On the public citation graph
Whole Resistome Analysis in Campylobacter jejuni and C. coli Genomes Available in Public Repositories
0 signed · 116 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/b978-0-12-803623-5.00005-8openalex-snapshot
Campylobacter epidemiology—sources and routes of transmission for human infection
inferredcites →https://doi.org/10.1016/j.heliyon.2020.e03537openalex-snapshot
Epidemiology and antimicrobial resistance of Campylobacter spp. in animals in Sub-Saharan Africa: A systematic review
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.vetmic.2009.07.022openalex-snapshot
Multilocus sequence typing of Campylobacter jejuni from broilers
inferredcites →https://doi.org/10.1016/s0140-6736(13)60222-6openalex-snapshot
Global burden of childhood pneumonia and diarrhoea
inferredcites →https://doi.org/10.1016/s0140-6736(14)61698-6openalex-snapshot
Global, regional, and national causes of child mortality in 2000–13, with projections to inform post-2015 priorities: an updated systematic analysis
inferredcites →https://doi.org/10.1016/s0378-1097(00)00306-2openalex-snapshot
Characterization of gyrA mutations associated with fluoroquinolone resistance in Campylobacter coli by DNA sequence analysis and MAMA PCR
inferredcites →https://doi.org/10.1017/s0950268811002676openalex-snapshot
Source attribution of human campylobacteriosis using a meta-analysis of case-control studies of sporadic infections
inferredcites →https://doi.org/10.1038/ismej.2015.149openalex-snapshot
Rapid host switching in generalist Campylobacter strains erodes the signal for tracing human infections
inferredcites →https://doi.org/10.1038/s41598-019-44454-2openalex-snapshot
Source attribution of Campylobacter jejuni shows variable importance of chicken and ruminants reservoirs in non-invasive and invasive French clinical isolates
inferredcites →https://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
inferredcites →https://doi.org/10.1073/pnas.1503141112openalex-snapshot
Global trends in antimicrobial use in food animals
inferredcites →https://doi.org/10.1073/pnas.1917168117openalex-snapshot
Agricultural intensification and the evolution of host specialism in the enteric pathogen Campylobacter jejuni
inferredcites →https://doi.org/10.1089/fpd.2016.2257openalex-snapshot
Outbreak of Campylobacteriosis Following a Dairy Farm Visit: Confirmation by Genotyping
inferredcites →https://doi.org/10.1089/fpd.2019.2752openalex-snapshot
Antimicrobial Resistance of Campylobacter in Broiler Chicken Along the Food Chain in Canada
inferredcites →https://doi.org/10.1093/cid/civ431openalex-snapshot
Partial Failure of Milk Pasteurization as a Risk for the Transmission ofCampylobacterFrom Cattle to Humans
inferredcites →https://doi.org/10.1093/jac/dks261openalex-snapshot
Identification of acquired antimicrobial resistance genes
inferredcites →https://doi.org/10.1093/jac/dkv001openalex-snapshot
Novel gentamicin resistance genes in Campylobacter isolated from humans and retail meats in the USA
inferredcites →https://doi.org/10.1093/jac/dkv382openalex-snapshot
Species shift and multidrug resistance of Campylobacter from chicken and swine, China, 2008–14
inferredcites →https://doi.org/10.1093/jac/dkx217openalex-snapshot
PointFinder: a novel web tool for WGS-based detection of antimicrobial resistance associated with chromosomal point mutations in bacterial pathogens
inferredcites →https://doi.org/10.1093/jac/dkz539openalex-snapshot
Comparison of phenotypic and WGS-derived antimicrobial resistance profiles of Campylobacter jejuni and Campylobacter coli isolated from cases of diarrhoeal disease in England and Wales, 2015–16
inferredcites →https://doi.org/10.1111/1462-2920.13628openalex-snapshot
Genome‐wide association of functional traits linked with C ampylobacter jejuni survival from farm to fork
inferredcites →https://doi.org/10.1111/1462-2920.14760openalex-snapshot
Gene pool transmission of multidrug resistance among Campylobacter from livestock, sewage and human disease
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/10.1111/mec.12742openalex-snapshot
Cryptic ecology among host generalist Campylobacter jejuni in domestic animals
inferredcites →https://doi.org/10.1111/zph.12039openalex-snapshot
Risk of Infectious Gastroenteritis in Young Children Living in Québec Rural Areas with Intensive Animal Farming: Results of a Case–Control Study (2004–2007)
inferredcites →https://doi.org/10.1128/aac.01655-08openalex-snapshot
β-Lactamase-Mediated β-Lactam Resistance in Campylobacter Species: Prevalence of Cj0299 ( bla OXA-61 ) and Evidence for a Novel β-Lactamase in C . jejuni
inferredcites →https://doi.org/10.1128/aac.49.2.690-698.2005openalex-snapshot
Prevalence and Subtypes of Ciprofloxacin-Resistant Campylobacter spp. in Commercial Poultry Flocks before, during, and after Treatment with Fluoroquinolones
inferredcites →https://doi.org/10.1128/aem.02765-19openalex-snapshot
Emergence of Fluoroquinolone-Resistant Campylobacter jejuni and Campylobacter coli among Australian Chickens in the Absence of Fluoroquinolone Use
inferredcites →https://doi.org/10.1128/aem.02873-15openalex-snapshot
Whole-Genome Sequencing Analysis Accurately Predicts Antimicrobial Resistance Phenotypes in Campylobacter spp
inferredcites →https://doi.org/10.1128/aem.03085-16openalex-snapshot
Genome-Wide Identification of Host-Segregating Epidemiological Markers for Source Attribution in Campylobacter jejuni
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/cmr.00006-15openalex-snapshot
Global Epidemiology of Campylobacter Infection
inferredcites →https://doi.org/10.1128/jcm.00042-08openalex-snapshot
Multilocus Sequence Typing of Campylobacter jejuni Isolates from Humans, Chickens, Raw Milk, and Environmental Water in Quebec, Canada
inferredcites →https://doi.org/10.1128/jcm.01086-12openalex-snapshot
A Longitudinal 6-Year Study of the Molecular Epidemiology of Clinical Campylobacter Isolates in Oxfordshire, United Kingdom
inferredcites →https://doi.org/10.1155/2013/340605openalex-snapshot
Antimicrobial Resistance Mechanisms among Campylobacter
inferredcites →https://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
inferredcites →https://doi.org/10.1186/1471-2334-12-193openalex-snapshot
Campylobacterantimicrobial resistance in Peru: a ten-year observational study
inferredcites →https://doi.org/10.1186/s12864-016-3340-8openalex-snapshot
Genomic insights from whole genome sequencing of four clonal outbreak Campylobacter jejuni assessed within the global C. jejuni population
inferredcites →https://doi.org/10.1186/s12879-017-2535-1openalex-snapshot
MLST genotypes of Campylobacter jejuni isolated from broiler products, dairy cattle and human campylobacteriosis cases in Lithuania
inferredcites →https://doi.org/10.1186/s13099-016-0100-xopenalex-snapshot
Genotyping and antibiotic resistance of thermophilic Campylobacter isolated from chicken and pig meat in Vietnam
inferredcites →https://doi.org/10.12688/wellcomeopenres.14826.1openalex-snapshot
Open-access bacterial population genomics: BIGSdb software, the PubMLST.org website and their applications
inferredcites →https://doi.org/10.1289/ehp.7647openalex-snapshot
Fluoroquinolone-Resistant Campylobacter Isolates from Conventional and Antibiotic-Free Chicken Products
inferredcites →https://doi.org/10.1371/journal.pntd.0008533openalex-snapshot
Genomic epidemiology of Campylobacter jejuni associated with asymptomatic pediatric infection in the Peruvian Amazon
inferredcites →https://doi.org/10.1371/journal.pone.0026880openalex-snapshot
Finnish Campylobacter jejuni Strains of Multilocus Sequence Type ST-22 Complex Have Two Lineages with Different Characteristics
inferredcites →https://doi.org/10.1371/journal.pone.0227535openalex-snapshot
Increasing prevalence of a fluoroquinolone resistance mutation amongst Campylobacter jejuni isolates from four human infectious intestinal disease studies in the United Kingdom
inferredcites →https://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
inferredcites →https://doi.org/10.2807/1560-7917.es.2019.24.31.1800357openalex-snapshot
Campylobacter species prevalence, characterisation of antimicrobial resistance and analysis of whole-genome sequence of isolates from livestock and humans, Latvia, 2008 to 2016
inferredcites →https://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
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/eid0812.020115openalex-snapshot
Increasing Fluoroquinolone Resistance inCampylobacter jejuni,Pennsylvania, USA,1982–20011
inferredcites →https://doi.org/10.3201/eid1302.060587openalex-snapshot
Campylobacter Antimicrobial Drug Resistance among Humans, Broiler Chickens, and Pigs, France
inferredcites →https://doi.org/10.3201/eid1701.p11101openalex-snapshot
Foodborne Illness Acquired in the United States—Major Pathogens
inferredcites →https://doi.org/10.3201/eid1902.121147openalex-snapshot
CampylobacterInfection in Poultry-Processing Workers, Virginia, USA, 2008–2011
inferredcites →https://doi.org/10.3201/eid2603.190947openalex-snapshot
Whole-Genome Sequencing to Detect Numerous Campylobacter jejuni Outbreaks and Match Patient Isolates to Sources, Denmark, 2015–2017
inferredcites →https://doi.org/10.3389/fcimb.2020.592512openalex-snapshot
Genotyping and Antibiotic Resistance Traits in Campylobacter jejuni and coli From Pigs and Wild Boars in Italy
inferredcites →https://doi.org/10.3389/fmicb.2011.00200openalex-snapshot
Campylobacter spp. as a Foodborne Pathogen: A Review
inferredcites →https://doi.org/10.3389/fmicb.2016.01002openalex-snapshot
Adhesion, Biofilm Formation, and Genomic Features of Campylobacter jejuni Bf, an Atypical Strain Able to Grow under Aerobic Conditions
inferredcites →https://doi.org/10.3389/fmicb.2018.02432openalex-snapshot
Genomic Epidemiology of Campylobacter jejuni Transmission in Israel
inferredcites →https://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
inferredcites →https://doi.org/10.3389/fmicb.2020.513070openalex-snapshot
Genomic Analysis Reveals the Genetic Determinants Associated With Antibiotic Resistance in the Zoonotic Pathogen Campylobacter spp. Distributed Globally
inferredcites →https://doi.org/10.3389/fmicb.2020.571064openalex-snapshot
Whole-Genome Sequencing and Bioinformatic Analysis of Environmental, Agricultural, and Human Campylobacter jejuni Isolates From East Tennessee
inferredcites →https://doi.org/10.3390/pathogens8020087openalex-snapshot
Campylobacter at the Human–Food Interface: The African Perspective
inferredcites →https://doi.org/10.4102/jsava.v81i4.153openalex-snapshot
Antimicrobial susceptibility in thermophilic Campylobacter species isolated from pigs and chickens in South Africa
inferredcites →https://doi.org/10.4315/0362-028x-73.5.825openalex-snapshot
Prevalence and Antimicrobial Resistance of Campylobacter jejuni and Campylobacter coli Isolated from Cattle between 2002 and 2006 in France
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/10.1016/j.afres.2026.102701openalex-snapshot
Genomic tracking of Campylobacter jejuni along poultry and pig value chains in Northeast India: Implications for food safety
inferred← citeshttps://doi.org/10.1016/j.cmi.2024.06.027openalex-snapshot
Occurrence of in vivo carbapenem-resistant Campylobacter coli mediated by porA point mutation and overexpression of blaOXA-489 under meropenem treatment
inferred← citeshttps://doi.org/10.1016/j.foohum.2026.101369openalex-snapshot
Farm-to-fork genomic analysis of Campylobacter coli in poultry and pig systems: A one health challenge in Northeast India
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2025.111469openalex-snapshot
Broad-host-range bacteriophages CBP1 and CBP2 with dual-species activity against Campylobacter jejuni and Campylobacter coli
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2026.111941openalex-snapshot
Genomic analysis of Campylobacter risk in retail chicken isolated from Beijing in 2024
inferred← citeshttps://doi.org/10.1016/j.jfp.2025.100540openalex-snapshot
Campylobacter in Raw Chicken Meat at Retail Level: Quantitative and Qualitative Assessment, Genomic Profiling, and Comparison With Isolates From Human Infections
inferred← citeshttps://doi.org/10.1016/j.jgar.2022.07.001openalex-snapshot
Draft genome sequence of a multidrug-resistant Campylobacter coli ST825 carrying several acquired antibiotic resistance genes isolated from poultry in China
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.lwt.2026.119810openalex-snapshot
Global genomic epidemiology of the β-lactamase gene blaOXA in Campylobacter
inferred← citeshttps://doi.org/10.1016/j.meegid.2024.105578openalex-snapshot
Whole genome sequence-based characterization of Campylobacter isolated from broiler carcasses over a three-year period in a big poultry slaughterhouse reveals high genetic diversity and a recurring genomic lineage 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.2025.105302openalex-snapshot
Phenotypic and whole genome-based characterization of antibiotic resistance of Campylobacter jejuni isolates from chicken livers
inferred← citeshttps://doi.org/10.1016/j.psj.2026.107271openalex-snapshot
Phenotypic and whole genome characterization of multidrug-resistant Campylobacter coli from chicken liver
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/10.1089/fpd.2022.0043openalex-snapshot
Prevalence and Antimicrobial Resistance of Campylobacter spp. Isolated from Broilers Throughout the Supply Chain in Valencia, Spain
inferred← citeshttps://doi.org/10.1089/fpd.2023.0099openalex-snapshot
Contribution of Food to the Human Health Burden of Antimicrobial Resistance
inferred← citeshttps://doi.org/10.1089/fpd.2024.0173openalex-snapshot
Phenotypic and Whole-Genome Sequencing-Based Profiling of Antimicrobial Resistance and Virulence in Campylobacter spp. Isolated from Human Stool in a Croatian University Hospital
inferred← citeshttps://doi.org/10.1093/bioadv/vbag130openalex-snapshot
Impact of sequencing read quality on whole-genome sequencing outcomes for foodborne pathogens using a BacWORK standardized analysis workflow
inferred← citeshttps://doi.org/10.1099/mgen.0.000875openalex-snapshot
Emerging patterns of fluoroquinolone resistance in Campylobacter jejuni in the UK [1998–2018]
inferred← citeshttps://doi.org/10.1099/mgen.0.001073openalex-snapshot
Pangenomic analyses of antibiotic-resistant Campylobacter jejuni reveal unique lineage distributions and epidemiological associations
inferred← citeshttps://doi.org/10.1099/mgen.0.001190openalex-snapshot
Prevalence, antibiotic resistance, and genomic characterisation of Campylobacter spp. in retail chicken in Hanoi, Vietnam
inferred← citeshttps://doi.org/10.1099/mgen.0.001444openalex-snapshot
Large-scale global molecular epidemiology of antibiotic resistance determinants in Streptococcus pneumoniae
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/10.1111/zph.12994openalex-snapshot
Host‐associated variability of the cdtABC operon, coding for the cytolethal distending toxin, in Campylobacter jejuni
inferred← citeshttps://doi.org/10.1128/aac.01108-24openalex-snapshot
Genomic epidemiology and genetic characteristics of clinical Campylobacter species cocirculating in West Bengal, India, 2019, using whole genome analysis
inferred← citeshttps://doi.org/10.1128/aac.01687-21openalex-snapshot
Genomic Screening of Antimicrobial Resistance Markers in UK and US Campylobacter Isolates Highlights Stability of Resistance over an 18-Year Period
inferred← citeshttps://doi.org/10.1128/aem.01614-24openalex-snapshot
Campylobacter jejuni ST353 and ST464 cause localized gut inflammation, crypt damage, and extraintestinal spread during large- and small-scale infection in broiler chickens
inferred← citeshttps://doi.org/10.1128/mra.00316-22openalex-snapshot
Draft Genome Sequence of Campylobacter jejuni ST-508 Strain Shizu21005, Isolated from an Asymptomatic Food Handler in Japan, 2021
inferred← citeshttps://doi.org/10.1128/spectrum.01028-24openalex-snapshot
Genotypic characterization and antimicrobial susceptibility of human Campylobacter jejuni isolates in Southern Spain
inferred← citeshttps://doi.org/10.1128/spectrum.02659-22openalex-snapshot
Whole-Genome and Plasmid Comparative Analysis of Campylobacter jejuni from Human Patients in Toyama, Japan, from 2015 to 2019
inferred← citeshttps://doi.org/10.1155/ijm/2763026openalex-snapshot
Campylobacter jejuni Across the Food Chain: Integrating Pathogenesis, Persistence, Antimicrobial Resistance, and Emerging One Health Control Strategies
inferred← citeshttps://doi.org/10.1186/s13099-022-00517-wopenalex-snapshot
Genomic insights into zoonotic transmission and antimicrobial resistance in Campylobacter jejuni from farm to fork: a one health perspective
inferred← citeshttps://doi.org/10.15212/zoonoses-2024-0060openalex-snapshot
Longitudinal Trends and Drivers of Antimicrobial Resistance in Campylobacter Worldwide (1954-2023)
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1208825openalex-snapshot
Whole-genome sequencing reveals changes in genomic diversity and distinctive repertoires of T3SS and T6SS effector candidates in Chilean clinical Campylobacter strains
inferred← citeshttps://doi.org/10.3389/fcimb.2024.1449856openalex-snapshot
Campylobacter coli of porcine origin exhibits an open pan-genome within a single clonal complex: insights from comparative genomic analysis
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1074548openalex-snapshot
Whole genome characterization of thermophilic Campylobacter species isolated from dairy manure in small specialty crop farms of Northeast Ohio
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1285236openalex-snapshot
Combined genomic-proteomic approach in the identification of Campylobacter coli amoxicillin-clavulanic acid resistance mechanism in clinical isolates
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1293666openalex-snapshot
Antibiotic resistance, plasmids, and virulence-associated markers in human strains of Campylobacter jejuni and Campylobacter coli isolated in Italy
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1540210openalex-snapshot
A One Health approach for the genomic characterization of antibiotic-resistant Campylobacter isolates using Nanopore whole-genome sequencing
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1599555openalex-snapshot
Genomic analysis and antimicrobial resistance in human- and poultry-derived Campylobacter jejuni isolates from Hangzhou, China
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1717297openalex-snapshot
Role of microplastics in the survival and antimicrobial susceptibility of Campylobacter jejuni
inferred← citeshttps://doi.org/10.3389/fvets.2023.1092179openalex-snapshot
Genomic insight into Campylobacter jejuni isolated from commercial turkey flocks in Germany using whole-genome sequencing analysis
inferred← citeshttps://doi.org/10.3390/antibiotics11111632openalex-snapshot
Antimicrobial Resistance Genes Analysis of Publicly Available Staphylococcus aureus Genomes
inferred← citeshttps://doi.org/10.3390/ijms26104657openalex-snapshot
Antimicrobial Activity of a Synthetic Brevibacillin Analog Against Multidrug-Resistant Campylobacter spp.
inferred← citeshttps://doi.org/10.3390/microorganisms10051067openalex-snapshot
Antibiotic Resistance in Campylobacter spp. Isolated from Broiler Chicken Meat and Human Patients in Estonia
inferred← citeshttps://doi.org/10.3390/microorganisms10071410openalex-snapshot
Resistome Analysis of Campylobacter jejuni Strains Isolated from Human Stool and Primary Sterile Samples in Croatia
inferred← citeshttps://doi.org/10.3390/microorganisms12040709openalex-snapshot
Analysis of Antimicrobial Resistance in Bacterial Pathogens Recovered from Food and Human Sources: Insights from 639,087 Bacterial Whole-Genome Sequences in the NCBI Pathogen Detection Database
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/10.70675/c2632e44zf646z46b7za24bz6d73c78f1944openalex-snapshot
Développement d'une méthode d'analyse protéomique par spectrométrie de masse pour le diagnostic médical des infections bactériennes du sang
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.