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B. Loeys · SciRah

Researcher profile · Semantic Scholar

B. Loeys

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B. Loeys — researcher profile on SciRah

h-index: 78
Works: 365
Citations: 28K

Most-cited papers

2023 ESC Guidelines for the management of cardiomyopathies.
E. Arbelo, A. Protonotarios, J. Gimeno, E. Arbustini +23 more
2023European Heart Journal2,428 citations Open access
Semantic Scholar
Genome-wide association analyses identify novel Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
J. Barc, R. Tadros, C. Glinge, David Y. Chiang +152 more
2022Nature Genetics113 citations Open access
Semantic Scholar
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
N. Lahrouchi, R. Tadros, L. Crotti, Y. Mizusawa +102 more
2020Circulation105 citations Open access
Semantic Scholar
Extracellular Matrix in Vascular Disease, Part 2/4: JACC Focus Seminar.
J. Barallobre-Barreiro, B. Loeys, M. Mayr, M. Rienks +2 more
2020Journal of the American College of Cardiology92 citations Open access
Semantic Scholar
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
R. Walsh, N. Lahrouchi, R. Tadros, F. Kyndt +126 more
2020Genetics in Medicine82 citations Open access
Semantic Scholar
LOEYS–DIETZ SYNDROME
A. Verstraeten, H. Dietz, B. Loeys
2020Cassidy and Allanson's Management of Genetic Syndromes77 citations
Semantic Scholar
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
D. Greene, D. Pirri, K. Frudd, E. Sackey +29 more
2023Nature Medicine68 citations Open access
Semantic Scholar
The Genetics and Typical Traits of Thoracic Aortic Aneurysm and Dissection.
Jotte Rodrigues Bento, J. Meester, I. Luyckx, Silke Peeters +2 more
2022Annual review of genomics and human genetics (Print)52 citations Open access
Semantic Scholar
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction
L. Lenaerts, S. Reynhout, Iris Verbinnen, F. Laumonnier +48 more
2020Genetics in Medicine47 citations Open access
Semantic Scholar
Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia.
A. Persu, P. Dobrowolski, H. Gornik, J. Olin +21 more
2021Cardiovascular Research40 citations Open access
Semantic Scholar
Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy
I. Luyckx, G. MacCarrick, M. Kempers, J. Meester +18 more
2019European Journal of Human Genetics40 citations Open access
Semantic Scholar
Biglycan in the Skeleton
V. Kram, Reut Shainer, Priyam Jani, J. Meester +2 more
2020Journal of Histochemistry and Cytochemistry39 citations Open access
Semantic Scholar
The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2
Silke Peeters, Pauline De Kinderen, J. Meester, A. Verstraeten +1 more
2022Human Mutation38 citations Open access
Semantic Scholar
A dynamic mucin mRNA signature associates with COVID-19 disease presentation and severity
A. Smet, T. Breugelmans, Johan Michiels, K. Lamote +18 more
2021JCI Insight30 citations Open access
Semantic Scholar
Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.
A. Verstraeten, M. Perik, A. Baranowska, J. Meester +73 more
2020Circulation30 citations Open access
Semantic Scholar
SMAD6-deficiency in human genetic disorders
I. Luyckx, A. Verstraeten, M. Goumans, B. Loeys
2022npj Genomic Medicine29 citations Open access
Semantic Scholar
The emerging role of endothelial cells in the pathogenesis of thoracic aortic aneurysm and dissection
A. Verstraeten, I. Fedoryshchenko, B. Loeys
2023European Heart Journal28 citations Open access
Semantic Scholar
Defining the Clinical, Molecular and Ultrastructural Characteristics in Occipital Horn Syndrome: Two New Cases and Review of the Literature
A. Beyens, Kyaran Van Meensel, L. Pottie, R. De Rycke +8 more
2019Genes28 citations Open access
Semantic Scholar
Predictors of Bicuspid Aortic Valve–Associated Aortopathy in Childhood
M. Grattan, Andrea Prince, Rawan Ruman, C. Morgan +12 more
2020Circulation Cardiovascular Imaging25 citations Open access
Semantic Scholar
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort
J. Meester, Silke Peeters, Lotte J. F. Van Den Heuvel, G. Vandeweyer +23 more
2022Genetics in Medicine24 citations Open access
Semantic Scholar
iPSC-Cardiomyocyte Models of Brugada Syndrome—Achievements, Challenges and Future Perspectives
A. Nijak, J. Saenen, A. Labro, D. Schepers +2 more
2021International Journal of Molecular Sciences22 citations Open access
Semantic Scholar
NOTCH Pathway Regulator MIB1: A Novel Gene for Bicuspid Aortic Valve
Idit Tessler, J. Albuisson, Rebeca Piñeiro-Sabarís, A. Verstraeten +33 more
2023JAMA cardiology21 citations Open access
Semantic Scholar
HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) a statement from the HTAD working group of VASCERN.
M. Caruana, M. Baars, E. Bashiardes, K. Benke +25 more
2022European Journal of Medical Genetics21 citations Open access
Semantic Scholar
Differentiation of Induced Pluripotent Stem Cells Into Chondrocytes: Methods and Applications for Disease Modeling and Drug Discovery
Pauline De Kinderen, J. Meester, B. Loeys, Silke Peeters +4 more
2022Journal of Bone and Mineral Research20 citations
Semantic Scholar
Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy
H. Boen, B. Loeys, M. Alaerts, J. Saenen +9 more
2022The Journal of Heart and Lung Transplantation20 citations Open access
Semantic Scholar
Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN).
I. M. van de Laar, A. Baas, J. De Backer, Jan D. Blankenstein +9 more
2022European Journal of Medical Genetics18 citations Open access
Semantic Scholar
Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases
Sofia Papadimitriou, Barbara Gravel, Charlotte Nachtegael, E. De Baere +4 more
2022HGG advances18 citations Open access
Semantic Scholar
A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.
I. Van Gucht, J. Meester, J. R. Bento, M. Bastiaansen +43 more
2021American Journal of Human Genetics18 citations Open access
Semantic Scholar
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics.
E. Arbustini, E. Behr, L. Carrier, C. M. van Duijn +17 more
2022European Heart Journal17 citations Open access
Semantic Scholar
Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy
Sarah Duerinckx, J. Désir, Camille Perazzolo, C. Badoer +34 more
2021Molecular Genetics & Genomic Medicine17 citations Open access
Semantic Scholar
iPSC-Derived Cardiomyocytes in Inherited Cardiac Arrhythmias: Pathomechanistic Discovery and Drug Development
E. Simons, B. Loeys, M. Alaerts
2023Biomedicines16 citations Open access
Semantic Scholar
Luminescent Human iPSC-Derived Neurospheroids Enable Modeling of Neurotoxicity After Oxygen–glucose Deprivation
Elise Van Breedam, A. Nijak, Tamariche Buyle-Huybrecht, J. Di Stefano +19 more
2022Neurotherapeutics16 citations Open access
Semantic Scholar
Indications and utility of cardiac genetic testing in athletes.
S. Castelletti, B. Gray, C. Basso, E. Behr +15 more
2022European Journal of Preventive Cardiology16 citations Open access
Semantic Scholar
Loeys-Dietz Syndrome.
J. Velchev, L. Van Laer, I. Luyckx, H. Dietz +1 more
2021Advances in Experimental Medicine and Biology16 citations
Semantic Scholar
Aortic Valve Surgery in Non-Elderly Patients: Insights Gained from AVIATOR.
E. Lansac, P. Youssefi, F. de Heer, J. Bavaria +127 more
2019Seminars in Thoracic and Cardiovascular Surgery14 citations Open access
Semantic Scholar
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome
S. L. Van Driest, L. Sleeper, B. Gelb, S. Morris +20 more
2020Jornal de Pediatria13 citations Open access
Semantic Scholar
Delineation of a new fibrillin-2-opathy with evidence for a role of FBN2 in the pathogenesis of carpal tunnel syndrome
Silke Peeters, A. Decramer, Stuart A. Cain, P. Houpt +13 more
2020Journal of Medical Genetics12 citations
Semantic Scholar
Comparability of different Z-score equations for aortic root dimensions in children with Marfan syndrome
Dominiek W E Rutten, Ilse J H Aarts-Janssen, M. Kempers, A. Reimer +3 more
2021Cardiology in the Young11 citations Open access
Semantic Scholar
Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings
I. Van Gucht, A. Krebsová, B. Diness, S. Laga +15 more
2021International Journal of Molecular Sciences11 citations Open access
Semantic Scholar
Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing
Shalini S. Nayak, Pauline E. Schneeberger, S. Patil, K. Arun +16 more
2021Scientific Reports11 citations Open access
Semantic Scholar
Meester-Loeys Syndrome.
J. Meester, Pauline De Kinderen, A. Verstraeten, B. Loeys
2021Advances in Experimental Medicine and Biology11 citations
Semantic Scholar
Phenotype of COL3A1/COL5A2 deletion patients.
M. Kempers, M. Wessels, A. V. Van Berendoncks, I. M. van de Laar +2 more
2022European Journal of Medical Genetics8 citations Open access
Semantic Scholar
Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping
E. Sieliwończyk, B. Vandendriessche, C. Claes, E. Mayeur +6 more
2023Scientific Reports7 citations Open access
Semantic Scholar
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes
A. Nijak, E. Simons, B. Vandendriessche, D. V. Van de Sande +13 more
2022Biology Open7 citations Open access
Semantic Scholar
Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder.
M. Meuwissen, A. Verstraeten, E. Ranza, Justyna Iwaszkiewicz +37 more
2022Genetics in Medicine7 citations Open access
Semantic Scholar
Blood biomarkers in patients with bicuspid aortic valve disease.
L. Bons, L. W. Geenen, A. T. van den Hoven, W. Dik +11 more
2020Journal of Cardiology7 citations Open access
Semantic Scholar
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report
A. Nijak, A. Labro, H. De Wilde, W. Dewals +11 more
2020Frontiers in Cardiovascular Medicine7 citations Open access
Semantic Scholar
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
R. Walsh, N. Lahrouchi, R. Tadros, F. Kyndt +127 more
2020Genetics in Medicine7 citations Open access
Semantic Scholar
Comparison of biomechanical properties in ascending aortic aneurysms of patients with congenital bicuspid aortic valve and Marfan syndrome.
Junfeng Yan, Ann-Cathrin Lehsau, Benjamin Sauer, B. Pieper +10 more
2019International Journal of Cardiology7 citations
Semantic Scholar
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.
Lisa M. van den Bersselaar, J. Verhagen, J. Bekkers, M. Kempers +15 more
2022Genetics in Medicine6 citations Open access
Semantic Scholar

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