Citation Impact
Citing Papers
Extracellular Matrix Reorganization During Wound Healing and Its Impact on Abnormal Scarring
2013 Standout
GATA2 is required for lymphatic vessel valve development and maintenance
2015
Crystallographic Insight into Collagen Recognition by Discoidin Domain Receptor 2
2009
Nucleoside-modified VEGFC mRNA induces organ-specific lymphatic growth and reverses experimental lymphedema
2021 StandoutNobel
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
2020 Standout
Lymphatic vasculature mediates macrophage reverse cholesterol transport in mice
2013 Standout
Human genetics of infectious diseases: Unique insights into immunological redundancy
2017
The mechanisms of Hedgehog signalling and its roles in development and disease
2013 Standout
Host susceptibility to non-tuberculous mycobacterial infections
2015
Inhibition of Collagen Fibrillogenesis by Cells Expressing Soluble Extracellular Domains of DDR1 and DDR2
2009
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity
2015
The NLRP3 inflammasome: molecular activation and regulation to therapeutics
2019 Standout
The Neurovascular Unit Coming of Age: A Journey through Neurovascular Coupling in Health and Disease
2017 Standout
A novel role for 12/15-lipoxygenase in regulating autophagy
2014 StandoutNobel
British Thoracic Society guidelines for the management of non-tuberculous mycobacterial pulmonary disease (NTM-PD)
2017 Standout
Role of Cardiolipin in Mitochondrial Signaling Pathways
2017
Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders
2018 Standout
Skin Biopsy: A Useful Tool in the Diagnosis of Lysosomal Storage Diseases
2006
Structural and functional features of central nervous system lymphatic vessels
2015 StandoutNature
Mechanically Activated Ion Channels
2015 StandoutNobel
Inherited Predisposition to Acute Myeloid Leukemia
2014
The lymphatic vasculature in disease
2011
Discoidin domain receptor tyrosine kinases: new players in cancer progression
2012
Sex and gender: modifiers of health, disease, and medicine
2020 Standout
Ubiquitin-dependent regulation of COPII coat size and function
2012 StandoutNatureNobel
Extracellular matrix structure
2015 Standout
Analysis of the brain mural cell transcriptome
2016
Transcriptional Control of Lymphatic Endothelial Cell Type Specification
2013
The Collagen Family
2010 Standout
Remodelling the extracellular matrix in development and disease
2014 Standout
Structural snapshots of TRPV1 reveal mechanism of polymodal functionality
2021 StandoutNobel
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
Autism
2013 Standout
Lessons learned from the study of human inborn errors of innate immunity
2018
Sex differences in autism spectrum disorders
2013
The primary cilium: a signalling centre during vertebrate development
2010 Standout
Acute Myeloid Leukemia
2015 Standout
The Lymphatic System: Integral Roles in Immunity
2016 Standout
Transmembrane Collagen Receptors
2011
New developments in clinical aspects of lymphatic disease
2014
Getting out and about: the emergence and morphogenesis of the vertebrate lymphatic vasculature
2013
High‐resolution structures of transient receptor potential vanilloid channels: Unveiling a functionally diverse group of ion channels
2020
Making sense of cilia in disease: The human ciliopathies
2009
Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation
2018 StandoutNobel
Familial myelodysplastic syndrome/acute leukemia syndromes: a review and utility for translational investigations
2014
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia
2016 Standout
Lymphatic System in Cardiovascular Medicine
2016
Works of Sarah Smithson being referenced
TRPV6 compound heterozygous variants result in impaired placental calcium transport and severe undermineralization and dysplasia of the fetal skeleton
2018
Diagnosis in dysmorphology: clues from the skin
2004
De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome
2012
DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III
2009
Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications
2008
Barth syndrome: an X‐linked cause of fetal cardiomyopathy and stillbirth
2010
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
2011
Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype
2011
Autism, language and communication in children with sex chromosome trisomies
2010