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Author Details

Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
1995
44
18
PMIDPaper TitleJournal TitlePublished Year
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37308929Development of HPV16 mouse and dog models for more accurate prediction of human vaccine efficacy.Lab Anim Res2023
34328547INFRAFRONTIER quality principles in systemic phenotyping.Mamm Genome2022
36551904Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.Biomedicines2022
35195951Behavioral Testing Design for Evaluation of Cognitive Disabilities.Curr Protoc2022
33476328Identifying causative mechanisms linking early-life stress to psycho-cardio-metabolic multi-morbidity: The EarlyCause project.PLoS One2021
34862403ProMetIS, deep phenotyping of mouse models by combined proteomics and metabolomics analysis.Sci Data2021
34587162Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.PLoS Genet2021
34356832High Resolution Episcopic Microscopy for Qualitative and Quantitative Data in Phenotyping Altered Embryos and Adult Mice Using the New "Histo3D" System.Biomedicines2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
31145554Ultrasound-Guided Approaches to Improve Orthotopic Mouse Xenograft Models for Hepatocellular Carcinoma.Curr Protoc Mouse Biol2019
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
29659809A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterations.Hum Mol Genet2018
29113787Nox4 genetic inhibition in experimental hypertension and metabolic syndrome.Arch Cardiovasc Dis2018
28065649Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.Neuron2017
28288815RF313, an orally bioavailable neuropeptide FF receptor antagonist, opposes effects of RF-amide-related peptide-3 and opioid-induced hyperalgesia in rodents.Neuropharmacology2017
28266534Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE.Sci Rep2017
29066853Non-invasive quantitative imaging of hepatocellular carcinoma growth in mice by micro-CT using liver-targeted iodinated nano-emulsions.Sci Rep2017
28650954Prevalence of sexual dimorphism in mammalian phenotypic traits.Nat Commun2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28704368Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.PLoS Genet2017
28851918Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies.Sci Rep2017
27088730How Does Circadian Rhythm Impact Salt Sensitivity of Blood Pressure in Mice? A Study in Two Close C57Bl/6 Substrains.PLoS One2016
27739457Multimodal imaging of a humanized orthotopic model of hepatocellular carcinoma in immunodeficient mice.Sci Rep2016
27621313Physiological Expression of AMPKγ2RG Mutation Causes Wolff-Parkinson-White Syndrome and Induces Kidney Injury in Mice.J Biol Chem2016
26938916Role of the BAHD1 Chromatin-Repressive Complex in Placental Development and Regulation of Steroid Metabolism.PLoS Genet2016
25992600Applying the ARRIVE Guidelines to an In Vivo Database.PLoS Biol2015
26214591Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Nat Genet2015
24811761Hyperactivation of Alk induces neonatal lethality in knock-in AlkF1178L mice.Oncotarget2014
25405900Regulator of G-protein signaling 18 controls both platelet generation and function.PLoS One2014
23359549Repression of osteoblast maturation by ERRα accounts for bone loss induced by estrogen deficiency.PLoS One2013
23911743Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors.Neuropharmacology2013
23902802A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.Genome Biol2013
22323709Absence of TI-VAMP/Vamp7 leads to increased anxiety in mice.J Neurosci2012
22961258Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project.Mamm Genome2012
18392653Genetic background determines metabolic phenotypes in the mouse.Mamm Genome2008
17937900[Functional genomics of the mouse: the European dynamics].Med Sci (Paris)2007
15667338Expression of human IL-1alpha after intramarrow gene transfer into healthy non-human primate by adenoviral vector.J Med Primatol2005
12181061Retroviral interleukin 1alpha gene transfer in bone marrow stromal cells in a primate model: induction of myelopoiesis stimulation.Br J Haematol2002
11266964How can adenovirus-mediated catalase and superoxide dismutase gene transfer improve the outcome of pancreatic cells for transplantation?Transplant Proc2001
10174693Gene therapy for AIDS.Transfus Sci1997
8787346[Gene therapy for hereditary and acquired human diseases].Ann Endocrinol (Paris)1995
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Collaborators

Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 27
Guillaume Pavlovic
CNRS, INSERM, Universite de Strasbourg, PHENOMIN-Institut Clinique de la Souris (ICS)
Co-authored papers 13
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 12
Ann-Marie Mallon
The Turing Institute
Co-authored papers 11
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 10
Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 10
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 10
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 9
Colin McKerlie
The Hospital for Sick Children
Co-authored papers 9
Kent C Lloyd
University of California davis
Co-authored papers 8
Helmut Fuchs
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 8
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 8
Terrence F Meehan
European Bioinformatics Institute
Co-authored papers 7
Jan Rozman
German Center for Diabetes Research (DZD)
Co-authored papers 7
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 7
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 6
Luis Santos
The Turing Institute
Co-authored papers 6
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 6
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 6
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 6
Simon Greenaway
Harwell Institute
Co-authored papers 5
Robert E Braun
University of Maine
Co-authored papers 5
Hugh Morgan
MRC Harwell Institute
Co-authored papers 5
Natasha A Karp
Wellcome Sanger Institute
Co-authored papers 5
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 5
Je Kyung Seong
Seoul National University
Co-authored papers 5
Stephen A Murray
Columbia University.
Co-authored papers 5
Karen L Svenson
Co-authored papers 5
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 5
Corey L Reynolds
Baylor College of Medicine
Co-authored papers 5
Release 1.2