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Inge Liebaers

Explore the profile of Inge Liebaers including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 61
Citations 1428
Followers 0
Related Specialties
Reproductive Medicine
Genetics
Pediatrics
Top 10 Co-Authors
Andre Van Steirteghem
Martine De Rycke
Karen Sermon
Paul Devroey
Maryse Bonduelle
Willy Lissens
Catherine Staessen
Herman Tournaye
Hilde Van de Velde
Claudia Spits
Published In
Hum Reprod
Fertil Steril
Eur J Hum Genet
Am J Med Genet A
Mol Hum Reprod
Affiliations
Soon will be listed here.
Recent Articles
21.
Two-year auxological and medical outcome of singletons born after embryo biopsy applied in preimplantation genetic diagnosis or preimplantation genetic screening
Desmyttere S, De Schepper J, Nekkebroeck J, De Vos A, De Rycke M, Staessen C, et al.
Hum Reprod . 2008 Dec; 24(2):470-6. PMID: 19054780
Background: Embryo biopsy is an essential but invasive procedure to perform preimplantation genetic diagnosis (PGD) or preimplantation genetic screening (PGS). The major objective of this study was to determine whether...
22.
Recurrent chromosomal abnormalities in human embryonic stem cells
Spits C, Mateizel I, Geens M, Mertzanidou A, Staessen C, Vandeskelde Y, et al.
Nat Biotechnol . 2008 Nov; 26(12):1361-3. PMID: 19029912
Cultured human embryonic stem (hES) cells have a known predisposition to aneuploidy of chromosomes 12, 17 and X. We studied 17 hES cell lines by array-based comparative genomic hybridization (aCGH)...
23.
First successful bone marrow transplantation for X-linked chronic granulomatous disease by using preimplantation female gender typing and HLA matching
Reichenbach J, Van de Velde H, De Rycke M, Staessen C, Platteau P, Baetens P, et al.
Pediatrics . 2008 Sep; 122(3):e778-82. PMID: 18762514
Allogeneic hematopoietic stem cell transplantation from an human leukocyte antigen (HLA)-identical donor is currently the only proven curative treatment for chronic granulomatous disease. Hematopoietic stem cell transplantation with alternative donors...
24.
The four blastomeres of a 4-cell stage human embryo are able to develop individually into blastocysts with inner cell mass and trophectoderm
Van de Velde H, Cauffman G, Tournaye H, Devroey P, Liebaers I
Hum Reprod . 2008 May; 23(8):1742-7. PMID: 18503052
Background: Early mammalian blastomeres are thought to be flexible and totipotent allowing the embryo to overcome perturbations in its organization during preimplantation development. In the past, experiments using single blastomeres...
25.
Efficient differentiation of human embryonic stem cells into a homogeneous population of osteoprogenitor-like cells
Mateizel I, De Becker A, Van de Velde H, De Rycke M, Van Steirteghem A, Cornelissen R, et al.
Reprod Biomed Online . 2008 May; 16(5):741-53. PMID: 18492382
The use of human embryonic stem cells (hESC) in both research and therapeutic applications requires relatively large homogeneous populations of differentiated cells. The differentiation of three hESC lines into highly...
26.
Do we need to search for gr/gr deletions in infertile men in a clinical setting?
Stouffs K, Tournaye H, Van der Elst J, Haentjens P, Liebaers I, Lissens W
Hum Reprod . 2008 Mar; 23(5):1193-9. PMID: 18326516
Background: Partial deletions of the AZFc region of the Y chromosome such as gr/gr deletions have been detected in infertile patients as well as in control groups. The impact of...
27.
Is there a role for the nuclear export factor 2 gene in male infertility?
Stouffs K, Tournaye H, Van der Elst J, Liebaers I, Lissens W
Fertil Steril . 2008 Feb; 90(5):1787-91. PMID: 18258234
Objective: To determine the presence of mutations in the NXF2 gene of patients with nonobstructive azoospermia. Design: Molecular analysis of male infertility. Setting: University genetic laboratory and reproductive clinic. Patient(s):...
28.
Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis
Goossens V, De Rycke M, De Vos A, Staessen C, Michiels A, Verpoest W, et al.
Hum Reprod . 2007 Dec; 23(3):481-92. PMID: 18156649
Background: Preimplantation genetic diagnosis or screening (PGD, PGS) involves embryo biopsy on Day 3. Opting for one- or two-cell biopsy is a balance between the lowest risk for misdiagnosis on...
29.
Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene
Jansen A, Cao H, Kaplan P, Silver K, Leonard G, De Meirleir L, et al.
Arch Neurol . 2007 Nov; 64(11):1629-34. PMID: 17998446
Background: Mucopolysaccharidosis type IIID (MPS-IIID), or Sanfilippo syndrome type D, is a rare autosomal recessive lysosomal storage disorder caused by mutations in the N-acetylglucosamine-6-sulfatase (GNS) gene, leading to impaired degradation...
30.
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) region
Lissens W, Arena A, Seneca S, Rafi M, Sorge G, Liebaers I, et al.
Hum Mutat . 2007 Jun; 28(7):742. PMID: 17579360
A high proportion of patients with late onset forms of Krabbe disease is observed in a region north of Catania in Sicily. Molecular analysis in five families from this region...