J. Sawyer

J. Sawyer, D. Parham, J. Bridge, 2004, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

A Biochemical Marker for Preosseous Fibroproliferative Lesions in Patients With Fibrodysplasia Ossificans Progressiva

J. Folkman, M. Zasloff, J. Sawyer, 2003 .

Literature-curated marker genes References

J. Mackey, J. Sawyer, G. Baldwin, 2015 .

Dose-dense and less dose-intense total therapy 5 for gene expression profiling-defined high-risk multiple myeloma

J. Crowley, B. Barlogie, E. Tian, 2016, Blood cancer journal.

Primary plasma cell leukemia: clinical and laboratory presentation, gene-expression profiling, and clinical outcome with Total Therapy protocols

B. Barlogie, J. Shaughnessy, J. Sawyer, 2012, Leukemia.

A novel reciprocal chromosome translocation t(11;22)(p13;q12) in an intraabdominal desmoplastic small round-cell tumor.

J. Sawyer, J. Lewis, A. Tryka, 1992, The American journal of surgical pathology.

Secondary acute myelogenous leukemia following safe exposure to etoposide.

J. Sawyer, K. Stine, D. Becton, 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Unique role of cytogenetics in the prognosis of patients with myeloma receiving high-dose therapy and autotransplants.

B. Barlogie, S. Jagannath, D. Siegel, 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Cytogenetic findings in 200 patients with multiple myeloma.

B. Barlogie, S. Jagannath, J. Sawyer, 1995, Cancer genetics and cytogenetics.

Chromosome 11 aberrations in small colony L5178Y TK-/- mutants early in their clonal history.

D. Clive, M. Moore, J. Sawyer, 1985, Mutation research.

Characterization of banding patterns of metaphase-prophase G-banded chromosomes and their use in gene mapping.

D. W. Ball, J. Sawyer, J. Yunis, 1978, Cytogenetics and cell genetics.

Deletion of the retinoblastoma gene in multiple myeloma.

B. Barlogie, G. Tricot, J. Sawyer, 1994, Leukemia.

Both hypodiploidy and deletion of chromosome 13 independently confer poor prognosis in multiple myeloma

B. Barlogie, E. Anaissie, G. Tricot, 2002, British journal of haematology.

Secondary genomic rearrangements involving immunoglobulin or MYC loci show similar prevalences in hyperdiploid and nonhyperdiploid myeloma tumors

B. Barlogie, J. Shaughnessy, J. Sawyer, 2008, Genes, chromosomes & cancer.

Aberrations of 6q13 Mapped to the COL12A1 Locus in Chondromyxoid Fibroma

J. Nishio, J. Sawyer, J. Reith, 2009, Modern Pathology.

Radiation-induced meningiomas: clinical, pathological, cytokinetic, and cytogenetic characteristics.

J. Sawyer, O. Al-Mefty, M. Harrison, 2004, Journal of neurosurgery.

Adult T-cell leukemia/lymphoma with a complex karyotype and central nervous system involvement.

S. Suh, J. Sawyer, Hyeoung-Joon Kim, 2007, Cancer genetics and cytogenetics.

Telomeric associations in the progression of chromosome aberrations in pediatric solid tumors.

J. Sawyer, W. Chadduck, J. Thomas, 1996, Cancer genetics and cytogenetics.

detected by multiprobe interphase FISH High incidence of chromosome 13 deletion in multiple myeloma

B. Barlogie, G. Tricot, E. Tian, 2013 .

A novel reciprocal (10;17)(p11.2;q23) in myxoid fibrosarcoma.

J. Sawyer, R. Nicholas, J. Thomas, 2001, Cancer genetics and cytogenetics.

Clinical implications of loss of bone marrow minimal residual disease negativity in multiple myeloma

G. Tricot, E. Tian, M. Zangari, 2021, Blood advances.

Translocation (7;7)(p13;q21) in a Wilms' tumor.

J. Sawyer, J. Redman, G. Roloson, 1993, Cancer genetics and cytogenetics.

Unusual type of TLS/FUS-ERG chimeric transcript in a pediatric acute myelocytic leukemia with 47,XX,+10,t(16;21)(p11;q22).

S. Suh, J. Sawyer, Hyeoung-Joon Kim, 2006, Cancer genetics and cytogenetics.

A reciprocal t(4;9)(q31;p22) in a solitary neurofibroma.

J. Sawyer, N. Gokden, R. Nicholas, 2005, Cancer genetics and cytogenetics.

A novel t(X;2)(q13;q35) in clear cell sugar tumor of bone.

J. Sawyer, D. Parham, R. Nicholas, 2004, Cancer genetics and cytogenetics.

The mouse lymphoma assay detects recombination, deletion, and aneuploidy.

N. Mei, Tao Chen, M. Moore, 2009, Toxicological sciences : an official journal of the Society of Toxicology.

High-resolution cytogenetic characterization of the L5178Y TK+/- mouse lymphoma cell line.

M. Moore, J. Sawyer, J. Hozier, 1989, Mutation research.

Cytogenetic analysis of the L5178Y/TK+/- leads to TK-/- mouse lymphoma mutagenesis assay system.

D. Clive, M. Moore, J. Sawyer, 1981, Mutation research.

Cytogenetic analysis of two C-1300 murine neuroblastoma cell lines expressing discordant malignant behavior.

M. Tuchman, J. Sawyer, 1989, Cancer genetics and cytogenetics.

Congenital aneurysmal hemorrhage and astrocytoma in an infant.

J. Sawyer, F. Boop, M. Husain, 1991, Pediatric neurosurgery.

Localization of the mouse thymidine kinase gene to the distal portion of chromosome 11.

D. Clive, J. Sawyer, J. Hozier, 1991, Genomics.

High-resolution cytogenetic analysis of L5178Y TK+/- 3.7.2C cells: variation in chromosome 11 breakpoints among small-colony TK-/- mutants.

M. Moore, J. Sawyer, J. Hozier, 1989, Mutation research.

Cytogenetic characterization of the L5178Y TK+/-3.7.2C mouse lymphoma cell line.

D. Clive, M. Moore, J. Sawyer, 1985, Mutation research.

CYTOGENETIC ANALYSIS OF SMALL‐COLONY L5178Y TK‐/‐ MUTANTS EARLY IN THEIR CLONAL HISTORY

D. Clive, M. Moore, J. Sawyer, 1983 .

Cytogenetic analysis of the L5178Y/TK+/− → TK−/− mouse lymphoma mutagenesis assay system

D. Clive, M. Moore, J. Sawyer, 1981 .

Prediction of cytogenetic abnormalities with gene expression profiles.

O. Stephens, B. Barlogie, J. Shaughnessy, 2012, Blood.

Evidence of an epigenetic origin for high-risk 1q21 copy number aberrations in multiple myeloma.

B. Barlogie, G. Morgan, E. Tian, 2014, Blood.

The Vitamin E Analog Gamma-Tocotrienol (GT3) Suppresses Radiation-Induced Cytogenetic Damage

I. Koturbash, M. Boerma, J. Sawyer, 2016, Pharmaceutical Research.

Strange bedfellows: mitotically active chronic myeloid leukemia in molecular complete remission, detected in focal lesion of myeloma.

B. Barlogie, J. Sawyer, R. Samant, 2014, Clinical Lymphoma, Myeloma & Leukemia.

Metaphase cytogenetic techniques in multiple myeloma.

J. Sawyer, 2011, Methods in molecular biology.

Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.

J. Sawyer, C. Cunniff, C. Swanson, 1995, American journal of medical genetics.

J. Dudley, A. Laganà, J. Keats, 2020, Science advances.

A clonal reciprocal t(2;7)(p13;p13) in plantar fibromatosis.

J. Sawyer, N. Gokden, R. Nicholas, 2005, Cancer genetics and cytogenetics.

Jumping translocations of chromosome 1q in multiple myeloma: evidence for a mechanism involving decondensation of pericentromeric heterochromatin.

B. Barlogie, S. Jagannath, G. Tricot, 1998, Blood.

Telomeric fusion and chromosome instability in multiple tissues of a patient with mosaic Ullrich-Turner syndrome.

J. Sawyer, C. Pihoker, P. North, 1997, American journal of medical genetics.

DNA hypomethylation and unusual chromosome instability in cell lines fromICF syndrome patients

M. Ehrlich, E. Fiala, A. Narayan, 2000, Cytogenetic and Genome Research.

BRAF and DIS3 Mutations Associate with Adverse Outcome in a Long-term Follow-up of Patients with Multiple Myeloma

B. Barlogie, G. Morgan, E. Tian, 2020, Clinical Cancer Research.

Jumping translocations of 1q12 in multiple myeloma: a novel mechanism for deletion of 17p in cytogenetically defined high-risk disease.

B. Barlogie, E. Tian, D. Johann, 2014, Blood.

Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma.

B. Barlogie, J. Shaughnessy, P. L. Bergsagel, 2001, Blood.

Evi27 encodes a novel membrane protein with homology to the IL17 receptor

J. Shaughnessy, D. Largaespada, N. Copeland, 2000, Oncogene.

Identification of isochromosome 1q as a recurring chromosome aberration in skull base chordomas: a new marker for aggressive tumors?

J. Sawyer, O. Al-Mefty, M. Husain, 2001, Neurosurgical focus.

In multiple myeloma, 14q32 translocations are nonrandom chromosomal fusions driving high expression levels of the respective partner genes

B. Barlogie, E. Tian, J. Sawyer, 2014, Genes, chromosomes & cancer.

Cyclin D dysregulation: an early and unifying pathogenic event in multiple myeloma.

Bart Barlogie, F. Zhan, B. Barlogie, 2005, Blood.

Duplication and deletion of chromosome band 2(p21p22) resulting from a familial interstitial insertion (2;11)(p21;p15).

J. Sawyer, C. Cunniff, J. Quirk, 1994, American journal of medical genetics.

Highly conserved segments in mammalian chromosomes.

J. Sawyer, J R Sawyer, 1991, The Journal of heredity.

Satellite DNA hypomethylation in karyotyped Wilms tumors.

Christian B. Woods, N. Hopkins, M. Ehrlich, 2003, Cancer genetics and cytogenetics.

Gene mapping and leader polypeptide sequence of human glucocerebrosidase: implications for Gaucher disease.

S. Tsuji, E. Ginns, P. Choudary, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Cytogenetics of Plasma Cell Neoplasms

J. Sawyer, 2016 .

immunoglobulin loci in multiple myeloma Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to

B. Barlogie, P. L. Bergsagel, M. Kuehl, 2013 .

Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma

B. Barlogie, J. Shaughnessy, N. Munshi, 2001, British journal of haematology.

Trisomy 9: review and report of two new cases.

J. Sawyer, R. Kirby, G. Arnold, 1995, American journal of medical genetics.

High resolution of mouse chromosomes: banding conservation between man and mouse.

J. Sawyer, J. Hozier, 1986, Science.

Poor overall survival in hyperhaploid multiple myeloma is defined by double-hit bi-allelic inactivation of TP53

Yan Wang, Gareth J. Morgan, Cody Ashby, 2019, Oncotarget.

Frequent gain of chromosome band 1q21 in plasma-cell dyscrasias detected by fluorescence in situ hybridization: incidence increases from MGUS to relapsed myeloma and is related to prognosis and disease progression following tandem stem-cell transplantation.

Yongsheng Huang, J. Stewart, F. Zhan, 2006, Blood.

progression following tandem stem cell transplantation MGUS to relapsed myeloma and is related to prognosis and disease hybridization : Incidence increases from in situ detected by fluorescence Frequent gain of chromosome band 1 q 21 in plasma cell dyscrasias

Yongsheng Huang, J. Stewart, F. Zhan, 2006 .

Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping

B. Barlogie, J. Shaughnessy, D. Siegel, 1998 .

Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping.

B. Barlogie, J. Shaughnessy, N. Munshi, 1998, Blood.

Malignant progression in meningioma: documentation of a series and analysis of cytogenetic findings.

J. Sawyer, O. Al-Mefty, S. Pravdenkova, 2004, Journal of neurosurgery.

Evidence of an association between 6q13‐21 chromosome aberrations and locally aggressive behavior in patients with cartilage tumors

J. Sawyer, P. North, R. Nicholas, 1998, Cancer.

Karyotype evolution in a patient with Down syndrome and acute leukemia following a congenital leukemoid reaction.

D. Head, J. Sawyer, G. Roloson, 1994, Medical and pediatric oncology.

Clonal telomeric fusions and chromosome instability in a subcutaneous sacrococcygeal myxopapillary ependymoma.

J. Sawyer, J. P. Miller, D. A. Ellison, 1998, Cancer genetics and cytogenetics.

Telomere fusion as a mechanism for the progressive loss of the short arm of chromosome 11 in an anaplastic wilms' tumor

J. Sawyer, K. Stine, J. Thomas, 1994, Cancer.

High resolution G-banded chromosomes of the mouse

M. Moore, J. Sawyer, J. Hozier, 2004, Chromosoma.

Magnetic resonance imaging in multiple myeloma: diagnostic and clinical implications.

B. Barlogie, J. Shaughnessy, E. Anaissie, 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The characterization of high-resolution G-banded chromosomes of man

D. W. Ball, J. Yunis, J. Sawyer, 1978, Chromosoma.

Evolution of tumor chromosome abnormalities after therapy in a pediatric astrocytoma.

J. Sawyer, W. Chadduck, C. Swanson, 1991, Cancer genetics and cytogenetics.

De novo proximal duplication of 1(q12q22) in a female infant with multiple congenital anomalies

J. Sawyer, C. Lim, C. Swanson, 2007, American journal of medical genetics. Part A.

The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee.

J. Sawyer, J. Yunis, K. Dunham, 1980, Science.

Mitochondrial DNA determines androgen dependence in prostate cancer cell lines

A. Gotoh, T. Shirakawa, J. Sawyer, 2006, Oncogene.

An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome

B. Barlogie, G. Morgan, E. Tian, 2018, Blood Cancer Journal.

Adverse Metaphase Cytogenetics Can Be Overcome by Adding Bortezomib and Thalidomide to Fractionated Melphalan Transplants

B. Barlogie, G. Morgan, E. Tian, 2016, Clinical Cancer Research.

Risk factors for MDS and acute leukemia following total therapy 2 and 3 for multiple myeloma.

B. Barlogie, D. Johann, J. Sawyer, 2013, Blood.

in the context of global gene expression survival in multiple myeloma treated with Total Therapy I: interpretation especially of chromosome 13 and hypodiploidy, ensures long-term Continuous absence of metaphase-defined cytogenetic abnormalities,

B. Barlogie, J. Shaughnessy, S. Jagannath, 2013 .

patients treated since 1989 stem-cell mobilization: the Arkansas experience in more than 3000 autotransplantation for multiple myeloma linked to poor hematopoietic Cytogenetically defined myelodysplasia after melphalan-based

B. Barlogie, E. Anaissie, G. Tricot, 2013 .

Cytogenetically defined myelodysplasia after melphalan-based autotransplantation for multiple myeloma linked to poor hematopoietic stem-cell mobilization: the Arkansas experience in more than 3,000 patients treated since 1989.

B. Barlogie, E. Anaissie, G. Tricot, 2008, Blood.

Prognostic impact of cytogenetic and interphase fluorescence in situ hybridization‐defined chromosome 13 deletion in multiple myeloma: early results of total therapy II

B. Barlogie, J. Shaughnessy, E. Anaissie, 2003, British journal of haematology.

Predicting long‐term (≥ 5 years) event‐free survival in multiple myeloma patients following planned tandem autotransplants

B. Barlogie, N. Munshi, R. Desikan, 2002, British journal of haematology.

Multicolor Spectral Karyotyping Identification of New Nonrandom Translocations in Multiple Myeloma With

B. Barlogie, J. Shaughnessy, D. Siegel, 2011 .

Establishment and exploitation of hyperdiploid and non‐hyperdiploid human myeloma cell lines

F. Zhan, J. Shaughnessy, J. Sawyer, 2007, British journal of haematology.

Soft-Tissue Aneurysmal Bone Cyst: Report of a Case with t(5;17)(q33;p13)

J. Sawyer, D. Parham, R. Nicholas, 2007, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

P. Bray-Ward, D. Ward, J. Wienberg, 1996, Human molecular genetics.

Bone marrow transplant engraftment analysis with loss of an informative allele.

S. Schichman, J. Sawyer, Carla S. Wilson, 2002, The Journal of molecular diagnostics : JMD.

Telomeric fusion as a mechanism for the loss of 1p in meningioma.

J. Sawyer, O. Al-Mefty, M. Husain, 2003, Cancer genetics and cytogenetics.

A role for telomeric and centromeric instability in the progression of chromosome aberrations in meningioma patients

J. Sawyer, O. Al-Mefty, A. Krisht, 2000, Cancer.

The prognostic significance of cytogenetics and molecular profiling in multiple myeloma.

J. Sawyer, 2011, Cancer genetics.

A Complete Remission (CR) Is Not a Prerequisite for Prolonged Survival after Autotransplants for Multiple Myeloma.

B. Barlogie, G. Tricot, J. Sawyer, 2004 .

Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.

S. Gollin, J. Sawyer, J. Overhauser, 1992, American journal of medical genetics.

Centromeric instability of chromosome 1 resulting in multibranched chromosomes, telomeric fusions, and “jumping translocations” of 1 q in a human immunodeficiency virus‐related non‐Hodgkin's lymphoma

J. Sawyer, P. North, M. Koller, 1995, Cancer.

Nonrandom chromosome breakpoints at Xq26 and 2q33 characterize cemento‐ossifying fibromas of the orbit

J. Sawyer, F. Boop, J. M. Bell, 1995, Cancer.

Cytogenetic Findings in Pediatric T-Lymphoblastic Lymphomas: One Institution’s Experience and a Review of the Literature

J. Sawyer, D. Parham, D. A. Ellison, 2005, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Genetic modifiers of CHEK 2 * 1100 delC-associated breast cancer risk

Marina, Bogdanova, A. Whittemore, 2017 .

Preceding standard therapy is the likely cause of MDS after autotransplants for multiple myeloma

B. Barlogie, S. Jagannath, G. Tricot, 1996, British journal of haematology.

Clonal chromosome aberrations in a case of nodular fasciitis.

J. Sawyer, J. M. Bell, G. Sammartino, 1994, Cancer genetics and cytogenetics.

Metastatic myxopapillary ependymoma: Report of a case with fine‐needle aspiration findings

R. Mrak, J. Sawyer, R. Bardales, 1994, Diagnostic cytopathology.

Involvement of the short arm of chromosome 1 in a myxopapillary ependymoma.

J. Sawyer, W. Chadduck, M. Crowson, 1991, Cancer genetics and cytogenetics.

Localization of a unique DNA sequence to band p16 of human chromosome 4.

R. E. Thayer, O. Mcbride, J. Sawyer, 1987, Cytogenetics and cell genetics.

Chromosome aberrations in four ependymomas.

J. Sawyer, W. Chadduck, F. Boop, 1994, Cancer genetics and cytogenetics.

Molecular cytogenetic analysis of a medulloblastoma with isochromosome 17 and double minutes.

J. Sawyer, W. Chadduck, F. Boop, 1991, Cancer genetics and cytogenetics.

Cytogenetic studies of pediatric brain and spinal cord tumors.

J. Sawyer, F. Boop, W. Chadduck, 1991, Pediatric neurosurgery.

Trisomy for chromosome 1q in a pontine astrocytoma.

J. Sawyer, W. Chadduck, G. Roloson, 1990, Cancer genetics and cytogenetics.

A novel reciprocal translocation (14;15)(q11;q24) in a congenital mesoblastic nephroma.

J. Sawyer, J. P. Miller, G. Roloson, 1996, Cancer genetics and cytogenetics.

Exploitation of Novel Hyperdiploid and Nonhyperdiploid Myeloma Cell Lines for Studying Innovative Interventions for Myeloma and Its Associated Bone Disease.

F. Zhan, B. Barlogie, J. Shaughnessy, 2007 .

Confirmation of autosomal dominant transmission of the DiGeorge malformation complex.

A. Burks, S. Gollin, J. Sawyer, 1988, The Journal of pediatrics.

Pericentric inversion (2)(p15q35) in an alveolar rhabdomyosarcoma.

J. Sawyer, M. Kletzel, F. Crussi, 1994, Cancer genetics and cytogenetics.

Dose-dense and less dose-intense total therapy 5 for gene expression profiling-defined high-risk multiple myeloma

J. Crowley, B. Barlogie, E. Tian, 2016, Blood Cancer Journal.

High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19

J. Sawyer, C. Cunniff, S. Hassed, 1993, Human Genetics.

High resolution mid-prophase human chromosomes induced by echinomycin and ethidium bromide

J. Sawyer, 2004, Human Genetics.

Genomic instability in multiple myeloma: Evidence for jumping segmental duplications of chromosome arm 1q

B. Barlogie, J. Shaughnessy, G. Tricot, 2005, Genes, chromosomes & cancer.

Persistent bone marrow minimal residual disease as a “high‐risk” disease feature in multiple myeloma

G. Tricot, E. Tian, M. Zangari, 2021, American journal of hematology.

Hematopoietic progenitor cell collection after autologous transplant for multiple myeloma: low platelet count predicts for poor collection and sole use of resulting graft enhances risk of myelodysplasia

B. Barlogie, J. Sawyer, M. Cottler-Fox, 2014, Leukemia.

Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon

B. Barlogie, J. Shaughnessy, E. Tian, 2009, British journal of haematology.

Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone.

J. Sawyer, R. Nicholas, C. Swanson, 2005, Cancer genetics and cytogenetics.

Daratumumab in high‐risk relapsed/refractory multiple myeloma patients: adverse effect of chromosome 1q21 gain/amplification and GEP70 status on outcome

E. Tian, M. Zangari, J. Sawyer, 2019, British journal of haematology.

Fulminant onset of acute leukemia from normal hematopoiesis within 3 months of follow up for multiple myeloma treated with total therapy protocols

B. Barlogie, J. Sawyer, F. van Rhee, 2015, Clinical case reports.

G-banding patterns of high-resolution human chromosomes 6–22, X, and Y

D. W. Ball, J. Yunis, J. Sawyer, 1979, Human Genetics.

Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephaly.

M. Muenke, J. Sawyer, G. Arnold, 1996, American journal of medical genetics.

Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype

J. Sawyer, K. McKelvey, J. Clothier, 2018, American journal of medical genetics. Part A.

MCT-1 oncogene downregulates p53 and destabilizes genome structure in the response to DNA double-strand damage.

C. Shu, R. Gartenhaus, H. Hsu, 2007, DNA repair.

Molecular and Cytogenetic Evaluation of a Patient with Ring Chromosome 13 and Discordant Results

J. Sawyer, Charles Sailey, Julie Kaylor, 2014, Cytogenetic and Genome Research.

Impact of cytogenetic abnormalities on the management of skull base chordomas.

J. Sawyer, O. Al-Mefty, S. Pravdenkova, 2009, Journal of neurosurgery.

Analysis of trifluorothymidine-resistant (TFTr) mutants of L5178Y/TK+/- mouse lymphoma cells.

D. Clive, M. Moore, J. Sawyer, 1985, Mutation research.

Cytogenetic findings in a pleomorphic xanthoastrocytoma.

J. Sawyer, W. Chadduck, F. Boop, 1991, Cancer genetics and cytogenetics.

The Vitamin E Analog Gamma-Tocotrienol (GT3) Suppresses Radiation-Induced Cytogenetic Damage

I. Koturbash, M. Boerma, J. Sawyer, 2016, Pharmaceutical Research.

Elevated Expression of CKS1B at 1q21 Is Highly Correlated with Short Survival in Myeloma.

F. Zhan, B. Barlogie, E. Anaissie, 2004 .

Identification of Three Novel Chromosomal Translocation Partners Involving the Immunoglobulin Loci in Newly Diagnosed Myeloma and Human Myeloma Cell Lines.

John D. Shaughnessy, Bart Barlogie, Ryuzo Ueda, 2005 .

Progression of chromosome abnormalities after radiation therapy in a patient with Askin's tumor.

J. Sawyer, W. Chadduck, M. Keltzel, 1990, Cancer genetics and cytogenetics.

Hyperhaploid karyotypes in multiple myeloma

G. Morgan, J. Sawyer, 2017, Oncotarget.

Constitutional t(16;22)(p13.3;q11.2 approximately 12) in a primitive neuroectodermal tumor of the pineal region.

M. Linskey, J. Sawyer, G. Sammartino, 2003, Cancer genetics and cytogenetics.

Telomeric associations evolving to ring chromosomes in a recurrent pleomorphic xanthoastrocytoma.

J. Sawyer, W. Chadduck, F. Boop, 1992, Cancer genetics and cytogenetics.

Ring chromosome 12 resulting from nonrandom telomeric associations with the short arm of chromosome 15 in a cerebellar astrocytoma

J. Sawyer, F. Boop, G. Sammartino, 1993, Genes, chromosomes & cancer.

High incidence of chromosome 13 deletion in multiple myeloma detected by multiprobe interphase FISH.

B. Barlogie, J. Shaughnessy, G. Tricot, 2000, Blood.

Results of high-dose therapy for 1000 patients with multiple myeloma: durable complete remissions and superior survival in the absence of chromosome 13 abnormalities.

B. Barlogie, J. Shaughnessy, S. Jagannath, 2000, Blood.

Allelic mutations in noncoding genomic sequences construct novel transcription factor binding sites that promote gene overexpression

B. Barlogie, J. Shaughnessy, E. Tian, 2015, Genes, chromosomes & cancer.

Cytogenetic findings in a case of pediatric glioblastoma.

J. Sawyer, W. Chadduck, D. Longee, 1992, Cancer genetics and cytogenetics.

Multicolor spectral karyotyping of the L5178Y Tk+/−‐3.7.2C mouse lymphoma cell line

M. Moore, J. Sawyer, Jianyong Wang, 2006, Environmental and molecular mutagenesis.

Translocation (1;19)(q21;q13.3) is a recurrent reciprocal translocation in meningioma.

J. Sawyer, O. Al-Mefty, E. Thomas, 2002, Cancer Genetics and Cytogenetics.

Cyclin D 3 at 6 p 21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma

B. Barlogie, J. Shaughnessy, P. L. Bergsagel, 2001 .

Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon

B. Barlogie, J. Shaughnessy, E. Tian, 2009, British journal of haematology.

Cytogenetic distinction between the TK+ and TK- chromosomes in the L5178Y TK+/- 3.7.2C mouse-lymphoma cell line.

D. Clive, M. Moore, J. Sawyer, 1982, Mutation research.

Allelic mutations in noncoding genomic sequences construct novel transcription factor binding sites that promote gene overexpression

B. Barlogie, J. Shaughnessy, E. Tian, 2015, Genes, chromosomes & cancer.

The role of cytogenetics in myeloma

F. Zhan, G. Tricot, J. Sawyer, 2006, Leukemia.