Citation Impact
Citing Papers
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
The RNA Binding Protein Quaking Regulates Formation of circRNAs
2015 Standout
The mechanisms of Hedgehog signalling and its roles in development and disease
2013 Standout
Osteoporosis
2019 Standout
Bone development
2015
Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways
2014
WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta
2013
The role of genes domesticated from LTR retrotransposons and retroviruses in mammals
2012
Significance of glycosylation in Notch signaling
2014
Biological roles of glycans
2016 Standout
Mapping Sites of O-Glycosylation and Fringe Elongation on Drosophila Notch
2016
Mutations in NOTCH1 Cause Adams-Oliver Syndrome
2014
A Smoothened-Evc2 Complex Transduces the Hedgehog Signal at Primary Cilia
2012
Smoothened transduces Hedgehog signal by forming a complex with Evc/Evc2
2012
Surrogate Wnt agonists that phenocopy canonical Wnt and β-catenin signalling
2017 StandoutNatureNobel
A 4.6 kb genomic duplication on 20p12.2–12.3 is associated with brachydactyly type A2 in a Chinese family
2011
TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease
2016 Standout
Dock-family exchange factors in cell migration and disease
2014
Glycosylation in cancer: mechanisms and clinical implications
2015 Standout
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities
2017 Standout
Identification of copy number variants in whole-genome data using Reference Coverage Profiles
2015 StandoutNobel
MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation
2017
The Fibroblast Growth Factor signaling pathway
2015 Standout
Ionizable Lipid Nanoparticles for In Vivo mRNA Delivery to the Placenta during Pregnancy
2023 StandoutNobel
Specification of osteoblast cell fate by canonical Wnt signaling requires Bmp2
2016
Chemical Glycoproteomics
2016 StandoutNobel
Works of Mona Aglan being referenced
Brachydactyly
2008
Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta
2010
The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1
2009
Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta
2011
Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome
2013
Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence
2008
Widening the mutation spectrum ofEVCandEVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts hedgehog signaling
2009
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum
2012
A Novel Homozygous Mutation in FGFR3 Causes Tall Stature, Severe Lateral Tibial Deviation, Scoliosis, Hearing Impairment, Camptodactyly, and Arachnodactyly
2014