Eva Berglund

Fioretos T, Wirta V, Cavelier L, Berglund E, Friedman M, Akhras M, Botling J, Ehrencrona H, Engstrand L, Helenius G, Fagerqvist T, Gisselsson D, Gruvberger-Saal S, Gyllensten U, Heidenblad M, Höglund K, Jacobsson B, Johansson M, Johansson Å, Soller MJ, Landström M, Larsson P, Levin LÅ, Lindstrand A, Lovmar L, Lyander A, Melin M, Nordgren A, Nordmark G, Mölling P, Palmqvist L, Palmqvist R, Repsilber D, Sikora P, Stenmark B, Söderkvist P, Stranneheim H, Strid T, Wheelock CE, Wadelius M, Wedell A, Edsjö A, Rosenquist R. (2022) Implementing precision medicine in a regionally organized healthcare system in Sweden. Nat Med. 2022 Oct;28(10):1980-1982

Berglund E.C., Barbany G, Orsmark-Pietras C., Fogelstrand L., Abrahamsson J., Golovleva I., Hallböök H., Höglund M., Lazarevic V., Levin L-Å., Nordlund J., Norèn-Nyström U., Palle J., Thangavelu T., Palmqvist L., Wirta V, Cavelier L., Fioretos T., Rosenquist R. (2022). A study protocol for validation and implementation of whole-genome and -transcriptome sequencing as a comprehensive precision diagnostic test in acute leukemias. Front Med. Mar 24;9:842507

Lindqvist C.M., Lundmark A., Nordlund J., Freyhult E., Ekman D., Carlsson Almlöf J., Raine A., Övernäs E., Abrahamsson J., Frost B.M., Grandér D., Heyman M., Palle J., Forestier E., Lönnerholm G., Berglund E.C., Syvänen A.C. (2016). Deep targeted sequencing in pediatric acute lymphoblastic leukemia unveils distinct mutational patterns between genetic subtypes and novel relapse-associated genes. Oncotarget 7(39):64071-64088

Lindqvist C.M., Nordlund J., Ekman D., Johansson A., Moghadam B.T., Raine A., Övernäs E., Dahlberg J., Wahlberg P., Henriksson N., Abrahamsson J., Frost B.M., Grandér D., Heyman M., Larsson R., Palle J., Söderhäll S., Forestier E., Lönnerholm G., Syvänen A-C., Berglund E.C. (2015). The mutational landscape in pediatric acute lymphoblastic leukemia deciphered by whole genome sequencing. Human Mutation 36(1):118-28

Berglund E.C., Lindqvist C.M., Hayat S., Overnas E., Henriksson N., Nordlund J., Wahlberg P., Forestier E., Lonnerholm G., Syvanen A-C. (2013). Accurate detection of subclonal single nucleotide variants in whole genome amplified and pooled cancer samples using HaloPlex target enrichment. BMC Genomics 14:856

Berglund E.C., Kiialainen A., Syvänen A-C. (2011). Next generation sequencing technologies and applications for human genetic history and forensics. Investig Genet. 242 (1): 23

Berglund E.C., Ehrenborg C., Vinnere Pettersson O., Granberg F., Näslund K., Holmberg M., Andersson S.G.E. (2010). Genome dynamics of Bartonella grahamii in micropopulations of woodland rodents. BMC genomics 11:152

Berglund E.C., Ellegaard K., Granberg F., Xie Z., Kosoy M.Y., Birtles R., Andersson S.G.E. (2010). Rapid diversification by recombination in Bartonella grahamii from wild rodents in Asia contrasts with low levels of genomic divergence in Northern Europe and America. Molecular Ecology 19(11)

Berglund E.C., Frank A.C., Calteau A., Vinnere Pettersson O., Granberg F., Eriksson A-S., Näslund K., Holmberg M., Lindroos H., Andersson S.G.E. (2009). Run-off Replication of Host-adaptability Genes is Associated with Gene Transfer Agents in the Genome of Mouse-Infecting Bartonella grahamii. PLoS Genetics 5:e1000546

Berglund E.C., Nystedt B., Andersson S.G.E. (2009). Computational Resources in Infectious Disease: Limitations and Challenges. PLoS Comput Biol 5:e1000481