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JOHN FRATER, MD
MD
Anatomic Pathology & Clinical Pathology Physician
NPI: 1407873920IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hematology (Pathology) Physician
Pathology — Hematology
Code: 207ZH0000X
2003011845(MO)
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
2003011845(MO)
CMS Specialties
PrimaryPATHOLOGY
Education
UNIVERSITY OF TOLEDO COLLEGE OF MEDICINE
Class of 1996
Research & Publications (20)
Lymphoplasmacytic lymphoma/Waldenström macroglobulinemia with inv(16)(p13q22) as a sole genetic abnormality.
PMID 17452259·Cancer Genet Cytogenet·2007
5-case
Deletion of MYC and presence of double minutes with MYC amplification in a morphologic acute promyelocytic leukemia-like case lacking RARA rearrangement: could early exclusion of double-minute chromosomes be a prognostic factor?
PMID 16631470·Cancer Genet Cytogenet·2006
5-case
Histiocytic sarcoma with secondary involvement of the skin and expression of CD1a: evidence of indeterminate cell differentiation?
PMID 16776720·J Cutan Pathol·2006
5-case
Lymphoblastic leukemia with mature B-cell phenotype in infancy.
PMID 15454841·J Pediatr Hematol Oncol·2004
5-case
Chronic myeloid leukemia following therapy with imatinib mesylate (Gleevec). Bone marrow histopathology and correlation with genetic status.
PMID 12817431·Am J Clin Pathol·2003
3-trial
Biphenotypic acute leukemia with coexpression of CD79a and markers of myeloid lineage.
PMID 12653584·Arch Pathol Lab Med·2003
5-case
Peripheral eosinophilia camouflaging anaplastic large cell lymphoma.
PMID 18805872·Int J Surg Pathol·2011
5-case
Pathologic and clinical features of Hodgkin lymphoma--like posttransplant lymphoproliferative disease.
PMID 19578050·Int J Surg Pathol·2010
5-case
Cutaneous and systemic plasmacytosis in an Asian male born in the North American continent: a controversial entity potentially related to multicentric Castleman disease.
PMID 19614735·J Cutan Pathol·2010
5-case
Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis.
PMID 19240791·PLoS One·2009
8-other
Cutaneous rosai-dorfman disease and morphea: coincidence or association?
PMID 19542928·Am J Dermatopathol·2009
5-case
The spectrum of adult B-lymphoid leukemias with BCR-ABL: molecular diagnostic, cytogenetic, and clinical laboratory perspectives.
PMID 18932238·Am J Hematol·2008
8-other
Dysregulated angiogenesis in B-chronic lymphocytic leukemia: morphologic, immunohistochemical, and flow cytometric evidence.
PMID 18423023·Diagn Pathol·2008
8-other
A transient benign lymph node-based proliferation of T-cells simulating non-Hodgkin lymphoma in a patient with psoriasis treated with tumor necrosis factor alpha and CD11a antagonists.
PMID 18366773·Diagn Pathol·2008
8-other
CD8+ T-cell responses to different HIV proteins have discordant associations with viral load.
PMID 17173051·Nat Med·2007
8-other
Precise identification of a human immunodeficiency virus type 1 antigen processing mutant.
PMID 17108020·J Virol·2007
4-observational
Coexistence of neocentromeric marker 3q and trisomy 3 in two different tissues in a 3-year-old boy with peripheral T-cell lymphoma: support for a gene dosage effect hypothesis.
PMID 17011987·Cancer Genet Cytogenet·2006
5-case
Is procalcitonin useful in early diagnosis of serious bacterial infections in children?
PMID 15981747·Acta Paediatr·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1 BARNES JEWISH HOSPITAL PLZ, DIV PA ANATOMIC AND MOLECULAR PATH
SAINT LOUIS, MO 63110 - Phone
- (314) 362-5641
Quick Facts
- NPI
- 1407873920
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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