Citation Impact
Citing Papers
2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients With Thoracic Aortic Disease
2010 Standout
Differential Roles of Macrophages in Diverse Phases of Skin Repair
2010 Standout
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
2012
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
Tuning the Transcriptional Response to Hypoxia by Inhibiting Hypoxia-inducible Factor (HIF) Prolyl and Asparaginyl Hydroxylases
2016 StandoutNobel
Potent and Selective Triazole-Based Inhibitors of the Hypoxia-Inducible Factor Prolyl-Hydroxylases with Activity in the Murine Brain
2015 StandoutNobel
Ehlers-Danlos syndrome type IV
2007
Xylosyltransferase II is the predominant isoenzyme which is responsible for the steady-state level of xylosyltransferase activity in human serum
2015 StandoutNobel
Osteoporosis
2019 Standout
Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG)
2011
Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type
2010
The cerebellum and cognition
2018 Standout
Fibulin-4 and fibulin-5 in elastogenesis and beyond: Insights from mouse and human studies
2014
Genetics, epigenetics and pharmaco‐(epi)genomics in angiogenesis
2008
Dual-action inhibitors of HIF prolyl hydroxylases that induce binding of a second iron ion
2012 StandoutNobel
Inhibition of 2-oxoglutarate dependent oxygenases
2011
TGFβ signalling in context
2012 Standout
New Therapeutic Approaches to Mendelian Disorders
2010
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
2020 Standout
Mechanotransduction and extracellular matrix homeostasis
2014 Standout
Extracellular control of TGFβ signalling in vascular development and disease
2007
Arrestin Development: Emerging Roles for β-arrestins in Developmental Signaling Pathways
2009 StandoutNobel
Fibrillin‐rich microfibrils: Structural determinants of morphogenetic and homeostatic events
2007
Integrated design, execution, and analysis of arrayed and pooled CRISPR genome-editing experiments
2018
Extracellular Matrix Degradation and Remodeling in Development and Disease
2011 Standout
Role of transforming growth factor-β superfamily signaling pathways in human disease
2008
Biological roles of glycans
2016 Standout
Hypoxia and the extracellular matrix: drivers of tumour metastasis
2014 StandoutNobel
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
Extracellular matrix structure
2015 Standout
Pharmacological targeting of the HIF hydroxylases – A new field in medicine development
2016 StandoutNobel
Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin
2016 Standout
Cystic fibrosis genetics: from molecular understanding to clinical application
2014 Standout
TGF-β and fibrosis in different organs — molecular pathway imprints
2009 Standout
Hepatic expression and cellular distribution of the glucose transporter family
2012
Dynamic Combinatorial Chemistry Employing Boronic Acids/Boronate Esters Leads to Potent Oxygenase Inhibitors
2012 StandoutNobel
TGF-β and the TGF-β Family: Context-Dependent Roles in Cell and Tissue Physiology
2016 Standout
Lessons on the pathogenesis of aneurysm from heritable conditions
2011 Nature
Carotid body hyperplasia and enhanced ventilatory responses to hypoxia in mice with heterozygous deficiency of PHD2
2013 StandoutNobel
Molecular mechanisms and clinical applications of angiogenesis
2011 StandoutNature
The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation
2013
Elastic fibres in health and disease
2013
LRG1 promotes angiogenesis by modulating endothelial TGF-β signalling
2013 StandoutNature
MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation
2017
2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients With Thoracic Aortic Disease
2010 Standout
Betti reaction enables efficient synthesis of 8-hydroxyquinoline inhibitors of 2-oxoglutarate oxygenases
2015 StandoutNobel
New Genes in Bone Development: What's New in Osteogenesis Imperfecta
2013
Structure‐Activity Relationship and Crystallographic Studies on 4‐Hydroxypyrimidine HIF Prolyl Hydroxylase Domain Inhibitors
2019 StandoutNobel
The cerebellar cognitive affective/Schmahmann syndrome scale
2017
Selective Small Molecule Probes for the Hypoxia Inducible Factor (HIF) Prolyl Hydroxylases
2013 StandoutNobel
Lrp6 Hypomorphic Mutation Affects Bone Mass Through Bone Resorption in Mice and Impairs Interaction With Mesd
2008 StandoutNobel
Guidelines for the Primary Prevention of Stroke
2014 Standout
PHD3-mediated prolyl hydroxylation of nonmuscle actin impairs polymerization and cell motility
2014 StandoutNobel
The Genetics of Low-Density Lipoprotein Receptor-Related Protein 5 in Bone: A Story of Extremes
2007
Stroke Risk Factors, Genetics, and Prevention
2017
Dynamic Combinatorial Chemistry Employing Boronic Acids/Boronate Esters Leads to Potent Oxygenase Inhibitors
2012 StandoutNobel
Stroke Risk Prediction with Machine Learning Techniques
2022 Standout
CRISPOR: intuitive guide selection for CRISPR/Cas9 genome editing experiments and screens
2018 Standout
Inhibition of the oxygen sensor PHD2 in the liver improves survival in lactic acidosis by activating the Cori cycle
2015 StandoutNobel
Human Genetic Disorders and Knockout Mice Deficient in Glycosaminoglycan
2014
Report of the National Heart, Lung, and Blood Institute and National Marfan Foundation Working Group on Research in Marfan Syndrome and Related Disorders
2008
Works of Andy Willaert being referenced
Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder
2013
GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling
2011
CRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalis
2016
BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment
2016
The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)
2010
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation
2008
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
2006
Missense Mutations in LRP5 Are Not a Common Cause of Idiopathic Osteoporosis in Adult Men
2005
Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
2010
RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder
2015