Professor, Pathology and Microbiology, University of Nebraska Medical Center College of Medicine
Pathology
Dr. Julia A. Bridge, MD
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Julia A. Bridge is an expert in the field of Pathology. She went to University of Kansas School of Medicine. Julia Bridge is a published physician as well. She has 91 publications published. The latest was: Sinonasal small round blue cell tumors: An approach to diagnosis. She is registered with Medicare and accepts Medicare payments.
Publications
- Liposarcomatous differentiation in malignant phyllodes tumors is unassociated with MDM2 or CDK4 amplification.
- Sinonasal small round blue cell tumors: An approach to diagnosis.
- Tumoral TP53 and/or CDKN2A alterations are not reliable prognostic biomarkers in patients with localized Ewing sarcoma: A report from the children's oncology group.
- MUC 4-negative FUS-CREB3L2 rearranged low-grade fibromyxoid sarcoma.
- A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.
- VCL-ALK Renal Cell Carcinoma in Children With Sickle-cell Trait: The Eighth Sickle-cell Nephropathy?
- Myogenin, AP2β, NOS-1, and HMGA2 Are Surrogate Markers of Fusion Status in Rhabdomyosarcoma: A Report From the Soft Tissue Sarcoma Committee of the Children's Oncology...
- The role of cytogenetics and molecular diagnostics in the diagnosis of soft-tissue tumors.
- Dense pattern of embryonal rhabdomyosarcoma, a lesion easily confused with alveolar rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Children's...
- Osseous myxochondroid sarcoma: a detailed study of 5 cases of extraskeletal myxoid chondrosarcoma of the bone.
- Intracranial malignant triton tumor in a patient with neurofibromatosis type 1: case report and review of the literature.
- Pharmacologic Inhibition of Epigenetic Modification Reveals Targets of Aberrant Promoter Methylation in Ewing Sarcoma.
- Soft tissue angiofibroma: report of 2 cases of a recently described tumor.
- Cytogenetic abnormalities in follicular dendritic cell sarcoma: report of two cases and literature review.
- PAX-FOXO1 Fusion Status Drives Unfavorable Outcome for Children With Rhabdomyosarcoma: A Children's Oncology Group Report.
- Primary intrathoracic dermatofibrosarcoma protuberans.
- Composite uterine neoplasm with embryonal rhabdomyosarcoma and primitive neuroectodermal tumor components: rhabdomyosarcoma with divergent differentiation, variant of ...
- Identification of a Novel, Recurrent SLC44A1-PRKCA Fusion in Papillary Glioneuronal Tumor.
- Genomic imbalances in benign metastasizing leiomyoma: characterization by conventional karyotypic, fluorescence in situ hybridization, and whole genome SNP array analy...
- PAX3/7-FOXO1 fusion status in older rhabdomyosarcoma patient population by fluorescent in situ hybridization.
- Primary intranodal epithelioid rhabdomyosarcoma.
- Unusual presentation of congenital infantile fibrosarcoma in seven infants with molecular-genetic analysis.
- Renal medullary carcinomas: histopathologic phenotype associated with diverse genotypes.
- A CD117 and CD34 immunoreactive sarcoma masquerading as a gastrointestinal stromal tumor: diagnostic pitfalls of ancillary studies in sarcoma.
- Extraskeletal Ewing's sarcoma of the thoracic epidural space: Case report and review of the literature.
- Molecular diagnostics of soft tissue tumors.
- Array-based comparative genomic hybridization identifies CDK4 and FOXM1 alterations as independent predictors of survival in malignant peripheral nerve sheath tumor.
- Renal cell carcinoma with novel VCL-ALK fusion: new representative of ALK-associated tumor spectrum.
- A novel t(4;22)(q31;q12) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor.
- Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes.
- C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma.
- Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator...
- Contributions of pediatrics and pediatric pathology to the body of knowledge regarding human disease.
- The small round blue cell tumors of the sinonasal area.
- Osteoblastoma characterized by a three-way translocation: report of a case and review of the literature.
- Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism micr...
- Aberrations of 6q13 mapped to the COL12A1 locus in chondromyxoid fibroma.
- Virtual-karyotyping with SNP microarrays in morphologically challenging renal cell neoplasms: a practical and useful diagnostic modality.
- Clear cell sarcoma of soft tissue metastatic to the ovaries: a heretofore unreported occurrence.
- Liposarcomas in young patients: a study of 82 cases occurring in patients younger than 22 years of age.
- Alveolar rhabdomyosarcoma of the head and neck region in older adults: genetic characterization and a review of the literature.
- Prevalence and clinical impact of anaplasia in childhood rhabdomyosarcoma : a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group.
- Best cases from the AFIP: Adamantinoma of the tibia and fibula with cytogenetic analysis.
- Contribution of cytogenetics to the management of poorly differentiated sarcomas.
- Aggressive angiomyxoma with t(12;21) and HMGA2 rearrangement: report of a case and review of the literature.
- Loss of the PTCH1 gene locus in cardiac fibroma.
- Lack of a common or characteristic cytogenetic anomaly in solitary fibrous tumor.
- Imbalances of chromosomes 4, 9, and 12 are recurrent in the thecoma-fibroma group of ovarian stromal tumors.
- Analysis of HER2 gene amplification using an automated fluorescence in situ hybridization signal enumeration system.
- Embryonal rhabdomyosarcoma with a der(16)t(1;16) translocation.
- Use of a multitarget fluorescence in situ hybridization assay to diagnose bladder cancer in patients with hematuria.
- Use of a novel FISH assay on paraffin-embedded tissues as an adjunct to diagnosis of alveolar rhabdomyosarcoma.
- Intracranial Ewing sarcoma.
- Cytogenetic findings in clear cell chondrosarcoma.
- C-erb-B2 (HER2/neu) expression in synovial sarcoma of the head and neck.
- Identification of a ring chromosome with spectral karyotyping in a pleural synovial sarcoma.
- Renal carcinomas with the t(6;11)(p21;q12): clinicopathologic features and demonstration of the specific alpha-TFEB gene fusion by immunohistochemistry, RT-PCR, and DN...
- Monosomy 22 as a diagnostic aid in a case of late recurrence of adult granulosa cell tumor of the ovary.
- Paraganglioma-like dermal melanocytic tumor: a unique entity distinct from cellular blue nevus, clear cell sarcoma, and cutaneous melanoma.
- Cytogenetic and molecular cytogenetic findings in 43 aneurysmal bone cysts: aberrations of 17p mapped to 17p13.2 by fluorescence in situ hybridization.
- USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst.
- Translocation (2;11)(q31;q12) is recurrent in collagenous fibroma (desmoplastic fibroblastoma).
- Cytogenetic distinction among benign fibro-osseous lesions of bone in children and adolescents: value of karyotypic findings in differential diagnosis.
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors.
- Loss of 13q14-q21 and gain of 5p14-pter in the progression of leiomyosarcoma.
- Inconspicuous insertion 22;12 in myxoid/round cell liposarcoma accompanied by the secondary structural abnormality der(16)t(1;16).
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: chondrosarcoma and other cartilaginous neoplasms.
- Fusion of ALK to the Ran-binding protein 2 (RANBP2) gene in inflammatory myofibroblastic tumor.
- Translocation (1;4)(p31;q34) in nonossifying fibroma.
- Cytogenetic findings in benign cartilaginous neoplasms.
- The homeotic protein Six3 is a coactivator of the nuclear receptor NOR-1 and a corepressor of the fusion protein EWS/NOR-1 in human extraskeletal myxoid chondrosarcomas.
- Chromosome 6 abnormalities are recurrent in synovial chondromatosis.
- Performance characteristics of a reverse transcriptase-polymerase chain reaction assay for the detection of tumor-specific fusion transcripts from archival tissue.
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. Dermatofibrosarcoma protuberans and giant cell fibroblastoma.
- Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas.
- Clinical evaluation of a multi-target fluorescent in situ hybridization assay for detection of bladder cancer.
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. desmoplastic small round-cell tumors.
- Cytogenetic and molecular cytogenetic evidence of recurrent 8q24.1 loss in osteochondroma.
- Sclerosing rhabdomyosarcoma in adults: report of four cases of a hyalinizing, matrix-rich variant of rhabdomyosarcoma that may be confused with osteosarcoma, chondrosa...
- Genetic heterogeneity in the alveolar rhabdomyosarcoma subset without typical gene fusions.
- PAX3-FKHR and PAX7-FKHR gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: a report from the children's oncology group.
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. gastrointestinal stromal tumors.
- Translocation der(13;21)(q10;q10) in skeletal and extraskeletal mesenchymal chondrosarcoma.
- Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar...
- EWS/FLI-1 fusion signal inserted into chromosome 11 in one patient with morphologic features of Ewing sarcoma, but lacking t(11;22).
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. Synovial sarcoma.
- Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
- Impact of SYT-SSX fusion type on the clinical behavior of synovial sarcoma: a multi-institutional retrospective study of 243 patients.
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: congenital (infantile) fibrosarcoma and mesoblastic nephroma.
- Optimal z-axis scanning parameters for gynecologic cytology specimens.
Schools
University of Nebraska College of Medicine
University Kans Med Center
University Nebr Med Center
Doctors Specialties
- Anatomic Pathology
- Clinical Cytogenetics
- Pathology
Accepted Insurances
Education
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University of Kansas School of Medicine -
University of Nebraska College of Medicine
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1811954175 |
| Last Name Of The Provider | BRIDGE |
| First Name Of The Provider | JULIA |
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