Citation Impact
Citing Papers
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
High-throughput muscle fiber typing from RNA sequencing data
2022 StandoutNobel
Idiopathic pulmonary fibrosis
2017 Standout
Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development
2006
Regulation of microRNA function in animals
2018 Standout
Population frequencies of inherited neuromuscular diseases—A world survey
1991 Standout
Hedgehog signaling update
2010
Wound Complications After Cleft Repair in Children With Van der Woude Syndrome
2010
Identification of microdeletions in candidate genes for cleft lip and/or palate
2009
PVRL1 variants contribute to non‐syndromic cleft lip and palate in multiple populations
2006
Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts
2008
Role of platelet-derived growth factors in physiology and medicine
2008 Standout
Atopic dermatitis
2015 Standout
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
2020 Standout
PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase
2009 StandoutNobel
Sequence evaluation of FGF and FGFR gene conserved non‐coding elements in non‐syndromic cleft lip and palate cases
2007
Arrestin Development: Emerging Roles for β-arrestins in Developmental Signaling Pathways
2009 StandoutNobel
A Human Skeletal Muscle Atlas Identifies the Trajectories of Stem and Progenitor Cells across Development and from Human Pluripotent Stem Cells
2020
A-to-I editing of coding and non-coding RNAs by ADARs
2015
MTHFRandMSX1contribute to the risk of nonsyndromic cleft lip/palate
2010
Subclinical features in non‐syndromic cleft lip with or without cleft palate (CL/P): review of the evidence that subepithelial orbicularis oris muscle defects are part of an expanded phenotype for CL/P*
2007
Testing reported associations of genetic risk factors for oral clefts in a large Irish study population
2009
Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results
2009
Cellular senescence in ageing: from mechanisms to therapeutic opportunities
2020 Standout
A-to-I RNA editing — immune protector and transcriptome diversifier
2018
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Metazoan MicroRNAs
2018 Standout
Cleft lip and palate
2009 Standout
A reference single-cell transcriptomic atlas of human skeletal muscle tissue reveals bifurcated muscle stem cell populations
2020
Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate
2007
Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate
2007
Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population
2010
Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate
2010
The genetics of isolated orofacial clefts: from genotypes to subphenotypes
2009
Unraveling the therapeutic potential of the Hedgehog pathway in cancer
2013 Standout
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
2007
Dual Strategies for Argonaute2-Mediated Biogenesis of Erythroid miRNAs Underlie Conserved Requirements for Slicing in Mammals
2018
Addressing the challenges of cleft lip and palate research in India
2009
DNA methylation-based biomarkers and the epigenetic clock theory of ageing
2018 Standout
In medio stat virtus : unanticipated consequences of telomere dysequilibrium
2018
The biogenesis, biology and characterization of circular RNAs
2019 Standout
TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease
2016 Standout
Human atopic dermatitis complicated by eczema herpeticum is associated with abnormalities in IFN-γ response
2011
Interstitial Cell Remodeling Promotes Aberrant Adipogenesis in Dystrophic Muscles
2020
Facioscapulohumeral muscular dystrophy
2013
Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate
2009
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate
2008
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P
2008
Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population
2011
Genetic Determinants of Facial Clefting: Analysis of 357 Candidate Genes Using Two National Cleft Studies from Scandinavia
2009
Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
2017
The Fibroblast Growth Factor signaling pathway
2015 Standout
Lrp6-mediated canonical Wnt signaling is required for lip formation and fusion
2009
Anoctamins/TMEM16 Proteins: Chloride Channels Flirting with Lipids and Extracellular Vesicles
2016
Association between TGFB3 and Nonsyndromic Cleft Lip with or Without Cleft Palate in a Chilean Population
2010
Analysis of Candidate Genes for Lineage-Specific Expression Changes in Humans and Primates
2014 StandoutNobel
Functionally heterogeneous human satellite cells identified by single cell RNA sequencing
2020
Heterozygous nonsense mutationSATB2 associated with cleft palate, osteoporosis, and cognitive defects
2007
The Glial Nature of Embryonic and Adult Neural Stem Cells
2009 Standout
Cilia and Developmental Signaling
2007
Ethnic Heterogeneity of IRF6 AP-2a Binding Site Promoter SNP Association with Nonsyndromic Cleft Lip and Palate
2010
Telomeropathies: An emerging spectrum disorder
2014
Isolation and characterization of muscle stem cells, fibro-adipogenic progenitors, and macrophages from human skeletal muscle biopsies
2021
Impaired FGF signaling contributes to cleft lip and palate
2007
OSCA/TMEM63 are an evolutionarily conserved family of mechanically activated ion channels
2018 StandoutNobel
Telomere-driven diseases and telomere-targeting therapies
2017
Inhibition of Microtubule Assembly in Osteoblasts Stimulates Bone Morphogenetic Protein 2 Expression and Bone Formation through Transcription Factor Gli2
2008
Wound healing - A literature review
2016 Standout
Works of Fedik Rahimov being referenced
CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies
2016
A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function
2011
Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate
2005
Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy
2013
GLI2 mutations in four Brazilian patients: How wide is the phenotypic spectrum?
2006
Comparative RNA editing in autistic and neurotypical cerebella
2012
Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis
2012
Genetic variants in IRF6 and the risk of facial clefts: single‐marker and haplotype‐based analyses in a population‐based case‐control study of facial clefts in Norway
2008
Cellular and molecular mechanisms underlying muscular dystrophy
2013
Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
2012
MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms
2014