Deborah Morris-Rosendahl

Consultant Clinical Scientist and Head

Royal Marsden NHS Foundation Trust

United Kingdom

Research Interests

Explore related searches

Professors in United Kingdom Professors in Medical Science Medical Science professors in United Kingdom

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Deborah Morris-Rosendahl is a Consultant Clinical Scientist and Head at the Royal Brompton and Harefield NHS Foundation Trust in the UK. Her research areas include primary ciliary dyskinesia, inherited cardiomyopathies, and genetic variants associated with Noonan syndrome and thoracic aortic disease. She has contributed to several recent articles focused on clinical phenotypes and genetic testing recommendations in various conditions.

Articles (10)

Year:

2025

Year:

2025

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Collaborators (4)

Claire Shovlin

Imperial College London

UNITED KINGDOM

View details

Adam Shapiro

Associate Professor

McGill University Faculty of Medicine

CANADA

View details

Eric Huang

Professor

University of California, San Francisco

UNITED STATES

View details

Marie-Coralie Cornet

Assistant Professor

University of California, San Francisco

UNITED STATES

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Deborah Morris-Rosendahl

Research Interests

Explore related searches

Contact this professor

About

Articles (10)

Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta Syndrome

Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood

A novel variant in PTPN11, c.1277A>G p.(His426Arg), in a patient with Noonan syndrome with multiple lentigines

Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy

Pathogenic Variant Frequencies in Hereditary Haemorrhagic Telangiectasia Support Clinical Evidence of Protection from Myocardial Infarction

EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias

Primary ciliary dyskinesia as a common cause of bronchiectasis in the Canadian Inuit population

The genetic basis of thoracic aortic disease: The future of aneurysm classification?

Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma (Scientific Reports, (2021), 11, 1, (19138), 10.1038/s41598-021-98414-w)

COPD in the chromosomes

Collaborators (4)

Claire Shovlin

Adam Shapiro

Eric Huang

Marie-Coralie Cornet

Make your next move.

Deborah Morris-Rosendahl

Research Interests

Explore related searches

Contact this professor

About

Articles (10)

Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta Syndrome

Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood

A novel variant in PTPN11, c.1277A&gt;G p.(His426Arg), in a patient with Noonan syndrome with multiple lentigines

Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy

Pathogenic Variant Frequencies in Hereditary Haemorrhagic Telangiectasia Support Clinical Evidence of Protection from Myocardial Infarction

EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias

Primary ciliary dyskinesia as a common cause of bronchiectasis in the Canadian Inuit population

The genetic basis of thoracic aortic disease: The future of aneurysm classification?

Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma (Scientific Reports, (2021), 11, 1, (19138), 10.1038/s41598-021-98414-w)

COPD in the chromosomes

Collaborators (4)

Claire Shovlin

Adam Shapiro

Eric Huang

Marie-Coralie Cornet

Make your next move.

A novel variant in PTPN11, c.1277A>G p.(His426Arg), in a patient with Noonan syndrome with multiple lentigines