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Profile

Debra Saxe PhD

  • Department of Pathology and Laboratory Medicine
    Professor Emeritus
  • (404) 712-4810
  • dsaxe01@emory.edu
Head shot of Debra Saxe

Academic Appointment

  • Associate Professor /Adjunct Professor, Emory University School of Medicine
  • Associate Professor, Department of Pathology and Laboratory Medicine, Emory University School of Medicine
  • Associate Professor /Adjunct Professor, Emory University School of Medicine

Education

Degrees

  • PhD from University of Arizona
  • BA from University of Texas
  • MS from University of Arizona

Research

Focus

  • I am collaborating with Emory Biomarker Service Center to develop a single nucleotide polymorphic (SNP) microarray for leukemias and lymphomas that can be transitioned into clinical use. I am also a co-investigator on a study to correlate flourescent in situ hybridation (FISH) and whole genome analysis on specific lung tumors with disease progression and response to therapies. I am developing cytogenomic microarray testing for clinical use in oncology.

Publications

  • Transposon DNA sequences facilitate the tissue-specific gene transfer of circulating tumor DNA between human cells.
    Nucleic Acids Res Volume: 52 Page(s): 7539 - 7555
    07/22/2024 Authors: Cinar M; Martinez-Medina L; Puvvula PK; Arakelyan A; Vardarajan BN; Anthony N; Nagaraju GP; Park D; Feng L; Sheff F
  • Loss of heterozygosity leading to incorrect HLA typing for platelet-transfusion refractory patient.
    Volume: 63 Page(s): 263 - 268
    01/01/2023 Authors: Horwath M; Tvrdik T; Saxe D; Deeb KK; Roback JD; Gebel HM; Bray RA; Sullivan HC
  • Clinical Validation and Diagnostic Utility of Optical Genome Mapping for Enhanced Cytogenomic Analysis of Hematological Neoplasms.
    J Mol Diagn Volume: 24 Page(s): 1279 - 1291
    12/01/2022 Authors: Sahajpal NS; Mondal AK; Tvrdik T; Hauenstein J; Shi H; Deeb KK; Saxe D; Hastie AR; Chaubey A; Savage NM
  • Cryptic t(6;11) KMT2A rearrangement in a pediatric acute myeloid leukemia patient detected by next-generation sequencing and dual-fusion FISH analysis.
    Pediatr Blood Cancer Volume: 69 Page(s): e29428
    03/01/2022 Authors: Raghunandan S; Jain J; Saxe D; Pauly M; Aljudi AA; Ketterling RP; Carter AB; Raikar SS
  • Sustained Complete Molecular Remission With Imatinib Monotherapy in a Child Presenting With Blast Phase FIP1L1-PDGFRA-Associated Myeloid Neoplasm With Eosinophilia.
    Hemasphere Volume: 4 Page(s): e486
    12/01/2020 Authors: Jain J; Weinzierl EP; Saxe D; Bergsagel J; Gotlib J; Reiter A; Raikar SS
  • Copy number assessment in the genomic analysis of CNS neoplasia: An evidence-based review from the cancer genomics consortium (CGC) working group on primary CNS tumors.
    Cancer Genet Volume: 243 Page(s): 19 - 47
    05/01/2020 Authors: Neill SG; Hauenstein J; Li MM; Liu YJ; Luo M; Saxe DF; Ligon AH
  • Genomic copy number variation correlates with survival outcomes in WHO grade IV glioma.
    Sci Rep Volume: 10 Page(s): 7355
    04/30/2020 Authors: Buchwald ZS; Tian S; Rossi M; Smith GH; Switchenko J; Hauenstein JE; Moreno CS; Press RH; Prabhu RS; Zhong J
  • Clonal Evolution of B-Cell Acute Lymphoblastic Leukemia with del(9)(p13p21) into Mixed Phenotype Acute Leukemia Presenting as an Isolated Testicular Relapse.
    Reports (MDPI) Volume: 2
    09/01/2019 Authors: Miller LH; Park SI; Saxe D; Lew G; Raikar SS
  • Gliosarcoma: distinct molecular pathways and genomic alterations identified by DNA copy number/SNP microarray analysis.
    J Neurooncol Volume: 143 Page(s): 381 - 392
    07/01/2019 Authors: Lowder L; Hauenstein J; Woods A; Chen H-R; Rupji M; Kowalski J; Olson JJ; Saxe D; Schniederjan M; Neill S
  • Evaluating approaches to enhance survival in children with hypodiploid acute lymphoblastic leukaemia (ALL).
    Br J Haematol Volume: 185 Page(s): 613 - 616
    05/01/2019 Authors: Miller L; Kobayashi S; Pauly M; Lew G; Saxe D; Keller F; Qayed M; Castellino S
  • Recent advances in cytogenetic characterization of multiple myeloma.
    Int J Lab Hematol Volume: 41 Page(s): 5 - 14
    02/01/2019 Authors: Saxe D; Seo E-J; Bergeron MB; Han J-Y
  • Acute Myeloid Leukemia in an Infant with t(8;19)(p11.2;q13) Translocation: Case Report and a Review of the Literature.
    Case Rep Hematol Volume: 2019 Page(s): 4198415
    01/01/2019 Authors: Eason AC; Bunting ST; Peterson JF; Saxe D; Sabnis HS
  • Complex karyotype in patients with mantle cell lymphoma predicts inferior survival and poor response to intensive induction therapy.
    Cancer Volume: 124 Page(s): 2306 - 2315
    06/01/2018 Authors: Greenwell IB; Staton AD; Lee MJ; Switchenko JM; Saxe DF; Maly JJ; Blum KA; Grover NS; Mathews SP; Gordon MJ
  • Utility of Fluorescence In Situ Hybridization Panel for Myelodysplastic Syndrome in Evaluation of Cytopenia in a Pediatric Hospital: A 5-Year Retrospective Review and Utilization Management.
    Lab Med Volume: 48 Page(s): 266 - 270
    08/01/2017 Authors: Bunting CT; Senior T; Susson Y; Rivera A; Saxe D; Bunting ST
  • Molecular and cytogenomic profiling of hepatic adenocarcinoma expressing inhibinA, a mimicker of neuroendocrine tumors: proposal to reclassify as "cholangioblastic variant of intrahepatic cholangiocarcinoma".
    Volume: 62 Page(s): 232 - 241
    04/01/2017 Authors: Braxton DR; Saxe D; Damjanov N; Stashek K; Shroff S; Morrissette JD; Tondon R; Furth EE
  • A variant c-KIT mutation, D816H, fundamental to the sequential development of an ovarian mixed germ cell tumor and systemic mastocytosis with chronic myelomonocytic leukemia.
    Pediatr Blood Cancer Volume: 64
    04/01/2017 Authors: Mitchell SG; Bunting ST; Saxe D; Olson T; Keller FG
  • Multimodality Technologies in the Assessment of Hematolymphoid Neoplasms.
    Arch Pathol Lab Med Volume: 141 Page(s): 341 - 354
    03/01/2017 Authors: Li S; Jaye DL; Bradley KT; Zhang L; Saxe D; Deeb G; Hill CE; Mann KP
  • Genomic Analysis in the Practice of Surgical Neuropathology: The Emory Experience.
    Arch Pathol Lab Med Volume: 141 Page(s): 355 - 365
    03/01/2017 Authors: Neill SG; Saxe DF; Rossi MR; Schniederjan MJ; Brat DJ
  • MYC Immunohistochemistry Predicts MYC Rearrangements by FISH.
    Front Oncol Volume: 7 Page(s): 209
    01/01/2017 Authors: Nwanze J; Siddiqui MT; Stevens KA; Saxe D; Cohen C
  • Genomic Copy Number Complexity Correlates With Overall Survival in Glioblastoma Patients
    Volume: 96 Page(s): S92 - S93
    10/01/2016 Authors: Buchwald ZS; Rossi M; Smith G; Abugideiri M; Hauenstein JE; Saxe DF; Neill SG; Ali AN; Brat DJ; Olson JJ
  • Genomic Copy Number Complexity Correlates With Overall Survival in Glioblastoma Patients
    Volume: 96 Page(s): S92 - S93
    10/01/2016 Authors: Buchwald ZS; Rossi M; Smith G; Abugideiri M; Hauenstein JE; Saxe DF; Neill SG; Ali AN; Brat DJ; Olson JJ
  • Genomic Copy Number Complexity Correlates With Overall Survival in Glioblastoma Patients.
    Volume: 96 Page(s): S92 - S93
    10/01/2016 Authors: Buchwald ZS; Rossi M; Smith G; Abugideiri M; Hauenstein JE; Saxe DF; Neill SG; Ali AN; Brat DJ; Olson JJ
  • An evaluation of NGS to identify gene fusions using RNA from FFPE solid tumor samples
    Volume: 76
    07/01/2016 Authors: Parks JT; Byron L; Crain B; June S; Chen Z; Du T; Sica GL; Owonikoko TK; Neill SG; Newman S
  • Adult-onset Leukoencephalopathy with Cerebral Calcifications and Cysts (Labrune Syndrome): A Case With Novel Copy Number Abnormalities
    Volume: 75 Page(s): 613 - 613
    06/01/2016 Authors: Vega JV; Neill S; Schniederjan M; Hunter S; Brat D; Saxe D; Rossi M; Holder C; Olson J
  • Section E6.5-6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor-acquired chromosomal abnormalities.
    Genet Med Volume: 18 Page(s): 643 - 648
    06/01/2016 Authors: Cooley LD; Morton CC; Sanger WG; Saxe DF; Mikhail FM
  • Clinical Validation and Implementation of a Targeted Next-Generation Sequencing Assay to Detect Somatic Variants in Non-Small Cell Lung, Melanoma, and Gastrointestinal Malignancies.
    J Mol Diagn Volume: 18 Page(s): 299 - 315
    03/01/2016 Authors: Fisher KE; Zhang L; Wang J; Smith GH; Newman S; Schneider TM; Pillai RN; Kudchadkar RR; Owonikoko TK; Ramalingam SS
  • Molecular and Cytogenomic Profiling of Hepatic Adenocarcinoma Expressing Inhibin, a Mimicker of Neuroendocrine Tumors: Proposal to Reclassify as "Cholangioblastic Variant of Intrahepatic Cholangiocarcinoma"
    Volume: 29 Page(s): 416A - 416A
    02/01/2016 Authors: Braxton DR; Saxe DF; Stashek K; Shroff SG; Damjanov N; Morrissette JJD; Tondon R; Furth EE
  • The role of immunohistochemical analysis in the evaluation of EML4-ALK gene rearrangement in lung cancer.
    Volume: 23 Page(s): 239 - 244
    04/01/2015 Authors: Sullivan HC; Fisher KE; Hoffa AL; Wang J; Saxe D; Siddiqui MT; Cohen C
  • CAP/ASCO Low HER2 Guidelines 2013-Immunohistochemistry Quantitation Visually and By Image Cytometry (ACIS) Versus FISH
    Volume: 95 Page(s): 505A - 506A
    02/01/2015 Authors: Myers C; Guerzon G; Lawson D; Saxe D; Cohen C
  • CAP/ASCO Low HER2 Guidelines 2013-Immunohistochemistry Quantitation Visually and By Image Cytometry (ACIS) Versus FISH
    Volume: 28 Page(s): 505A - 506A
    02/01/2015 Authors: Myers C; Guerzon G; Lawson D; Saxe D; Cohen C
  • The SNP-CN Microarray Shows High Concordance and Greater Sensitivity in Detecting Molecular Alterations Compared To FISH and SNaPshot
    Volume: 95 Page(s): 428A - 428A
    02/01/2015 Authors: Appin C; Neill S; Schniederjan M; Hunter S; Saxe D; Hill C; Rossi M; Brat D
  • The SNP-CN Microarray Shows High Concordance and Greater Sensitivity in Detecting Molecular Alterations Compared To FISH and SNaPshot
    Volume: 28 Page(s): 428A - 428A
    02/01/2015 Authors: Appin C; Neill S; Schniederjan M; Hunter S; Saxe D; Hill C; Rossi M; Brat D
  • A Precursor Lesion To AT/RT? A Case of AT/RT in Association With a Lower Grade SMARCB1-Deficient Neoplasm
    Volume: 95 Page(s): 434A - 434A
    02/01/2015 Authors: Neill S; Vigneswaran K; Holder C; Saxe D; Rossi M; Schniederjan M
  • A Precursor Lesion To AT/RT? A Case of AT/RT in Association With a Lower Grade SMARCB1-Deficient Neoplasm
    Volume: 28 Page(s): 434A - 434A
    02/01/2015 Authors: Neill S; Vigneswaran K; Holder C; Saxe D; Rossi M; Schniederjan M
  • Detection of NFKB2 3'end Loos By Quantitative PCR (QPCR) or Detection of NFKB2 Rearrangements Correlate with Bortezomib Response in Multiple Myeloma
    Volume: 124
    12/06/2014 Authors: Ramachandiran S; Koff JL; Garderet L; Saxe D; Ikhlef S; Kelkar N; Kaplan L; El-Cheikh J; Switchenko JM; Sunay S
  • Analysis of graft survival in a trial of stem cell transplant in ALS.
    Ann Clin Transl Neurol Volume: 1 Page(s): 900 - 908
    11/01/2014 Authors: Tadesse T; Gearing M; Senitzer D; Saxe D; Brat DJ; Bray R; Gebel H; Hill C; Boulis N; Riley J
  • Consolidation and maintenance therapy with lenalidomide, bortezomib and dexamethasone (RVD) in high-risk myeloma patients.
    Leukemia Volume: 28 Page(s): 690 - 693
    03/01/2014 Authors: Nooka AK; Kaufman JL; Muppidi S; Langston A; Heffner LT; Gleason C; Casbourne D; Saxe D; Boise LH; Lonial S
  • Subjectivity in chromosome band-level estimation: a multicenter study.
    Genet Med Volume: 16 Page(s): 170 - 175
    02/01/2014 Authors: Geiersbach KB; Gardiner AE; Wilson A; Shetty S; Bruyre H; Zabawski J; Saxe DF; Gaulin R; Williamson C; Van Dyke DL
  • c-Met Immunohistochemistry in EGFR Mutant Adenocarcinoma: Comparison with Fluorescence In-Situ Hybridization
    Volume: 27 Page(s): 499A - 499A
    02/01/2014 Authors: Willis BC; Martin DR; Saxe D; Ramalingam SS; Khuri F; Fisher KE; Rossi MR; Cohen C; Sica G
  • c-Met Immunohistochemistry in EGFR Mutant Adenocarcinoma: Comparison with Fluorescence In-Situ Hybridization
    Volume: 94 Page(s): 499A - 499A
    02/01/2014 Authors: Willis BC; Mortin DR; Saxe D; Ramalingam SS; Khuri F; Fisher KE; Rossi MR; Cohen C; Sica G
  • Using RNA-Seq, SNP-CN and Targeted Deep Sequencing To Improve The Diagnostic Paradigm In Multiple Myeloma
    Volume: 122
    11/15/2013 Authors: Rossi MR; Newman S; Nooka AK; Kaufman JL; Bahlis NJ; Neri P; Matulis SM; Bernal-Mizrachi L; Gupta VA; Varma A
  • Genomic Characterization of Diffuse Astrocytoma by SNP-CN Arrays and Hot-Spot Mutation Sequencing
    Volume: 72 Page(s): 540 - 541
    06/01/2013 Authors: Rossi M; Appin C; Bellail A; Mann K; Saxe D; Hill C; Olson J; Hadjipanayis C; Hunter S; Brat D
  • Characteristics and outcomes of diffuse large B-cell lymphoma presenting in leukaemic phase.
    Br J Haematol Volume: 158 Page(s): 608 - 614
    09/01/2012 Authors: Muringampurath-John D; Jaye DL; Flowers CR; Saxe D; Chen Z; Lechowicz MJ; Weisenburger DD; Bast M; Arellano ML; Bernal-Mizrachi L
  • Validation of fluorescence in situ hybridization using an analyte-specific reagent for detection of abnormalities involving the mixed lineage leukemia gene.
    Arch Pathol Lab Med Volume: 136 Page(s): 47 - 52
    01/01/2012 Authors: Saxe DF; Persons DL; Wolff DJ; Theil KS; Cytogenetics Resource Committee of the College of American Pathologists
  • College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis.
    Genet Med Volume: 13 Page(s): 765 - 769
    09/01/2011 Authors: Brothman AR; Dolan MM; Goodman BK; Park JP; Persons DL; Saxe DF; Tepperberg JH; Tsuchiya KD; Van Dyke DL; Wilson KS
  • Does pretreatment fluorescence in situ hybridization for BCR-ABL predict imatinib-associated hematologic toxicity in chronic myeloid leukemia?
    Leuk Lymphoma Volume: 52 Page(s): 1010 - 1016
    06/01/2011 Authors: Lima LM; Sampat K; Assouline S; Saxe D; Nault S; Tighiouart M; McLemore M; Arellano M; Winton E; Bernal-Mizrachi L
  • Peripheral blood monitoring of chronic myeloid leukemia during treatment with imatinib, second-line agents, and beyond.
    Cancer Volume: 117 Page(s): 1245 - 1252
    03/15/2011 Authors: Lima L; Bernal-Mizrachi L; Saxe D; Mann KP; Tighiouart M; Arellano M; Heffner L; McLemore M; Langston A; Winton E
  • The role of CD11c expression in the diagnosis of mantle cell lymphoma.
    Am J Clin Pathol Volume: 134 Page(s): 271 - 277
    08/01/2010 Authors: Kraus TS; Sillings CN; Saxe DF; Li S; Jaye DL
  • A novel flow cytometric antibody panel for distinguishing Burkitt lymphoma from CD10+ diffuse large B-cell lymphoma.
    Am J Clin Pathol Volume: 133 Page(s): 718 - 726
    05/01/2010 Authors: Schniederjan SD; Li S; Saxe DF; Lechowicz MJ; Lee KL; Terry PD; Mann KP
  • NUT midline carcinoma in a newborn with multiorgan disseminated tumor and a 2-year-old with a pancreatic/hepatic primary.
    Pediatr Dev Pathol Volume: 13 Page(s): 481 - 485
    01/01/2010 Authors: Shehata BM; Steelman CK; Abramowsky CR; Olson TA; French CA; Saxe DF; Ricketts RR; Katzenstein HM
  • Section E6.5 of the ACMG technical standards and guidelines: chromosome studies for solid tumor abnormalities.
    Genet Med Volume: 11 Page(s): 890 - 897
    12/01/2009 Authors: Cooley LD; Mascarello JT; Hirsch B; Jacky PB; Rao PN; Saxe D; Rao KW; Working Group of the American College of Medical Genetics (ACMG) Laboratory Quality Assurance Committee
  • Does pre-imatinib (IM) fluorescence in situ hybridization (FISH) predict myelosuppression and outcomes in chronic myeloid leukemia (CML)?
    Volume: 27
    05/20/2009 Authors: Lima L; Assouline SE; Saxe D; Mann K; McLemore M; Souza L; Arellano M; Winton EF; Bernal-Mizrachi L; Khoury HJ
  • Monitoring chronic myeloid leukemia (CML) response to tyrosine kinase inhibitors (TKI) and homoharringtonine (HHT) using peripheral blood (PB) fluorescence in situ hybridization (FISH) and quantitative RT-PCR (Q-PCR): Are bone marrow biopsies still needed?
    J Clin Oncol Volume: 27 Page(s): 7064
    05/20/2009 Authors: Khoury HJ; Lima L; Saxe D; Mann KP; Arellano M; Heffner L; Bernal-Mizrachi L; McLemore M; Langston A; Winton E
  • Does pre-imatinib (IM) fluorescence in situ hybridization (FISH) predict myelosuppression and outcomes in chronic myeloid leukemia (CML)?
    J Clin Oncol Volume: 27 Page(s): 7071
    05/20/2009 Authors: Lima L; Assouline SE; Saxe D; Mann K; McLemore M; Souza L; Arellano M; Winton EF; Bernal-Mizrachi L; Khoury HJ
  • Monitoring chronic myeloid leukemia (CML) response to tyrosine kinase inhibitors (TKI) and homoharringtonine (HHT) using peripheral blood (PB) fluorescence in situ hybridization (FISH) and quantitative RT-PCR (Q-PCR): Are bone marrow biopsies still needed?
    Volume: 27
    05/20/2009 Authors: Khoury HJ; Lima L; Saxe D; Mann KP; Arellano M; Heffner L; Bernal-Mizrachi L; McLemore M; Langston A; Winton E
  • A Novel Flow Cytometric Antibody Panel for Distinguishing Burkitt Lymphoma from CD10-Positive Diffuse Large B-Cell Lymphoma
    Volume: 22 Page(s): 285A - 285A
    01/01/2009 Authors: Schniederjan SD; Li S; Lechowicz MJ; Saxe DF; Terry PD; Mann KP
  • A Novel Flow Cytometric Antibody Panel for Distinguishing Burkitt Lymphoma from CD10-Positive Diffuse Large B-Cell Lymphoma
    Volume: 89 Page(s): 285A - 285A
    01/01/2009 Authors: Schniederjan SD; Li S; Lechowicz MJ; Saxe DF; Terry PD; Mann KP
  • Quality watch: Detection and reporting program to assist quality genetic testing
    Volume: 121
    01/01/2008 Authors: Saxe DF; Benkendorf J; Cowan TM; Prior TW; Richards CS; Rao KW; Watson MS
  • Quality watch: A new program of the American College of Medical Genetics laboratory quality assurance committee to enhance quality genetic testing
    Volume: 116
    01/01/2007 Authors: Saxe DF; Benkendorf J; Cowan TM; Prior TW; Richards CS; Watson MS
  • Assessment of banding resolution for a case
    Volume: 106 Page(s): 128 - 128
    01/01/2004 Authors: Saxe D; Wolff D
  • Familial case of duplication 10p without phenotypic effects.
    Volume: 73 Page(s): 308 - 308
    11/01/2003 Authors: Saxe D; Coleman K; Miley D; Yearall A; Sanders T; May K
  • Comparison of three cases of deletion and duplication in 5p.
    Volume: 71 Page(s): 295 - 295
    10/01/2002 Authors: May KM; Saxe D; Yearell A; Taylor C; Uhas K
  • Mosaicism for trisomy 21 and sex chromosome monosomy (45,X/47,XX,+21) detected prenatally.
    AMERICAN JOURNAL OF HUMAN GENETICS Volume: 65 Page(s): A368 - A368
    10/01/1999 Authors: Palaniappan SN; Yearell A; Bunke B; Boschen M; Kupke K; May KM; Saxe DF
  • Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.
    Genet Med Volume: 1 Page(s): 94 - 97
    01/01/1999 Authors: Ing PS; Van Dyke DL; Caudill SP; Reidy JA; Bice G; Bieber FR; Buchanan PD; Carroll AJ; Cheung SW; DeWald G
  • Prenatal diagnosis of two rare familial heteromorphisms
    CYTOGENETICS AND CELL GENETICS Volume: 82 Page(s): 140 - 140
    01/01/1998 Authors: Saxe DF; May KM; Trepanier AM; Talley P
  • Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant.
    Am J Med Genet Volume: 62 Page(s): 243 - 246
    03/29/1996 Authors: Roberts HE; Saxe DF; Muralidharan K; Coleman KB; Zacharias JF; Fernhoff PM
  • A 14-year survey of chromosome abnormalities seen in products of conception
    CYTOGENETICS AND CELL GENETICS Volume: 74 Page(s): 310 - 310
    01/01/1996 Authors: Saxe D; Berkowitz Z
  • Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
    Prenat Diagn Volume: 16 Page(s): 1 - 28
    01/01/1996 Authors: Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA
  • INITIAL REPORT OF PARTIAL TRISOMY-8 PRESENTING AS A RING CHROMOSOME
    AMERICAN JOURNAL OF HUMAN GENETICS Volume: 57 Page(s): 602 - 602
    10/01/1995 Authors: BLACKSTON RD; SAXE D
  • THE NATURE OF RECURRENT TRIPLOIDY IN HUMANS
    AMERICAN JOURNAL OF HUMAN GENETICS Volume: 57 Page(s): 689 - 689
    10/01/1995 Authors: PRIEST JH; ADAMS WR; SANFORDHANNA J; HOBART HH; SAXE DF; SANDERS T; MCGAVRAN L; PERSZYK AA; SPECTOR EB; STONE JF
  • A UNIQUE MOSAICISM OF TETRAPLOIDY AND TRISOMY-8 IN A LIVEBORN
    CYTOGENETICS AND CELL GENETICS Volume: 71 Page(s): 395 - 395
    01/01/1995 Authors: SAXE D; ROBERTS H; MURALIDHARAN K; COLEMAN K; ZACHARIAS J; FERNHOFF P
  • CONGENITAL CUTANEOUS VASCULAR-LESIONS REPORTED FROM THE COOK OB-GYN CATHETER MULTICENTER CHORIONIC VILLUS SAMPLING (CVS) TRIAL
    AMERICAN JOURNAL OF HUMAN GENETICS Volume: 53 Page(s): 1795 - 1795
    09/01/1993 Authors: FILKINS K; BLAKEMORE K; LUTHY D; PRIEST J; KOROTKIN J; SAXE D; PLATT L; CARLSON D; MEDEARIS A; VERP M
  • CHARACTERIZATION OF UNUSUAL CHROMOSOME VARIANTS UTILIZING FLUORESCENCE IN-SITU HYBRIDIZATION
    CYTOGENETICS AND CELL GENETICS Volume: 63 Page(s): 255 - 255
    01/01/1993 Authors: SAXE DF; HELFRICK DH; MAY KM
  • DNA methylation represses FMR-1 transcription in fragile X syndrome.
    Hum Mol Genet Volume: 1 Page(s): 397 - 400
    09/01/1992 Authors: Sutcliffe JS; Nelson DL; Zhang F; Pieretti M; Caskey CT; Saxe D; Warren ST
  • Confirmation of CVS mosaicism.
    Prenat Diagn Volume: 12 Page(s): 626 - 627
    07/01/1992 Authors: May KM; Saxe DF; Priest JH
  • AN UNUSUAL MOSAIC KARYOTYPE IN A PATIENT WITH R(18) SYNDROME
    AMERICAN JOURNAL OF HUMAN GENETICS Volume: 49 Page(s): 274 - 274
    10/01/1991 Authors: SAXE DF; MAY KM; BLACKSTON RD
  • Mapping and gene order of U1 small nuclear RNA, endogenous viral env sequence, amylase, and alcohol dehydrogenase-3 on mouse chromosome 3.
    Somat Cell Mol Genet Volume: 14 Page(s): 133 - 142
    03/01/1988 Authors: Blatt C; Saxe D; Marzluff WF; Lobo S; Nesbitt MN; Simon MI
  • Assignment of the Ly-6--Ril-1--Sis--H-30--Pol-5/Xmmv-72--Ins-3--Krt-1--Int-1 --Gdc-1 region to mouse chromosome 15.
    Immunogenetics Volume: 25 Page(s): 361 - 372
    01/01/1987 Authors: Meruelo D; Rossomando A; Scandalis S; D'Eustachio P; Fournier RE; Roop DR; Saxe D; Blatt C; Nesbitt MN
  • Aniridia and Wilms' tumor in a child constitutionally mosaic for 11p-;12q+: a new chromosomal change also present in Wilms' tumor cells of the blastema type.
    Hum Pathol Volume: 17 Page(s): 1074 - 1077
    10/01/1986 Authors: Trigg ME; Padilla-Nash H; Saxe D; Friedman A; Uehling D; France T; Gilbert E
  • Effect of rabbit antimouse brain serum on marrow cells capable of curing W/Wv mice.
    Exp Hematol Volume: 13 Page(s): 581 - 585
    07/01/1985 Authors: Saxe DF; Boggs DR; Monette FC; Boggs SS
  • Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion.
    Proc Natl Acad Sci U S A Volume: 82 Page(s): 2344 - 2348
    04/01/1985 Authors: Kant JA; Fornace AJ; Saxe D; Simon MI; McBride OW; Crabtree GR
  • Localization of the human myelin basic protein gene (MBP) to region 18q22----qter by in situ hybridization.
    Cytogenet Cell Genet Volume: 39 Page(s): 246 - 249
    01/01/1985 Authors: Saxe DF; Takahashi N; Hood L; Simon MI
  • The T cell receptor beta chain genes are located on chromosome 6 in mice and chromosome 7 in humans.
    Cell Volume: 37 Page(s): 1091 - 1099
    07/01/1984 Authors: Caccia N; Kronenberg M; Saxe D; Haars R; Bruns GA; Goverman J; Malissen M; Willard H; Yoshikai Y; Simon M
  • Transplantation of chromosomally marked syngeneic marrow cells into mice not subjected to hematopoietic stem cell depletion.
    Exp Hematol Volume: 12 Page(s): 277 - 283
    05/01/1984 Authors: Saxe DF; Boggs SS; Boggs DR
  • Aging and hematopoiesis. II. The ability of bone marrow cells from young and aged mice to cure and maintain cure in W/Wv.
    Transplantation Volume: 37 Page(s): 300 - 306
    03/01/1984 Authors: Boggs DR; Saxe DF; Boggs SS
  • Trisomy of chromosome 6.15 is not necessary for proliferation of AKR(Rb6.15)1Ald lymphoma cells.
    Cancer Genet Cytogenet Volume: 9 Page(s): 151 - 166
    06/01/1983 Authors: Boggs SS; Patrene KD; Downer WR; Schwartz GN; Saxe DF
  • Hematopoietic stem cells with high proliferative potential. Assay of their concentration in marrow by the frequency and duration of cure of W/Wv mice.
    J Clin Invest Volume: 70 Page(s): 242 - 253
    08/01/1982 Authors: Boggs DR; Boggs SS; Saxe DF; Gress LA; Canfield DR
  • In vitro clonal assay for human metastatic melanoma cells.
    Stem Cells (1981) Volume: 1 Page(s): 61 - 72
    01/01/1981 Authors: Meyskens FL; Soehnlen BJ; Saxe DF; Casey WJ; Salmon SE
  • Biological and biochemical properties of a human uveal melanocyte-derived cell line.
    In Vitro Volume: 16 Page(s): 775 - 780
    09/01/1980 Authors: Meyskens FL; Berglund EB; Saxe DF; Fuller BB; Pacelli LZ; Hall JD; Ray CG
  • ABNORMAL CHROMOSOMAL SEGREGATION IN HUMAN-MELANOMA
    AMERICAN JOURNAL OF HUMAN GENETICS Volume: 31 Page(s): A108 - A108
    01/01/1979 Authors: SAXE DF; MEYSKENS FL
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