Publications by authors named "Roger Schultz"

52Publications

Genomic microarray analysis on formalin-fixed paraffin-embedded material for uveal melanoma prognostication.

Authors:
Eugen C Minca Raymond R Tubbs Bryce P Portier Zhen Wang Christopher Lanigan Mary E Aronow Pierre L Triozzi Arun Singh James R Cook Yogen Saunthararajah Thomas P Plesec Lynn Schoenfield Victoria Cawich Scott Sulpizio Roger A Schultz

Cancer Genet 2014 Jul-Aug;207(7-8):306-15. Epub 2014 Aug 29.

Signature Genomics Laboratories, Perkin Elmer, Spokane, WA, USA. Electronic address:

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January 2015

Experience using a rapid assay for aneuploidy and microdeletion/microduplication detection in over 2,900 prenatal specimens.

Authors:
Jill A Rosenfeld S Anne Morton Cathryn Hummel Scott G Sulpizio Lisa D McDaniel Roger A Schultz Beth S Torchia J Britt Ravnan Jay W Ellison Allan J Fisher

Fetal Diagn Ther 2014 8;36(3):231-41. Epub 2014 Aug 8.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Wash., USA.

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June 2015

Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndrome.

Authors:
Justin Overhoff Marina M Rabideau Lynne M Bird Daniela N Schweitzer Karla Haynes Roger A Schultz Lisa G Shaffer Jill A Rosenfeld Jay W Ellison

Am J Med Genet A 2014 Jan 20;164A(1):259-63. Epub 2013 Nov 20.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington.

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January 2014

Characterization of a case of follicular lymphoma transformed into B-lymphoblastic leukemia.

Authors:
Yi Ning Aubry Foss Amy S Kimball Nicholas Neill Tricia Matz Roger Schultz

Mol Cytogenet 2013 Aug 28;6(1):34. Epub 2013 Aug 28.

Signature Genomic Laboratories/Perkin Elmer, 2820 N Astor, Spokane, WA, 99207, USA.

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August 2013

Value of oligonucleotide-based array comparative genomic hybridization for diagnosis of acute promyelocytic leukemia in a patient negative for t(15;17)(q24.1;q21.2)/promyelocytic leukemia-retinoic acid receptor, alpha by conventional cytogenetics and fluorescence in situ hybridization.

Authors:
Khaled Alayed L Jeffrey Medeiros Roger A Schultz Jorge Cortes Gary Lu Carlos E Bueso-Ramos Sergej Konoplev

Clin Lymphoma Myeloma Leuk 2013 Aug 14;13(4):507-10. Epub 2013 Jun 14.

Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

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August 2013

Cryptic chromosome abnormalities in a patient with mixed phenotype acute leukemia.

Authors:
Yi Ning Marilyn L Slovak Roger A Schultz Ivana Gojo Maria R Baer

Leuk Lymphoma 2014 Mar 10;55(3):680-2. Epub 2013 Jul 10.

Department of Pathology, Johns Hopkins University , Baltimore, MD , USA.

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March 2014

The use of cytogenetic microarrays in myelodysplastic syndrome characterization.

Authors:
Lisa G Shaffer Blake C Ballif Roger A Schultz

Methods Mol Biol 2013 ;973:69-85

Signature Genomic Laboratories, PerkinElmer Inc., Spokane, WA, USA.

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July 2013

MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways.

Authors:
Alex R Paciorkowski Ryan N Traylor Jill A Rosenfeld Jacqueline M Hoover Catharine J Harris Susan Winter Yves Lacassie Martin Bialer Allen N Lamb Roger A Schultz Elizabeth Berry-Kravis Brenda E Porter Marni Falk Anu Venkat Rena J Vanzo Julie S Cohen Ali Fatemi William B Dobyns Lisa G Shaffer Blake C Ballif Eric D Marsh

Neurogenetics 2013 May 7;14(2):99-111. Epub 2013 Feb 7.

Department of Neurology, Pediatrics, and Biomedical Genetics, Center for Neural Development & Disease, University of Rochester Medical Center, 601 Elmwood Ave, Rochester, NY 14642, USA.

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May 2013

Modified array-based comparative genomic hybridization detects cryptic and variant PML-RARA rearrangements in acute promyelocytic leukemia lacking classic translocations.

Authors:
Aaron M Gruver Heesun J Rogers James R Cook Blake C Ballif Roger A Schultz Jacqueline R Batanian Mark J Fesler Raymond R Tubbs

Diagn Mol Pathol 2013 Mar;22(1):10-21

Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH 44195, USA.

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March 2013

The use of new technologies in the detection of balanced translocations in hematologic disorders.

Authors:
Lisa G Shaffer Roger A Schultz Blake C Ballif

Curr Opin Genet Dev 2012 Jun 13;22(3):264-71. Epub 2012 Feb 13.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, WA, USA.

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June 2012

Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.

Authors:
Allen N Lamb Jill A Rosenfeld Nicholas J Neill Michael E Talkowski Ian Blumenthal Santhosh Girirajan Debra Keelean-Fuller Zheng Fan Jill Pouncey Cathy Stevens Loren Mackay-Loder Deborah Terespolsky Patricia I Bader Kenneth Rosenbaum Stephanie E Vallee John B Moeschler Roger Ladda Susan Sell Judith Martin Shawnia Ryan Marilyn C Jones Rocio Moran Amy Shealy Suneeta Madan-Khetarpal Juliann McConnell Urvashi Surti Andrée Delahaye Bénédicte Heron-Longe Eva Pipiras Brigitte Benzacken Sandrine Passemard Alain Verloes Bertrand Isidor Cedric Le Caignec Gwen M Glew Kent E Opheim Maria Descartes Evan E Eichler Cynthia C Morton James F Gusella Roger A Schultz Blake C Ballif Lisa G Shaffer

Hum Mutat 2012 Apr;33(4):728-40

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington 99207, USA.

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April 2012

NF1 microduplications: identification of seven nonrelated individuals provides further characterization of the phenotype.

Authors:
Kimberly J Moles Gordon C Gowans Satyanarayana Gedela David Beversdorf Arthur Yu Laurie H Seaver Roger A Schultz Jill A Rosenfeld Beth S Torchia Lisa G Shaffer

Genet Med 2012 May 12;14(5):508-14. Epub 2012 Jan 12.

Signature Genomic Laboratories, PerkinElmer Inc., Spokane, Washington, USA.

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May 2012

Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromes.

Authors:
Kathryn A Kolquist Roger A Schultz Aubry Furrow Theresa C Brown Jin-Yeong Han Lynda J Campbell Meaghan Wall Marilyn L Slovak Lisa G Shaffer Blake C Ballif

Cancer Genet 2011 Nov;204(11):603-28

Sacred Heart Medical Center, Spokane, WA, USA.

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November 2011

Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis.

Authors:
Kathryn A Kolquist Roger A Schultz Marilyn L Slovak Lisa D McDaniel Theresa C Brown Raymond R Tubbs James R Cook Karl S Theil Victoria Cawich Caitlin Valentin Sara Minier Nicholas J Neill Steve Byerly S Annie Morton Trilochan Sahoo Blake C Ballif Lisa G Shaffer

Mol Cytogenet 2011 Nov 16;4:25. Epub 2011 Nov 16.

Signature Genomic Laboratories, PerkinElmer Inc,, 2820 North Astor Street, Spokane, WA, 99207, USA.

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November 2011

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.

Authors:
Blake C Ballif Jill A Rosenfeld Ryan Traylor Aaron Theisen Patricia I Bader Roger L Ladda Susan L Sell Michelle Steinraths Urvashi Surti Marianne McGuire Shelley Williams Sandra A Farrell James Filiano Rhonda E Schnur Lauren B Coffey Raymond C Tervo Tracy Stroud Michael Marble Michael Netzloff Kristen Hanson Arthur S Aylsworth J S Bamforth Deepti Babu Dmitriy M Niyazov J Britt Ravnan Roger A Schultz Allen N Lamb Beth S Torchia Bassem A Bejjani Lisa G Shaffer

Hum Genet 2012 Jan 29;131(1):145-56. Epub 2011 Jul 29.

Signature Genomic Laboratories, Spokane, WA 99207, USA.

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January 2012

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

Authors:
Trilochan Sahoo Aaron Theisen Jill A Rosenfeld Allen N Lamb J Britt Ravnan Roger A Schultz Beth S Torchia Nicholas Neill Ian Casci Bassem A Bejjani Lisa G Shaffer

Genet Med 2011 Oct;13(10):868-80

Signature Genomic Laboratories, 2820 N. Astor St., Spokane, WA 99207, USA.

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October 2011

Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes.

Authors:
Jill A Rosenfeld Joanne Milisa Drautz Carol L Clericuzio Tom Cushing Salmo Raskin Judith Martin Raymond C Tervo Jose A Pitarque Dorota M Nowak Justyna A Karolak Allen N Lamb Roger A Schultz Blake C Ballif Bassem A Bejjani Marzena Gajecka Lisa G Shaffer

Am J Med Genet A 2011 Aug 8;155A(8):1906-16. Epub 2011 Jul 8.

Signature Genomic Laboratories, Spokane, Washington, USA.

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August 2011

The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.

Authors:
Lisa G Shaffer Justine Coppinger S Annie Morton Sarah Alliman Jessica Burleson Ryan Traylor Cathryn Walker Steve Byerly Allen N Lamb Roger Schultz J Britt Ravnan Catherine D Kashork Beth S Torchia Scott Sulpizio Kyle Sundin Mack Schermer Karl Adler Stephanie Dallaire Blake C Ballif

Prenat Diagn 2011 Aug 21;31(8):778-87. Epub 2011 Jun 21.

Signature Genomic Laboratories, Spokane, WA 99207, USA.

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August 2011

Activated NOTCH2 is overexpressed in hepatoblastomas: an immunohistochemical study.

Authors:
Jason B Litten Tina T-L Chen Roger Schultz Karl Herman Jessica Comstock Joshua Schiffman Gail E Tomlinson Dinesh Rakheja

Pediatr Dev Pathol 2011 Sep-Oct;14(5):378-83. Epub 2011 Jun 3.

Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA.

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February 2012

Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.

Authors:
Nicholas J Neill Blake C Ballif Allen N Lamb Sumit Parikh J Britt Ravnan Roger A Schultz Beth S Torchia Jill A Rosenfeld Lisa G Shaffer

Genome Res 2011 Apr 7;21(4):535-44. Epub 2011 Mar 7.

Signature Genomic Laboratories, Spokane, WA 99207, USA.

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April 2011