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Vincent Magrini

James S. McDonnell Foundation · US
Area of research
Molecular Biology · Cancer Research
Research interest
Research interests include Cancer Genomics and Diagnostics, Genomics and Phylogenetic Studies, Acute Myeloid Leukemia Research, and RNA modifications and cancer.
h-index
56
citations
62,288
works
174
NIH funding
primary concept
email

Recent publications

Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth
Genetics in Medicine 2021cited by 59position: middledoi
Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas
Acta Neuropathologica Communications 2021cited by 24position: middledoi
Correction to: Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma
Acta Neuropathologica Communications 2020cited by 30position: middledoi
Characterizing the Major Structural Variant Alleles of the Human Genome
Cell 2019cited by 575position: middledoi
Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma
Acta Neuropathologica Communications 2019cited by 175position: middledoi
The prognostic effects of somatic mutations in ER-positive breast cancer
Nature Communications 2018cited by 140position: middledoi
Whole genome analysis of a schistosomiasis-transmitting freshwater snail
Nature Communications 2017cited by 311position: middledoi
A dendritic cell vaccine increases the breadth and diversity of melanoma neoantigen-specific T cells
Science 2015cited by 1,281position: middledoi
Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo
Cancer Cell 2015cited by 283position: middledoi
RNA Sequencing of Tumor-Associated Microglia Reveals Ccl5 as a Stromal Chemokine Critical for Neurofibromatosis-1 Glioma Growth
Neoplasia 2015cited by 97position: middledoi
Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci
PLoS Genetics 2014cited by 55position: middledoi
The Oxytricha trifallax Macronuclear Genome: A Complex Eukaryotic Genome with 16,000 Tiny Chromosomes
PLoS Biology 2013cited by 231position: middledoi
Structure, function and diversity of the healthy human microbiome
Nature 2012cited by 11,854position: middledoi
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
Nature 2012cited by 2,005position: middledoi
The Origin and Evolution of Mutations in Acute Myeloid Leukemia
Cell 2012cited by 1,564position: middledoi
De Novo Gene Disruptions in Children on the Autistic Spectrum
Neuron 2012cited by 1,513position: middledoi
Cancer exome analysis reveals a T-cell-dependent mechanism of cancer immunoediting
Nature 2012cited by 1,277position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Elaine R. Mardis · James S. McDonnell Foundation5 papers (2012–2020) · 3 papers (2015–2020)Jason Walker · 10X Genomics (United States)3 papers (2015–2020)David H. Gutmann · Lantmännen3 papers (2015–2020) · 3 papers (2015–2020)Helmut Kettenmann · Shenzhen University2 papers (2019–2020)Daniel Pérez-Hernández · Max Delbrück Center2 papers (2019–2020)Zhihong Chen · Chinese Academy of Medical Sciences & Peking Union Medical College2 papers (2019–2020)Sean McGrath · Royal Marsden Hospital2 papers (2015–2019)Ramón Vidal · Max Delbrück Center2 papers (2019–2020)Philipp Mertins · Abterra Biosciences (United States)2 papers (2019–2020)Malachi Griffith · Alvin J. Siteman Cancer Center2 papers (2015–2015)Marcus Semtner · Max Delbrück Center2 papers (2019–2020)Jasreet Hundal · Washington University in St. Louis2 papers (2012–2015)Todd Wylie · Washington University in St. Louis2 papers (2012–2015)Sascha Sauer · Max Delbrück Center2 papers (2019–2020)Verena Haage · University of California, Berkeley2 papers (2019–2020)Dolores Hambardzumyan · Cancer Institute (WIA)2 papers (2019–2020) · 1 papers (2021–2021) · 1 papers (2015–2015)