Jonas A Gustafson (Jonas Gustafson)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 8

Top Topics

Top Venues

International journal of molecular sciences

medRxiv : the preprint server for health sciences

Case reports in genetics

Proceedings of the National Academy of Sciences of the United States of America

This page only lists publications with an associated author ORCID identifier.

Publications

Jonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, Miranda Perez-Galey Zalusky, Kendra Hoekzema, David Twesigomwe, Lei Yang, Anthony A Snead, Phillip Andrew Richmond, Wouter De Coster, Nathan D Olson, Andrea Guarracino, Qiuhui Li, Angela L Miller, Joy Goffena, Zachery Anderson, Sophie Hr Storz, Sydney A Ward, Maisha Sinha, Claudia Gonzaga-Jauregui, Wayne E Clarke, Anna O Basile, André Corvelo, Catherine E Reeves, Adrienne Helland, Rajeeva Lochan Musunuri, Mahler Revsine, Karynne E Patterson, Cate Paschal, Christina Zakarian, Sara Goodwin, Tanner D Jensen, Esther Robb, null null, null null, null null, W Richard McCombie, Fritz J Sedlazeck, Justin M Zook, Stephen B Montgomery, Erik P Garrison, Mikhail Kolmogorov, Michael C Schatz, Richard N McLaughlin, Harriet Dashnow, Michael C Zody, Matthew William Loose, Miten Jain, Evan E Eichler, Danny E Miller
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation. medRxiv : the preprint server for health sciences (2024)
Jonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, Miranda Perez-Galey Zalusky, Kendra Hoekzema, David Twesigomwe, Lei Yang, Anthony A Snead, Phillip Andrew Richmond, Wouter De Coster, Nathan D Olson, Andrea Guarracino, Qiuhui Li, Angela L Miller, Joy Goffena, Zachery Anderson, Sophie Hr Storz, Sydney A Ward, Maisha Sinha, Claudia Gonzaga-Jauregui, Wayne E Clarke, Anna O Basile, André Corvelo, Catherine E Reeves, Adrienne Helland, Rajeeva Lochan Musunuri, Mahler Revsine, Karynne E Patterson, Cate R Paschal, Christina Zakarian, Sara Goodwin, Tanner D Jensen, Esther Robb, null null, null null, null null, W Richard McCombie, Fritz J Sedlazeck, Justin M Zook, Stephen B Montgomery, Erik P Garrison, Mikhail Kolmogorov, Michael C Schatz, Richard N McLaughlin, Harriet Dashnow, Michael C Zody, Matthew William Loose, Miten Jain, Evan E Eichler, Danny E Miller
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation. medRxiv : the preprint server for health sciences (2024)
Samantha Lapehn, Jonas A Gustafson, Andrew E Timms, Michael L Cunningham, Alison G Paquette
Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes. International journal of molecular sciences 24 (6) (2023)
Samantha Lapehn, Jonas A Gustafson, Andrew E Timms, Michael L Cunningham, Alison G Paquette
Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes. International journal of molecular sciences 24 (6) (2023)
Samantha Lapehn, Jonas A Gustafson, Andrew E Timms, Michael L Cunningham, Alison G Paquette
Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes. International journal of molecular sciences 24 (6) (2023)
Zahra A Aldawood, Luigi Mancinelli, Xuehui Geng, Shu-Chi A Yeh, Roberta Di Carlo, Taiana C Leite, Jonas A Gustafson, Katarzyna Wilk, Joseph Yozgatian, Sasan Garakani, Seyed Hossein Bassir, Michael L Cunningham, Charles P Lin, Giuseppe Intini
Expansion of the sagittal suture induces proliferation of skeletal stem cells and sustains endogenous calvarial bone regeneration. Proceedings of the National Academy of Sciences of the United States of America 120 (16) (2023)
Jonas A Gustafson, Maria Bjork, Conny M A van Ravenswaaij-Arts, Michael L Cunningham
Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis. Case reports in genetics 2022 (2022)
Andrew T Timberlake, Casey Griffin, Carrie L Heike, Anne V Hing, Michael L Cunningham, David Chitayat, Mark R Davis, Soghra J Doust, Amelia F Drake, Milagros M Dueñas-Roque, Jack Goldblatt, Jonas A Gustafson, Paula Hurtado-Villa, Alexis Johns, Natalya Karp, Nigel G Laing, Leanne Magee, null null, Sureni V Mullegama, Harry Pachajoa, Gloria L Porras-Hurtado, Rhonda E Schnur, Jennie Slee, Steven L Singer, David A Staffenberg, Andrew E Timms, Cheryl A Wise, Ignacio Zarante, Jean-Pierre Saint-Jeannet, Daniela V Luquetti
Haploinsufficiency of SF3B2 causes craniofacial microsomia. Nature communications 12 (1) (2021)