Christine R. Bryke
Medical Genetics
330 Brookline Ave
Beth Israel Deaconess Medical Center
Boston, MA 02215
Beth Israel Deaconess Medical Center
Boston, MA 02215
Last Updated: 09/26/2026
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Found 15 publications
Cytogenetic and Molecular Characterization of IDH-Wildtype Glioblastomas and Grade 4 IDH-Mutant Astrocytomas with Unusual Histology.
Journal: Journal of neuropathology and experimental neurology
Published: October 19, 2022
JAK2 Mutations Are Rare and Diverse in Myelodysplastic Syndromes: Case Series and Review of the Literature.
Journal: Hematology reports
Published: October 04, 2022
Cytogenetically cryptic PML::RARA fusion in acute promyelocytic leukemia: Testing strategies in the modern era.
Journal: Leukemia research reports
Published: February 11, 2022
Multiple Whole Chromosomal Gains Define Angiomatous Meningiomas and Are Absent From the Tumor Vasculature.
Journal: Journal of neuropathology and experimental neurology
Published: January 27, 2020
A high-grade glioma with SOS1 amplification.
Journal: Clinical neuropathology
Published: December 17, 2019
Papillary haemangioma in the spinal canal of a patient with a germline 12p microdeletion.
Journal: Histopathology
Published: March 19, 2019
Characteristics of myeloproliferative neoplasms in patients exposed to ionizing radiation following the Chernobyl nuclear accident.
Journal: American journal of hematology
Published: September 24, 2018
EBV-positive, HHV8-negative large B-cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient.
Journal: Clinical case reports
Published: March 21, 2018
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.
Journal: Cancer genetics
Published: March 11, 2018
Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.
Journal: Cancer genetics
Published: March 05, 2018
Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAFV600E.
Journal: Oncotarget
Published: July 14, 2017
Last Updated: 09/26/2026