Fernanda M. Bosada

Amsterdam, NH 1105AZ, Netherlands

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

Journal: Circulation
Published: October 11, 2024

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.

Journal: Nature communications
Published: February 17, 2023

An atrial fibrillation-associated regulatory region modulates cardiac Tbx5 levels and arrhythmia susceptibility.

An atrial fibrillation-associated regulatory region modulates cardiac Tbx5 levels and arrhythmia susceptibility.

Journal: eLife
Published: May 27, 2022

Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction.

Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction.

Journal: Circulation
Published: February 03, 2022

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Journal: Circulation research
Published: December 10, 2021

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 15, 2021

A Variant Noncoding Region Regulates Prrx1 and Predisposes to Atrial Arrhythmias.

A Variant Noncoding Region Regulates Prrx1 and Predisposes to Atrial Arrhythmias.

Journal: Circulation research
Published: June 07, 2021

Variant Intronic Enhancer Controls SCN10A-short Expression and Heart Conduction.

Variant Intronic Enhancer Controls SCN10A-short Expression and Heart Conduction.

Journal: Circulation
Published: April 29, 2021

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 27, 2020

Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker Enhancer.

Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker Enhancer.

Journal: Circulation research
Published: October 12, 2020

Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation.

Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation.

Journal: Circulation research
Published: July 28, 2020
Showing 1-12 of 16

Last Updated: 09/26/2026