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Mervi Aavikko

Showing results (11-20 of 38) with videos related to

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Blood|March 5, 2013
Primary mediastinal large B-cell lymphoma segregating in a family: exome sequencing identifies MLL as a candidate predisposition geneSilva Saarinen, Eevi Kaasinen, Marja-Liisa Karjalainen-Lindsberg, et al.
Molecular Oncology|August 21, 2012
Accumulation of genomic alterations in 2p16, 9q33.1 and 19p13 in lung tumours of asbestos-exposed patientsPenny Nymark, Mervi Aavikko, Jussi Mäkilä, et al.
European Journal of Medical Genetics|August 1, 2014
Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndromeEevi Kaasinen, Elisa Rahikkala, Peppi Koivunen, et al.
Familial Cancer|May 2, 2015
3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivityJohanna Kondelin, Sari Tuupanen, Alexandra E Gylfe, et al.
Plos One|February 1, 2013
Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcomaEevi Kaasinen, Mervi Aavikko, Pia Vahteristo, et al.
Open Forum Infectious Diseases|October 30, 2019
Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome SequencingSanni J Rinne, Lauri J Sipilä, Päivi Sulo, et al.
Nature Communications|June 20, 2026
PGS Browser: a public platform for personalized polygenic score analysis and interpretationNikita Kolosov, Mary P Reeve, Pietro Della Briotta Parolo, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2016
Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkersMiika Mehine, Eevi Kaasinen, Hanna-Riikka Heinonen, et al.
Cell Host & Microbe|December 20, 2011
KSHV-initiated notch activation leads to membrane-type-1 matrix metalloproteinase-dependent lymphatic endothelial-to-mesenchymal transitionFang Cheng, Pirita Pekkonen, Simonas Laurinavicius, et al.
American Journal of Human Genetics|September 11, 2012
Loss of SUFU function in familial multiple meningiomaMervi Aavikko, Song-Ping Li, Silva Saarinen, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Blood|March 5, 2013
Primary mediastinal large B-cell lymphoma segregating in a family: exome sequencing identifies MLL as a candidate predisposition geneSilva Saarinen, Eevi Kaasinen, Marja-Liisa Karjalainen-Lindsberg, et al.
Molecular Oncology|August 21, 2012
Accumulation of genomic alterations in 2p16, 9q33.1 and 19p13 in lung tumours of asbestos-exposed patientsPenny Nymark, Mervi Aavikko, Jussi Mäkilä, et al.
European Journal of Medical Genetics|August 1, 2014
Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndromeEevi Kaasinen, Elisa Rahikkala, Peppi Koivunen, et al.
Familial Cancer|May 2, 2015
3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivityJohanna Kondelin, Sari Tuupanen, Alexandra E Gylfe, et al.
Plos One|February 1, 2013
Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcomaEevi Kaasinen, Mervi Aavikko, Pia Vahteristo, et al.
Open Forum Infectious Diseases|October 30, 2019
Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome SequencingSanni J Rinne, Lauri J Sipilä, Päivi Sulo, et al.
Nature Communications|June 20, 2026
PGS Browser: a public platform for personalized polygenic score analysis and interpretationNikita Kolosov, Mary P Reeve, Pietro Della Briotta Parolo, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2016
Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkersMiika Mehine, Eevi Kaasinen, Hanna-Riikka Heinonen, et al.
Cell Host & Microbe|December 20, 2011
KSHV-initiated notch activation leads to membrane-type-1 matrix metalloproteinase-dependent lymphatic endothelial-to-mesenchymal transitionFang Cheng, Pirita Pekkonen, Simonas Laurinavicius, et al.
American Journal of Human Genetics|September 11, 2012
Loss of SUFU function in familial multiple meningiomaMervi Aavikko, Song-Ping Li, Silva Saarinen, et al.
Pageof 4