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Author Details
Full Name
Christopher D Gocke
Affiliation
Johns Hopkins University School of Medicine
ORCID
Career Start Year
1992
Papers
188
H Index
40
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37236162
Current clinical practices and challenges in molecular testing: a GOAL Consortium Hematopathology Working Group report.
Blood Adv
2023
37841697
Plexiform neurofibroma of the liver, with malignant transformation to MPNST, in a pediatric patient without neurofibromatosis type 1.
Neurooncol Adv
2023
37926709
Donor cell-derived genetic abnormalities after sex mismatched allogeneic cell transplantation: a unique challenge of donor cell leukemia.
Blood Cancer J
2023
37583476
The Genomics Organization for Academic Laboratories (GOAL): A vision for a genomics future for academic pathology.
Acad Pathol
2023
38001699
Ring Chromosomes in Hematological Malignancies Are Associated with <i>TP53</i> Gene Mutations and Characteristic Copy Number Variants.
Cancers (Basel)
2023
37806433
Recommendations for Cell-Free DNA Assay Validations: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.
J Mol Diagn
2023
37090662
The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts.
Res Sq
2023
37276081
Cell-free DNA measurable residual disease as a predictor of postallogeneic hematopoietic cell transplant outcomes.
Blood Adv
2023
37140166
Familial Clonal Hematopoiesis in a Long Telomere Syndrome.
N Engl J Med
2023
37440250
Novel PAX3::INO80D Fusion in Biphenotypic Sinonasal Sarcoma in an Adult.
JAMA Otolaryngol Head Neck Surg
2023
37372318
Complex/cryptic <i>EWSR1::FLI1/ERG</i> Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas.
Genes (Basel)
2023
37236162
Current clinical practices and challenges in molecular testing: a GOAL Consortium Hematopathology Working Group report.
Blood Adv
2023
37354804
Co-occurring mutations in ASXL1, SRSF2, and SETBP1 define a subset of myelodysplastic/ myeloproliferative neoplasm with neutrophilia.
Leuk Res
2023
37350948
Colorectal cancer in patients of advanced age is associated with increased incidence of <i>BRAF</i> p.V600E mutation and mismatch repair deficiency.
Front Oncol
2023
37806433
Recommendations for Cell-Free DNA Assay Validations: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.
J Mol Diagn
2023
38001699
Ring Chromosomes in Hematological Malignancies Are Associated with <i>TP53</i> Gene Mutations and Characteristic Copy Number Variants.
Cancers (Basel)
2023
37583476
The Genomics Organization for Academic Laboratories (GOAL): A vision for a genomics future for academic pathology.
Acad Pathol
2023
37841697
Plexiform neurofibroma of the liver, with malignant transformation to MPNST, in a pediatric patient without neurofibromatosis type 1.
Neurooncol Adv
2023
37926709
Donor cell-derived genetic abnormalities after sex mismatched allogeneic cell transplantation: a unique challenge of donor cell leukemia.
Blood Cancer J
2023
37354804
Co-occurring mutations in ASXL1, SRSF2, and SETBP1 define a subset of myelodysplastic/ myeloproliferative neoplasm with neutrophilia.
Leuk Res
2023
37090662
The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts.
Res Sq
2023
37350948
Colorectal cancer in patients of advanced age is associated with increased incidence of <i>BRAF</i> p.V600E mutation and mismatch repair deficiency.
Front Oncol
2023
37440250
Novel PAX3::INO80D Fusion in Biphenotypic Sinonasal Sarcoma in an Adult.
JAMA Otolaryngol Head Neck Surg
2023
37372318
Complex/cryptic <i>EWSR1::FLI1/ERG</i> Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas.
Genes (Basel)
2023
37276081
Cell-free DNA measurable residual disease as a predictor of postallogeneic hematopoietic cell transplant outcomes.
Blood Adv
2023
37140166
Familial Clonal Hematopoiesis in a Long Telomere Syndrome.
N Engl J Med
2023
34107771
Short Communication: Persistence of HIV After Allogeneic Bone Marrow Transplant in a Dually Infected Individual.
AIDS Res Hum Retroviruses
2022
35561840
Utility of targeted next-generation sequencing assay to detect 1p/19q co-deletion in formalin-fixed paraffin-embedded glioma specimens.
Hum Pathol
2022
35730391
Clonal hematopoiesis in men living with HIV and association with subclinical atherosclerosis.
AIDS
2022
34107771
Short Communication: Persistence of HIV After Allogeneic Bone Marrow Transplant in a Dually Infected Individual.
AIDS Res Hum Retroviruses
2022
34519764
Double PIK3CA Alterations and Parallel Evolution in Colorectal Cancers.
Am J Clin Pathol
2022
35312750
Artificial Intelligence-Assisted Serial Analysis of Clinical Cancer Genomics Data Identifies Changing Treatment Recommendations and Therapeutic Targets.
Clin Cancer Res
2022
34793200
Donor Clonal Hematopoiesis and Recipient Outcomes After Transplantation.
J Clin Oncol
2022
35149321
Lynch syndrome caused by a novel deletion of the promoter and exons 1-13 of MLH1 gene.
Cancer Genet
2022
34753870
Brief Report: Rebound HIV Viremia With Meningoencephalitis After Antiretroviral Therapy Interruption After Allogeneic Bone Marrow Transplant.
J Acquir Immune Defic Syndr
2022
35730391
Clonal hematopoiesis in men living with HIV and association with subclinical atherosclerosis.
AIDS
2022
35561840
Utility of targeted next-generation sequencing assay to detect 1p/19q co-deletion in formalin-fixed paraffin-embedded glioma specimens.
Hum Pathol
2022
35312750
Artificial Intelligence-Assisted Serial Analysis of Clinical Cancer Genomics Data Identifies Changing Treatment Recommendations and Therapeutic Targets.
Clin Cancer Res
2022
35149321
Lynch syndrome caused by a novel deletion of the promoter and exons 1-13 of MLH1 gene.
Cancer Genet
2022
34793200
Donor Clonal Hematopoiesis and Recipient Outcomes After Transplantation.
J Clin Oncol
2022
34519764
Double PIK3CA Alterations and Parallel Evolution in Colorectal Cancers.
Am J Clin Pathol
2022
34753870
Brief Report: Rebound HIV Viremia With Meningoencephalitis After Antiretroviral Therapy Interruption After Allogeneic Bone Marrow Transplant.
J Acquir Immune Defic Syndr
2022
34233240
Concomitance of a novel RMDN2-ALK fusion and an EML4-ALK fusion in a lung adenocarcinoma.
Cancer Genet
2021
33909482
Feasibility of Cell-Free DNA Collection and Clonal Immunoglobulin Sequencing in South African Patients With HIV-Associated Lymphoma.
JCO Glob Oncol
2021
34233240
Concomitance of a novel RMDN2-ALK fusion and an EML4-ALK fusion in a lung adenocarcinoma.
Cancer Genet
2021
33577993
Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies.
J Mol Diagn
2021
34209587
Germline <i>ERBB2</i>/<i>HER2</i> Coding Variants Are Associated with Increased Risk of Myeloproliferative Neoplasms.
Cancers (Basel)
2021
33929516
IDH1 and IDH2 Mutations in Colorectal Cancers.
Am J Clin Pathol
2021
34358677
Diagnostic Utility of Gene Fusion Panel to Detect Gene Fusions in Fresh and Formalin-Fixed, Paraffin-Embedded Cancer Specimens.
J Mol Diagn
2021
34491318
CloneRetriever: An Automated Algorithm to Identify Clonal B and T Cell Gene Rearrangements by Next-Generation Sequencing for the Diagnosis of Lymphoid Malignancies.
Clin Chem
2021
1 - 50 of 376
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4
Christine A Pratilas
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4
Sarah J Wheelan
National Human Genome Research Institute, National Institutes of Health
Co-authored papers
4
Fausto J Rodriguez
University of California Los Angeles
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4
Emmanuel S Antonarakis
The Sidney Kimmel Cancer Comprehensive Cancer Center at Johns Hopkins
Co-authored papers
2
Peter C Burger
Co-authored papers
2
Srinivasan Yegnasubramanian
Johns Hopkins University School of Medicine
Co-authored papers
2
Hua Ling
Chongqing Center for Disease Control and Prevention.
Co-authored papers
2
Peter K Rogan
CytoGnomix Inc.
Co-authored papers
2
Donald Small
Johns Hopkins University School of Medicine
Co-authored papers
2
Nara Sobreira
Johns Hopkins University
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2
Vered Stearns
Co-authored papers
2
Donna M Williams
Johns Hopkins University School of Medicine
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2
Christian F Meyer
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Elaine S Jaffe
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