Long Chen

Tianjin Enterprise Key Laboratory Of AI Aided Hematopathology Diagnosis
Tianjin, China

Last Updated: 09/26/2026

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Found 22 publications

Acute myeloid leukemia with 4q12 rearrangements involving CHIC2: "pitfalls" in fluorescence in situ hybridization diagnosis of PDGFRA rearrangements.

Acute myeloid leukemia with 4q12 rearrangements involving CHIC2: "pitfalls" in fluorescence in situ hybridization diagnosis of PDGFRA rearrangements.

Journal: American journal of clinical pathology

Published: March 26, 2026

Diagnostic pitfalls and molecular insights in a rare RUNX1::TACC1-positive AML with t(8;21)(p11;q22).

Diagnostic pitfalls and molecular insights in a rare RUNX1::TACC1-positive AML with t(8;21)(p11;q22).

Journal: Journal of hematopathology

Published: January 08, 2026

Adverse outcomes and high incidence of therapy-related neoplasms in patients with the t(16;21)/RUNX1::RUNX1T3 fusion.

Adverse outcomes and high incidence of therapy-related neoplasms in patients with the t(16;21)/RUNX1::RUNX1T3 fusion.

Journal: Leukemia & lymphoma

Published: December 22, 2025

A novel splicing variant of CNTRL::FGFR1 in myeloid/lymphoid neoplasm with eosinophilia and rearrangement of FGFR1.

A novel splicing variant of CNTRL::FGFR1 in myeloid/lymphoid neoplasm with eosinophilia and rearrangement of FGFR1.

Journal: Journal of hematopathology

Published: July 09, 2025

Detection of leukemia gene fusions on DNA-level through targeted Next-Generation Sequencing.

Detection of leukemia gene fusions on DNA-level through targeted Next-Generation Sequencing.

Journal: PloS one

Published: May 16, 2025

The t(18;22)/IGL::BCL2 translocation defines a unique CLL subtype: association with early treatment initiation.

The t(18;22)/IGL::BCL2 translocation defines a unique CLL subtype: association with early treatment initiation.

Journal: Journal of hematopathology

Published: February 11, 2025

A Novel Frameshift Mutation of HBB Causing Dominant β-Thalassemia in a Chinese Individual.

A Novel Frameshift Mutation of HBB Causing Dominant β-Thalassemia in a Chinese Individual.

Journal: Hemoglobin

Published: August 05, 2024

Clinical laboratory characteristics and gene mutation spectrum of Ph-negative MPN patients with atypical variants of JAK2, MPL, or CALR.

Clinical laboratory characteristics and gene mutation spectrum of Ph-negative MPN patients with atypical variants of JAK2, MPL, or CALR.

Journal: Cancer medicine

Published: November 16, 2023

WNT inhibitory factor 1 (WIF1) is a novel fusion partner of RUNX family transcription factor 1 (RUNX1) in acute myeloid leukemia with t(12;21)(q14;q22).

WNT inhibitory factor 1 (WIF1) is a novel fusion partner of RUNX family transcription factor 1 (RUNX1) in acute myeloid leukemia with t(12;21)(q14;q22).

Journal: Journal of hematopathology

Published: November 14, 2023

The application of targeted RNA sequencing for the analysis of fusion genes, gene mutations, IKZF1 intragenic deletion, and CRLF2 overexpression in acute lymphoblastic leukemia.

The application of targeted RNA sequencing for the analysis of fusion genes, gene mutations, IKZF1 intragenic deletion, and CRLF2 overexpression in acute lymphoblastic leukemia.

Journal: International journal of laboratory hematology

Published: September 07, 2023

Identification of novel mutations in patients with Diamond-Blackfan anemia and literature review of RPS10 and RPS26 mutations.

Identification of novel mutations in patients with Diamond-Blackfan anemia and literature review of RPS10 and RPS26 mutations.

Journal: International journal of laboratory hematology

Published: February 27, 2023

Mutational features of immunoglobulin heavy chain variable region gene in patients with chronic lymphocytic leukemia

Mutational features of immunoglobulin heavy chain variable region gene in patients with chronic lymphocytic leukemia

Journal: Zhonghua bing li xue za zhi = Chinese journal of pathology

Published: November 02, 2022

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Last Updated: 09/26/2026