M. Baetens

发表

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

K. Devriendt, B. Menten, J. Vermeesch, 2021, Genetics in Medicine.

PREFACE: In silico pipeline for accurate cell‐free fetal DNA fraction prediction

B. Menten, A. Dheedene, M. Baetens, 2019, Prenatal diagnosis.

Practical Tools to Implement Massive Parallel Pyrosequencing of PCR Products in Next Generation Molecular Diagnostics

J. Vandesompele, J. Hellemans, L. Clement, 2011, PloS one.

Low feasibility of in vitro matured oocytes originating from cumulus complexes found during ovarian tissue preparation at the moment of gender confirmation surgery and during testosterone treatment for fertility preservation in transgender men.

B. Menten, S. Lierman, P. De Sutter, 2021, Fertility and sterility.

Flexible, Scalable, and Efficient Targeted Resequencing on a Benchtop Sequencer for Variant Detection in Clinical Practice

J. Vandesompele, J. Hellemans, E. Baere, 2015, Human mutation.

Massive parallel amplicon sequencing of the breast cancer genes BRCA1 and BRCA2: opportunities, challenges, and limitations

J. Hellemans, K. Claes, A. De Paepe, 2011, Human mutation.

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

Justin L Cotney, T. Cox, Ellen Roets, 2022, bioRxiv.

Comparison of the positivity rate of anti-spike and anti-nucleocapsid SARS-CoV-2 IgG in asymptomatic pregnant women

B. Menten, L. Heireman, I. Dehaene, 2021, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.

Paul Coucke, Marjolijn Renard, Bart Loeys, 2013, International journal of cardiology.

Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles

K. Devriendt, J. Vermeesch, K. Janssens, 2023, European journal of human genetics : EJHG.

GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction.

B. Menten, N. Callewaert, K. Tilleman, 2022, Human Reproduction.

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys‐Dietz syndromes

B. Menten, J. Hellemans, A. De Paepe, 2011, Human mutation.

Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations

K. Devriendt, J. Vermeesch, J. Gatot, 2021, Obstetrics and gynecology.

Characterization of ovarian tissue oocytes from transgender men reveals poor calcium release and embryo development, which might be overcome by spindle transfer.

B. Menten, B. Heindryckx, A. Van Soom, 2023, Human reproduction.

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

S. Brugmann, Ellen Roets, S. Vergult, 2024, Nature communications.

Pronuclear transfer rescues poor embryo development of in vitro-grown secondary mouse follicles

B. Heindryckx, A. Van Soom, C. De Roo, 2024, Human reproduction open.