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 · 681 citations

Renal Function, Molecular Physiology, Biochemistry +8

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

Karin E. Finberg, Matthew M. Heeney, Dean R. Campagna et al. · Nature Genetics · 2008 · 670 citations · Full text

Anemia, Heme Homeostasis, Iron Metabolism +8

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 · 492 citations · Full text

Genetics, Genomic Mechanism, Molecular Biology +22

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 · 257 citations · Full text

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

Tumor Biology, Kras Mutation, Pathology +8