Scott Mahan

发表

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

Joshua M. Korn, Christopher A. Miller, Derek Y. Chiang, 2008, Nature.

The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity

Adam A. Margolin, Michael P. Morrissey, S. Gabriel, 2012, Nature.

Initial genome sequencing and analysis of multiple myeloma

Trevor J Pugh, A. Sivachenko, K. Cibulskis, 2011, Nature.

Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity

Adam A. Margolin, Michael P. Morrissey, S. Gabriel, 2012, Nature.

Melanoma genome sequencing reveals frequent PREX2 mutations

T. Fennell, A. Sivachenko, K. Cibulskis, 2012, Nature.

The genomic complexity of primary human prostate cancer

Eric S. Lander, Kristian Cibulskis, Todd R. Golub, 2010, Nature.

Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records.

Peter Szolovits, Tianxi Cai, Shawn N Murphy, 2011, American journal of human genetics.

Characterization of Nigerian breast cancer reveals prevalent homologous recombination deficiency and aggressive molecular features

Michael P. Morrissey, K. White, Scott Mahan, 2018, Nature Communications.

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

Tanya M. Teslovich, Amy L. Williams, Ian C. Smith, 2013, Nature.

Characterization of Nigerian breast cancer reveals prevalent homologous recombination deficiency and aggressive molecular features

Michael P. Morrissey, K. White, Scott Mahan, 2018, Nature Communications.

Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.

Beth K. Martin, Michael P. Morrissey, J. Shendure, 2016, JAMA neurology.

Collaborative design for automated DNA storage that allows for rapid, accurate, large-scale studies.

Scott Mahan, Kristin G Ardlie, Kevin F Krenitsky, 2004, Assay and drug development technologies.

Melanoma genome sequencing reveals frequent PREX2 mutations

Trevor J Pugh, T. Fennell, A. Sivachenko, 2012, Nature.