Karin E. Finberg
Yale University(US)
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Ion Transport and Channel Regulation, Erythrocyte Function and Pathophysiology, Trace Elements in Health
Most-Cited Works
- → Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness(1999)684 cited
- → Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)(2008)673 cited
- → Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae.(1994)492 cited
- → Renal Vacuolar H+-ATPase(2004)441 cited
- → A Founder Mutation as a Cause of Cerebral Cavernous Malformation in Hispanic Americans(1996)258 cited
- → Mucinous Differentiation Correlates with Absence of EGFR Mutation and Presence of KRAS Mutation in Lung Adenocarcinomas with Bronchioloalveolar Features(2007)218 cited
- → Mutations in the Na-Cl Cotransporter Reduce Blood Pressure in Humans(2001)173 cited
- → Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status(2002)173 cited
- → Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis(2010)163 cited
- → Analytical Validation of the Next-Generation Sequencing Assay for a Nationwide Signal-Finding Clinical Trial(2017)153 cited