Citation Impact
Citing Papers
CCBE1 Enhances Lymphangiogenesis via A Disintegrin and Metalloprotease With Thrombospondin Motifs-3–Mediated Vascular Endothelial Growth Factor-C Activation
2014
Literature Watch
2004
Walker-Warburg syndrome
2006
Nucleoside-modified VEGFC mRNA induces organ-specific lymphatic growth and reverses experimental lymphedema
2021 StandoutNobel
β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the Skin
2001 Standout
The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis
2009 Standout
Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H
2009
Mechanisms, regulation and functions of the unfolded protein response
2020 Standout
Mental Health Problems Among Schoolchildren in United Arab Emirates: Prevalence and Risk Factors
1998
Carbimazole embryopathy: An emerging phenotype
2004
Xylosyltransferase II is the predominant isoenzyme which is responsible for the steady-state level of xylosyltransferase activity in human serum
2015 StandoutNobel
Osteoporosis
2019 Standout
ECLAMC: The Latin-American Collaborative Study of Congenital Malformations
2004 Standout
Epidermal homeostasis: a balancing act of stem cells in the skin
2009 Standout
Clinical Course of Genetic Diseases of the Insulin Receptor (Type A and Rabson-Mendenhall Syndromes)
2004
GP130/OSMR is the only LIF/IL‐6 family receptor complex to promote osteoblast differentiation of calvaria progenitors
2005
Folic acid in pregnancy and fetal outcomes
2008
Diversity in expression of glucose‐6‐phosphate dehydrogenase deficiency in females
1999
Molecular principles of hair follicle induction and morphogenesis
2005
T1 /podoplanin deficiency disrupts normal lymphatic vasculature formation and causes lymphedema
2003 Standout
Polycystic ovary syndrome: definition, aetiology, diagnosis and treatment
2018 Standout
Lymphangiogenesis: Molecular Mechanisms and Future Promise
2010 Standout
TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita
2008
A Comprehensive Guide for the Accurate Classification of Murine Hair Follicles in Distinct Hair Cycle Stages
2001 Standout
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia
2015 StandoutNobel
Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders
2018 Standout
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension
2014 Standout
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Berberine lowers blood glucose in type 2 diabetes mellitus patients through increasing insulin receptor expression
2009
Cleft lip and palate
2009 Standout
GP130 cytokines and bone remodelling in health and disease
2010
Keratinocyte–Fibroblast Interactions in Wound Healing
2007 Standout
Cytokine-Like Factor 1 Gene Expression Is Enriched in Idiopathic Pulmonary Fibrosis and Drives the Accumulation of CD4+ T Cells in Murine Lungs
2012
Parental consanguinity in specific types of congenital anomalies
2001
Roles of CHOP/GADD153 in endoplasmic reticulum stress
2003 Standout
An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress
2003 Standout
Oncostatin M promotes bone formation independently of resorption when signaling through leukemia inhibitory factor receptor in mice
2010
EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome
2000
Idiopathic pulmonary fibrosis
2017 Standout
Sixteen years and counting: The current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasias
2011
The Effect of Polygamous Marital Structure on Behavioral, Emotional, and Academic Adjustment in Children: A Comprehensive Review of the Literature
2002 Standout
A Comprehensive Guide for the Recognition and Classification of Distinct Stages of Hair Follicle Morphogenesis
1999
A Pragmatic Guide to Enrichment Strategies for Mass Spectrometry–Based Glycoproteomics
2020 StandoutNobel
Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans
2009
The Hallmarks of Aging
2013 Standout
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
2000 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
A Putative Src Homology 3 Domain Binding Motif but Not the C-terminal Dystrophin WW Domain Binding Motif Is Required for Dystroglycan Function in Cellular Polarity in Drosophila
2007 StandoutNobel
Moyamoya Disease and Moyamoya Syndrome
2009 Standout
Birth defects in Arkansas: Is folic acid fortification making a difference?
2004
Mutations in fam20b and xylt1 Reveal That Cartilage Matrix Controls Timing of Endochondral Ossification by Inhibiting Chondrocyte Maturation
2011
The primary cilium: a signalling centre during vertebrate development
2010 Standout
Golgi Glycosylation and Human Inherited Diseases
2011
Inflammatory bone loss: pathogenesis and therapeutic intervention
2012 Standout
The integrated stress response
2016 Standout
Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and Postpartum
2011 Standout
2016 American Thyroid Association Guidelines for Diagnosis and Management of Hyperthyroidism and Other Causes of Thyrotoxicosis
2016 Standout
2017 Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and the Postpartum
2017 Standout
Wound repair and regeneration: Mechanisms, signaling, and translation
2014 Standout
Delineation of the Clinical, Molecular and Cellular Aspects of Novel JAM 3 Mutations Underlying the Autosomal Recessive Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts
2012
MECHANISMS IN ENDOCRINOLOGY: Genetics of human bone formation
2017
The Fibroblast Growth Factor signaling pathway
2015 Standout
Dystroglycan: from biosynthesis to pathogenesis of human disease
2006
The Chemical Composition and Biological Properties of Coconut (Cocos nucifera L.) Water
2009 Standout
THE MAMMALIAN UNFOLDED PROTEIN RESPONSE
2005 Standout
Controls of Hair Follicle Cycling
2001 Standout
Endoplasmic Reticulum Stress Links Obesity, Insulin Action, and Type 2 Diabetes
2004 StandoutScience
Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications
2012 Standout
Moyamoya Syndrome Associated With Down Syndrome: Outcome After Surgical Revascularization
2005
Bone mineralization is regulated by signaling cross talk between molecular factors of local and systemic origin: The role of fibroblast growth factor 23
2014
Works of L.I. Al-Gazali being referenced
Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development
2007
An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy
2002
A study of possible deleterious effects of consanguinity
1997
Further delineation of Hennekam syndrome
2003
Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome
2004
Gerodermia osteodysplastica and wrinkly skin syndrome: Are they the same?
2001
Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect
2001
Are the strokes in moyamoya syndrome associated with Down syndrome due to protein C deficiency?
2002
Mutations in Cytokine Receptor-Like Factor 1 (CRLF1) Account for Both Crisponi and Cold-Induced Sweating Syndromes
2007
Mutations inPOMT1 are found in a minority of patients with Walker-Warburg syndrome
2005
A Rare Bone Dysplasia and Chronic Lung Disease
1999
Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?
1992
Homozygosity for a new mutation (Ile119-->Met) in the insulin receptor gene in five sibs with familial insulin resistance.
1994
The profile of major congenital abnormalities in the United Arab Emirates (UAE) population.
1995
A syndrome of insulin resistance resembling leprechaunism in five sibs of consanguineous parents.
1993
Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes
1999
Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome.
1998