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Author Details

Christoph Preuss
Universite de Montreal
2007
33
17
PMIDPaper TitleJournal TitlePublished Year
35233576Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19.bioRxiv2023
37491352Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19.Nat Commun2023
36641439A novel human tau knock-in mouse model reveals interaction of Abeta and human tau under progressing cerebral amyloidosis in 5xFAD mice.Alzheimers Res Ther2023
34886679Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.Circ Res2022
34027015Transfer learning-trained convolutional neural networks identify novel MRI biomarkers of Alzheimer's disease progression.Alzheimers Dement (Amst)2021
32492070Transcriptomic stratification of late-onset Alzheimer's cases reveals novel genetic modifiers of disease pathology.PLoS Genet2020
33172468A novel systems biology approach to evaluate mouse models of late-onset Alzheimer's disease.Mol Neurodegener2020
33188183Molecular estimation of neurodegeneration pseudotime in older brains.Nat Commun2020
33273466Author Correction: Molecular estimation of neurodegeneration pseudotime in older brains.Nat Commun2020
32668255Meta-Analysis of the Alzheimer's Disease Human Brain Transcriptome and Functional Dissection in Mouse Models.Cell Rep2020
30455415ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.Nat Genet2019
31878951Genetic perturbations of disease risk genes in mice capture transcriptomic signatures of late-onset Alzheimer's disease.Mol Neurodegener2019
31369031Meox2 Haploinsufficiency Accelerates Axonal Degeneration in DBA/2J Glaucoma.Invest Ophthalmol Vis Sci2019
31510680Identifying and ranking potential driver genes of Alzheimer's disease using multiview evidence aggregation.Bioinformatics2019
31150388Enhancing face validity of mouse models of Alzheimer's disease with natural genetic variation.PLoS Genet2019
30854227Variable outcomes of human heart attack recapitulated in genetically diverse mice.NPJ Regen Med2019
30820038Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene.Eur J Hum Genet2019
30526866Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.Am J Hum Genet2018
28659821Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.Front Physiol2017
28459858Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice.PLoS Genet2017
28376948Relationship between interatrial communication, ductus arteriosus, and pulmonary flow patterns in fetuses with transposition of the great arteries: prediction of neonatal desaturation.Cardiol Young2017
28974934Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.Front Physiol2017
26148450Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.Can J Cardiol2016
27760138Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.PLoS Genet2016
24461919Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.Can J Cardiol2014
25282101Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.Nat Genet2014
23249132Serotonergic overstimulation in a preterm infant after sertraline intake via breastmilk.Breastfeed Med2013
23706783Genetics of heart failure in congenital heart disease.Can J Cardiol2013
22606245Evolutionary dynamics of co-segregating gene clusters associated with complex diseases.PLoS One2012
21573245Gp130-dependent release of acute phase proteins is linked to the activation of innate immune signaling pathways.PLoS One2011
22187409Inherited risk factors for thrombotic diseases in children: the genome-wide perspective.Semin Thromb Hemost2011
18239962Comparative analysis of expressed sequence tag (EST) libraries in the seagrass Zostera marina subjected to temperature stress.Mar Biotechnol (NY)2008
17234726Angiotensin II induces endothelial xanthine oxidase activation: role for endothelial dysfunction in patients with coronary disease.Arterioscler Thromb Vasc Biol2007
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Collaborators

Tufts University School of Medicine
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Fred Hutchinson Cancer Research Center
Co-authored papers 7
The Johns Hopkins University
Co-authored papers 5
Tufts University Graduate School of Biomedical Sciences
Co-authored papers 5
Children's Hospital Oakland Research Institute
Co-authored papers 5
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Hospital for Sick Children
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University of Washington
Co-authored papers 4
Mayo Clinic
Co-authored papers 3
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Columbia University Medical Center
Co-authored papers 3
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F. Hoffmann-La Roche Ltd
Co-authored papers 3
Johns Hopkins University School of Medicine
Co-authored papers 3
National Institute of Allergy and Infectious Diseases
Co-authored papers 2
Center for Computational Sciences
Co-authored papers 2
National Institute of Allergy and Infectious Diseases
Co-authored papers 2
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers 2
Cornell University
Co-authored papers 2
University of Washington
Co-authored papers 2
University of Washington School of Medicine
Co-authored papers 2
Chongqing Center for Disease Control and Prevention.
Co-authored papers 2
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers 2
Johns Hopkins University
Co-authored papers 2
National Institute of Allergy and Infectious Diseases
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Ontario Institute for Cancer Research
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University of British Columbia
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Fred Hutchinson Cancer Research Center
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Institute for Cell Engineering, Johns Hopkins University School of Medicine
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SUNY Upstate Medical University
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