SubmiRine: assessing variants in microRNA targets using clinical genomic data sets

por Maxwell, Evan K., Campbell, Joshua D., Spira, Avrum, Baxevanis, Andreas D.
Publicado 2015

MicroRNAs and essential components of the microRNA processing machinery are not encoded in the genome of the ctenophore Mnemiopsis leidyi

por Maxwell, Evan K, Ryan, Joseph F, Schnitzler, Christine E, Browne, William E, Baxevanis, Andreas D
Publicado 2012

Evolutionary profiling reveals the heterogeneous origins of classes of human disease genes: implications for modeling disease genetics in animals

por Maxwell, Evan K, Schnitzler, Christine E, Havlak, Paul, Putnam, Nicholas H, Nguyen, Anh-Dao, Moreland, R Travis, Baxevanis, Andreas D
Publicado 2014

CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data

por Packer, Jonathan S., Maxwell, Evan K., O’Dushlaine, Colm, Lopez, Alexander E., Dewey, Frederick E., Chernomorsky, Rostislav, Baras, Aris, Overton, John D., Habegger, Lukas, Reid, Jeffrey G.
Publicado 2016

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population

por Martin, Christa Lese, Wain, Karen E., Oetjens, Matthew T., Tolwinski, Kasia, Palen, Emily, Hare-Harris, Abby, Habegger, Lukas, Maxwell, Evan K., Reid, Jeffrey G., Walsh, Lauren Kasparson, Myers, Scott M., Ledbetter, David H.
Publicado 2020