J. Meester

发表

Differentiation of Induced Pluripotent Stem Cells Into Chondrocytes: Methods and Applications for Disease Modeling and Drug Discovery

G. Mortier, Steven Woods, B. Loeys, 2022, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder.

A. V. Vulto-van Silfhout, S. Antonarakis, B. Asselbergh, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

The Role of Genetics in Risk Stratification of Thoracic Aortic Aneurysm Dissection

B. Loeys, J. Meester, A. Verstraeten, 2020, Hearts.

The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2

B. Loeys, Pauline De Kinderen, J. Meester, 2022, Human mutation.

Meester-Loeys Syndrome.

B. Loeys, Pauline De Kinderen, J. Meester, 2021, Advances in experimental medicine and biology.

Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular Intersection.

G. Mortier, B. Loeys, J. Meester, 2020, Trends in molecular medicine.

Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.

B. Loeys, M. Alaerts, L. Van Laer, 2017, Annals of cardiothoracic surgery.

Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections

G. Mortier, H. Dietz, W. Wuyts, 2016, Genetics in Medicine.

A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.

Anthony R. Dallosso, J. Rosenfeld, A. Pagnamenta, 2021, American journal of human genetics.

Biglycan in the Skeleton

B. Loeys, M. Young, V. Kram, 2020, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings

N. Samani, T. Webb, M. Kempers, 2021, International journal of molecular sciences.

The Genetics and Typical Traits of Thoracic Aortic Aneurysm and Dissection.

B. Loeys, J. Meester, Silke Peeters, 2022, Annual review of genomics and human genetics.

Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants

M. Macek, B. Loeys, A. Van Berendoncks, 2022, Human mutation.

Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease

B. Loeys, M. Alaerts, L. Van Laer, 2018, Clinical genetics.

Elucidating the genetic architecture of Adams–Oliver syndrome in a large European cohort

W. Reardon, F. McKenzie, P. Itin, 2018, Human mutation.

Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor

Emmanuel Messas, Luc Mertens, Dmytro Zerbino, 2017, Front. Physiol..

Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing

F. Kortüm, K. Girisha, A. Shukla, 2021, Scientific Reports.

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections.

L. Lagae, J. Casanova, G. Mortier, 2017, The Journal of clinical investigation.

Structural genomic variants in thoracic aortic disease

B. Loeys, J. Meester, Anne Hebert, 2023, Current opinion in cardiology.

Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy

K. Devriendt, M. Kempers, M. Baldewijns, 2021, Molecular genetics & genomic medicine.

Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort

D. Roden, H. Dietz, B. Gelb, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

A mutation update on the LDS‐associated genes TGFB2/3 and SMAD2/3

S. Mehta, J. Roos‐Hesselink, M. Kempers, 2018, Human mutation.

Performant Mutation Identification Using Targeted Next‐Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes

D. Roden, G. Mortier, H. Dietz, 2015, Human mutation.

Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome.

D. Roden, H. Dietz, L. Sleeper, 2020, The Journal of pediatrics.

Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.

J. Roach, B. D. de Vries, K. Prescott, 2015, American journal of human genetics.

Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy

A. Hoischen, J. Timmermans, H. Dietz, 2019, European Journal of Human Genetics.

Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.

N. Samani, L. Mazzolai, A. Maas, 2020, Circulation.

Adams–Oliver syndrome caused by mutations of the EOGT gene

M. Tekin, D. Duman, W. Wuyts, 2019, American journal of medical genetics. Part A.

Heterozygous Loss-of-Function Mutations in DLL 4 Cause Adams-Oliver Syndrome Report

J. Roach, K. Prescott, P. Itin, 2018 .

Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients.

B. Loeys, L. Van Laer, J. Meester, 2016, Genetics research.

IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC)

G. Mortier, B. Loeys, P. Ponsaerts, 2023, Stem Cell Research.

Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient.

B. Loeys, P. Ponsaerts, M. Alaerts, 2022, Stem cell research.

Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool

P. Jorens, J. Hendriks, B. Loeys, 2019, Front. Med..

Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier

E. Govaerts, B. Loeys, I. Rodrigus, 2023, Frontiers in genetics.

A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation.

B. Loeys, P. Coucke, M. Perik, 2023, Stem cell research.

Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation.

B. Loeys, L. Van Laer, J. Meester, 2023, Stem cell research.

Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy

A. Hoischen, J. Timmermans, H. Dietz, 2019, European Journal of Human Genetics.

Elucidating the genetic architecture of Adams–Oliver syndrome in a large European cohort

W. Reardon, F. McKenzie, P. Itin, 2018, Human mutation.

Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome

J. Meester, Silke Peeters, A. Verstraeten, 2024, International journal of molecular sciences.