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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

https://doi.org/10.1038/srep20939
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What this work says

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

inferredcites →https://doi.org/10.1002/nmi2.58openalex-snapshot
Enteroaggregative Shiga toxin-producing Escherichia coli of serotype O104:H4 in Belgium and Luxembourg
inferredcites →https://doi.org/10.1007/s10654-014-9917-0openalex-snapshot
A tradition and an epidemic: determinants of the campylobacteriosis winter peak in Switzerland
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2006.12.012openalex-snapshot
A seven-year survey of Campylobacter contamination in meat at different production stages in Belgium
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.prevetmed.2009.09.015openalex-snapshot
Trends in Campylobacter incidence in broilers and humans in six European countries, 1997–2007
inferredcites →https://doi.org/10.1017/s0950268805005406openalex-snapshot
Risk factors for Salmonella Enteritidis and Typhimurium (DT104 and non-DT104) infections in The Netherlands: predominant roles for raw eggs in Enteritidis and sandboxes in Typhimurium infections
inferredcites →https://doi.org/10.1017/s0950268806007576openalex-snapshot
A multi-centre prospective case-control study of campylobacter infection in persons aged 5 years and older in Australia
inferredcites →https://doi.org/10.1017/s0950268809991579openalex-snapshot
Molecular and spatial epidemiology of human campylobacteriosis: source association and genotype-related risk factors
inferredcites →https://doi.org/10.1017/s095026881000052xopenalex-snapshot
Risk factors for indigenousCampylobacter jejuniandCampylobacter coliinfections in The Netherlands: a case-control study
inferredcites →https://doi.org/10.1017/s0950268812000568openalex-snapshot
Estimating the true incidence of campylobacteriosis and salmonellosis in the European Union, 2009
inferredcites →https://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
inferredcites →https://doi.org/10.1017/s0950268813002069openalex-snapshot
Campylobacteriosis in returning travellers and potential secondary transmission of exotic strains
inferredcites →https://doi.org/10.1017/s0950268813002719openalex-snapshot
Source attribution of human campylobacteriosis in Denmark
inferredcites →https://doi.org/10.1017/s0950268814003410openalex-snapshot
Genotypes and antibiotic resistance of bovineCampylobacterand their contribution to human campylobacteriosis
inferredcites →https://doi.org/10.1046/j.1365-2672.94.s1.12.xopenalex-snapshot
Cattle and sheep farms as reservoirs ofCampylobacter
inferredcites →https://doi.org/10.1080/10408410802636017openalex-snapshot
Immunity to Campylobacter: its role in risk assessment and epidemiology
inferredcites →https://doi.org/10.1080/1065657x.2004.10702188openalex-snapshot
Inactivation of Giardia Cysts and Cryptosporidium Oocysts in Beef Feedlot Manure By Thermophilic Windrow Composting
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/10.1086/597402openalex-snapshot
Campylobacter Genotyping to Determine the Source of Human Infection
inferredcites →https://doi.org/10.1086/597417openalex-snapshot
Attribution ofCampylobacterInfections in Northeast Scotland to Specific Sources by Use of Multilocus Sequence Typing
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/10.1111/j.1472-765x.2008.02496.xopenalex-snapshot
Survival ofCampylobacterspp. in bovine faeces on pasture
inferredcites →https://doi.org/10.1111/j.1539-6924.2009.01224.xopenalex-snapshot
Source Attribution of Food‐Borne Zoonoses in New Zealand: A Modified Hald Model
inferredcites →https://doi.org/10.1111/mec.12144openalex-snapshot
Marked host specificity and lack of phylogeographic population structure of Campylobacter jejuni in wild birds
inferredcites →https://doi.org/10.1111/mec.12742openalex-snapshot
Cryptic ecology among host generalist Campylobacter jejuni in domestic animals
inferredcites →https://doi.org/10.1128/9781555815554.ch9openalex-snapshot
Epidemiology of Campylobacter jejuni Infections in Industrialized Nations
inferredcites →https://doi.org/10.1128/aem.00865-08openalex-snapshot
Multilocus Sequence Typing, Pulsed-Field Gel Electrophoresis, and fla Short Variable Region Typing of Clonal Complexes of Campylobacter jejuni Strains of Human, Bovine, and Poultry Origins in Luxembourg
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.01902-09openalex-snapshot
Prolonged Survival ofCampylobacterSpecies in Bovine Manure Compost
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/jcm.39.1.14-23.2001openalex-snapshot
Multilocus Sequence Typing System for Campylobacter jejuni
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/10.1186/1471-2105-11-595openalex-snapshot
BIGSdb: Scalable analysis of bacterial genome variation at the population level
inferredcites →https://doi.org/10.1186/1471-2334-12-80openalex-snapshot
Using sequence data to identify alternative routes and risk of infection: a case-study of campylobacter in Scotland
inferredcites →https://doi.org/10.1186/2042-5783-2-8openalex-snapshot
Analysis of evolutionary patterns of genes in Campylobacter jejuni and C. coli
inferredcites →https://doi.org/10.1186/s12866-014-0205-7openalex-snapshot
Investigating the host specificity of Campylobacter jejuni and Campylobacter coli by sequencing gyrase subunit A
inferredcites →https://doi.org/10.1371/journal.pgen.1000203openalex-snapshot
Tracing the Source of Campylobacteriosis
inferredcites →https://doi.org/10.1371/journal.pone.0042599openalex-snapshot
Risk Factors for Campylobacteriosis of Chicken, Ruminant, and Environmental Origin: A Combined Case-Control and Source Attribution Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0055029openalex-snapshot
Practicalities of Using Non-Local or Non-Recent Multilocus Sequence Typing Data for Source Attribution in Space and Time of Human Campylobacteriosis
inferredcites →https://doi.org/10.2134/jeq2003.1508openalex-snapshot
Fate of Coliform Bacteria in Composted Beef Cattle Feedlot Manure
inferredcites →https://doi.org/10.2134/jeq2008.0168openalex-snapshot
A Biosecure Composting System for Disposal of Cattle Carcasses and Manure Following Infectious Disease Outbreak
inferredcites →https://doi.org/10.2903/j.efsa.2010.1437openalex-snapshot
Scientific Opinion on Quantification of the risk posed by broiler meat to human campylobacteriosis in the EU
inferredcites →https://doi.org/10.2903/j.efsa.2015.3991openalex-snapshot
The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2013
inferredcites →https://doi.org/10.2903/j.efsa.2018.5500openalex-snapshot
The European Union summary report on trends and sources of zoonoses, zoonotic agents and food‐borne outbreaks in 2017
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/eid0910.020584openalex-snapshot
Characterization of Waterborne Outbreak–associated Campylobacter jejuni , Walkerton, Ontario
inferredcites →https://doi.org/10.3201/eid1302.060620openalex-snapshot
Host-associated Genetic Import inCampylobacter jejuni
inferredcites →https://doi.org/10.3201/eid1803.111024openalex-snapshot
Poultry Culling and Campylobacteriosis Reduction among Humans, the Netherlands
inferredcites →https://doi.org/10.3390/ijerph120100032openalex-snapshot
Agricultural and Management Practices and Bacterial Contamination in Greenhouse versus Open Field Lettuce Production

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/10.1007/978-3-030-65481-8_2openalex-snapshot
The Data Behind Risk Analysis of Campylobacter Jejuni and Campylobacter Coli Infections
inferred← citeshttps://doi.org/10.1007/978-3-030-85877-3_6-1openalex-snapshot
Campylobacter: Animal Reservoirs, Human Infections, and Options for Control
inferred← citeshttps://doi.org/10.1007/978-3-031-27164-9_6openalex-snapshot
Campylobacter: Animal Reservoirs, Human Infections, and Options for Control
inferred← citeshttps://doi.org/10.1007/978-3-319-61688-9_18openalex-snapshot
What Is Known About Zoonotic Bacteria in Cattle and Pig Farms, and What Should Be Done to Prevent Occupational Infections
inferred← citeshttps://doi.org/10.1007/978-981-16-9723-4_16-1openalex-snapshot
Antimicrobial Resistance in Food-Borne Campylobacter spp.
inferred← citeshttps://doi.org/10.1007/978-981-19-9279-7_16openalex-snapshot
Antimicrobial Resistance in Food-Borne Campylobacter spp.
inferred← citeshttps://doi.org/10.1007/s11259-022-09981-wopenalex-snapshot
Identification of genes associated with environmental persistence in Campylobacter jejuni and Campylobacter coli isolates from processing in a broiler abattoir
inferred← citeshttps://doi.org/10.1007/s11259-024-10455-4openalex-snapshot
Harnessing medicinal plant compounds for the control of Campylobacter in foods: a comprehensive review
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/bs.aambs.2018.01.001openalex-snapshot
Antimicrobial Resistance in Campylobacter Species: Mechanisms and Genomic Epidemiology
inferred← citeshttps://doi.org/10.1016/j.cmi.2016.08.014openalex-snapshot
Molecular epidemiology of Campylobacter jejuni infection in Israel—a nationwide study
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.fm.2025.104812openalex-snapshot
Source attribution studies of foodborne pathogens, 2010–2023: a review and collection of estimates
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.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.2018.04.004openalex-snapshot
Orthogonal typing methods identify genetic diversity among Belgian Campylobacter jejuni strains isolated over a decade from poultry and cases of sporadic human illness
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2020.108656openalex-snapshot
Prevalence, antibiotic resistance and genotypes of Campylobacter jejuni and Campylobacter coli isolated from chickens in Irbid governorate, Jordan
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2024.110953openalex-snapshot
Source attribution of Listeria monocytogenes in the Netherlands
inferred← citeshttps://doi.org/10.1016/j.jinf.2018.04.016openalex-snapshot
Immune response-eliciting exposure to Campylobacter vastly exceeds the incidence of clinically overt campylobacteriosis but is associated with similar risk factors: A nationwide serosurvey in the Netherlands
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.mran.2020.100118openalex-snapshot
Risk factors for sporadic campylobacteriosis: A systematic review and meta-analysis
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/10.1038/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/s41598-021-02423-8openalex-snapshot
Investigating the Campylobacter enteritis winter peak in Germany, 2018/2019
inferred← citeshttps://doi.org/10.1038/s41598-025-94453-9openalex-snapshot
Antimicrobial resistance and genomic characteristics of Campylobacter spp. From Australian meat chickens with A follow up investigation
inferred← citeshttps://doi.org/10.1038/srep28737openalex-snapshot
Insights into Campylobacter jejuni colonization and enteritis using a novel infant rabbit model
inferred← citeshttps://doi.org/10.1097/ede.0000000000001504openalex-snapshot
Nearest-Neighbors Matching for Case–Control Study Analyses: Better Risk Factor Identification From a Study of Sporadic Campylobacteriosis in the United States
inferred← citeshttps://doi.org/10.1097/mog.0000000000000329openalex-snapshot
The consequences of Campylobacter infection
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/10.1101/2021.09.24.461243openalex-snapshot
Local accessory gene sharing drives lineage-specific acquisition of antimicrobial resistance in Egyptian Campylobacter spp .
inferred← citeshttps://doi.org/10.1111/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.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/10.1111/zph.13063openalex-snapshot
UK ‐wide risk factor study of broiler carcases highly contaminated with Campylobacter
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.02365-18openalex-snapshot
Population Genetics and Characterization of Campylobacter jejuni Isolates from Western Jackdaws and Game Birds in Finland
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/10.1155/2020/2092478openalex-snapshot
Prevalence, Risk Factors, and Antimicrobial Resistance Profiles of Thermophilic Campylobacter Species in Humans and Animals in Sub-Saharan Africa: A Systematic Review
inferred← citeshttps://doi.org/10.1186/s12879-022-07553-6openalex-snapshot
Risk factors for campylobacteriosis in Australia: outcomes of a 2018–2019 case–control study
inferred← citeshttps://doi.org/10.1186/s12879-025-12057-0openalex-snapshot
Prevalence and antimicrobial resistance patterns of Campylobacter spp. Causing human gastroenteritis in Iran (2000–2025): a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1186/s12889-016-3679-4openalex-snapshot
Non food-related risk factors of campylobacteriosis in Canada: a matched case-control study
inferred← citeshttps://doi.org/10.1186/s12967-019-1781-yopenalex-snapshot
Climate, human behaviour or environment: individual-based modelling of Campylobacter seasonality and strategies to reduce disease burden
inferred← citeshttps://doi.org/10.1186/s13104-017-2587-8openalex-snapshot
The recurrent campylobacteriosis epidemic over Christmas and New Year in European countries, 2006–2014
inferred← citeshttps://doi.org/10.1264/jsme2.me18115openalex-snapshot
Phylogenetic Diversity and Antimicrobial Resistance of Campylobacter coli from Humans and Animals in Japan
inferred← citeshttps://doi.org/10.1371/journal.pone.0183790openalex-snapshot
Source attribution of human campylobacteriosis at the point of exposure by combining comparative exposure assessment and subtype comparison based on comparative genomic fingerprinting
inferred← citeshttps://doi.org/10.1371/journal.pone.0235841openalex-snapshot
The source attribution analysis revealed the prevalent role of poultry over cattle and wild birds in human campylobacteriosis cases in the Baltic States
inferred← citeshttps://doi.org/10.1371/journal.pone.0266976openalex-snapshot
Prevalence, determinants, and antimicrobial susceptibility patterns of Campylobacter infection among under-five children with diarrhea at Governmental Hospitals in Hawassa city, Sidama, Ethiopia. A cross-sectional study
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1387051/v1openalex-snapshot
Risk Factors for Campylobacteriosis in Australia: Outcomes of a 2018–2019 Case-Control Study
inferred← citeshttps://doi.org/10.22099/ijvr.2022.42199.6135openalex-snapshot
Virulence, MLST analysis, and antimicrobial resistance of Campylobacter coli isolated from broiler chickens in Tamil Nadu, India.
inferred← citeshttps://doi.org/10.2807/1560-7917.es.2019.24.43.1800696openalex-snapshot
A systematic review of source attribution of human campylobacteriosis using multilocus sequence typing
inferred← citeshttps://doi.org/10.2903/j.efsa.2019.5598openalex-snapshot
The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2017
inferred← citeshttps://doi.org/10.2903/j.efsa.2019.5709openalex-snapshot
Technical specifications on harmonised monitoring of antimicrobial resistance in zoonotic and indicator bacteria from food‐producing animals and food
inferred← citeshttps://doi.org/10.2903/j.efsa.2020.6007openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2017/2018
inferred← citeshttps://doi.org/10.2903/j.efsa.2021.6490openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2018/2019
inferred← citeshttps://doi.org/10.3382/ps/pez286openalex-snapshot
Prevalence and genetic diversity of Campylobacter spp. in the production chain of broiler chickens in Lebanon and its association with the intestinal protozoan Blastocystis sp
inferred← citeshttps://doi.org/10.3389/fcimb.2020.608020openalex-snapshot
Investigating Major Recurring Campylobacter jejuni Lineages in Luxembourg Using Four Core or Whole Genome Sequencing Typing Schemes
inferred← citeshttps://doi.org/10.3389/fmicb.2018.01983openalex-snapshot
Source Attribution of Foodborne Diseases: Potentialities, Hurdles, and Future Expectations
inferred← citeshttps://doi.org/10.3389/fmicb.2019.02578openalex-snapshot
Critical Orientation in the Jungle of Currently Available Methods and Types of Data for Source Attribution of Foodborne Diseases
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01799openalex-snapshot
Antimicrobial Resistance and Virulence-Associated Markers in Campylobacter Strains From Diarrheic and Non-diarrheic Humans in Poland
inferred← citeshttps://doi.org/10.3389/fmicb.2021.662144openalex-snapshot
Whole Resistome Analysis in Campylobacter jejuni and C. coli Genomes Available in Public Repositories
inferred← citeshttps://doi.org/10.3389/fmicb.2021.689262openalex-snapshot
Monitoring of Antimicrobial Resistance to Aminoglycosides and Macrolides in Campylobacter coli and Campylobacter jejuni From Healthy Livestock in Spain (2002–2018)
inferred← citeshttps://doi.org/10.3389/fmicb.2021.780559openalex-snapshot
Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
inferred← citeshttps://doi.org/10.3390/ani10050838openalex-snapshot
Dogs and Cats: Reservoirs for Highly Diverse Campylobacter jejuni and a Potential Source of Human Exposure
inferred← citeshttps://doi.org/10.3390/app131810257openalex-snapshot
The Bactericidal Activity of a Novel Aneurinibacillus aneurinilyticus Isolate Effectively Controls Foodborne Pathogens Campylobacter jejuni and Listeria monocytogenes
inferred← citeshttps://doi.org/10.3390/diagnostics11111949openalex-snapshot
Investigation of MALDI-TOF Mass Spectrometry for Assessing the Molecular Diversity of Campylobacter jejuni and Comparison with MLST and cgMLST: A Luxembourg One-Health Study
inferred← citeshttps://doi.org/10.3390/foods6120105openalex-snapshot
Campylobacter in Broiler Chicken and Broiler Meat in Sri Lanka: Influence of Semi-Automated vs. Wet Market Processing on Campylobacter Contamination of Broiler Neck Skin Samples
inferred← citeshttps://doi.org/10.3390/microorganisms11061540openalex-snapshot
Antimicrobial Resistance of Campylobacter coli Isolated from Caecal Samples of Fattening Pigs at Slaughter
inferred← citeshttps://doi.org/10.3390/microorganisms13061420openalex-snapshot
Genome Analysis of the Multidrug-Resistant Campylobacter coli BCT3 of the Sequence Type (ST) 872 Isolated from a Pediatric Diarrhea Case
inferred← citeshttps://doi.org/10.3390/microorganisms9112300openalex-snapshot
Phylogenetic Analysis Reveals Source Attribution Patterns for Campylobacter spp. in Tennessee and Pennsylvania
inferred← citeshttps://doi.org/10.3390/pathogens12010048openalex-snapshot
Surveillance of Human Cases of Salmonellosis, Campylobacteriosis, Listeriosis, and Hepatitis A in Campania (Southern Italy): Seven-Year Monitoring (2013–2019)
inferred← citeshttps://doi.org/10.3390/pathogens12091069openalex-snapshot
Comparative Analysis of Campylobacter jejuni and C. coli Isolated from Livestock Animals to C. jejuni and C. coli Isolated from Surface Water Using DNA Sequencing and MALDI-TOF
inferred← citeshttps://doi.org/10.3390/pathogens15050539openalex-snapshot
Sources of Human Campylobacteriosis Cases in Estonia and the Genomic Associations with Broiler Chicken Meat Isolates
inferred← citeshttps://doi.org/10.3390/vetsci4030036openalex-snapshot
Inquiring into the Gaps of Campylobacter Surveillance Methods
inferred← citeshttps://doi.org/10.3390/w17182767openalex-snapshot
Prevalence and Resistance Patterns of Campylobacter spp. and Arcobacter spp. in Portuguese Water Bodies
inferred← citeshttps://doi.org/10.4038/java.v3i1.119openalex-snapshot
Impact of antibiotic resistant Campylobacter isolated from poultry: A concise review
inferred← citeshttps://doi.org/10.4236/aim.2021.115016openalex-snapshot
Prevalence of Campylobacter spp. Isolated from Pigs in Three Slaughterhouses of Yaounde Cameroon
inferred← citeshttps://doi.org/10.4315/jfp-20-151openalex-snapshot
Attributing Human Foodborne Diseases to Food Sources and Water in Japan Using Analysis of Outbreak Surveillance Data
inferred← citeshttps://doi.org/10.46756/sci.fsa.ksj135openalex-snapshot
Enhanced molecular-based (MLST/whole genome) surveillance and source attribution of Campylobacter infections in the UK
inferred← citeshttps://doi.org/10.6084/m9.figshare.20208269openalex-snapshot
Additional file 1 of Risk factors for campylobacteriosis in Australia: outcomes of a 2018–2019 case–control study
inferred← citeshttps://doi.org/10.6084/m9.figshare.20208272openalex-snapshot
Additional file 2 of Risk factors for campylobacteriosis in Australia: outcomes of a 2018–2019 case–control study
inferred← citeshttps://doi.org/10.6084/m9.figshare.20208293openalex-snapshot
Additional file 6 of Risk factors for campylobacteriosis in Australia: outcomes of a 2018–2019 case–control study
inferred← citeshttps://doi.org/10.70675/124b2534z6ee8z401dzb484ze8cb9f6b03e2openalex-snapshot
Capacité de différents outils de typage moléculaire pour tracer Campylobacter jejuni et identifier l’origine de contamination en cas de campylobactériose
inferred← citeshttps://doi.org/10.70675/430b01bdz5ca7z4d53zb8cdz32d38a494205openalex-snapshot
Population structure and phenotypical traits of Campylobacter jejuni circulating in Luxembourg
inferred← citeshttps://doi.org/10.70675/796c8f56z61d6z4e1bza90dz9ca86e302dd9openalex-snapshot
Contributions de l'évaluation des risques et de la génomique à la recherche de stratégies de contrôle de Campylobacter dans les abattoirs de poulets de chair
inferred← citeshttps://doi.org/10.70675/989a2c34z1d5ez4bcaz9433z62d0b7a6d4a4openalex-snapshot
Génomique appliquée à l'étude des infections par les bactéries des genres Campylobacter et Helicobacter.
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