Vincent Magrini

Career Trajectory

Research Cluster Map

Direct collaborators. Node size = influence, colour = community, dashed = past collaboration.

• 23. Paired exome analysis in Mosaic Disease yields expanded Genotype-Phenotype Associations

  Cancer Genetics · 2022-11-01

• 117. Clinical lessons learned from Translational Molecular Profiling of Cancer and Somatic Disease

  Cancer Genetics · 2022-11-01

• Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome–Based Resolution of Isoform Complexity

  Journal of Molecular Diagnostics · 2022-09-30 · 11 citations

• Author Correction: Comparative and demographic analysis of orang-utan genomes

  Nature · 2022-08-12 · 2 citations

• Leveraging gene therapy to achieve long-term continuous or controllable expression of biotherapeutics

  Science Advances · 2022-07-13 · 27 citations

• Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case‐based review

  Genes Chromosomes and Cancer · 2022-06-18 · 1 citations

• Detection of brain somatic variation in epilepsy‐associated developmental lesions

  Epilepsia · 2022-06-10 · 53 citations

• Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers

  Cancer Genetics · 2022-04-30 · 11 citations

• Expanding the Clinical Phenotype of FGFR1 Internal Tandem Duplication

  Molecular Case Studies · 2022-02-11 · 10 citations

• 26. Co-occurrence of rosette-forming glioneuronal tumors with Noonan Syndrome

  Cancer Genetics · 2022-01-01

• A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2

  Diagnostic Microbiology and Infectious Disease · 2021-12-29 · 17 citations

• Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic liversPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2021-12-16 · 1 citations

• Detection of brain somatic variation in epilepsy-associated developmental lesionsPreprint

  medRxiv · 2021-12-09 · 11 citations

• Long‐read whole genome sequencing reveals HOXD13 alterations in synpolydactyly

  Human Mutation · 2021-12-03 · 12 citations

• Discovery of clinically relevant fusions in pediatric cancer

  BMC Genomics · 2021-12-01 · 32 citations

• Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas

  Acta Neuropathologica Communications · 2021-12-01 · 24 citations

• Somatic variation as an incidental finding in the pediatric next-generation sequencing era

  Molecular Case Studies · 2021-10-29 · 5 citations

• Gastroblastoma with a novel <scp><i>EWSR1‐CTBP1</i></scp> fusion presenting in adolescence

  Genes Chromosomes and Cancer · 2021-05-27 · 31 citations

• PTEN somatic mutations contribute to spectrum of cerebral overgrowth

  Brain · 2021-04-26 · 44 citations

• Novel morphologic findings in <scp>PLAG1‐rearranged</scp> soft tissue tumors

  Genes Chromosomes and Cancer · 2021-04-24 · 20 citations