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Daynna Wolff

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Charles Butler; Yubin Kang; Robert K Stuart; Daynna J Wolff; Luciano J Costa
Association of age with fluorescence in situ hybridization abnormalities in multiple myeloma reveals higher rate of IGH translocations among older patients.
Denise I Quigley; Stephanie N Carter; Joyce A Foster; Daynna J Wolff
Cytogenetics caseload survey summary 2012.
Linsheng Zhang; Iya Znoyko; Laura K Conlin; Luciano J Costa; Robert D Daber; Sally E Self; Daynna J Wolff
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia.

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2012: Charles Butler; Yubin Kang; Robert K Stuart; Daynna J Wolff; Luciano J Costa
Association of age with fluorescence in situ hybridization abnormalities in multiple myeloma reveals higher rate of IGH translocations among older patients.
Leukemia & lymphoma 2012;53(12):2444-8.
2012: Denise I Quigley; Stephanie N Carter; Joyce A Foster; Daynna J Wolff
Cytogenetics caseload survey summary 2012.
Journal of the Association of Genetic Technologists 2012;38(4):199-202.
2011: Linsheng Zhang; Iya Znoyko; Laura K Conlin; Luciano J Costa; Robert D Daber; Sally E Self; Daynna J Wolff
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia.
Cancer genetics 2011;204(12):654-65.
2011: Arthur R Brothman; Michelle M Dolan; Barbara K Goodman; Jonathan P Park; Diane L Persons; Debra F Saxe; James H Tepperberg; Karen D Tsuchiya; Daniel L Van Dyke; Kathleen S Wilson; Daynna J Wolff; Karl S Theil
College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis.
Genetics in medicine : official journal of the American College of Medical Genetics 2011;13(9):765-9.
2011: Linsheng Zhang; Sherine Chan; Daynna J Wolff
Mitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosis.
Archives of pathology & laboratory medicine 2011;135(7):925-34.
2011: Hutton M Kearney; Allen Lamb; Kathleen W Rao; Sarah T South; Daynna J Wolff; Ada Hamosh
American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities.
Genetics in medicine : official journal of the American College of Medical Genetics 2011;13(7):676-9.
2011: Ginell R Post; Daynna J Wolff; Joshua S Black; Gil Y Cortes; Ross Brian Pollack; John Lazarchick
The utility of fluorescence in situ hybridization (FISH) analysis in diagnosing graft versus host disease following orthotopic liver transplant.
Annals of clinical and laboratory science 2011;41(2):188-92.
2010: Daynna J Wolff; Daniel L Van Dyke; CM Powell
Laboratory guideline for Turner syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2010;12(1):52-5.
2009: Daynna J Wolff; Denise LaMarche Heaney; Paul D Neuwald; Kathleen A Stellrecht; Richard D Press
Multi-Site PCR-based CMV viral load assessment-assays demonstrate linearity and precision, but lack numeric standardization: a report of the association for molecular pathology.
The Journal of molecular diagnostics : JMD 2009;11(2):87-92.
2008: Iya Znoyko; Robert Stuart; Tara Ellingham; Jennifer Winters; Daynna J Wolff; Denise I Quigley
Tetraploidy and 5q deletion in myelodysplastic syndrome: a case report.
Cancer genetics and cytogenetics 2008;183(1):64-8.
2007: Daynna J Wolff; Adam Bagg; Linda D Cooley; Gordon W Dewald; Betsy A Hirsch; Peter B Jacky; Kathleen W Rao; P Nagesh Rao
Guidance for fluorescence in situ hybridization testing in hematologic disorders.
The Journal of molecular diagnostics : JMD 2007;9(2):134-43.
2007: Daynna J Wolff
The genetics of bladder cancer: a cytogeneticist's perspective.
Cytogenetic and genome research 2007;118(2-4):177-81.
2007: Denise I Quigley; Jessica K Booker; Daynna J Wolff
The Prothrombin 20209C>T Sequence Variant: To Test or Not to Test.
Journal of the Association of Genetic Technologists 2007;33(2):1-3.
2007: Jennifer Laudadio; Denise I Quigley; Raymond Tubbs; Daynna J Wolff
HER2 testing: a review of detection methodologies and their clinical performance.
Expert review of molecular diagnostics 2007;7(1):53-64.
2007: Masha H. Bilic; Denise I Quigley; Robert Stuart; Daynna J Wolff
Jumping translocation of 1q in BCR/ABL-positive acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 2007;172(1):90-1.
2006: Christopher C Benz; Vita Fedele; Fan Xu; Bauke Ylstra; David Ginzinger; Mamie Yu; Dan Moore; Rayna Kneuper Hall; Daynna J Wolff; Mary L Disis; Serenella Eppenberger-Castori; Urs Eppenberger; Francesco Schittulli; Stefania Tommasi; angelo paradiso; Gary K Scott; Donna G Albertson
Altered promoter usage characterizes monoallelic transcription arising with ERBB2 amplification in human breast cancers.
Genes, chromosomes & cancer 2006;45(11):983-94.
2006: Michael D Graf; Laurie A Christ; James T Mascarello; P Mowrey; M Pettenati; Gail Stetten; P Storto; Urvashi Surti; Daniel L Van Dyke; Gail H Vance; Daynna J Wolff; Stuart Schwartz
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
Journal of medical genetics 2006;43(8):660-4.
2006: Arthur R Brothman; Nancy R Schneider; Irene Saikevych; Linda D Cooley; Merlin G Butler; Shivanand Patil; James T Mascarello; Kathleen W Rao; Gordon W Dewald; Jonathan P Park; Diane L Persons; Daynna J Wolff; Gail H Vance
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.
Archives of pathology & laboratory medicine 2006;130(7):947-9.
2006: Denise I Quigley; Daynna J Wolff
Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci.
Cancer genetics and cytogenetics 2006;168(1):77-9.
2006: Diane L Persons; Raymond R Tubbs; Linda D Cooley; Gordon W Dewald; Patricia K Dowling; Emma Du; James T Mascarello; Kathleen W Rao; Kathleen S Wilson; Daynna J Wolff; Gail Habegger-Vance
HER-2 fluorescence in situ hybridization: results from the survey program of the College of American Pathologists.
Archives of pathology & laboratory medicine 2006;130(3):325-31.
2006: Denise LaMarche Heaney; Patrick A Flume; Lauren Hamilton; Elaine Lyon; Daynna J Wolff
Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screen.
The Journal of molecular diagnostics : JMD 2006;8(1):137-40.
2005: Jennifer Laudadio; Thomas E Keane; Hugh M Reeves; Stephen J. Savage; Rana S Hoda; Janice M Lage; Daynna J Wolff
Fluorescence in situ hybridization for detecting transitional cell carcinoma: implications for clinical practice.
BJU international 2005;96(9):1280-5.
2005: Jin Yu; Mark S Kindy; Blake C Ellis; John E Baatz; Margie M Peden-Adams; Tara J Ellingham; Daynna J Wolff; Patricia A Fair; Sebastiano Gattoni-Celli
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, and evolutionary biology 2005;287(2):1246-55.
2005: Ryan Parker; H Mallory Reeves; Sunil Sudarshan; Daynna J Wolff; Thomas E Keane
Abnormal fluorescence in situ hybridization analysis in collecting duct carcinoma.
Urology 2005;66(5):1110.
2005: Bin Chen; Catherine D O' Connell; D Joe Boone; Jean A Amos; Jeanne C Beck; Maria M Chan; Daniel H Farkas; Roger V Lebo; Carolyn S (Sue) Richards; Benjamin B Roa; Lawrence M Silverman; David Barton; Bassem A Bejjani; Dorothy R Belloni; Susan H Bernacki; Michele Caggana; PATRICIA CHARACHE; Elisabeth Dequeker; Andrea Ferreira-Gonzalez; Kenneth Friedman; Carol L Greene; Wayne W Grody; W Edward Highsmith; Cecelia S Hinkel; Lisa V Kalman; Ira M Lubin; Elaine Lyon; Deborah A Payne; Victoria M Pratt; Elizabeth Rohlfs; Clark A Rundell; Erasmus Schneider; Ann M Willey; Laurina O Williams; James Willey; Emily S Winn-Deen; Daynna J Wolff
Developing a sustainable process to provide quality control materials for genetic testing.
Genetics in medicine : official journal of the American College of Medical Genetics 2005;7(8):534-49.
2005: Betsy Hirsh; Arthur R Brothman; Peter B Jacky; Kathleen W Rao; Daynna J Wolff
Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalities.
Genetics in medicine : official journal of the American College of Medical Genetics 2005;7(7):509-13.
2005: Elaine B Spector; Wayne W Grody; Carla J Matteson; Glenn E Palomaki; Daniel B Bellissimo; Daynna J Wolff; Linda A Bradley; Thomas W Prior; Gerald L Feldman; Bradley W Popovich; Michael S Watson; Carolyn S (Sue) Richards
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.
Genetics in medicine : official journal of the American College of Medical Genetics 2005;7(6):444-53.
2005: Lydia Christiansen; Richard A Allen; S Terence Dunn; Daynna J Wolff
A case of infantile acute myelogenous leukemia with MLL-MLL10 fusion caused by insertion of 11q into 10p.
Cancer genetics and cytogenetics 2005;159(2):181-3.
2005: Amy Skorupa; Joanna Metzner-Sadurski; Daynna J Wolff; Rashim Gupta; Rayna Kneuper-Hall
HER-2/neu amplified breast cancers in South Carolina.
Journal of the South Carolina Medical Association (1975) 2005;101(4):97-9.
2005: Lydia R Christiansen; Janice M Lage; Daynna J Wolff; G Shashidhar Pai; Russell A Harley
Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranes.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2005;8(1):115-23.
2004: Siby Sebastian; Silvia G Spitzer; Leonard E Grosso; Jean Amos; Frederick V Schaefer; Elaine Lyon; Daynna J Wolff; Atieh Hajianpour; Annette K Taylor; Alison Millson; Timothy T Stenzel
Multicenter characterization and validation of the intron-8 poly(T) tract (IVS8-T) status in 25 Coriell cell repository cystic fibrosis reference cell lines for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation assays.
Clinical chemistry 2004;50(1):251-4.
2003: Walter H Johnson; Ping Yang; Tao Yang; Yung R Lau; Barbara A Mostella; Daynna J Wolff; Dan Mark Roden; D Woodrow Benson
Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
Pediatric research 2003;53(5):744-8.
2002: Julianne Collins; Rick L Olson; Barbara R DuPont; Daynna J Wolff; Robert G Best; Roger E Stevenson
Prevalence of aneuploidies in South Carolina in the 1990s.
Genetics in medicine : official journal of the American College of Medical Genetics 2002;4(3):131-5.
2002: Dawn W Nichols; Daynna J Wolff; Sally Self; John S Metcalf; Donna Jacobs; Rayna Kneuper-Hall; John C Cate
A testing algorithm for determination of HER2 status in patients with breast cancer.
Annals of clinical and laboratory science 2002;32(1):3-11.
2002: Daynna J Wolff; Kimberly Clifton; Cynthia Ann Karr; Jane M Charles
Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion.
Genetics in medicine : official journal of the American College of Medical Genetics 2002;4(1):10-4.
2001: Brian A Gray; Angela Bent-Williams; Daynna J Wolff; Roberto T Zori
A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX.
Clinical genetics 2001;60(1):73-6.
2001: A Maddalena; Carolyn S (Sue) Richards; M J McGinniss; Arthur R Brothman; Robert J Desnick; R E Grier; B Hirsch; Peter B Jacky; Geraldine A McDowell; Bradley W Popovich; M Watson; Daynna J Wolff
Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of the Laboratory Practice Committee.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(3):200-5.
2000: Daynna J Wolff
Advances in laboratory evaluation of Turner syndrome and its variants: beyond cytogenetics studies.
Indian journal of pediatrics 2000;67(11):825-9.
2000: Daynna J Wolff; Stuart Schwartz; Laura Carrel
Molecular determination of X inactivation pattern correlates with phenotype in women with a structurally abnormal X chromosome.
Genetics in medicine : official journal of the American College of Medical Genetics 2000;2(2):136-41.
1999: Baruch Feldman; RL Kramer; Salah A Ebrahim; Daynna J Wolff; Mark I Evans
Prenatal evaluation of a de novo X;9 translocation.
American journal of medical genetics 1999;85(5):476-8.
1998: Arun Kumar; L A Becker; TW Depinet; J M Haren; C L Kurtz; Nathaniel H Robin; Suzanne B Cassidy; Daynna J Wolff; Stuart Schwartz
Molecular characterization and delineation of subtle deletions in de novo "balanced" chromosomal rearrangements.
Human genetics 1998;103(2):173-8.
1998: W M White; Huntington F Willard; Daniel L Van Dyke; Daynna J Wolff
The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA.
American journal of human genetics 1998;63(1):20-8.
1998: Daynna J Wolff; Stuart Schwartz; T Montgomery; JL Zackowski
Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.
American journal of medical genetics 1998;77(5):401-4.
1998: Zeynep Tümer; Daynna J Wolff; Asli N Silahtaroglu; A Orum; Karen Brøndum-Nielsen
Characterization of a supernumerary small marker X chromosome in two females with similar phenotypes.
American journal of medical genetics 1998;76(1):45-50.
1997: RS James; P Dalton; Karen M Gustashaw; Daynna J Wolff; Huntington F Willard; C Mitchell; Patricia A Jacobs
Molecular characterization of isochromosomes of Xq.
Annals of human genetics 1997;61(Pt 6):485-90.
1997: Nathaniel H Robin; A Harari-Shacham; Stuart Schwartz; Daynna J Wolff
Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region.
American journal of medical genetics 1997;71(3):361-5.
1997: Daynna J Wolff; Karen M Gustashaw; VL Zurcher; L Ko; W White; L Weiss; Daniel L Van Dyke; Stuart Schwartz; Huntington F Willard
Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern.
Human genetics 1997;100(2):256-61.
1997: Stuart Schwartz; TW Depinet; J Leana-Cox; N B Isada; E M Karson; V M Park; L M Pasztor; L C Sheppard; R Stallard; Daynna J Wolff; A B Zinn; VL Zurcher; JL Zackowski
Sex chromosome markers: characterization using fluorescence in situ hybridization and review of the literature.
American journal of medical genetics 1997;71(1):1-7.
1996: M A Micale; Daynna J Wolff; L H Dickerman; Raymond W Redline; JM Conroy; Stuart Schwartz
Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
Prenatal diagnosis 1996;16(10):893-7.
1996: Daynna J Wolff; A P Miller; Daniel L Van Dyke; Stuart Schwartz; Huntington F Willard
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
American journal of human genetics 1996;58(1):154-60.
1995: A P Miller; Karen M Gustashaw; Daynna J Wolff; S H Rider; Anthony P Monaco; B Eble; David Schlessinger; J L Gorski; G J van Ommen; J Weissenbach
Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22.
Human molecular genetics 1995;4(4):731-9.
1994: B A Sullivan; Daynna J Wolff; Stuart Schwartz
Analysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy.
Chromosoma 1994;103(7):459-67.
1994: Daynna J Wolff; Carolyn J Brown; Stuart Schwartz; A M Duncan; U Surti; Huntington F Willard
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
American journal of human genetics 1994;55(1):87-95.
1993: AM Duncan; A Macdonald; C J Brown; Daynna J Wolff; H F Willard; B Sutton
Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization.
American journal of medical genetics 1993;47(8):1153-6.
1993: Daynna J Wolff; M F Schwartz; M M Cohen; Stuart Schwartz
Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
American journal of medical genetics 1993;46(5):520-3.
1993: Daynna J Wolff; Stuart Schwartz
The effect of Robertsonian translocation on recombination on chromosome 21.
Human molecular genetics 1993;2(6):693-9.
1992: Daynna J Wolff; Stuart Schwartz
Characterization of Robertsonian translocations by using fluorescence in situ hybridization.
American journal of human genetics 1992;50(1):174-81.
1991: Daynna J Wolff; L J Raffel; M M Ferré; Stuart Schwartz
Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype.
American journal of medical genetics 1991;41(3):319-21.
1991: Daynna J Wolff; B W Needleman; Steven Wasserman; Stuart Schwartz
Spontaneous and clastogen induced chromosomal breakage in scleroderma.
The Journal of rheumatology 1991;18(6):837-40.