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Yoann Seeleuthner

Showing results (1-10 of 58) with videos related to

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Scientific Reports|September 25, 2021
Controlling for human population stratification in rare variant association studiesMatthieu Bouaziz, Jimmy Mullaert, Benedetta Bigio, et al.
Genetic Epidemiology|August 17, 2021
Taking population stratification into account by local permutations in rare-variant association studies on small samplesJimmy Mullaert, Matthieu Bouaziz, Yoann Seeleuthner, et al.
Bioinformatics Advances|June 25, 2026
GDIv2: improving variant selection from human exomesEstelle Talouarn, Yoann Seeleuthner, Astrid Marchal, et al.
NAR Genomics and Bioinformatics|May 28, 2021
Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencingBenedetta Bigio, Yoann Seeleuthner, Gaspard Kerner, et al.
Scientific Reports|January 28, 2017
Accessing the genomic information of unculturable oceanic picoeukaryotes by combining multiple single cellsJean-François Mangot, Ramiro Logares, Pablo Sánchez, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2019
Homozygosity for <i>TYK2</i> P1104A underlies tuberculosis in about 1% of patients in a cohort of European ancestryGaspard Kerner, Noe Ramirez-Alejo, Yoann Seeleuthner, et al.
Scientific Reports|December 1, 2016
Survey of the green picoalga Bathycoccus genomes in the global oceanThomas Vannier, Jade Leconte, Yoann Seeleuthner, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 4, 2020
Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genesAntonio Rausell, Yufei Luo, Marie Lopez, et al.
Frontiers in Immunology|November 29, 2024
Case report: A novel <i>JAK3</i> homozygous variant in a patient with severe combined immunodeficiency and persistent COVID-19Renan Cesar Sbruzzi, Mayara Jorgens Prado, Bibiana Fam, et al.
Journal of Human Immunity|May 29, 2026
STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapyNima Parvaneh, Rasol Molatefi, Conor Gruber, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Scientific Reports|September 25, 2021
Controlling for human population stratification in rare variant association studiesMatthieu Bouaziz, Jimmy Mullaert, Benedetta Bigio, et al.
Genetic Epidemiology|August 17, 2021
Taking population stratification into account by local permutations in rare-variant association studies on small samplesJimmy Mullaert, Matthieu Bouaziz, Yoann Seeleuthner, et al.
Bioinformatics Advances|June 25, 2026
GDIv2: improving variant selection from human exomesEstelle Talouarn, Yoann Seeleuthner, Astrid Marchal, et al.
NAR Genomics and Bioinformatics|May 28, 2021
Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencingBenedetta Bigio, Yoann Seeleuthner, Gaspard Kerner, et al.
Scientific Reports|January 28, 2017
Accessing the genomic information of unculturable oceanic picoeukaryotes by combining multiple single cellsJean-François Mangot, Ramiro Logares, Pablo Sánchez, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2019
Homozygosity for <i>TYK2</i> P1104A underlies tuberculosis in about 1% of patients in a cohort of European ancestryGaspard Kerner, Noe Ramirez-Alejo, Yoann Seeleuthner, et al.
Scientific Reports|December 1, 2016
Survey of the green picoalga Bathycoccus genomes in the global oceanThomas Vannier, Jade Leconte, Yoann Seeleuthner, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 4, 2020
Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genesAntonio Rausell, Yufei Luo, Marie Lopez, et al.
Frontiers in Immunology|November 29, 2024
Case report: A novel <i>JAK3</i> homozygous variant in a patient with severe combined immunodeficiency and persistent COVID-19Renan Cesar Sbruzzi, Mayara Jorgens Prado, Bibiana Fam, et al.
Journal of Human Immunity|May 29, 2026
STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapyNima Parvaneh, Rasol Molatefi, Conor Gruber, et al.
Pageof 6