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Infectious Agents and Cancer|August 3, 2022
Incidence of oncogenic HPV and HPV-related dysplasia five years after a negative HPV test by self-sampling in elderly womenRuth S Hermansson, Matts Olovsson, Inger Gustavsson, et al.
Virology Journal|October 8, 2020
Temporal changes in the vaginal microbiota in self-samples and its association with persistent HPV16 infection and CIN2Malin Berggrund, Inger Gustavsson, Riina Aarnio, et al.
BMC Infectious Diseases|February 4, 2014
Increased alpha-9 human papillomavirus species viral load in human immunodeficiency virus positive womenZizipho Z A Mbulawa, Leigh F Johnson, Dianne J Marais, et al.
British Journal of Cancer|February 14, 2018
Randomised study shows that repeated self-sampling and HPV test has more than two-fold higher detection rate of women with CIN2+ histology than Pap smear cytologyInger Gustavsson, Riina Aarnio, Malin Berggrund, et al.
Nature Communications|February 3, 2022
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generationsIda Höijer, Anastasia Emmanouilidou, Rebecka Östlund, et al.
American Journal of Hematology|June 8, 2012
Next generation RNA-sequencing in prognostic subsets of chronic lymphocytic leukemiaLarry Mansouri, Rebeqa Gunnarsson, Lesley-Ann Sutton, et al.
Plos One|November 10, 2020
Acceptability of self- collection for human papillomavirus detection in the Eastern Cape, South AfricaOngeziwe Taku, Tracy L Meiring, Inger Gustavsson, et al.
Genetics Research|September 15, 2015
Determination of obesity associated gene variants related to TMEM18 through ultra-deep targeted re-sequencing in a case-control cohort for pediatric obesityMathias Rask-Andersen, Markus Sällman Almén, Josefin A Jacobsson, et al.
Virology Journal|August 24, 2019
Clinical validation of the HPVIR high-risk HPV test on cervical samples according to the international guidelines for human papillomavirus DNA test requirements for cervical cancer screeningInger Gustavsson, Riina Aarnio, Mattias Myrnäs, et al.
Genes|October 12, 2018
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing DataAdam Ameur, Huiwen Che, Marcel Martin, et al.
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