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Maria Johansson-Soller

Showing results (1-10 of 29) with videos related to

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Genes|September 28, 2024
Pregnancy Planning and Genetic Testing: Exploring Advantages, and ChallengesUlf Kristoffersson, Maria Johansson-Soller
Journal of Community Genetics|December 13, 2025
Midwives 'views of parents' questions and expectations on prenatal genetic testing - identifying informational needs in prenatal genetic counsellingLisa Åkerman, Maria Johansson Soller, Charlotta Ingvoldstad Malmgren
Journal of Community Genetics|January 15, 2026
Preparedness for working with genomic medicine among Swedish non-genetics physicians - a nation-wide survey studyJoar Björk, Mikaela Friedman, Amy Nisselle, et al.
Journal of Community Genetics|July 18, 2025
Self-assessed knowledge of genomic medicine among non-genetics physicians - results from a nationwide Swedish surveyJoar Björk, Mikaela Friedman, Amy Nisselle, et al.
Genes, Chromosomes & Cancer|April 1, 2006
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancerMaria Johansson Soller, Margareth Isaksson, Peter Elfving, et al.
Cancer Genetics and Cytogenetics|February 8, 2007
Cytogenetic findings in pediatric renal cell carcinomaMaria Johansson Soller, Carl-Magnus Kullendorff, Albert N Békássy, et al.
Lakartidningen|May 11, 2021
[The utility of whole genome sequencing in rare disease diagnostics]Maria Johansson Soller, Ann Nordgren, Hans Ehrencrona, et al.
Scientific Reports|December 5, 2024
Multi-omics analysis detail a submicroscopic inv(15)(q14q15) generating fusion transcripts and MEIS2 and NUSAP1 haploinsufficiencyMarlene Ek, Malin Kvarnung, Maria Pettersson, et al.
Scientific Reports|April 27, 2023
The cost-effectiveness of whole genome sequencing in neurodevelopmental disordersHannes Runheim, Maria Pettersson, Anna Hammarsjö, et al.
British Journal of Cancer|November 5, 2025
Risk of malignant melanoma and colorectal cancer in Birt-Hogg-Dubé syndrome - a matched cohort studyAnna Skarin Nordenvall, Fredrik Persson, Anna Martling, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Genes|September 28, 2024
Pregnancy Planning and Genetic Testing: Exploring Advantages, and ChallengesUlf Kristoffersson, Maria Johansson-Soller
Journal of Community Genetics|December 13, 2025
Midwives 'views of parents' questions and expectations on prenatal genetic testing - identifying informational needs in prenatal genetic counsellingLisa Åkerman, Maria Johansson Soller, Charlotta Ingvoldstad Malmgren
Journal of Community Genetics|January 15, 2026
Preparedness for working with genomic medicine among Swedish non-genetics physicians - a nation-wide survey studyJoar Björk, Mikaela Friedman, Amy Nisselle, et al.
Journal of Community Genetics|July 18, 2025
Self-assessed knowledge of genomic medicine among non-genetics physicians - results from a nationwide Swedish surveyJoar Björk, Mikaela Friedman, Amy Nisselle, et al.
Genes, Chromosomes & Cancer|April 1, 2006
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancerMaria Johansson Soller, Margareth Isaksson, Peter Elfving, et al.
Cancer Genetics and Cytogenetics|February 8, 2007
Cytogenetic findings in pediatric renal cell carcinomaMaria Johansson Soller, Carl-Magnus Kullendorff, Albert N Békássy, et al.
Lakartidningen|May 11, 2021
[The utility of whole genome sequencing in rare disease diagnostics]Maria Johansson Soller, Ann Nordgren, Hans Ehrencrona, et al.
Scientific Reports|December 5, 2024
Multi-omics analysis detail a submicroscopic inv(15)(q14q15) generating fusion transcripts and MEIS2 and NUSAP1 haploinsufficiencyMarlene Ek, Malin Kvarnung, Maria Pettersson, et al.
Scientific Reports|April 27, 2023
The cost-effectiveness of whole genome sequencing in neurodevelopmental disordersHannes Runheim, Maria Pettersson, Anna Hammarsjö, et al.
British Journal of Cancer|November 5, 2025
Risk of malignant melanoma and colorectal cancer in Birt-Hogg-Dubé syndrome - a matched cohort studyAnna Skarin Nordenvall, Fredrik Persson, Anna Martling, et al.
Pageof 3