Establishment of F1 hybrid mortality in real time

Por Saulsberry, Ashley, Pinchas, Marisa, Noll, Aaron, Lynch, Jeremy A., Bordenstein, Seth R., Brucker, Robert M.
Publicado no BMC Evol Biol (2017)

Aneuploidy and polyploidy underlie adaptive evolution of yeast cells deprived of a conserved cytokinesis motor

Por Rancati, Giulia, Pavelka, Norman, Fleharty, Brian, Noll, Aaron, Allen, Rhonda, Walton, Kendra, Perera, Anoja, Staehling-Hampton, Karen, Seidel, Chris W., Li, Rong
Publicado em 2008

Identification of EMS-Induced Mutations in Drosophila melanogaster by Whole-Genome Sequencing

Por Blumenstiel, Justin P., Noll, Aaron C., Griffiths, Jennifer A., Perera, Anoja G., Walton, Kendra N., Gilliland, William D., Hawley, R. Scott, Staehling-Hampton, Karen
Publicado em 2009

A Whole-Chromosome Analysis of Meiotic Recombination in Drosophila melanogaster

Por Miller, Danny E., Takeo, Satomi, Nandanan, Kavyasree, Paulson, Ariel, Gogol, Madelaine M., Noll, Aaron C., Perera, Anoja G., Walton, Kendra N., Gilliland, William D., Li, Hua, Staehling, Karen K., Blumenstiel, Justin P., Hawley, R. Scott
Publicado em 2012

Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units

Por Saunders, Carol Jean, Miller, Neil Andrew, Soden, Sarah Elizabeth, Dinwiddie, Darrell Lee, Noll, Aaron, Alnadi, Noor Abu, Andraws, Nevene, Patterson, Melanie LeAnn, Krivohlavek, Lisa Ann, Fellis, Joel, Humphray, Sean, Saffrey, Peter, Kingsbury, Zoya, Weir, Jacqueline Claire, Betley, Jason, Grocock, Russell James, Margulies, Elliott Harrison, Farrow, Emily Gwendolyn, Artman, Michael, Safina, Nicole Pauline, Petrikin, Joshua Erin, Hall, Kevin Peter, Kingsmore, Stephen Francis
Publicado no Sci Transl Med (2012)

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

Por Willig, Laurel K, Petrikin, Josh E, Smith, Laurie D, Saunders, Carol J, Thiffault, Isabelle, Miller, Neil A, Soden, Sarah E, Cakici, Julie A, Herd, Suzanne M, Twist, Greyson, Noll, Aaron, Creed, Mitchell, Alba, Patria M, Carpenter, Shannon L, Clements, Mark A, Fischer, Ryan T, Hays, J Allyson, Kilbride, Howard, McDonough, Ryan J, Rosterman, Jamie L, Tsai, Sarah L, Zellmer, Lee, Farrow, Emily G, Kingsmore, Stephen F
Publicado no Lancet Respir Med (2015)

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

Por Soden, Sarah E., Saunders, Carol J., Willig, Laurel K., Farrow, Emily G., Smith, Laurie D., Petrikin, Josh E., LePichon, Jean-Baptiste, Miller, Neil A., Thiffault, Isabelle, Dinwiddie, Darrell L., Twist, Greyson, Noll, Aaron, Heese, Bryce A., Zellmer, Lee, Atherton, Andrea M., Abdelmoity, Ahmed T., Safina, Nicole, Nyp, Sarah S., Zuccarelli, Britton, Larson, Ingrid A., Modrcin, Ann, Herd, Suzanne, Creed, Mitchell, Ye, Zhaohui, Yuan, Xuan, Brodsky, Robert A., Kingsmore, Stephen F.
Publicado no Sci Transl Med (2014)