Shawn E Levy (S E Levy, Shawn Levy)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 14

Top Venues

Nature communications

bioRxiv : the preprint server for biology

NPJ genomic medicine

Nature biotechnology

HudsonAlpha Institute for Biotechnology

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

Affiliation History

HudsonAlpha Institute for Biotechnology Sep 01 2009

United States

Investigator

Publications

Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
David Porubsky, Harriet Dashnow, Thomas A Sasani, Glennis A Logsdon, Pille Hallast, Michelle D Noyes, Zev N Kronenberg, Tom Mokveld, Nidhi Koundinya, Cillian Nolan, Cody J Steely, Andrea Guarracino, Egor Dolzhenko, William T Harvey, William J Rowell, Kirill Grigorev, Thomas J Nicholas, Keisuke K Oshima, Jiadong Lin, Peter Ebert, W Scott Watkins, Tiffany Y Leung, Vincent C T Hanlon, Sean McGee, Brent S Pedersen, Michael E Goldberg, Hannah C Happ, Hyeonsoo Jeong, Katherine M Munson, Kendra Hoekzema, Daniel D Chan, Yanni Wang, Jordan Knuth, Gage H Garcia, Cairbre Fanslow, Christine Lambert, Charles Lee, Joshua D Smith, Shawn E Levy, Christopher E Mason, Erik P Garrison, Peter M Lansdorp, Deborah W Neklason, Lynn B Jorde, Aaron R Quinlan, Michael A Eberle, Evan E Eichler
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree. bioRxiv : the preprint server for biology (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
David Porubsky, Harriet Dashnow, Thomas A Sasani, Glennis A Logsdon, Pille Hallast, Michelle D Noyes, Zev N Kronenberg, Tom Mokveld, Nidhi Koundinya, Cillian Nolan, Cody J Steely, Andrea Guarracino, Egor Dolzhenko, William T Harvey, William J Rowell, Kirill Grigorev, Thomas J Nicholas, Keisuke K Oshima, Jiadong Lin, Peter Ebert, W Scott Watkins, Tiffany Y Leung, Vincent C T Hanlon, Sean McGee, Brent S Pedersen, Michael E Goldberg, Hannah C Happ, Hyeonsoo Jeong, Katherine M Munson, Kendra Hoekzema, Daniel D Chan, Yanni Wang, Jordan Knuth, Gage H Garcia, Cairbre Fanslow, Christine Lambert, Charles Lee, Joshua D Smith, Shawn E Levy, Christopher E Mason, Erik P Garrison, Peter M Lansdorp, Deborah W Neklason, Lynn B Jorde, Aaron R Quinlan, Michael A Eberle, Evan E Eichler
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree. bioRxiv : the preprint server for biology (2024)
David Porubsky, Harriet Dashnow, Thomas A Sasani, Glennis A Logsdon, Pille Hallast, Michelle D Noyes, Zev N Kronenberg, Tom Mokveld, Nidhi Koundinya, Cillian Nolan, Cody J Steely, Andrea Guarracino, Egor Dolzhenko, William T Harvey, William J Rowell, Kirill Grigorev, Thomas J Nicholas, Keisuke K Oshima, Jiadong Lin, Peter Ebert, W Scott Watkins, Tiffany Y Leung, Vincent C T Hanlon, Sean McGee, Brent S Pedersen, Michael E Goldberg, Hannah C Happ, Hyeonsoo Jeong, Katherine M Munson, Kendra Hoekzema, Daniel D Chan, Yanni Wang, Jordan Knuth, Gage H Garcia, Cairbre Fanslow, Christine Lambert, Charles Lee, Joshua D Smith, Shawn E Levy, Christopher E Mason, Erik P Garrison, Peter M Lansdorp, Deborah W Neklason, Lynn B Jorde, Aaron R Quinlan, Michael A Eberle, Evan E Eichler
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree. bioRxiv : the preprint server for biology (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
David Porubsky, Harriet Dashnow, Thomas A Sasani, Glennis A Logsdon, Pille Hallast, Michelle D Noyes, Zev N Kronenberg, Tom Mokveld, Nidhi Koundinya, Cillian Nolan, Cody J Steely, Andrea Guarracino, Egor Dolzhenko, William T Harvey, William J Rowell, Kirill Grigorev, Thomas J Nicholas, Keisuke K Oshima, Jiadong Lin, Peter Ebert, W Scott Watkins, Tiffany Y Leung, Vincent C T Hanlon, Sean McGee, Brent S Pedersen, Michael E Goldberg, Hannah C Happ, Hyeonsoo Jeong, Katherine M Munson, Kendra Hoekzema, Daniel D Chan, Yanni Wang, Jordan Knuth, Gage H Garcia, Cairbre Fanslow, Christine Lambert, Charles Lee, Joshua D Smith, Shawn E Levy, Christopher E Mason, Erik P Garrison, Peter M Lansdorp, Deborah W Neklason, Lynn B Jorde, Aaron R Quinlan, Michael A Eberle, Evan E Eichler
A familial, telomere-to-telomere reference for human de novo mutation and recombination from a four-generation pedigree. bioRxiv : the preprint server for biology (2024)
Medhat Mahmoud, Y Huang, K Garimella, Peter A Audano, W Wan, N Prasad, Robert E Handsaker, S Hall, A Pionzio, Michael C Schatz, Michael E Talkowski, Evan E Eichler, Shawn E Levy, Fritz J Sedlazeck
Utility of long-read sequencing for All of Us. Nature communications 15 (1) (2024)
Jonathan Foox, Scott W Tighe, Charles M Nicolet, Justin M Zook, Marta Byrska-Bishop, Wayne E Clarke, Michael M Khayat, Medhat Mahmoud, Phoebe K Laaguiby, Zachary T Herbert, Derek Warner, George S Grills, Jin Jen, Shawn E Levy, Jenny Xiang, Alicia Alonso, Xia Zhao, Wenwei Zhang, Fei Teng, Yonggang Zhao, Haorong Lu, Gary P Schroth, Giuseppe Narzisi, William Farmerie, Fritz J Sedlazeck, Don A Baldwin, Christopher E Mason
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nature biotechnology 39 (9) (2021)
Xiaoming Jia, Fernando S Goes, Adam E Locke, Duncan S Palmer, Weiqing Wang, Sarah Cohen-Woods, Giulio Genovese, Anne U Jackson, Chen Jiang, Mark Kvale, Niamh Mullins, Tan-Hoang Nguyen, Mehdi Pirooznia, Margarita Rivera, Douglas M Ruderfer, Ling Shen, Khanh Thai, Matthew Zawistowski, Yongwen Zhuang, Gonçalo R Abecasis, Huda Akil, Sarah E Bergen, Margit Burmeister, Sinéad Chapman, Melissa DelaBastide, Anders Juréus, Hyun Min Kang, Pui-Yan Kwok, Jun Z Li, Shawn E Levy, Eric T Monson, Jennifer Moran, Janet Sobell, Stanley J Watson, Virginia Willour, Sebastian Zöllner, Rolf Adolfsson, Douglas H R Blackwood, Michael Boehnke, Gerome D Breen, Aiden Corvin, Nick Craddock, Arianna DiFlorio, Christina M Hultman, Mikaél Landén, Cathryn M Lewis, Steven A McCarroll, W Richard McCombie, Peter McGuffin, Andrew M McIntosh, Andrew McQuillin, Derek W Morris, Richard M Myers, Michael C O'Donovan, Roel Ophoff, Marco P M Boks, Rene S Kahn, Willem Hendrik Ouwehand, Michael J Owen, Carlos Pato, Michele Pato, Danielle Posthuma, James B Potash, Andreas Reif, Pamela Sklar, Jordan Smoller, Patrick F Sullivan, John B Vincent, James Walters, Benjamin M Neale, Shaun M Purcell, Neil Risch, Catherine Schaefer, Eli A Stahl, Peter P Zandi, Laura J Scott
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular psychiatry 26 (9) (2021)
Daniel Butler, Christopher Mozsary, Cem Meydan, Jonathan Foox, Joel Rosiene, Alon Shaiber, David Danko, Ebrahim Afshinnekoo, Matthew MacKay, Fritz J Sedlazeck, Nikolay A Ivanov, Maria Sierra, Diana Pohle, Michael Zietz, Undina Gisladottir, Vijendra Ramlall, Evan T Sholle, Edward J Schenck, Craig D Westover, Ciaran Hassan, Krista Ryon, Benjamin Young, Chandrima Bhattacharya, Dianna L Ng, Andrea C Granados, Yale A Santos, Venice Servellita, Scot Federman, Phyllis Ruggiero, Arkarachai Fungtammasan, Chen-Shan Chin, Nathaniel M Pearson, Bradley W Langhorst, Nathan A Tanner, Youngmi Kim, Jason W Reeves, Tyler D Hether, Sarah E Warren, Michael Bailey, Justyna Gawrys, Dmitry Meleshko, Dong Xu, Mara Couto-Rodriguez, Dorottya Nagy-Szakal, Joseph Barrows, Heather Wells, Niamh B O'Hara, Jeffrey A Rosenfeld, Ying Chen, Peter A D Steel, Amos J Shemesh, Jenny Xiang, Jean Thierry-Mieg, Danielle Thierry-Mieg, Angelika Iftner, Daniela Bezdan, Elizabeth Sanchez, Thomas R Campion, John Sipley, Lin Cong, Arryn Craney, Priya Velu, Ari M Melnick, Sagi D Shapira, Iman Hajirasouliha, Alain C Borczuk, Thomas Iftner, Mirella Salvatore, Massimo Loda, Lars F Westblade, Melissa Cushing, Shixiu Wu, Shawn E Levy, Charles Y Chiu, Robert E Schwartz, Nicholas P Tatonetti, Hanna Rennert, Marcin Imielinski, Christopher E Mason
Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions. Nature communications 12 (1) (2021)
Delia Tomoiaga, Vanessa Aguiar-Pulido, Shristi Shrestha, Paul Feinstein, Shawn E Levy, Christopher E Mason, Jeffrey A Rosenfeld
Single-cell sperm transcriptomes and variants from fathers of children with and without autism spectrum disorder. NPJ genomic medicine 5 (2020)
Jedidiah Carlson, Adam E Locke, Matthew Flickinger, Matthew Zawistowski, Shawn E Levy, Richard M Myers, Michael Boehnke, Hyun Min Kang, Laura J Scott, Jun Z Li, Sebastian Zöllner, null null
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans. Nature communications 9 (1) (2018)

Shawn E Levy.css-eqlu8i{font-size:small;padding-left:4px;} (S E Levy, Shawn Levy)

Publication Activity (10 Years)

Top Topics

Top Venues

Shawn E Levy (S E Levy, Shawn Levy)