Contact Information

295 Congress Avenue
BCMM Room 147
New Haven, CT 06510

Education

Yale University, New Haven, CT
B.S. in Biology 1993

Yale School of Medicine, New Haven, CT
M.D./Ph.D. Program, Department of Genetics, September 1994-present

Research Interest
 The genetic basis of the syndrome of renal tubular acidosis with sensorineural deafness.
 

Publications

Karet, F.E., Finberg, K.E., Nayir, A., et al. Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing (rdRTA) to 7q33-34. Am J Hum Gen 65, 1656-1665.

Karet, F.E., Finberg, K.E., Nelson, R.D., et al.  Mutations in the Gene Encoding B1 Subunit of H+-ATPase Cause Renal Tubular Acidosis with Sensorineural Deafness.  Nature Genetics 21, 84-90.

Gunel, M., Awad, I.A., Finberg, K., et al.  Genetic Heterogeneity of Inherited Cerebral Cavernous Malformation.  Neurosurgery 38, 1265-1271.

Gunel, M., Awad, I.A., Finberg, K., et al.  A Founder Mutation as a Cause of Cerebral Cavernous Malformation in Hispanic Americans.  The New England Journal of Medicine 334, 946-951.

Finberg, K.E., Muth, T.R., Young, S.P., et al.  Interactions of VirB9, -10, and  -11 with the membrane fraction of Agrobacterium tumefaciens:  solubility studies provide evidence for tight associations.  Journal of Bacteriology 177, 4881-9.

Burns, N., Grimwade, B., Ross-Macdonald, P.B., Choi, E.Y., Finberg, K., Roeder, G.S., and Snyder, M.  Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae.  Genes & Development 8, 1087-105.