Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss
Diaz-Horta, Oscar, Duman, Duygu, Foster, 2nd, 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
Published in PloS one (30.11.2012)
Published in PloS one (30.11.2012)
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Journal Article
GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis
Gonzalez, Michael A., Lebrigio, Rafael F. Acosta, Van Booven, Derek, Ulloa, Rick H., Powell, Eric, Speziani, Fiorella, Tekin, Mustafa, Schüle, Rebecca, Züchner, Stephan
Published in Human mutation (01.06.2013)
Published in Human mutation (01.06.2013)
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The mtDNA Mutation Spectrum of the Progeroid Polg Mutator Mouse Includes Abundant Control Region Multimers
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
Published in Cell metabolism (01.12.2010)
Published in Cell metabolism (01.12.2010)
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Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss
Diaz-Horta, Oscar, Duman, Duygu, Foster, Joseph, Sırmacı, Aslı, Gonzalez, Michael, Mahdieh, Nejat, Fotouhi, Nikou, Bonyadi, Mortaza, Cengiz, Filiz BaÅak, Menendez, Ibis, Ulloa, Rick H., Edwards, Yvonne J. K., Züchner, Stephan, Blanton, Susan, Tekin, Mustafa
Published in PloS one (17.05.2013)
Published in PloS one (17.05.2013)
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Whole Genome Sequencing and a New Bioinformatics Platform Allow for Rapid Gene Identification in D. melanogaster EMS Screens
Gonzalez, Michael A, Van Booven, Derek, Hulme, William, Ulloa, Rick H, Lebrigio, Rafael F Acosta, Osterloh, Jeannette, Logan, Mary, Freeman, Marc, Zuchner, Stephan
Published in Biology (Basel, Switzerland) (05.12.2012)
Published in Biology (Basel, Switzerland) (05.12.2012)
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