A common mechanism by which type 2A von Willebrand disease mutations enhance ADAMTS13 proteolysis revealed with a von Willebrand factor A2 domain FRET construct von Lynch, Christopher J, Cawte, Adam D, Millar, Carolyn M, Rueda, David, Lane, David A

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Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding von Westbury, Sarah K., Canault, Matthias, Greene, Daniel, Bermejo, Emilse, Hanlon, Katharine, Lambert, Michele P., Millar, Carolyn M., Nurden, Paquita, Obaji, Samya G., Revel-Vilk, Shoshana, Van Geet, Chris, Downes, Kate, Papadia, Sofia, Tuna, Salih, Watt, Christopher, Freson, Kathleen, Laffan, Michael A., Ouwehand, Willem H., Alessi, Marie-Christine, Turro, Ernest, Mumford, Andrew D.

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Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor von Riddell, Anne F., Gomez, Keith, Millar, Carolyn M., Mellars, Gillian, Gill, Saher, Brown, Simon A., Sutherland, Megan, Laffan, Mike A., McKinnon, Thomas A.J.

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Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses von van Oorschot, Rinske, Marneth, Anna E, Bergevoet, Saskia M, van Bergen, Maaike G J M, Peerlinck, Kathelijne, Lentaigne, Claire E, Millar, Carolyn M, Westbury, Sarah K, Favier, Remi, Erber, Wendy N, Turro, Ernest, Jansen, Joop H, Ouwehand, Willem H, McKinney, Harriet L, Downes, Kate, Freson, Kathleen, van der Reijden, Bert A

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The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haemat... von Laffan, Mike A., Lester, Will, O'Donnell, James S., Will, Andrew, Tait, Robert Campbell, Goodeve, Anne, Millar, Carolyn M., Keeling, David M.

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Efficacy, safety, and quality of life 4 years after valoctocogene roxaparvovec gene transfer for severe hemophilia A in the phase 3 GENEr8-1 trial von Leavitt, Andrew D., Mahlangu, Johnny, Raheja, Priyanka, Symington, Emily, Quon, Doris V., Giermasz, Adam, López Fernández, Maria Fernanda, Kenet, Gili, Lowe, Gillian, Key, Nigel S., Millar, Carolyn M., Pipe, Steven W., Madan, Bella, Chou, Sheng-Chieh, Klamroth, Robert, Mason, Jane, Chambost, Hervé, Peyvandi, Flora, Majerus, Elaine, Pepperell, Dominic, Rivat, Christine, Yu, Hua, Robinson, Tara M., Ozelo, Margareth C.

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A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders von 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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Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency von Peyvandi, Flora, Auerswald, Guenter, Austin, Steven K., Liesner, Ri, Kavakli, Kaan, Álvarez Román, Maria Teresa, Millar, Carolyn M.

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A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss von Stritt, Simon, Nurden, Paquita, Turro, Ernest, Greene, Daniel, Jansen, Sjoert B., Westbury, Sarah K., Petersen, Romina, Astle, William J., Marlin, Sandrine, Bariana, Tadbir K., Kostadima, Myrto, Lentaigne, Claire, Maiwald, Stephanie, Papadia, Sofia, Kelly, Anne M., Stephens, Jonathan C., Penkett, Christopher J., Ashford, Sofie, Tuna, Salih, Austin, Steve, Bakchoul, Tamam, Collins, Peter, Favier, Rémi, Lambert, Michele P., Mathias, Mary, Millar, Carolyn M., Mapeta, Rutendo, Perry, David J., Schulman, Sol, Simeoni, Ilenia, Thys, Chantal, Gomez, Keith, Erber, Wendy N., Stirrups, Kathleen, Rendon, Augusto, Bradley, John R., van Geet, Chris, Raymond, F.Lucy, Laffan, Michael A., Nurden, Alan T., Nieswandt, Bernhard, Richardson, Sylvia, Freson, Kathleen, Ouwehand, Willem H., Mumford, Andrew D.

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A need to increase von Willebrand disease awareness: vwdtest.com – A global initiative to help address this gap von Corrales-Medina, Fernando F., Federici, Augusto B., Srivastava, Alok, Dougall, Alison, Millar, Carolyn M., Roberts, Jonathan C., Jaffray, Julie, Berntorp, Erik

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Three-year outcomes of valoctocogene roxaparvovec gene therapy for hemophilia A von Madan, Bella, Ozelo, Margareth C., Raheja, Priyanka, Symington, Emily, Quon, Doris V., Leavitt, Andrew D., Pipe, Steven W., Lowe, Gillian, Kenet, Gili, Reding, Mark T., Mason, Jane, Wang, Michael, von Drygalski, Annette, Klamroth, Robert, Shapiro, Susan, Chambost, Hervé, Dunn, Amy L., Oldenburg, Johannes, Chou, Sheng-Chieh, Peyvandi, Flora, Millar, Carolyn M., Osmond, Dane, Yu, Hua, Dashiell-Aje, Ebony, Robinson, Tara M., Mahlangu, Johnny

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Dealing with the uncertain risk of variant Creutzfeldt-Jakob disease transmission by coagulation replacement products von Millar, Carolyn M., Makris, Mike

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Next‐generation sequencing for the diagnosis of MYH9‐RD: Predicting pathogenic variants von Bury, Loredana, Megy, Karyn, Stephens, Jonathan C., Grassi, Luigi, Greene, Daniel, Gleadall, Nick, Althaus, Karina, Allsup, David, Bariana, Tadbir K., Bonduel, Mariana, Butta, Nora V., Collins, Peter, Curry, Nicola, Deevi, Sri V. V., Downes, Kate, Duarte, Daniel, Elliott, Kim, Falcinelli, Emanuela, Furie, Bruce, Keeling, David, Lambert, Michele P., Linger, Rachel, Mangles, Sarah, Mapeta, Rutendo, Millar, Carolyn M., Penkett, Christopher, Perry, David J., Stirrups, Kathleen E., Turro, Ernest, Westbury, Sarah K., Wu, John, BioResource, NIHR, Gomez, Keith, Freson, Kathleen, Ouwehand, Willem H., Gresele, Paolo, Simeoni, Ilenia

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Cellular and molecular basis of von Willebrand disease: studies on blood outgrowth endothelial cells von Starke, Richard D., Paschalaki, Koralia E., Dyer, Clare E.F., Harrison-Lavoie, Kimberly J., Cutler, Jacqueline A., McKinnon, Thomas A.J., Millar, Carolyn M., Cutler, Daniel F., Laffan, Mike A., Randi, Anna M.

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Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders von Westbury, Sarah K, Turro, Ernest, Greene, Daniel, Lentaigne, Claire, Kelly, Anne M, Bariana, Tadbir K, Simeoni, Ilenia, Pillois, Xavier, Attwood, Antony, Austin, Steve, Jansen, Sjoert Bg, Bakchoul, Tamam, Crisp-Hihn, Abi, Erber, Wendy N, Favier, Rémi, Foad, Nicola, Gattens, Michael, Jolley, Jennifer D, Liesner, Ri, Meacham, Stuart, Millar, Carolyn M, Nurden, Alan T, Peerlinck, Kathelijne, Perry, David J, Poudel, Pawan, Schulman, Sol, Schulze, Harald, Stephens, Jonathan C, Furie, Bruce, Robinson, Peter N, van Geet, Chris, Rendon, Augusto, Gomez, Keith, Laffan, Michael A, Lambert, Michele P, Nurden, Paquita, Ouwehand, Willem H, Richardson, Sylvia, Mumford, Andrew D, Freson, Kathleen

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Drug therapy in anticoagulation: which drug for which patient? von Millar, Carolyn M, Laffan, Mike A

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Treatment burden, haemostatic strategies and real world inhibitor screening practice in non‐severe haemophilia A von Batty, Paul, Austin, Steve K., Khair, Kate, Millar, Carolyn M., Palmer, Ben, Rangarajan, Savita, Stümpel, Jan‐Phillip, Thanigaikumar, Murugaiyan, Yee, Thynn T., Hart, Daniel P.

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Blocking direct inhibitor bleeding von Millar, Carolyn M., Lane, David A.

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Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variation von Joyce, Katie E., Onabanjo, Ebun, Brownlow, Sheila, Nur, Fadumo, Olupona, Kike, Fakayode, Kehinde, Sroya, Manveer, Thomas, Geraldine A., Ferguson, Teena, Redhead, Julian, Millar, Carolyn M., Cooper, Nichola, Layton, D. Mark, Boardman-Pretty, Freya, Caulfield, Mark J., Shovlin, Claire L.

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Publisher Correction: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data von Farmery, James H. R., Smith, Mike L., Lynch, Andy G.

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