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Campylobacter Genotyping to Determine the Source of Human Infection
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A case–control study of risk factors for sporadic campylobacter infections in Denmark
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Campylobacter jejuni Infections: Update on Emerging Issues and Trends
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A Risk Assessment Model for Campylobacter in Broiler Meat
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Multilocus Sequence Typing of Bacteria
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Tracing the Source of Campylobacteriosis
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Campylobacter source attribution by exposure assessment
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The Dioxin Crisis as Experiment To Determine Poultry-Related Campylobacter Enteritis
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Molecular Characterization ofCampylobacter jejuniClones: A Basis for Epidemiologic Investigation
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Host-associated Genetic Import inCampylobacter jejuni
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Campylobacter Contamination of Raw Meat and Poultry at Retail Sale: Identification of Multiple Types and Comparison with Isolates from Human Infection
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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An epidemiological investigation of Campylobacter in pig and poultry farms in the Mekong delta of Vietnam
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Ruminant and chicken: important sources of campylobacteriosis in France despite a variation of source attribution in 2009 and 2015
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Parallel sequencing of porA reveals a complex pattern of Campylobacter genotypes that differs between broiler and broiler breeder chickens
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Source attribution of Campylobacter jejuni shows variable importance of chicken and ruminants reservoirs in non-invasive and invasive French clinical isolates
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Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host
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Mining whole genome sequence data to efficiently attribute individuals to source populations
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Whole genome-based characterisation of antimicrobial resistance and genetic diversity in Campylobacter jejuni and Campylobacter coli from ruminants
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First molecular characterization and antimicrobial resistance profiles of Campylobacter jejuni isolated from poultry meat in Yemen
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Molecular epidemiology of Campylobacter jejuni associated with Guillain–Barré syndrome
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Campylobacter jejuni genotypes are associated with post-infection irritable bowel syndrome in humans
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Human Campylobacteriosis in Luxembourg, 2010–2013: A Case-Control Study Combined with Multilocus Sequence Typing for Source Attribution and Risk Factor Analysis
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Agricultural intensification and the evolution of host specialism in the enteric pathogen Campylobacter jejuni
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Accelerating Campylobacter zoonosis in the Anthropocene
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Comparison of bacterial identification by MALDI-TOF mass spectrometry and conventional diagnostic microbiology methods: agreement, speed and cost implications
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Gut microbiome dysbiosis and functional alterations in Campylobacter -associated gastroenteritis using metagenomic approaches
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Study of Cytolethal Distending Toxin ( cdt ) in Campylobacter coli Using a Multiplex Polymerase Chain Reaction Assay and Its Distribution Among Clinical and Food Strains
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Campylobacter Excreted into the Environment by Animal Sources: Prevalence, Concentration Shed, and Host Association
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Genetic Similarity of Campylobacter Isolates in Humans, Food, and Water Sources in Central Poland
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Antimicrobial Resistance Profiles of Campylobacter from Humans, Retail Chicken Meat, and Cattle Feces
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Using Outbreak Data for Source Attribution of Human Salmonellosis and Campylobacteriosis in Europe
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Diversity of Campylobacter in Retail Meat and Liver of Lambs and Goat Kids
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Drivers of Uncertainty in Estimates of Foodborne Gastroenteritis Incidence
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Typing of Campylobacter jejuni Isolated from Turkey by Genotypic Methods, Antimicrobial Susceptibility, and Virulence Gene Patterns: A Retrospective Study
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Genetic Relatedness Among Shiga Toxin–Producing Escherichia coli Isolated Along the Animal Food Supply Chain and in Gastroenteritis Cases in Qatar Using Multilocus Sequence Typing
inferred← citeshttps://doi.org/10.1089/fpd.2019.2681openalex-snapshot
Laboratory Study on the Gastroenteritis Outbreak Caused by a Multidrug-Resistant Campylobacter coli in China
inferred← citeshttps://doi.org/10.1089/fpd.2023.0046openalex-snapshot
Predicting Food Sources of Listeria monocytogenes Based on Genomic Profiling Using Random Forest Model
inferred← citeshttps://doi.org/10.1089/fpd.2023.0137openalex-snapshot
Detection of Escherichia coli O157H7 and Campylobacter jejuni in Bovine Carcasses in Two Slaughterhouses in Bio-Bío District, Chile
inferred← citeshttps://doi.org/10.1089/mdr.2012.0099openalex-snapshot
Antimicrobial Resistance Patterns and Corresponding Multilocus Sequence Types of the Campylobacter jejuni Isolates from Human Diarrheal Samples
inferred← citeshttps://doi.org/10.1093/cid/civ431openalex-snapshot
Partial Failure of Milk Pasteurization as a Risk for the Transmission ofCampylobacterFrom Cattle to Humans
inferred← citeshttps://doi.org/10.1093/gbe/evy026openalex-snapshot
Convergent Amino Acid Signatures in Polyphyletic Campylobacter jejuni Subpopulations Suggest Human Niche Tropism
inferred← citeshttps://doi.org/10.1093/nar/gkw019openalex-snapshot
Phase variation of a Type IIG restriction-modification enzyme alters site-specific methylation patterns and gene expression inCampylobacter jejunistrain NCTC11168
inferred← citeshttps://doi.org/10.1097/inf.0000000000000989openalex-snapshot
Risk Factors for Sporadic Infection With Campylobacter Spp. Among Children in Israel
inferred← citeshttps://doi.org/10.1098/rspb.2015.2323openalex-snapshot
Monitoring chicken flock behaviour provides early warning of infection by human pathogen Campylobacter
inferred← citeshttps://doi.org/10.1099/jmm.0.002053openalex-snapshot
Growth rates and metabolic traits differ by diarrhoeal manifestation in Campylobacter jejuni strains
inferred← citeshttps://doi.org/10.1099/mgen.0.000198openalex-snapshot
Trends in fluoroquinolone resistance in Campylobacter
inferred← citeshttps://doi.org/10.1099/mgen.0.000834openalex-snapshot
Local accessory gene sharing among Egyptian Campylobacter potentially promotes the spread of antimicrobial resistance
inferred← citeshttps://doi.org/10.1099/mgen.0.001121openalex-snapshot
Evidence of potential Campylobacter jejuni zooanthroponosis in captive macaque populations
inferred← citeshttps://doi.org/10.1099/mgen.0.001714openalex-snapshot
GeneScanner: profiling genetic variation across bacterial populations
inferred← citeshttps://doi.org/10.1099/mic.0.031047-0openalex-snapshot
Genetic diversity and stability of the porA allele as a genetic marker in human Campylobacter infection
inferred← citeshttps://doi.org/10.1099/mic.0.045153-0openalex-snapshot
Introgression in the genus Campylobacter: generation and spread of mosaic alleles
inferred← citeshttps://doi.org/10.1099/mic.0.062000-0openalex-snapshot
Campylobacter sequence typing databases: applications and future prospects
inferred← citeshttps://doi.org/10.1101/2020.06.10.141978openalex-snapshot
Deep sequencing reveals Campylobacter in commercial meat chickens less than 8 days old
inferred← citeshttps://doi.org/10.1101/2020.12.02.407999openalex-snapshot
Quantifying bacterial evolution in the wild: a birthday problem for Campylobacter lineages
inferred← citeshttps://doi.org/10.1101/2021.03.15.435406openalex-snapshot
A two-hit epistasis model prevents core genome disharmony in recombining bacteria
inferred← citeshttps://doi.org/10.1101/2021.09.24.461243openalex-snapshot
Local accessory gene sharing drives lineage-specific acquisition of antimicrobial resistance in Egyptian Campylobacter spp .
inferred← citeshttps://doi.org/10.1101/2023.07.11.548564openalex-snapshot
Urbanization spreads antimicrobial resistant enteric pathogens in wild bird microbiomes
inferred← citeshttps://doi.org/10.1101/2023.11.09.566360openalex-snapshot
Genomic tailoring of autogenous poultry vaccines to reduce Campylobacter from farm to fork
inferred← citeshttps://doi.org/10.1101/2025.04.24.650550openalex-snapshot
Growth Rates and Metabolic Traits Differ by Diarrheal Manifestation in Campylobacter jejuni Strains
inferred← citeshttps://doi.org/10.1101/332544openalex-snapshot
High-resolution sweep metagenomics using fast probabilistic inference
inferred← citeshttps://doi.org/10.1101/cshperspect.a018119openalex-snapshot
The Evolution of Campylobacter jejuni and Campylobacter coli
inferred← citeshttps://doi.org/10.1111/1462-2920.12415openalex-snapshot
The long‐term dynamics of C ampylobacter colonizing a free‐range broiler breeder flock: an observational study
inferred← citeshttps://doi.org/10.1111/1462-2920.13051openalex-snapshot
Enhanced biofilm formation and multi‐host transmission evolve from divergent genetic backgrounds in C ampylobacter jejuni
inferred← citeshttps://doi.org/10.1111/1462-2920.13092openalex-snapshot
Major contribution of the type II beta carbonic anhydrase CanB ( C j0237) to the capnophilic growth phenotype of C ampylobacter jejuni
inferred← citeshttps://doi.org/10.1111/1462-2920.13628openalex-snapshot
Genome‐wide association of functional traits linked with C ampylobacter jejuni survival from farm to fork
inferred← citeshttps://doi.org/10.1111/1462-2920.13930openalex-snapshot
Transcriptome and proteome dynamics in chemostat culture reveal how Campylobacter jejuni modulates metabolism, stress responses and virulence factors upon changes in oxygen availability
inferred← citeshttps://doi.org/10.1111/1462-2920.14760openalex-snapshot
Gene pool transmission of multidrug resistance among Campylobacter from livestock, sewage and human disease
inferred← citeshttps://doi.org/10.1111/1574-6968.12488openalex-snapshot
Role of environmental survival in transmission ofCampylobacter jejuni
inferred← citeshttps://doi.org/10.1111/1758-2229.12314openalex-snapshot
Wild bird‐associated C ampylobacter jejuni isolates are a consistent source of human disease, in O xfordshire, U nited K ingdom
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2009.04444.xopenalex-snapshot
MLST clustering of Campylobacter jejuni isolates from patients with gastroenteritis, reactive arthritis and Guillain–Barré syndrome
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2010.04883.xopenalex-snapshot
Campylobacter genotypes from poultry transportation crates indicate a source of contamination and transmission
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2011.05038.xopenalex-snapshot
Potential sources of Campylobacter infection on chicken farms: contamination and control of broiler-harvesting equipment, vehicles and personnel
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05179.xopenalex-snapshot
Niche segregation and genetic structure of Campylobacter jejuni populations from wild and agricultural host species
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2011.02461.xopenalex-snapshot
Genomic variations define divergence of water/wildlife‐associated Campylobacter jejuni niche specialists from common clonal complexes
inferred← citeshttps://doi.org/10.1111/j.1472-765x.2011.03121.xopenalex-snapshot
Following an imaginary Campylobacter population from farm to fork and beyond: a bacterial perspective
inferred← citeshttps://doi.org/10.1111/j.1758-2229.2011.00265.xopenalex-snapshot
Campylobacter populations in wild and domesticated Mallard ducks ( Anas platyrhynchos )
inferred← citeshttps://doi.org/10.1111/j.1863-2378.2010.01373.xopenalex-snapshot
Genetic Diversity among Campylobacter jejuni Isolates from Healthy Livestock and Their Links to Human Isolates in Spain
inferred← citeshttps://doi.org/10.1111/j.1863-2378.2012.01525.xopenalex-snapshot
Multilocus Sequence Types of EnvironmentalCampylobacter jejuniIsolates and their Similarities to those of Human, Poultry and BovineC. jejuniIsolates
inferred← citeshttps://doi.org/10.1111/jam.14132openalex-snapshot
Relation between broiler and humanCampylobacter jejunistrains isolated in Belgium from 2011 to 2013
inferred← citeshttps://doi.org/10.1111/jam.14914openalex-snapshot
Occurrence of Campylobacter spp. in Swedish calves, common sequence types and antibiotic resistance patterns
inferred← citeshttps://doi.org/10.1111/jam.15753openalex-snapshot
Genomic diversity, virulence and source of Campylobacter jejuni contamination in Irish poultry slaughterhouses by whole genome sequencing
inferred← citeshttps://doi.org/10.1111/mec.12144openalex-snapshot
Marked host specificity and lack of phylogeographic population structure of Campylobacter jejuni in wild birds
inferred← citeshttps://doi.org/10.1111/mec.12162openalex-snapshot
Progressive genome‐wide introgression in agricultural Campylobacter coli
inferred← citeshttps://doi.org/10.1111/mec.13001openalex-snapshot
Evidence of land‐sea transfer of the zoonotic pathogen Campylobacter to a wildlife marine sentinel species
inferred← citeshttps://doi.org/10.1111/mec.14176openalex-snapshot
Local genes for local bacteria: Evidence of allopatry in the genomes of transatlantic Campylobacter populations
inferred← citeshttps://doi.org/10.1111/mmi.14715openalex-snapshot
The flavodoxin FldA activates the class Ia ribonucleotide reductase of Campylobacter jejuni
inferred← citeshttps://doi.org/10.1111/tbed.12931openalex-snapshot
Genetic characterization and epidemiological implications of Campylobacter isolates from wild birds in South Korea
inferred← citeshttps://doi.org/10.1111/tbed.13046openalex-snapshot
Molecular epidemiology and antimicrobial resistance mechanisms ofCampylobacter colifrom diarrhoeal patients and broiler carcasses in Belgium
inferred← citeshttps://doi.org/10.1111/tbed.14165openalex-snapshot
A pilot study revealing host‐associated genetic signatures for source attribution of sporadic Campylobacter jejuni infection in Egypt
inferred← citeshttps://doi.org/10.1111/zph.12141openalex-snapshot
Characterization of the Campylobacter jejuni Population in the Barnacle Geese Reservoir
inferred← citeshttps://doi.org/10.1111/zph.12300openalex-snapshot
Outbreak of Campylobacteriosis Associated with Raccoon Contact at a Wildlife Rehabilitation Centre, Minnesota, 2013
inferred← citeshttps://doi.org/10.1111/zph.12366openalex-snapshot
Population structure and attribution of human clinical Campylobacter jejuni isolates from central Europe to livestock and environmental sources
inferred← citeshttps://doi.org/10.1111/zph.12403openalex-snapshot
Attribution of human infections with Shiga toxin‐producing Escherichia coli ( STEC ) to livestock sources and identification of source‐specific risk factors, The Netherlands (2010–2014)
inferred← citeshttps://doi.org/10.1111/zph.12786openalex-snapshot
Epidemiology of Campylobacter jejuni in raccoons (Procyon lotor) on swine farms and in conservation areas in southern Ontario
inferred← citeshttps://doi.org/10.1111/zph.12802openalex-snapshot
Establishment of sentinel surveillance of human clinical campylobacteriosis in Ireland
inferred← citeshttps://doi.org/10.1111/zph.13063openalex-snapshot
UK ‐wide risk factor study of broiler carcases highly contaminated with Campylobacter
inferred← citeshttps://doi.org/10.1128/9781555817114.ch3openalex-snapshot
The Impact of Horizontal Genetic Exchange on Bacterial Population Structure: Insights from the GeneraNeisseriaandCampylobacter
inferred← citeshttps://doi.org/10.1128/aac.00669-13openalex-snapshot
Whole-Genome Sequencing of Gentamicin-Resistant Campylobacter coli Isolated from U.S. Retail Meats Reveals Novel Plasmid-Mediated Aminoglycoside Resistance Genes
inferred← citeshttps://doi.org/10.1128/aem.00124-10openalex-snapshot
Host Association of Campylobacter Genotypes Transcends Geographic Variation
inferred← citeshttps://doi.org/10.1128/aem.00162-17openalex-snapshot
Novel Sampling Method for Assessing Human-Pathogen Interactions in the Natural Environment Using Boot Socks and Citizen Scientists, with Application to Campylobacter Seasonality
inferred← citeshttps://doi.org/10.1128/aem.00428-11openalex-snapshot
Temporal Variation and Host Association in the Campylobacter Population in a Longitudinal Ruminant Farm Study
inferred← citeshttps://doi.org/10.1128/aem.00499-09openalex-snapshot
Spatiotemporal Homogeneity of Campylobacter Subtypes from Cattle and Sheep across Northeastern and Southwestern Scotland
inferred← citeshttps://doi.org/10.1128/aem.00537-14openalex-snapshot
Multilocus Sequence Typing Confirms Wild Birds as the Source of a Campylobacter Outbreak Associated with the Consumption of Raw Peas
inferred← citeshttps://doi.org/10.1128/aem.00546-15openalex-snapshot
Gene Loss and Lineage-Specific Restriction-Modification Systems Associated with Niche Differentiation in the Campylobacter jejuni Sequence Type 403 Clonal Complex
inferred← citeshttps://doi.org/10.1128/aem.00581-10openalex-snapshot
Decreasing Trend of Overlapping Multilocus Sequence Types between Human and Chicken Campylobacter jejuni Isolates over a Decade in Finland
inferred← citeshttps://doi.org/10.1128/aem.00813-10openalex-snapshot
Genotype and Antibiotic Resistance Analyses of Campylobacter Isolates from Ceca and Carcasses of Slaughtered Broiler Flocks
inferred← citeshttps://doi.org/10.1128/aem.00862-09openalex-snapshot
Molecular Epidemiology ofCampylobacter jejuniin a Geographically Isolated Country with a Uniquely Structured Poultry Industry
inferred← citeshttps://doi.org/10.1128/aem.00934-16openalex-snapshot
Molecular Epidemiology of Campylobacter coli Strains Isolated from Different Sources in New Zealand between 2005 and 2014
inferred← citeshttps://doi.org/10.1128/aem.01023-12openalex-snapshot
Association of Campylobacter jejuni Metabolic Traits with Multilocus Sequence Types
inferred← citeshttps://doi.org/10.1128/aem.01060-21openalex-snapshot
Parallel Sequencing Reveals Campylobacter spp. in Commercial Meat Chickens Less than 8 Days Old
inferred← citeshttps://doi.org/10.1128/aem.01388-10openalex-snapshot
Longitudinal Molecular Epidemiological Study of Thermophilic Campylobacters on One Conventional Broiler Chicken Farm
inferred← citeshttps://doi.org/10.1128/aem.01532-10openalex-snapshot
Survival of Campylobacter jejuni under Conditions of Atmospheric Oxygen Tension with the Support of Pseudomonas spp
inferred← citeshttps://doi.org/10.1128/aem.01753-09openalex-snapshot
Expanded Multilocus Sequence Typing and Comparative Genomic Hybridization of Campylobacter coli Isolates from Multiple Hosts
inferred← citeshttps://doi.org/10.1128/aem.01753-19openalex-snapshot
Shifts in the Molecular Epidemiology of Campylobacter jejuni Infections in a Sentinel Region of New Zealand following Implementation of Food Safety Interventions by the Poultry Industry
inferred← citeshttps://doi.org/10.1128/aem.01787-20openalex-snapshot
Genome-Wide Identification of Host-Segregating Single-Nucleotide Polymorphisms for Source Attribution of Clinical Campylobacter coli Isolates
inferred← citeshttps://doi.org/10.1128/aem.02162-14openalex-snapshot
Campylobacter Colonization and Proliferation in the Broiler Chicken upon Natural Field Challenge Is Not Affected by the Bird Growth Rate or Breed
inferred← citeshttps://doi.org/10.1128/aem.02521-12openalex-snapshot
Evidence for Phenotypic Plasticity among Multihost Campylobacter jejuni and C. coli Lineages, Obtained Using Ribosomal Multilocus Sequence Typing and Raman Spectroscopy
inferred← citeshttps://doi.org/10.1128/aem.03085-16openalex-snapshot
Genome-Wide Identification of Host-Segregating Epidemiological Markers for Source Attribution in Campylobacter jejuni
inferred← citeshttps://doi.org/10.1128/aem.03693-15openalex-snapshot
Genetic Diversity of Campylobacter jejuni and Campylobacter coli Isolates from Conventional Broiler Flocks and the Impacts of Sampling Strategy and Laboratory Method
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