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Recent
Publications:
- Christiansen LR, Lage JM, Wolff DJ, Pai GS, Harley
RA. Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis
and mineralization of extraplacental membranes. Pediatr Dev Pathol.
8:115-23, 2005
- Christiansen L, Allen RA, Dunn T, Wolff DJ. A case
of infantile AML with MLL-MLL10 fusion caused by insertion of 11q into
10p. Canc Genet Cytogenet, 159:181-183, 2005.
- Quigley DI, Wolff DJ. Cytogenetics caseload and
FTE survey summary 2005. J Assoc Genet Tech, 31:59-62, 2005.
- Laudadio J, Keane TE, Reeves HM, Savage SJ, Hoda RS, Lage JM, Wolff
DJ. Fluorescence in situ hybridization for detecting transitional
cell carcinoma: implications for clinical practice. Brit J Urol,
Internat 96:1280-1285, 2005.
- Chen B, O’Connell CD, Boone DJ, Amos JA, Beck JC, Chan MM,
Farkas DH, Lebo RV, Richards CS, Roa BB, Silverman LM, Barton DE, Bejjani
BA, Belloni DR, Bernacki SH, Caggana M, Charache P, Dequeker E, Ferreira-Gonzalez
A, Friedman KJ, Greene CL, Grody WW, Highsmith WE, Jr., Hinkel CS,
Kalman LV, Lubin IM, Lyon E, Payne DA, Pratt VM, Rohlfs E, Rundell
CA, Schneider E, Willey AM, Williams LO, Willey JC, Winn-Deen ES, Wolff
DJ. Developing a sustainable process to provide quality
control materials for genetic testing. Genet Med, 7:534-549, 2005.
- Skorupa A, Metzner-Sadurski J, Wolff DJ, Gupta R,
Hall RK. HER-2/neu amplified breast cancers in South Carolina. J South
Carolina Med Assoc., 101:97-99, 2005.
- Spector EB, Grody WW, Matteson CJ, Palomaki GE, Bellissimo DB, Wolff
DJ, Bradley LA, Prior TW, Feldman G, Popovich BW, Watson
MS, Richards CS. Technical standards and guidelines: Venous thromboembolism
(Factor V Leiden and prothrombin 20210G>A testing): A disease-specific
supplement to the standards and guidelines for clinical genetics
laboratories. Genet Med. 7:444-453, 2005.
- Yu J, Kindy MS, Ellis BC, Baatz JE, Peden-Adams M, Ellingham TJ, Wolff
DJ, Fair PA, Gattoni-Celli S. Establishment of epidermal
cell Lines derived from the skin of the Atlantic bottlenose dolphin
(Tursiops Truncatus). The Anatomical Record, Part A, Discoveries
in Molecular, Cellular & Evolutionary Biology. 287:1246-55, 2005.
- Parker R, Reeves H, Sudarshan S, Wolff D, Keane
T. Abnormal in situ hybridization analysis in collecting duct carcinoma.
Urology 66:1110, 2005.
- Hirsh B, Brothman AR, Jacky PB, Rao KW, Wolff DJ.
Section E6 of the ACMG technical standards and guidelines: chromosome
studies for acquired abnormalities. Genet Med. 7:509-513, 2005.
- Brothman AR, Schneider NR,, Saikevych I, Cooley LD, Butler MG, Patil
S, Mascarello J, Rao K, Dewald G, Park JP, Persons D, Wolff
DJ, Vance GH. Cytogenetic Heteromorphisms: Survey results
and reporting practices of G-band regions that we have pondered for
years. Arch Path Lab Med, 130:947-949, 2006.
- Heaney DL, Flume P, Hamilton L, Lyon E, Wolff DJ.
Detection of an apparent homozygous 3120G>A cystic fibrosis mutation
on a routine carrier screen. J Mol Diag 8:137-40, 2006.
- Persons
DL, Tubbs
RR, Cooley
LD, Dewald
GW, Dowling
PK, Du
E, Mascarello
JT, Rao
KW, Wilson
KS, Wolff
DJ, Habegger-Vance
G. HER-2 fluorescence in situ hybridization:
results from the survey program of the College
of American Pathologists. Arch
Pathol Lab Med. 130:325-31, 2006.
- Graf MD, Christ L, Mascarello JT, Mowrey P, Pettenati
M, Stetten G, Storto P, Surti U, Van Dyke DL, Vance GH, Wolff
D, Schwartz S. Redefining the risks for prenatally ascertained
supernumary marker chromosomes: A collaborative study. J Med Genet.43:660-4,
2006.
- Quigley DI, Wolff DJ. Pediatric T-cell Acute Lymphoblastic
Leukemia with Aberrations of both MLL Loci, Cancer Genetics and Cytogenetics,
168:77-79, 2006.
- Benz CC, Fedele V, Xu F, Yistra B, Ginzinger B, Yu M, Moore D, Hall
RK, Wolff DJ, Disis ML, Eppenberger-Castori S, Eppenberger
U, Schittulli F, Tommassi S, Paradiso A, Scott GK, Albertson DG. Altered
promoter usage characterizes monoallelic transcription arising with
ERBB2 amplification in human breast cancers. Genes, Chromosomes & Cancer
45:983-994, 2006.
- Wolff DJ, Bagg A, Cooley AD, Dewald GW, Hirsch BA,
Jacky PB, Rao KW, Rao PN. Guidance for fluorescence in situ hybridization
(FISH) testing in hematologic disorders. J Mol Diagn. 9:134-43, 2007
and joint publication in J Mol Diagn. 9:134-43, 2007.
- Bilic M, Quigley DI, Stuart RK, Wolff DJ. Jumping
translocation of 1q in BCR/ABL-positive acute lymphoblastic leukemia.
Cancer Genet Cytogenet. 172:90-91, 2007.
- Quigley DI, Brooker J, Wolff DJ. The Prothrombin
20209C>T Sequence Variant: To Test or Not to Test? J Assoc
Genet Technol. 33:1-3, 2007.
- Znoyko I, Stuart RK, Ellingham T, Winters J, Wolff
DJ, Quigley DI.
Tetraploidy and 5q deletion in MDS: A case report. Cancer Genet Cytogenet,
in press.
Book
Chapters:
- Wolff DJ, Brothman A, Hirsch B, Jacky P. Clinical
Cytogenetics. In, American College of Medical Genetics Standards
and Guidelines for Clinical Genetics Laboratories, edited by M Watson, www.acmg.net,
2004.
- Wolff DJ, Schwartz S. Clinical Applications
of Fluorescence In Situ Hybridization. In, The Principles of Clinical
Cytogenetics, Second Edition, edited by S.Gerson and M Keagle.
Humana Press, Inc., Totowa, NJ, 2005.
- Wolff DJ. Advances in Clinical Cytogenetics.
In, Encyclopedia of Genomics, Proteomics and Bioinformatics, edited
by M Dunn, L Jorde, P Little and S Subramaniam. John Wiley & Sons,
Ltd., West Sussex, UK, 2006.
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