Publications by authors named "Daynna J Wolff"

53Publications

Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia.

Cancer Genet 2020 Aug 7;246-247:44-47. Epub 2020 Aug 7.

Medical University of South Carolina, Department of Pathology and Laboratory Medicine, 165 Ashley Ave, MSC 908, Charleston, SC 29425, United States. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.cancergen.2020.08.004DOI Listing
August 2020

Assessing Genomic Copy Number Alterations as Best Practice for Renal Cell Neoplasia: An Evidence-Based Review from the Cancer Genomics Consortium Workgroup.

Cancer Genet 2020 Jun 1;244:40-54. Epub 2020 May 1.

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, 165 Ashley Avenue, MSC 908, Charleston, SC 29425.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.cancergen.2020.04.004DOI Listing
June 2020

Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.

Genes Chromosomes Cancer 2020 07 26;59(7):422-427. Epub 2020 Mar 26.

Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gcc.22842DOI Listing
July 2020

Whole-Genome Single Nucleotide Polymorphism Microarray for Copy Number and Loss of Heterozygosity Analysis in Tumors.

Methods Mol Biol 2019 ;1908:89-111

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-1-4939-9004-7_7DOI Listing
June 2019

Authors' Reply.

J Mol Diagn 2018 01;20(1):125-126

Interpretation of Sequence Variants in Somatic Conditions Working Group of the Clinical Practice Committee, Association for Molecular Pathology, Bethesda, Maryland; University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jmoldx.2017.11.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818630PMC
January 2018

First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination.

Pediatr Dev Pathol 2018 Nov-Dec;21(6):561-567. Epub 2017 Dec 7.

1 Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1093526617744714DOI Listing
December 2018

Urothelial carcinoma of donor origin in a kidney transplant patient.

J Immunother Cancer 2016 18;4:63. Epub 2016 Oct 18.

Division of Hematology and Oncology, Medical University of South Carolina, 173 Ashley Ave, Suite 102 BSB, Charleston, SC 29425 USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s40425-016-0167-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067888PMC
February 2018

Comparison Between HER2, Estrogen Receptors and Progesterone Receptors in Primary Breast Carcinomas and Matched Lymph Node Metastases.

Turk Patoloji Derg 2016 ;32(3):178-85

Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, NASHVILLE, TN, UNITED STATES.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5146/tjpath.2015.01354DOI Listing
April 2017

Chromothripsis in Two Patients With Renal Cell Carcinoma: A Case Series.

Clin Genitourin Cancer 2017 02 23;15(1):e137-e143. Epub 2016 Jun 23.

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clgc.2016.06.005DOI Listing
February 2017

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.

Authors:
Przemyslaw Szafranski Tomasz Gambin Avinash V Dharmadhikari Kadir Caner Akdemir Shalini N Jhangiani Jennifer Schuette Nihal Godiwala Svetlana A Yatsenko Jessica Sebastian Suneeta Madan-Khetarpal Urvashi Surti Rosanna G Abellar David A Bateman Ashley L Wilson Melinda H Markham Jill Slamon Fernando Santos-Simarro María Palomares Julián Nevado Pablo Lapunzina Brian Hon-Yin Chung Wai-Lap Wong Yoyo Wing Yiu Chu Gary Tsz Kin Mok Eitan Kerem Joel Reiter Namasivayam Ambalavanan Scott A Anderson David R Kelly Joseph Shieh Taryn C Rosenthal Kristin Scheible Laurie Steiner M Anwar Iqbal Margaret L McKinnon Sara Jane Hamilton Kamilla Schlade-Bartusiak Dawn English Glenda Hendson Elizabeth R Roeder Thomas S DeNapoli Rebecca Okashah Littlejohn Daynna J Wolff Carol L Wagner Alison Yeung David Francis Elizabeth K Fiorino Morris Edelman Joyce Fox Denise A Hayes Sandra Janssens Elfride De Baere Björn Menten Anne Loccufier Lieve Vanwalleghem Philippe Moerman Yves Sznajer Amy S Lay Jennifer L Kussmann Jasneek Chawla Diane J Payton Gael E Phillips Erwin Brosens Dick Tibboel Annelies de Klein Isabelle Maystadt Richard Fisher Neil Sebire Alison Male Maya Chopra Jason Pinner Girvan Malcolm Gregory Peters Susan Arbuckle Melissa Lees Zoe Mead Oliver Quarrell Richard Sayers Martina Owens Charles Shaw-Smith Janet Lioy Eileen McKay Nicole de Leeuw Ilse Feenstra Liesbeth Spruijt Frances Elmslie Timothy Thiruchelvam Carlos A Bacino Claire Langston James R Lupski Partha Sen Edwina Popek Paweł Stankiewicz

Hum Genet 2016 May 12;135(5):569-586. Epub 2016 Apr 12.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm. R809, Houston, TX, 77030, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-016-1655-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518754PMC
May 2016

"Low-Fat" Pseudoangiomatous Spindle Cell Lipoma: A Rare Variant With Loss of 13q14 Region.

Am J Dermatopathol 2015 Dec;37(12):920-3

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DAD.0000000000000286DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894806PMC
December 2015

Evaluation of urovysion and cytology for bladder cancer detection: a study of 1835 paired urine samples with clinical and histologic correlation.

Cancer Cytopathol 2013 Oct 25;121(10):591-7. Epub 2013 Jun 25.

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/cncy.21327DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800248PMC
October 2013

American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders.

Genet Med 2013 Jun 25;15(6):484-94. Epub 2013 Apr 25.

Department of Pathology and Laboratory Medicine, Children's Mercy Hospital and University of Missouri Medical School, Kansas City, Missouri, USA.

View Article

Download full-text PDF

Source
http://www.nature.com/articles/gim201349
Publisher Site
http://dx.doi.org/10.1038/gim.2013.49DOI Listing
June 2013

Cytogenetics caseload survey summary 2012.

J Assoc Genet Technol 2012 ;38(4):199-202

Kaiser Permanente Northwest, Portland, OR.

View Article

Download full-text PDF

Source
November 2012

Association of age with fluorescence in situ hybridization abnormalities in multiple myeloma reveals higher rate of IGH translocations among older patients.

Leuk Lymphoma 2012 Dec 31;53(12):2444-8. Epub 2012 May 31.

Division of Hematology/Oncology, Department of Medicine, Medical University of South Carolina, Charleston, SC, USA.

View Article

Download full-text PDF

Source
http://www.tandfonline.com/doi/full/10.3109/10428194.2012.69
Publisher Site
http://dx.doi.org/10.3109/10428194.2012.691483DOI Listing
December 2012

Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia.

Cancer Genet 2011 Dec;204(12):654-65

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, USA.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S221077621100305
Publisher Site
http://dx.doi.org/10.1016/j.cancergen.2011.10.012DOI Listing
December 2011

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 2012 Jan;136(1):47-52

Department of Pathology and Laboratory Medicine, Emory School of Medicine, Atlanta, Georgia 30022, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5858/arpa.2010-0645-SADOI Listing
January 2012

The utility of fluorescence in situ hybridization (FISH) analysis in diagnosing graft versus host disease following orthotopic liver transplant.

Ann Clin Lab Sci 2011 ;41(2):188-92

Department of Pathology, University of Arkansas for Medical Sciences, 4301 W. Markham Street, Little Rock, AR 72205-7199, USA.

View Article

Download full-text PDF

Source
January 2012

Mitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosis.

Arch Pathol Lab Med 2011 Jul;135(7):925-34

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1043/2010-0356-RAR.1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158670PMC
July 2011

Laboratory guideline for Turner syndrome.

Genet Med 2010 Jan;12(1):52-5

Department of Pathology and Laboratory Medicine, University of South Carolina, Charleston, South Carolina 29425, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/GIM.0b013e3181c684b2DOI Listing
January 2010

Tetraploidy and 5q deletion in myelodysplastic syndrome: a case report.

Cancer Genet Cytogenet 2008 May;183(1):64-8

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, 165 Ashley Ave, Ste. 309, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S016546080800098
Publisher Site
http://dx.doi.org/10.1016/j.cancergencyto.2008.01.022DOI Listing
May 2008

The Prothrombin 20209C>T Sequence Variant: To Test or Not to Test.

J Assoc Genet Technol 2007 ;33(2):1-3

Department of Pathology and Laboratory Medicine.

View Article

Download full-text PDF

Source
July 2011

Guidance for fluorescence in situ hybridization testing in hematologic disorders.

J Mol Diagn 2007 Apr;9(2):134-43

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2353/jmoldx.2007.060128DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867444PMC
April 2007

HER2 testing: a review of detection methodologies and their clinical performance.

Expert Rev Mol Diagn 2007 Jan;7(1):53-64

University of South Carolina, Department of Pathology and Laboratory Medicine, 165 Ashley Avenue, Suite 309, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
http://www.tandfonline.com/doi/full/10.1586/14737159.7.1.53
Publisher Site
http://dx.doi.org/10.1586/14737159.7.1.53DOI Listing
January 2007

Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci.

Cancer Genet Cytogenet 2006 Jul;168(1):77-9

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S016546080600101
Publisher Site
http://dx.doi.org/10.1016/j.cancergencyto.2006.02.004DOI Listing
July 2006

Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screen.

J Mol Diagn 2006 Feb;8(1):137-40

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, 165 Ashley Ave., Suite 309, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S15251578106030
Publisher Site
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867569PMC
http://dx.doi.org/10.2353/jmoldx.2006.050065DOI Listing
February 2006

Fluorescence in situ hybridization for detecting transitional cell carcinoma: implications for clinical practice.

BJU Int 2005 Dec;96(9):1280-5

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1464-410X.2005.05826.xDOI Listing
December 2005

Establishment of epidermal cell lines derived from the skin of the Atlantic bottlenose dolphin (Tursiops truncatus).

Anat Rec A Discov Mol Cell Evol Biol 2005 Dec;287(2):1246-55

Department of Neurosciences and Neuroscience Institute, Medical University of South Carolina, Charleston, South Carolina 29403, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ar.a.20266DOI Listing
December 2005

Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalities.

Genet Med 2005 Sep;7(7):509-13

ACMG Laboratory Quality Assurance Cytogenetic Subcommittee, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/01.gim.0000177416.12323.58DOI Listing
September 2005

Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranes.

Pediatr Dev Pathol 2005 Jan-Feb;8(1):115-23. Epub 2004 Dec 6.

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, 165 Ashley Avenue, Suite 309, Charleston, SC 29425, USA.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s10024-003-9098-4
Publisher Site
http://dx.doi.org/10.1007/s10024-003-9098-4DOI Listing
June 2005

Utility of Interphase FISH Panels for Routine Clinical Cytogenetic Evaluation of Chronic Lymphocytic Leukemia and Multiple Myeloma.

J Assoc Genet Technol 2004 ;30(3):77-81

Department of Pathology and Medical University of South Carolina (MUSC) Laboratory Medicine, 165 Ashley Avenue, Suite 309, Charleston, SC 29425.

View Article

Download full-text PDF

Source
January 2004

Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.

Pediatr Res 2003 May 5;53(5):744-8. Epub 2003 Mar 5.

Department of Pediatrics, L.M. Bargeron Division of Pediatric Cardiology, University of Alabama at Birmingham, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1203/01.PDR.0000059750.17002.B6DOI Listing
May 2003

Prevalence of aneuploidies in South Carolina in the 1990s.

Genet Med 2002 May-Jun;4(3):131-5

Greenwood Genetic Center, 1 Gregor Mendel Circle, Greenwood, SC 29646, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00125817-200205000-00006DOI Listing
August 2003

A testing algorithm for determination of HER2 status in patients with breast cancer.

Ann Clin Lab Sci 2002 ;32(1):3-11

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston 29425, USA.

View Article

Download full-text PDF

Source
August 2002

Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion.

Genet Med 2002 Jan-Feb;4(1):10-4

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina 29425, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00125817-200201000-00002DOI Listing
April 2002