Pia Ostergaard

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Professor of Human Genetics

St George’s, University of London

United Kingdom

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About

Professor Pia Ostergaard is a faculty member in the field of Human Genetics at St George's University of London, UK. Her research focuses on lymphatic anomalies, genetic associations in rare diseases, and advanced imaging techniques in lymphatic disorders. She has recently published articles examining lymphoedema diagnosis, genetic risk factors in lipedema, and the significance of lymphatic-lymphocyte interactions.

Recent Grants

Grant: Close

Metabolic programs of lymphatic endothelial cells and their disturbance in lymphedema

Open Date: 2018-01-01

Close Date: 2021-12-31

Grant: Close

Deep phenotyping to improve understanding of causal mechanisms and underlying gene mutations in primary lymphoedema and lymphatic malformations

Open Date: 2017-09-30

Close Date: 2022-09-29

Grant: Close

Genetic Analysis of Lipoedema

Open Date: 2016-03-01

Close Date: 2018-02-01

Grant: Close

Functional analysis of GATA2 and KIF11

Open Date: 2014-01-01

Close Date: 2018-12-01

Grant: Close

Analysis of candidate genes for primary lymphoedema

Open Date: 2013-10-01

Close Date: 2015-09-01

Articles (18)

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2025

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2024

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2024

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2021

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2021

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2020

Collaborators (9)

Taija Makinen

Professor

Uppsala University

SWEDEN

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kathleen freson

Prof

Katholieke Universiteit Leuven

BELGIUM

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Nils Rouven Hansmeier

GERMANY

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Ernest Turro

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Alan Pittman

University College London

UNITED KINGDOM

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Jenny Lord

University of Southampton

UNITED KINGDOM

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Roland Fleck

King’s College London

UNITED KINGDOM

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Richard Monaghan

The University of Manchester

UNITED KINGDOM

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René Hägerling

GERMANY

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Pia Ostergaard

Research Interests

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About

Recent Grants

Articles (18)

A systematic review of indocyanine green lymphography imaging for the diagnosis of primary lymphoedema

The utility of dynamic contrast-enhanced intranodal magnetic resonance lymphangiography (MRL) in the investigation of primary lymphatic anomalies

Magnetic resonance lymphangiography: Establishing normal

Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies

Genetic association analysis of 77,539 genomes reveals rare disease etiologies.

Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors

Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts

Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions.

Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort.

Image registration and subtraction in dynamic magnetic resonance lymphangiography (MRL) of the legs.

Correction: Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes

Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes

Mutations in EPHB4 cause human venous valve aplasia.

The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases

Systematic Review of Magnetic Resonance Lymphangiography From a Technical Perspective

Development and Physiological Functions of the Lymphatic System - Insights from Genetic Studies of Lymphedema.

The St George's Classification Algorithm of Primary Lymphatic Anomalies.

Update and audit of the St George's classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis.

Collaborators (9)

Taija Makinen

kathleen freson

Nils Rouven Hansmeier

Ernest Turro

Alan Pittman

Jenny Lord

Roland Fleck

Richard Monaghan

René Hägerling

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