Tessa Homfray

London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 64 publications

Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?

Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?

Journal: Prenatal diagnosis
Published: February 03, 2026

Fetal Bradycardia Prompting the Diagnosis and Management of Parental Long QT Syndrome.

Fetal Bradycardia Prompting the Diagnosis and Management of Parental Long QT Syndrome.

Journal: Circulation. Arrhythmia and electrophysiology
Published: December 02, 2025

RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.

RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2025

RNU4ATAC-opathy: Clinical, molecular, and transcriptomic insights from a large cohort.

RNU4ATAC-opathy: Clinical, molecular, and transcriptomic insights from a large cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2025

A feasibility study of whole genome germline testing as an adjunct screening tool in a UK general private practice.

A feasibility study of whole genome germline testing as an adjunct screening tool in a UK general private practice.

Journal: Scientific reports
Published: May 29, 2025

Prenatal presentation of fetal bradycardia and long QT syndrome.

Prenatal presentation of fetal bradycardia and long QT syndrome.

Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: October 24, 2024

Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort.

Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort.

Journal: Prenatal diagnosis
Published: June 14, 2024

Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant.

Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant.

Journal: HeartRhythm case reports
Published: January 11, 2024

Enhancement of phenotyping for fetal investigation using next-generation sequencing.

Enhancement of phenotyping for fetal investigation using next-generation sequencing.

Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: May 20, 2023

De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage.

De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage.

Journal: American journal of medical genetics. Part A
Published: November 23, 2022

The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum.

The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum.

Journal: Journal of medical genetics
Published: October 31, 2022

Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation.

Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation.

Journal: Nature communications
Published: October 31, 2022
Showing 1-12 of 64

Last Updated: 09/26/2026