Pia Ostergaard

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 22

Top Venues

Human molecular genetics

Nature medicine

Nature communications

European journal of human genetics : EJHG

St. George's University of London

Imperial College London (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

St. George's University of London Aug 01 2017

United Kingdom

Reader :: Molecular and Clinical Sciences Research Institute

St George's University of London Apr 01 2015 - Jul 31 2017

United Kingdom

Senior Lecturer :: Molecular and Clinical Sciences Institute

St. George's, University of London Jul 01 2013 - Mar 31 2015

United Kingdom

Lecturer :: Cardiovascular and Cell Sciences

Education History

Imperial College London May 01 1999 - Nov 01 2004

United Kingdom

PHD :: Division of Ecology and Evolution

Publications

Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Jiarna Rose Zerella, Claire C Homan, Peer Arts, Xuzhu Lin, Sam John Spinelli, Parvathy Venugopal, Milena Babic, Peter Brautigan, Lynda Truong, Luis Alberto Arriola-Martinez, Sarah Moore, Rachel Hollins, Wendy Parker, Hung Nguyen, Karin S Kassahn, Susan Branford, Simone K Feurstein, Lise Larcher, Flore Sicre de Fontbrune, Serwet Demirdas, Sonja de Munnik, Helene A Poirel, Benedicte Brichard, Shehla Mohammed, Kristiana Gordon, Erg Variants Research Network, Marcin W Wlodarski, Ashwin Lakshman Koppayi, Sara E Dobbins, Pim G N J Mutsaers, Kim E Nichols, Ninad Oak, Desiree DeMille, Rong Mao, Ali Crawford, Julie McCarrier, Donald Basel, Josue Flores-Daboub, Michael W Drazer, Kerry Phillips, Nicola Poplawski, Graeme M Birdsey, Daniela Pirri, Pia Ostergaard, Annet Simons, Lucy A Godley, David Morrall Ross, Devendra K Hiwase, Jean Soulier, Anna L Brown, Catherine L Carmichael, Hamish S Scott, Christopher N Hahn
Germline ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition. Blood (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics 33 (14) (2024)
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, Arie van Haeringen, Gabriela M Repetto, Kathelijn Keymolen, Laurence M Boon, Florence Belva, Guido Giacalone, Nicole Revencu, Yves Sznajer, Katie Riches, Vaughan Keeley, Shehla Mohammed, Kristiana Gordon, Silvia Martin-Almedina, Sara E Dobbins, Pia Ostergaard, Isabelle Quéré, Pascal Brouillard, Miikka Vikkula
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. Human molecular genetics (2024)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine 29 (3) (2023)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine (2023)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine 29 (3) (2023)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine 29 (3) (2023)
Dionysios Grigoriadis, Ege Sackey, Katie Riches, Malou van Zanten, Glen Brice, Ruth England, Michael Mills, Sara E Dobbins, Li Ling Lee, null null, null null, Steve Jeffery, Liang Dong, David B Savage, Peter S Mortimer, Vaughan Keeley, Alan Pittman, Kristiana Gordon, Pia Ostergaard
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort. PloS one 17 (10) (2022)
Michael Mills, Kristiana Gordon, Lakshmi Ratnam, Malou Van Zanten, Peter S Mortimer, Pia Ostergaard, Franklyn A Howe
Image registration and subtraction in dynamic magnetic resonance lymphangiography (MRL) of the legs. BJR case reports 8 (4) (2022)
Yann C Klimentidis, Zhao Chen, Manuel L Gonzalez-Garay, Dionysios Grigoriadis, Ege Ozkan, Alan M Pittman, Pia Ostergaard, Karen L Herbst
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors. European journal of human genetics : EJHG (2022)
Richard M Monaghan, Donna Joanne Page, Pia Ostergaard, Bernard D Keavney
The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases. Cardiovascular research 117 (8) (2022)
Silvia Martin-Almedina, Kazim Ogmen, Ege Ozkan, Dionysios Grigoriadis, Christina Karapouliou, Noeline Nadarajah, Cathrine Ebbing, Jenny Lord, Rhiannon Mellis, Fanny Kortuem, Mary Beth Dinulos, Cassandra Polun, Sherri Bale, Giles Atton, Alexandra Robinson, Hallvard Reigstad, Gunnar Houge, Axel von der Wense, Wolf-Henning Becker, Steve Jeffery, Peter S Mortimer, Kristiana Gordon, Katherine S Josephs, Sarah Robart, Mark David Kilby, Stephanie Vallee, Jerome L Gorski, Maja Hempel, Siren Berland, Shehla Mohammed, Pia Ostergaard
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes. Genetics in medicine : official journal of the American College of Medical Genetics 23 (7) (2021)
Shehla Mohammed, Katherine S Josephs, Pia Ostergaard, Kristiana Gordon, Malou Van Zanten, Julian Pearce, Steve Jeffery, Vaughan Keeley, Katie Riches, Alexander Kreuter, Ulrike Wieland, René Hägerling, Lakshmi Ratnam, Ege Sackey, Dionysios Grigoriadis, Bernard Ho, Frances Smith, Elisabeth Rauter, Peter Mortimer, Derek Macallan
Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts. Journal of medical genetics (2021)
Silvia Martin-Almedina, Peter S Mortimer, Pia Ostergaard
Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema. Physiological reviews 101 (4) (2021)
Michael Mills, Malou Van Zanten, Marco Borri, Peter S Mortimer, Kristiana Gordon, Pia Ostergaard, Franklyn A Howe
Systematic Review of Magnetic Resonance Lymphangiography From a Technical Perspective. Journal of magnetic resonance imaging : JMRI 53 (6) (2021)
Naushin H Waseem, Sancy Low, Amna Z Shah, Deepa Avisetti, Pia Ostergaard, Michael Simpson, Katarzyna A Niemiec, Belen Martin-Martin, Hebah Aldehlawi, Saima Usman, Pak Sang Lee, Anthony P Khawaja, Jonathan B Ruddle, Ameet Shah, Ege Ozkan, Alexander C Day, Yuzhen Jiang, Geoff Swinfield, Ananth Viswanathan, Giovanna Alfano, Christina Chakarova, Heather J Cordell, David F Garway-Heath, Peng T Khaw, Shomi S Bhattacharya, Ahmad Waseem, Paul J Foster
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma. PLoS genetics 16 (4) (2020)
Maike Frye, Andrea Taddei, Cathrin Dierkes, Ines Martinez-Corral, Matthew Fielden, Henrik Ortsäter, Jan Kazenwadel, Dinis P Calado, Pia Ostergaard, Marjo Salminen, Liqun He, Natasha L Harvey, Friedemann Kiefer, Taija Mäkinen
Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program. Nature communications 9 (1) (2018)
Noeline Nadarajah, Dörte Schulte, Vivienne McConnell, Silvia Martin-Almedina, Christina Karapouliou, Peter S Mortimer, Steve Jeffery, Stefan Schulte-Merker, Kristiana Gordon, Sahar Mansour, Pia Ostergaard
A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon. International journal of molecular sciences 19 (8) (2018)
Silvia Martin-Almedina, Sahar Mansour, Pia Ostergaard
Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes? The Journal of physiology 596 (6) (2018)
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, Michael P Snyder, Stanley G Rockson, Steve Jeffery, Peter S Mortimer, Sahar Mansour, Pia Ostergaard
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. Nature communications 6 (2015)
Sarah Joyce, Kristiana Gordon, Glen Brice, Pia Ostergaard, Rani Nagaraja, John Short, Sandra Moore, Peter Mortimer, Sahar Mansour
The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome. European journal of human genetics : EJHG 24 (5) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Pia Ostergaard