Barbara K. Goodman

Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter

Jose A. Camacho, Cassandra Obie, Barbara J. Biery et al. · Nature Genetics · 1999 · 204 citations

Mitochondrial Ornithine Transporter, Urology, Mendelian Disorder +8

Deletion ofPTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease

Ellen Arch, Barbara K. Goodman, Robert A. Van Wesep et al. · American Journal of Medical Genetics · 1997 · 134 citations

Mendelian Disorder, Genetic Disorder, Cowden Disease +8

SET oncoprotein overexpression in B-cell chronic lymphocytic leukemia and non-Hodgkin lymphoma: a predictor of aggressive disease and a new treatment target

Dale J. Christensen, Youwei Chen, Jessica Oddo et al. · Blood · 2011 · 128 citations · Full text

Identification of the α-Aminoadipic Semialdehyde Synthase Gene, Which Is Defective in Familial Hyperlysinemia

Katherine A. Sacksteder, Barbara J. Biery, James C. Morrell et al. · The American Journal of Human Genetics · 2000 · 113 citations · Full text

Mendelian Disorder, Biochemistry, Genetic Disorder +9

ATR functions as a gene dosage‐dependent tumor suppressor on a mismatch repair‐deficient background

Yanan Fang, Cheng-Chung Tsao, Barbara K. Goodman et al. · The EMBO Journal · 2004 · 110 citations · Full text