Wen Shuai

Journal Article Cancer · March 15, 2023 BACKGROUND: ETNK1 mutation has been suggested as a useful tool to support the diagnosis of atypical chronic myeloid leukemia. ETNK1 mutations, however, occur in other myeloid neoplasms. METHODS: The authors assessed the clinicopathologic and molecular gene ... Full text Link to item Cite

BRAF-negative, CD103-negative hairy cell leukemia.

Journal Article Blood · February 16, 2023 Full text Link to item Cite

Postchemotherapy Histiocyte-rich Pseudotumor Mimicking Residual Lymphoma

Journal Article American Journal of Surgical Pathology · February 2021 Postchemotherapy histiocyte-rich pseudotumor is a rare event in lymphoma patients and can cause elevated metabolic activity on positron emission tomography-computed tomography scan mimicking residual tumor. Here, we reported 11 lymphoma cases showi ... Full text Cite

Ultra-Rapid Reporting of TP53 Mutation in Myeloid Neoplasms by Using Next Generation Sequencing.

Journal Article Modern Pathology · 2021 Cite

The Diagnostic and Prognostic Roles of EBER for Patients With HIV-Associated Aggressive Non-Hodgkin Lymphomas In The Era of HAART

Journal Article Modern Pathology · 2021 Cite

Clinicopathological characterization of chronic lymphocytic leukemia with MYD88 mutations: L265P and non-L265P mutations are associated with different features

Journal Article Blood Cancer Journal · August 26, 2020 AbstractMYD88 mutations in chronic lymphocytic leukemia (CLL) are not well characterized. Earlier reports yielded conflicting results in terms of clinicopathologic presentation and prognostic impa ... Full text Cite

CD138− plasma cell myeloma

Journal Article Blood · September 12, 2019 Full text Cite

Gaucher disease type 1 first recognized in an elderly patient with thrombocytopenia and lung adenocarcinoma

Journal Article Clinical Case Reports · September 2019 AbstractRecognizing Gaucher disease in elderly patients can be challenging. We present a Gaucher disease type 1 case diagnosed in an elderly patient with thrombocytopenia and lung adenocarcinoma. The diagnosis of Gaucher di ... Full text Cite

Distinct Clinicopathologic Features of Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Based on MYD88 Mutations at Hotspot versus Non-Hotspot Codons.

Journal Article Modern Pathology · 2019 Cite

Primary Bone Diffuse Large B-Cell Lymphoma.

Journal Article Modern Pathology · 2018 Cite

Exclusion of Primer Sequence in the Alignment Process of the NGS Reads Could Miss the Insertion Detection of KIT Gene in GIST.

Journal Article Modern Pathology · 2018 Cite

Read phase related error could cause strand bias in NGS sequencing.

Journal Article Modern Pathology · 2018 Cite

Validation of NGS Detection of the Mutations in the Hematopoietic Disorders with Large Myeloid Panel.

Journal Article Modern Pathology · 2017 Cite

A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome

Journal Article Heart Rhythm · January 2013 Full text Cite

Wen Shuai

Selected Publications

ETNK1 mutation occurs in a wide spectrum of myeloid neoplasms and is not specific for atypical chronic myeloid leukemia.

BRAF-negative, CD103-negative hairy cell leukemia.

Postchemotherapy Histiocyte-rich Pseudotumor Mimicking Residual Lymphoma

Ultra-Rapid Reporting of TP53 Mutation in Myeloid Neoplasms by Using Next Generation Sequencing.

The Diagnostic and Prognostic Roles of EBER for Patients With HIV-Associated Aggressive Non-Hodgkin Lymphomas In The Era of HAART

Clinicopathological characterization of chronic lymphocytic leukemia with MYD88 mutations: L265P and non-L265P mutations are associated with different features

CD138− plasma cell myeloma

Gaucher disease type 1 first recognized in an elderly patient with thrombocytopenia and lung adenocarcinoma

Distinct Clinicopathologic Features of Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Based on MYD88 Mutations at Hotspot versus Non-Hotspot Codons.

Primary Bone Diffuse Large B-Cell Lymphoma.

Exclusion of Primer Sequence in the Alignment Process of the NGS Reads Could Miss the Insertion Detection of KIT Gene in GIST.

Read phase related error could cause strand bias in NGS sequencing.

Validation of NGS Detection of the Mutations in the Hematopoietic Disorders with Large Myeloid Panel.

A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome

Trafficking-competent KCNQ1 variably influences the function of HERG long QT alleles

Genetic screening in C. elegans identifies rho-GTPase activating protein 6 as novel HERG regulator

HERG Is Protected from Pharmacological Block by α-1,2-Glucosyltransferase Function