Marlin Y. Touma

Neonatology | Pediatrics

200 Medical Plz
Los Angeles, CA 90095

Last Updated: 09/26/2026

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Found 34 publications

Mosaic pathogenic PRKAG2 variant and pathologic diagnosis of glycogen storage disease in an infant with negative whole-genome sequencing.

Mosaic pathogenic PRKAG2 variant and pathologic diagnosis of glycogen storage disease in an infant with negative whole-genome sequencing.

Journal: JHLT open

Published: May 08, 2026

Novel Missense Variants in TRIM37 Associated with Mulibrey Nanism and Complex Congenital Heart Disease.

Novel Missense Variants in TRIM37 Associated with Mulibrey Nanism and Complex Congenital Heart Disease.

Journal: Cardiology and cardiovascular medicine

Published: March 30, 2026

Heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1) maintains muscle progenitor identity by stabilizing the Ppp1r1b-lncRNA-PRC2 complex.

Heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1) maintains muscle progenitor identity by stabilizing the Ppp1r1b-lncRNA-PRC2 complex.

Journal: Nucleic acids research

Published: November 28, 2025

Genetic drivers of congenital cardiac fibrosis.

Genetic drivers of congenital cardiac fibrosis.

Journal: Communications biology

Published: October 22, 2025

Wnt11 Positively Regulates Neonatal Cardiomyocyte Maturation at the Interphase of Life via Frizzled 4 Receptor.

Wnt11 Positively Regulates Neonatal Cardiomyocyte Maturation at the Interphase of Life via Frizzled 4 Receptor.

Journal: bioRxiv : the preprint server for biology

Published: June 12, 2025

Endocardial Fibrosis Elastosis: Long-Standing Mystery and Promising Therapy.

Endocardial Fibrosis Elastosis: Long-Standing Mystery and Promising Therapy.

Journal: JACC. Basic to translational science

Published: May 15, 2025

Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects.

Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects.

Journal: International journal of molecular sciences

Published: January 30, 2025

High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.

High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.

Journal: International journal of molecular sciences

Published: April 16, 2024

Gestational exposure to air pollutants perturbs metabolic and placenta-fetal phenotype.

Gestational exposure to air pollutants perturbs metabolic and placenta-fetal phenotype.

Journal: Reproductive toxicology (Elmsford, N.Y.)

Published: March 23, 2024

Stromal Cell-SLIT3/Cardiomyocyte-ROBO1 Axis Regulates Pressure Overload-Induced Cardiac Hypertrophy.

Stromal Cell-SLIT3/Cardiomyocyte-ROBO1 Axis Regulates Pressure Overload-Induced Cardiac Hypertrophy.

Journal: Circulation research

Published: February 28, 2024

Mapping Chromatin Occupancy of Ppp1r1b-lncRNA Genome-Wide Using Chromatin Isolation by RNA Purification (ChIRP)-seq.

Mapping Chromatin Occupancy of Ppp1r1b-lncRNA Genome-Wide Using Chromatin Isolation by RNA Purification (ChIRP)-seq.

Journal: bioRxiv : the preprint server for biology

Published: November 14, 2023

Mapping Chromatin Occupancy of Ppp1r1b-lncRNA Genome-Wide Using Chromatin Isolation by RNA Purification (ChIRP)-seq.

Mapping Chromatin Occupancy of Ppp1r1b-lncRNA Genome-Wide Using Chromatin Isolation by RNA Purification (ChIRP)-seq.

Journal: Cells

Published: October 25, 2023

Showing 1-12 of 34

Last Updated: 09/26/2026