J. Stone

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Development of a Prognostic Genetic Signature to Predict the Metastatic Risk Associated with Cutaneous Melanoma

Robert W Cook, Pedram Gerami, R. Amaria, 2015, Clinical Cancer Research.

Unbalanced chromosomal translocation, der(17)t(13;17)(q14;p11) in a solid and cystic papillary epithelial neoplasm of the pancreas.

A. Sandberg, G. Lauwers, J. Stone, 1996, The American journal of surgical pathology.

FISH: a useful technique in the verification of clonality of random chromosome abnormalities.

J. Stone, R. Morgan, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Sex chromosome aneuploidy and aging.

A. Sandberg, J. Stone, Avery A. Sandberg, 1995, Mutation research.

Hematologic masquerade of rhabdomyosarcoma

A. Sandberg, J. Stone, L. Czarnecki, 2001, American journal of hematology.

Some observations on fluorescence in situ hybridization evaluation of chronic myelocytic leukemia.

J. Stone, R. Morgan, P. Richards, 1997, Cancer genetics and cytogenetics.

The Philadelphia chromosome as a secondary change in leukemia: three case reports and an overview of the literature.

A. Meloni-Ehrig, J. Stone, R. Morgan, 1998, Cancer genetics and cytogenetics.

Identification of complex t(15;17) in APL by FISH.

J. Stone, R. Morgan, A. Sandberg, 1994, Cancer genetics and cytogenetics.

Identification of masked and variant Ph (complex type) translocations in CML and classic Ph in AML and ALL by fluorescence in situ hybridization with the use of bcr/abl cosmid probes.

J. Stone, R. Morgan, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Gene expression profiling in uveal melanoma: technical reliability and correlation of molecular class with pathologic characteristics

F. Monzon, R. Cook, K. Oelschlager, 2017, Diagnostic Pathology.

Medulloblastoma, Primitive Neuroectodermal Tumors, and Pineal Tumors

A. Sandberg, J. Stone, 2008 .

True hermaphroditism with partial duplication of chromosome 22 and without SRY.

R. Erickson, J. Hackel, J. Stone, 1999, American journal of medical genetics.

Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies

M. Eccles, R. Erickson, L. McNoe, 1997, Clinical genetics.

Identification of a novel amplicon at 1q31 in pancreatic cancer cell lines.

C. Tirado, J. Stone, A. Sandberg, 1999, Cancer genetics and cytogenetics.

A Gene Signature to Determine Metastatic Behavior in Thymomas

S. Badve, C. Goswami, P. Loehrer, 2013, PloS one.

Validation of a Gene Expression Test for Mesothelioma Prognosis in Formalin-Fixed Paraffin-Embedded Tissues.

M. Becich, W. Richards, R. Bueno, 2017, The Journal of molecular diagnostics : JMD.

Translocation (12;14) in lipoma: a case report and review of the literature.

A. Meloni-Ehrig, M. Malawer, J. Stone, 1998, Cancer genetics and cytogenetics.

Spontaneous expression of the chromosome fragile site at 10q23 in leiomyoma.

U. Surti, Y. Ozisik, A. Sandberg, 1994, Cancer genetics and cytogenetics.

Involvement of 10q22 and 11q13 in hibernoma.

C. H. Bush, A. Sandberg, S. Spanier, 1994, Cancer genetics and cytogenetics.

Epigenetic reprogramming and aberrant expression of PRAME are associated with increased metastatic risk in Class 1 and Class 2 uveal melanomas

Michael A. Durante, A. Bowcock, J. Harbour, 2016, Oncotarget.

Clinical Performance and Management Outcomes with the DecisionDx-UM Gene Expression Profile Test in a Prospective Multicenter Study

T. Aaberg, Y. Shildkrot, R. Cook, 2016, Journal of oncology.

A "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome.

T. Glover, R. Erickson, J. Stone, 1995, Cytogenetics and cell genetics.

Gene expression profiling for molecular staging of cutaneous melanoma in patients undergoing sentinel lymph node biopsy.

L. Ferris, R. Amaria, K. Delman, 2015, Journal of the American Academy of Dermatology.

FISH in the evaluation of pleural and ascitic fluids.

A. Peier, A. Sandberg, J. Stone, 1995, Cancer genetics and cytogenetics.

Increased chromosome 20 copy number detected by fluorescence in situ hybridization (FISH) in malignant melanoma

J. Trent, D. Pinkel, Jin-Ming Yang, 1997, Genes, chromosomes & cancer.

Analytic validity of DecisionDx-Melanoma, a gene expression profile test for determining metastatic risk in melanoma patients

K. Covington, F. Monzon, R. Cook, 2018, Diagnostic Pathology.

Appreciation of the significance of cytogenetic and FISH analysis of bone marrow in clinical oncology.

J. Stone, R. Morgan, A. Sandberg, 1994, Cancer genetics and cytogenetics.

Increased chromosome 20 copy number detected by fluorescence in situ hybridization (FISH) in malignant melanoma

J. Trent, D. Pinkel, Jin-Ming Yang, 1997, Genes, chromosomes & cancer.

Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.

J. Trent, X. Guan, A. Sandberg, 1997, American journal of medical genetics.

Analytical Validation and Performance of a 7-Gene Next-Generation Sequencing Panel in Uveal Melanoma

K. Covington, J. Harbour, F. Monzon, 2020, Ocular Oncology and Pathology.

A case of therapy-related extramedullary acute promyelocytic leukemia.

J. Stone, R. Morgan, H. Mostafavi, 1996, Cancer genetics and cytogenetics.

Trisomy 10: age and leukemic lineage associations.

J. Stone, R. Morgan, A. Sandberg, 1996, Cancer genetics and cytogenetics.