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Antimicrobial resistance patterns in Streptococcus dysgalactiae in a One Health perspective

Frontiers in microbiology, 2024-06, Vol.15, p.1423762

2024

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Emergence of Inducible Macrolide Resistance in Mycobacterium chelonae Due to Broad-Host-Range Plasmid and Chromosomal Variants of the Novel 23S rRNA Methylase Gene, erm (55)

Journal of clinical microbiology, 2023-07, Vol.61 (7), p.e0042823-e0042823

2023

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Klotho Overexpression Is Frequently Associated With Upstream Rearrangements in Fusion-Negative Phosphaturic Mesenchymal Tumors of Bone and Sinonasal Tract

Modern pathology, 2023-12, Vol.36 (12), p.100336-100336, Article 100336

2023

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Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?

Frontiers in genetics, 2021-06, Vol.12, p.682980-682980

Liehr, Thomas

2021

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Whole genome sequencing–based copy number variations reveal novel pathways and targets in Alzheimer's disease

Alzheimer's & dementia, 2022-10, Vol.18 (10), p.1846-1867

2022

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Case Report: A novel IRF2BP2 mutation in an IEI patient with recurrent infections and autoimmune disorders

Frontiers in immunology, 2023-06, Vol.14, p.967345-967345

2023

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Frequent Methicillin-Resistant Staphylococcus aureus Introductions Into an Inner-city Jail: Indications of Community Transmission Networks

Clinical infectious diseases, 2020-07, Vol.71 (2), p.323-331

2020

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First parechovirus reported case in Saudi Arabia in hospitalized immunocompromised adult patient

Virology journal, 2024-05, Vol.21 (1), p.102-102, Article 102

2024

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Assessing the Costs and Cost-Effectiveness of Genomic Sequencing

Journal of personalized medicine, 2015-12, Vol.5 (4), p.470-486

2015

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Frozen Vegetable Processing Plants Can Harbour Diverse Listeria monocytogenes Populations: Identification of Critical Operations by WGS

Foods, 2022-05, Vol.11 (11), p.1546

2022

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Next-Generation Sequencing Whole-Genome Analysis for Targeted Treatment Approach of Metastatic Bartholin Gland Adenocarcinoma: An Emblematic Case Report and Review of the Literature

Diagnostics (Basel), 2021-11, Vol.11 (11), p.2085

2021

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Premier cas de séquençage complet du génome dans le cancer de la prostate

Progrès en urologie (Paris), 2014-12, Vol.24 (16), p.1041-1042

2014

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Genomic analysis-integrated whole-exome sequencing of neuroblastomas identifies genetic mutations in axon guidance pathway

Oncotarget, 2017-08, Vol.8 (34), p.56684-56697

2017

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Approach to the Differential Diagnosis of Cerebellar Ataxias

Handbook of the Cerebellum and Cerebellar Disorders, p.2053-2075

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A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants

American journal of human genetics, 2019-10, Vol.105 (4), p.719-733

2019

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Whole‐genome sequencing approaches for conservation biology: Advantages, limitations and practical recommendations

Molecular ecology, 2017-10, Vol.26 (20), p.5369-5406

2017

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Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies

American journal of human genetics, 2021-05, Vol.108 (5), p.919-928

2021

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VFDB 2019: a comparative pathogenomic platform with an interactive web interface

Nucleic acids research, 2019-01, Vol.47 (D1), p.D687-D692

2019

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Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature

Genetics in medicine, 2019-01, Vol.21 (1), p.3-16

2019

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Comprehensive evaluation and characterisation of short read general-purpose structural variant calling software

Nature communications, 2019-07, Vol.10 (1), p.3240-11, Article 3240

2019

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Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing

Genetics in medicine, 2018-11, Vol.20 (11), p.1328-1333

2018

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New Tools for Mendelian Disease Gene Identification: PhenoDB Variant Analysis Module; and GeneMatcher, a Web-Based Tool for Linking Investigators with an Interest in the Same Gene

Human mutation, 2015-04, Vol.36 (4), p.425-431

2015

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Genomic Analysis in the Age of Human Genome Sequencing

Cell, 2019-03, Vol.177 (1), p.70-84

2019

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Transmission, infectivity, and neutralization of a spike L452R SARS-CoV-2 variant

Cell, 2021-06, Vol.184 (13), p.3426-3437.e8

2021

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Next-Generation Sequencing and Emerging Technologies

Seminars in thrombosis and hemostasis, 2019-10, Vol.45 (7), p.661-673

2019

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Antimicrobial resistance patterns in Streptococcus dysgalactiae in a One Health perspective

Emergence of Inducible Macrolide Resistance in Mycobacterium chelonae Due to Broad-Host-Range Plasmid and Chromosomal Variants of the Novel 23S rRNA Methylase Gene, erm (55)

Klotho Overexpression Is Frequently Associated With Upstream Rearrangements in Fusion-Negative Phosphaturic Mesenchymal Tumors of Bone and Sinonasal Tract

Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?

Whole genome sequencing–based copy number variations reveal novel pathways and targets in Alzheimer's disease

Case Report: A novel IRF2BP2 mutation in an IEI patient with recurrent infections and autoimmune disorders

Frequent Methicillin-Resistant Staphylococcus aureus Introductions Into an Inner-city Jail: Indications of Community Transmission Networks

First parechovirus reported case in Saudi Arabia in hospitalized immunocompromised adult patient

Assessing the Costs and Cost-Effectiveness of Genomic Sequencing

Frozen Vegetable Processing Plants Can Harbour Diverse Listeria monocytogenes Populations: Identification of Critical Operations by WGS

Next-Generation Sequencing Whole-Genome Analysis for Targeted Treatment Approach of Metastatic Bartholin Gland Adenocarcinoma: An Emblematic Case Report and Review of the Literature

Premier cas de séquençage complet du génome dans le cancer de la prostate

Genomic analysis-integrated whole-exome sequencing of neuroblastomas identifies genetic mutations in axon guidance pathway

Approach to the Differential Diagnosis of Cerebellar Ataxias

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants

Whole‐genome sequencing approaches for conservation biology: Advantages, limitations and practical recommendations

Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies

VFDB 2019: a comparative pathogenomic platform with an interactive web interface

Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature

Comprehensive evaluation and characterisation of short read general-purpose structural variant calling software

Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing

New Tools for Mendelian Disease Gene Identification: PhenoDB Variant Analysis Module; and GeneMatcher, a Web-Based Tool for Linking Investigators with an Interest in the Same Gene

Genomic Analysis in the Age of Human Genome Sequencing

Transmission, infectivity, and neutralization of a spike L452R SARS-CoV-2 variant

Next-Generation Sequencing and Emerging Technologies

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