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Items where Author is "Porteous, David J."

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Number of items: 4.

2019

Shrine, Nick and Guyatt, Anna L. and Erzurumluoglu, A. Mesut and Jackson, Victoria E. and Hobbs, Brian D. and Melbourne, Carl A. and Batini, Chiara and Fawcett, Katherine A. and Song, Kijoung and Sakornsakolpat, Phuwanat and Li, Xingnan and Boxall, Ruth and Reeve, Nicola F. and Obeidat, Ma'en and Zhao, Jing Hua and Wielscher, Matthias and Understanding Society Scientific Group, and Weiss, Stefan and Kentistou, Katherine A. and Cook, James P. and Sun, Benjamin B. and Zhou, Jian and Hui, Jennie and Karrasch, Stefan and Imboden, Medea and Harris, Sarah E. and Marten, Jonathan and Enroth, Stefan and Kerr, Shona M. and Surakka, Ida and Vitart, Veronique and Lehtimäki, Terho and Allen, Richard J. and Bakke, Per S. and Beaty, Terri H. and Bleecker, Eugene R. and Bossé, Yohan and Brandsma, Corry-Anke and Chen, Zhengming and Crapo, James D. and Danesh, John and DeMeo, Dawn L. and Dudbridge, Frank and Ewert, Ralf and Gieger, Christian and Gulsvik, Amund and Hansell, Anna L. and Hao, Ke and Hoffman, Joshua D. and Hokanson, John E. and Homuth, Georg and Joshi, Peter K. and Joubert, Philippe and Langenberg, Claudia and Li, Xuan and Li, Liming and Lin, Kuang and Lind, Lars and Locantore, Nicholas and Luan, Jian'an and Mahajan, Anubha and Maranville, Joseph C. and Murray, Alison and Nickle, David C. and Packer, Richard and Parker, Margaret M. and Paynton, Megan L. and Porteous, David J. and Prokopenko, Dmitry and Qiao, Dandi and Rawal, Rajesh and Runz, Heiko and Sayers, Ian and Sin, Don D. and Smith, Blair H. and Soler Artigas, María and Sparrow, David and Tal-Singer, Ruth and Timmers, Paul R. H. J. and Van den Berge, Maarten and Whittaker, John C. and Woodruff, Prescott G. and Yerges-Armstrong, Laura M. and Troyanskaya, Olga G. and Raitakari, Olli T. and Kähönen, Mika and Polašek, Ozren and Gyllensten, Ulf and Rudan, Igor and Deary, Ian J. and Probst-Hensch, Nicole M. and Schulz, Holger and James, Alan L. and Wilson, James F. and Stubbe, Beate and Zeggini, Eleftheria and Jarvelin, Marjo-Riitta and Wareham, Nick and Silverman, Edwin K. and Hayward, Caroline and Morris, Andrew P. and Butterworth, Adam S. and Scott, Robert A. and Walters, Robin G. and Meyers, Deborah A. and Cho, Michael H. and Strachan, David P. and Hall, Ian P. and Tobin, Martin D. and Wain, Louise V.. (2019) New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nature genetics, 51 (3). pp. 481-493.

2018

Jackson, Victoria E. and Latourelle, Jeanne C. and Wain, Louise V. and Smith, Albert V. and Grove, Megan L. and Bartz, Traci M. and Obeidat, Ma'en and Province, Michael A. and Gao, Wei and Qaiser, Beenish and Porteous, David J. and Cassano, Patricia A. and Ahluwalia, Tarunveer S. and Grarup, Niels and Li, Jin and Altmaier, Elisabeth and Marten, Jonathan and Harris, Sarah E. and Manichaikul, Ani and Pottinger, Tess D. and Li-Gao, Ruifang and Lind-Thomsen, Allan and Mahajan, Anubha and Lahousse, Lies and Imboden, Medea and Teumer, Alexander and Prins, Bram and Lyytikäinen, Leo-Pekka and Eiriksdottir, Gudny and Franceschini, Nora and Sitlani, Colleen M. and Brody, Jennifer A. and Bossé, Yohan and Timens, Wim and Kraja, Aldi and Loukola, Anu and Tang, Wenbo and Liu, Yongmei and Bork-Jensen, Jette and Justesen, Johanne M. and Linneberg, Allan and Lange, Leslie A. and Rawal, Rajesh and Karrasch, Stefan and Huffman, Jennifer E. and Smith, Blair H. and Davies, Gail and Burkart, Kristin M. and Mychaleckyj, Josyf C. and Bonten, Tobias N. and Enroth, Stefan and Lind, Lars and Brusselle, Guy G. and Kumar, Ashish and Stubbe, Beate and Understanding Society Scientific Group, and Kähönen, Mika and Wyss, Annah B. and Psaty, Bruce M. and Heckbert, Susan R. and Hao, Ke and Rantanen, Taina and Kritchevsky, Stephen B. and Lohman, Kurt and Skaaby, Tea and Pisinger, Charlotta and Hansen, Torben and Schulz, Holger and Polasek, Ozren and Campbell, Archie and Starr, John M. and Rich, Stephen S. and Mook-Kanamori, Dennis O. and Johansson, Åsa and Ingelsson, Erik and Uitterlinden, André G. and Weiss, Stefan and Raitakari, Olli T. and Gudnason, Vilmundur and North, Kari E. and Gharib, Sina A. and Sin, Don D. and Taylor, Kent D. and O'Connor, George T. and Kaprio, Jaakko and Harris, Tamara B. and Pederson, Oluf and Vestergaard, Henrik and Wilson, James G. and Strauch, Konstantin and Hayward, Caroline and Kerr, Shona and Deary, Ian J. and Barr, R. Graham and de Mutsert, Renée and Gyllensten, Ulf and Morris, Andrew P. and Ikram, M. Arfan and Probst-Hensch, Nicole and Gläser, Sven and Zeggini, Eleftheria and Lehtimäki, Terho and Strachan, David P. and Dupuis, Josée and Morrison, Alanna C. and Hall, Ian P. and Tobin, Martin D. and London, Stephanie J.. (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome Open Research, 3. p. 4.

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.

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 Mon Nov 18 06:08:28 2019 CET.