Zhongxia M. Qi

Medical Genetics

185 Berry Street, Suite 290, Room 2421
San Francisco, CA 94107

Last Updated: 09/26/2026

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Found 38 publications

Development of a Fully Non-Viral 1XX-enhanced BCMA CAR-T Cell Therapy for Multiple Myeloma.

Development of a Fully Non-Viral 1XX-enhanced BCMA CAR-T Cell Therapy for Multiple Myeloma.

Journal: bioRxiv : the preprint server for biology

Published: May 04, 2026

Development of a Fully Non-Viral 1XX-enhanced BCMA CAR-T Cell Therapy for Multiple Myeloma.

Development of a Fully Non-Viral 1XX-enhanced BCMA CAR-T Cell Therapy for Multiple Myeloma.

Journal: bioRxiv : the preprint server for biology

Published: May 04, 2026

Molecular Characterization of MECOM Rearrangements in Two Cases with Myelodysplastic Syndrome and t(2;3)(p23;q26.2).

Molecular Characterization of MECOM Rearrangements in Two Cases with Myelodysplastic Syndrome and t(2;3)(p23;q26.2).

Journal: Cytogenetic and genome research

Published: August 30, 2025

Gene-corrected regulatory T cell therapy for IL2RA deficiency.

Gene-corrected regulatory T cell therapy for IL2RA deficiency.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: June 02, 2025

Cell type specificity of mosaic chromosome 1q gain resolved by snRNA-seq in a case of epilepsy with hyaline protoplasmic astrocytopathy.

Cell type specificity of mosaic chromosome 1q gain resolved by snRNA-seq in a case of epilepsy with hyaline protoplasmic astrocytopathy.

Journal: bioRxiv : the preprint server for biology

Published: February 08, 2024

Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy.

Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy.

Journal: Neurology. Genetics

Published: August 25, 2023

Complex Genomic Rearrangements Involving ETV6::ABL1 Gene Fusion in an Individual with Myeloid Neoplasm.

Complex Genomic Rearrangements Involving ETV6::ABL1 Gene Fusion in an Individual with Myeloid Neoplasm.

Journal: Genes

Published: August 12, 2023

Editorial: Unravelling the basis of non-invasive prenatal screening results.

Editorial: Unravelling the basis of non-invasive prenatal screening results.

Journal: Frontiers in genetics

Published: June 26, 2023

Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening.

Synthesis of positive plasmas with known chromosomal abnormalities for validation of non-invasive prenatal screening.

Journal: Frontiers in genetics

Published: June 16, 2022

Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia.

Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia.

Journal: Cytogenetic and genome research

Published: February 25, 2022

Distinct pathologic feature of myeloid neoplasm with t(v;11p15); NUP98 rearrangement.

Distinct pathologic feature of myeloid neoplasm with t(v;11p15); NUP98 rearrangement.

Journal: Human pathology

Published: November 23, 2021

Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders.

Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders.

Journal: NPJ genomic medicine

Published: October 13, 2021

Showing 1-12 of 38

Last Updated: 09/26/2026