Citation Impact
Citing Papers
Characterizing and explaining the impact of disease-associated mutations in proteins without known structures or structural homologs
2022 StandoutNobel
Regulation of Osteogenesis-Angiogenesis Coupling by HIFs and VEGF
2009 StandoutNobel
Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness
2017 Standout
Degeneration of the intervertebral disc.
2003 Standout
107th ENMC International Workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th–9th June 2002, Naarden, the Netherlands
2003
Ror2 Receptor Requires Tyrosine Kinase Activity to Mediate Wnt5A Signaling
2009
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark
2008
WNT5A mutations in patients with autosomal dominant Robinow syndrome
2009
Auto-antibodies to the receptor tyrosine kinase MuSK in patients with myasthenia gravis without acetylcholine receptor antibodies
2001 Standout
171st ENMC International Workshop: Standards of care and management of facioscapulohumeral muscular dystrophy
2010
Molecular biology of distal muscular dystrophies—Sarcomeric proteins on top
2006
Brachy–syndactyly caused by loss of Sfrp2 function
2008
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome
2000
Cell biology of Ca2+-triggered exocytosis
2010 StandoutNobel
Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B
2010
The Receptor Tyrosine Kinase Ror2 Associates with and Is Activated by Casein Kinase Iϵ
2004
Bone morphogenetic protein receptors and signal transduction
2009 Standout
TGFβ signalling in context
2012 Standout
WNT signalling pathways as therapeutic targets in cancer
2012 Standout
PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase
2009 StandoutNobel
New Insights into the Biology of Renal Cell Carcinoma
2011 StandoutNobel
Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development
2000
Facioscapulohumeral muscular dystrophy
2006
Defective membrane repair in dysferlin-deficient muscular dystrophy
2003 Nature
The muscular dystrophies
2002 Standout
Wnt signaling in osteoblasts and bone diseases
2004
Taking it to the max: The genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology
2004
A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN
2007
Osteoporosis: now and the future
2011 Standout
Extracellular Matrix Degradation and Remodeling in Development and Disease
2011 Standout
EFNS guideline on diagnosis and management of limb girdle muscular dystrophies
2007
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Dysferlin and muscle membrane repair
2007
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
2009
Wnt/β-Catenin Signaling and Disease
2012 Standout
Pain and Neuromuscular Disease
2006
RTK mutations and human syndromes
2000
Circletail, a New Mouse Mutant with Severe Neural Tube Defects: Chromosomal Localization and Interaction with the Loop-Tail Mutation
2001
Muscular dystrophy into the new millennium
2002
Expression and subcellular localization of Ror tyrosine kinase receptors are developmentally regulated in cultured hippocampal neurons
2003
TGF-β and BMP Signaling in Osteoblast Differentiation and Bone Formation
2012 Standout
Modulation of GDF5/BRI‐b signalling through interaction with the tyrosine kinase receptor Ror2
2004
The frequency of limb girdle muscular dystrophy 2A in northeastern Italy
2005
The receptor tyrosine kinase Ror2 is involved in non‐canonical Wnt5a/JNK signalling pathway
2003
The Deleted in Brachydactyly B Domain of ROR2 Is Required for Receptor Activation by Recruitment of Src
2008
Respiratory involvement in inherited primary muscle conditions
2006
ROR1 Is Expressed in Human Breast Cancer and Associated with Enhanced Tumor-Cell Growth
2012
TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease
2016 Standout
Adipocyte differentiation from the inside out
2006 Standout
Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variants
2021
Systematic analysis of genes required for synapse structure and function
2005 StandoutNatureNobel
Selection Signatures in Worldwide Sheep Populations
2014 Standout
Mice lacking the orphan receptor ror1 have distinct skeletal abnormalities and are growth retarded
2010
Molecular Bases of the Regulation of Bone Remodeling by the Canonical Wnt Signaling Pathway
2006
Ror‐family receptor tyrosine kinases in noncanonical Wnt signaling: Their implications in developmental morphogenesis and human diseases
2009
Self-healing polymeric materials
2013 Standout
Update on Wnt signaling in bone cell biology and bone disease
2011
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities
2017 Standout
Sec24b selectively sorts Vangl2 to regulate planar cell polarity during neural tube closure
2009 StandoutNobel
The genetic basis for skeletal diseases
2003 Nature
ToppGene Suite for gene list enrichment analysis and candidate gene prioritization
2009 Standout
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
2003
Self-healing polymers
2020 Standout
RELIEVING PAIN IN AMERICA: A BLUEPRINT FOR TRANSFORMING PREVENTION, CARE, EDUCATION, AND RESEARCH
2012 Standout
The orphan tyrosine kinase receptor, ROR2, mediates Wnt5A signaling in metastatic melanoma
2009
A comprehensive review of reported heritable noggin‐associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term:NOG‐related‐symphalangism spectrum disorder (NOG‐SSD)
2011
The muscular dystrophies
2012
Impact of Biopsychosocial Factors on Chronic Pain in Persons With Myotonic and Facioscapulohumeral Muscular Dystrophy
2009
Molecular‐pathogenetic classification of genetic disorders of the skeleton
2001
Toward simpler and faster genome-wide mutagenesis in mice
2007 StandoutNobel
Non-Smad TGF-β signals
2005 Standout
Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies
2008
From Estrogen-Centric to Aging and Oxidative Stress: A Revised Perspective of the Pathogenesis of Osteoporosis
2010 Standout
RTK mutations and human syndromes: when good receptors turn bad
2000
Satellite Cells and the Muscle Stem Cell Niche
2013 Standout
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Generation of skeletal muscle stem/progenitor cells from murine induced pluripotent stem cells
2010 StandoutNobel
Works of C. Pollitt being referenced
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies
2001
Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports
1998
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
2000
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach
2001
Multicore myopathy: respiratory failure and paraspinal muscle contractures are important complications
2000
Multicore myopathy: respiratory failure and paraspinal muscle contractures are important complications
2000