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Jonas A Gustafson

Showing results (1-10 of 20) with videos related to

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Plos One|August 24, 2019
Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse modelJonas A Gustafson, Sarah S Park, Michael L Cunningham
Arxiv|December 19, 2025
needLR: Long-read structural variant annotation with population-scale frequency estimationJonas A Gustafson, Jiadong Lin, Evan E Eichler, et al.
International Journal of Molecular Sciences|March 29, 2023
Transcriptomic Signatures of Single-Suture Craniosynostosis PhenotypesSamantha Lapehn, Jonas A Gustafson, Andrew E Timms, et al.
Bioinformatics (Oxford, England)|June 17, 2026
needLR: Long-read structural variant annotation with population-scale frequency estimationJonas A Gustafson, Jiadong Lin, Miranda P G Zalusky, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Principles and functional consequences of plasmid chromatinization in mammalian cellsBenjamin J Mallory, Thomas W Tullius, Carina G Biar, et al.
Journal of Neurosurgery. Pediatrics|June 21, 2024
AXIN1 mutations in nonsyndromic craniosynostosisAndrew T Timberlake, Kshipra Hemal, Jonas A Gustafson, et al.
Molecular Cell|May 22, 2026
Chromatin architectures underlying plasmid-based assays for regulatory variant effectsBenjamin J Mallory, Thomas W Tullius, Carina G Biar, et al.
Biorxiv : the Preprint Server for Biology|August 6, 2025
Pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamicsChaofan Zhang, Rituparna Sinha Roy, Ming Yin Lun, et al.
Annals of Clinical and Translational Neurology|February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural VariantsAndré Fienemann, Theresa Lüth, Susen Schaake, et al.
Journal of Medical Genetics|January 13, 2021
Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disordersEduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Plos One|August 24, 2019
Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse modelJonas A Gustafson, Sarah S Park, Michael L Cunningham
Arxiv|December 19, 2025
needLR: Long-read structural variant annotation with population-scale frequency estimationJonas A Gustafson, Jiadong Lin, Evan E Eichler, et al.
International Journal of Molecular Sciences|March 29, 2023
Transcriptomic Signatures of Single-Suture Craniosynostosis PhenotypesSamantha Lapehn, Jonas A Gustafson, Andrew E Timms, et al.
Bioinformatics (Oxford, England)|June 17, 2026
needLR: Long-read structural variant annotation with population-scale frequency estimationJonas A Gustafson, Jiadong Lin, Miranda P G Zalusky, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Principles and functional consequences of plasmid chromatinization in mammalian cellsBenjamin J Mallory, Thomas W Tullius, Carina G Biar, et al.
Journal of Neurosurgery. Pediatrics|June 21, 2024
AXIN1 mutations in nonsyndromic craniosynostosisAndrew T Timberlake, Kshipra Hemal, Jonas A Gustafson, et al.
Molecular Cell|May 22, 2026
Chromatin architectures underlying plasmid-based assays for regulatory variant effectsBenjamin J Mallory, Thomas W Tullius, Carina G Biar, et al.
Biorxiv : the Preprint Server for Biology|August 6, 2025
Pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamicsChaofan Zhang, Rituparna Sinha Roy, Ming Yin Lun, et al.
Annals of Clinical and Translational Neurology|February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural VariantsAndré Fienemann, Theresa Lüth, Susen Schaake, et al.
Journal of Medical Genetics|January 13, 2021
Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disordersEduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
Pageof 2