Citation Impact
Citing Papers
Plasma membrane translocation of a protein needle based on a triple-stranded β-helix motif
2014 StandoutNobel
Intrinsic disorder of the extracellular matrix
2011
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
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
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants
2013
Multifunctional Lipid/Quantum Dot Hybrid Nanocontainers for Controlled Targeting of Live Cells
2006 StandoutNobel
Characterization of a putative fusogenic sequence in the E2 hepatitis G virus protein
2005
Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type
2010
Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives
2019
Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates
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
Cellular uptake of Antennapedia Penetratin peptides is a two-step process in which phase transfer precedes a tryptophan-dependent translocation
2003
ClinVar: public archive of relationships among sequence variation and human phenotype
2013 Standout
Biological roles of glycans
2016 Standout
Mammalian display screening of diverse cystine-dense peptides for difficult to drug targets
2017 StandoutNobel
Hypoxia and the extracellular matrix: drivers of tumour metastasis
2014 StandoutNobel
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
2014 Standout
Designing antimicrobial peptides: form follows function
2011 Standout
Pharmacological targeting of the HIF hydroxylases – A new field in medicine development
2016 StandoutNobel
Relationships between Membrane Binding, Affinity and Cell Internalization Efficacy of a Cell-Penetrating Peptide: Penetratin as a Case Study
2011
Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin
2016 Standout
Transduction peptides: from technology to physiology
2004
The Collagen Family
2010 Standout
A Cell-Penetrating Scorpion Toxin Enables Mode-Specific Modulation of TRPA1 and Pain
2019 StandoutNobel
Ehlers-Danlos syndromes and Marfan syndrome
2008
Glycotherapy: New Advances Inspire a Reemergence of Glycans in Medicine
2013 StandoutNobel
The signal peptide as a new target for drug design
2020
High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal
2005 Standout
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
TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease
2016 Standout
Lessons on the pathogenesis of aneurysm from heritable conditions
2011 Nature
Interaction of synthetic peptides corresponding to hepatitis G virus (HGV/GBV‐C) E2 structural protein with phospholipid vesicles
2005
Delivery of bioactive molecules into the cell: the Trojan horse approach
2004
Carotid body hyperplasia and enhanced ventilatory responses to hypoxia in mice with heterozygous deficiency of PHD2
2013 StandoutNobel
Chemistry and Function of Glycosaminoglycans in the Nervous System
2014
The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation
2013
Key challenges for delivering clinical impact with artificial intelligence
2019 Standout
MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation
2017
Cell-Penetrating Peptides: Design, Synthesis, and Applications
2014
SignalP 6.0 predicts all five types of signal peptides using protein language models
2022 Standout
Modifications of Glycans: Biological Significance and Therapeutic Opportunities
2011
A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)
2011
A Novel Mutation ofSMAD3Identified in a Chinese Family with Aneurysms-Osteoarthritis Syndrome
2015
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 role of cancer-associated myofibroblasts in intrahepatic cholangiocarcinoma
2011
Selective Small Molecule Probes for the Hypoxia Inducible Factor (HIF) Prolyl Hydroxylases
2013 StandoutNobel
Nonviral Vectors for Gene Delivery
2008 Standout
Surface-Enhanced Raman Spectroscopy for Bioanalysis: Reliability and Challenges
2018 Standout
Collagen Structure and Stability
2009 Standout
Classification of Intrinsically Disordered Regions and Proteins
2014 Standout
PHD3-mediated prolyl hydroxylation of nonmuscle actin impairs polymerization and cell motility
2014 StandoutNobel
Dynamic Combinatorial Chemistry Employing Boronic Acids/Boronate Esters Leads to Potent Oxygenase Inhibitors
2012 StandoutNobel
Single-Molecule Motions of Oligoarginine Transporter Conjugates on the Plasma Membrane of Chinese Hamster Ovary Cells
2008 StandoutNobel
Chronic Inflammation and Cytokines in the Tumor Microenvironment
2014 Standout
Characterization of an Immunodominant Antigenic Site on GB Virus C Glycoprotein E2 That Is Involved in Cell Binding
2006 StandoutNobel
Multifunctional Lipid/Quantum Dot Hybrid Nanocontainers for Controlled Targeting of Live Cells
2006 StandoutNobel
Comparison of Penetratin and Other Homeodomain-Derived Cell-Penetrating Peptides: Interaction in a Membrane-Mimicking Environment and Cellular Uptake Efficiency
2006
Human Genetic Disorders and Knockout Mice Deficient in Glycosaminoglycan
2014
Works of Sofie Symoens being referenced
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta
2011
The molecular basis of classic Ehlers-Danlos syndrome: A comprehensive study of biochemical and molecular findings in 48 unrelated patients
2004
Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood
2007
Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans
2013
Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder
2013
Tryptophan fluorescence study of the interaction of penetratin peptides with model membranes
2002
COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers-Danlos syndrome
2008
Musculocontractural Ehlers-Danlos Syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan-4-sulfotransferase 1 encoding CHST14 gene
2010
Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients
2015
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation
2008
Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
2010
Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome
2018
Identification of binding partners interacting with the α1-N-propeptide of type V collagen
2010