The effect of drawdown on suspended solids and phosphorus export from Columbia Lake, Waterloo, Canada von Shantz, Mike, Dowsett, Elizabeth, Canham, Emma, Tavernier, Guillaume, Stone, Mike, Price, Jonathan

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Expedited evaluation of hereditary hematopoietic malignancies in the setting of stem cell transplantation von Roloff, Gregory W, Kosuri, Satyajit, Nawas, Mariam T, DuVall, Adam S, Patel, Anand A, Riedell, Peter A, Odenike, Olatoyosi, Stock, Wendy, Larson, Richard A, Bishop, Michael R, Nunley, Emma, Godley, Lucy A, Hathaway, Feighanne, Del Gaudio, Daniela, Das, Soma, Canham, Lorraine E, Drazer, Michael W

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Clinical and genetic aspects of KBG syndrome von Low, Karen, Ashraf, Tazeen, Canham, Natalie, Clayton-Smith, Jill, Deshpande, Charu, Donaldson, Alan, Fisher, Richard, Flinter, Frances, Foulds, Nicola, Fryer, Alan, Gibson, Kate, Hayes, Ian, Hills, Alison, Holder, Susan, Irving, Melita, Joss, Shelagh, Kivuva, Emma, Lachlan, Kathryn, Magee, Alex, McConnell, Vivienne, McEntagart, Meriel, Metcalfe, Kay, Montgomery, Tara, Newbury-Ecob, Ruth, Stewart, Fiona, Turnpenny, Peter, Vogt, Julie, Fitzpatrick, David, Williams, Maggie, Smithson, Sarah

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A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma von Rattenberry, Eleanor, Vialard, Lindsey, Yeung, Anna, Bair, Hayley, McKay, Kirsten, Jafri, Mariam, Canham, Natalie, Cole, Trevor R, Denes, Judit, Hodgson, Shirley V, Irving, Richard, Izatt, Louise, Korbonits, Márta, Kumar, Ajith V, Lalloo, Fiona, Morrison, Patrick J, Woodward, Emma R, Macdonald, Fiona, Wallis, Yvonne, Maher, Eamonn R

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Dual diagnosis of achondroplasia and mandibulofacial dysostosis with microcephaly von Lyulcheva-Bennett, Ekaterina, Kershaw, Christopher, Baker, Eleanor, Gillies, Stuart, McCarthy, Emma, Higgs, Jenny, Canham, Natalie, Hennigan, Dawn, Parks, Chris, Bennett, Daimark

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease von Stephens, Jonathan, Dewhurst, Eleanor, Malka, Samantha, Plagnol, Vincent, Rizzo, Roberta, Scott, Richard H., Henderson, Robert H.H., MacLaren, Robert E., Paterson, Joan, Aitman, Timothy, Ali, Sonia, Ambegaonkar, Gautum, Arno, Gavin, Astle, William, Attwood, Antony, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Boggard, Harm, Carss, Keren, Clements-Brod, Naomi, DaCosta, Rosa, De Vries, Minka, Dewhurst, Eleanor, Drewe, Elizabeth, Egner, William, Erber, Wendy N., Everington, Tamara, Fletcher, Debra, Freson, Kathleen, Gale, Daniel, Ghali, Neeti, Ghurye, Rohit, Gräf, Stefan, Greene, Daniel, Grigoriadou, Sofia, Grozeva, Detelina, Hackett, Scott, Hadinnapola, Charaka, Hague, Rosie, Hammerton, Tracey, Heemskerk, Johan W.M., Holder, Muriel, Holder, Susan, Huissoon, Aarnoud, Hurst, Jane, Jolles, Stephen, Keeling, David, Kennedy, Fiona, Kiely, David, Lawrie, Allan, Lear, Sara, Lees, Melissa, Lentaigne, Claire, Lorenzo, Lorena, Mangles, Sarah, Mapeta, Rutendo, Masati, Larahmie, Mathias, Mary, Michaelides, Michel, Millar, Carolyn M., Moledina, Shahin, Moore, Anthony, Murng, Sai, Oksenhendler, Eric, Park, Soo-Mi, Patch, Chris, Paterson, Joan, Penkett, Christopher J., Pepke-Zaba, Joanna, Pollock, Val, Qasim, Waseem, Quinti, Isabella, Reid, Evan, Rondina, Matthew, Rosser, Elisabeth, Santra, Saikat, Sargur, Ravishankar, Savic, Sinisa, Scully, Marie, Sewell, Carrock, Smith, Kenneth, Southgate, Laura, Stauss, Hans, Stein, Penelope, Talks, Kate, Thomas, Ellen, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Turro, Ernest, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Welch, Steve, Westbury, Sarah, Woods, Geoffrey, Yong, Patrick, Webster, Andrew R.

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Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals' views and experiences von Peter, Michelle, Mellis, Rhiannon, McInnes-Dean, Hannah, Daniel, Morgan, Walton, Holly, Fisher, Jane, Leeson-Beevers, Kerry, Allen, Stephanie, Baple, Emma L, Beleza-Meireles, Ana, Bertoli, Marta, Campbell, Jennifer, Canham, Natalie, Cilliers, Deirdre, Cobben, Jan, Eason, Jacqueline, Harrison, Victoria, Holder-Espinasse, Muriel, Male, Alison, Mansour, Sahar, McEwan, Alec, Park, Soo-Mi, Smith, Audrey, Stewart, Alison, Tapon, Dagmar, Vasudevan, Pradeep, Williams, Denise, Wu, Wing Han, Chitty, Lyn S, Hill, Melissa

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Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation von Bernkopf, Marie, Abdullah, Ummi B., Bush, Stephen J., Wood, Katherine A., Ghaffari, Sahar, Giannoulatou, Eleni, Koelling, Nils, Maher, Geoffrey J., Thibaut, Loïc M., Williams, Jonathan, Blair, Edward M., Kelly, Fiona Blanco, Bloss, Angela, Burkitt-Wright, Emma, Canham, Natalie, Deng, Alexander T., Dixit, Abhijit, Eason, Jacqueline, Elmslie, Frances, Gardham, Alice, Hay, Eleanor, Holder, Muriel, Homfray, Tessa, Hurst, Jane A., Johnson, Diana, Jones, Wendy D., Kini, Usha, Kivuva, Emma, Kumar, Ajith, Lees, Melissa M., Leitch, Harry G., Morton, Jenny E. V., Németh, Andrea H., Ramachandrappa, Shwetha, Saunders, Katherine, Shears, Deborah J., Side, Lucy, Splitt, Miranda, Stewart, Alison, Stewart, Helen, Suri, Mohnish, Clouston, Penny, Davies, Robert W., Wilkie, Andrew O. M., Goriely, Anne

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Community Consultations to Support Scoping Review Knowledge Dissemination von Canham, Sarah L., Weldrick, Rachel, Siantz, Elizabeth, Rose, Jeffrey N., Littman, Danielle Maude, Cruz Erisman, Morgan, Rehn, Kyle, Jones, Shannon, Anderson, Sumiko, McNamara, Anne, Greenwood, Emma

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122 Objective evaluation of plan quality in the PATHOS clinical trial using automated treatment planning von Berenato, Salvatore, Evans, Mererid, Webster, Richard, Palaniappan, Nachi, Nixon, Lisette, Higgins, Emma, Patel, Rush, Millin, Anthony E, Hurt, Christian, Heiberg, Christie, Canham, Joanna, Jones, Terence M, Miles, Elizabeth, Beasley, Matthew, Wheeler, Philip A

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49 Development of a Normal Tissue Complication Probability Model for Dysphagia in PATHOS trial patients von Higgins, Emma, Webster, Richard, Palaniappan, Nachi, Hurt, Chris, Nabi, Zohal, Rizos, Kostas, Elliott, Kate, Miles, Elizabeth, Patterson, Joanne, Hutcheson, Kate, Canham, Joanne, Nixon, Lisette, Heiberg, Christie, Beasley, Matthew, Jones, Terry M, Evans, Mererid

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Does variation in swallowing organs-at-risk (SWOAR) delineation impact on predicted swallowing dysfunction for PATHOS trial patients? von Higgins, Emma, Palaniappan, Nachi, Nabi, Zohal, Elliott, Kate, Miles, Liz, Lad, Rikki, Nixon, Lisette, Canham, Jo, Hurt, Chris, Heiberg, Christie, Beasley, Matthew, Jones, Terry, Webster, Richard, Evans, Mererid

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Normal DNA methylation dynamics in DICER1-deficient mouse embryonic stem cells von Ip, Jonathan, Canham, Paul, Choo, K H Andy, Inaba, Yoshimi, Jacobs, Shelley A, Kalitsis, Paul, Mattiske, Deidre M, Ng, Jane, Saffery, Richard, Wong, Nicholas C, Wong, Lee H, Mann, Jeffrey R

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The impact of inversions across 33,924 families with rare disease from a national genome sequencing project von Pagnamenta, Alistair T., Yu, Jing, Walker, Susan, Noble, Alexandra J., Lord, Jenny, Dutta, Prasun, Hashim, Mona, Camps, Carme, Green, Hannah, Devaiah, Smrithi, Nashef, Lina, Parr, Jason, Fratter, Carl, Ibnouf Hussein, Rana, Lindsay, Sarah J., Lalloo, Fiona, Banos-Pinero, Benito, Evans, David, Mallin, Lucy, Waite, Adrian, Evans, Julie, Newman, Andrew, Allen, Zoe, Perez-Becerril, Cristina, Ryan, Gavin, Hart, Rachel, Taylor, John, Bedenham, Tina, Clement, Emma, Blair, Ed, Hay, Eleanor, Forzano, Francesca, Higgs, Jenny, Canham, Natalie, Majumdar, Anirban, McEntagart, Meriel, Lahiri, Nayana, Stewart, Helen, Smithson, Sarah, Calpena, Eduardo, Jackson, Adam, Banka, Siddharth, Titheradge, Hannah, McGowan, Ruth, Rankin, Julia, Shaw-Smith, Charles, Evans, D. Gareth, Burghel, George J., Smith, Miriam J., Anderson, Emily, Madhu, Rajesh, Firth, Helen, Ellard, Sian, Brennan, Paul, Anderson, Claire, Taupin, Doug, Rogers, Mark T., Cook, Jackie A., Durkie, Miranda, East, James E., Fowler, Darren, Wilson, Louise, Igbokwe, Rebecca, Gardham, Alice, Tomlinson, Ian, Baralle, Diana, Uhlig, Holm H., Taylor, Jenny C.

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes von West, Hannah, Carss, Keren, Shakeel, Hassan, Adlard, Julian, Cole, Trevor, Kwong, Ava, Paterson, Joan, Searle, Claire, Skytte, Anne-Bine, Aitman, Timothy, Ambegaonkar, Gautum, Antrobus, Richard, Arno, Gavin, Astle, William, Attwood, Antony, Austin, Steve, Bakchoul, Tamam, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Bolton-Maggs, Paula, Booth, Claire, Clements-Brod, Naomi, Clowes, Virginia, Collins, Peter, Cookson, Victoria, Creaser-Myers, Amanda, DaCosta, Rosa, Davies, Sophie, Deegan, Patrick, Dewhurst, Eleanor, Doffinger, Rainer, Drewe, Elizabeth, Favier, Remi, Firth, Helen, Furie, Bruce, Furnell, Abigail, Gardham, Alice, Gissen, Paul, Gomez, Keith, Graf, Stefan, Gräf, Stefan, Greenhalgh, Alan, Hackett, Scott, Haimel, Matthias, Herwadkar, Archana, Holder, Muriel, Huissoon, Aarnoud, James, Roger, Kennedy, Fiona, Kingston, Nathalie, Kuijpers, Taco, Lawrie, Allan, Lentaigne, Claire, Machado, Rajiv, Maher, Eamonn, Mangles, Sarah, Manson, Ania, Matser, Vera, McDermott, Elizabeth, Megy, Karyn, Millar, Carolyn M., Morrell, Nicholas, Ouwehand, Willem H., Papadia, Sofia, Payne, Jeanette, Peacock, Andrew, Pollock, Val, Quinti, Isabella, Rayner-Matthews, Paula, Rehnstrom, Karola, Rhodes, Christopher J., Richardson, Sylvia, Richter, Alex, Rondina, Matthew, Rosser, Elisabeth, Rue-Albrecht, Kevin, Sargur, Ravishankar, Savic, Sinisa, Schotte, Gwen, Schulze, Harald, Seneviratne, Suranjith, Shamardina, Olga, Simeoni, Ilenia, Staines, Simon, Stark, Hannah, Stock, Sophie, Thaventhiran, James, Thompson, Dorothy, Toh, Cheng-Hock, Turek, Wojciech, Wassmer, Evangeline, Watt, Christopher, Wharton, John, Williamson, Catherine, Woods, Geoff, Wort, John, Yeatman, Nigel, Tischkowitz, Marc D., Maher, Eamonn R.

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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth von Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

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Developmental trajectories in infants and pre-school children with Neurofibromatosis 1 von Slevin, Hannah, Kehinde, Fiona, Begum-Ali, Jannath, Ellis, Ceri, Burkitt-Wright, Emma, Green, Jonathan, Johnson, Mark H, Pasco, Greg, Charman, Tony, Jones, Emily J H, Garg, Shruti

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Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation von Ramakrishnan, Rema, Mallinson, Corinne, Hardy, Steven, Broughan, Jennifer, Blyth, Maisie, Melis, Gabriella, Franklin, Catherine, Hill, Melissa, Mellis, Rhiannon, Wu, Wing Han, Allen, Stephanie, Chitty, Lyn S, Knight, Marian

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Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration von Arno, Gavin, Zihni, Ceniz, Robson, Anthony G., Fiorentino, Alessia, Black, Graeme, Ponitkos, Nikos, Holder, Graham E., Aitman, Timothy, Alachkar, Hana, Allsup, David, Anderson, Julie, Armstrong, Ruth, Arumugakani, Gururaj, Ashford, Sofie, Bakchoul, Tamam, Bariana, Tadbir K., Bibi, Shahnaz, Bitner-Glindzicz, Maria, Bolton-Maggs, Paula, Brady, Angie, Brown, Matthew, Caulfield, Mark, Chitre, Manali, Clowes, Virginia, Coghlan, Gerry, Collins, Peter, Creaser-Myers, Amanda, DaCosta, Rosa, Davies, Sophie, Deegan, Patrick, Deshpande, Charu, Doffinger, Rainer, Egner, William, Erwood, Marie, Favier, Remi, Flinter, Frances, Furie, Bruce, Furnell, Abigail, Gardham, Alice, Gattens, Michael, Ghataorhe, Pavandeep K., Gibbs, Simon, Gilmour, Kimberley, Gissen, Paul, Goddard, Sarah, Gordins, Pavel, Greinacher, Andreas, Grigoriadou, Sofia, Hayman, Grant, Henderson, Robert, Henskens, Yvonne, Holden, Simon, Hu, Fengyuan, Jolles, Stephen, Josifova, Dragana, Keeling, David, Kelleher, Peter, Kelly, Anne M., Kuijpers, Taco W., Kumararatne, Dinakantha, Kurian, Manju, Laffan, Michael A., Linger, Rachel, Machado, Rajiv, Manson, Ania, Markus, Hugh S., Meehan, Sharon, Ouwehand, Willem H., Park, Soo-Mi, Parker, Alasdair, Paterson, Joan, Peerlinck, Kathelijne, Perry, David J., Qasim, Waseem, Rankin, Julia, Rehnstrom, Karola, Roberts, Irene, Roughley, Catherine, Rue-Albrecht, Kevin, Schulze, Harald, Shamardina, Olga, Shipley, Debbie, Simeoni, Ilenia, Stephens, Jonathan, Suntharalingam, Jay, Thachil, Jecko, Thaventhiran, James, Thomas, Ellen, Titterton, Catherine, Toh, Cheng-Hock, Turek, Wojciech, Turro, Ernest, Van Geet, Chris, Wakeling, Emma, Warner, Timothy Q., Webster, Andrew, Wilkins, Martin, Young, Tim, Yu, Ping, Webster, Andrew R.

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

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