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British Journal of Haematology|September 10, 2011
Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocolsMette K Andersen, Kirsi Autio, Gisela Barbany, et al.
The Journal of Biological Chemistry|January 22, 2003
Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactionsIrina Golovleva, Sanjoy Bhattacharya, Zhiping Wu, et al.
British Journal of Haematology|February 5, 2008
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survivalErik Forestier, Mats Heyman, Mette K Andersen, et al.
Haematologica|May 7, 2013
High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocolsKajsa Paulsson, Erik Forestier, Mette K Andersen, et al.
Genes, Chromosomes & Cancer|June 17, 2009
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcomeKristina Karrman, Erik Forestier, Mats Heyman, et al.
Genes, Chromosomes & Cancer|November 9, 2007
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literatureErik Forestier, Fredrika Gauffin, Mette K Andersen, et al.
Human Mutation|August 7, 2018
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsiaNicole Weisschuh, Katarina Stingl, Isabelle Audo, et al.
Frontiers in Medicine|April 11, 2022
A Study Protocol for Validation and Implementation of Whole-Genome and -Transcriptome Sequencing as a Comprehensive Precision Diagnostic Test in Acute LeukemiasEva Berglund, Gisela Barbany, Christina Orsmark-Pietras, et al.
Molecular Therapy. Nucleic Acids|January 15, 2026
Using RNA-targeting CRISPR-Cas13 and engineered U1 systems to target ABCA4 splice variants in Stargardt diseaseRoxanne Hsiang-Chi Liou, Daniel Urrutia-Cabrera, Chia-Fei Liu, et al.
Human Mutation|August 16, 2013
Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlationsDonna S Mackay, Arundhati Dev Borman, Ruifang Sui, et al.
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