 21. PubMed PMID: 20966462.

Seriola A, Spits C, Simard JP, Hilven P, Haentjens P, Pearson CE, Sermon K. Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation. Hum Mol Genet. 2011 Jan 1;20(1):176-85. Epub 2010 Oct 8