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Pia Østergaard | doi.page

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Pia Østergaard

St George's, University of London(GB)Genomics England(GB)City St George's, University of London(GB)

Publications by Year

Research Areas

Lymphatic System and Diseases, Vascular Malformations and Hemangiomas, Skin and Cellular Biology Research, Lymphatic Disorders and Treatments, Parasite Biology and Host Interactions

Most-Cited Works

→ Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)(2011)499 cited
→ The phylogeny of the Schistosomatidae based on three genes with emphasis on the interrelationships of Schistosoma Weinland, 1858(2003)347 cited
→ Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis(2015)316 cited
→ Lipedema: An inherited condition(2010)308 cited
→ Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy(2012)188 cited
→ Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program(2018)170 cited

→ The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings(2013)168 cited

→ Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema(2013)167 cited

→ Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype(2011)116 cited

→ EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis(2016)103 cited