Citation Impact
Citing Papers
DiarrheagenicEscherichia coli
1998 Standout
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
Origins and Divergence of the Roma (Gypsies)
2001 Standout
Sclerosis multiplex in gypsies
1991
High incidence of serum antibodies to Escherichia coli O157 lipopolysaccharide in children with hemolytic-uremic syndrome
1991
Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia
2000 Standout
ECLAMC: The Latin-American Collaborative Study of Congenital Malformations
2004 Standout
HLA and in vitro susceptibility to HIV infection
2002
Clinical and Molecular Genetics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
1991
Sexual behaviour in context: a global perspective
2006 Standout
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
1996 Standout
C4A deficiency and nonresponse to hepatitis B vaccination
2002
The β-Thalassemias
1999 Standout
Strong Amerind/White Sex Bias and a Possible Sephardic Contribution among the Founders of a Population in Northwest Colombia
2000 Standout
Women and Aids in Zimbabwe: The Making of an Epidemic
1991
A systematic review of current knowledge of HIV epidemiology and of sexual behaviour in Nepal
2002
The role of sexually transmitted diseases in HIV transmission
2004 Standout
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.
1989
A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual
1988
8 The population genetics of the haemoglobinopathies
1993
Epidemiology and the web of causation: Has anyone seen the spider?
1994 Standout
Systemic Lupus Erythematosus
2011 Standout
Chicken Consumption Is a Newly Identified Risk Factor for SporadicSalmonella entericaSerotype Enteritidis Infections in the United States: A Case‐Control Study in FoodNet Sites
2004
Sickle-cell disease
2010 Standout
Sarcoidosis
1997 Standout
Complement
2001 Standout
Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4
2001
Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies
1998 Standout
World distribution of factor V Leiden
1995 Standout
HLA Class I, II, and III Polymorphism in Italian Patients With Sarcoidosis
1993
Autosomal, mtDNA, and Y-Chromosome Diversity in Amerinds: Pre- and Post-Columbian Patterns of Gene Flow in South America
2000
Why are some genetic diseases common?
1993
Global Prevalence of Celiac Disease: Systematic Review and Meta-analysis
2018 Standout
The P450 Superfamily: Update on New Sequences, Gene Mapping, Accession Numbers, Early Trivial Names of Enzymes, and Nomenclature
1993 Standout
Complement deficiency and disease
1991
A major histocompatibility complex Class III allotype (C4B 2) associated with Primary Biliary Cirrhosis (PBC)
1987
Indirect hemagglutination assay for diagnosis of Escherichia coli O157 infection in patients with hemolytic-uremic syndrome
1992
Two HLA-linked loci controlling the fourth component of human complement.
1978
Genetic Differences between the Salt-Wasting, Simple Virilizing, and Nonclassical Types of Congenital Adrenal Hyperplasia*
1985
Human Retinoblastoma Susceptibility Gene: Cloning, Identification, and Sequence
1987 StandoutScience
21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.
1989
Primary Biliary Cirrhosis
2011 Standout
The many faces and factors oforofacial clefts
1999
Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia.
1987 Nobel
H deficiency in two brothers with atypical dense intramembranous deposit disease
1986
Purification, biochemical characterization, and biological function of human esterase D.
1986
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus
2003 Standout
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq
1990
Diversity in Intrinsic Strengths of the Human Complement System: Serum C4 Protein Concentrations Correlate withC4Gene Size and Polygenic Variations, Hemolytic Activities, and Body Mass Index
2003
Celiac disease in native Indians from Brazil: A clinical and epidemiological survey.
2010
2013 IDSA Clinical Practice Guideline for Vaccination of the Immunocompromised Host
2013 Standout
THE MOLECULAR GENETICS OF 21-HYDROXYLASE DEFICIENCY
1989
Pathogenesis and Diagnosis of Shiga Toxin-Producing Escherichia coli Infections
1998 Standout
Isolation of cDNA clones specifying the fourth component of mouse complement and its isotype, sex-limited protein.
1984 StandoutNobel
Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.
1986 Nobel
Incidence and trends of infection with pathogens transmitted commonly through food--Foodborne Diseases Active Surveillance Network, 10 U.S. sites, 2006-2013.
2014 Standout
GENETICS OF SYSTEMIC LUPUS ERYTHEMATOSUS
1992
Works of G. Mauff being referenced
Yersinia enterocolitica serodiagnosis: A dual role of specific IgA. Evaluation of microagglutination and ELISA
1987
Major Histocompatibility Complex Class I to III Allotypes in Patients with AIDS‐Related Complex/Walter‐Reed 5, Disseminated Kaposi's Sarcoma and in Normal Controls
1990
The study of a French family with two duplicated C4A haplotypes
1987
Epidemiology of HIV and hepatitis B virus (HBV) in selected African and Asian populations
1989
Reference Typing Report for Complement Component C4
1998
Factor B Reference Typing Report
1990
Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from Southern Brazil: the Kaingang and the Guarani
1997
Campylobacter and Salmonella Contaminating Fresh Chicken Meat
1996
C4 Nomenclature Statement (1990)
1990
Human BF*F-subtypes: segregation analysis with inclusion of MHC haplotypes
1989
An estimate on the frequency of duplicated haplotypes and silent alleles of human C4 protein polymorphism. I. Investigations in healthy Caucasoid families
1989
C4 AND HLA HAPLOTYPES ASSOCIATED WITH PARTIAL INHIBITION OF ANTI‐RG AND ANTI‐CH
1984
Detection of the Genetic Polymorphism of Human C2 (Native Protein and C2a Fragment) by Immunoblotting after Polyacrylamide Gel Isoelectric Focusing
1985
Properdin factor B (glycine-rich beta-glycoprotein or C3 proactivator)-polymorphism: genetic and biochemical aspects. First application to paternity cases.
1975
Multiple Sclerosis: Immunogenetic Analyses of Sib-Pair Double Case Families. II. Studies on the Association of Multiple Sclerosis with C2, C4, BF, C3, C6, and GLO Polymorphisms
1983
Clinical and immunological studies in a case of selective complete C1q deficiency.
1979
The C4 ?-chain: Evidence for a genetically determined polymorphism
1983
A Hemolytically Inactive Gene Product of Factor B
1980
Esterase D polymorphism: High-voltage agarose-gel electrophoresis and distribution of phenotypes in different European populations
1975
Genetic Polymorphism of the Fourth Component of Human Complement1
1978
Linkage studies in a pedigree with Van der Woude syndrome.
1987