Laurie B. Griffin

Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy

Claudia Gonzaga‐Jauregui, Tamar Harel, Tomasz Gambin et al. · Cell Reports · 2015 · 240 citations · Full text

Identification of an Inhibitor of the EWS-FLI1 Oncogenic Transcription Factor by High-Throughput Screening

Patrick J. Grohar, Girma M. Woldemichael, Laurie B. Griffin et al. · JNCI Journal of the National Cancer Institute · 2011 · 202 citations · Full text

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Alexander J. Abrams, Robert B. Hufnagel, Adriana Rebelo et al. · Nature Genetics · 2015 · 200 citations · Full text

Somatic Variant, Mendelian Disorder, Genetic Disorder +7

Mutation in Mouse Hei10, an E3 Ubiquitin Ligase, Disrupts Meiotic Crossing Over

Jeremy O Ward, Laura G. Reinholdt, William W. Motley et al. · PLoS Genetics · 2007 · 128 citations · Full text

Spermatogenesis, Cytogenetics, Genetics +19

Ecteinascidin 743 Interferes with the Activity of EWS-FLI1 in Ewing Sarcoma Cells

Patrick J. Grohar, Laurie B. Griffin, Choh Yeung et al. · Neoplasia · 2011 · 121 citations · Full text