Ilari Scheinin

Helsinki, Finland

Last Updated: 09/26/2026

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Found 9 publications

Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing.

Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing.

Journal: Lung

Published: June 14, 2015

Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours.

Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours.

Journal: Neuropathology and applied neurobiology

Published: December 15, 2014

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.

Journal: Genome research

Published: September 20, 2014

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas.

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas.

Journal: Genome biology

Published: July 11, 2014

Erratum to: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH result.

Erratum to: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH result.

Journal: BMC medical genetics

Published: January 01, 2014

Clinical value of chromosome arms 19q and 11p losses in low-grade gliomas.

Clinical value of chromosome arms 19q and 11p losses in low-grade gliomas.

Journal: Neuro-oncology

Published: December 17, 2013

Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias.

Copy number alterations and neoplasia-specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias.

Journal: Genes, chromosomes & cancer

Published: October 14, 2013

Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations.

Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations.

Journal: Genomics

Published: September 25, 2012

Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study.

Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study.

Journal: Cancer genetics

Published: June 28, 2012

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Last Updated: 09/26/2026