Whole Genome Sequencing and a New Bioinformatics Platform Allow for Rapid Gene Identification in D. melanogaster EMS Screens

Por Gonzalez, Michael A., Van Booven, Derek, Hulme, William, Ulloa, Rick H., Lebrigio, Rafael F. Acosta, Osterloh, Jeannette, Logan, Mary, Freeman, Marc, Zuchner, Stephan
Publicado em 2012

GEnomes Management Application (GEM.app): A new software tool for large-scale collaborative genome analysis

Por Gonzalez, Michael A., Acosta Lebrigio, Rafael F., Van Booven, Derek, Ulloa, Rick H., Powell, Eric, Speziani, Fiorella, Tekin, Mustafa, Schule, Rebecca, Zuchner, Stephan
Publicado no Hum Mutat (2013)

The mtDNA mutation spectrum of the progeroid Polg mutator mouse includes abundant control region multimers

Por Williams, Siôn L., Huang, Jia, Edwards, Yvonne J.K., Ulloa, Rick H., Dillon, Lloye M., Prolla, Tomas A., Vance, Jeffery M., Moraes, Carlos T., Züchner, Stephan
Publicado em 2010

Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Por Diaz-Horta, Oscar, Duman, Duygu, Foster, Joseph, Sırmacı, Aslı, Gonzalez, Michael, Mahdieh, Nejat, Fotouhi, Nikou, Bonyadi, Mortaza, Cengiz, Filiz Başak, Menendez, Ibis, Ulloa, Rick H., Edwards, Yvonne J. K., Züchner, Stephan, Blanton, Susan, Tekin, Mustafa
Publicado em 2012

Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Por Diaz-Horta, Oscar, Duman, Duygu, Foster, Joseph, Sırmacı, Aslı, Gonzalez, Michael, Mahdieh, Nejat, Fotouhi, Nikou, Bonyadi, Mortaza, Cengiz, Filiz Başak, Menendez, Ibis, Ulloa, Rick H., Edwards, Yvonne J. K., Züchner, Stephan, Blanton, Susan, Tekin, Mustafa
Publicado em 2013