Catharina Larsson

Overview

Best Publications

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

  Catharina Larsson;Britt Skogseid;Kjell Öberg;Yusuke Nakamura

  1248
  Citations

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

  Johannes N. Spelbrink;Fang Yuan Li;Valeria Tiranti;Kaisu Nikali

  988
  Citations

• Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene. The European Consortium on MEN1

  Irma Lemmens;Wim J. M. Van de Ven;Koen Kas;Chang X. Zhang

  809
  Citations

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

  J.D. Carpten;C.M. Robbins;A. Villablanca;L. Forsberg

  788
  Citations

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

  Trisha M. Shattuck;Stiina Välimäki;Takao Obara;Randall D. Gaz

  577
  Citations

• BRCA2 mutations in primary breast and ovarian cancers

  Johnathan M. Lancaster;Richard Wooster;Jonathon Mangion;Catherine M. Phelan;Catherine M. Phelan;Catherine M. Phelan

  448
  Citations

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

  Kerstin Lindblad-Toh;David M. Tanenbaum;Mark J. Daly;Ellen Winchester

  419
  Citations

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

  Camilla Bystrom;Catharina Larsson;Carl Blomberg;Kerstin Sandelin

  389
  Citations

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

  Xiaotian Yuan;Xiaotian Yuan;Catharina Larsson;Dawei Xu

  384
  Citations

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

  Patricia L M Dahia;Debbie J. Marsh;Zimu Zheng;Jan Zedenius

  358
  Citations

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

  John W. Kunstman;C. Christofer Juhlin;Gerald Goh;Taylor C. Brown

  349
  Citations

• LUMA (LUminometric Methylation Assay)--a high throughput method to the analysis of genomic DNA methylation.

  Mohsen Karimi;Sofia Johansson;Dirk Stach;Martin Corcoran

  336
  Citations

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

  C M Phelan;J M Lancaster;P Tonin;C Gumbs

  327
  Citations

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

  Stefano Caramuta;Suzanne Egyházi;Monica Rodolfo;Daniela Witten

  286
  Citations

• Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

  Catherine M. Phelan;Catherine M. Phelan;Timothy R. Rebbeck;Barbara L. Weber;Peter Devilee

  279
  Citations

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

  T Liu;N Wang;J Cao;A Sofiadis

  271
  Citations

• Genetic Aberrations in Adrenocortical Tumors Detected Using Comparative Genomic Hybridization Correlate with Tumor Size and Malignancy

  Magnus Kjellman;Olli-P. Kallioniemi;Ritva Karhu;Anders Höög

  268
  Citations

• Involvement of the PAX8/peroxisome proliferator-activated receptor γ rearrangement in follicular thyroid tumors

  Trisha Dwight;Srinivasan R. Thoppe;Theodoros Foukakis;Weng O. Lui

  265
  Citations

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

  Hunter Heath;Shannon Odelberg;Charles E. Jackson;Bin Tean Teh

  264
  Citations

• Thymic carcinoids in multiple endocrine neoplasia type 1

  Bin Tean Teh;Jan Zedenius;Soili Kytölä;Britt Skogseid

  262
  Citations