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Endocrine-Related Cancer|June 12, 2024
Genetic variants and down-regulation of CACNA1H in pheochromocytomaFredrika Svahn, Karolina Solhusløkk Höse, Adam Stenman, et al.
Clinical Epigenetics|July 10, 2020
The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instabilityHolly Russell, Katarzyna Kedzierska, Daniel D Buchanan, et al.
NPJ Precision Oncology|February 26, 2026
Novel activating SNRNP70-ALK fusion in congenital infant-type hemispheric glioma displays clinical response to lorlatinib: a case-reportCecilia Arthur, Kleopatra Georgantzi, Teresita Díaz de Ståhl, et al.
Cancers|January 21, 2022
Whole-Body MRI Surveillance-Baseline Findings in the Swedish Multicentre Hereditary TP53-Related Cancer Syndrome Study (SWEP53)Meis Omran, Emma Tham, Yvonne Brandberg, et al.
BMJ Open|November 10, 2025
Mesalamine for Colorectal Cancer Prevention Programme in Lynch syndrome (MesaCAPP): a multicentre, multinational, randomised, two-arm, double-blind, phase II clinical study with mesalamine or placebo in carriers with Lynch syndrome - a study protocolAnn-Sofie Backman, Alexander Frank, Lars Joachim Lindberg, et al.
BMC Cancer|August 10, 2023
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancerAnna Öfverholm, Therese Törngren, Anna Rosén, et al.
European Journal of Human Genetics : EJHG|May 14, 2015
A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9Emma Tham, Erik A Eklund, Anna Hammarsjö, et al.
Molecular Aspects of Medicine|June 13, 2019
Circulating biomarkers for early detection and clinical management of colorectal cancerMaría Marcuello, Veronika Vymetalkova, Rui P L Neves, et al.
Frontiers in Oncology|June 19, 2023
Whole-genome informed circulating tumor DNA analysis by multiplex digital PCR for disease monitoring in B-cell lymphomas: a proof-of-concept studyZahra Haider, Tove Wästerlid, Linn Deleskog Spångberg, et al.
Plos One|March 18, 2025
A Swedish genome-wide haplotype association analysis identifies novel candidate loci associated with endometrial cancer riskElin Barnekow, Wen Liu, Emil Andersson, et al.
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