On the public citation graph

Tracing the Source of Campylobacteriosis

https://doi.org/10.1371/journal.pgen.1000203
0 signed · 457 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00239-004-0316-0openalex-snapshot
Analysis of Recombination in Campylobacter jejuni from MLST Population Data
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2007.01.006openalex-snapshot
Campylobacters as zoonotic pathogens: A food production perspective
inferredcites →https://doi.org/10.1016/j.tree.2004.10.009openalex-snapshot
Germs, genomes and genealogies
inferredcites →https://doi.org/10.1017/s0950268803008495openalex-snapshot
Outbreaks of infectious disease associated with private drinking water supplies in England and Wales 1970–2000
inferredcites →https://doi.org/10.1017/s0950268805005509openalex-snapshot
Most Campylobacter subtypes from sporadic infections can be found in retail poultry products and food animals
inferredcites →https://doi.org/10.1017/s0950268806006406openalex-snapshot
Outbreaks of waterborne infectious intestinal disease in England and Wales, 1992–2003
inferredcites →https://doi.org/10.1046/j.1365-2672.2001.01355.xopenalex-snapshot
Campylobacters in water, sewage and the environment
inferredcites →https://doi.org/10.1073/pnas.0503252102openalex-snapshot
Comparative phylogenomics of the food-borne pathogen Campylobacter jejuni reveals genetic markers predictive of infection source
inferredcites →https://doi.org/10.1086/381598openalex-snapshot
Risk Factors for SporadicCampylobacterInfection in the United States: A Case‐Control Study in FoodNet Sites
inferredcites →https://doi.org/10.1086/513785openalex-snapshot
The Economic Burden ofCampylobacter‐AssociatedGuillain‐Barré Syndrome
inferredcites →https://doi.org/10.1093/aje/kwg139openalex-snapshot
Factors Associated with Increased and Decreased Risk of Campylobacter Infection: A Prospective Case-Control Study in Norway
inferredcites →https://doi.org/10.1093/genetics/131.2.479openalex-snapshot
Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data.
inferredcites →https://doi.org/10.1093/genetics/155.1.451openalex-snapshot
The Coalescent With Gene Conversion
inferredcites →https://doi.org/10.1093/genetics/156.2.879openalex-snapshot
Consequences of Recombination on Traditional Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/genetics/163.1.367openalex-snapshot
Bayesian Analysis of Genetic Differentiation Between Populations
inferredcites →https://doi.org/10.1093/genetics/164.4.1567openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data: Linked Loci and Correlated Allele Frequencies
inferredcites →https://doi.org/10.1093/genetics/49.4.725openalex-snapshot
THE NUMBER OF ALLELES THAT CAN BE MAINTAINED IN A FINITE POPULATION
inferredcites →https://doi.org/10.1093/genetics/59.4.565openalex-snapshot
A MIGRATION MATRIX MODEL FOR THE STUDY OF RANDOM GENETIC DRIFT
inferredcites →https://doi.org/10.1093/rheumatology/keg303openalex-snapshot
Health problems following Campylobacter jejuni enteritis in a Lancashire population
inferredcites →https://doi.org/10.1111/j.1365-2672.2007.03437.xopenalex-snapshot
Statistical comparison of Campylobacter jejuni subtypes from human cases and environmental sources
inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00782.xopenalex-snapshot
Spatial epidemiology and natural population structure of Campylobacter jejuni colonizing a farmland ecosystem
inferredcites →https://doi.org/10.1126/science.286.5448.2275openalex-snapshot
Food Irradiation--The Neglected Solution to Food-Borne Illness
inferredcites →https://doi.org/10.1128/aem.01488-06openalex-snapshot
Longitudinal Study of Finnish Campylobacter jejuni and C. coli Isolates from Humans, Using Multilocus Sequence Typing, Including Comparison with Epidemiological Data and Isolates from Poultry and Cattle
inferredcites →https://doi.org/10.1128/aem.69.11.6370-6379.2003openalex-snapshot
MultilocusSequence Typing for Comparison of Veterinary and HumanIsolates of Campylobacter jejuni
inferredcites →https://doi.org/10.1128/aem.69.12.7409-7413.2003openalex-snapshot
Genetic Diversity of Campylobacter jejuni Isolates from Farm Animals and the FarmEnvironment
inferredcites →https://doi.org/10.1128/aem.71.1.85-92.2005openalex-snapshot
Temperature-Driven Campylobacter Seasonality in England and Wales
inferredcites →https://doi.org/10.1128/aem.72.1.645-652.2006openalex-snapshot
Sources of Campylobacter spp. Colonizing Housed Broiler Flocks during Rearing
inferredcites →https://doi.org/10.1128/aem.72.5.3309-3313.2006openalex-snapshot
Genetic Diversity and Quinolone Resistance in Campylobacter jejuni Isolates from Poultry in Senegal
inferredcites →https://doi.org/10.1128/jcm.39.1.14-23.2001openalex-snapshot
Multilocus Sequence Typing System for Campylobacter jejuni
inferredcites →https://doi.org/10.1128/jcm.43.11.5705-5714.2005openalex-snapshot
Campylobacter coliin Swine Production: Antimicrobial Resistance Mechanisms and Molecular Epidemiology
inferredcites →https://doi.org/10.1128/jcm.43.5.2080-2091.2005openalex-snapshot
Use of the Oxford Multilocus Sequence Typing Protocol and Sequencing of the Flagellin Short Variable Region To Characterize Isolates from a Large Outbreak of Waterborne Campylobacter sp. Strains in Walkerton, Ontario, Canada
inferredcites →https://doi.org/10.1128/jcm.43.5.2315-2329.2005openalex-snapshot
Extended Multilocus Sequence Typing System for Campylobacter coli , C. lari , C. upsaliensis , and C. helveticus
inferredcites →https://doi.org/10.1128/jcm.43.8.4221-4224.2005openalex-snapshot
Genetic Diversity of Campylobacter sp. Isolates from Retail Chicken Products and Humans with Gastroenteritis in Central Michigan
inferredcites →https://doi.org/10.2175/106143006x95483openalex-snapshot
Published Case Studies of Waterborne Disease Outbreaks—Evidence of a Recurrent Threat
inferredcites →https://doi.org/10.2527/jas.2006-612openalex-snapshot
Preharvest control of Escherichia coli O157 in cattle1
inferredcites →https://doi.org/10.3201/eid0809.010817openalex-snapshot
A Case-Case Comparison ofCampylobacter coliandCampylobacter jejuniInfection: A Tool for Generating Hypotheses
inferredcites →https://doi.org/10.3201/eid0809.02-0122openalex-snapshot
Molecular Characterization ofCampylobacter jejuniClones: A Basis for Epidemiologic Investigation
inferredcites →https://doi.org/10.3201/eid1103.040191openalex-snapshot
Disease Risks from Foods, England and Wales, 1996–2000
inferredcites →https://doi.org/10.3201/eid1302.060620openalex-snapshot
Host-associated Genetic Import inCampylobacter jejuni

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4671846openalex-extracted
Machine Learning the Source Campylobacter Infection in the United States of America
inferred← citeshttps://doi.org/10.1002/9780470600122.ch10openalex-snapshot
Population Genetics ofCampylobacter
inferred← citeshttps://doi.org/10.1002/9781118644843.ch28openalex-snapshot
Campylobacter jejuni: Molecular Mechanisms and Animal Models of Colonization and Disease
inferred← citeshttps://doi.org/10.1002/cpmc.64openalex-snapshot
Isolation and Whole‐Genome Sequencing of Environmental Campylobacter
inferred← citeshttps://doi.org/10.1002/efs3.2014.11.issue-4openalex-snapshot
inferred← citeshttps://doi.org/10.1002/mbo3.102openalex-snapshot
C ampylobacter jejuni colonization and population structure in urban populations of ducks and starlings in N ew Z ealand
inferred← citeshttps://doi.org/10.1007/5584_2020_531openalex-snapshot
Intracellular Survival and Translocation Ability of Human and Avian Campylobacter jejuni and Campylobacter coli Strains
inferred← citeshttps://doi.org/10.1007/978-1-4939-2004-4_22openalex-snapshot
Characterization of Campylobacter jejuni and Campylobacter coli Genotypes in Poultry Flocks by Restriction Fragment Length Polymorphism (RFLP) Analysis
inferred← citeshttps://doi.org/10.1007/978-3-030-65481-8_2openalex-snapshot
The Data Behind Risk Analysis of Campylobacter Jejuni and Campylobacter Coli Infections
inferred← citeshttps://doi.org/10.1007/978-3-030-65481-8_5openalex-snapshot
Emission Sources of Campylobacter from Agricultural Farms, Impact on Environmental Contamination and Intervention Strategies
inferred← citeshttps://doi.org/10.1007/978-3-030-97291-2_18openalex-snapshot
The Link Between Animal Manure and Zoonotic Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-43751-4_8openalex-snapshot
Campylobacter
inferred← citeshttps://doi.org/10.1007/978-3-319-54051-1_3openalex-snapshot
Bacteriophage Biocontrol in Poultry
inferred← citeshttps://doi.org/10.1007/978-94-017-9457-2_6openalex-snapshot
Campylobacter: Animal Reservoirs, Human Infections, and Options for Control
inferred← citeshttps://doi.org/10.1007/s00580-014-1981-zopenalex-snapshot
Distribution of Salmonella, Arcobacter, and thermophilic Campylobacter spp. among Persian fallow deer (Dama mesopotamica) population in Dasht-e-Arzhan Wildlife refuge, southern Iran
inferred← citeshttps://doi.org/10.1007/s10068-014-0162-9openalex-snapshot
Occurrence of multidrug resistance in Campylobacter from Ivorian poultry and analysis of bacterial response to acid shock
inferred← citeshttps://doi.org/10.1007/s10096-014-2184-xopenalex-snapshot
Comparative population structure analysis of Campylobacter jejuni from human and poultry origin in Bangladesh
inferred← citeshttps://doi.org/10.1007/s12571-012-0230-zopenalex-snapshot
The risk of transfer of foodborne bacterial hazards in Turkey through the consumption of meat; risk ranking of muscle foods with the potential to transfer Campylobacter spp.
inferred← citeshttps://doi.org/10.1016/b978-0-12-416041-5.00002-0openalex-snapshot
The Foods Most Often Associated with Major Foodborne Pathogens
inferred← citeshttps://doi.org/10.1016/b978-0-12-416041-5.00009-3openalex-snapshot
Campylobacter
inferred← citeshttps://doi.org/10.1016/b978-0-12-800245-2.00005-8openalex-snapshot
A Descriptive Tool for Tracing Microbiological Contaminations
inferred← citeshttps://doi.org/10.1016/b978-0-12-800723-5.00003-6openalex-snapshot
Bacterial Contamination in Food Production
inferred← citeshttps://doi.org/10.1016/b978-0-12-801214-7.00004-1openalex-snapshot
Antimicrobial Resistance and Campylobacter jejuni and C. coli
inferred← citeshttps://doi.org/10.1016/b978-0-12-803623-5.00005-8openalex-snapshot
Campylobacter epidemiology—sources and routes of transmission for human infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-811444-5.00004-xopenalex-snapshot
Foodborne Pathogen–Produced Toxins and Their Signal Transduction
inferred← citeshttps://doi.org/10.1016/b978-0-12-818619-0.00075-7openalex-snapshot
Campylobacter
inferred← citeshttps://doi.org/10.1016/b978-0-12-819519-2.00013-xopenalex-snapshot
Campylobacter
inferred← citeshttps://doi.org/10.1016/j.cimid.2012.05.002openalex-snapshot
Campylobacter spp., C. jejuni and C. upsaliensis infection-associated factors in healthy and ill dogs from clinics in Cordoba, Spain. Screening tests for antimicrobial susceptibility
inferred← citeshttps://doi.org/10.1016/j.cimid.2014.01.001openalex-snapshot
Campylobacter infection in wild artiodactyl species from southern Spain: Occurrence, risk factors and antimicrobial susceptibility
inferred← citeshttps://doi.org/10.1016/j.cofs.2016.04.004openalex-snapshot
Significance of whole genome sequencing for surveillance, source attribution and microbial risk assessment of foodborne pathogens
inferred← citeshttps://doi.org/10.1016/j.copbio.2009.03.004openalex-snapshot
Comparative studies of Campylobacter jejuni genomic diversity reveal the importance of core and dispensable genes in the biology of this enigmatic food-borne pathogen
inferred← citeshttps://doi.org/10.1016/j.diagmicrobio.2012.06.004openalex-snapshot
Detection of antibodies to Campylobacter in humans using enzyme-linked immunosorbent assays: a review of the literature
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2011.04.008openalex-snapshot
New hydroepidemiological models of indicator organisms and zoonotic pathogens in agricultural watersheds
inferred← citeshttps://doi.org/10.1016/j.fm.2015.05.006openalex-snapshot
Real-time PCR detection of Campylobacter spp.: A comparison to classic culturing and enrichment
inferred← citeshttps://doi.org/10.1016/j.fm.2017.03.002openalex-snapshot
New paradigms for Salmonella source attribution based on microbial subtyping
inferred← citeshttps://doi.org/10.1016/j.foodcont.2015.02.044openalex-snapshot
Towards the production of reliable quantitative microbiological data for risk assessment: Direct quantification of Campylobacter in naturally infected chicken fecal samples using selective culture and real-time PCR
inferred← citeshttps://doi.org/10.1016/j.foodcont.2019.01.003openalex-snapshot
A quantitative microbial risk assessment model of Campylobacter in broiler chickens: Evaluating processing interventions
inferred← citeshttps://doi.org/10.1016/j.foodres.2020.109253openalex-snapshot
Variability in lag-duration of Campylobacter spp. during enrichment after cold and oxidative stress and its impact on growth kinetics and reliable detection
inferred← citeshttps://doi.org/10.1016/j.heliyon.2019.e02814openalex-snapshot
Human campylobacteriosis: A public health concern of global importance
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.01.033openalex-snapshot
EFSA's 12th Scientific Colloquium — Assessing health benefits of controlling Campylobacter in the food chain
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.06.014openalex-snapshot
Evaluation of the “testing and scheduling” strategy for control of Campylobacter in broiler meat in The Netherlands
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.10.015openalex-snapshot
Future challenges to microbial food safety
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2009.12.021openalex-snapshot
Comparison of Campylobacter populations isolated from a free-range broiler flock before and after slaughter
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2010.12.015openalex-snapshot
Challenges of Campylobacter jejuni in poultry production
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2014.07.002openalex-snapshot
Exploiting the explosion of information associated with whole genome sequencing to tackle Shiga toxin-producing Escherichia coli (STEC) in global food production systems
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2016.03.009openalex-snapshot
Tracing isolates from domestic human Campylobacter jejuni infections to chicken slaughter batches and swimming water using whole-genome multilocus sequence typing
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2016.08.026openalex-snapshot
Campylobacters and their bacteriophages from chicken liver: The prospect for phage biocontrol
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2018.03.010openalex-snapshot
A representative overview of the genetic diversity and lipooligosaccharide sialylation in Campylobacter jejuni along the broiler production chain in France and its comparison with human isolates
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2020.108984openalex-snapshot
Cross-contamination events of Campylobacter spp. in domestic kitchens associated with consumer handling practices of raw poultry
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2021.109075openalex-snapshot
Comparative history of Campylobacter contamination on chicken meat and campylobacteriosis cases in the United States: 1994–2018
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2021.109518openalex-snapshot
Role of substrate availability in the growth of Campylobacter co-cultured with extended spectrum beta-lactamase-producing Escherichia coli in Bolton broth
inferred← citeshttps://doi.org/10.1016/j.ijheh.2018.03.005openalex-snapshot
Pathogens transmitted in animal feces in low- and middle-income countries
inferred← citeshttps://doi.org/10.1016/j.ijid.2015.11.005openalex-snapshot
A seventeen-year observation of the antimicrobial susceptibility of clinical Campylobacter jejuni and the molecular mechanisms of erythromycin-resistant isolates in Beijing, China
inferred← citeshttps://doi.org/10.1016/j.ijmm.2009.07.002openalex-snapshot
Campylobacter jejuni: A brief overview on pathogenicity-associated factors and disease-mediating mechanisms
inferred← citeshttps://doi.org/10.1016/j.ijmm.2019.04.003openalex-snapshot
Enhanced microbiological surveillance reveals that temporal case clusters contribute to the high rates of campylobacteriosis in a model agroecosystem
inferred← citeshttps://doi.org/10.1016/j.jcpa.2015.08.003openalex-snapshot
Disease Risk Assessments Involving Companion Animals: an Overview for 15 Selected Pathogens Taking a European Perspective
inferred← citeshttps://doi.org/10.1016/j.jgar.2015.03.010openalex-snapshot
Isolation of a point mutation associated with altered expression of the CmeABC efflux pump in a multidrug-resistant Campylobacter jejuni population of poultry origin
inferred← citeshttps://doi.org/10.1016/j.jgar.2019.02.001openalex-snapshot
Long-term observation of antimicrobial susceptibility and molecular characterisation of Campylobacter jejuni isolated in a Japanese general hospital 2000–2017
inferred← citeshttps://doi.org/10.1016/j.jinf.2020.09.039openalex-snapshot
Sources and transmission routes of campylobacteriosis: A combined analysis of genome and exposure data
inferred← citeshttps://doi.org/10.1016/j.jinf.2024.106265openalex-snapshot
Machine learning to attribute the source of Campylobacter infections in the United States: A retrospective analysis of national surveillance data
inferred← citeshttps://doi.org/10.1016/j.mbs.2018.07.007openalex-snapshot
Designing group dose-response studies in the presence of transmission
inferred← citeshttps://doi.org/10.1016/j.meegid.2009.05.014openalex-snapshot
Phylogenetic understanding of clonal populations in an era of whole genome sequencing
inferred← citeshttps://doi.org/10.1016/j.meegid.2009.09.003openalex-snapshot
Assigning the source of human campylobacteriosis in New Zealand: A comparative genetic and epidemiological approach
inferred← citeshttps://doi.org/10.1016/j.meegid.2014.10.003openalex-snapshot
Tracing the sources of human salmonellosis: A multi-model comparison of phenotyping and genotyping methods
inferred← citeshttps://doi.org/10.1016/j.micinf.2019.07.004openalex-snapshot
Symposium report: One Health meets sequencing
inferred← citeshttps://doi.org/10.1016/j.micpath.2017.12.057openalex-snapshot
Detection of virulence genes determining the ability to adhere and invade in Campylobacter spp. from cattle and swine in Poland
inferred← citeshttps://doi.org/10.1016/j.micpath.2020.104398openalex-snapshot
Designing an efficient multi-epitope vaccine against Campylobacter jejuni using immunoinformatics and reverse vaccinology approach
inferred← citeshttps://doi.org/10.1016/j.mimet.2013.06.024openalex-snapshot
Use of phages to control Campylobacter spp.
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2011.07.011openalex-snapshot
Utilizing a combination of molecular and spatial tools to assess the effect of a public health intervention
inferred← citeshttps://doi.org/10.1016/j.psj.2023.102592openalex-snapshot
In silico prediction and expression analysis of vaccine candidate genes of Campylobacter jejuni
inferred← citeshttps://doi.org/10.1016/j.psj.2024.104380openalex-snapshot
Campylobacter jejuni from no antibiotics ever (NAE) broilers: prevalence, antibiotic resistance, and virulence genes analysis
inferred← citeshttps://doi.org/10.1016/j.psj.2026.107483openalex-snapshot
Characterization of Campylobacter isolates from chicken farms and retail poultry meat
inferred← citeshttps://doi.org/10.1016/j.rvsc.2018.06.016openalex-snapshot
Exploring the oxidative, antimicrobial and genomic properties of Campylobacter jejuni strains isolated from poultry
inferred← citeshttps://doi.org/10.1016/j.soh.2026.100147openalex-snapshot
Seasonal dynamics, antimicrobial resistance, and genetic lineages of thermotolerant Campylobacter isolates from South American camelids
inferred← citeshttps://doi.org/10.1016/j.sste.2011.07.005openalex-snapshot
The integration of molecular tools into veterinary and spatial epidemiology
inferred← citeshttps://doi.org/10.1016/j.sste.2011.07.008openalex-snapshot
The detection of spatially localised outbreaks in campylobacteriosis notification data
inferred← citeshttps://doi.org/10.1016/j.tifs.2009.03.002openalex-snapshot
An introduction to biotracing in food chain systems
inferred← citeshttps://doi.org/10.1016/j.tvjl.2014.08.001openalex-snapshot
Longitudinal prevalence, faecal shedding and molecular characterisation of Campylobacter spp. and Salmonella enterica in sheep
inferred← citeshttps://doi.org/10.1016/j.vaccine.2009.10.018openalex-snapshot
Evaluation of live-attenuated Salmonella vaccines expressing Campylobacter antigens for control of C. jejuni in poultry
inferred← citeshttps://doi.org/10.1016/j.vaccine.2025.128116openalex-snapshot
Mucosal delivery (in ovo and oral) of chitosan nanoparticle-based subunit vaccine enhances resistance against Campylobacter jejuni colonization in broiler chickens
inferred← citeshttps://doi.org/10.1016/j.vetimm.2014.09.003openalex-snapshot
Interaction between Campylobacter and intestinal epithelial cells leads to a different proinflammatory response in human and porcine host
inferred← citeshttps://doi.org/10.1016/j.vetmic.2008.10.018openalex-snapshot
Genomic and phenotypic changes of Campylobacter jejuni strains after passage of the chicken gut
inferred← citeshttps://doi.org/10.1016/j.vetmic.2012.08.016openalex-snapshot
Experimental infection of weaned piglets with Campylobacter coli – Excretion and translocation in a pig colonisation trial
inferred← citeshttps://doi.org/10.1016/j.vetmic.2013.10.006openalex-snapshot
Genotypes and antibiotic resistance of canine Campylobacter jejuni isolates
inferred← citeshttps://doi.org/10.1016/j.watres.2016.05.069openalex-snapshot
Quantifying potential sources of surface water contamination with Campylobacter jejuni and Campylobacter coli
inferred← citeshttps://doi.org/10.1016/j.watres.2020.116421openalex-snapshot
Tracing the animal sources of surface water contamination with Campylobacter jejuni and Campylobacter coli
inferred← citeshttps://doi.org/10.1016/s0140-6736(10)60708-8openalex-snapshot
The growing UK epidemic of human campylobacteriosis
inferred← citeshttps://doi.org/10.1016/s1473-3099(12)70324-9openalex-snapshot
An epidemiological view of microbial genomic data
inferred← citeshttps://doi.org/10.1016/s2095-3119(19)62844-3openalex-snapshot
Molecular detection of virulence genes in Campylobacter species isolated from livestock production systems in South Africa
inferred← citeshttps://doi.org/10.1016/s2222-1808(13)60076-6openalex-snapshot
Emergence of Campylobacter spp. in grasscutter (Thryonomys swinderianus, Temminck, 1827)
inferred← citeshttps://doi.org/10.1017/s0950268809991051openalex-snapshot
Temporal and farm-management-associated variation in the faecal-pat prevalence ofCampylobacter jejuniin ruminants
inferred← citeshttps://doi.org/10.1017/s0950268809991075openalex-snapshot
Binary genomotyping using lipooligosaccharide biosynthesis genes distinguishes betweenCampylobacter jejuniisolates within poultry-associated multilocus sequence types
inferred← citeshttps://doi.org/10.1017/s0950268809991579openalex-snapshot
Molecular and spatial epidemiology of human campylobacteriosis: source association and genotype-related risk factors
inferred← citeshttps://doi.org/10.1017/s0950268810000488openalex-snapshot
Spatio-temporal epidemiology of Campylobacter jejuni enteritis, in an area of Northwest England, 2000–2002
inferred← citeshttps://doi.org/10.1017/s095026881000155xopenalex-snapshot
Risk attribution ofCampylobacterinfection by age group using exposure modelling
inferred← citeshttps://doi.org/10.1017/s0950268810002736openalex-snapshot
Molecular epidemiology and genetic diversity ofCampylobacter jejuniin ruminants
inferred← citeshttps://doi.org/10.1017/s0950268811000628openalex-snapshot
Environmental characteristics associated with campylobacteriosis: accounting for the effect of age and season
inferred← citeshttps://doi.org/10.1017/s0950268811002159openalex-snapshot
The spatial and temporal determinants of campylobacteriosis notifications in New Zealand, 2001–2007
inferred← citeshttps://doi.org/10.1017/s0950268811002676openalex-snapshot
Source attribution of human campylobacteriosis using a meta-analysis of case-control studies of sporadic infections
inferred← citeshttps://doi.org/10.1017/s0950268812000192openalex-snapshot
Molecular epidemiology of humanCampylobacter jejunishows association between seasonal and international patterns of disease
inferred← citeshttps://doi.org/10.1017/s0950268812002063openalex-snapshot
Identifying the seasonal origins of human campylobacteriosis
inferred← citeshttps://doi.org/10.1017/s0950268813000356openalex-snapshot
Increased risk forCampylobacter jejuniandC. coliinfection of pet origin in dog owners and evidence for genetic association between strains causing infection in humans and their pets
inferred← citeshttps://doi.org/10.1017/s095026881300160xopenalex-snapshot
Temporal and farm-management-associated variation in faecal pat prevalence ofArcobacterspp. in ruminants
inferred← citeshttps://doi.org/10.1017/s0950268813002069openalex-snapshot
Campylobacteriosis in returning travellers and potential secondary transmission of exotic strains
inferred← citeshttps://doi.org/10.1017/s0950268813002719openalex-snapshot
Source attribution of human campylobacteriosis in Denmark
inferred← citeshttps://doi.org/10.1017/s0950268814003410openalex-snapshot
Genotypes and antibiotic resistance of bovineCampylobacterand their contribution to human campylobacteriosis
inferred← citeshttps://doi.org/10.1017/s0950268819002292openalex-snapshot
Campylobacteriosis associated with the consumption of unpasteurised milk: findings from a sentinel surveillance site
inferred← citeshttps://doi.org/10.1017/s0950268822001042openalex-snapshot
Temporal changes in the proportion ofSalmonellaoutbreaks associated with 12 food commodity groups in the United States
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c02581openalex-snapshot
Development of Recombinase-Aided Amplification (RAA)-Exo-Probe and RAA-CRISPR/Cas12a Assays for Rapid Detection of Campylobacter jejuni in Food Samples
inferred← citeshttps://doi.org/10.1038/hdy.2009.150openalex-snapshot
Extensive linkage disequilibrium in a wild bird population
inferred← citeshttps://doi.org/10.1038/ismej.2015.149openalex-snapshot
Rapid host switching in generalist Campylobacter strains erodes the signal for tracing human infections
inferred← citeshttps://doi.org/10.1038/s41579-024-01051-zopenalex-snapshot
Foodborne bacterial pathogens: genome-based approaches for enduring and emerging threats in a complex and changing world
inferred← citeshttps://doi.org/10.1038/s41598-017-00584-zopenalex-snapshot
Rising fluoroquinolone resistance in Campylobacter isolated from feedlot cattle in the United States
inferred← citeshttps://doi.org/10.1038/s41598-017-05227-xopenalex-snapshot
A combined case-control and molecular source attribution study of human Campylobacter infections in Germany, 2011–2014
inferred← citeshttps://doi.org/10.1038/s41598-018-27558-zopenalex-snapshot
Ruminant and chicken: important sources of campylobacteriosis in France despite a variation of source attribution in 2009 and 2015
inferred← citeshttps://doi.org/10.1038/s41598-020-68740-6openalex-snapshot
Mining whole genome sequence data to efficiently attribute individuals to source populations
inferred← citeshttps://doi.org/10.1038/s41598-021-02423-8openalex-snapshot
Investigating the Campylobacter enteritis winter peak in Germany, 2018/2019
inferred← citeshttps://doi.org/10.1038/srep20939openalex-snapshot
Human Campylobacteriosis in Luxembourg, 2010–2013: A Case-Control Study Combined with Multilocus Sequence Typing for Source Attribution and Risk Factor Analysis
inferred← citeshttps://doi.org/10.1073/pnas.2536554123openalex-snapshot
Genomic epidemiology of Salmonella and Campylobacter in poultry production: Quantifying the contribution of primary breeders
inferred← citeshttps://doi.org/10.1080/00288330.2011.587822openalex-snapshot
Motueka River plume facilitates transport of ruminant faecal contaminants into shellfish growing waters, Tasman Bay, New Zealand
inferred← citeshttps://doi.org/10.1080/10408398.2011.605231openalex-snapshot
Microbial Source Tracking: A Tool for Identifying Sources of Microbial Contamination in the Food Chain
inferred← citeshttps://doi.org/10.1080/10408398.2021.1984200openalex-snapshot
A systematic review from basics to omics on bacteriophage applications in poultry production and processing
inferred← citeshttps://doi.org/10.1080/19476337.2012.722564openalex-snapshot
Campylobacter jejuniisolated from human cases in Chile showed indistinguishable pulsed field gel electrophoresis profiles with strains isolated from poultry and bovine sources
inferred← citeshttps://doi.org/10.1080/23311983.2024.2392399openalex-snapshot
Human migration, infectious diseases, plague, global health crisis - historical evidence
inferred← citeshttps://doi.org/10.1080/23779497.2024.2358756openalex-snapshot
Biosecurity infectious diseases of the returning Indonesian migrant workers
inferred← citeshttps://doi.org/10.1086/597402openalex-snapshot
Campylobacter Genotyping to Determine the Source of Human Infection
inferred← citeshttps://doi.org/10.1089/fpd.2008.0247openalex-snapshot
Novel Approaches for Campylobacter Control in Poultry
inferred← citeshttps://doi.org/10.1089/fpd.2009.0327openalex-snapshot
Campylobacter Excreted into the Environment by Animal Sources: Prevalence, Concentration Shed, and Host Association
inferred← citeshttps://doi.org/10.1089/fpd.2010.0564openalex-snapshot
Using Outbreak Data for Source Attribution of Human Salmonellosis and Campylobacteriosis in Europe
inferred← citeshttps://doi.org/10.1089/fpd.2010.0637openalex-snapshot
Molecular Characterization and Environmental Mapping of Campylobacter Isolates in a Subset of Intensive Poultry Flocks in Ireland
inferred← citeshttps://doi.org/10.1089/fpd.2010.0640openalex-snapshot
Efficacy of High-Intensity Pulsed Light for the Microbiological Decontamination of Chicken, Associated Packaging, and Contact Surfaces
inferred← citeshttps://doi.org/10.1089/fpd.2010.0676openalex-snapshot
Rapid Detection of Point Mutations in Domain V of the 23S rRNA Gene in Erythromycin-Resistant Campylobacter Isolates by Pyrosequencing
inferred← citeshttps://doi.org/10.1089/fpd.2012.1134openalex-snapshot
Assessing the Applicability of Currently Available Methods for Attributing Foodborne Disease to Sources, Including Food and Food Commodities
inferred← citeshttps://doi.org/10.1089/fpd.2012.1293openalex-snapshot
Molecular Epidemiology and Public Health Relevance of Campylobacter Isolated from Dairy Cattle and European Starlings in Ohio, USA
inferred← citeshttps://doi.org/10.1089/fpd.2016.2121openalex-snapshot
The Fecal Microbial Communities of Dairy Cattle Shedding Shiga Toxin–Producing Escherichia coli or Campylobacter jejuni
inferred← citeshttps://doi.org/10.1089/fpd.2016.2209openalex-snapshot
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.2016.2229openalex-snapshot
Campylobacter Species Isolated from Pigs in Grenada Exhibited Novel Clones: Genotypes and Antimicrobial Resistance Profiles of Sequence Types
inferred← citeshttps://doi.org/10.1089/fpd.2018.2493openalex-snapshot
Emerging and Re-Emerging Foodborne Pathogens
inferred← citeshttps://doi.org/10.1089/fpd.2023.0042openalex-snapshot
Outbreaks of Campylobacteriosis Caused by Drinking Raw Milk in Japan: Evidence of Relationship Between Milk and Patients by Using Whole Genome Sequencing
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.2023.0075openalex-snapshot
A Review on Microbiological Source Attribution Methods of Human Salmonellosis: From Subtyping to Whole-Genome Sequencing
inferred← citeshttps://doi.org/10.1089/vbz.2011.0676openalex-snapshot
Poultry as a Host for the Zoonotic Pathogen Campylobacter jejuni
inferred← citeshttps://doi.org/10.1089/vbz.2020.2640openalex-snapshot
The Role of Peridomestic Rodents as Reservoirs for Zoonotic Foodborne Pathogens
inferred← citeshttps://doi.org/10.1093/cid/cir249openalex-snapshot
Outbreak of Campylobacteriosis Associated With Consumption of Raw Peas
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/cid/civ727openalex-snapshot
Molecular Approaches to Understanding Transmission and Source Attribution in NontyphoidalSalmonellaand Their Application in Africa
inferred← citeshttps://doi.org/10.1093/molbev/msn264openalex-snapshot
Rapid Evolution and the Importance of Recombination to the Gastroenteric Pathogen Campylobacter jejuni
inferred← citeshttps://doi.org/10.1093/oso/9780197683293.003.0007openalex-snapshot
Waterborne Diseases
inferred← citeshttps://doi.org/10.1098/rsif.2018.0534openalex-snapshot
Extending statistical models for source attribution of zoonotic diseases: a study of campylobacteriosis
inferred← citeshttps://doi.org/10.1099/jmm.0.016576-0openalex-snapshot
Species-specific identification and differentiation of Arcobacter, Helicobacter and Campylobacter by full-spectral matrix-associated laser desorption/ionization time of flight mass spectrometry analysis
inferred← citeshttps://doi.org/10.1099/jmm.0.072892-0openalex-snapshot
Prevalence and genotypes of Campylobacter jejuni from urban environmental sources in comparison with clinical isolates from children
inferred← citeshttps://doi.org/10.1099/mgen.0.000366openalex-snapshot
AB_SA: Accessory genes-Based Source Attribution – tracing the source of Salmonella enterica Typhimurium environmental strains
inferred← citeshttps://doi.org/10.1099/mgen.0.001553openalex-snapshot
Evidence of diversification and geographic separation in a lineage of Campylobacter jejuni co-circulating in cattle and humans
inferred← citeshttps://doi.org/10.1099/mic.0.062000-0openalex-snapshot
Campylobacter sequence typing databases: applications and future prospects
inferred← citeshttps://doi.org/10.1101/2020.06.03.132191openalex-snapshot
A mathematical modelling approach to uncover factors influencing the spread of Campylobacter in a flock of chickens
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/10.1101/2023.07.05.547857openalex-snapshot
Dissecting components of the Campylobacter jejuni fetMP-fetABCDEF gene cluster in iron scavenging
inferred← citeshttps://doi.org/10.1101/2024.11.08.24316954openalex-snapshot
A systematic review of the methodological considerations in Campylobacter burden of disease studies
inferred← citeshttps://doi.org/10.1101/2025.11.11.25340000openalex-snapshot
Genomic Epidemiology of Salmonella and Campylobacter in Poultry Production: Quantifying the Contribution of Primary Breeders
inferred← citeshttps://doi.org/10.11109/jaes.2021.23.3.129openalex-snapshot
Analysis of air temperature distribution according to the application of porous media in the animal occupied zone using CFD
inferred← citeshttps://doi.org/10.1111/1462-2920.12111openalex-snapshot
Characterization of water and wildlife strains as a subgroup of C ampylobacter jejuni using DNA microarrays
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/10.1111/1462-2920.13628openalex-snapshot
Genome‐wide association of functional traits linked with C ampylobacter jejuni survival from farm to fork
inferred← citeshttps://doi.org/10.1111/1541-4337.12124openalex-snapshot
Thermotolerant Campylobacter during Broiler Rearing: Risk Factors and Intervention
inferred← citeshttps://doi.org/10.1111/1574-6968.12488openalex-snapshot
Role of environmental survival in transmission ofCampylobacter jejuni
inferred← citeshttps://doi.org/10.1111/1750-3841.12788openalex-snapshot
The Antimicrobial Effect of Spice‐Based Marinades against Campylobacter jejuni on Contaminated Fresh Broiler Wings
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.1364-5072.2010.04883.xopenalex-snapshot
Campylobacter genotypes from poultry transportation crates indicate a source of contamination and transmission.
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2010.04883.xopenalex-snapshot
Campylobacter genotypes from poultry transportation crates indicate a source of contamination and transmission
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2010.04906.xopenalex-snapshot
Comparison of genotypes and antibiotic resistance of Campylobacter jejuni isolated from humans and slaughtered chickens in Switzerland
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2010.04934.xopenalex-snapshot
Expression and characterization of cell-signalling molecules in Campylobacter jejuni
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.1365-2672.2011.05100.xopenalex-snapshot
Comparison of Campylobacter jejuni isolates from human, food, veterinary and environmental sources in Iceland using PFGE, MLST and fla-SVR sequencing
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.1539-6924.2009.01224.xopenalex-snapshot
Source Attribution of Food‐Borne Zoonoses in New Zealand: A Modified Hald Model
inferred← citeshttps://doi.org/10.1111/j.1539-6924.2009.01291.xopenalex-snapshot
Integrated Approaches for the Public Health Prioritization of Foodborne and Zoonotic Pathogens
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.12986openalex-snapshot
Control strategies against Campylobacter at the poultry production level: biosecurity measures, feed additives and vaccination
inferred← citeshttps://doi.org/10.1111/jam.13185openalex-snapshot
Multilocus sequence typing of Campylobacter jejuni and Campylobacter coli isolates from poultry, cattle and humans in Nigeria
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/jfpp.14251openalex-snapshot
Processing and retail strategies to minimizeCampylobactercontamination in retail chicken
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/risa.12483openalex-snapshot
Application of Molecular Typing Results in Source Attribution Models: The Case of Multiple Locus Variable Number Tandem Repeat Analysis (MLVA) of Salmonella Isolates Obtained from Integrated Surveillance in Denmark
inferred← citeshttps://doi.org/10.1111/risa.14138openalex-snapshot
Source attribution of campylobacteriosis in Australia, 2017–2019
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.12295openalex-snapshot
Molecular and Statistical Analysis of Campylobacter spp. and Antimicrobial‐Resistant Campylobacter Carriage in Wildlife and Livestock from Ontario Farms
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.12937openalex-snapshot
A statistical modelling approach for source attribution meta-analysis of sporadic infection with foodborne pathogens.
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/10.1128/9781555818463.ch11openalex-snapshot
CampylobacterSpecies
inferred← citeshttps://doi.org/10.1128/9781555818852.ch2openalex-snapshot
Statistical Considerations in Environmental Microbial Forensics
inferred← citeshttps://doi.org/10.1128/9781555819804.ch29openalex-snapshot
Source Attribution and Risk Assessment of Antimicrobial Resistance
inferred← citeshttps://doi.org/10.1128/9781555819972.ch10openalex-snapshot
ElevenCampylobacterSpecies
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.00168-09openalex-snapshot
Clonal Population Structure and Antimicrobial Resistance ofCampylobacter jejuniin Chicken Meat from Belgium
inferred← citeshttps://doi.org/10.1128/aem.00374-09openalex-snapshot
Chickens and Cattle as Sources of Sporadic Domestically Acquired Campylobacter jejuni Infections in Finland
showing the first 200 of 418
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.