Jeffrey R. Sawyer
Department of Pathology
University of Arkansas for Medical Sciences
Little Rock
Arkansas
USA
Name/email consistency: high
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage-fusion-bridge cycles of a 1q12 approximately 23 amplicon. Sawyer, J.R., Tian, E., Thomas, E., Koller, M., Stangeby, C., Sammartino, G., Goosen, L., Swanson, C., Binz, R.L., Barlogie, B., Shaughnessy, J. Br. J. Haematol. (2009)
- De novo proximal duplication of 1(q12q22) in a female infant with multiple congenital anomalies. Sawyer, J.R., Binz, R.L., Swanson, C.M., Lim, C. Am. J. Med. Genet. A (2007)
- Genomic instability in multiple myeloma: evidence for jumping segmental duplications of chromosome arm 1q. Sawyer, J.R., Tricot, G., Lukacs, J.L., Binz, R.L., Tian, E., Barlogie, B., Shaughnessy, J. Genes. Chromosomes. Cancer (2005)
- A clonal reciprocal t(2;7)(p13;p13) in plantar fibromatosis. Sawyer, J.R., Sammartino, G., Gokden, N., Nicholas, R.W. Cancer Genet. Cytogenet. (2005)
- Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone. Sawyer, J.R., Goosen, L.S., Binz, R.L., Swanson, C.M., Nicholas, R.W. Cancer Genet. Cytogenet. (2005)
- A novel t(X;2)(q13;q35) in clear cell sugar tumor of bone. Sawyer, J.R., Nicholas, R.W., Parham, D.M. Cancer Genet. Cytogenet. (2004)
- Constitutional t(16;22)(p13.3;q11.2 approximately 12) in a primitive neuroectodermal tumor of the pineal region. Sawyer, J.R., Sammartino, G., Husain, M., Linskey, M.E. Cancer Genet. Cytogenet. (2003)
- Telomeric fusion as a mechanism for the loss of 1p in meningioma. Sawyer, J.R., Husain, M., Lukacs, J.L., Stangeby, C., Binz, R.L., Al-Mefty, O. Cancer Genet. Cytogenet. (2003)
- Recurring breakpoints of 1p13 approximately p22 in osteochondroma. Sawyer, J.R., Thomas, E.L., Lukacs, J.L., Swanson, C.M., Ding, Y., Parham, D.M., Thomas, J.R., Nicholas, R.W. Cancer Genet. Cytogenet. (2002)
- Identification of isochromosome 1q as a recurring chromosome aberration in skull base chordomas: a new marker for aggressive tumors?. Sawyer, J.R., Husain, M., Al-Mefty, O. Neurosurg. Focus (2001)