Citation Impact
Citing Papers
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
2006
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
2022 Standout
ROS-induced R loops trigger a transcription-coupled but BRCA1/2-independent homologous recombination pathway through CSB
2018
Pulmonary Complications of Down Syndrome during Childhood
2010
Osteoporosis
2019 Standout
The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects
2015
Burden of liver diseases in the world
2018 Standout
Histone methylation: a dynamic mark in health, disease and inheritance
2012 Standout
Mechanotransduction and extracellular matrix homeostasis
2014 Standout
Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis
2016
Ageing as a risk factor for neurodegenerative disease
2019 Standout
Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis
2017
Inducible expression of Wnt7b promotes bone formation in aged mice and enhances fracture healing
2020
Piezos thrive under pressure: mechanically activated ion channels in health and disease
2017 StandoutNobel
Surrogate Wnt agonists that phenocopy canonical Wnt and β-catenin signalling
2017 StandoutNatureNobel
The Hallmarks of Aging
2013 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
Cockayne syndrome: Clinical features, model systems and pathways
2016
Piezo2 senses airway stretch and mediates lung inflation-induced apnoea
2016 StandoutNatureNobel
ROS and the DNA damage response in cancer
2018 Standout
Receptor subtype discrimination using extensive shape complementary designed interfaces
2019 StandoutNobel
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities
2017 Standout
MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation
2017
2014
Down Syndrome
2020 Standout
Wilson Disease Mutation Pattern with Genotype‐Phenotype Correlations from Western India: Confirmation of p.C271* as a Common Indian Mutation and Identification of 14 Novel Mutations
2013
New Genes in Bone Development: What's New in Osteogenesis Imperfecta
2013
A promiscuous biotin ligase fusion protein identifies proximal and interacting proteins in mammalian cells
2012 Standout
Nrf2 attenuates inflammatory response in COPD /emphysema: Crosstalk with Wnt3a/β‐catenin and AMPK pathways
2018 Standout
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF‐β expression and connective tissue features
2014
Works of Solaf M. Elsayed being referenced
Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients
2011
Maternal MTHFR C677T genotype and septal defects in offspring with Down syndrome: A pilot study
2013
WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta
2013
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care
2015
Neuroradiologic Manifestations of Loeys-Dietz Syndrome Type 1
2009
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations
2013
Phenotype of apoptotic lymphocytes in children with Down syndrome
2009
Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia
2004