Catharina Larsson

Research interests

Publications

• Mechanisms underlying the activation of TERT transcription and telomerase activity in human cancer: old actors and new players

  Oncogene · 2019 · https://doi.org/10.1038/s41388-019-0872-9

• Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention

  JAMA Oncology · 2017 · https://doi.org/10.1001/jamaoncol.2017.0223

• Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

  Human Molecular Genetics · 2015 · https://doi.org/10.1093/hmg/ddu749

• Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma

  The Journal of Clinical Endocrinology & Metabolism · 2014 · https://doi.org/10.1210/jc.2014-3282

• The age- and shorter telomere-dependent TERT promoter mutation in follicular thyroid cell-derived carcinomas

  Oncogene · 2013 · https://doi.org/10.1038/onc.2013.446

• The role of microRNA deregulation in the pathogenesis of adrenocortical carcinoma

  Endocrine Related Cancer · 2011 · https://doi.org/10.1530/erc-11-0082

• MicroRNA Expression Profiles Associated with Mutational Status and Survival in Malignant Melanoma

  Journal of Investigative Dermatology · 2010 · https://doi.org/10.1038/jid.2010.63

• LUMA (LUminometric Methylation Assay)—A high throughput method to the analysis of genomic DNA methylation

  Experimental Cell Research · 2006 · https://doi.org/10.1016/j.yexcr.2006.03.006

• Involvement of the PAX8/Peroxisome Proliferator-Activated Receptor γ Rearrangement in Follicular Thyroid Tumors

  The Journal of Clinical Endocrinology & Metabolism · 2003 · https://doi.org/10.1210/jc.2002-021690

• Somatic and Germ-Line Mutations of the HRPT2 Gene in Sporadic Parathyroid Carcinoma

  New England Journal of Medicine · 2003 · https://doi.org/10.1056/nejmoa031237

• HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

  Nature Genetics · 2002 · https://doi.org/10.1038/ng1048

• Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

  Nature Genetics · 2001 · https://doi.org/10.1038/90058

• Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays

  Nature Biotechnology · 2000 · https://doi.org/10.1038/79269

• Thymic Carcinoids in Multiple Endocrine Neoplasia Type 1

  Annals of Surgery · 1998 · https://doi.org/10.1097/00000658-199807000-00015

• Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors.

  PubMed · 1997

• Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains.

  The Journal of Clinical Endocrinology & Metabolism · 1996 · https://doi.org/10.1210/jcem.81.4.8636323

• BRCA2 mutations in primary breast and ovarian cancers

  Nature Genetics · 1996 · https://doi.org/10.1038/ng0696-238

• Mutation analysis of the BRCA2 gene in 49 site–specific breast cancer families

  Nature Genetics · 1996 · https://doi.org/10.1038/ng0596-120

• Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1.

  The Journal of Clinical Endocrinology & Metabolism · 1992 · https://doi.org/10.1210/jcem.75.1.1352309

• Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.

  Proceedings of the National Academy of Sciences · 1990 · https://doi.org/10.1073/pnas.87.5.1968

• Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

  Nature · 1988 · https://doi.org/10.1038/332085a0

Current projects

No projects listed.