Brendan J. Floyd

Pediatric Cardiology | Pediatrics | Medical Genetics

9000 W Wisconsin Ave
Milwaukee, WI 53226

Last Updated: 09/26/2026

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Found 21 publications

Damaging RBM20 E-rich domain variants are not rescued by gene replacement.

Damaging RBM20 E-rich domain variants are not rescued by gene replacement.

Journal: bioRxiv : the preprint server for biology

Published: July 29, 2026

Scaled Multidimensional Assays of Variant Effect Identify Sequence-Function Relationships in Hypertrophic Cardiomyopathy.

Scaled Multidimensional Assays of Variant Effect Identify Sequence-Function Relationships in Hypertrophic Cardiomyopathy.

Journal: Circulation

Published: July 12, 2026

RBM20 Truncating Variants and Human Cardiomyopathy.

RBM20 Truncating Variants and Human Cardiomyopathy.

Journal: JAMA cardiology

Published: April 08, 2026

SHOC2 Is a Novel Cause of Central Conducting Lymphatic Anomaly.

SHOC2 Is a Novel Cause of Central Conducting Lymphatic Anomaly.

Journal: American journal of medical genetics. Part A

Published: January 30, 2026

Multiparametric Assessment of TNNI3 Variant Phenotypes in Human iPSC-Cardiomyocytes Correlates with Disease Severity in Patients.

Multiparametric Assessment of TNNI3 Variant Phenotypes in Human iPSC-Cardiomyocytes Correlates with Disease Severity in Patients.

Journal: bioRxiv : the preprint server for biology

Published: December 25, 2025

The contribution of RBM20 truncating variants to human cardiomyopathy.

The contribution of RBM20 truncating variants to human cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences

Published: August 08, 2025

Scaled multidimensional assays of variant effect identify sequence-function relationships in hypertrophic cardiomyopathy.

Scaled multidimensional assays of variant effect identify sequence-function relationships in hypertrophic cardiomyopathy.

Journal: bioRxiv : the preprint server for biology

Published: June 12, 2025

Cardiologists' Perceptions of Cardiogenetic Testing and Management.

Cardiologists' Perceptions of Cardiogenetic Testing and Management.

Journal: JACC. Advances

Published: January 10, 2025

Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants.

Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants.

Journal: Circulation. Genomic and precision medicine

Published: July 02, 2024

Multi-site validation of a functional assay to adjudicate SCN5A Brugada Syndrome-associated variants.

Multi-site validation of a functional assay to adjudicate SCN5A Brugada Syndrome-associated variants.

Journal: medRxiv : the preprint server for health sciences

Published: January 10, 2024

Correction: Exploring the feasibility of using long-term stored newborn dried blood spots to identify metabolic features for congenital heart disease screening.

Correction: Exploring the feasibility of using long-term stored newborn dried blood spots to identify metabolic features for congenital heart disease screening.

Journal: Biomarker research

Published: November 23, 2023

Exploring the feasibility of using long-term stored newborn dried blood spots to identify metabolic features for congenital heart disease screening.

Exploring the feasibility of using long-term stored newborn dried blood spots to identify metabolic features for congenital heart disease screening.

Journal: Biomarker research

Published: October 21, 2023

Showing 1-12 of 21

Last Updated: 09/26/2026