Citation Impact

Citing Papers

Intracellular Ca 2+ signaling and store-operated Ca 2+ entry are required in Drosophila neurons for flight
2009
Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2
2003 StandoutScience
Kinetics of FKBP12.6 Binding to Ryanodine Receptors in Permeabilized Cardiac Myocytes and Effects on Ca Sparks
2010
A pupal transcriptomic screen identifies Ral as a target of store-operated calcium entry in Drosophila neurons
2017 StandoutNobel
Genetics of bipolar disorder
1999
Ryanodine receptors and ventricular arrhythmias: Emerging trends in mutations, mechanisms and therapies
2006
The Retinal Pigment Epithelium in Visual Function
2005 Standout
International Union of Pharmacology. XLIX. Nomenclature and Structure-Function Relationships of Transient Receptor Potential Channels
2005 StandoutNobel
CD44: From adhesion molecules to signalling regulators
2003 Standout
Epidermal homeostasis: a balancing act of stem cells in the skin
2009 Standout
Skeletal Muscle Fatigue: Cellular Mechanisms
2008 Standout
TRPV3 and TRPV4 Mediate Warmth-evoked Currents in Primary Mouse Keratinocytes
2004
DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24
2001
Classical and new roles of β-arrestins in the regulation of G-PROTEIN-COUPLED receptors
2001 StandoutNobel
Calcium signalling: dynamics, homeostasis and remodelling
2003 Standout
Nanostructure of the Epidermal Extracellular Space as Observed by Cryo-Electron Microscopy of Vitreous Sections of Human Skin
2005 StandoutNobel
TRPV3 in keratinocytes transmits temperature information to sensory neurons via ATP
2009 StandoutNobel
Early cardiac hypertrophy in mice with impaired calmodulin regulation of cardiac muscle Ca2+ release channel
2007 StandoutNobel
P2X Purinergic Receptor Antagonist Accelerates SkinBarrier Repair and Prevents Epidermal Hyperplasia Inducedby Skin Barrier Disruption
2002
The Human Brainnetome Atlas: A New Brain Atlas Based on Connectional Architecture
2016 Standout
Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease-Causing Point Mutations
2000
Are desmosomes more than tethers for intermediate filaments?
2000
Constitutive neuregulin‐1/ErbB signaling contributes to human vestibular schwannoma proliferation
2006
ERM proteins and merlin: integrators at the cell cortex
2002 Standout
Cryo‐electron microscopy of vitreous sections
2004 StandoutNobel
Cryo-electron microscopy of vitreous sections of native biological cells and tissues
2004 StandoutNobel
Transient receptor potential channels: targeting pain at the source
2008 StandoutNobel
Human skeletal muscle fibres: molecular and functional diversity
2000
Update on the molecular genetics of retinitis pigmentosa
2001
Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele
1997
Molecular physiology of the SERCA and SPCA pumps
2002
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
2000
EGF–ERBB signalling: towards the systems level
2006 Standout
Superresolution microscopy in heart — Cardiac nanoscopy
2012 StandoutNobel
Putting tumours in context
2001 Standout
Virus associated malignancies: The role of viral hepatitis in hepatocellular carcinoma
2014 StandoutNobel
Store-Operated Calcium Channels
2005 Standout
Mutations in the Sarcoplasmic/Endoplasmic Reticulum Ca2+ ATPase Isoform Cause Darier's Disease
2003
Tissue Kallikrein Inhibitors Based on the Sunflower Trypsin Inhibitor Scaffold – A Potential Therapeutic Intervention for Skin Diseases
2016 StandoutNobel
The cornified envelope: a model of cell death in the skin
2005 Standout
Screening for germ‐line mutations in the NF2 Gene
1995
Hepatitis B virus-related insertional mutagenesis implicates SERCA1 gene in the control of apoptosis
2000
Retinitis pigmentosa
2006 Standout
Human Keratinocyte ATP2C1 Localizes to the Golgi and Controls Golgi Ca2+ Stores
2003
Diverse Viruses Require the Calcium Transporter SPCA1 for Maturation and Spread
2017 StandoutNobel
Strategems in vitro for gene therapies directed to dominant mutations
1997
Physiology and Pathophysiology of Purinergic Neurotransmission
2007 Standout
Regulation of the Neurofibromatosis Type 2 Tumor Suppressor Protein, Merlin, by Adhesion and Growth Arrest Stimuli
1998
SERCA pump isoforms: Their role in calcium transport and disease
2007
Neurofibromatosis 2: loss of merlin's protective spell
1996
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
Molecular genetics of Ca2+ stores and intracellular Ca2+ signalling
2001
Head and traumatic brain injuries among Australian youth and young adults, July 2000–June 2006
2012
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
2011 Standout
Functional organization of human subgenual cortical areas: Relationship between architectonical segregation and connectional heterogeneity
2015
Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa
1995
A Core Complex of BBS Proteins Cooperates with the GTPase Rab8 to Promote Ciliary Membrane Biogenesis
2007 Standout
CNV Concordance in 1,097 MZ Twin Pairs
2015
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa
2002
The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
2003 Standout
Sensors and regulators of intracellular pH
2009 Standout
Diseases involving the Golgi calcium pump
2007
Nanoparticles, Proteins, and Nucleic Acids: Biotechnology Meets Materials Science
2001 Standout
Transient Receptor Potential Cation Channels in Disease
2007 Standout
A Yeast Genetic Screen Reveals a Critical Role for the Pore Helix Domain in TRP Channel Gating
2008 StandoutNobel
Differential contribution of TRPV1 to thermal responses and tissue injury-induced sensitization of dorsal horn neurons in laminae I and V in the mouse
2006 StandoutNobel
TGF-β-induced epithelial to mesenchymal transition
2009 Standout
Plasticity and adaptation of Ca2+ signaling and Ca2+-dependent exocytosis in SERCA2+/- mice
2001
Regulation of desmosome assembly and adhesion
2004
Effects of PMCA and SERCA pump overexpression on the kinetics of cell Ca2+ signalling
2000
Physiological Functions of Plasma Membrane and Intracellular Ca2+ Pumps Revealed by Analysis of Null Mutants
2003
TRPV3 regulates nitric oxide synthase-independent nitric oxide synthesis in the skin
2011 StandoutNobel
Desmosomal cadherins
2002
Retinitis Pigmentosa
1999
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.
1996
Estimating the global incidence of traumatic brain injury
2018 Standout
Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/ RDS and ROM1 Loci
1994 Science
The Diagnostic Evaluation and Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
1997 Standout
Diagnostic issues in a family with late onset type 2 neurofibromatosis.
1995
Fiber Types in Mammalian Skeletal Muscles
2011 Standout
Impaired Thermosensation in Mice Lacking TRPV3, a Heat and Camphor Sensor in the Skin
2005 StandoutScienceNobel
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.
1996
Genetic Dissection of Complex Traits
1994 StandoutScience
The Neuroimaging and Clinical Spectrum of Neurofibromatosis 2
1996
The Ca2+/Mn2+ pumps in the Golgi apparatus
2004
TRP ION CHANNELS AND TEMPERATURE SENSATION
2006 StandoutNobel
Sertoli-Sertoli and Sertoli-Germ Cell Interactions and Their Significance in Germ Cell Movement in the Seminiferous Epithelium during Spermatogenesis
2004 Standout
Investigating the functional link between TMEM165 and SPCA1
2019 StandoutNobel
Severe Retinal Degeneration Caused by a Novel Rhodopsin Mutation
2010 StandoutNobel
TRP Channels
2007 Standout
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump
2000
LINKAGEANALYSIS INPSYCHIATRICDISORDERS: The Emerging Picture
2002
The gene gun: current applications in cutaneous gene therapy
2000

Works of Simon Carter being referenced

The management of trauma victims in England and Wales: a study by the National Confidential Enquiry into Patient Outcome and Death☆☆☆
2009
Germline mutations in the neurofibromatosis type 2 tumour suppressor gene
1994
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p
1993
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
1999
Anterior cingulate cortex abnormalities associated with a first psychotic episode in bipolar disorder
2009
Maximum Phosphorylation of the Cardiac Ryanodine Receptor at Serine-2809 by Protein Kinase A Produces Unique Modifications to Channel Gating and Conductance Not Observed at Lower Levels of Phosphorylation
2006
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