Automatic fish population counting by artificial neural network von Newbury, Paul F., Culverhouse, Philip F., Pilgrim, Derek A.

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Leitfähiger Maskierungsverbundstoff von JONES, PETER M., LONDONDERRY, NEW HAMPSHIRE 03053, US, KEYSER, PAUL F., W. NEWBURY, MASSACHUSETTS 01985, US, FARRELL, THERESA, N. ANDOVER, MASSACHUSETTS 01845, US, HUBBARD, JOHN DANA, BILLERICA, MASSACHUSETTS 01821, US

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data von Wright, Caroline F, Dr, Fitzgerald, Tomas W, MS, Jones, Wendy D, MBBS, Clayton, Stephen, MRes, McRae, Jeremy F, PhD, van Kogelenberg, Margriet, PhD, King, Daniel A, MD, Ambridge, Kirsty, BSc, Barrett, Daniel M, BSc, Bayzetinova, Tanya, BSc, Bevan, A Paul, PhD, Bragin, Eugene, MSc, Chatzimichali, Eleni A, PhD, Gribble, Susan, PhD, Jones, Philip, MSc, Krishnappa, Netravathi, MSc, Mason, Laura E, BSc, Miller, Ray, PhD, Morley, Katherine I, PhD, Parthiban, Vijaya, PhD, Prigmore, Elena, PhD, Rajan, Diana, MSc, Sifrim, Alejandro, PhD, Swaminathan, G Jawahar, PhD, Tivey, Adrian R, MSc, Middleton, Anna, PhD, Parker, Michael, Prof, Carter, Nigel P, PhD, Barrett, Jeffrey C, PhD, Hurles, Matthew E, PhD, FitzPatrick, David R, Prof, Firth, Helen V, DM

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Identification of EpCAM as the Gene for Congenital Tufting Enteropathy von Sivagnanam, Mamata, Mueller, James L, Lee, Hane, Chen, Zugen, Nelson, Stanley F, Turner, Dan, Zlotkin, Stanley H, Pencharz, Paul B, Ngan, Bo–Yee, Libiger, Ondrej, Schork, Nicholas J, Lavine, Joel E, Taylor, Sharon, Newbury, Robert O, Kolodner, Richard D, Hoffman, Hal M

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Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment von Pettigrew, Kerry A, Reeves, Emily, Leavett, Ruth, Hayiou-Thomas, Marianna E, Sharma, Anahita, Simpson, Nuala H, Martinelli, Angela, Thompson, Paul, Hulme, Charles, Snowling, Margaret J, Newbury, Dianne F, Paracchini, Silvia

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Expression and proteolytic processing of the amyloid precursor protein is unaffected by the expression of the three human apolipoprotein E alleles in the brains of mice von Novy, Mariah J., Newbury, Samantha F., Liemisa, Braison, Morales-Corraliza, Jose, Alldred, Melissa J., Ginsberg, Stephen D., Mathews, Paul M.

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Brain apolipoprotein E levels in mice challenged by a Western diet increase in an allele-dependent manner von Liemisa, Braison, Newbury, Samantha F, Novy, Mariah J, Pasato, Jonathan A, Morales-Corraliza, Jose, Peng, Katherine Y, Mathews, Paul M

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PAPSS2‐related brachyolmia: Clinical and radiological phenotype in 18 new cases von Bownass, Lucy, Abbs, Stephen, Armstrong, Ruth, Baujat, Genevieve, Behzadi, Gry, Berentsen, Ragnhild Drage, Burren, Christine, Calder, Alistair, Cormier‐Daire, Valérie, Newbury‐Ecob, Ruth, Foulds, Nicola, Juliusson, Petur B., Kant, Sarina G., Lefroy, Henrietta, Mehta, Sarju G., Merckoll, Else, Michot, Caroline, Monsell, Fergal, Offiah, Amaka C., Richards, Allan, Rosendahl, Karen, Rustad, Cecilie F., Shears, Deborah, Tveten, Kristian, Wellesley, Diana, Wordsworth, Paul, Smithson, Sarah

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Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders von Faundes, Víctor, Demos, Michelle K., Goldman, Amy, Lehman, Anna, McKee, Shane, Morton, Jenny, Rankin, Julia, Temple, I. Karen, Adam, Shelin, van Karnebeek, Clara, Aitken, Stuart, Alvi, Mohsan, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Mason, Laura E., Tivey, Adrian R., Ahmed, Munaza, Balasubramanian, Meena, Barnicoat, Angela, Bitner-Glindzicz, Maria, Bourdon, Louise, Bradley, Lisa, Burn, John, Colgiu, Irina, Collins, Amanda, Collinson, Morag N., Connell, Fiona, Crow, Yanick, Dabir, Tabib, Davidson, Rosemarie, de Vries, Dylan, Deshpande, Charu, Dixit, Abhijit, Dobbie, Angus, Douzgou, Sofia, Duncan, Alexis, Eason, Jacqueline, Ellard, Sian, Elmslie, Frances, Evans, Karenza, Everest, Sarah, Flinter, Frances, Foulds, Nicola, Ghali, Neeti, Gibbons, Richard, Gill, Harinder, Greene, Philip, Gribble, Susan, Holder, Muriel, Hollingsworth, Georgina, Ingram, Stuart, Jenkins, Lucy, Joss, Shelagh, Kerr, Bronwyn, Kini, Usha, Kraus, Alison, Lachlan, Katherine, Marks, Karen, McConnell, Vivienne, McEntagart, Meriel, McGowan, Ruth, Middleton, Anna, Mohammed, Shehla, O’Shea, Rosie, Ogilvie, Caroline, Ong, Kai-Ren, Parker, Michael J., Patel, Chirag, Paterson, Joan, Payne, Stewart, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Randall, Josh, Rankin, Julia, Raymond, Lucy, Rice, Debbie, Robert, Leema, Samant, Shalaka, Selby, Ann, Sequeira, Cheryl, Shears, Debbie, Smith, Audrey, Smith, Kath, Splitt, Miranda, Squires, Miranda, Tomkins, Susan, Treacy, Becky, Tysoe, Carolyn, Vasudevan, Pradeep, Vijayarangakannan, Parthiban, Vogt, Julie, Wakeling, Emma, Whiteford, Margo, Wilcox, Sarah, Wilkinson, Emily, Firth, Helen V., Wright, Caroline F., FitzPatrick, David R.

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Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis von Newbury, Dianne F., Simpson, Nuala H., Thompson, Paul A., Bishop, Dorothy V. M.

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Logical and Methodological Issues Affecting Genetic Studies of Humans Reported in Top Neuroscience Journals von Grabitz, Clara R., Button, Katherine S., Munafò, Marcus R., Newbury, Dianne F., Pernet, Cyril R., Thompson, Paul A., Bishop, Dorothy V. M.

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Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance von Seitan, Vlad C, Banks, Peter, Laval, Steve, Majid, Nazia A, Dorsett, Dale, Rana, Amer, Smith, Jim, Bateman, Alex, Krpic, Sanja, Hostert, Arnd, Rollins, Robert A, Erdjument-Bromage, Hediye, Tempst, Paul, Benard, Claire Y, Hekimi, Siegfried, Newbury, Sarah F, Strachan, Tom

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A multicentre study of patients with Timothy syndrome von Walsh, Mark A, Turner, Christian, Timothy, Katherine W, Seller, Neil, Hares, Dominic L, James, Andrew F, Hancox, Jules C, Uzun, Orhan, Boyce, Dean, Stuart, Alan G, Brennan, Paul, Sarton, Caroline, McGuire, Karen, Newbury-Ecob, Ruth A, Mcleod, Karen

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De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental Disorder von Calpena, Eduardo, Hervieu, Alexia, Kaserer, Teresa, Swagemakers, Sigrid M.A., Goos, Jacqueline A.C., Popoola, Olajumoke, Ortiz-Ruiz, Maria Jesus, Barbaro-Dieber, Tina, Bownass, Lucy, Brilstra, Eva H., Brimble, Elise, Foulds, Nicola, Grebe, Theresa A., Harder, Aster V.E., Lees, Melissa M., Monaghan, Kristin G., Newbury-Ecob, Ruth A., Ong, Kai-Ren, Osio, Deborah, Reynoso Santos, Francis Jeshira, Ruzhnikov, Maura R.Z., Telegrafi, Aida, van Binsbergen, Ellen, van Dooren, Marieke F., van der Spek, Peter J., Blagg, Julian, Twigg, Stephen R.F., Mathijssen, Irene M.J., Clarke, Paul A., Wilkie, Andrew O.M.

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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes von Pettigrew, Kerry A, Frinton, Emily, Nudel, Ron, Chan, May T M, Thompson, Paul, Hayiou-Thomas, Marianna E, Talcott, Joel B, Stein, John, Monaco, Anthony P, Hulme, Charles, Snowling, Margaret J, Newbury, Dianne F, Paracchini, Silvia

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Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis von Newbury, Dianne F, Simpson, Nuala H, Thompson, Paul A, Bishop, Dorothy V M

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Generalized Structured Component Analysis in candidate gene association studies: applications and limitations von Thompson, Paul A, Bishop, Dorothy V M, Eising, Else, Fisher, Simon E, Newbury, Dianne F

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Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis von Newbury, Dianne F., Simpson, Nuala H., Thompson, Paul A., Bishop, Dorothy V. M.

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Need for recovery amongst emergency physicians in the UK and Ireland: a cross-sectional survey von Cottey, Laura, Lyttle, Mark David, Latour, Jos, Kane, L, Richter, S, Selway, J, Rimmer, C, Ayres, M, Kaur, K, Hartshorn, S, McGregor, K, Gardner, G, Clingo, T, Stewart, R, Mullen, N, Mirza, K, Cuthbert, P, Veeramuthu, K, Lipton, G, Umana, E, Agosti, V, Kerr, J, Dhutia, SJ, Cherian, B, Williams, O, Lindsay, C, Manou, S, Nunn, C, Fuller, R, Reynard, C, Daly, J, Boggaram, G, McConnell, D, Hirst, R, Muller, J, Chatha, H, Ramsundar, S, Sparkes, T, Barrett, L, Driessen, J, Meredith, S, Grimsmo-Powney, H, Malik, H, Gwatkin, L, Blackburn, R, Gillies, F, McLoughlin, TF, Hopping, K, Challen, K, Macdonald, M, Randle, A, Fairbairn, H, Thompson, J, Gray, S, Foley, J, Gardner, S, Pintus, S, Brammer, K, Raghunathan, A, Langston, S, Cooper, H, Arumugam, A, Moulds, Y, Thom, DL, Ali, N, Mackay, A, Frost, E, Wright, R, Saunders, A, Malik, KI, Fatkin, A, Naeem, S, Basu, A, Hill, O, Boulind, C, Williams, P, Hardwick, S, Gandolfi, C, Everitt, E, Ghosh, A, McKeever, D, Savage, L, Bailey, S, Sharr, R, Loffhagen, R, Rivers, V, Khan, HD, Baird, H, Bury, S, Gaiawyn, J, Johnson, G, Akhtar, A, Clarke, B, Colmar, M, Morrison, M, Raffo, D, Griffiths, OR, McIlwham, B, Cunningham, K, Clegg, E

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