Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort von Grigoriadis, Dionysios, Sackey, Ege, Riches, Katie, van Zanten, Malou, Brice, Glen, England, Ruth, Mills, Mike, Dobbins, Sara E, Lee, Li Ling, Jeffery, Steve, Dong, Liang, Savage, David B, Mortimer, Peter S, Keeley, Vaughan, Pittman, Alan, Gordon, Kristiana, Ostergaard, Pia

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EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis von Martin-Almedina, Silvia, Martinez-Corral, Ines, Holdhus, Rita, Vicente, Andres, Fotiou, Elisavet, Lin, Shin, Petersen, Kjell, Simpson, Michael A, Hoischen, Alexander, Gilissen, Christian, Jeffery, Heather, Atton, Giles, Karapouliou, Christina, Brice, Glen, Gordon, Kristiana, Wiseman, John W, Wedin, Marianne, Rockson, Stanley G, Jeffery, Steve, Mortimer, Peter S, Snyder, Michael P, Berland, Siren, Mansour, Sahar, Makinen, Taija, Ostergaard, Pia

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Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort von Dionysios Grigoriadis, Ege Sackey, Katie Riches, Malou van Zanten, Glen Brice, Ruth England, Mike Mills, Sara E. Dobbins, Li Ling Lee, Steve Jeffery, Liang Dong, David B. Savage, Peter S. Mortimer, Vaughan Keeley, Alan Pittman, Kristiana Gordon, Pia Ostergaard

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Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia von Jamshidi, Yalda, PhD, Nolte, Ilja M., PhD, Dalageorgou, Chrysoula, BSc, Zheng, Dongling, PhD, Johnson, Toby, PhD, Bastiaenen, Rachel, MBBS, Ruddy, Suzanne, PhD, Talbott, Daniel, BSc, Norris, Kris J., RN, Snieder, Harold, PhD, George, Alfred L., MD, Marshall, Vanessa, MBBS, Shakir, Saad, MD, Kannankeril, Prince J., MD, Munroe, Patricia B., PhD, Camm, A. John, MD, Jeffery, Steve, PhD, Roden, Dan M., MD, Behr, Elijah R., MBBS, MD

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Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis von Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia

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Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions von Pearce, Julian, Hadcocks, Linda, Mansour, Sahar, van Zanten, Malou, Jeffery, Steve, Gordon, Kristiana, Ostergaard, Pia, Mortimer, Peter, Macallan, Derek C

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Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome von Tartaglia, Marco, Mehler, Ernest L, Goldberg, Rosalie, Zampino, Giuseppe, Brunner, Han G, Kremer, Hannie, van der Burgt, Ineke, Crosby, Andrew H, Ion, Andra, Jeffery, Steve, Kalidas, Kamini, Patton, Michael A, Kucherlapati, Raju S, Gelb, Bruce D

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PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity von Tartaglia, Marco, Kalidas, Kamini, Shaw, Adam, Song, Xiaoling, Musat, Dan L., van der Burgt, Ineke, Brunner, Han G., Bertola, Débora R., Crosby, Andrew, Ion, Andra, Kucherlapati, Raju S., Jeffery, Steve, Patton, Michael A., Gelb, Bruce D.

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A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon von Nadarajah, Noeline, Schulte, Dörte, McConnell, Vivienne, Martin-Almedina, Silvia, Karapouliou, Christina, Mortimer, Peter S, Jeffery, Steve, Schulte-Merker, Stefan, Gordon, Kristiana, Mansour, Sahar, Ostergaard, Pia

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Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas von Connell, F. C, Ostergaard, P, Carver, C, Brice, G, Williams, N, Mansour, S, Mortimer, P. S, Jeffery, Steve

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Epidemiology of U.K. Military Burns von ANTHONY FOSTER, Mark, MOLEDINA, Jamil, JEFFERY, Steve L. A

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Diagnosis of Vascular Skin Lesions in Children: An Audit and Review von MacFie, Caroline C., Jeffery, Steve L.A.

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Mutations in EPHB4 cause human venous valve aplasia von Lyons, Oliver, Walker, James, Seet, Christopher, Ikram, Mohammed, Kuchta, Adam, Arnold, Andrew, Hernández-Vásquez, Magda, Frye, Maike, Vizcay-Barrena, Gema, Fleck, Roland A, Patel, Ashish S, Padayachee, Soundrie, Mortimer, Peter, Jeffery, Steve, Berland, Siren, Mansour, Sahar, Ostergaard, Pia, Makinen, Taija, Modarai, Bijan, Saha, Prakash, Smith, Alberto

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Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy von Raju, Hariharan, Ware, James S, Skinner, Jonathan R, Hedley, Paula L, Arno, Gavin, Love, Donald R, van der Werf, Christian, Tfelt-Hansen, Jacob, Winkel, Bo Gregers, Cohen, Marta C, Li, Xinzhong, John, Shibu, Sharma, Sanjay, Jeffery, Steve, Wilde, Arthur A M, Christiansen, Michael, Sheppard, Mary N, Behr, Elijah R

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Changing Work and Community Identities in European Regions: Perspectives on the Past and Present von John Kirk, Sylvie Contrepois, Steve Jefferys

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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2 von Jeffery, Steve, Afzal, Ali R, Rajab, Anna, Fenske, Christiane D, Oldridge, Michael, Elanko, Navaratnam, Ternes-Pereira, Eliana, Tüysüz, Beyhan, Murday, Victoria A, Patton, Michael A, Wilkie, Andrew O.M

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Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis von Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia

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Energy dissipation in atomic force microscopy and atomic loss processes von Hoffmann, P M, Jeffery, S, Pethica, J B, Ozer, H O, Oral, A

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Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome von Tartaglia, Marco, Cordeddu, Viviana, Chang, Hong, Shaw, Adam, Kalidas, Kamini, Crosby, Andrew, Patton, Michael A., Sorcini, Mariella, van der Burgt, Ineke, Jeffery, Steve, Gelb, Bruce D.

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Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency von Mellor, Russell H., Tate, Naomi, Stanton, Anthony W.B., Hubert, Charlotte, Mäkinen, Taija, Smith, Alberto, Burnand, Kevin G., Jeffery, Steve, Levick, J. Rodney, Mortimer, Peter S.

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