Karin E. Finberg

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Fiona E. Karet, Karin E. Finberg, Raoul D. Nelson et al. · Nature Genetics · 1999 · 694 citations

Medicine, Genetics, Molecular Genetics +13

Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)

Karin E. Finberg, Matthew M. Heeney, Dean R. Campagna et al. · Nature Genetics · 2008 · 678 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae.

Nigel Burns, Brian G. Grimwade, Petra Ross‐Macdonald et al. · Genes & Development · 1994 · 493 citations · Full text

Life Sciences, Genetics, Molecular Biology +13

A Founder Mutation as a Cause of Cerebral Cavernous Malformation in Hispanic Americans

Murat Günel, Issam A. Awad, Karin E. Finberg et al. · New England Journal of Medicine · 1996 · 258 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mucinous Differentiation Correlates with Absence of EGFR Mutation and Presence of KRAS Mutation in Lung Adenocarcinomas with Bronchioloalveolar Features

Karin E. Finberg, Lecia V. Sequist, Victoria A. Joshi et al. · Journal of Molecular Diagnostics · 2007 · 218 citations · Full text

Medicine, Oncology, Pathology +16