Yuan Chen - Publications

Response alone does not define optimal bridging before brexucabtagene autoleucel in mantle cell lymphoma.

Journal: British journal of haematology

Published: April 05, 2026

Analysis of a Chinese pedigree with Hereditary coagulation factor Ⅻ deficiency due to compound heterozygous variants of Ⅻ gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 15, 2025

Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 01, 2024

A Novel Heterozygous IHH c.331_333del Mutation Identified in a Fetus with Brachydactyly Type A1 Causes IHH Protein Maturation Failure in HEK293T Cells.

Journal: Phenomics (Cham, Switzerland)

Published: December 07, 2023

Genetic Analysis of Prekallikrein Deficiency in a Consanguineously Married Chinese Family.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: December 05, 2023

Metabolomics profiling of maternal and umbilical cord blood in normoglycemia macrosomia.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: October 17, 2023

Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency.

Journal: Hamostaseologie

Published: September 15, 2023

Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events.

Journal: International journal of laboratory hematology

Published: August 27, 2023

Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations.

Journal: Hamostaseologie

Published: June 15, 2023

Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*).

Journal: Blood cells, molecules & diseases

Published: June 11, 2023

A Novel Homozygous Missense Mutation (Ile583Asn) in a Consanguineous Marriage Family with Hereditary Factor XII Deficiency: A Case Report.

Journal: Hamostaseologie

Published: December 09, 2022

Analysis of PROC gene variant in a Chinese pedigree affected with hereditary protein C deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: November 01, 2022