Gordana Raca

Gordana Raca

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Gordana Raca

Gordana Raca

Publications by authors named "Gordana Raca"

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A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants.

Cold Spring Harb Mol Case Stud 2019 Apr 1;5(2). Epub 2019 Apr 1.

Center for Personalized Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California 90027, USA.

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http://dx.doi.org/10.1101/mcs.a003756DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549575PMC
April 2019

OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.

J Mol Diagn 2018 11 20;20(6):765-776. Epub 2018 Aug 20.

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California; Department of Pathology, Keck School of Medicine of USC, Los Angeles, California.

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https://linkinghub.elsevier.com/retrieve/pii/S15251578183010
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http://dx.doi.org/10.1016/j.jmoldx.2018.06.009DOI Listing
November 2018

Myeloid lineage switch following chimeric antigen receptor T-cell therapy in a patient with TCF3-ZNF384 fusion-positive B-lymphoblastic leukemia.

Pediatr Blood Cancer 2018 09 24;65(9):e27265. Epub 2018 May 24.

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.

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http://doi.wiley.com/10.1002/pbc.27265
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http://dx.doi.org/10.1002/pbc.27265DOI Listing
September 2018

A neoplasm with FIP1L1-PDGFRA fusion presenting as pediatric T-cell lymphoblastic leukemia/lymphoma without eosinophilia.

Cancer Genet 2017 Oct 3;216-217:91-99. Epub 2017 Aug 3.

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California. Electronic address:

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http://dx.doi.org/10.1016/j.cancergen.2017.07.007DOI Listing
October 2017

Congenital B-lymphoblastic leukemia with a cryptic MLL rearrangement and post-treatment evolution to mixed phenotype acute leukemia.

Leuk Res Rep 2016 2;6:29-32. Epub 2016 Aug 2.

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd., Los Angeles, CA 90027, USA.

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http://dx.doi.org/10.1016/j.lrr.2016.07.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982915PMC
August 2016

MYC Amplification in Angiosarcoma Arising from an Arteriovenous Graft Site.

Case Rep Pathol 2015 24;2015:537297. Epub 2015 Nov 24.

Department of Pathology, University of Chicago, 5841 S Maryland Avenue, MC 6161, Chicago, IL 60637, USA.

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http://dx.doi.org/10.1155/2015/537297DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670641PMC
December 2015

RCSD1-ABL1 Translocation Associated with IKZF1 Gene Deletion in B-Cell Acute Lymphoblastic Leukemia.

Case Rep Hematol 2015 27;2015:353247. Epub 2015 Oct 27.

Combined Military Hospital, Kharian 50090, Pakistan.

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http://dx.doi.org/10.1155/2015/353247DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639642PMC
November 2015

Predicting Prognosis in Chronic Lymphocytic Leukemia in the Contemporary Era.

JAMA Oncol 2015 Oct;1(7):965-74

Division of Genomic and Molecular Pathology, Department of Pathology, University of Chicago, Chicago, Illinois.

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https://pathology.uchicago.edu/sites/pathology.uchicago.edu/
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http://oncology.jamanetwork.com/article.aspx?doi=10.1001/jam
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http://dx.doi.org/10.1001/jamaoncol.2015.0779DOI Listing
October 2015

Prognosis in Chronic Lymphocytic Leukemia-Reply.

JAMA Oncol 2015 Oct;1(7):988-9

Division of Genomic and Molecular Pathology, Department of Pathology, University of Chicago, Chicago, Illinois.

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http://dx.doi.org/10.1001/jamaoncol.2015.2532DOI Listing
October 2015

MLL Rearrangment and EVI1 Deletion in BCR/ABL1 Positive Chronic Myeloid Leukemia.

J Assoc Genet Technol 2013 ;39(4):190-4

Cancer Cytogenetics, Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL.

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June 2015

RCSD1-ABL2 fusion resulting from a complex chromosomal rearrangement in high-risk B-cell acute lymphoblastic leukemia.

Leuk Lymphoma 2015 Apr 26;56(4):1145-7. Epub 2014 Aug 26.

Department of Medicine, The University of Chicago , Chicago, IL , USA.

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http://dx.doi.org/10.3109/10428194.2014.951851DOI Listing
April 2015

MECP2 duplication: possible cause of severe phenotype in females.

Am J Med Genet A 2014 Apr 23;164A(4):1029-34. Epub 2014 Jan 23.

Department of Pediatrics, University of Wisconsin, Madison, Wisconsin.

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http://dx.doi.org/10.1002/ajmg.a.36380DOI Listing
April 2014

The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.

Cancer Genet 2013 Sep-Oct;206(9-10):317-26. Epub 2013 Oct 24.

University of Wisconsin Cytogenetic Services, Wisconsin State Laboratory of Hygiene, Madison, WI, USA; Department of Pediatrics, University of Wisconsin-Madison, Madison, WI, USA.

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http://dx.doi.org/10.1016/j.cancergen.2013.09.001DOI Listing
January 2014

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

J Neurodev Disord 2013 Oct 2;5(1):29. Epub 2013 Oct 2.

Waisman Center, University of Wisconsin-Madison, 1500 Highland Avenue, Madison, WI, 53705, USA.

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http://dx.doi.org/10.1186/1866-1955-5-29DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851280PMC
October 2013

A Unique "Composite" PTLD with Diffuse Large B-Cell and T/Anaplastic Large Cell Lymphoma Components Occurring 17 Years after Transplant.

Case Rep Hematol 2013 7;2013:386147. Epub 2013 May 7.

Department of Pathology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.

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http://dx.doi.org/10.1155/2013/386147DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662176PMC
June 2013

Two cases of localized neuroblastoma with multiple segmental chromosomal alterations and metastatic progression.

Pediatr Blood Cancer 2013 Feb 19;60(2):332-5. Epub 2012 Sep 19.

Department of Neuro-Oncology, Dana Farber Cancer Institute/Boston Children's Hospital, Boston, Massachusetts, USA.

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http://doi.wiley.com/10.1002/pbc.24311
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http://dx.doi.org/10.1002/pbc.24311DOI Listing
February 2013

Acute myeloid leukemia: the challenge of unfavorable cytogenetics.

Oncology (Williston Park) 2012 Aug;26(8):724, 726-7

Section of Hematology/Oncology, Department of Medicine and Comprehensive Cancer Center, The University of Chicago, Chicago, Illinois, USA.

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August 2012

Typical renal-coloboma syndrome phenotype in a patient with a submicroscopic deletion of the PAX2 gene.

Am J Med Genet A 2012 Jun 11;158A(6):1437-41. Epub 2012 May 11.

Institute of Biological Systems and Genetics Research, Lithuanian University of Health Sciences, Kaunas, Lithuania.

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http://dx.doi.org/10.1002/ajmg.a.35342DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098919PMC
June 2012

DNA methylation assay for X-chromosome inactivation in female human iPS cells.

Stem Cell Rev Rep 2011 Nov;7(4):969-75

Clinical Genetic Laboratories, Wisconsin State Laboratory of Hygiene, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA.

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http://dx.doi.org/10.1007/s12015-011-9238-6DOI Listing
November 2011

Chromosomal abnormalities in 2 cases of testicular failure.

J Androl 2011 May-Jun;32(3):226-31. Epub 2010 Oct 21.

Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, USA.

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http://dx.doi.org/10.2164/jandrol.110.010280DOI Listing
July 2011

Array comparative genomic hybridization analysis in patients with anophthalmia, microphthalmia, and coloboma.

Genet Med 2011 May;13(5):437-42

UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

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http://dx.doi.org/10.1097/GIM.0b013e318204cfd2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237064PMC
May 2011

Next generation sequencing in research and diagnostics of ocular birth defects.

Mol Genet Metab 2010 Jun 15;100(2):184-92. Epub 2010 Mar 15.

UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, 465 Henry Mall, Madison, WI 53706, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671921000095
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http://dx.doi.org/10.1016/j.ymgme.2010.03.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871986PMC
June 2010

Mild clinical presentation in a child with prenatally diagnosed 45,X/47,XX,+18 mosaicism.

Am J Med Genet A 2009 Nov;149A(11):2588-92

Department of Obstetrics and Gynecology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53715-1599, USA.

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http://dx.doi.org/10.1002/ajmg.a.33084DOI Listing
November 2009

Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth.

Am J Med Genet A 2009 Nov;149A(11):2437-43

UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, Madison, Wisconsin 53706, USA.

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http://dx.doi.org/10.1002/ajmg.a.33083DOI Listing
November 2009

Progressive dystonia in a 12-year-old boy.

Eur J Paediatr Neurol 2003 ;7(2):85-8

Department of Paediatrics and Paediatric Neurology, University of Essen, Germany.

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July 2003