| Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) P Ostergaard, MA Simpson, FC Connell, CG Steward, G Brice, ... Nature genetics 43 (10), 929-931, 2011 | 577 | 2011 |
| The phylogeny of the Schistosomatidae based on three genes with emphasis on the interrelationships of Schistosoma Weinland, 1858 AE Lockyer, PD Olson, P Østergaard, D Rollinson, DA Johnston, ... Parasitology 126 (3), 203-224, 2003 | 345 | 2003 |
| Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis E Fotiou, S Martin-Almedina, MA Simpson, S Lin, K Gordon, G Brice, ... Nature communications 6 (1), 8085, 2015 | 298 | 2015 |
| Lipedema: an inherited condition AH Child, KD Gordon, P Sharpe, G Brice, P Ostergaard, S Jeffery, ... American Journal of Medical Genetics Part A 152 (4), 970-976, 2010 | 272 | 2010 |
| The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings FC Connell, K Gordon, G Brice, V Keeley, S Jeffery, PS Mortimer, ... Clinical genetics 84 (4), 303-314, 2013 | 198 | 2013 |
| 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 K Gordon, D Schulte, G Brice, MA Simpson, MG Roukens, A Van Impel, ... Circulation research 112 (6), 956-960, 2013 | 192 | 2013 |
| Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy P Ostergaard, MA Simpson, A Mendola, P Vasudevan, FC Connell, ... The American Journal of Human Genetics 90 (2), 356-362, 2012 | 183 | 2012 |
| Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program M Frye, A Taddei, C Dierkes, I Martinez-Corral, M Fielden, H Ortsäter, ... Nature communications 9 (1), 1-16, 2018 | 141 | 2018 |
| Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas FC Connell, P Ostergaard, C Carver, G Brice, N Williams, S Mansour, ... Human genetics 124, 625-631, 2009 | 130 | 2009 |
| Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype P Ostergaard, MA Simpson, G Brice, S Mansour, FC Connell, ... Journal of medical genetics 48 (4), 251-255, 2011 | 122 | 2011 |
| Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia F Connell, K Kalidas, P Ostergaard, G Brice, T Homfray, L Roberts, ... Human genetics 127, 231-241, 2010 | 112 | 2010 |
| Contrasting feeding patterns among species of fish larvae from the tropical Andaman Sea P Østergaard, P Munk, V Janekarn Marine Biology 146, 595-606, 2005 | 112 | 2005 |
| EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis S Martin-Almedina, I Martinez-Corral, R Holdhus, A Vicente, E Fotiou, ... The Journal of clinical investigation 126 (8), 3080-3088, 2016 | 103 | 2016 |
| FLT4/VEGFR3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update K Gordon, SL Spiden, FC Connell, G Brice, S Cottrell, J Short, R Taylor, ... Human mutation 34 (1), 23-31, 2013 | 96 | 2013 |
| Emberger syndrome—Primary lymphedema with myelodysplasia: Report of seven new cases S Mansour, F Connell, C Steward, P Ostergaard, G Brice, S Smithson, ... American Journal of Medical Genetics Part A 152 (9), 2287-2296, 2010 | 92 | 2010 |
| The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome S Joyce, K Gordon, G Brice, P Ostergaard, R Nagaraja, J Short, S Moore, ... European Journal of Human Genetics 24 (5), 690-696, 2016 | 85 | 2016 |
| A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family G Brice, P Ostergaard, S Jeffery, K Gordon, PS Mortimer, S Mansour Clinical Genetics 84 (4), 378-381, 2013 | 84 | 2013 |
| Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations GE Jones, P Ostergaard, AT Moore, FC Connell, D Williams, O Quarrell, ... European Journal of Human Genetics 22 (7), 881-887, 2014 | 82 | 2014 |
| Update and audit of the St George’s classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis K Gordon, R Varney, V Keeley, K Riches, S Jeffery, M Van Zanten, ... Journal of Medical Genetics 57 (10), 653-659, 2020 | 80 | 2020 |
| The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review G Atton, K Gordon, G Brice, V Keeley, K Riches, P Ostergaard, P Mortimer, ... European Journal of Human Genetics 23 (12), 1634-1639, 2015 | 69 | 2015 |
