The genetic basis of von Willebrand disease by Goodeve, Anne C

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Specific and global coagulation assays in the diagnosis of discrepant mild hemophilia A by Bowyer, Annette E, Van Veen, Joost J, Goodeve, Anne C, Kitchen, Steve, Makris, Michael

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Incidence and prognosis of c‐KIT and FLT3 mutations in core binding factor (CBF) acute myeloid leukaemias by Care, Rory S., Valk, Peter J. M., Goodeve, Anne C., Abu‐Duhier, Faisel M., Geertsma‐Kleinekoort, Wendy M. C., Wilson, Giu A., Gari, Mamdooh A., Peake, Ian R., Löwenberg, Bob, Reilly, John T.

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Next Generation Sequencing in Newborn Screening in the United Kingdom National Health Service by van Campen, Julia C, Sollars, Elizabeth S A, Thomas, Rebecca C, Bartlett, Clare M, Milano, Antonio, Parker, Matthew D, Dawe, Jennifer, Winship, Peter R, Peck, Gerrard, Grafham, Darren, Kirk, Richard J, Bonham, James R, Goodeve, Anne C, Dalton, Ann

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Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease by Stockley, Jacqueline, Nisar, Shaista P, Leo, Vincenzo C, Sabi, Essa, Cunningham, Margaret R, Eikenboom, Jeroen C, Lethagen, Stefan, Schneppenheim, Reinhard, Goodeve, Anne C, Watson, Steve P, Mundell, Stuart J, Daly, Martina E

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Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders by Fourouclas, Nasios, Li, Juan, Gilby, Daniel C, Campbell, Peter J, Beer, Philip A, Boyd, Elaine M, Goodeve, Anne C, Bareford, David, Harrison, Claire N, Reilly, John T, Green, Anthony R, Bench, Anthony J

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The molecular basis of von Willebrand disease: the under investigated, the unexpected and the overlooked by Hampshire, Daniel J, Goodeve, Anne C

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Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH by Megy, Karyn, Downes, Kate, Simeoni, Ilenia, Bury, Loredana, Morales, Joannella, Mapeta, Rutendo, Bellissimo, Daniel B., Bray, Paul F., Goodeve, Anne C., Gresele, Paolo, Lambert, Michele, Reitsma, Pieter, Ouwehand, Willem H., Freson, Kathleen

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Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States by Flood, Veronica H., Christopherson, Pamela A., Gill, Joan Cox, Friedman, Kenneth D., Haberichter, Sandra L., Bellissimo, Daniel B., Udani, Rupa A., Dasgupta, Mahua, Hoffmann, Raymond G., Ragni, Margaret V., Shapiro, Amy D., Lusher, Jeanne M., Lentz, Steven R., Abshire, Thomas C., Leissinger, Cindy, Hoots, W. Keith, Manco-Johnson, Marilyn J., Gruppo, Ralph A., Boggio, Lisa N., Montgomery, Kate T., Goodeve, Anne C., James, Paula D., Lillicrap, David, Peake, Ian R., Montgomery, Robert R.

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VWF sequence variants: a data goldmine by Goodeve, Anne C.

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Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD c... by HAMPSHIRE, Daniel J, BURGHEL, George J, GOUDEMAND, Jenny, BOUVET, Laura C. S, EIKENBOOM, Jeroen C. J, SCHNEPPENHEIM, Reinhard, BUDDE, Ulrich, PEAKE, Ian R, GOODEVE, Anne C

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The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance by Mufti, Ahmad H., Ogiwara, Kenichi, Swystun, Laura L., Eikenboom, Jeroen C.J., Budde, Ulrich, Hopman, Wilma M., Halldén, Christer, Goudemand, Jenny, Peake, Ian R., Goodeve, Anne C., Lillicrap, David, Hampshire, Daniel J.

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Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease–causing variants of von Willebrand factor by Michaux, Grégoire, Hewlett, Lindsay J., Messenger, Sarah L., Goodeve, Anne C., Peake, Ian R., Daly, Martina E., Cutler, Daniel F.

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When 1 plus 1 equals 3 in VWD by Goodeve, Anne C.

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p.P2063S: a neutral VWF variant masquerading as a mutation by Hampshire, Daniel J., Goodeve, Anne C.

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Identification and characterization of a novel P2Y12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study by Daly, Martina E., Dawood, Ban B., Lester, William A., Peake, Ian R., Rodeghiero, Francesco, Goodeve, Anne C., Makris, Michael, Wilde, Jonathan T., Mumford, Andrew D., Watson, Stephen P., Mundell, Stuart J.

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Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms by Cartwright, Ashley, Webster, Simon J., de Jong, Annika, Dirven, Richard J., Bloomer, Lisa D.S., AL-Buhairan, Ahlam M., Budde, Ulrich, Halldén, Christer, Habart, David, Goudemand, Jenny, Peake, Ian R., Eikenboom, Jeroen C.J., Goodeve, Anne C., Hampshire, Daniel J.

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Tribbles-1 and -2 are tumour suppressors, down-regulated in human acute myeloid leukaemia by Gilby, Daniel C, Sung, Hye Youn, Winship, Peter R, Goodeve, Anne C, Reilly, John T, Kiss-Toth, Endre

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A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders by Simeoni, Ilenia, Stephens, Jonathan C., Hu, Fengyuan, Deevi, Sri V.V., Megy, Karyn, Bariana, Tadbir K., Lentaigne, Claire, Schulman, Sol, Sivapalaratnam, Suthesh, Vries, Minka J.A., Westbury, Sarah K., Greene, Daniel, Papadia, Sofia, Alessi, Marie-Christine, Attwood, Antony P., Ballmaier, Matthias, Baynam, Gareth, Bermejo, Emilse, Bertoli, Marta, Bray, Paul F., Bury, Loredana, Cattaneo, Marco, Collins, Peter, Daugherty, Louise C., Favier, Rémi, French, Deborah L., Furie, Bruce, Gattens, Michael, Germeshausen, Manuela, Ghevaert, Cedric, Goodeve, Anne C., Guerrero, Jose A., Hampshire, Daniel J., Hart, Daniel P., Heemskerk, Johan W.M., Henskens, Yvonne M.C., Hill, Marian, Hogg, Nancy, Jolley, Jennifer D., Kahr, Walter H., Kelly, Anne M., Kerr, Ron, Kostadima, Myrto, Kunishima, Shinji, Lambert, Michele P., Liesner, Ri, López, José A., Mapeta, Rutendo P., Mathias, Mary, Millar, Carolyn M., Nathwani, Amit, Neerman-Arbez, Marguerite, Nurden, Alan T., Nurden, Paquita, Othman, Maha, Peerlinck, Kathelijne, Perry, David J., Poudel, Pawan, Reitsma, Pieter, Rondina, Matthew T., Smethurst, Peter A., Stevenson, William, Szkotak, Artur, Tuna, Salih, van Geet, Christel, Whitehorn, Deborah, Wilcox, David A., Zhang, Bin, Revel-Vilk, Shoshana, Gresele, Paolo, Bellissimo, Daniel B., Penkett, Christopher J., Laffan, Michael A., Mumford, Andrew D., Rendon, Augusto, Gomez, Keith, Freson, Kathleen, Ouwehand, Willem H., Turro, Ernest

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Second hit mutations in the RTK/RAS signaling pathway in acute myeloid leukemia with inv(16) by Valk, Peter J M, Bowen, David T, Frew, Marion E, Goodeve, Anne C, Löwenberg, Bob, Reilly, John T

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