Publications by authors named "Laura Rabaut"

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Generation of a homozygous and heterozygous iPSC line carrying a variant of uncertain significance in CACNA1C, associated with Brugada syndrome.
Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Peter Ponsaerts, Bart Loeys

Stem Cell Res· December 2025

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An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells.
Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, Tycho Canter Cremers, Kevin De Man, Laura Rabaut

Methods· September 2025

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Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin.
Hanne M Boen, Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Aleksandra Nijak-Paeske

Stem Cell Res· December 2024

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Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome.
Josephina A N Meester, Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen

NPJ Genom Med· March 2024

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Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation.
Ilse Van Gucht, Lucia Buccioli, Laura Rabaut, Ivanna Fedoryshchenko, Josephina Meester

Stem Cell Res· June 2023

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IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC).
Pauline De Kinderen, Laura Rabaut, Melanie H A M Perik, Silke Peeters, Peter Ponsaerts

Stem Cell Res· June 2023

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Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variant.
Silke Peeters, Ivanna Fedoryshchenko, Laura Rabaut, Aline Verstraeten, Bart L Loeys

Stem Cell Res· April 2023

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IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type).
Pauline De Kinderen, Silke Peeters, Laura Rabaut, Geert Mortier, Peter Ponsaerts

Stem Cell Res· March 2023

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Generation of an induced pluripotent stem cell (iPSC) line (BBANTWi009-A) from a Meester-Loeys syndrome patient carrying a BGN mutation.
Pauline De Kinderen, Laura Rabaut, Anne Hebert, Peter Ponsaerts, Melanie Perik

Stem Cell Res· February 2023

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Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
Ewa Sieliwonczyk, Maaike Alaerts, Eline Simons, Dirk Snyders, Aleksandra Nijak, Laura Rabaut

Orphanet J Rare Dis· January 2023

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Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient.
Melanie Perik, Aline Verstraeten, Aleksandra Nijak-Paeske, Laura Rabaut, Lut Van Laer

Stem Cell Res· December 2022

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