Citation Impact
Citing Papers
Probing mucin-type O-linked glycosylation in living animals
2006 StandoutNobel
The mucin-selective protease StcE enables molecular and functional analysis of human cancer-associated mucins
2019 StandoutNobel
Limits of long-term selection against Neandertal introgression
2019 StandoutNobel
A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation
2003 StandoutNobel
X-linked cholestasis in mouse due to mutations of the P4-ATPase ATP11C
2011 StandoutNobel
Targeting of Cyclic AMP Degradation to β 2 -Adrenergic Receptors by β-Arrestins
2002 StandoutScienceNobel
Structural Basis of Carbohydrate Transfer Activity by Human UDP-GalNAc: Polypeptide α-N-Acetylgalactosaminyltransferase (pp-GalNAc-T10)
2006
Characterization of a novel human UDP‐GalNAc transferase, pp‐GalNAc‐T15
2004
The Human Chitotriosidase Gene
1998
Physiological functions of the HECT family of ubiquitin ligases
2009
Mechanism of met oncogene activation
1986
Exploring the glycan repertoire of genetically modified mice by isolation and profiling of the major glycan classes and nano-NMR analysis of glycan mixtures
2000
Assembly and self-association of Oxytricha telomeric nucleoprotein complexes
1989 StandoutNobel
The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains
1988 StandoutScience
Improved eye- and skin-color prediction based on 8 SNPs
2013
The chemistry and biology of mucin-type O-linked glycosylation
2005 StandoutNobel
Characterization of a novel human UDP‐GalNAc transferase, pp‐GalNAc‐T101
2002
Initiation of O-Glycan Synthesis in IgA1 Hinge Region Is Determined by a Single Enzyme, UDP-N-Acetyl-α-d-galactosamine:PolypeptideN-Acetylgalactosaminyltransferase 2
2003
The Lectin Domain of UDP-N-acetyl-d-galactosamine:PolypeptideN-acetylgalactosaminyltransferase-T4 Directs Its Glycopeptide Specificities
2000
Physical Principles of Membrane Shape Regulation by the Glycocalyx
2019 StandoutNobel
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
1996 Standout
The Molecular Biology of Cyclic Nucleotide Phosphodiesterases
1999
Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis
1999
Conservation of peptide acceptor preferences between Drosophila and mammalian polypeptide-GalNAc transferase ortholog pairs
2008
cDNA cloning and expression of UDP-N-acetyl-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase T1 from Toxoplasma gondii
2003 StandoutNobel
Structural basis for triplet repeat disorders: a computational analysis
1999 StandoutNobel
Glycopeptide-preferring Polypeptide GalNAc Transferase 10 (ppGalNAc T10), Involved in Mucin-type O-Glycosylation, Has a Unique GalNAc-O-Ser/Thr-binding Site in Its Catalytic Domain Not Found in ppGalNAc T1 or T2
2009 StandoutNobel
Patterns of polymorphism and linkage disequilibrium for cystic fibrosis
1987
Molecular cloning and characterization of a novel member of the UDP‐GalNAc:polypeptide N‐acetylgalactosaminyltransferase family, pp‐GalNAc‐T121
2002
Molecular and genetic analysis of cystic fibrosis*1
1988
Localization of O-glycans in MUC1 glycoproteins using electron-capture dissociation fragmentation mass spectrometry
2008
High Density O-Glycosylation on Tandem Repeat Peptide from Secretory MUC1 of T47D Breast Cancer Cells
1999
A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers
1988
CLN3 is required for the clearance of glycerophosphodiesters from lysosomes
2022 Nature
The telomere terminal transferase of tetrahymena is a ribonucleoprotein enzyme with two kinds of primer specificity
1987 StandoutNobel
Functional characterization of a novel Toxoplasma gondii glycosyltransferase: UDP-N-acetyl-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase-T3
2004
The lectin domains of polypeptide GalNAc-transferases exhibit carbohydrate-binding specificity for GalNAc: lectin binding to GalNAc-glycopeptide substrates is required for high density GalNAc-O-glycosylation
2007
Characterization of a UDP-GalNAc:Polypeptide N-Acetylgalactosaminyltransferase That Displays Glycopeptide N-Acetylgalactosaminyltransferase Activity
1999
Cloning and characterization of a novel UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, pp-GalNAc-T14
2003
CLINIC EXPERIENCE OF PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY USE OF LINKED DNA PROBES
1987
Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene
2000
Cloning and Characterization of a Close Homologue of Human UDP-N-acetyl-α-d-galactosamine:Polypeptide N-Acetylgalactosaminyltransferase-T3, Designated GalNAc-T6
1999
O-Linked Glycosylation in the Mammary Gland: Changes that Occur During Malignancy
2001
Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.
1989
Mucin Core O-Glycosylation Is Modulated by Neighboring Residue Glycosylation Status
2002
MUC1: the polymorphic appearance of a human mucin
2000
Salmonella typhi uses CFTR to enter intestinal epithelial cells
1998 StandoutNatureNobel
The Lectin Domain of UDP-GalNAc:Polypeptide N-Acetylgalactosaminyltransferase 1 Is Involved in O-Glycosylation of a Polypeptide with Multiple Acceptor Sites
2002
Evidence for glycosylation-dependent activities of polypeptide N-acetylgalactosaminyltransferases rGalNAc-T2 and -T4 on mucin glycopeptides
2001
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
1995 Nature
Constructing genomic maps of positive selection in humans: Where do we go from here?
2009
Defective Urinary Concentrating Ability Due to a Complete Deficiency of Aquaporin-1
2001 StandoutNobel
A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color
2008
O-Glycosylation of the Mucin Type
2001
Crossovers in two German cystic fibrosis families determine probe order for MET, 7C22 and XV-2c/CS.7
1987
Function of the lectin domain of polypeptide N-acetylgalactosaminyltransferase 1
2002
The Hallmarks of Aging
2013 Standout
A 12 megabase restriction map at the cystic fibrosis locus
1989
MUC1 and the MUCs: A Family of Human Mucins with Impact in Cancer Biology
2004
Mechanisms of trinucleotide repeat instability during human development
2010
Lectin Domains of Polypeptide GalNAc Transferases Exhibit Glycopeptide Binding Specificity
2011 StandoutNobel
A novel human UDP‐N‐acetyl‐D ‐galactosamine:polypeptide N‐acetylgalactosaminyltransferase, GalNAc‐T7, with specificity for partial GalNAc‐glycosylated acceptor substrates
1999
Allelic inactivation regulates olfactory receptor gene expression
1994 StandoutNobel
Identification of Common and Unique Peptide Substrate Preferences for the UDP-GalNAc:Polypeptide α-N-acetylgalactosaminyltransferases T1 and T2 Derived from Oriented Random Peptide Substrates
2006
Expression of polypeptide GalNAc-transferases in stratified epithelia and squamous cell carcinomas: immunohistological evaluation using monoclonal antibodies to three members of the GalNAc-transferase family
1999
Functional Conservation of Subfamilies of Putative UDP-N-acetylgalactosamine:Polypeptide N-Acetylgalactosaminyltransferases inDrosophila, Caenorhabditis elegans, and Mammals
2002
The Human Condition—A Molecular Approach
2014 StandoutNobel
Cloning and Characterization of a Ninth Member of the UDP-GalNAc:Polypeptide N-Acetylgalactosaminyltransferase Family, ppGaNTase-T9
2001
Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis
2006
Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis
1988
The Cystic Fibrosis Transmembrane Conductance Regulator Gene
1995
An Animal Model for Cystic Fibrosis Made by Gene Targeting
1992 StandoutScienceNobel
Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells
2010 StandoutNobel
Linkage disequilibrium, cystic fibrosis, and genetic counseling.
1989
Localization to Mature Melanosomes by Virtue of Cytoplasmic Dileucine Motifs Is Required for Human OCA2 Function
2008
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene.
1988
Recombinations between IRP and cystic fibrosis.
1988
Studies of cystic fibrosis in Hutterite families by using linked DNA probes.
1987
Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney.
1996 StandoutNobel
The application of molecular genetics to detection of craniofacial abnormality
1988
Further linkage data on cystic fibrosis: the Utah Study.
1986
Delineation of DNA replication time zones by fluorescence in situ hybridization.
1992
Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population.
1996 StandoutNobel
FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WITH LINKED DNA PROBES
1986
The rate of telomere sequence loss in human leukocytes varies with age
1998 StandoutNobel
Lysosomal cathepsin D mediates endogenous mucin glycodomain catabolism in mammals
2022 StandoutNobel
Probing polypeptide GalNAc-transferase isoform substrate specificities by in vitro analysis
2014
The telomeres of the linear mitochondrial DNA of tetrahymena thermophila consist of 53 bp tandem repeats
1986 StandoutNobel
Microdissection and microcloning of the long arm of human chromosome 7
1987
Bacterial Biofilms: A Common Cause of Persistent Infections
1999 StandoutScience
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7.
1987
Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray
1995 StandoutScience
Isolation of cDNA clones for the catalytic gamma subunit of mouse muscle phosphorylase kinase: expression of mRNA in normal and mutant Phk mice.
1987
CRISPR-CasΦ from huge phages is a hypercompact genome editor
2020 StandoutScienceNobel
Cystic fibrosis: typing 48 German families with linked DNA probes
1987
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
1989 Standout
Programmed DNA destruction by miniature CRISPR-Cas14 enzymes
2018 StandoutScienceNobel
Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8.
1989
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands
1987 Nature
Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations
2018 StandoutScienceNobel
Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.
1986
PRENATAL DIAGNOSIS OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE WITH A DNA PROBE
1986
Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study.
1988
CHIP Deficiency Decreases Longevity, with Accelerated Aging Phenotypes Accompanied by Altered Protein Quality Control
2008
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.
1989
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Cell-type-specific and hypoxia-inducible expression of the human erythropoietin gene in transgenic mice.
1991 StandoutNobel
Potential of preventing Pseudomonas aeruginosa lung infections in cystic fibrosis patients: Experimental studies in animals
1996
Linkage of DNA markers to cystic fibrosis in 26 families.
1986
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study.
1986
Chemically tunable mucin chimeras assembled on living cells
2015 StandoutNobel
Physical localization of two DNA markers closely linked to the cystic fibrosis locus by pulsed-field gel electrophoresis.
1989
Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene.
1989
The beginnings of mucin biosynthesis: The crystal structure of UDP-GalNAc:polypeptide α- N -acetylgalactosaminyltransferase-T1
2004
Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
1989 StandoutScience
Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location
1986 Nature
DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis.
1989
The Molecular Genetics of Cancer
1987 StandoutScienceNobel
Nuclear repartitioning of galectin-1 by an extracellular glycan switch regulates mammary morphogenesis
2016 StandoutNobel
Regional mapping of six cloned DNA sequences on human chromosome 7.
1986
Reverse genetics and human disease
1986
A genetic analysis of the Gibraltar Neanderthals
2019 StandoutNobel
Characterization of a UDP-N-acetyl-D -galactosamine:polypeptide N-acetylgalactosaminyltransferase with an unusual lectin domain from the platyhelminth parasite Echinococcus granulosus
2004
Mutation detection with MutH, MutL, and MutS mismatch repair proteins.
1996 StandoutNobel
Derivation of Clones Close to met by Preparative Field Inversion Gel Electrophoresis
1987 Science
Linkage between the Colton blood group locus and ASSP11 on chromosome 7
1990
Initiation of Protein O Glycosylation by the Polypeptide GalNAcT-1 in Vascular Biology and Humoral Immunity
2007
Genetic linkage map of human chromosome 7 with 63 DNA markers.
1987
Genetic analysis of cystic fibrosis using linked DNA markers.
1986
Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation
2013 StandoutNobel
Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer.
1987
Construction of a General Human Chromosome Jumping Library, with Application to Cystic Fibrosis
1987 Science
Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP.
1989
Circadian control of XPA and excision repair of cisplatin-DNA damage by cryptochrome and HERC2 ubiquitin ligase
2010 StandoutNobel
Polycythemia in transgenic mice expressing the human erythropoietin gene.
1989 StandoutNobel
A High-Throughput O-Glycopeptide Discovery Platform for Seromic Profiling
2010
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.
1988
Telomere replication, kinetochore organizers, and satellite DNA evolution.
1979
High-resolution structures of a chitinase complexed with natural product cyclopentapeptide inhibitors: Mimicry of carbohydrate substrate
2002 StandoutNobel
Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysis
1987
The Structure of Haplotype Blocks in the Human Genome
2002 StandoutScience
Genetic homogeneity of cystic fibrosis
1986
Targeted Investigation of the Neandertal Genome by Array-Based Sequence Capture
2010 StandoutScienceNobel
Chemical Glycoproteomics
2016 StandoutNobel
The Human Genome Project
1991
Cleft palate in mice with a targeted mutation in the γ-aminobutyric acid-producing enzyme glutamic acid decarboxylase 67
1997 StandoutNobel
Works of Hans Eiberg being referenced
Cloning of a Human UDP-N-Acetyl-α-d-Galactosamine:PolypeptideN-Acetylgalactosaminyltransferase That Complements Other GalNAc-Transferases in Complete O-Glycosylation of the MUC1 Tandem Repeat
1998
Localization of cystic fibrosis locus to human chromosome 7cen–q22
1985 Nature
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression
2008
Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract
2002
Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1
1998
Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16
1990
Human eye colour and HERC2, OCA2 and MATP
2010
A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family
2008
Batten disease (Spielmeyer‐Sjogren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16
1989
Genomic organization and chromosomal localization of three members of the UDP-N-acetylgalactosamine: Polypeptide N-acetylgalactosaminyltransferase family
1998
Linkage Studies of Cholestasis Familiaris Groenlandica/Byler-Like Disease with Polymorphic Protein and Blood Group Markers
1993
Cag Repeat Expansion in Autosomal Dominant Pure Spastic Paraplegia Linked to Chromosome 2p21-p24
1997
Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the β-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3
1994
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
1987
Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1q by a linkage study
1997
Assignment of Genes Coding forBrown Eye Colour (BEY2) andBrown Hair Colour (HCL3) onChromosome 15q
1996
Linkage of cystic fibrosis to the proα 2(I) collagen gene, COL1A2, on chromosome 7
1986
Linkage between the loci for cystic fibrosis and paraoxonase
1986
Colton blood groups: indication of linkage with the Kidd (Jk) system as support for assignment to chromosome 7
1977
Linkage relationships of paraoxonase (PON) with other markers: indication of PON‐cystic fibrosis synteny
1985
New selective Giemsa technique for human chromosomes, Cd staining
1974 Nature
Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker
1985 Science