Browse by all authors Browse By Author/Contributor/Editor Name - Brown,+Morris+J.

Browse Results (19 results found)

Subscribe to the RSS feed for this result setSubscribe to the RSS feed for this result set

  Abstract Views File Downloads Thomson Reuters Web of Science Citation Count Scopus Citation Count Altmetric Score
Houlden, H., Rizzu, P., Stevens, M., De Knijff, P., Van Duijn, C. M., Van Swieten, J. C., Heutink, P., Perez-Tur, J., Thomas, V., Baker, M., Morris, H., Rossor, M., Jannsen, J. C., Petersen, R. C., Dodd, P. R., Dark, F., Boeve, B., Dickson, D., Davies, P., Pickering-Brown, S., Mann, D. and Adamson, J. (1999) Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations. Neuroscience Letters, 260 3: 193-195. doi:10.1016/S0304-3940(98)00931-8     17 Cited 20 times in Scopus20 0
Hutton, M, Lendon, CL, Rizzu, P, Baker, M, Froelich, S, Houlden, H, Pickering-Brown, S, Chakraverty, S, Isaacs, A, Grover, A, Hackett, J, Adamson, J, Lincoln, S, Dickson, D, Davies, P, Petersen, RC, Stevens, M, de Graaff, E, Wauters, E, van Baren, J, Hillebrand, M, Joosse, M, Kwon, JM, Nowotny, P, Che, LK, Norton, J, Morris, JC, Reed, LA, Trojanowski, J, Basun, H, Lannfelt, L, Neystat, M, Fahn, S, Dark, F, Tannenberg, T, Dodd, PR, Hayward, N, Kwok, JBJ, Schofield, PR, Andreadis, A, Snowden, J, Craufurd, D, Neary, D, Owen, F, Oostra, BA, Hardy, J, Goate, A, van Swieten, J, Mann, D, Lynch, T and Heutink, P (1998) Association of missense and 5 '-splice-site mutations in tau with the inherited dementia FTDP-17. Nature, 393 6686: 702-705. doi:10.1038/31508     2282 Cited 2380 times in Scopus2380 28
Burgess, S., Thompson, S. G., Andrews, G., Samani, N. J., Hall, A., Whincup, P., Morris, R., Lawlor, D. A., Davey Smith, G., Timpson, N., Ebrahim, S., Ben-Shlomo, Y., Brown, M., Ricketts, S., Sandhu, M., Reiner, A., Psaty, B., Lange, L., Cushman, M., Hung, J., Thompson, P., Beilby, J., Warrington, N., Palmer, L. J., Nordestgaard, B. G., Tybjaerg-Hansen, A., Zacho, J., Wu, C., Lowe, G., Tzoulaki, I., Kumari, M., Yamamoto, J. F., Chiodini, B., Franzosi, M., Hankey, G. J., Jamrozik, K., Palmer, L., Rimm, E., Pai, J., Heckbert, S., Bis, J., Anand, S., Engert, J., Collins, R., Clarke, R., Melander, O., Berglund, G., Ladenvall, P., Johansson, L., Jansson, J.-H., Hallmans, G., Hingorani, A., Humphries, S., Manson, J., Watkins, H., Hopewell, J., Saleheen, D., Frossard, R., Danesh, J., Sattar, N., Robertson, M., Shepherd, J., Schaefer, E., Hofman, A., Witteman ,J. C. M., Kardys, I., De Faire, U., Bennet, A., Ford, I., Packard, C., Casas, J. P., Smeeth, L., Wensley, F., Bowden, J., Di Angelantonio, E., Gao, P., Shah, T., Verzilli, C., Walker, M. and Whittaker, J. (2010) Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variables. Statistics in Medicine, 29 12: 1298-1311. doi:10.1002/sim.3843     15 Cited 16 times in Scopus16 1
Maller, Julian B., McVean, Gilean, Byrnes, Jake, Vukcevic, Damjan, Palin, Kimmo, Su, Zhan, Howson, Joanna M. M., Auton, Adam, Myers, Simon, Morris, Andrew, Pirinen, Matti, Brown, Matthew A., Burton, Paul R., Caulfield, Mark J., Compston, Alastair, Farrall, Martin, Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Mathew, Christopher G., Pembrey, Marcus, Satsangi, Jack, Stratton, Michael R., Worthington, Jane, Craddock, Nick, Hurles, Matthew, Ouwehand, Willem, Parkes, Miles, Rahman, Nazneen, Duncanson, Audrey, Todd, John A., Kwiatkowski, Dominic P., Samani, Nilesh J., Gough, Stephen C. L., McCarthy, Mark I., Deloukas, Panagiotis and Donnelly, Peter (2012) Bayesian refinement of association signals for 14 loci in 3 common diseases. Nature Genetics, 44 12: 1294-1301. doi:10.1038/ng.2435     160 Cited 187 times in Scopus187 14
Johnson, Toby, Gaunt, Tom R., Newhouse, Stephen J., Padmanabhan, Sandosh, Tomaszewski, Marciej, Kumari, Meena, Morris, Richard W., Tzoulaki, Ioanna, O'Brien, Eoin T., Poulter, Neil R., Sever, Peter, Shields, Denis C., Thom, Simon, Wannamethee, Sasiwarang G., Whincup, Peter H., Brown, Morris J., Connell, John M., Dobson, Richard J., Howard, Philip J., Mein, Charles A., Onipinla, Abiodun, Shaw-Hawkins, Sue, Zhang, Yun, Smith, George Davey, Day, Ian N. M., Lawlor, Debbie A., Goodall, Alison H.., Fowkes, F. Gerald, Abecasis, Goncalo R., Elliott, Paul, Gateva, Vesela, Braund, Peter S., Burton, Paul R., Nelson, Christopher P., Tobin, Martin D., Van Der Harst, Pim, Glorioso, Nicola, Neuvrith, Hani, Salvi, Erika, Staessen, Jan A., Stucchi, Andrea, Devos, Nabila, Jeunemaitre, Xavier, Plouin, Pierre-Francois, Tichet, Jean, Juhanson, Peeter, Org, Elin, Putku, Margus, Sober, Siim, Veldre, Gudrun, Viigimaa, Margus, Levinsson, Anna, Rosengren, Annika, Thelle, Dag S., Hastie, Claire E., Hedner, Thomas, Lee, Wai K., Melander, Olle, Wahlstrand, Bjorn, Hardy, Rebecca, Wong, Andrew, Cooper, Jackie A., Palmen, Jutta, Chen, Li, Stewart, Alexandre F. R., Wells, George A., Westra, Harm-Jan, Wolfs, Marcel G. M., Clarke, Robert, Franzosi, Maria Grazia, Goel, Anuj, Hamsten, Anders, Lathrop, Mark, Peden, John F., Seedorf, Udo, Watkins, Hugh, Ouwehand, Willem H., Sambrook, Jennifer, Stephens, Jonathan, Casas, Juan-Pablo, Drenos, Fotios, Holmes, Michael V., Kivimaki, Mika, Shah, Sonia, Shah, Tina, Talmud, Philippa J., Whittaker, John, Wallace, Chris, Delles, Christian, Laan, Maris, Kuh, Diana, Humphries, Steve E., Nyberg, Fredrik, Cusi, Daniele, Roberts, Robert, Newton-Cheh, Christopher, Franke, Lude, Stanton, Alive V., Dominiczak, Anna F., Farrall, Martin, Hingorani, Aroon D., Samani, Nilesh J., Caulfield, Mark J. and Munroe, Patricia B. (2011) Blood pressure loci identified with a gene-centric array. American Journal of Human Genetics, 89 6: 688-700. doi:10.1016/j.ajhg.2011.10.013     104 Cited 108 times in Scopus108 5
Nolte, Ilja M., Wallace, Chris, Newhouse, Stephen J., Waggott, Daryl, Fu, Jingyuan, Soranzo, Nicole, Gwilliam, Rhian, Deloukas, Panos, Savelieva, Irina, Zheng, Dongling, Dalageorgou, Chrysoula, Farrall, Martin, Samani, Nilesh J., Connell, John, Brown, Morris, Dominiczak, Anna, Lathrop, Mark, Zeggini, Eleftheria, Wain, Louise V., The DCCT/EDIC Research Group, Newton-Cheh, Christopher, Eijgelsheim, Mark, Rice, Kenneth, de Bakke, Paul I. W., Pfeufer, Arne, Sanna, Serena, Arking, Dan E., Asselbergs, Folkert W., Spector, Tim D., Carter, Nicholas D., Jeffery, Steve, Tobin, Martin, Caulfield, Mark, Snieder, Harold, Paterson, Andrew D., Munroe, Patricia B., Jamshidi, Yalda, The Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda (2009) Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: Meta-analysis of three genome-wide association studies. PLoS One, 4 7: e6138-1-e6138-10. doi:10.1371/journal.pone.0006138     40 Cited 44 times in Scopus44 3
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group, Wellcome Trust Case Control Consortium 2, Zhou, Kaixin, Tavendale, Roger, Donnelly, Louise A., Schofield, Chris, Burch, Lindsay, Carr, Fiona, Colhoun, Helen, Morris, Andrew D., Sutherland, Calum, Palmer, Colin N. A., Pearson, Ewan, Bellenguez Celine, Spencer, Chris C. A., Strange, Amy, Freeman, Colin, Rautanen, Anna, McCarthy, Mark I., Donnelly, Peter, Bennett, Amanda J., Coleman, Ruth L., Groves, Christopher J., McCarthy, Mark I., Holman, Rury R., Hawley, Simon A., Hardie, Grahame, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Edkins, Sarah, Gray, Emma, Hunt, Sarah, Langford, Cordelia, Peltonen, Leena, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G, Trembath, Richard, Plomin, Robert, Sawcer, Stephen J., Samani, Nilesh J., Viswanathan, Aananth C., Wood, Nicholas W., Harries, Lorna W., Hattersley, Andrew T., Doney, Alex S. F., McCarthy, Mark I. and Donnelly, Peter (2011) Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nature Genetics, 43 2: 117-120. doi:10.1038/ng.735     224 Cited 262 times in Scopus262 2
Bailey, Emily J., Cates, Christopher J., Kruske, Sue G., Morris, Peter S., Chang, Anne B. and Brown, Ngiare (2009) Culture-specific programs for children and adults from minority groups who have asthma. Cochrane Database of Systematic Reviews, 2: . doi:10.1002/14651858.CD006580.pub4     3 Cited 50 times in Scopus50 0
van de Bunt, Martijn, Cortes, Adrian, Brown, Matthew A., Morris, Andrew P., McCarthy, Mark I., IGAS Consortium, Hadler, Johanna, Robinson, Philip C., Leo, Paul, Cremin, Katie, Pryce, Karena, Harris, Jessica, Bradbury, Linda A., Kenna, Tony J. and Yang, Jian (2015) Evaluating the performance of fine-mapping strategies at common variant GWAS Loci. PL o S Genetics, 11 9: 1-14. doi:10.1371/journal.pgen.1005535     14 Cited 16 times in Scopus16 15
Taylor, Paul J., Brown, Scott R., Cooper, Donald P., Salm, Paul, Morris, Michael R., Pillans, Peter I. and Lynch, Stephen V. (2005) Evaluation of 3 internal standards for the measurement of cyclosporin by HPLC-mass spectrometry. Clinical Chemistry, 51 10: 1890-1893. doi:10.1373/clinchem.2005.055160     31 Cited 33 times in Scopus33 0
Koettgen, Anna, Albrecht, Eva, Teumer, Alexander, Vitart, Veronique, Krumsiek, Jan, Hundertmark, Claudia, Pistis, Giorgio, Ruggiero, Daniela, O'Seaghdha, Conall M., Haller, Toomas, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltan, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Pirastu, Nicola, Li, Guo, Hayward, Caroline, Zemunik, Tatijana, Huffman, Jennifer, Yengo, Loic, Zhao, Jing Hua, Demirkan, Ayse, Feitosa, Mary F., Liu, Xuan, Malerba, Giovanni, Lopez, Lorna M., van der Harst, Pim, Li, Xinzhong, Kleber, Marcus E., Hicks, Andrew A., Nolte, Ilja M., Johansson, Asa, Murgia, Federico, Wild, Sarah H., Bakker, Stephan J. L., Peden, John F., Dehghan, Abbas, Steri, Maristella, Tenesa, Albert, Lagou, Vasiliki, Salo, Perttu, Mangino, Massimo, Rose, Lynda M., Lehtimaki, Terho, Woodward, Owen M., Okada, Yukinori, Tin, Adrienne, Mueller, Christian, Oldmeadow, Christopher, Putku, Margus, Czamara, Darina, Kraft, Peter, Frogheri, Laura, Thun, Gian Andri, Grotevendt, Anne, Gislason, Gauti Kjartan, Harris, Tamara B., Launer, Lenore J., McArdle, Patrick, Shuldiner, Alan R., Boerwinkle, Eric, Coresh, Josef, Schmidt, Helena, Schallert, Michael, Martin, Nicholas G., Montgomery, Grant W., Kubo, Michiaki, Nakamura, Yusuke, Tanaka, Toshihiro, Munroe, Patricia B., Samani, Nilesh J., Jacobs, David R., Jr., Liu, Kiang, D'Adamo, Pio, Ulivi, Sheila, Rotter, Jerome I., Psaty, Bruce M., Vollenweider, Peter, Waeber, Gerard, Campbell, Susan, Devuyst, Olivier, Navarro, Pau, Kolcic, Ivana, Hastie, Nicholas, Balkau, Beverley, Froguel, Philippe, Esko, Tonu, Salumets, Andres, Khaw, Kay Tee, Langenberg, Claudia, Wareham, Nicholas J., Isaacs, Aaron, Kraja, Aldi, Zhang, Qunyuan, Wild, Philipp S., Scott, Rodney J., Holliday, Elizabeth G., Org, Elin, Viigimaa, Margus, Bandinelli, Stefania, Metter, Jeffrey E., Lupo, Antonio, Trabetti, Elisabetta, Sorice, Rossella, Doering, Angela, Lattka, Eva, Strauch, Konstantin, Theis, Fabian, Waldenberger, Melanie, Wichmann, H-Erich, Davies, Gail, Gow, Alan J., Bruinenberg, Marcel, Stolk, Ronald P., Kooner, Jaspal S., Zhang, Weihua, Winkelmann, Bernhard R., Boehm, Bernhard O., Lucae, Susanne, Penninx, Brenda W., Smit, Johannes H., Curhan, Gary, Mudgal, Poorva, Plenge, Robert M., Portas, Laura, Persico, Ivana, Kirin, Mirna, Wilson, James F., Leach, Irene Mateo, van Gilst, Wiek H., Goel, Anuj, Ongen, Halit, Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Imboden, Medea, von Eckardstein, Arnold, Cucca, Francesco, Nagaraja, Ramaiah, Piras, Maria Grazia, Nauck, Matthias, Schurmann, Claudia, Budde, Kathrin, Ernst, Florian, Farrington, Susan M., Theodoratou, Evropi, Prokopenko, Inga, Stumvoll, Michael, Jula, Antti, Perola, Markus, Salomaa, Veikko, Shin, So-Youn, Spector, Tim D., Sala, Cinzia, Ridker, Paul M., Kaehoenen, Mika, Viikari, Jorma, Hengstenberg, Christian, Nelson, Christopher P., Meschia, James F., Nalls, Michael A., Sharma, Pankaj, Singleton, Andrew B., Kamatani, Naoyuki, Zeller, Tanja, Burnier, Michel, Attia, John, Laan, Maris, Klopp, Norman, Hillege, Hans L., Kloiber, Stefan, Choi, Hyon, Pirastu, Mario, Tore, Silvia, Probst-Hensch, Nicole M., Voelzke, Henry, Gudnason, Vilmundur, Parsa, Afshin, Schmidt, Reinhold, Whitfield, John B., Fornage, Myriam, Gasparini, Paolo, Siscovick, David S., Polasek, Ozren, Campbell, Harry, Rudan, Igor, Bouatia-Naji, Nabila, Metspalu, Andres, Loos, Ruth J. F., van Duijn, Cornelia M., Borecki, Ingrid B., Ferrucci, Luigi, Gambaro, Giovanni, Deary, Ian J., Wolffenbuttel, Bruce H. R., Chambers, John C., Maerz, Winfried, Pramstaller, Peter P., Snieder, Harold, Gyllensten, Ulf, Wright, Alan F., Navis, Gerjan, Watkins, Hugh, Witteman, Jacqueline C. M., Sanna, Serena, Schipf, Sabine, Dunlop, Malcolm G., Toenjes, Anke, Ripatti, Samuli, Soranzo, Nicole, Toniolo, Daniela, Chasman, Daniel I., Raitakari, Olli, Kao, W. H. Linda, Ciullo, Marina, Fox, Caroline S., Caulfield, Mark, Bochud, Murielle and Gieger, Christian (2013) Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics, 45 2: 145-154. doi:10.1038/ng.2500     283 Cited 284 times in Scopus284 45
Gregson, Celia L., Newell, Felicity, Leo, Paul J., Clark, Graeme R., Paternoster, Lavinia, Marshall, Mhairi, Forgetta, Vincenzo, Morris, John A., Ge, Bing, Bao, Xiao, Duncan Bassett, J. H., Williams, Graham R., Youlten, Scott E., Croucher, Peter I., Davey Smith, George, Evans, David M., Kemp, John P., Brown, Matthew A., Tobias, Jon H. and Duncan, Emma L. (2018) Genome-wide association study of extreme high bone mass: contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Bone, 114 62-71. doi:10.1016/j.bone.2018.06.001     0 0 3
Hare, K. M., Leach, A. J., Morris, P. S., Smith-Vaughan, H., Torzillo, P., Bauert, P., Cheng, A. C., McDonald, M. I., Brown, N., Chang, A. B. and Grimwood, K. (2012) Impact of recent antibiotics on nasopharyngeal carriage and lower airway infection in Indigenous Australian children with non-cystic fibrosis bronchiectasis. International Journal of Antimicrobial Agents, 40 4: 365-369. doi:10.1016/j.ijantimicag.2012.05.018     20 Cited 20 times in Scopus20 2
Hare, Kim M., Singleton, Rosalyn J., Grimwood, Keith, Valery, Patricia C., Cheng, Allen C., Morris, Peter S., Leach, Amanda J., Smith-Vaughan, Heidi C., Chatfield, Mark, Redding, Greg, Reasonover, Alisa L., McCallum, Gabrielle B., Chikoyak, Lori, McDonald, Malcolm I., Brown, Ngiare, Torzillo, Paul J. and Chang, Anne B. (2013) Longitudinal Nasopharyngeal Carriage and Antibiotic Resistance of Respiratory Bacteria in Indigenous Australian and Alaska Native Children with Bronchiectasis. Plos One, 8 8: e70478.1-e70478.8. doi:10.1371/journal.pone.0070478     19 Cited 20 times in Scopus20 1
Doyle, Lex W., Anderson, Peter J., Battin, Malcolm, Bowen, Jennifer R., Brown, Nisha, Callanan, Catherine, Campbell, Catherine, Chandler, Samantha, Cheong, Jeanie, Darlow, Brian, Davis, Peter G., DePaoli, Tony, French, Noel, McPhee, Andy, Morris, Shusannah, O'Callaghan, Michael, Rieger, Ingrid, Roberts, Gehan, Spittle, Alicia J., Wolke, Dieter and Woodward, Lianne J. (2014) Long term follow up of high risk children: who, why and how?. BMC Pediatrics, 14 279: 1-15. doi:10.1186/1471-2431-14-279     24 Cited 33 times in Scopus33 1
King, Daniel A., Jones, Wendy D., Crow, Yanick J., Dominiczak, Anna F., Foster, Nicola A., Gaunt, Tom R., Harris, Jade, Hellens, Stephen W., Homfray, Tessa, Innes, Josie, Jones, Elizabeth A., Joss, Shelagh, Kulkarni, Abhijit, Mansour, Sahar, Andrew D. Morris, D. Morris, Parker, Michael J., Porteous, David J., Shihab, Hashem A., Smith, Blair H., Tatton-Brown, Katrina, Tolmie, John L., Trzaskowski, Maciej, Vasudevan, Pradeep C., Wakeling, Emma, Wright, Michael, Plomin, Robert, Timpson, Nicholas J. and Hurles, Matthew E. (2015) Mosaic structural variation in children with developmental disorders. Human Molecular Genetics, 24 10: 2733-2745. doi:10.1093/hmg/ddv033     18 Cited 21 times in Scopus21 9
Bailey, Emily J., Maclennan, Carolyn, Morris, Peter S., Kruske, Sue G., Brown, Ngiare and Chang, Anne B. (2009) Risks of severity and readmission of Indigenous and non-Indigenous children hospitalised for bronchiolitis. Journal of Paediatrics and Child Health, 45 10: 593-597. doi:10.1111/j.1440-1754.2009.01571.x     15 Cited 15 times in Scopus15 0
Azizan, Elena A.B., Murthy, Meena, Stowasser, Michael, Gordon, Richard, Kowalski, Bartosz, Xu, Shengxin, Brown, Morris J. and O'Shaughnessy, Kevin M. (2012) Somatic mutations affecting the selectivity filter of KCNJ5 are frequent in 2 large unselected collections of adrenal aldosteronomas. Hypertension, 59 3: 587-591. doi:10.1161/HYPERTENSIONAHA.111.186239     89 Cited 101 times in Scopus101 1
Azizan, Elena A., Murthy, Meena, Stowasser, Michael, Gordon, Richard D., Kowalski, Bartosz, Xu, Shengxin, Brown, Morris J. and O'Shaughnessy, Kevin M. (2012). Somatic mutations affecting the selectivity filter of KCNJ5 are frequent in aldosterone-producing adenomas and associated with lack of aldosterone response to upright posture. In: Abstracts for the Aldosterone & Salt: Heart and Kidney International Society of Hypertension 2012 Satellite Symposium. Satellite Symposium of the International-Society-of-Hypertension on Aldosterone and Salt - Heart and Kidney, Palm Cove, QLD, Australia, (1318-1318). 5-7 October 2012. doi:10.1038/ajh.2012.134     0 0