Identification and characterization of a novel human vanilloid receptor-like protein, VRL-2 by DELANY, NATALIE S, HURLE, MICHAEL, FACER, PAUL, ALNADAF, TANJA, PLUMPTON, CHRISTOPHER, KINGHORN, IAN, SEE, CHEE GEE, COSTIGAN, MICHAEL, ANAND, PRAVEEN, WOOLF, CLIFFORD J, CROWTHER, DANIEL, SANSEAU, PHILIPPE, TATE, SIMON N

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Reverse Transcriptase-PCR Analysis of Bacterial rRNA for Detection and Characterization of Bacterial Species in Arthritis Synovial Tissue by KEMPSELL, Karen E, COX, Charles J, HURLE, Michael, WONG, Anthony, WILKIE, Scott, ZANDERS, Edward D, GASTON, J. S, CROWE, J. Scott

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Isolation and characterisation of potential respiratory syncytial virus receptor(s) on epithelial cells by Malhotra, Rajneesh, Ward, Malcolm, Bright, Helen, Priest, Richard, Foster, Martyn R., Hurle, Michael, Blair, Eddie, Bird, Michael

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En bloc re-resection of high-risk NMIBC after en bloc resection: results of a multicenter observational study by Hurle, Rodolfo, Casale, Paolo, Lazzeri, Massimo, Paciotti, Marco, Saita, Alberto, Colombo, Piergiuseppe, Morenghi, Emanuela, Oswald, David, Colleselli, Daniela, Mitterberger, Michael, Kunit, Thomas, Hager, Martina, Herrmann, Thomas R. W., Lusuardi, Lukas

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Crack growth rates in lithium disilicates with bulk (mis)alignment of the Li2Si2O5 phase in the [001] direction by Kirsten, Julia, Belli, Renan, Wendler, Michael, Petschelt, Anselm, Hurle, Katrin, Lohbauer, Ulrich

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Xpert Bladder Cancer Monitor May Avoid Cystoscopies in Patients Under "Active Surveillance" for Recurrent Bladder Cancer (BIAS Project): Longitudinal Cohort Study by Fasulo, Vittorio, Paciotti, Marco, Lazzeri, Massimo, Contieri, Roberto, Casale, Paolo, Saita, Alberto, Lughezzani, Giovanni, Diana, Pietro, Frego, Nicola, Avolio, Pier Paolo, Colombo, Piergiuseppe, Elefante, Grazia Maria, Guazzoni, Giorgio, Buffi, Nicolò Maria, Bates, Michael, Hurle, Rodolfo

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Synaptic, transcriptional and chromatin genes disrupted in autism by De Rubeis, Silvia, He, Xin, Goldberg, Arthur P, Poultney, Christopher S, Samocha, Kaitlin, Cicek, A Erucment, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarinder, Klei, Lambertus, Kosmicki, Jack, Shih-Chen, Fu, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F, Brownfeld, Jessica M, Cai, Jinlu, Campbell, Nicholas G, Carracedo, Angel, Chahrour, Maria H, Chiocchetti, Andreas G, Coon, Hilary, Crawford, Emily L, Curran, Sarah R, Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A, Gallagher, Louise, Geller, Evan, Guter, Stephen J, Hill, R Sean, Ionita-Laza, Juliana, Jimenz Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M, Kolevzon, Alexander, Lee, Irene, Lei, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R, McInnes, Alison L, Neale, Benjamin, Owen, Michael J, Ozaki, Noriio, Parellada, Mara, Parr, Jeremy R, Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J, Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Li-San, Wang, Weiss, Lauren A, Willsey, A Jeremy, Yu, Timothy W, Yuen, Ryan K C, Cook, Edwin H, Freitag, Christine M, Gill, Michael, Hultman, Christina M, Lehner, Thomas, Palotie, Aaarno, Schellenberg, Gerard D, Sklar, Pamela, State, Matthew W, Sutcliffe, James S, Walsh, Christiopher A, Scherer, Stephen W, Zwick, Michael E, Barett, Jeffrey C, Cutler, David J, Roeder, Kathryn, Devlin, Bernie, Daly, Mark J, Buxbaum, Joseph D

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Precision farming technologies for crop protection: A meta-analysis by Anastasiou, Evangelos, Fountas, Spyros, Voulgaraki, Matina, Psiroukis, Vasilios, Koutsiaras, Michael, Kriezi, Olga, Lazarou, Erato, Vatsanidou, Anna, Fu, Longsheng, Bartolo, Fabiola Di, Barreiro-Hurle, Jesus, Gómez-Barbero, Manuel

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study by 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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The UK10K project identifies rare variants in health and disease by Walter, Klaudia, Min, Josine L, Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R B, Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E, Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V, Barroso, Inês, Humphries, Steve E, Hurles, Matthew E, Zeggini, Eleftheria, Barrett, Jeffrey C, Plagnol, Vincent, Richards, J Brent, Greenwood, Celia M T, Timpson, Nicholas J, Durbin, Richard, Soranzo, Nicole

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An integrated map of genetic variation from 1,092 human genomes by Abecasis, Goncalo R, Auton, Adam, Brooks, Lisa D, DePristo, Mark A, Durbin, Richard M, Handsaker, Robert E, Kang, Hyun Min, Marth, Gabor T, McVean, Gil A

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Precision farming technologies on crop protection: A stakeholders survey by Anastasiou, Evangelos, Fountas, Spyros, Koutsiaras, Michael, Voulgaraki, Matina, Vatsanidou, Anna, Barreiro-Hurle, Jesus, Bartolo, Fabiola Di, Gómez-Barbero, Manuel

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Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data by 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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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel by Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L, Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J Brent, Durbin, Richard, Timpson, Nicholas J, Marchini, Jonathan, Soranzo, Nicole

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X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 by Olcese, Chiara, Patel, Mitali P, Shoemark, Amelia, Kiviluoto, Santeri, Legendre, Marie, Williams, Hywel J, Vaughan, Cara K, Hayward, Jane, Goldenberg, Alice, Emes, Richard D, Munye, Mustafa M, Dyer, Laura, Cahill, Thomas, Bevillard, Jeremy, Gehrig, Corinne, Guipponi, Michel, Chantot, Sandra, Duquesnoy, Philippe, Thomas, Lucie, Jeanson, Ludovic, Copin, Bruno, Tamalet, Aline, Thauvin-Robinet, Christel, Papon, Jean-François, Garin, Antoine, Pin, Isabelle, Vera, Gabriella, Aurora, Paul, Fassad, Mahmoud R, Jenkins, Lucy, Boustred, Christopher, Cullup, Thomas, Dixon, Mellisa, Onoufriadis, Alexandros, Bush, Andrew, Chung, Eddie M K, Antonarakis, Stylianos E, Loebinger, Michael R, Wilson, Robert, Armengot, Miguel, Escudier, Estelle, Hogg, Claire, Amselem, Serge, Sun, Zhaoxia, Bartoloni, Lucia, Blouin, Jean-Louis, Mitchison, Hannah M

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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel by Delaneau, Olivier, Marchini, Jonathan

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Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics by Khurana, Ekta, Fu, Yao, Colonna, Vincenza, Mu, Xinmeng Jasmine, Kang, Hyun Min, Lappalainen, Tuuli, Sboner, Andrea, Lochovsky, Lucas, Chen, Jieming, Harmanci, Arif, Das, Jishnu, Abyzov, Alexej, Balasubramanian, Suganthi, Beal, Kathryn, Chakravarty, Dimple, Challis, Daniel, Chen, Yuan, Clarke, Declan, Clarke, Laura, Cunningham, Fiona, Evani, Uday S., Flicek, Paul, Fragoza, Robert, Garrison, Erik, Gibbs, Richard, Gümüş, Zeynep H., Herrero, Javier, Kitabayashi, Naoki, Kong, Yong, Lage, Kasper, Liluashvili, Vaja, Lipkin, Steven M., MacArthur, Daniel G., Marth, Gabor, Muzny, Donna, Pers, Tune H., Ritchie, Graham R. S., Rosenfeld, Jeffrey A., Sisu, Cristina, Wei, Xiaomu, Wilson, Michael, Xue, Yali, Yu, Fuli, Dermitzakis, Emmanouil T., Yu, Haiyuan, Rubin, Mark A., Tyler-Smith, Chris, Gerstein, Mark

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Estimating telomere length from whole genome sequence data by Ding, Zhihao, Mangino, Massimo, Aviv, Abraham, Spector, Tim, Durbin, Richard

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GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements by Dixon, Peter H, Levine, Adam P, Cebola, Inês, Chan, Melanie M Y, Amin, Aliya S, Aich, Anshul, Mozere, Monika, Maude, Hannah, Mitchell, Alice L, Zhang, Jun, Chambers, Jenny, Syngelaki, Argyro, Donnelly, Jennifer, Cooley, Sharon, Geary, Michael, Nicolaides, Kypros, Thorsell, Malin, Hague, William M, Estiu, Maria Cecilia, Marschall, Hanns-Ulrich, Gale, Daniel P, Williamson, Catherine

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Mutations in CCDC39 and CCDC40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms by Antony, Dinu, Becker-Heck, Anita, Zariwala, Maimoona A., Schmidts, Miriam, Onoufriadis, Alexandros, Forouhan, Mitra, Wilson, Robert, Taylor-Cox, Theresa, Dewar, Ann, Jackson, Claire, Goggin, Patricia, Loges, Niki T., Olbrich, Heike, Jaspers, Martine, Jorissen, Mark, Leigh, Margaret W., Wolf, Whitney E., Daniels, M. Leigh Anne, Noone, Peadar G., Ferkol, Thomas W., Sagel, Scott D., Rosenfeld, Margaret, Rutman, Andrew, Dixit, Abhijit, O'Callaghan, Christopher, Lucas, Jane S., Hogg, Claire, Scambler, Peter J., Emes, Richard D., UK10K, Chung, Eddie M.K., Shoemark, Amelia, Knowles, Michael R., Omran, Heymut, Mitchison, Hannah M.

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