Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Johansson

Showing results (81-90 of 99) with videos related to

Pageof 10
Sort By:
Human Mutation|April 10, 2013
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnosticsBirgit Sikkema-Raddatz, Lennart F Johansson, Eddy N de Boer, et al.
NAR Genomics and Bioinformatics|February 13, 2026
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflowWillem T K Maassen, Charlotte C E T Pape, Carlos G Urzua-Traslavina, et al.
Clinical Chemistry|May 26, 2018
Genetic Screening Test to Detect Translocations in Acute Leukemias by Use of Targeted Locus AmplificationMohamed Z Alimohamed, Lennart F Johansson, Eddy N de Boer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 28, 2007
Multicentre European study of thalamic stimulation for parkinsonian tremor: a 6 year follow-upM I Hariz, P Krack, F Alesch, et al.
Scientific Reports|May 14, 2017
Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal TestingL F Johansson, E N de Boer, H A de Weerd, et al.
International Journal of Cardiology|March 4, 2021
Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patientsMohamed Z Alimohamed, Lennart F Johansson, Anna Posafalvi, et al.
NAR Genomics and Bioinformatics|June 30, 2025
MOLGENIS VIP: an end-to-end DNA variant interpretation pipeline for research and diagnostics configurable to support rapid implementation of new methodsWillem T K Maassen, Lennart F Johansson, Bart Charbon, et al.
Targeted Oncology|February 19, 2021
Clinical Value of EGFR Copy Number Gain Determined by Amplicon-Based Targeted Next Generation Sequencing in Patients with EGFR-Mutated NSCLCJiacong Wei, Pei Meng, Miente Martijn Terpstra, et al.
The Lancet Regional Health. Europe|June 26, 2023
Vaccine-induced correlate of protection against fatal COVID-19 in older and frail adults during waves of neutralization-resistant variants of concern: an observational studyLinnea Vikström, Peter Fjällström, Yong-Dae Gwon, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|March 30, 2023
At-home sampling to meet geographical challenges for serological assessment of SARS-CoV-2 exposure in a rural region of northern Sweden, March to May 2021: a retrospective cohort studyJulia Wigren Byström, Linnea Vikström, Ebba Rosendal, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Human Mutation|April 10, 2013
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnosticsBirgit Sikkema-Raddatz, Lennart F Johansson, Eddy N de Boer, et al.
NAR Genomics and Bioinformatics|February 13, 2026
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflowWillem T K Maassen, Charlotte C E T Pape, Carlos G Urzua-Traslavina, et al.
Clinical Chemistry|May 26, 2018
Genetic Screening Test to Detect Translocations in Acute Leukemias by Use of Targeted Locus AmplificationMohamed Z Alimohamed, Lennart F Johansson, Eddy N de Boer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 28, 2007
Multicentre European study of thalamic stimulation for parkinsonian tremor: a 6 year follow-upM I Hariz, P Krack, F Alesch, et al.
Scientific Reports|May 14, 2017
Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal TestingL F Johansson, E N de Boer, H A de Weerd, et al.
International Journal of Cardiology|March 4, 2021
Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patientsMohamed Z Alimohamed, Lennart F Johansson, Anna Posafalvi, et al.
NAR Genomics and Bioinformatics|June 30, 2025
MOLGENIS VIP: an end-to-end DNA variant interpretation pipeline for research and diagnostics configurable to support rapid implementation of new methodsWillem T K Maassen, Lennart F Johansson, Bart Charbon, et al.
Targeted Oncology|February 19, 2021
Clinical Value of EGFR Copy Number Gain Determined by Amplicon-Based Targeted Next Generation Sequencing in Patients with EGFR-Mutated NSCLCJiacong Wei, Pei Meng, Miente Martijn Terpstra, et al.
The Lancet Regional Health. Europe|June 26, 2023
Vaccine-induced correlate of protection against fatal COVID-19 in older and frail adults during waves of neutralization-resistant variants of concern: an observational studyLinnea Vikström, Peter Fjällström, Yong-Dae Gwon, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|March 30, 2023
At-home sampling to meet geographical challenges for serological assessment of SARS-CoV-2 exposure in a rural region of northern Sweden, March to May 2021: a retrospective cohort studyJulia Wigren Byström, Linnea Vikström, Ebba Rosendal, et al.
Pageof 10