Citation Impact
Citing Papers
CTLA-4 and PD-1 Receptors Inhibit T-Cell Activation by Distinct Mechanisms
2005 Standout
Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance
2018 Standout
Tumour-cell invasion and migration: diversity and escape mechanisms
2003 Standout
Force of infection: a determinant of vaccine efficacy?
2021
Latrophilins Function as Heterophilic Cell-adhesion Molecules by Binding to Teneurins
2013 StandoutNobel
Control of Regulatory T Cells by Co-signal Molecules
2019 StandoutNobel
Effect of Human Rotavirus Vaccine on Severe Diarrhea in African Infants
2010
A Systematic Review of the Effect of Rotavirus Vaccination on Diarrhea Outcomes Among Children Younger Than 5 Years
2016
Regulation of SLAM-mediated signal transduction by SAP, the X-linked lymphoproliferative gene product
2001
All Four Members of the Ten-m/Odz Family of Transmembrane Proteins Form Dimers
2002
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
1998
The Common Feature of Leukemia-Associated IDH1 and IDH2 Mutations Is a Neomorphic Enzyme Activity Converting α-Ketoglutarate to 2-Hydroxyglutarate
2010 Standout
Intracellular zinc homeostasis and zinc signaling
2008
Global, regional, and national causes of under-5 mortality in 2000–15: an updated systematic analysis with implications for the Sustainable Development Goals
2016 Standout
Glutamate uptake
2001 Standout
Zinc transporters and the cellular trafficking of zinc
2006
TAFI polymorphisms at amino acids 147 and 325 are not risk factors for cerebral infarction
2004 StandoutNobel
The NLRP3 inflammasome: molecular activation and regulation to therapeutics
2019 Standout
Nicotinic acetylcholine receptor α7 subunit is an essential regulator of inflammation
2002 StandoutNature
TGF-β signaling in tumor suppression and cancer progression
2001 Standout
The Human Obesity Gene Map: The 2005 Update
2006
Childhood obesity: public-health crisis, common sense cure
2002 Standout
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
1996 Standout
Advances in the use of nucleic acid probes in diagnosis of viral diseases of man
1987
New insights into nNOS regulation of vascular homeostasis
2005 StandoutNobel
Cancer invasion and tissue remodeling: common themes in proteolytic matrix degradation
1998
Human Models of Inherited Immunoglobulin Class Switch Recombination and Somatic Hypermutation Defects (Hyper-IgM Syndromes)
2004
The Hallmarks of Cancer
2000 Standout
Molecular and cellular pathogenesis of X‐linked lymphoproliferative disease
2005
Newer Methods for Diagnosis of Cytomegalovirus Infection
1990
Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
2009 StandoutNature
Gsα Mutations and Imprinting Defects in Human Disease
2002
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
Genetics of congenital hypothyroidism
2005
Prediction of structures of zinc‐binding proteins through explicit modeling of metal coordination geometry
2010 StandoutNobel
Extracellular matrix structure
2015 Standout
Cancer as an overhealing wound: an old hypothesis revisited
2008 Standout
SLAM Family Receptors Distinguish Hematopoietic Stem and Progenitor Cells and Reveal Endothelial Niches for Stem Cells
2005 Standout
Regulation of NKT cell development by SAP, the protein defective in XLP
2005
New insights into the structure and function of the plasminogen/plasmin system
2013
Matrix Metalloproteinases Regulate Neovascularization by Acting as Pericellular Fibrinolysins
1998
Molecular mechanisms of T cell co-stimulation and co-inhibition
2013 Standout
Safety, Reactogenicity, and Immunogenicity of Human Rotavirus Vaccine RIX4414 in Human Immunodeficiency Virus-positive Infants in South Africa
2010
New functions for nicotinic acetylcholine receptors?
1998
Negative regulators of T‐cell activation: potential targets for therapeutic intervention in cancer, autoimmune disease, and persistent infections
2009 StandoutNobel
A constitutively open potassium channel formed by KCNQ1 and KCNE3
2000 StandoutNature
D‐2‐hydroxyglutaric acid induces oxidative stress in cerebral cortex of young rats
2003
The Human Obesity Gene Map: The 2001 Update
2002
BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1
2003 StandoutNobel
NLRP3 inflammasome inhibition is disrupted in a group of auto-inflammatory disease CAPS mutations
2016
The Human Obesity Gene Map: The 2003 Update
2004
Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study
2013 Standout
The dual-function CD150 receptor subfamily: the viral attraction
2002
Impaired humoral immunity in X-linked lymphoproliferative disease is associated with defective IL-10 production by CD4+ T cells
2005
Obesity in children and young people: a crisis in public health
2004 Standout
Response to influenza virus vaccination during chemotherapy in patients with breast cancer
2011
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
2013 Standout
Infection in Organ-Transplant Recipients
1998 Standout
New functions for the matrix metalloproteinases in cancer progression
2002 Standout
Hepatitis B vaccination: A completed schedule enough to control HBV lifelong?
2012
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
1998
Thrombosis as an intravascular effector of innate immunity
2012 Standout
Update on the pathophysiology of the epilepsies
2000
The Human Obesity Gene Map: The 2004 Update
2005
Functional overlap between two classes of matrix-degrading proteases in wound healing
1999
Matrix Metalloproteinases
1999 Standout
NK CELL RECOGNITION
2004 Standout
Pathophysiology of Human Visceral Obesity: An Update
2013 Standout
PD-1 Inhibits Antiviral Immunity at the Effector Phase in the Liver
2003 StandoutNobel
Impaired humoral immunity in X-linked lymphoproliferative disease is associated with defective IL-10 production by CD4+ T cells
2005
Obesity and Cardiovascular Disease: Pathophysiology, Evaluation, and Effect of Weight Loss
2005 Standout
The NLRP3 Inflammasome: An Overview of Mechanisms of Activation and Regulation
2019 Standout
The Biology of NKT Cells
2006 Standout
Cutting Edge: Defective NK Cell Activation in X-Linked Lymphoproliferative Disease
2000
Cutting Edge: Activation of NK Cell-Mediated Cytotoxicity by a SAP-Independent Receptor of the CD2 Family
2001
Familial Hemiplegic Migraine: A Clinical Comparison of Families Linked and Unlinked to Chromosome 19
1996
Follicular Helper CD4 T Cells (TFH)
2011 Standout
CD150 Association with Either the SH2-Containing Inositol Phosphatase or the SH2-Containing Protein Tyrosine Phosphatase Is Regulated by the Adaptor Protein SH2D1A
2001
Degradable Controlled-Release Polymers and Polymeric Nanoparticles: Mechanisms of Controlling Drug Release
2016 Standout
THE B7 FAMILY REVISITED
2005 Standout
BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Mass Vaccination Setting
2021 Standout
Thrombin activatable fibrinolysis inhibitor and the risk for deep vein thrombosis
2000
SLAM Family Receptors and SAP Adaptors in Immunity
2011
Matrix Proteases in Health and Disease
2012
Regulation of matrix metalloproteinase expression in tumor invasion
1999 Standout
Rapid and simple method for purification of nucleic acids
1990 Standout
Plasmin as a proinflammatory cell activator
2012
How Matrix Metalloproteinases Regulate Cell Behavior
2001 Standout
Enrichment of cereal grains with zinc: Agronomic or genetic biofortification?
2007 Standout
2013 IDSA Clinical Practice Guideline for Vaccination of the Immunocompromised Host
2013 Standout
PD-1 and Its Ligands in Tolerance and Immunity
2008 Standout
Plasminogen Is a Critical Host Pathogenicity Factor for Group A Streptococcal Infection
2004 Science
Works of Volker Schuster being referenced
Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP)
1999
Mutation spectrum of humanSLC39A4in a panel of patients with acrodermatitis enteropathica
2003
Efficacy and Immunogenicity of Live-attenuated Human Rotavirus Vaccine in Breast-fed and Formula-fed European Infants
2012
Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia
2011
Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy
1993
Unimpaired Activation of c-Jun NH2-Terminal Kinase (JNK) 1 upon CD40 Stimulation in B Cells of Patients with X-Linked Agammaglobulinemia
2002
Plasminogen deficiency
2007
Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled study
2007
Twenty Year Follow up of a Patient with a New De-NovoNLRP3Mutation (S595G) and CINCA Syndrome
2009
Immunogenicity and reactogenicity of a trivalent influenza split vaccine in previously unvaccinated children aged 6–9 and 10–13 years
2007
Lasting immune memory against hepatitis B in children after primary immunization with 4 doses of DTPa-HBV-IPV/Hib in the first and 2nd year of life
2010
Homozygous Type I Plasminogen Deficiency
1997
X‐linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain‐containing signal transduction adaptor protein
2000
Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q
1995
Therapy with a Purified Plasminogen Concentrate in an Infant with Ligneous Conjunctivitis and Homozygous Plasminogen Deficiency
1998
Monitoring of 4‐hydroxybutyric acid levels in body fluids during vigabatrin treatment in succinic semialdehyde dehydrogenase deficiency
2003
Homozygous Mutations in the Plasminogen Gene of Two Unrelated Girls With Ligneous Conjunctivitis
1997
Homozygous Mutations in the Plasminogen Gene of Two Unrelated Girls With Ligneous Conjunctivitis
1997
Compound-Heterozygous Mutations in the Plasminogen Gene Predispose to the Development of Ligneous Conjunctivitis
1999
Identification of Two Novel Deletion Mutations within the Gsα Gene (GNAS1) in Albright Hereditary Osteodystrophy1
1999
Detection of Human Cytomegalovirus in Urine by DNA-DNA and RNA-DNA Hybridization
1986