edoc

Items where Author is "Evans, David M."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type | Refereed
Jump to: 2017 | 2015 | 2014 | 2011
Number of items: 6.

2017

Wain, Louise V. and Shrine, Nick and Artigas, María Soler and Erzurumluoglu, A. Mesut and Noyvert, Boris and Bossini-Castillo, Lara and Obeidat, Ma'en and Henry, Amanda P. and Portelli, Michael A. and Hall, Robert J. and Billington, Charlotte K. and Rimington, Tracy L. and Fenech, Anthony G. and John, Catherine and Blake, Tineka and Jackson, Victoria E. and Allen, Richard J. and Prins, Bram P. and Understanding Society Scientific Group, and Campbell, Archie and Porteous, David J. and Jarvelin, Marjo-Riitta and Wielscher, Matthias and James, Alan L. and Hui, Jennie and Wareham, Nicholas J. and Zhao, Jing Hua and Wilson, James F. and Joshi, Peter K. and Stubbe, Beate and Rawal, Rajesh and Schulz, Holger and Imboden, Medea and Probst-Hensch, Nicole M. and Karrasch, Stefan and Gieger, Christian and Deary, Ian J. and Harris, Sarah E. and Marten, Jonathan and Rudan, Igor and Enroth, Stefan and Gyllensten, Ulf and Kerr, Shona M. and Polasek, Ozren and Kähönen, Mika and Surakka, Ida and Vitart, Veronique and Hayward, Caroline and Lehtimäki, Terho and Raitakari, Olli T. and Evans, David M. and Henderson, A. John and Pennell, Craig E. and Wang, Carol A. and Sly, Peter D. and Wan, Emily S. and Busch, Robert and Hobbs, Brian D. and Litonjua, Augusto A. and Sparrow, David W. and Gulsvik, Amund and Bakke, Per S. and Crapo, James D. and Beaty, Terri H. and Hansel, Nadia N. and Mathias, Rasika A. and Ruczinski, Ingo and Barnes, Kathleen C. and Bossé, Yohan and Joubert, Philippe and van den Berge, Maarten and Brandsma, Corry-Anke and Paré, Peter D. and Sin, Don D. and Nickle, David C. and Hao, Ke and Gottesman, Omri and Dewey, Frederick E. and Bruse, Shannon E. and Carey, David J. and Kirchner, H. Lester and Jonsson, Stefan and Thorleifsson, Gudmar and Jonsdottir, Ingileif and Gislason, Thorarinn and Stefansson, Kari and Schurmann, Claudia and Nadkarni, Girish and Bottinger, Erwin P. and Loos, Ruth J. F. and Walters, Robin G. and Chen, Zhengming and Millwood, Iona Y. and Vaucher, Julien and Kurmi, Om P. and Li, Liming and Hansell, Anna L. and Brightling, Chris and Zeggini, Eleftheria and Cho, Michael H. and Silverman, Edwin K. and Sayers, Ian and Trynka, Gosia and Morris, Andrew P. and Strachan, David P. and Hall, Ian P. and Tobin, Martin D.. (2017) Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nature genetics, 49 (3). pp. 416-425.

2015

Gharib, Sina A. and Loth, Daan W. and Soler Artigas, María and Birkland, Timothy P. and Wilk, Jemma B. and Wain, Louise V. and Brody, Jennifer A. and Obeidat, Ma'en and Hancock, Dana B. and Tang, Wenbo and Rawal, Rajesh and Boezen, H. Marike and Imboden, Medea and Huffman, Jennifer E. and Lahousse, Lies and Alves, Alexessander C. and Manichaikul, Ani and Hui, Jennie and Morrison, Alanna C. and Ramasamy, Adaikalavan and Smith, Albert Vernon and Gudnason, Vilmundur and Surakka, Ida and Vitart, Veronique and Evans, David M. and Strachan, David P. and Deary, Ian J. and Hofman, Albert and Gläser, Sven and Wilson, James F. and North, Kari E. and Zhao, Jing Hua and Heckbert, Susan R. and Jarvis, Deborah L. and Probst-Hensch, Nicole and Schulz, Holger and Barr, R. Graham and Jarvelin, Marjo-Riitta and O'Connor, George T. and Kähönen, Mika and Cassano, Patricia A. and Hysi, Pirro G. and Dupuis, Josée and Hayward, Caroline and Psaty, Bruce M. and Hall, Ian P. and Parks, William C. and Tobin, Martin D. and London, Stephanie J.. (2015) Integrative pathway genomics of lung function and airflow obstruction. Human molecular genetics, 24 (23). pp. 6836-6848.

Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjörg and Hotze, Melanie and Strachan, David P. and Curtin, John A. and Bønnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P. and den Dekker, Herman T. and Ferreira, Manuel A. and Altmaier, Elisabeth and Sleiman, Patrick M. and Xiao, Feng Li and Gonzalez, Juan R. and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Cheng Jian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M. and Venturini, Cristina and Pennell, Craig E. and Barton, Sheila J. and Levin, Arbet M. and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Møller, Eskil and Lockett, Gabrielle A. and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A. and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L. and Henderson, A. John and Kemp, John P. and Zheng, Jie and Smith, George Davey and Rüschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O. and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Rodríguez, Elke and Peters, Annette and Franke, Andre and Lieb, Wolfgang and Novak, Natalija and Fölster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L. and Grarup, Niels and de Jongste, Johan C. and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V. and Pasmans, Suzanne G. M. A. and Elbert, Niels J. and Uitterlinden, André G. and Marks, Guy B. and Thompson, Philip J. and Matheson, Melanie C. and Robertson, Colin F. and Australian Asthma Genetics, Consortium (AAGC) and Ried, Janina S. and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong Yin and Sun, Liang Dan and McAleer, Maeve A. and O'Regan, Grainne M. and Fahy, Caoimhe M. R. and Campbell, Linda E. and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S. and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M. and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T. and Thiering, Elisabeth and Pahukasahasram, Badri and Yang, James J. and Imboden, Madea and Huntsman, Scott and Vilor-Tejedor, Natàlia and Relton, Caroline L. and Myhre, Ronny and Nystad, Wenche and Custovic, Adnan and Weiss, Scott T. and Meyers, Deborah A. and Soderhall, Cilla and Melén, Erik and Ober, Carole and Raby, Benjamin A. and Simpson, Angela and Jacobsson, Bo and Holloway, John W. and Bisgaard, Hans and Sunyer, Jordi and Probst-Hensch, Nicole M. and Williams, L. Keoki and Godfrey, Keith M. and Wang, Carol A. and Boomsma, Dorret I. and Melbye, Mads and Koppelman, Gerard H. and Jarvis, Deborah and McLean, W. H. Irwin and Irvine, Alan D. and Zhang, Xue Jun and Hakonarson, Hakon and Gieger, Christian and Burchard, Esteban G. and Martin, Nicholas G. and Duijts, Liesbeth and Linneberg, Allan and Jarvelin, Marjo-Riitta and Noethen, Markus M. and Lau, Susanne and Hübner, Norbert and Lee, Young-Ae and Tamari, Mayum and Hinds, David A. and Glass, Daniel and Brown, Sara J. and Heinrich, Joachim and Evans, David M. and Weidinger, Stephan and EArly Genetics, and Lifecourse Epidemiology (EAGLE) Eczema Consortium, . (2015) Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, 47 (12). pp. 1449-1456.

Artigas, María Soler and Wain, Louise V. and Miller, Suzanne and Kheirallah, Abdul Kader and Huffman, Jennifer E. and Ntalla, Ioanna and Shrine, Nick and Obeidat, Ma'en and Trochet, Holly and McArdle, Wendy L. and Alves, Alexessander Couto and Hui, Jennie and Zhao, Jing Hua and Joshi, Peter K. and Teumer, Alexander and Albrecht, Eva and Imboden, Medea and Rawal, Rajesh and Lopez, Lorna M. and Marten, Jonathan and Enroth, Stefan and Surakka, Ida and Polasek, Ozren and Lyytikäinen, Leo-Pekka and Granell, Raquel and Hysi, Pirro G. and Flexeder, Claudia and Mahajan, Anubha and Beilby, John and Bossé, Yohan and Brandsma, Corry-Anke and Campbell, Harry and Gieger, Christian and Gläser, Sven and González, Juan R. and Grallert, Harald and Hammond, Chris J. and Harris, Sarah E. and Hartikainen, Anna-Liisa and Heliövaara, Markku and Henderson, John and Hocking, Lynne and Horikoshi, Momoko and Hutri-Kähönen, Nina and Ingelsson, Erik and Johansson, Åsa and Kemp, John P. and Kolcic, Ivana and Kumar, Ashish and Lind, Lars and Melén, Erik and Musk, Arthur W. and Navarro, Pau and Nickle, David C. and Padmanabhan, Sandosh and Raitakari, Olli T. and Ried, Janina S. and Ripatti, Samuli and Schulz, Holger and Scott, Robert A. and Sin, Don D. and Starr, John M. and BiLeve, U. K. and Viñuela, Ana and Völzke, Henry and Wild, Sarah H. and Wright, Alan F. and Zemunik, Tatijana and Jarvis, Deborah L. and Spector, Tim D. and Evans, David M. and Lehtimäki, Terho and Vitart, Veronique and Kähönen, Mika and Gyllensten, Ulf and Rudan, Igor and Deary, Ian J. and Karrasch, Stefan and Probst-Hensch, Nicole M. and Heinrich, Joachim and Stubbe, Beate and Wilson, James F. and Wareham, Nicholas J. and James, Alan L. and Morris, Andrew P. and Jarvelin, Marjo-Riitta and Hayward, Caroline and Sayers, Ian and Strachan, David P. and Hall, Ian P. and Tobin, Martin D.. (2015) Sixteen new lung function signals identified through 1000 genomes project reference panel imputation. Nature communications, 6. p. 8658.

2014

Hoggart, Clive J. and Venturini, Giulia and Mangino, Massimo and Gomez, Felicia and Ascari, Giulia and Zhao, Jing Hua and Teumer, Alexander and Winkler, Thomas W. and Tšernikova, Natalia and Luan, Jian'an and Mihailov, Evelin and Ehret, Georg B. and Zhang, Weihua and Lamparter, David and Esko, Tõnu and Macé, Aurelien and Rüeger, Sina and Bochud, Pierre-Yves and Barcella, Matteo and Dauvilliers, Yves and Benyamin, Beben and Evans, David M. and Hayward, Caroline and Lopez, Mary F. and Franke, Lude and Russo, Alessia and Heid, Iris M. and Salvi, Erika and Vendantam, Sailaja and Arking, Dan E. and Boerwinkle, Eric and Chambers, John C. and Fiorito, Giovanni and Grallert, Harald and Guarrera, Simonetta and Homuth, Georg and Huffman, Jennifer E. and Porteous, David and Generation Scotland Consortium, and LifeLines Cohort study, and Giant Consortium, and Moradpour, Darius and Iranzo, Alex and Hebebrand, Johannes and Kemp, John P. and Lammers, Gert J. and Aubert, Vincent and Heim, Markus H. and Martin, Nicholas G. and Montgomery, Grant W. and Peraita-Adrados, Rosa and Santamaria, Joan and Negro, Francesco and Schmidt, Carsten O. and Scott, Robert A. and Spector, Tim D. and Strauch, Konstantin and Völzke, Henry and Wareham, Nicholas J. and Yuan, Wei and Bell, Jordana T. and Chakravarti, Aravinda and Kooner, Jaspal S. and Peters, Annette and Matullo, Giuseppe and Wallaschofski, Henri and Whitfield, John B. and Paccaud, Fred and Vollenweider, Peter and Bergmann, Sven and Beckmann, Jacques S. and Tafti, Mehdi and Hastie, Nicholas D. and Cusi, Daniele and Bochud, Murielle and Frayling, Timothy M. and Metspalu, Andres and Jarvelin, Marjo-Riitta and Scherag, André and Smith, George Davey and Borecki, Ingrid B. and Rousson, Valentin and Hirschhorn, Joel N. and Rivolta, Carlo and Loos, Ruth J. F. and Kutalik, Zoltán. (2014) Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index. PLoS Genetics, 10 (7). e1004508.

2011

Rizzi, Thais S. and Arias-Vasquez, Alejandro and Rommelse, Nanda and Kuntsi, Jonna and Anney, Richard and Asherson, Philip and Buitelaar, Jan and Banaschewski, Tobias and Ebstein, Richard and Ruano, Dina and Van der Sluis, Sophie and Markunas, Christina A. and Garrett, Melanie E. and Ashley-Koch, Allison E. and Kollins, Scott H. and Anastopoulos, Arthur D. and Hansell, Narelle K. and Wright, Margaret J. and Montgomery, Grant W. and Martin, Nicholas G. and Harris, Sarah E. and Davies, Gail and Tenesa, Albert and Porteous, David J. and Starr, John M. and Deary, Ian J. and St Pourcain, Beate and Davey Smith, George and Timpson, Nicholas J. and Evans, David M. and Gill, Michael and Miranda, Ana and Mulas, Fernando and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Sonuga-Barke, Edmund and Steinhausen, Hans Christoph and Taylor, Eric and Faraone, Stephen V. and Franke, Barbara and Posthuma, Danielle. (2011) The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background : evidence from a large collaborative study totaling 4,963 subjects. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 156, H. 2. pp. 145-157.

This list was generated on Fri Mar 29 13:00:51 2024 CET.