Inge Liebaers
Overview
Explore the profile of Inge Liebaers including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
61
Citations
1428
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Hens K, Bonduelle M, de Die-Smulders C, Liebaers I
Eur J Med Genet
. 2018 Dec;
62(12):103604.
PMID: 30572173
Objective: Comprehensive chromosome examination is a promising approach to Preimplantation Genetic Testing (PGT). Next to testing of specific chromosomes, such as in the case of reduced fertility due to chromosomal...
2.
Verdyck P, Berckmoes V, De Vos A, Verpoest W, Liebaers I, Bonduelle M, et al.
Am J Med Genet A
. 2015 May;
167A(10):2306-13.
PMID: 25953684
Fragile X syndrome (FXS), the most common inherited intellectual disability syndrome, is caused by expansion and hypermethylation of the CGG repeat in the 5' UTR of the FMR1 gene. This...
3.
Harper J, Geraedts J, Borry P, Cornel M, Dondorp W, Gianaroli L, et al.
Hum Reprod
. 2014 Jul;
29(8):1603-9.
PMID: 25006203
Study Question: How has the interface between genetics and assisted reproduction technology (ART) evolved since 2005? Summary Answer: The interface between ART and genetics has become more entwined as we...
4.
Winand R, Hens K, Dondorp W, de Wert G, Moreau Y, Vermeesch J, et al.
Hum Reprod
. 2014 Feb;
29(4):842-51.
PMID: 24491297
Study Question: What are the analytical and clinical validity and the clinical utility of in vitro screening of embryos by whole-genome sequencing? Summary Answer: At present there are still many...
5.
Harper J, Geraedts J, Borry P, Cornel M, Dondorp W, Gianaroli L, et al.
Eur J Hum Genet
. 2013 Nov;
21 Suppl 2:S1-21.
PMID: 24225486
In March 2005, a group of experts from the European Society of Human Genetics and European Society of Human Reproduction and Embryology met to discuss the interface between genetics and...
6.
De Paepe C, Cauffman G, Verloes A, Sterckx J, Devroey P, Tournaye H, et al.
Hum Reprod
. 2012 Dec;
28(3):740-9.
PMID: 23257394
Study Question: Are human trophectoderm (TE) cells committed or still able to develop into inner cell mass (ICM) cells? Summary Answer: Human full blastocyst TE cells still have the capacity...
7.
van Rij M, De Rademaeker M, Moutou C, Dreesen J, De Rycke M, Liebaers I, et al.
Eur J Hum Genet
. 2011 Nov;
20(4):368-75.
PMID: 22071896
This study provides an overview of 13 years of experience of preimplantation genetic diagnosis (PGD) for Huntington's disease (HD) at three European PGD centres in Brussels, Maastricht and Strasbourg. Information...
8.
Keymolen K, Staessen C, Verpoest W, Liebaers I, Bonduelle M
Eur J Hum Genet
. 2011 Nov;
20(4):376-80.
PMID: 22071893
Carriers of reciprocal translocations (rcp) are known to be at risk for reproductive difficulties. Preimplantation genetic diagnosis (PGD) is one of the options these carriers have to try in order...
9.
Keymolen K, Van Berkel K, Vorsselmans A, Staessen C, Liebaers I
Am J Med Genet A
. 2011 Sep;
155A(10):2381-5.
PMID: 21910218
Robertsonian translocation carriers are at increased risk for infertility, spontaneous abortions, or chromosomally unbalanced offspring. Reproductive counseling of these carriers is challenging. We performed a retrospective analysis of all prenatal...
10.
Kyrou D, Verpoest W, Staessen C, De Vos A, Haentjens P, Liebaers I, et al.
Fertil Steril
. 2010 Jun;
95(2):563-7.
PMID: 20576261
Objective: To investigate whether the incidence of chromosomally abnormal blastomeres is related to the type of pituitary suppression used in ovarian stimulation. Design: Retrospective study. Setting: Tertiary referral center. Patient(s):...