Tommy Martinsson

Research interests

Publications

• Sense-Antisense lncRNA Pair Encoded by Locus 6p22.3 Determines Neuroblastoma Susceptibility via the USP36-CHD7-SOX9 Regulatory Axis

  Cancer Cell · 2018 · https://doi.org/10.1016/j.ccell.2018.01.020

• Emergence of New ALK Mutations at Relapse of Neuroblastoma

  Journal of Clinical Oncology · 2014 · https://doi.org/10.1200/jco.2013.54.0674

• The Risk-Associated Long Noncoding RNA NBAT-1 Controls Neuroblastoma Progression by Regulating Cell Proliferation and Neuronal Differentiation

  Cancer Cell · 2014 · https://doi.org/10.1016/j.ccell.2014.09.014

• Anaplastic Lymphoma Kinase (ALK) regulates initiation of transcription of MYCN in neuroblastoma cells

  Oncogene · 2012 · https://doi.org/10.1038/onc.2012.12

• Meta-analysis of Neuroblastomas Reveals a Skewed ALK Mutation Spectrum in Tumors with MYCN Amplification

  Clinical Cancer Research · 2010 · https://doi.org/10.1158/1078-0432.ccr-09-2660

• High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset

  Proceedings of the National Academy of Sciences · 2010 · https://doi.org/10.1073/pnas.0910684107

• High incidence of DNA mutations and gene amplifications of the ALK gene in advanced sporadic neuroblastoma tumours

  Biochemical Journal · 2008 · https://doi.org/10.1042/bj20081834

• Age at onset and different types of psoriasis

  British Journal of Dermatology · 2006 · https://doi.org/10.1111/j.1365-2133.1995.tb02753.x

• Quality Assessment of Genetic Markers Used for Therapy Stratification

  Journal of Clinical Oncology · 2003 · https://doi.org/10.1200/jco.2003.03.025

• Essential fatty acid deficiency in relation to genotype in patients with cystic fibrosis

  The Journal of Pediatrics · 2001 · https://doi.org/10.1067/mpd.2001.118890

• RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

  Oncogene · 2001 · https://doi.org/10.1038/sj.onc.1204968

• Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene mutations

  Gastroenterology · 2001 · https://doi.org/10.1053/gast.2001.28707

• Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene

  Proceedings of the National Academy of Sciences · 2000 · https://doi.org/10.1073/pnas.250289597

• Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)

  Human Mutation · 2000 · https://doi.org/10.1002/1098-1004(200011)16:5<386::aid-humu2>3.0.co;2-y

• The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders

  Tissue Antigens · 2000 · https://doi.org/10.1034/j.1399-0039.2000.560407.x

• Psoriasis susceptibility locus in chromosome region 3q21 identified in patients from southwest Sweden

  European Journal of Human Genetics · 1999 · https://doi.org/10.1038/sj.ejhg.5200365

• Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms.

  PubMed · 1995

• A population genetic study of psoriasis

  British Journal of Dermatology · 1994 · https://doi.org/10.1111/j.1365-2133.1994.tb08454.x

• Neuroblastoma consensus deletion maps to 1p36.1–2

  Genes Chromosomes and Cancer · 1989 · https://doi.org/10.1002/gcc.2870010209

Current projects

No projects listed.