A common neonatal image phenotype predicts adverse neurodevelopmental outcome in children born preterm

by Boardman, J.P., Craven, C., Valappil, S., Counsell, S.J., Dyet, L.E., Rueckert, D., Aljabar, P., Rutherford, M.A., Chew, A.T.M., Allsop, J.M., Cowan, F., Edwards, A.D.
Published in NeuroImage (Orlando, Fla.)

Smaller Cerebellar Volumes in Very Preterm Infants at Term-Equivalent Age are Associated with the Presence of Supratentorial Lesions

by Srinivasan, L, Allsop, J, Counsell, S.J, Boardman, J.P, Edwards, A.D, Rutherford, M
Published in American Journal of Neuroradiology

High b-Value Diffusion Tensor Imaging of the Neonatal Brain at 3T

by Dudink, J, Larkman, D.J, Kapellou, O, Boardman, J.P, Allsop, J.M, Cowan, F.M, Hajnal, J.V, Edwards, A.D, Rutherford, M.A, Counsell, S.J
Published in American journal of neuroradiology : AJNR

A patient care system for early 3.0 Tesla magnetic resonance imaging of very low birth weight infants

by Merchant, N, Groves, A, Larkman, D.J, Counsell, S.J, Thomson, M.A, Doria, V, Groppo, M, Arichi, T, Foreman, S, Herlihy, D.J, Hajnal, J.V, Srinivasan, L, Foran, A, Rutherford, M, Edwards, A.D, Boardman, J.P
Published in Early human development

Brain Development in Fetuses of Mothers with Diabetes: A Case-Control MR Imaging Study

by Denison, F C, Macnaught, G, Semple, S I K, Terris, G, Walker, J, Anblagan, D, Serag, A, Reynolds, R M, Boardman, J P
Published in American journal of neuroradiology : AJNR

Assessment of brain growth in early childhood using deformation-based morphometry

by Aljabar, P., Bhatia, K.K., Murgasova, M., Hajnal, J.V., Boardman, J.P., Srinivasan, L., Rutherford, M.A., Dyet, L.E., Edwards, A.D., Rueckert, D.
Published in NeuroImage (Orlando, Fla.)

A multivariate statistical analysis of the developing human brain in preterm infants

by Thomaz, C.E., Boardman, J.P., Counsell, S., Hill, D.L.G., Hajnal, J.V., Edwards, A.D., Rutherford, M.A., Gillies, D.F., Rueckert, D.
Published in Image and vision computing

A patient care system for early 3.0Tesla magnetic resonance imaging of very low birth weight infants

by Merchant, N., Groves, A., Larkman, D.J., Counsell, S.J., Thomson, M.A., Doria, V., Groppo, M., Arichi, T., Foreman, S., Herlihy, D.J., Hajnal, J.V., Srinivasan, L., Foran, A., Rutherford, M., Edwards, A.D., Boardman, J.P.
Published in Early human development

Clustering and Dispersion of Duopolists in a Linear Market

by Pitts, Timothy C., Boardman, John P.
Published in Geographical analysis

Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

by HEARLE, Nicholas, SCHUMACHER, Valerie, TRIMBATH, Jill D, GIARDIELLO, Francis M, GRUBER, Stephen B, OFFERHAUS, G. Johan A, DE ROOIJ, Felix W. M, WILSON, J. H. Paul, HANSMANN, Anika, MÖSLEIN, Gabriela, ROYER-POKORA, Brigitte, TILMANVOGEL, MENKO, Fred H, PHILLIPS, Robin K. S, SPIGELMAN, Allan D, HOULSTON, Richard S, OLSCHWANG, Sylviane, BOARDMAN, Lisa A, GILLE, Johan J. P, KELLER, Josbert J, WESTERMAN, Anne Marie, SCOTT, Rodney J, LIM, Wendy
Published in Clinical cancer research

Mapping methane concentrations from a controlled release experiment using the next generation airborne visible/infrared imaging spectrometer (AVIRIS-NG)

by Thorpe, A.K., Frankenberg, C., Aubrey, A.D., Roberts, D.A., Nottrott, A.A., Rahn, T.A., Sauer, J.A., Dubey, M.K., Costigan, K.R., Arata, C., Steffke, A.M., Hills, S., Haselwimmer, C., Charlesworth, D., Funk, C.C., Green, R.O., Lundeen, S.R., Boardman, J.W., Eastwood, M.L., Sarture, C.M., Nolte, S.H., Mccubbin, I.B., Thompson, D.R., McFadden, J.P.
Published in Remote sensing of environment

Signatures of TOP1 transcription-associated mutagenesis in cancer and germline

by Reijns, Martin A M, Parry, David A, Williams, Thomas C, Nadeu, Ferran, Hindshaw, Rebecca L, Rios Szwed, Diana O, Nicholson, Michael D, Carroll, Paula, Boyle, Shelagh, Royo, Romina, Cornish, Alex J, Xiang, Hang, Ridout, Kate, Schuh, Anna, Aden, Konrad, Palles, Claire, Campo, Elias, Stankovic, Tatjana, Taylor, Martin S, Jackson, Andrew P
Published in Nature (London)

Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition

by Martins Custodio, Helena, Clayton, Lisa M, Bellampalli, Ravishankara, Pagni, Susanna, Silvennoinen, Katri, Caswell, Richard, Brunklaus, Andreas, Guerrini, Renzo, Koeleman, Bobby P C, Lemke, Johannes R, Møller, Rikke S, Scheffer, Ingrid E, Weckhuysen, Sarah, Zara, Federico, Zuberi, Sameer, Kuchenbaecker, Karoline, Balestrini, Simona, Mills, James D, Sisodiya, Sanjay M
Published in Brain (London, England : 1878)

A Biomechanical Analysis of Rotator Cuff Deficiency in a Cadaveric Model

by Thompson, William O., Debski, Richard E., Boardman, N. Douglas, Taskiran, Emin, Warner, Jon J. P., Fu, Freddie H., Woo, Savio L.-Y.
Published in American journal of sports medicine

Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration

by Vetro, Annalisa, Pelorosso, Cristiana, Balestrini, Simona, Masi, Alessio, Hambleton, Sophie, Argilli, Emanuela, Giubbolini, Simone, Barrick, Rebekah, Bergant, Gaber, Writzl, Karin, Bijlsma, Emilia K., Cacheiro, Pilar, Mei, Davide, Devlin, Anita, Machol, Keren, Mannaioni, Guido, Sakamoto, Masamune, Menezes, Manoj P., Courtin, Thomas, Sherr, Elliott, Parra, Riccardo, Richardson, Ruth, Roscioli, Tony, Scala, Marcello, von Stülpnagel, Celina, Smedley, Damian, Pochiero, Francesca, Ramesh, Venkateswaran, Capra, Valeria, Mancardi, Margherita, Keren, Boris, Mignot, Cyiril, Lulli, Matteo, Parks, Kendall, Griffin, Helen, Nigro, Vincenzo, Hirata, Yuko, Koichihara, Reiko, Peterlin, Borut, Maki, Ryuto, Nitta, Yohei, Ambrose, John C., Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boustred, Christopher R., Brittain, Helen, Brown, Matthew A., Caulfield, Mark J., Chan, Georgia C., Giess, Adam, Griffin, John N., Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Lakey, Anna, Lopez, Javier F., Maleady-Crowe, Fiona, Minneci, Federico, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Rahim, Tahrima, Rendon, Augusto, Sawant, Kushmita, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Zarowiecki, Magdalena, Torella, Annalaura, Tohyama, Jun, Hamada, Keisuke, Ogata, Kazuhiro, Sugie, Atsushi, van der Smagt, Jasper J., van Gassen, Koen, Valence, Stephanie, Vittery, Emma, Malone, Stephen, Kato, Mitsuhiro, Ratto, Gian Michele, Guerrini, Renzo
Published in American journal of human genetics

Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease

by Sadeghi-Alavijeh, Omid, Chan, Melanie M Y, Moochhala, Shabbir H, Howles, Sarah, Gale, Daniel P, Böckenhauer, Detlef
Published in Kidney international

Prevalence and significance of DDX41 gene variants in the general population

by Cheloor Kovilakam, Sruthi, Gu, Muxin, Dunn, William G., Marando, Ludovica, Barcena, Clea, Ambrose, J. C., Arumugam, P., Bevers, R., Bleda, M., Boardman-Pretty, F., Boustred, C. R., Brittain, H., Brown, M. A., Caulfield, M. J., Chan, G. C., Giess, A., Griffin, J. N., Hamblin, A., Henderson, S., Hubbard, T. J. P., Jackson, R., Jones, L. J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Lakey, A., Leigh, S. E. A., Leong, I. U. S., Lopez, F. J., Maleady-Crowe, F., McEntagart, M., Minneci, F., Mitchell, J., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A. C., O‘Donovan, P., Odhams, C. A., Patch, C., Perez-Gil, D., Pereira, M. B., Pullinger, J., Rahim, T., Rendon, A., Rogers, T., Savage, K., Sawant, K., Scott, R. H., Siddiq, A., Sieghart, A., Smith, S. C., Sosinsky, A., Stuckey, A., Tanguy, M., Taylor Tavares, A. L., Thomas, E. R. A., Thompson, S. R., Tucci, A., Welland, M. J., Williams, E., Witkowska, K., Wood, S. M., Zarowiecki, M., Nik-Zainal, Serena, Mohorianu, Irina, Kar, Siddhartha P., Fabre, Margarete A., Quiros, Pedro M., Vassiliou, George S.
Published in Blood

Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia

by Chen, Zhongbo, Tucci, Arianna, Cipriani, Valentina, Gustavsson, Emil K, Ibañez, Kristina, Reynolds, Regina H, Zhang, David, Vestito, Letizia, García, Alejandro Cisterna, Sethi, Siddharth, Brenton, Jonathan W, García-Ruiz, Sonia, Fairbrother-Browne, Aine, Gil-Martinez, Ana-Luisa, Wood, Nick, Hardy, John A, Smedley, Damian, Houlden, Henry, Botía, Juan, Ryten, Mina
Published in Brain (London, England : 1878)

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

by Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O'Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry
Published in Brain (London, England : 1878)

SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

by Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair
Published in Genetics in medicine