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Author Details
Full Name
Christoph Preuss
Affiliation
Universite de Montreal
ORCID
Career Start Year
2007
Papers
33
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35233576
Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19.
bioRxiv
2023
37491352
Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19.
Nat Commun
2023
36641439
A novel human tau knock-in mouse model reveals interaction of Abeta and human tau under progressing cerebral amyloidosis in 5xFAD mice.
Alzheimers Res Ther
2023
34886679
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.
Circ Res
2022
34027015
Transfer learning-trained convolutional neural networks identify novel MRI biomarkers of Alzheimer's disease progression.
Alzheimers Dement (Amst)
2021
32492070
Transcriptomic stratification of late-onset Alzheimer's cases reveals novel genetic modifiers of disease pathology.
PLoS Genet
2020
33172468
A novel systems biology approach to evaluate mouse models of late-onset Alzheimer's disease.
Mol Neurodegener
2020
33188183
Molecular estimation of neurodegeneration pseudotime in older brains.
Nat Commun
2020
33273466
Author Correction: Molecular estimation of neurodegeneration pseudotime in older brains.
Nat Commun
2020
32668255
Meta-Analysis of the Alzheimer's Disease Human Brain Transcriptome and Functional Dissection in Mouse Models.
Cell Rep
2020
30455415
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
Nat Genet
2019
31878951
Genetic perturbations of disease risk genes in mice capture transcriptomic signatures of late-onset Alzheimer's disease.
Mol Neurodegener
2019
31369031
Meox2 Haploinsufficiency Accelerates Axonal Degeneration in DBA/2J Glaucoma.
Invest Ophthalmol Vis Sci
2019
31510680
Identifying and ranking potential driver genes of Alzheimer's disease using multiview evidence aggregation.
Bioinformatics
2019
31150388
Enhancing face validity of mouse models of Alzheimer's disease with natural genetic variation.
PLoS Genet
2019
30854227
Variable outcomes of human heart attack recapitulated in genetically diverse mice.
NPJ Regen Med
2019
30820038
Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene.
Eur J Hum Genet
2019
30526866
Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.
Am J Hum Genet
2018
28659821
Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.
Front Physiol
2017
28459858
Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice.
PLoS Genet
2017
28376948
Relationship between interatrial communication, ductus arteriosus, and pulmonary flow patterns in fetuses with transposition of the great arteries: prediction of neonatal desaturation.
Cardiol Young
2017
28974934
Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: <i>SMAD6</i> as an Important Contributor.
Front Physiol
2017
26148450
Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.
Can J Cardiol
2016
27760138
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
PLoS Genet
2016
24461919
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.
Can J Cardiol
2014
25282101
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.
Nat Genet
2014
23249132
Serotonergic overstimulation in a preterm infant after sertraline intake via breastmilk.
Breastfeed Med
2013
23706783
Genetics of heart failure in congenital heart disease.
Can J Cardiol
2013
22606245
Evolutionary dynamics of co-segregating gene clusters associated with complex diseases.
PLoS One
2012
21573245
Gp130-dependent release of acute phase proteins is linked to the activation of innate immune signaling pathways.
PLoS One
2011
22187409
Inherited risk factors for thrombotic diseases in children: the genome-wide perspective.
Semin Thromb Hemost
2011
18239962
Comparative analysis of expressed sequence tag (EST) libraries in the seagrass Zostera marina subjected to temperature stress.
Mar Biotechnol (NY)
2008
17234726
Angiotensin II induces endothelial xanthine oxidase activation: role for endothelial dysfunction in patients with coronary disease.
Arterioscler Thromb Vasc Biol
2007
1 - 33 of 33
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