Bora E. Baysal
Department of Psychiatry
The University of Pittsburgh Medical Center
Pittsburgh
PA 15213-2593
USA
Name/email consistency: high
- Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. Baysal, B.E., Willett-Brozick, J.E., Lawrence, E.C., Drovdlic, C.M., Savul, S.A., McLeod, D.R., Yee, H.A., Brackmann, D.E., Slattery, W.H., Myers, E.N., Ferrell, R.E., Rubinstein, W.S. J. Med. Genet. (2002)
- A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family. Baysal, B.E., Willett-Brozick, J.E., Badner, J.A., Corona, W., Ferrell, R.E., Nimgaonkar, V.L., Detera-Wadleigh, S.D. Neurogenetics (2002)
- Hereditary paraganglioma targets diverse paraganglia. Baysal, B.E. J. Med. Genet. (2002)
- Etiopathogenesis and clinical presentation of carotid body tumors. Baysal, B.E., Myers, E.N. Microsc. Res. Tech. (2002)
- A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region. Baysal, B.E., Willett-Brozick, J.E., Taschner, P.E., Dauwerse, J.G., Devilee, P., Devlin, B. Eur. J. Hum. Genet. (2001)
- Genetics of familial paragangliomas: past, present, and future. Baysal, B.E. Otolaryngol. Clin. North Am. (2001)
- Phenotypic dichotomy in mitochondrial complex II genetic disorders. Baysal, B.E., Rubinstein, W.S., Taschner, P.E. J. Mol. Med. (2001)
- Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Baysal, B.E., Ferrell, R.E., Willett-Brozick, J.E., Lawrence, E.C., Myssiorek, D., Bosch, A., van der Mey, A., Taschner, P.E., Rubinstein, W.S., Myers, E.N., Richard, C.W., Cornelisse, C.J., Devilee, P., Devlin, B. Science (2000)
