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Anna-Maija Sulonen

Showing results (1-10 of 7) with videos related to

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Journal of Neuroimmunology|November 21, 2008
No evidence for shared etiology in two demyelinative disorders, MS and PLOSLAnna-Maija Sulonen, Suvi P Kallio, Pekka Ellonen, et al.
Genome Biology|September 30, 2011
Comparison of solution-based exome capture methods for next generation sequencingAnna-Maija Sulonen, Pekka Ellonen, Henrikki Almusa, et al.
Scientific Reports|February 21, 2024
Haplotype information of large neuromuscular disease genes provided by linked-read sequencing has a potential to increase diagnostic yieldJohanna Lehtonen, Anna-Maija Sulonen, Henrikki Almusa, et al.
Human Molecular Genetics|May 22, 2025
Genome sequencing reveals CCDC88A variants in malformations of cortical development and immune dysfunctionJohanna Lehtonen, Anna H Hakonen, Antti Hassinen, et al.
Plos One|February 14, 2008
mtDNA nt13708A variant increases the risk of multiple sclerosisXinhua Yu, Dirk Koczan, Anna-Maija Sulonen, et al.
American Journal of Human Genetics|February 18, 2010
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 geneEveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, et al.
Nature|August 12, 2011
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis, , Stephen Sawcer, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Neuroimmunology|November 21, 2008
No evidence for shared etiology in two demyelinative disorders, MS and PLOSLAnna-Maija Sulonen, Suvi P Kallio, Pekka Ellonen, et al.
Genome Biology|September 30, 2011
Comparison of solution-based exome capture methods for next generation sequencingAnna-Maija Sulonen, Pekka Ellonen, Henrikki Almusa, et al.
Scientific Reports|February 21, 2024
Haplotype information of large neuromuscular disease genes provided by linked-read sequencing has a potential to increase diagnostic yieldJohanna Lehtonen, Anna-Maija Sulonen, Henrikki Almusa, et al.
Human Molecular Genetics|May 22, 2025
Genome sequencing reveals CCDC88A variants in malformations of cortical development and immune dysfunctionJohanna Lehtonen, Anna H Hakonen, Antti Hassinen, et al.
Plos One|February 14, 2008
mtDNA nt13708A variant increases the risk of multiple sclerosisXinhua Yu, Dirk Koczan, Anna-Maija Sulonen, et al.
American Journal of Human Genetics|February 18, 2010
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 geneEveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, et al.
Nature|August 12, 2011
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis, , Stephen Sawcer, et al.
Pageof 1