Pia Østergaard

4.3k citations
56 papers · 2.5k · h-index 25

Impact in

Papers in

  • Oncology 26
    • Lymphatic System and Diseases 26
  • Surgery 13
    • Vascular Malformations and Hemangiomas 9
    • Lymphatic Disorders and Treatments 6
Co-authors
Sahar Mansour (27 shared papers)Steve Jeffery (20 shared papers)Glen Brice (15 shared papers)Peter Mortimer (24 shared papers)Kristiana Gordon (23 shared papers)Fiona Connell (7 shared papers)Michael A. Simpson (5 shared papers)Silvia Martin‐Almedina (6 shared papers)
Journals
Journal of Medical Genetics (3 papers)Human Genetics (3 papers)European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)Allergy (3 papers)
Partner nations
United KingdomUnited StatesGermany

In The Last Decade

Pia Østergaard

55 papers receiving 2.4k citations

Peers

Pia Østergaard
Comparison fields: 5 of 110
  • Oncology 1.1k
  • Parasitology 200
  • Cell Biology 376
  • Physiology 546
  • Hematology 193
Replace Richard Pannell with:
Richard Pannell United Kingdom
D. Hewett Australia
Francis Karanu Canada
Keiki Kumano Japan
Henry P. Adams United States
S Nishikawa Japan
David I. Stott United Kingdom
Guanling Huang China
Niels B. Atkin United Kingdom
Eleanor C. Weir United States
Pia Østergaard relative to Richard Pannell United Kingdom Richard Pannell's profile →
Citations per field
00.5×2×3.0×
Richard Pannell · 1×
Citations per year

Countries citing papers authored by Pia Østergaard

Since Specialization
Citations

This map shows the geographic impact of Pia Østergaard's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Pia Østergaard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pia Østergaard more than expected).

Fields of papers citing papers by Pia Østergaard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pia Østergaard. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Pia Østergaard. The network helps show where Pia Østergaard may publish in the future.

Co-authors

The 25 scholars most cited alongside Pia Østergaard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Pia Østergaard Line = papers co-authored together Pia Østergaard links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Nature Genetics ·Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour
2011374
2
The phylogeny of the Schistosomatidae based on three genes with emphasis on the interrelationships of Schistosoma Weinland, 1858
Parasitology ·Anne E. Lockyer, Peter D. Olson, Pia Østergaard, David Rollinson, David A. Johnston, Stephen W. Attwood, V. R. Southgate, Petr Horák, S. D. Snyder, Thanh Hoa Le, Takeshi Agatsuma, Donald P. McManus, A. Christopher Carmichael, S Naem, D. Timothy J. Littlewood
2003274
3
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
Nature Communications ·Elisavet Fotiou, Silvia Martin‐Almedina, Michael A. Simpson, Shin Lin, Kristiana Gordon, Glen Brice, Giles Atton, Iona Jeffery, David C. Rees, Cyril Mignot, Julie Vogt, Tessa Homfray, M Snyder, Stanley G. Rockson, Steve Jeffery, Peter Mortimer, Sahar Mansour, Pia Østergaard
2015234
4
Lipedema: An inherited condition
American Journal of Medical Genetics Part A ·Anne H. Child, Kristiana Gordon, Pip Sharpe, Glen Brice, Pia Østergaard, Steve Jeffery, Peter Mortimer
2010202
5
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
Circulation Research ·Kristiana Gordon, Dörte Schulte, Glen Brice, Michael A. Simpson, M. Guy Roukens, Andreas van Impel, Fiona Connell, Kamini Kalidas, Steve Jeffery, Peter Mortimer, Sahar Mansour, Stefan Schulte‐Merker, Pia Østergaard
2013133
6
Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program
Nature Communications ·Maike Frye, Andrea Taddei, Cathrin Dierkes, Inés Martínez‐Corral, Matthew Fielden, Henrik Ortsäter, Jan Kazenwadel, Dinis Pedro Calado, Pia Østergaard, Marjo Salminen, Liqun He, Natasha L. Harvey, Friedemann Kiefer, Taija Mäkinen
2018133
7
The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings
Clinical Genetics ·FC Connell, Kristiana Gordon, Glen Brice, Vaughan Keeley, Steve Jeffery, P.S. Mortimer, Sahar Mansour, Pia Østergaard
2013120
8
Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype
Journal of Medical Genetics ·Pia Østergaard, Michael A. Simpson, Glen Brice, Sahar Mansour, Fiona Connell, Alexandros Onoufriadis, A. H. Child, (unknown), Kamini Kalidas, Peter Mortimer, Richard C. Trembath, Steve Jeffery
201189
9
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia
Human Genetics ·Fiona Connell, Kamini Kalidas, Pia Østergaard, Glen Brice, Tessa Homfray, Lesley Roberts, David J. Bunyan, Sally G. Mitton, Sahar Mansour, Peter Mortimer, Steve Jeffery
200976
10
Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas
Human Genetics ·Fiona Connell, Pia Østergaard, Charles Carver, Glen Brice, N. Williams, Sahar Mansour, Peter Mortimer, Steve Jeffery
200876
11
Update and audit of the St George’s classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis
Journal of Medical Genetics ·Kristiana Gordon, Ruth Varney, Vaughan Keeley, Katie Riches, Steve Jeffery, Malou van Zanten, Peter Mortimer, Pia Østergaard, Sahar Mansour
202065
12
A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family
Clinical Genetics ·Glen Brice, Pia Østergaard, Steve Jeffery, Kristiana Gordon, P.S. Mortimer, Sahar Mansour
201363
13
FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update
Human Mutation ·Kristiana Gordon, Sarah L. Spiden, Fiona Connell, Glen Brice, Sally Cottrell, John Short, Rohan Taylor, Steve Jeffery, Peter Mortimer, Sahar Mansour, Pia Østergaard
201260
14
The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome
European Journal of Human Genetics ·Sarah Joyce, Kristiana Gordon, Glen Brice, Pia Østergaard, Rani Nagaraja, John Short, Sandra Moore, Peter Mortimer, Sahar Mansour
201558
15
Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy
The American Journal of Human Genetics ·Sophie Scheidecker, Christelle Etard, Laurence Haren, Corinne Stoetzel, Sarah Hull, Gavin Arno, Vincent Plagnol, Séverine Drunat, Sandrine Passemard, Annick Toutain, Cathy Obringer, Mériam Koob, Véronique Geoffroy, Vincent Marion, Uwe Strähle, Pia Østergaard, Alain Verloès, Andreas Merdes, Anthony T. Moore, Hélène Dollfus
201552
16
The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review
European Journal of Human Genetics ·Giles Atton, Kristiana Gordon, Glen Brice, Vaughan Keeley, Katie Riches, Pia Østergaard, Peter Mortimer, Sahar Mansour
201545
17
Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes?
The Journal of Physiology ·Silvia Martin‐Almedina, Sahar Mansour, Pia Østergaard
201838
18
The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases
Cardiovascular Research ·Richard M. Monaghan, Donna J. Page, Pia Østergaard, Bernard Keavney
202036
19
Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema
Physiological Reviews ·Silvia Martin‐Almedina, Peter Mortimer, Pia Østergaard
202132
20
VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations
JCI Insight ·René Hägerling, Dominik Drees, Aaron Scherzinger, Cathrin Dierkes, Silvia Martin‐Almedina, Stefan Butz, Kristiana Gordon, Michael Schäfers, Klaus Hinrichs, Pia Østergaard, Dietmar Vestweber, Tobias Goerge, Sahar Mansour, Xiaoyi Jiang, Peter Mortimer, Friedemann Kiefer
201731

About Pia Østergaard

Pia Østergaard is a scholar working on Oncology, Surgery, Molecular Biology, Physiology and Ecology, having authored 56 papers that have together received 2.5k indexed citations. Recurring topics across this work include Lymphatic System and Diseases (26 papers), Vascular Malformations and Hemangiomas (9 papers), Parasite Biology and Host Interactions (7 papers), Skin and Cellular Biology Research (7 papers), Lymphatic Disorders and Treatments (6 papers), Sympathectomy and Hyperhidrosis Treatments (4 papers), Congenital heart defects research (3 papers) and Marine Biology and Ecology Research (3 papers). The work is most often cited by research in Oncology (1.1k citations), Parasitology (200 citations), Cell Biology (376 citations), Physiology (546 citations) and Hematology (193 citations). Pia Østergaard has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Sahar Mansour, Steve Jeffery, Glen Brice, Peter Mortimer, Kristiana Gordon, Fiona Connell, Michael A. Simpson, Silvia Martin‐Almedina, Vaughan Keeley and P.S. Mortimer. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, European Journal of Human Genetics, Clinical Genetics and Allergy.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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