Not logged in Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework Ross, Justyne E.; Mohan, Shruthi; Zhang, Jing; Sullivan, Mia J.; Bury, Loredana; Lee, Kristy; Futchi, Isabella; Frantz, Annabelle; Mcdougal, Dara; Botero, Juliana Perez; Cattaneo, Marco; Cooper, Nichola; Downes, Kate; Gresele, Paolo; Keenan, Catriona; Lee, Alfred I.; Megy, Karyn; Morange, Pierre -Emmanuel; Morgan, Neil, V; Schulze, Harald; Zimowski, Karen; Freson, Kathleen; Lambert, Michele P. Share Save
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders Sanchis-Juan, Alba; Megy, Karyn; Stephens, Jonathan; Ricaurte, Camila Armirola; Dewhurst, Eleanor; Low, Kayyi; French, Courtney E.; Grozeva, Detelina; Stirrups, Kathleen; Erwood, Marie; McTague, Amy; Penkett, Christopher J.; Shamardina, Olga; Tuna, Salih; Daugherty, Louise C.; Gleadall, Nicholas; Duarte, Sofia T.; Hedrera-Fernandez, Antonio; Vogt, Julie; Ambegaonkar, Gautam; Chitre, Manali; Josifova, Dragana; Kurian, Manju A.; Parker, Alasdair; Rankin, Julia; Reid, Evan; Wakeling, Emma; Wassmer, Evangeline; Raymond, F. Lucy; Carss, Keren J. Share Save
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis (vol 19, pg 2612, 2021) Megy, Karyn; Downes, Kate; Morel-Kopp, Marie-Christine; Bastida, Jose M.; Brooks, Shannon; Bury, Loredana; Leinoe, Eva; Gomez, Keith; Morgan, Neil, V; Othman, Maha; Ouwehand, Willem H.; Botero, Juliana Perez; Rivera, Jose; Schulze, Harald; Tregouet, David-Alexandre; Freson, Kathleen Share Save
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohort Themistocleous, Andreas C.; Baskozos, Georgios; Blesneac, Iulia; Comini, Maddalena; Megy, Karyn; Chong, Sam; Deevi, Sri V. V.; Ginsberg, Lionel; Gosal, David; Hadden, Robert D. M.; Horvath, Rita; Mahdi-Rogers, Mohamed; Manzur, Adnan; Mapeta, Rutendo; Marshall, Andrew; Matthews, Emma; McCarthy, Mark, I; Reilly, Mary M.; Renton, Tara; Rice, Andrew S. C.; Vale, Tom A.; van Zuydam, Natalie; Walker, Suellen M.; Woods, Christopher Geoffrey; Bennett, David L. H. Share Save
Practical challenges for functional validation of STAT1 gain of function genetic variants Albuquerque, Adriana S.; Maimaris, Jesmeen; McKenna, Alexander J.; Lambourne, Jonathan; Moreira, Fernando; Workman, Sarita; Megy, Karyn; Simeoni, Ilenia; Allen, Hana Lango; NIHR BioResource-Rare Dis Consortium; Morris, Emma C.; Burns, Siobhan O. Share Save
First Genotype-Phenotype Study in TBX4 Syndrome Gain-of-Function Mutations Causative for Lung Disease Prapa, Matina; Lago-Docampo, Mauro; Swietlik, Emilia M.; Montani, David; Eyries, Melanie; Humbert, Marc; Welch, Carrie L.; Chung, Wendy K.; Berger, Rolf M. F.; Bogaard, Harm Jan; Danhaive, Olivier; Escribano-Subias, Pilar; Gall, Henning; Girerd, Barbara; Hernandez-Gonzalez, Ignacio; Holden, Simon; Hunt, David; Jansen, Samara M. A.; Kerstjens-Frederikse, Wilhelmina; Kiely, David G.; Lapunzina, Pablo; McDermott, John; Moledina, Shahin; Pepke-Zaba, Joanna; Polwarth, Gary J.; Schotte, Gwen; Tenorio-Castano, Jair; Thompson, A. A. Roger; Wharton, John; Wort, Stephen J.; Megy, Karyn; Mapeta, Rutendo; Treacy, Carmen M.; Martin, Jennifer M.; Li, Wei; Swift, Andrew J.; Upton, Paul D.; Morrell, Nicholas W.; Graf, Stefan; Valverde, Diana Share Save
Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood French, Courtney E.; Dolling, Helen; Megy, Karyn; Sanchis-Juan, Alba; Kumar, Ajay; Delon, Isabelle; Wakeling, Matthew; Mallin, Lucy; Agrawal, Shruti; Austin, Topun; Walston, Florence; Park, Soo-Mi; Parker, Alasdair; Piyasena, Chinthika; Bradbury, Kimberley; Ellard, Sian; Rowitch, David H.; Raymond, F. Lucy Share Save
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis Megy, Karyn; Downes, Kate; Morel-Kopp, Marie-Christine; Bastida, Jose M.; Brooks, Shannon; Bury, Loredana; Leinoe, Eva; Gomez, Keith; Morgan, Neil V.; Othman, Maha; Ouwehand, Willem H.; Perez Botero, Juliana; Rivera, Jose; Schulze, Harald; Tregouet, David-Alexandre; Freson, Kathleen Share Save
Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension Swietlik, Emilia M.; Greene, Daniel; Zhu, Na; Megy, Karyn; Cogliano, Marcella; Rajaram, Smitha; Pandya, Divya; Tilly, Tobias; Lutz, Katie A.; Welch, Carrie C. L.; Pauciulo, Michael W.; Southgate, Laura; Martin, Jennifer M.; Treacy, Carmen M.; Penkett, Christopher J.; Stephens, Jonathan C.; Bogaard, Harm J.; Church, Colin; Coghlan, Gerry; Coleman, Anna W.; Condliffe, Robin; Eichstaedt, Christina A.; Eyries, Melanie; Gall, Henning; Ghio, Stefano; Girerd, Barbara; Grunig, Ekkehard; Holden, Simon; Howard, Luke; Humbert, Marc; Kiely, David G.; Kovacs, Gabor; Lordan, Jim; Machado, Rajiv D.; Ross, Robert V. Mackenzie; McCabe, Colm; Moledina, Shahin; Montani, David; Olschewski, Horst; Pepke-Zaba, Joanna; Price, Laura; Rhodes, Christopher J.; Seeger, Werner; Soubrier, Florent; Suntharalingam, Jay; Toshner, Mark R.; Noordegraaf, Anton Vonk; Wharton, John; Wild, James M.; Wort, Stephen John; Lawrie, Allan; Wilkins, Martin R.; Trembath, Richard C.; Shen, Yufeng; Chung, Wendy K.; Swift, Andrew J.; Nichols, William C.; Morrell, Nicholas W.; Graf, Stefan Share Save
Development and validation of a universal blood donor genotyping platform: a multinational prospective study Gleadall, Nicholas S.; Veldhuisen, Barbera; Gollub, Jeremy; Butterworth, Adam S.; Ord, John; Penkett, Christopher J.; Timmer, Tiffany C.; Sauer, Carolin M.; van der Bolt, Nieke; Brown, Colin; Brugger, Kim; Dilthey, Alexander T.; Duarte, Daniel; Grimsley, Shane; van den Hurk, Katja; Jongerius, John M.; Luken, Jessie; Megy, Karyn; Miflin, Gail; Nelson, Christopher S.; Prinsze, Femmeke J.; Sambrook, Jennifer; Simeoni, Ilenia; Sweeting, Michael; Thornton, Nicole; Trompeter, Sara; Tuna, Salih; Varma, Ram; Walker, Matthew R.; Danesh, John; Roberts, David J.; Ouwehand, Willem H.; Stirrups, Kathleen E.; Rendon, Augusto; Westhoff, Connie M.; Di Angelantonio, Emanuele; van der Schoot, C. Ellen; Astle, William J.; Watkins, Nicholas A.; Lane, William J. Share Save
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy Levine, Adam P.; Chan, Melanie M. Y.; Sadeghi-Alavijeh, Omid; Wong, Edwin K. S.; Cook, H. Terence; Ashford, Sofie; Carss, Keren; Christian, Martin T.; Hall, Matthew; Harris, Claire Louise; McAlinden, Paul; Marchbank, Kevin J.; Marks, Stephen D.; Maxwell, Heather; Megy, Karyn; Penkett, Christopher J.; Mozere, Monika; Stirrups, Kathleen E.; Tuna, Salih; Wessels, Julie; Whitehorn, Deborah; Johnson, Sally A.; Gale, Daniel P. Share Save
How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study Tan, Rhea Y. Y.; Traylor, Matthew; Megy, Karyn; Duarte, Daniel; Deevi, Sri V. V.; Shamardina, Olga; Mapeta, Rutendo P.; Ouwehand, Willem H.; Graf, Stefan; Downes, Kate; Markus, Hugh S. Share Save
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants 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; Gomez, Keith; Freson, Kathleen; Ouwehand, Willem H.; Gresele, Paolo; Simeoni, Ilenia Share Save
Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH 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 Share Save
Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children French, Courtney E.; Delon, Isabelle; Dolling, Helen; Sanchis-Juan, Alba; Shamardina, Olga; Megy, Karyn; Abbs, Stephen; Austin, Topun; Bowdin, Sarah; Branco, Ricardo G.; Firth, Helen; Rowitch, David H.; Raymond, F. Lucy; Tuna, Salih; Aitman, Timothy J.; Ashford, Sofie; Astle, Willian J.; Bennet, David L.; Bleda, Marta; Carss, Keren J.; Chinnery, Patrick F.; Deevi, Sri V. V.; Fletcher, Debra; Gale, Daniel P.; Graf, Stefan F.; Hu, Fengyuan; James, Roger; Kasanicki, Mary A.; Kingston, Nathalie; Koziell, Ania B.; Allen, Hana Lango; Maher, Eamonn R.; Markus, Hugh S.; Meacham, Stuart; Morrell, Nicholas W.; Penkett, Christopher J.; Roberts, Irene; Sanchis-Juan, Alba; Smith, Kenneth G. C.; Stark, Hannah; Stirrups, Kathleen E.; Turro, Ernest; Watkins, Hugh; Williamson, Catherine; Young, Timothy; Bradley, John R.; Ouwehand, Willem H.; Raymond, F. Lucy; Agrawal, Shruti; Armstrong, Ruth; Beardsall, Kathryn; Belteki, Gusztav; Bohatschek, Marion; Broster, Susan; Campbell, Rosalie; Chaudhary, Rajiv; Costa, Cristine; D'Amore, Angela; Fitzsimmons, Annie; Hague, Jennifer; Harley, Joanne; Hoodbhoy, Shazia; Kayani, Riaz; Kelsall, Wilf; Mehta, Sarju G.; O'Donnell, Roddy; O'Hare, Samantha; Ogilvy-Stuart, Amanda; Papakostas, Stergios; Park, Soo-Mi; Parker, Alasdair; Pathan, Nazima; Prapa, Matina; Sammut, Audrienne; Sandford, Richard; Schon, Katherine; Singh, Yogen; Spike, Kelly; Tavares, Ana Lisa Taylor; Wari-Pepple, Doris; Wong, Hilary S.; Woods, C. Geoff Share Save
Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing Sanchis-Juan, Alba; Stephens, Jonathan; French, Courtney E.; Gleadall, Nicholas; Megy, Karyn; Penkett, Christopher; Shamardina, Olga; Stirrups, Kathleen; Delon, Isabelle; Dewhurst, Eleanor; Dolling, Helen; Erwood, Marie; Grozeva, Detelina; Stefanucci, Luca; Arno, Gavin; Webster, Andrew R.; Cole, Trevor; Austin, Topun; Branco, Ricardo Garcia; Ouwehand, Willem H.; Raymond, F. Lucy; Carss, Keren J. Share Save
Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018) Farmery, James H. R.; Smith, Mike L.; Lynch, Andy G.; Huissoon, Aarnoud; Furnell, Abigail; Mead, Adam; Levine, Adam P.; Manzur, Adnan; Thrasher, Adrian; Greenhalgh, Alan; Parker, Alasdair; Sanchis-Juan, Alba; Richter, Alex; Gardham, Alice; Lawrie, Allan; Sohal, Aman; Creaser-Myers, Amanda; Frary, Amy; Greinacher, Andreas; Themistocleous, Andreas; Peacock, Andrew J.; Marshall, Andrew; Mumford, Andrew; Rice, Andrew; Webster, Andrew; Brady, Angie; Koziell, Ania; Manson, Ania; Chandra, Anita; Hensiek, Anke; in't Veld, Anna Huis; Maw, Anna; Kelly, Anne M.; Moore, Anthony; Noordegraaf, Anton Vonk; Attwood, Antony; Herwadkar, Archana; Ghofrani, Ardi; Houweling, Arjan C.; Girerd, Barbara; Furie, Bruce; Treacy, Carmen M.; Millar, Carolyn M.; Sewell, Carrock; Roughley, Catherine; Titterton, Catherine; Williamson, Catherine; Hadinnapola, Charaka; Deshpande, Charu; Toh, Cheng-Hock; Bacchelli, Chiara; Patch, Chris; Van Geet, Chris; Babbs, Christian; Bryson, Christine; Penkett, Christopher J.; Rhodes, Christopher J.; Watt, Christopher; Bethune, Claire; Booth, Claire; Lentaigne, Claire; McJannet, Coleen; Church, Colin; French, Courtney; Samarghitean, Crina; Halmagyi, Csaba; Gale, Daniel; Greene, Daniel; Hart, Daniel; Allsup, David; Bennett, David; Edgar, David; Kiely, David G.; Gosal, David; Perry, David J.; Keeling, David; Montani, David; Shipley, Debbie; Whitehorn, Deborah; Fletcher, Debra; Krishnakumar, Deepa; Grozeva, Detelina; Kumararatne, Dinakantha; Thompson, Dorothy; Josifova, Dragana; Maher, Eamonn; Wong, Edwin K. S.; Murphy, Elaine; Dewhurst, Eleanor; Louka, Eleni; Rosser, Elisabeth; Chalmers, Elizabeth; Colby, Elizabeth; Drewe, Elizabeth; McDermott, Elizabeth; Thomas, Ellen; Staples, Emily; Clement, Emma; Matthews, Emma; Wakeling, Emma; Oksenhendler, Eric; Turro, Ernest; Reid, Evan; Wassmer, Evangeline; Raymond, F. Lucy; Hu, Fengyuan; Kennedy, Fiona; Soubrier, Florent; Flinter, Frances; Kovacs, Gabor; Polwarth, Gary; Ambegaonkar, Gautum; Arno, Gavin; Hudson, Gavin; Woods, Geoff; Coghlan, Gerry; Hayman, Grant; Arumugakani, Gururaj; Schotte, Gwen; Cook, H. Terry; Alachkar, Hana; Allen, Hana Lango; Lango-Allen, Hana; Stark, Hannah; Stauss, Hans; Schulze, Harald; Boggard, Harm J.; Baxendale, Helen; Dolling, Helen; Firth, Helen; Gall, Henning; Watson, Henry; Longhurst, Hilary; Markus, Hugh S.; Watkins, Hugh; Simeoni, Ilenia; Emmerson, Ingrid; Roberts, Irene; Quinti, Isabella; Wanjiku, Ivy; Gibbs, J. Simon R.; Thaventhiran, James; Whitworth, James; Hurst, Jane; Collins, Janine; Suntharalingam, Jay; Payne, Jeanette; Thachil, Jecko; Martin, Jennifer M.; Martin, Jennifer; Carmichael, Jenny; Maimaris, Jesmeen; Paterson, Joan; Pepke-Zaba, Joanna; Heemskerk, Johan W. M.; Gebhart, Johanna; Davis, John; Pasi, John; Bradley, John R.; Wharton, John; Stephens, Jonathan; Rankin, Julia; Anderson, Julie; Vogt, Julie; von Ziegenweldt, Julie; Rehnstrom, Karola; Megy, Karyn; Talks, Kate; Peerlinck, Kathelijne; Yates, Katherine; Freson, Kathleen; Stirrups, Kathleen; Gomez, Keith; Smith, Kenneth G. C.; Carss, Keren; Rue-Albrecht, Kevin; Gilmour, Kimberley; Masati, Larahmie; Scelsi, Laura; Southgate, Laura; Ranganathan, Lavanya; Ginsberg, Lionel; Devlin, Lisa; Willcocks, Lisa; Ormondroyd, Liz; Lorenzo, Lorena; Harper, Lorraine; Allen, Louise; Daugherty, Louise; Chitre, Manali; Kurian, Manju; Humbert, Marc; Tischkowitz, Marc; Bitner-Glindzicz, Maria; Erwood, Marie; Scully, Marie; Veltman, Marijke; Caulfield, Mark; Layton, Mark; McCarthy, Mark; Ponsford, Mark; Toshner, Mark; Bleda, Marta; Wilkins, Martin; Mathias, Mary; Reilly, Mary; Afzal, Maryam; Brown, Matthew; Rondina, Matthew; Stubbs, Matthew; Haimel, Matthias; Lees, Melissa; Laffan, Michael A.; Browning, Michael; Gattens, Michael; Richards, Michael; Michaelides, Michel; Lambert, Michele P.; Makris, Mike; De Vries, Minka; Mahdi-Rogers, Mohamed; Saleem, Moin; Thomas, Moira; Holder, Muriel; Eyries, Melanie; Clements-Brod, Naomi; Canham, Natalie; Dormand, Natalie; Van Zuydam, Natalie; Kingston, Nathalie; Ghali, Neeti; Cooper, Nichola; Morrell, Nicholas W.; Yeatman, Nigel; Roy, Noemi; Shamardina, Olga; Alavijeh, Omid S.; Gresele, Paolo; Nurden, Paquita; Chinnery, Patrick; Deegan, Patrick; Yong, Patrick; Yu-Wai-Man, Patrick; Corris, Paul A.; Calleja, Paul; Gissen, Paul; Bolton-Maggs, Paula; Rayner-Matthews, Paula; Ghataorhe, Pavandeep K.; Gordins, Pavel; Stein, Penelope; Collins, Peter; Dixon, Peter; Kelleher, Peter; Ancliff, Phil; Yu, Ping; Tait, R. Campbell; Linger, Rachel; Doffinger, Rainer; Machado, Rajiv; Kazmi, Rashid; Sargur, Ravishankar; Favier, Remi; Tan, Rhea; Liesner, Ri; Antrobus, Richard; Sandford, Richard; Scott, Richard; Trembath, Richard; Horvath, Rita; Hadden, Rob; MackenzieRoss, Rob V.; Henderson, Robert; MacLaren, Robert; James, Roger; Ghurye, Rohit; DaCosta, Rosa; Hague, Rosie; Mapeta, Rutendo; Armstrong, Ruth; Noorani, Sadia; Murng, Sai; Santra, Saikat; Tuna, Salih; Johnson, Sally; Chong, Sam; Lear, Sara; Walker, Sara; Goddard, Sarah; Mangles, Sarah; Westbury, Sarah; Mehta, Sarju; Hackett, Scott; Nejentsev, Sergey; Moledina, Shahin; Bibi, Shahnaz; Meehan, Sharon; Othman, Shokri; Revel-Vilk, Shoshana; Holden, Simon; McGowan, Simon; Staines, Simon; Savic, Sinisa; Burns, Siobhan; Grigoriadou, Sofia; Papadia, Sofia; Ashford, Sofie; Schulman, Sol; Ali, Sonia; Park, Soo-Mi; Davies, Sophie; Stock, Sophie; Ali, Souad; Deevi, Sri V. V.; Graf, Stefan; Ghio, Stefano; Wort, Stephen J.; Jolles, Stephen; Austin, Steve; Welch, Steve; Meacham, Stuart; Rankin, Stuart; Walker, Suellen; Seneviratne, Suranjith; Holder, Susan; Sivapalaratnam, Suthesh; Richardson, Sylvia; Kuijpers, Taco; Kuijpers, Taco W.; Bariana, Tadbir K.; Bakchoul, Tamam; Everington, Tamara; Renton, Tara; Young, Tim; Aitman, Timothy; Warner, Timothy Q.; Vale, Tom; Hammerton, Tracey; Pollock, Val; Matser, Vera; Cookson, Victoria; Clowes, Virginia; Qasim, Waseem; Wei, Wei; Erber, Wendy N.; Ouwehand, Willem H.; Astle, William; Egner, William; Turek, Wojciech; Henskens, Yvonne; Tan, Yvonne Share Save
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes Whitworth, James; Smith, Philip S.; Martin, Jose-Ezequiel; West, Hannah; Luchetti, Andrea; Rodger, Faye; Clark, Graeme; Carss, Keren; Stephens, Jonathan; Stirrups, Kathleen; Penkett, Chris; Mapeta, Rutendo; Ashford, Sofie; Megy, Karyn; Shakeel, Hassan; Ahmed, Munaza; Adlard, Julian; Barwell, Julian; Brewer, Carole; Casey, Ruth T.; Armstrong, Ruth; Cole, Trevor; Evans, Dafydd Gareth; Fostira, Florentia; Greenhalgh, Lynn; Hanson, Helen; Henderson, Alex; Hoffman, Jonathan; Izatt, Louise; Kumar, Ajith; Kwong, Ava; Lalloo, Fiona; Ong, Kai Ren; Paterson, Joan; Park, Soo-Mi; Chen-Shtoyerman, Rakefet; Searle, Claire; Side, Lucy; Skytte, Anne-Bine; Snape, Katie; Woodward, Emma R.; Tischkowitz, Marc D.; Maher, Eamonn R. Share Save
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease Carss, Keren J.; Arno, Gavin; Erwood, Marie; Stephens, Jonathan; Sanchis-Juan, Alba; Hull, Sarah; Megy, Karyn; Grozeva, Detelina; Dewhurst, Eleanor; Malka, Samantha; Plagnol, Vincent; Penkett, Christopher; Stirrups, Kathleen; Rizzo, Roberta; Wright, Genevieve; Josifova, Dragana; Bitner-Glindzicz, Maria; Scott, Richard H.; Clement, Emma; Allen, Louise; Armstrong, Ruth; Brady, Angela F.; Carmichael, Jenny; Chitre, Manali; Henderson, Robert H. H.; Hurst, Jane; MacLaren, Robert E.; Murphy, Elaine; Paterson, Joan; Rosser, Elisabeth; Thompson, Dorothy A.; Wakeling, Emma; Ouwehand, Willem H.; Michaelides, Michel; Moore, Anthony T.; Webster, Andrew R.; Raymond, F. Lucy Share Save
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