List of works - Paal S Andersen

A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.

scientific article published on 9 January 2008

A Novel Missense Mutation, Leu390Val, in the Cardiac ß-myosin Heavy Chain Associated with Pronounced Septal Hypertrophy in Two Families with Hypertrophic Cardiomyopathy

scientific article published on 01 December 2000

A broad range quorum sensing inhibitor working through sRNA inhibition

scientific article

A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity

scientific article published on 11 April 2012

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome

article

A universal primer-independent next-generation sequencing approach for investigations of norovirus outbreaks and novel variants

scientific article

Adaptation of Escherichia coli traversing from the faecal environment to the urinary tract.

scientific article published on 4 November 2016

Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene

article

Alpha-defensin DEFA1A3 gene copy number elevation in Danish Crohn's disease patients

scientific article published on 24 June 2011

Anti-TNF treatment response in rheumatoid arthritis patients is associated with genetic variation in the NLRP3-inflammasome

scientific article (publication date: 2014)

Apo E in multiple sclerosis and optic neuritis: the Apo E-o4 allele is associated with progression of multiple sclerosis

scientific article published on 01 October 2005

Association of Disease Severity With Skin Microbiome and Filaggrin Gene Mutations in Adult Atopic Dermatitis

scientific article published on 17 January 2018

Associations between COX-2 polymorphisms, blood cholesterol and risk of acute coronary syndrome

scientific article published on 28 August 2009

Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis

CACNA1C (rs1006737) is associated with schizophrenia

scientific article published on 01 February 2010

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening

scientific article

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

scientific article published on 20 January 2012

Characterisation of an IMP-7-producing ST357 Pseudomonas aeruginosa isolate detected in Denmark using whole genome sequencing

scientific article published on 29 November 2014

Characterization of the upp gene encoding uracil phosphoribosyltransferase of Escherichia coli K12.

scientific article published on February 1992

Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.

scientific article published in January 2004

Cohort description: The Danish Blood Donor Staphylococcus aureus Carriage Study

scientific article published on 19 September 2019

Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398.

scientific article published on 7 December 2017

Complete Genome Sequence of a CTX-M-15-Producing Escherichia coli Strain from the H30Rx Subclone of Sequence Type 131 from a Patient with Recurrent Urinary Tract Infections, Closely Related to a Lethal Urosepsis Isolate from the Patient's Sister

scientific article published on 12 May 2016

Complete Genome Sequence of the Epidemic and Highly Virulent CTX-M-15-Producing H30-Rx Subclone of Escherichia coli ST131.

scientific article published on 5 December 2013

Complicated Staphylococcus aureus Bacteremia (SAB) Is Associated with Genetic Variation in GLS2.

scientific article published on 4 October 2017

Corrigendum: Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

scientific article published on 8 June 2017

Corrigendum: Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

scientific article published on 5 October 2017

Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

scientific article published on 8 November 2016

Cross-sectional study identifies lower risk of Staphylococcus aureus nasal colonization in Danish blood donors with hidradenitis suppurativa symptoms

scientific article published on 20 February 2020

Demographic fluctuation of community-acquired antibiotic-resistant Staphylococcus aureus lineages: potential role of flimsy antibiotic exposure

scientific article published on 29 March 2018

Demographic fluctuation of community-acquired antibiotic-resistant Staphylococcus aureus lineages: potential role of flimsy antibiotic exposure

scholarly article published 19 October 2017

Description and characterization of a penicillin-resistant Streptococcus dysgalactiae subsp. equisimilis clone isolated from blood in three epidemiologically linked patients

scientific article published on September 2016

Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples.

scientific article

Determination of beta-defensin genomic copy number in different populations: A comparison of three methods

scientific article

Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy

scientific article published in March 2001

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

scientific article

Disease concordance, zygosity, and NOD2/CARD15 status: follow-up of a population-based cohort of Danish twins with inflammatory bowel disease

scientific article published in November 2005

Dissemination and Characteristics of a Novel Plasmid-Encoded Carbapenem-Hydrolyzing Class D β-Lactamase, OXA-436 from Four Patients Involving Six Different Hospitals in Denmark

scientific article published on 23 October 2017

Does KCNE5 play a role in long QT syndrome?

scientific article

Draft Genome Sequences of Two Avian Pathogenic Escherichia coli Strains of Clinical Importance, E44 and E51.

scientific article published on 4 August 2016

Echocardiographic evaluation of pre-diagnostic development in young relatives genetically predisposed to hypertrophic cardiomyopathy.

scientific article published in August 2015

Echocardiographic strain imaging to assess early and late consequences of sarcomere mutations in hypertrophic cardiomyopathy

scientific article

Effects of a 17q21 chromosome gene variant, tobacco smoke and furred pets on infant wheeze

article

Erratum: Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations

article

Erratum: One-third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region

scholarly article published in European Journal of Human Genetics

Evidence for Human Adaptation and Foodborne Transmission of Livestock-Associated Methicillin-Resistant Staphylococcus aureus

scientific article published on 20 September 2016

Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women

scientific article published in June 2010

Familial Clustering of Staphylococcus aureus Bacteremia in First-Degree Relatives: A Danish Nationwide Cohort Study

scientific article published on 5 July 2016

Genetic Variations in Pattern Recognition Receptor Loci Are Associated with Anti-TNF Response in Patients with Rheumatoid Arthritis

scientific article

Genetic and Environmental Factors in Monozygotic Twins with Crohn’s Disease and Their First-Degree Relatives: A Case Report

Genetic and environmental factors as predictors of disease severity and extent at time of diagnosis in an inception cohort of inflammatory bowel disease, Copenhagen County and City 2003–2005 ⬇️

scientific article published on March 4, 2008

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

scientific article

Genetic polymorphisms associated with psoriasis and development of psoriatic arthritis in patients with psoriasis

scientific article published in February 2018

Genetic susceptibility and genotype-phenotype association in 588 Danish children with inflammatory bowel disease

scientific article published on 3 January 2014

Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia

scientific article

Genetically determined high activities of the TNF-alpha, IL23/IL17, and NFkB pathways were associated with increased risk of ankylosing spondylitis

Genetically determined high activity of IL-12 and IL-18 in ulcerative colitis and TLR5 in Crohns disease were associated with non-response to anti-TNF therapy.

scientific article

Genome Sequence of Staphylococcus aureus Strain CA-347, a USA600 Methicillin-Resistant Isolate

scientific article published on 25 July 2013

Genome analysis of Clostridium perfringens isolates from healthy and necrotic enteritis infected chickens and turkeys

scientific article published on 11 July 2017

Genome analysis of Staphylococcus aureus ST291, a double locus variant of ST398, reveals a distinct genetic lineage

scientific article

Genome sequence of Staphylococcus aureus strain 11819-97, an ST80-IV European community-acquired methicillin-resistant isolate

scientific article published on March 2012

Genomic analyses of Staphylococcus aureus clonal complex 45 isolates does not distinguish nasal carriage from bacteraemia

scientific article published on 15 July 2020

Genomic analysis reveals different mechanisms of fusidic acid resistance in Staphylococcus aureus from Danish atopic dermatitis patients

scientific article published on 14 December 2017

Genomic characterization, phylogenetic analysis, and identification of virulence factors in Aerococcus sanguinicola and Aerococcus urinae strains isolated from infection episodes

scientific article

Genomic relatedness of Staphylococcus pettenkoferi isolates of different origins

scientific article published on May 2017

HLA-A alleles and infectious mononucleosis suggest a critical role for cytotoxic T-cell response in EBV-related Hodgkin lymphoma

scientific article

High Interlaboratory Reproducibility and Accuracy of Next-Generation-Sequencing-Based Bacterial Genotyping in a Ring Trial

scientific article

High throughput mutation screening by automated capillary electrophoresis.

scientific article

High-Throughput Mutation Screening

High-quality and -quantity DNA extraction from frozen archival blood clots for genotyping of single-nucleotide polymorphisms

scientific article published on 10 April 2013

High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

article by Paal S Andersen et al published February 2003 in Human Mutation

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

article

High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device

scientific article published in May 2005

Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study.

scientific article

Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia

scientific article published on 05 October 2018

Human β-defensin 3 (DEFB103) and its influence on Staphylococcus aureus nasal carriage

Human β-defensin-2 as a marker for disease severity and skin barrier properties in atopic dermatitis.

scientific article published in September 2013

Identification of a PVL-negative SCCmec-IVa sublineage of the methicillin-resistant Staphylococcus aureus CC80 lineage: understanding the clonal origin of CA-MRSA.

scientific article

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

scientific article

In vivo expression of antimicrobial peptides in atopic dermatitis

scientific article published on 13 August 2015

Infliximab dependency in children with Crohn’s disease

scientific article published on 13 January 2009

Infliximab dependency is related to decreased surgical rates in adult Crohnʼs disease patients

article

Influence of host genetics and environment on nasal carriage of staphylococcus aureus in danish middle-aged and elderly twins

scientific article

Investigation of a possible outbreak of NDM-5-producing ST16 Klebsiella pneumoniae among patients in Denmark with no history of recent travel using whole-genome sequencing

scientific article published on 29 June 2015

Investigation of a possible outbreak of carbapenem-resistant Acinetobacter baumannii in Odense, Denmark using PFGE, MLST and whole-genome-based SNPs

scientific article published on 19 March 2015

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2

scientific article published on 01 February 2000

Mapping the Evolution of Hypervirulent Klebsiella pneumoniae

scientific article published on 21 July 2015

Methicillin-Resistant Staphylococcus aureus CC398 in Humans and Pigs in Norway: A "One Health" Perspective on Introduction and Transmission

scientific article published on 11 August 2016

Methicillin-resistant and -susceptible Staphylococcus aureus from retail meat in Denmark

scientific article published on 6 March 2017

Meticillin-resistant Staphylococcus aureus CC398 is an increasing cause of disease in people with no livestock contact in Denmark, 1999 to 2011

scientific article published on September 2015

Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations

article

Molecular characterisation of the clonal emergence of high-level ciprofloxacin-monoresistant Haemophilus influenzae in the Region of Southern Denmark

scientific article published on 21 January 2016

Multiple transcriptional control of the Lactococcus lactis trp operon.

scientific article

Multiplex ligation-dependent probe amplification technique for copy number analysis on small amounts of DNA material.

scientific article published in December 2008

Mutation Detection by Cleavase in Combination With Capillary Electrophoresis Analysis: Application to Mutations Causing Hypertrophic Cardiomyopathy and Long-QT Syndrome

scientific article published on 01 June 1998

Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

scientific article published on 01 February 2005

Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients

scientific article

NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype-phenotype analysis in Danish and Portuguese patients and controls

scientific article published on 19 September 2005

Nasal and pharyngeal carriage of methicillin-resistant Staphylococcus sciuri among hospitalised patients and healthcare workers in a Serbian university hospital

scientific article published on 19 September 2017

Non-toxigenic tox gene-bearing Corynebacterium ulcerans in a traumatic ulcer from a human case and his asymptomatic dog.

scientific article published on 15 August 2015

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome

scientific article published in June 1998

Nucleotide metabolism in Lactococcus lactis: salvage pathways of exogenous pyrimidines.

scientific article

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region

scientific article published in February 2005

Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics

scientific article published on October 2006

Origin and evolution of European community-acquired methicillin-resistant Staphylococcus aureus

scientific article

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations

scientific article

PPARgamma Pro12Ala polymorphism and risk of acute coronary syndrome in a prospective study of Danes

scientific article

Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing

scientific article published on 28 November 2012

Polymorphisms in inflammation genes, tobacco smoke and furred pets and wheeze in children

article

Polymorphisms in the Toll-Like Receptor and the IL-23/IL-17 Pathways Were Associated with Susceptibility to Inflammatory Bowel Disease in a Danish Cohort

scientific article published on 23 December 2015

Polymorphisms in the inflammatory pathway genes TLR2, TLR4, TLR9, LY96, NFKBIA, NFKB1, TNFA, TNFRSF1A, IL6R, IL10, IL23R, PTPN22, and PPARG are associated with susceptibility of inflammatory bowel disease in a Danish cohort

scientific article

Predictors of coronary in-stent restenosis: importance of angiotensin-converting enzyme gene polymorphism and treatment with angiotensin-converting enzyme inhibitors

article

Prevalence of infective endocarditis in patients with Staphylococcus aureus bacteraemia: the value of screening with echocardiography

scientific article

Prospective study of interaction between alcohol, NSAID use and polymorphisms in genes involved in the inflammatory response in relation to risk of colorectal cancer

article

Rapid detection, differentiation and typing of methicillin-resistant Staphylococcus aureus harbouring either mecA or the new mecA homologue mecALGA251

scientific article published on 01 April 2012

Rapid differentiation between livestock-associated and livestock-independent Staphylococcus aureus CC398 clades

scientific article

Rapid tumour-like growth of giant filiform polyposis in a patient without a history of chronic bowel inflammation.

scientific article published in November 2007

ReadFilter - Filtering reads of interest for quicker downstream analysis

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene

scientific article published in September 1999

Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twins.

scientific article published on 09 May 2013

Role of urinary cathelicidin LL-37 and human β-defensin 1 in uncomplicated Escherichia coli urinary tract infections

scientific article published on 22 January 2014

Screening of 99 Danish patients with congenital heart disease for GATA4 mutations.

scientific article published in January 2006

Screening of congenital heart disease patients using multiplex ligation-dependent probe amplification: Early diagnosis of syndromic patients

Selection of unique Escherichia coli clones by random amplified polymorphic DNA (RAPD): Evaluation by whole genome sequencing

scientific article

Sharing data between LSDBs and central repositories

scientific article

Single-Strand Conformation Polymorphism Analysis Using Capillary Electrophoresis

Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detection

article

Spread of avian pathogenic Escherichia coli ST117 O78:H4 in Nordic broiler production

scientific article

Staphylococcus aureus Bacteremia in Children Aged 5-18 Years—Risk Factors in the New Millennium

Staphylococcus aureus CC395 harbours a novel composite staphylococcal cassette chromosome mec element

scientific article published on 14 January 2017

Staphylococcus aureus CC398: Host Adaptation and Emergence of Methicillin Resistance in Livestock

article

Staphylococcus aureus CC398: host adaptation and emergence of methicillin resistance in livestock

scientific article published on 21 February 2012

Staphylococcus aureus and the ecology of the nasal microbiome

scientific article

Staphylococcus aureus colonization in atopic eczema and its association with filaggrin gene mutations.

scientific article published on 19 March 2017

Surface Glycopolymers Are Crucial for In Vitro Anti-Wall Teichoic Acid IgG-Mediated Complement Activation and Opsonophagocytosis of Staphylococcus aureus

scientific article

Temporal and Spatial Variation of the Skin-Associated Bacteria from Healthy Participants and Atopic Dermatitis Patients

scientific article published on 23 February 2022

Temporal variation of Staphylococcus aureus clonal complexes in atopic dermatitis: a follow‐up study

scientific article published on 10 October 2018

The B form of dihydroorotate dehydrogenase from Lactococcus lactis consists of two different subunits, encoded by the pyrDb and pyrK genes, and contains FMN, FAD, and [FeS] redox centers.

scientific article

The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.

scientific article

The Skin Microbiome in Atopic Dermatitis—a Potential Treatment Target?

The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.

scientific article published in June 2001

The associations between socioeconomic status and risk of Staphylococcus aureus bacteremia and subsequent endocarditis - a Danish nationwide cohort study

scientific article

The epidemic of extended-spectrum-β-lactamase-producing Escherichia coli ST131 is driven by a single highly pathogenic subclone, H30-Rx

scientific article published on 17 December 2013

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

scientific article

Transcriptomic profiling of interacting nasal staphylococci species reveals global changes in gene and non-coding RNA expression

scientific article published on 9 January 2018

Two different dihydroorotate dehydrogenases in Lactococcus lactis.

scientific article published on July 1994

Two genes encoding uracil phosphoribosyltransferase are present in Bacillus subtilis.

scientific article

Type 1 diabetes risk analysis on dried blood spot samples from population-based newborns: design and feasibility of an unselected case-control study

scientific article

Use of WGS data for investigation of a long-term NDM-1-producing Citrobacter freundii outbreak and secondary in vivo spread of blaNDM-1 to Escherichia coli, Klebsiella pneumoniae and Klebsiella oxytoca

scientific article

Use of whole-genome sequencing for detection of the spread of VIM-4-producing Escherichia coli between two patients in Denmark

scientific article published on 22 December 2014

Using Whole Genome Analysis to Examine Recombination across Diverse Sequence Types of Staphylococcus aureus

scientific article published on 10 July 2015

Vancomycin gene selection in the microbiome of urban Rattus norvegicus from hospital environment

scientific article

Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems

scientific article published in January 2007

Whole-genome comparison of urinary pathogenic Escherichia coli and faecal isolates of UTI patients and healthy controls

scientific article published on 14 September 2017

Whole-genome sequencing of bloodstream Staphylococcus aureus isolates does not distinguish bacteraemia from endocarditis

scientific article published in November 2017

[Long QT syndrome--genes, mechanisms and risks. Indication for genetic family screening?].

scientific article published in June 2006

eHealth: Disease activity measures are related to the faecal gut microbiota in adult patients with ulcerative colitis

scientific article published on 12 October 2020

List of works by Paal S Andersen

A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.

A Novel Missense Mutation, Leu390Val, in the Cardiac ß-myosin Heavy Chain Associated with Pronounced Septal Hypertrophy in Two Families with Hypertrophic Cardiomyopathy

A broad range quorum sensing inhibitor working through sRNA inhibition

A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome

A universal primer-independent next-generation sequencing approach for investigations of norovirus outbreaks and novel variants

Adaptation of Escherichia coli traversing from the faecal environment to the urinary tract.

Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene

Alpha-defensin DEFA1A3 gene copy number elevation in Danish Crohn's disease patients

Anti-TNF treatment response in rheumatoid arthritis patients is associated with genetic variation in the NLRP3-inflammasome

Apo E in multiple sclerosis and optic neuritis: the Apo E-o4 allele is associated with progression of multiple sclerosis

Association of Disease Severity With Skin Microbiome and Filaggrin Gene Mutations in Adult Atopic Dermatitis

Associations between COX-2 polymorphisms, blood cholesterol and risk of acute coronary syndrome

Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis

CACNA1C (rs1006737) is associated with schizophrenia

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

Characterisation of an IMP-7-producing ST357 Pseudomonas aeruginosa isolate detected in Denmark using whole genome sequencing

Characterization of the upp gene encoding uracil phosphoribosyltransferase of Escherichia coli K12.

Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.

Cohort description: The Danish Blood Donor Staphylococcus aureus Carriage Study

Commercial Biocides Induce Transfer of Prophage Φ13 from Human Strains of Staphylococcus aureus to Livestock CC398.

Complete Genome Sequence of a CTX-M-15-Producing Escherichia coli Strain from the H30Rx Subclone of Sequence Type 131 from a Patient with Recurrent Urinary Tract Infections, Closely Related to a Lethal Urosepsis Isolate from the Patient's Sister

Complete Genome Sequence of the Epidemic and Highly Virulent CTX-M-15-Producing H30-Rx Subclone of Escherichia coli ST131.

Complicated Staphylococcus aureus Bacteremia (SAB) Is Associated with Genetic Variation in GLS2.

Corrigendum: Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

Corrigendum: Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

Cross-sectional study identifies lower risk of Staphylococcus aureus nasal colonization in Danish blood donors with hidradenitis suppurativa symptoms

Demographic fluctuation of community-acquired antibiotic-resistant Staphylococcus aureus lineages: potential role of flimsy antibiotic exposure

Demographic fluctuation of community-acquired antibiotic-resistant Staphylococcus aureus lineages: potential role of flimsy antibiotic exposure

Description and characterization of a penicillin-resistant Streptococcus dysgalactiae subsp. equisimilis clone isolated from blood in three epidemiologically linked patients

Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples.

Determination of beta-defensin genomic copy number in different populations: A comparison of three methods

Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

Disease concordance, zygosity, and NOD2/CARD15 status: follow-up of a population-based cohort of Danish twins with inflammatory bowel disease

Dissemination and Characteristics of a Novel Plasmid-Encoded Carbapenem-Hydrolyzing Class D β-Lactamase, OXA-436 from Four Patients Involving Six Different Hospitals in Denmark

Does KCNE5 play a role in long QT syndrome?

Draft Genome Sequences of Two Avian Pathogenic Escherichia coli Strains of Clinical Importance, E44 and E51.

Echocardiographic evaluation of pre-diagnostic development in young relatives genetically predisposed to hypertrophic cardiomyopathy.

Echocardiographic strain imaging to assess early and late consequences of sarcomere mutations in hypertrophic cardiomyopathy

Effects of a 17q21 chromosome gene variant, tobacco smoke and furred pets on infant wheeze

Erratum: Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations

Erratum: One-third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region

Evidence for Human Adaptation and Foodborne Transmission of Livestock-Associated Methicillin-Resistant Staphylococcus aureus

Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women

Familial Clustering of Staphylococcus aureus Bacteremia in First-Degree Relatives: A Danish Nationwide Cohort Study

Genetic Variations in Pattern Recognition Receptor Loci Are Associated with Anti-TNF Response in Patients with Rheumatoid Arthritis

Genetic and Environmental Factors in Monozygotic Twins with Crohn’s Disease and Their First-Degree Relatives: A Case Report

Genetic and environmental factors as predictors of disease severity and extent at time of diagnosis in an inception cohort of inflammatory bowel disease, Copenhagen County and City 2003–2005 ⬇️

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

Genetic polymorphisms associated with psoriasis and development of psoriatic arthritis in patients with psoriasis

Genetic susceptibility and genotype-phenotype association in 588 Danish children with inflammatory bowel disease

Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia

Genetically determined high activities of the TNF-alpha, IL23/IL17, and NFkB pathways were associated with increased risk of ankylosing spondylitis

Genetically determined high activity of IL-12 and IL-18 in ulcerative colitis and TLR5 in Crohns disease were associated with non-response to anti-TNF therapy.

Genome Sequence of Staphylococcus aureus Strain CA-347, a USA600 Methicillin-Resistant Isolate

Genome analysis of Clostridium perfringens isolates from healthy and necrotic enteritis infected chickens and turkeys

Genome analysis of Staphylococcus aureus ST291, a double locus variant of ST398, reveals a distinct genetic lineage

Genome sequence of Staphylococcus aureus strain 11819-97, an ST80-IV European community-acquired methicillin-resistant isolate

Genomic analyses of Staphylococcus aureus clonal complex 45 isolates does not distinguish nasal carriage from bacteraemia

Genomic analysis reveals different mechanisms of fusidic acid resistance in Staphylococcus aureus from Danish atopic dermatitis patients

Genomic characterization, phylogenetic analysis, and identification of virulence factors in Aerococcus sanguinicola and Aerococcus urinae strains isolated from infection episodes

Genomic relatedness of Staphylococcus pettenkoferi isolates of different origins

HLA-A alleles and infectious mononucleosis suggest a critical role for cytotoxic T-cell response in EBV-related Hodgkin lymphoma

High Interlaboratory Reproducibility and Accuracy of Next-Generation-Sequencing-Based Bacterial Genotyping in a Ring Trial

High throughput mutation screening by automated capillary electrophoresis.

High-Throughput Mutation Screening

High-quality and -quantity DNA extraction from frozen archival blood clots for genotyping of single-nucleotide polymorphisms

High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device

Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study.

Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia

Human β-defensin 3 (DEFB103) and its influence on Staphylococcus aureus nasal carriage

Human β-defensin-2 as a marker for disease severity and skin barrier properties in atopic dermatitis.

Identification of a PVL-negative SCCmec-IVa sublineage of the methicillin-resistant Staphylococcus aureus CC80 lineage: understanding the clonal origin of CA-MRSA.

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes