Citation Impact
Citing Papers
Complement Factor H Polymorphism and Age-Related Macular Degeneration
2005 StandoutScience
Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration
2005 StandoutScience
Complement Factor H Polymorphism in Age-Related Macular Degeneration
2005 StandoutScience
Intracellular Nucleic Acid Sensors and Autoimmunity
2011 StandoutNobel
Myeloid-Derived Suppressor Cells: Linking Inflammation and Cancer
2009 Standout
International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome: Report of an International workshop
1999 Standout
Actualización en síndrome hemolítico urémico atípico: diagnóstico y tratamiento. Documento de consenso
2015
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
Atypical hemolytic uremic syndrome
2011
Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients
2017
An integrated map of genetic variation from 1,092 human genomes
2012 StandoutNature
Therapeutic potential of complement modulation
2009
Progress in defining the molecular biology of age related macular degeneration
2007
Successful Split Liver-Kidney Transplant for Factor H Associated Hemolytic Uremic Syndrome
2008
Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome
2007 StandoutNobel
Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome
2007
The Role of Complement in Inflammatory Diseases From Behind the Scenes into the Spotlight
2007
Complement and its role in innate and adaptive immune responses
2009 Standout
Cellular and molecular mechanisms of fibrosis
2007 Standout
Role of Antioxidants and Natural Products in Inflammation
2016 Standout
Autoimmune forms of thrombotic micorangiopathy and membranoproliferative glomerulonephritis: Indications for a disease spectrum and common pathogenic principles
2009
Age-Related Macular Degeneration
2008 Standout
Therapeutic Roles of Curcumin: Lessons Learned from Clinical Trials
2012 Standout
Non-Transgenic Mouse Models of Kidney Disease
2016 Standout
Genetics and Outcome of Atypical Hemolytic Uremic Syndrome
2013
Hemolytic uremic syndrome recurrence after renal transplantation
2008
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Anti-complement-factor H-associated glomerulopathies
2016
Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome
2013
Complement: coming full circle
2009
Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura
2001
Tissue-resident macrophages
2013 Standout
STEC-HUS, atypical HUS and TTP are all diseases of complement activation
2012
Complement in human diseases: Lessons from complement deficiencies
2009
Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome
2005 Standout
Liver-Kidney Transplantation to Cure Atypical Hemolytic Uremic Syndrome
2008
Macular degeneration: recent advances and therapeutic opportunities
2006
Complement Genes Strongly Predict Recurrence and Graft Outcome in Adult Renal Transplant Recipients with Atypical Hemolytic and Uremic Syndrome
2013
Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
2012
Atypical Hemolytic–Uremic Syndrome
2009
Gene conversion causing human inherited disease: Evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair
2009
An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome
2014
Complement: a key system for immune surveillance and homeostasis
2010 Standout
Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID-19 infection: A report of five cases
2020 Standout
Complement deficiencies in humans and animals: Links to autoimmunity
2006
Hemolytic Uremic Syndrome in Pregnancy and Postpartum
2017
Sensors of the innate immune system: their link to rheumatic diseases
2010 StandoutNobel
Management of hemolytic uremic syndrome
2012
Discrimination between host and pathogens by the complement system
2008
Genetic and environmental factors influencing the human factor�H plasma levels
2004
Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases
2007 Standout
X-ray Crystal Structure of the C4d Fragment of Human Complement Component C4
2002
Vascular endothelial growth factor in eye disease
2008 Standout
Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p
2006
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration
2011
The Molecular Basis of Familial Hemolytic Uremic Syndrome
2001
Systemic Lupus Erythematosus
2011 Standout
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes
2016
Structure of complement fragment C3b–factor H and implications for host protection by complement regulators
2009
Age-related macular degeneration
2018 Standout
Haemolytic uraemic syndrome
2017
Myasthenia gravis
2019 Standout
Complement and coagulation: strangers or partners in crime?
2007
Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype
2010
Monoclonal Gammopathy of Undetermined Significance
2005
Complement
2001 Standout
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome
2004
Thrombotic microangiopathy after kidney transplantation
2006
The creation of an antithrombotic surface by apyrase immobilization
2010 StandoutNobel
Clinical outcomes and mechanism of action for rheopheresis treatment of age-related macular degeneration (AMD)
2005
Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion
2011
The immunopathology of sepsis and potential therapeutic targets
2017 Standout
Clinical Significance of Complement Deficiencies
2009
Membranoproliferative Glomerulonephritis — A New Look at an Old Entity
2012
Differential Diagnosis of Glomerular Disease: A Systematic and Inclusive Approach
2013 Standout
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency
1999
Age Sensitivity of NFκB Abundance and Programmed Cell Death in Erythrocytes Induced by NFκB Inhibitors
2013 Standout
The molecular biology of thrombotic microangiopathy
2006
Complement associated pathogenic mechanisms in myasthenia gravis
2013
Thrombosis as an intravascular effector of innate immunity
2012 Standout
Mechanisms and pathophysiological significance of eryptosis, the suicidal erythrocyte death
2015 Standout
Typical and Atypical Hemolytic Uremic Syndrome in the Critically Ill
2020
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
Mechanisms of Cell Protection by Heme Oxygenase-1
2010 Standout
Association of the Y402H Polymorphism in Complement Factor H Gene and Neovascular Age-Related Macular Degeneration in Chinese Patients
2006
Klebsiella pneumoniae: Going on the Offense with a Strong Defense
2016 Standout
Special Issue: KDIGO Clinical Practice Guideline for the Care of Kidney Transplant Recipients
2009 Standout
Haemostasis and innate immunity – a complementary relationship
2017
Complement System Part II: Role in Immunity
2015
An Evolutionary View of the Mechanism for Immune and Genome Diversity
2012 StandoutNobel
The Role of Complement in the Development of Systemic Lupus Erythematosus
2004
The human complement factor H: functional roles, genetic variations and disease associations
2004
The Role ofVldlrin Intraretinal Angiogenesis in Mice
2011 StandoutNobel
Evolutionary Comparison of the Mechanism of DNA Cleavage with Respect to Immune Diversity and Genomic Instability
2012 StandoutNobel
Dynamics of complement activation in aHUS and how to monitor eculizumab therapy
2014
Towards improved criteria for the antiphospholipid syndrome
1998
Hematological Problems in Pediatric Intensive Care
2013 Standout
Suicidal death of erythrocytes in recurrent hemolytic uremic syndrome
2006
Factor H and the pathogenesis of renal diseases
2000
Post‐transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation
2013
Works of Jacques Blouin being referenced
Genetic and Functional Analyses of Membrane Cofactor Protein (CD46) Mutations in Atypical Hemolytic Uremic Syndrome
2006
Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome
2006
Pediatric Systemic Lupus Erythematosus with C1q Deficiency
2007
Hereditary complement C7 deficiency in nine families: Subtotal C7 deficiency revisited
2007
Clinical Features of Anti-Factor H Autoantibody–Associated Hemolytic Uremic Syndrome
2010
Unusual Clinical Severity of Complement Membrane Cofactor Protein–Associated Hemolytic-Uremic Syndrome and Uniparental Isodisomy
2007
Prevalence of monoclonal gammopathy in patients presenting with acquired angioedema type 2
2002
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
2009
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
2009
Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome
2004
Heterozygous and Homozygous Factor H Deficiencies Associated with Hemolytic Uremic Syndrome or Membranoproliferative Glomerulonephritis
2004
Functional Complement C1q Abnormality Leads to Impaired Immune Complexes and Apoptotic Cell Clearance
2011
Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome
2008
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome
2009
Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE)
2001
Human complement factor H deficiency associated with hemolytic uremic syndrome.
1998
High frequency of C4 "null" alleles in primary antiphospholipid syndrome.
1996
Molecular Basis of a Selective C1s Deficiency Associated with Early Onset Multiple Autoimmune Diseases
2001
Restricted genetic defects underlie human complement C6 deficiency
2003