Nicolas Casadei
Reproducibility track record
1
assessed papers
87/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
2
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
Funders
—
Frequent co-authors
Aida Kalok 1Zhiqi Yang 1Alfred Lennart Bissinger 1Norashikin Abdul Fuad 1Tina Ganzenmueller 1Ersoy Kocak 1Stephan Ossowski 1Harivignesh Ganesan 1Omer Khalid 1Olaf Rieß 1
Institutions
Institute for Women's Policy Research 1University Kebangsaan Malaysia Medical Centre 1National University of Malaysia 1Science Oxford 1Institute of Medical Microbiology and Hygiene 1Bernstein Center for Computational Neuroscience Tübingen 1
Geography (author institutions)
US 1MY 1GB 1DE 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (171)
Request a reproduction →1 assessed by us (1 reproduced) · 170 not yet assessed — every PubMed paper on record, linked below.
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Comparing the impact of sample multiplexing approaches for single-cell RNA-sequencing on downstream analysis using cerebellar organoids ↗iScience · 2026 · PMID 41743667not yet assessed
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Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia ↗Nature Communications · 2026 · PMID 41690933not yet assessed
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Dysregulated NK-cell gene expression defines the enduring symptoms of long COVID-19 ↗Frontiers in Immunology · 2026 · PMID 41878441not yet assessed
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Single-Platform Nanopore Sequencing Enables Diploid Telomere-to-Telomere Genome Assembly and Haplotype-Resolved 3D Chromatin Maps ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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Prevention of ubiquitination at K6 and K9 in mutant huntingtin exacerbates disease pathology in a knock-in mouse model ↗Proceedings of the National Academy of Sciences · 2026 · PMID 41505525not yet assessed
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Comparing the impact of sample multiplexing approaches for single-cell RNA-sequencing on downstream analysis using cerebellar organoids ↗Repository KITopen (Karlsruhe Institute of Technology) · 2026not yet assessed
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Epigenetic control of S100A8/A9-driven monocytic inflammation licenses anti-leukemic functionality of immature NK cells during hematopoietic stem cell differentiation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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Altered light-dark phase-dependent behavioral responses and suprachiasmatic nucleus pathology in an α-synuclein rat model of Parkinson’s disease ↗npj Parkinson s Disease · 2026 · PMID 42321236not yet assessed
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MethylBench: A comprehensive benchmark of DNA methylation profiling methods across diverse sequencing platforms ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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No Evidence for an Association Between <i>DIP2B</i> Repeat Expansion and Neurological Disease ↗Movement Disorders · 2026 · PMID 42205056not yet assessed
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Gene expression and splicing counts from the Solve-RD study - blood, hg19, strand-specific ↗Zenodo (CERN European Organization for Nuclear Research) · 2026not yet assessed
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Gene expression and splicing counts from the Solve-RD study - blood, hg19, strand-specific ↗Zenodo (CERN European Organization for Nuclear Research) · 2026not yet assessed
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Genome-wide CRISPR-Cas9 screens identify BCL family members as modulators of response to regorafenib in experimental glioma ↗Neuro-Oncology · 2025 · PMID 39756423not yet assessed
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TDP-43 overexpression in the hypothalamus drives neuropathology, dysregulates metabolism and impairs behavior in mice ↗Acta Neuropathologica Communications · 2025 · PMID 40426231not yet assessed
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Long-read RNA-sequencing reveals transcript-specific regulation in human-derived cortical neurons ↗Open Biology · 2025 · PMID 40735840not yet assessed
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Cryogenic mouse tissue homogenization as an alternative to fresh-frozen biopsy use for genomics, transcriptomics, proteomics and metabolomics ↗Scientific Reports · 2025 · PMID 40550841not yet assessed
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Single-cell RNA-sequencing highlights a curtailed NK cell function in convalescent COVID-19 pregnant womenFrontiers in Immunology · 2025 · PMID 40661959L1 87/100
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Influence of ATXN2 intermediate CAG repeats, 9bp duplication and alternative splicing on SCA3 pathogenesis ↗Acta Neuropathologica Communications · 2025 · PMID 40684213not yet assessed
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sc-MULTI-omics approach in nano-rare diseases: understanding the pathophysiological mechanism of Mulvihill-Smith Syndrome ↗Functional & Integrative Genomics · 2025 · PMID 40343591not yet assessed
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Development of a QCM-D-Based Aptasensor for the Real-Time Detection of β-Lactoglobulin ↗Biosensors · 2025 · PMID 41002303not yet assessed
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Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits ↗The Breast · 2025 · PMID 40403485not yet assessed
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Unravelling axonal transcriptional landscapes: insights from induced pluripotent stem cell-derived cortical neurons and implications for motor neuron degeneration ↗Open Biology · 2025 · PMID 40495808not yet assessed
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Alpha-synuclein aggregation and dopaminergic neuron death in a new mouse model of Parkinson’s disease expressing human full-length and C-terminally truncated 1- 120 alpha-synuclein ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025not yet assessed
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not yet assessed
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RAG recombinase expression discriminates the development of natural killer cells. ↗PubMed · 2025 · PMID 40787451not yet assessed
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Extensive non-clonal CAR T-cell expansion causing fatal hyperinflammatory syndrome with immune effector cell-associated hemophagocytic lymphohistiocytosis, cytokine release syndrome, and neurotoxicity syndrome ↗Haematologica · 2025 · PMID 40874337not yet assessed
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JS04.7.A IDENTIFICATION OF BCL FAMILY MEMBERS AS MODULATORS OF REGORAFENIB EFFICACY IN EXPERIMENTAL GLIOMA ↗Neuro-Oncology · 2025not yet assessed
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Brain region-specific and systemic transcriptomic alterations in a human alpha-synuclein overexpressing rat model ↗Aging · 2025 · PMID 41117843not yet assessed
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Circadian disruption coincides with morphological changes in the suprachiasmatic nucleus in a genetic α-synuclein rat model of early Parkinson's disease ↗Research Square · 2025not yet assessed
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Chimeric organotypic brain slice cultures support the maturation and functional analysis of human iPSC-derived microglia ↗Research Square · 2025not yet assessed
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RAG recombinase expression discriminates the development of natural killer cells ↗Universitätsbibliothek Tübingen · 2025not yet assessed
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Altered light-dark phase-dependent behavioral responses and suprachiasmatic nucleus pathology in an α-synuclein rat model of Parkinson's disease ↗Zenodo (CERN European Organization for Nuclear Research) · 2025not yet assessed
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Altered light-dark phase-dependent behavioral responses and suprachiasmatic nucleus pathology in an α-synuclein rat model of Parkinson's disease ↗Zenodo (CERN European Organization for Nuclear Research) · 2025not yet assessed
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A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy ↗Nature Genetics · 2024 · PMID 38684900not yet assessed
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The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomics ↗npj Biodiversity · 2024 · PMID 39289538not yet assessed
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Genomes in clinical care ↗npj Genomic Medicine · 2024 · PMID 38485733not yet assessed
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Systemic inflammation accelerates neurodegeneration in a rat model of Parkinson’s disease overexpressing human alpha synuclein ↗npj Parkinson s Disease · 2024 · PMID 39500895not yet assessed
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Augmenting MEK inhibitor efficacy in BRAF wild-type melanoma: synergistic effects of disulfiram combination therapy ↗Journal of Experimental & Clinical Cancer Research · 2024 · PMID 38263136not yet assessed
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Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease ↗Neurobiology of Disease · 2024 · PMID 38423193not yet assessed
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Functional screening reveals genetic dependencies and diverging cell cycle control in atypical teratoid rhabdoid tumors ↗Genome biology · 2024 · PMID 39617889not yet assessed
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Resequencing the complete SNCA locus in Indian patients with Parkinson’s disease ↗npj Parkinson s Disease · 2024 · PMID 38622158not yet assessed
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A Novel <scp><i>PINK1</i></scp> p.<scp>F385S</scp> Loss‐of‐Function Mutation in an Indian Family with Parkinson's Disease ↗Movement Disorders · 2024 · PMID 38586902not yet assessed
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Concept and feasibility of the Augsburg Longitudinal Plasma Study (ALPS) – a prospective trial for comprehensive liquid biopsy-based longitudinal monitoring of solid cancer patients ↗Journal of Laboratory Medicine · 2024not yet assessed
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Systematic assessment of COVID-19 host genetics using whole genome sequencing data ↗PLoS Pathogens · 2024 · PMID 39715278not yet assessed
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Comparing the impact of sample multiplexing approaches for single-cell RNA-sequencing on downstream analysis using cerebellar organoids ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024not yet assessed
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Unraveling Axonal Transcriptional Landscapes: Insights from iPSC-Derived Cortical Neurons and Implications for Motor Neuron Degeneration ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024 · PMID 38585749not yet assessed
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Author Correction: The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomics ↗npj Biodiversity · 2024 · PMID 39407030not yet assessed
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Community effort to unravel the complex human neuronal landscape exemplified for the striatum ↗Research Square · 2024not yet assessed
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Long-Read RNA-sequencing reveals transcript-specific regulation in human-derived cortical neurons ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024not yet assessed
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Systemic inflammation accelerates neurodegeneration in a rat model of Parkinson’s disease overexpressing human alpha synuclein ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024not yet assessed
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not yet assessed
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not yet assessed
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Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy ↗International Journal of Molecular Sciences · 2024 · PMID 39409197not yet assessed
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Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases ↗Journal of Medical Genetics · 2023 · PMID 37734845not yet assessed
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Platelet-Derived MicroRNAs Regulate Cardiac Remodeling After Myocardial Ischemia ↗Circulation Research · 2023 · PMID 36891903not yet assessed
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Overexpression of human alpha-Synuclein leads to dysregulated microbiome/metabolites with ageing in a rat model of Parkinson disease ↗Molecular Neurodegeneration · 2023 · PMID 37403161not yet assessed
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Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study ↗npj Parkinson s Disease · 2023 · PMID 37996455not yet assessed
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Whole genome analysis of two sympatric human Mansonella: Mansonella perstans and Mansonella sp “DEUX” ↗Frontiers in Cellular and Infection Microbiology · 2023 · PMID 37124042not yet assessed
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Endogenous but not sensory-driven activity controls migration, morphogenesis and survival of adult-born juxtaglomerular neurons in the mouse olfactory bulb ↗Cellular and Molecular Life Sciences · 2023 · PMID 36932186not yet assessed
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Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3 ↗Brain · 2023 · PMID 37071051not yet assessed
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Lasting response by vertical inhibition with cetuximab and trametinib in<i>KRAS</i>‐mutated colorectal cancer patient‐derived xenografts ↗Molecular Oncology · 2023 · PMID 37604687not yet assessed
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Platelet-derived microRNAs play a pivotal role in cardiac remodeling after myocardial ischemia and reperfusion ↗European Heart Journal · 2023not yet assessed
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Genome sequencing identifies complex structural <scp><i>MLH1</i></scp> variant in unsolved Lynch syndrome ↗Molecular Genetics & Genomic Medicine · 2023 · PMID 36760167not yet assessed
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The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomics ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Reference genome of the ant <i>Lasius platythorax</i> ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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not yet assessed
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Augmenting MEK inhibitor Efficacy in BRAF Wild-Type Melanoma: Synergistic Effects of Disulfiram Combination Therapy ↗Research Square · 2023not yet assessed
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Blood and cerebellar abundance of <i>ATXN3</i> splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Author Correction: Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study ↗npj Parkinson s Disease · 2023 · PMID 38110362not yet assessed
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Accurate long-read sequencing identified GBA variants as a major genetic risk factor in the Luxembourg Parkinson’s study ↗medRxiv · 2023not yet assessed
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Accurate long-read sequencing identified GBA variants as a major genetic risk factor in the Luxembourg Parkinson’s study ↗Research Square · 2023not yet assessed
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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative ↗PLoS Genetics · 2022 · PMID 36327219not yet assessed
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Morpho‐Functional Changes of Nigral Dopamine Neurons in an α‐Synuclein Model of Parkinson's Disease ↗Movement Disorders · 2022 · PMID 36350188not yet assessed
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Host genetic loci LZTFL1 and CCL2 associated with SARS-CoV-2 infection and severity of COVID-19 ↗International Journal of Infectious Diseases · 2022 · PMID 35753602not yet assessed
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Miro1 R272Q disrupts mitochondrial calcium handling and neurotransmitter uptake in dopaminergic neurons ↗Frontiers in Molecular Neuroscience · 2022 · PMID 36533136not yet assessed
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Intronic enhancers of the human <i>SNCA</i> gene predominantly regulate its expression in brain in vivo ↗Science Advances · 2022 · PMID 36417521not yet assessed
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DYT6 mutated THAP1 is a cell type dependent regulator of the SP1 family ↗Brain · 2022 · PMID 35015830not yet assessed
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Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17 ↗Cellular and Molecular Life Sciences · 2022 · PMID 35482253not yet assessed
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Human Leucocyte Antigen G and Murine Qa-2 Are Critical for Myeloid Derived Suppressor Cell Expansion and Activation and for Successful Pregnancy Outcome ↗Frontiers in Immunology · 2022 · PMID 35111157not yet assessed
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SARS-CoV-2 B.1.214.1, B.1.214.2 and B.1.620 are predominant lineages between December 2020 and July 2021 in the Republic of Congo ↗IJID Regions · 2022 · PMID 35720148not yet assessed
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Identification and Functional Characterization of Argonaute (Ago) Proteins in Insect Genomes. ↗PubMed · 2022 · PMID 34495503not yet assessed
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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative ↗medRxiv · 2022not yet assessed
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Single-cell RNA sequencing highlights a reduced function of natural killer and cytotoxic T cell in recovered COVID-19 pregnant women ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Comparative multi-OMICS single cell atlas of five COVID-19 (rAdVV and mRNA) vaccines describe unique and distinct mechanisms of action ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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"DYT6 mutated THAP1 is a cell type dependent regulator of the SP1 family" ↗Zenodo (CERN European Organization for Nuclear Research) · 2022not yet assessed
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ATRT-19. Functional genomics reveal distinct modulators of response to CDK4/6 inhibitors in ATRTs ↗Neuro-Oncology · 2022not yet assessed
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Immune dynamics at single cell protein level after delta/omicron infection in COVID-19 vaccinated convalescent individuals ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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not yet assessed
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Swarm Learning for decentralized and confidential clinical machine learning ↗Nature · 2021 · PMID 34040261not yet assessed
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Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19 ↗Immunity · 2021 · PMID 34592166not yet assessed
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A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in Oligodendrocytes ↗Molecular Neurobiology · 2021 · PMID 34716557not yet assessed
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Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity ↗Human Genetics · 2021 · PMID 34889978not yet assessed
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Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection Clusters Based on Integrated Genomic Surveillance, Outbreak Analysis and Contact Tracing in an Urban Setting ↗Clinical Infectious Diseases · 2021 · PMID 34181711not yet assessed
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Genomic surveillance of SARS-CoV-2 in the Republic of Congo ↗International Journal of Infectious Diseases · 2021 · PMID 33737129not yet assessed
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SARS-CoV-2 infection paralyzes cytotoxic and metabolic functions of the immune cells ↗Heliyon · 2021 · PMID 34075347not yet assessed
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Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder ↗The American Journal of Human Genetics · 2021 · PMID 34022130not yet assessed
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Gene-corrected p.A30P SNCA patient-derived isogenic neurons rescue neuronal branching and function ↗Scientific Reports · 2021 · PMID 34754035not yet assessed
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Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Genome Medicine · 2021 · PMID 34271981not yet assessed
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SARS‐CoV‐2‐reactive T‐cell receptors isolated from convalescent COVID‐19 patients confer potent T‐cell effector function ↗European Journal of Immunology · 2021 · PMID 34424997not yet assessed
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Generation of R272Q, S156A and K572R RHOT1/Miro1 point mutations in iPSCs from a healthy individual using FACS-assisted CRISPR/Cas9 genome editing ↗Stem Cell Research · 2021 · PMID 34359002not yet assessed
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Imaging of α-Synuclein Aggregates in a Rat Model of Parkinson’s Disease Using Raman Microspectroscopy ↗Frontiers in Cell and Developmental Biology · 2021 · PMID 34568310not yet assessed
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Essential role of DNA-PKcs and plasminogen for the development of doxorubicin-induced glomerular injury in mice ↗Disease Models & Mechanisms · 2021 · PMID 34423816not yet assessed
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Endogenous but not sensory-driven activity controls migration, morphogenesis and survival of adult-born neurons in the mouse olfactory bulb ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Marker-free imaging of α-Synuclein aggregates in a rat model of Parkinson’s disease using Raman microspectroscopy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Human leucocyte antigen G (HLA-G) and its murine homologue Qa-2 protect from pregnancy loss ↗Research Square · 2021not yet assessed
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not yet assessed
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EXTH-69. FUNCTIONAL GENOMICS UNCOVER GENETIC DEPENDENCIES IN ATRTS ↗Neuro-Oncology · 2021not yet assessed
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A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in Oligodendrocytes ↗Research Square · 2021not yet assessed
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Additional file 6 of Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Figshare · 2021not yet assessed
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Additional file 1 of Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Figshare · 2021not yet assessed
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Additional file 3 of Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Figshare · 2021not yet assessed
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Additional file 7 of Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Figshare · 2021not yet assessed
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Additional file 5 of Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Figshare · 2021not yet assessed
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Additional file 4 of Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models ↗Figshare · 2021not yet assessed
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Immunophenotyping in pemphigus reveals a TH17/TFH17 cell–dominated immune response promoting desmoglein1/3-specific autoantibody production ↗Journal of Allergy and Clinical Immunology · 2020 · PMID 33221382not yet assessed
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Psychosis‐Like Behavior and Hyperdopaminergic Dysregulation in Human <b>α</b>‐Synuclein <scp>BAC</scp> Transgenic Rats ↗Movement Disorders · 2020 · PMID 33200461not yet assessed
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Comparative targeting analysis of KLF1, BCL11A, and HBG1/2 in CD34+ HSPCs by CRISPR/Cas9 for the induction of fetal hemoglobin ↗Scientific Reports · 2020 · PMID 32576837not yet assessed
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Human Dopaminergic Neurons Lacking PINK1 Exhibit Disrupted Dopamine Metabolism Related to Vitamin B6 Co-Factors ↗iScience · 2020 · PMID 33299968not yet assessed
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DJ-1 (Park7) affects the gut microbiome, metabolites and the development of innate lymphoid cells (ILCs) ↗Scientific Reports · 2020 · PMID 32999308not yet assessed
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The Endometrial Transcription Landscape of MRKH Syndrome ↗Frontiers in Cell and Developmental Biology · 2020 · PMID 33072755not yet assessed
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Calpain-1 ablation partially rescues disease-associated hallmarks in models of Machado-Joseph disease ↗Human Molecular Genetics · 2020 · PMID 31960910not yet assessed
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Comprehensive phenotyping revealed transient startle response reduction and histopathological gadolinium localization to perineuronal nets after gadodiamide administration in rats ↗Scientific Reports · 2020 · PMID 33372182not yet assessed
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Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia ↗Journal of Molecular Neuroscience · 2020 · PMID 32112337not yet assessed
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Increased expression of myelin-associated genes in frontal cortex of <i>SNCA</i> overexpressing rats and Parkinson&#x2019;s disease patients ↗Aging · 2020 · PMID 33017301not yet assessed
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Using Transcriptomic Analysis to Assess Double-Strand Break Repair Activity: Towards Precise in Vivo Genome Editing ↗International Journal of Molecular Sciences · 2020 · PMID 32085662not yet assessed
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A novel Ataxin-3 knock-in mouse model mimics the human SCA3 disease phenotype including neuropathological, behavioral, and transcriptional abnormalities ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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SARS-CoV-2 infection paralyzes cytotoxic and metabolic functions of the immune cells ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Genome-wide CRISPR and small-molecule screens uncover targetable dependencies in ATRT ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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The endometrial transcription landscape of MRKH syndrome ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Overexpression of human alpha-Synuclein leads to dysregulated microbiome/metabolites with ageing in a rat model of Parkinson disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Evidence for bidirectional and trans-synaptic parasympathetic and sympathetic propagation of alpha-synuclein in rats ↗Acta Neuropathologica · 2019 · PMID 31254094not yet assessed
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Blunting neuroinflammation with resolvin D1 prevents early pathology in a rat model of Parkinson’s disease ↗Nature Communications · 2019 · PMID 31477726not yet assessed
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α-Synuclein in Parkinson’s disease: causal or bystander? ↗Journal of Neural Transmission · 2019 · PMID 31240402not yet assessed
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Low mutational load in pediatric medulloblastoma still translates into neoantigens as targets for specific T-cell immunotherapy ↗Cytotherapy · 2019 · PMID 31351799not yet assessed
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LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis ↗Blood · 2019 · PMID 31366618not yet assessed
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Ubiquitin-specific protease USP36 knockdown impairs Parkin-dependent mitophagy via downregulation of Beclin-1-associated autophagy-related ATG14L ↗Experimental Cell Research · 2019 · PMID 31550441not yet assessed
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Enriched Environmental Conditions Modify the Gut Microbiome Composition and Fecal Markers of Inflammation in Parkinson’s Disease ↗Frontiers in Neuroscience · 2019 · PMID 31749671not yet assessed
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Systematic data analysis and data mining in CatWalk gait analysis by heat mapping exemplified in rodent models for neurodegenerative diseases ↗Journal of Neuroscience Methods · 2019 · PMID 31351096not yet assessed
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Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in Dystonia ↗Frontiers in Neurology · 2019 · PMID 31920950not yet assessed
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Silhouette-Length-Scaled Gait Parameters for Motor Functional Analysis in Mice and Rats ↗eNeuro · 2019 · PMID 31604813not yet assessed
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Distinct Stress Response and Altered Striatal Transcriptome in Alpha-Synuclein Overexpressing Mice ↗Frontiers in Neuroscience · 2019 · PMID 30686992not yet assessed
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not yet assessed
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Author Correction: Blunting neuroinflammation with resolvin D1 prevents early pathology in a rat model of Parkinson’s disease ↗Nature Communications · 2019 · PMID 31611555not yet assessed
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Enriched environmental conditions modify the gut microbiome composition and fecal markers of inflammation in Parkinson’s disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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PINK1 Regulates Dopamine and Lipids at Mitochondria to Maintain Synapses and Neuronal Function ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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DJ-1 (Park7) affects the gut microbiome, metabolites and development of Innate Lymphoid cells (ILCs) ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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Abstract B124: Personalized peptide vaccination based on patient-individual tumor-specific variants induces T-cell responses in pediatric patients ↗Cancer Immunology Research · 2019not yet assessed
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Blunting neuroinflammation with resolvin D1 prevents early pathology in a rat model of Parkinson's disease ↗Zenodo (CERN European Organization for Nuclear Research) · 2019not yet assessed
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Environmental Enrichment Prevents Transcriptional Disturbances Induced by Alpha-Synuclein Overexpression ↗Frontiers in Cellular Neuroscience · 2018 · PMID 29755323not yet assessed
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Treadmill exercise intervention improves gait and postural control in alpha-synuclein mouse models without inducing cerebral autophagy ↗Behavioural Brain Research · 2018 · PMID 30599154not yet assessed
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Dynamic nuclear envelope phenotype in rats overexpressing mutated human torsinA protein ↗Biology Open · 2018 · PMID 29739751not yet assessed
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Dynamic footprints of α-synucleinopathic mice recorded by CatWalk gait analysis ↗Data in Brief · 2018 · PMID 29876385not yet assessed
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Dynamic footprint based locomotion sway assessment in α-synucleinopathic mice using Fast Fourier Transform and Low Pass Filter ↗Journal of Neuroscience Methods · 2017 · PMID 29253577not yet assessed
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Mitochondrial defects and neurodegeneration in mice overexpressing wild-type or G399S mutant HtrA2 ↗Human Molecular Genetics · 2016not yet assessed
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Mitochondrial defects and neurodegeneration in mice overexpressing wild-type or G399S mutant HtrA2 ↗Human Molecular Genetics · 2015 · PMID 26604148not yet assessed
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Using enriched environment to identify critical genomic regions epigenetically altered in a Parkinson's disease mouse model ↗Basal Ganglia · 2015not yet assessed
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Overexpression of the calpain-specific inhibitor calpastatin reduces human alpha-Synuclein processing, aggregation and synaptic impairment in [A30P]αSyn transgenic mice ↗Human Molecular Genetics · 2014 · PMID 24619358not yet assessed
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Longitudinal follow-up and characterization of a robust rat model for Parkinson's disease based on overexpression of alpha-synuclein with adeno-associated viral vectors ↗Neurobiology of Aging · 2014 · PMID 25599874not yet assessed
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M06 Olesoxime Treatment Inhibits The Formation Of Mhtt Fragments Through Suppression Of Calpain Activity, And Leads To Behavioural And Neurological Improvements In The Bachd Rat ↗Journal of Neurology Neurosurgery & Psychiatry · 2014not yet assessed
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Characterization of Synphilin-1/alpha-Synuclein Double Transgenic Mice2014not yet assessed
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rAAV2/7 vector-mediated overexpression of alpha-synuclein in mouse substantia nigra induces protein aggregation and progressive dose-dependent neurodegeneration ↗Molecular Neurodegeneration · 2013 · PMID 24267638not yet assessed
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A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats ↗Brain · 2013 · PMID 23413261not yet assessed
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Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice ↗Human Molecular Genetics · 2013 · PMID 24064336not yet assessed
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Characterization of transgenic mice overexpressing wild type and G399S mutant HtrA2/Omi – Implications for PD ↗Basal Ganglia · 2013not yet assessed
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Dose-dependent therapeutic effects of FK506 on dopaminergic neurodegeneration and neuroinflammation in a viral vector-based α-synuclein rat model for Parkinson’s diseaseLirias · 2013not yet assessed
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Automated Behavioral Phenotyping Reveals Presymptomatic Alterations in a SCA3 Genetrap Mouse Model ↗Journal of genetics and genomics/Journal of Genetics and Genomics · 2012 · PMID 22749017not yet assessed
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FK506 decreases dopaminergic neurodegeneration and neuroinflammation in an optimized α-synuclein rat model for Parkinson’s disease2012not yet assessed
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Development of a robust alpha-synuclein-based rat model for Parkinson’s disease2012not yet assessed
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Therapeutic effects of FK506 in an optimized AAV-based rat model for α-synucleinopathy2011not yet assessed
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Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in mice ↗Neurogenetics · 2009 · PMID 19760259not yet assessed
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A humic acid stationary phase for the high performance liquid chromatography separation of buckminsterfullerenes: Theoretical and practical aspects ↗Analytica Chimica Acta · 2007 · PMID 17386820not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Casadei N” paper on PubMed ↗