Publications by authors named "Jan Meester"

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An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome.
Lotte J F Van Den Heuvel, Silke Peeters, Josephina A N Meester, Paul J Coucke, Bart L Loeys

Drug Discov Today· July 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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Variable clinical expression of a Belgian founder variant suggests the presence of a genetic modifier.
Melanie H A M Perik, Emmanuela Govaerts, Steven Laga, Inge Goovaerts, Johan Saenen, Josephina A N Meester

Front Genet· August 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, Josephina A N Meester

Stem Cell Res· June 2023

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Structural genomic variants in thoracic aortic disease.
Josephina A N Meester, Anne Hebert, Bart L Loeys

Curr Opin Cardiol· May 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, Josephina A N Meester

Stem Cell Res· March 2023

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A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation.
Lotte J F Van Den Heuvel, Silke Peeters, Josephina A N Meester, Melanie Perik, Paul Coucke

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, Josephina A N Meester

Stem Cell Res· February 2023

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Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants.
Jotte Rodrigues Bento, Alice Krebsová, Ilse Van Gucht, Irene Valdivia Callejon, An Van Berendoncks, Josephina A N Meester

Hum Mutat· December 2022

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The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2.
Silke Peeters, Pauline De Kinderen, Josephina A N Meester, Aline Verstraeten, Bart L Loeys

Hum Mutat· July 2022

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Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder.
Marije Meuwissen, Aline Verstraeten, Emmanuelle Ranza, Justyna Iwaszkiewicz, Maaike Bastiaansen, Josephina A N Meester

Genet Med· July 2022

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The role of biglycan in the healthy and thoracic aneurysmal aorta.
Josephina A N Meester, Pauline De Kinderen, Aline Verstraeten, Bart L Loeys

Am J Physiol Cell Physiol· June 2022

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Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort.
Josephina A N Meester, Silke Peeters, Lotte Van Den Heuvel, Geert Vandeweyer, Erik Fransen

Genet Med· May 2022

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Meester-Loeys Syndrome.
Josephina A N Meester, Pauline De Kinderen, Aline Verstraeten, Bart Loeys

Adv Exp Med Biol· November 2021

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A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.
Ilse Van Gucht, Josephina A N Meester, Jotte Rodrigues Bento, Maaike Bastiaansen, Jarl Bastianen

Am J Hum Genet· June 2021

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Biglycan in the Skeleton.
Vardit Kram, Reut Shainer, Priyam Jani, Josephina A N Meester, Bart Loeys

J Histochem Cytochem· November 2020

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Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.
Aline Verstraeten, Melanie H A M Perik, Anna A Baranowska, Josephina A N Meester, Lotte Van Den Heuvel

Circulation· September 2020

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Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome.
Sara L Van Driest, Lynn A Sleeper, Bruce D Gelb, Shaine A Morris, Harry C Dietz, Josephina A N Meester

J Pediatr· July 2020

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Evidence-based algorithm to treat patients with proximal humerus fractures-a prospective study with early clinical and overall performance results.
Christian Spross, Jan Meester, Ruben A Mazzucchelli, Gábor J Puskás, Vilijam Zdravkovic

J Shoulder Elbow Surg· June 2019

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[Differential diagnosis of heel pain].
Primoz Potocnik, Bettina Hochreiter, Norbert Harrasser, Jan Meester, An Dre As Toepfer

Orthopade· March 2019

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Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease.
J A N Meester, A Verstraeten, M Alaerts, D Schepers, L Van Laer

Clin Genet· January 2019

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Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
Josephina A N Meester, Maja Sukalo, Kim C Schröder, Denny Schanze, Gareth Baynam

Hum Mutat· September 2018

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Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.
Josephina A N Meester, Aline Verstraeten, Dorien Schepers, Maaike Alaerts, Lut Van Laer

Ann Cardiothorac Surg· November 2017

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Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections.
Josephina A N Meester, Geert Vandeweyer, Isabel Pintelon, Martin Lammens, Lana Van Hoorick

Genet Med· April 2017

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Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients.
Rustam Zhurayev, Dorien Proost, Dmytro Zerbino, Viktor Fedorenko, Josephina A N Meester

Genet Res (Camb)· October 2016

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