Biomarkers for Type 2 Diabetes and Impaired Fasting Glucose Using a Nontargeted Metabolomics Approach von MENNI, Cristina, FAUMAN, Eric, WEI YUAN, MILBURN, Mike, PALMER, Colin N. A, FRAYLING, Timothy M, TRIMMER, Jeff, BELL, Jordana T, GIEGER, Christian, MOHNEY, Rob P, BROSNAN, Mary Julia, SUHRE, Karsten, ERTE, Idil, SORANZO, Nicole, SPECTOR, Tim D, PERRY, John R. B, KASTENMÜLLER, Gabi, SHIN, So-Youn, PETERSEN, Ann-Kristin, HYDE, Craig, PSATHA, Maria, WARD, Kirsten J

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Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk von Lango, Hana, Palmer, Colin N A, Morris, Andrew D, Zeggini, Eleftheria, Hattersley, Andrew T, McCarthy, Mark I, Frayling, Timothy M, Weedon, Michael N

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Gene-environment interaction in the onset of eczema in infancy: filaggrin loss-of-function mutations enhanced by neonatal cat exposure von Bisgaard, Hans, Simpson, Angela, Palmer, Colin N A, Bønnelykke, Klaus, McLean, Irwin, Mukhopadhyay, Somnath, Pipper, Christian B, Halkjaer, Liselotte B, Lipworth, Brian, Hankinson, Jenny, Woodcock, Ashley, Custovic, Adnan

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Reduced-Function SLC22A1 Polymorphisms Encoding Organic Cation Transporter 1 and Glycemic Response to Metformin: A GoDARTS Study von Zhou, Kaixin, Donnelly, Louise A, Kimber, Charlotte H, Donnan, Peter T, Doney, Alex S F, Leese, Graham, Hattersley, Andrew T, McCarthy, Mark I, Morris, Andrew D, Palmer, Colin N A, Pearson, Ewan R

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Adiposity-Related Heterogeneity in Patterns of Type 2 Diabetes Susceptibility Observed in Genome-Wide Association Data von TIMPSON, Nicholas J, LINDGREN, Cecilia M, PALMER, Colin N. A, MORRIS, Andrew D, HATTERSLEY, Andrew T, ZEGGINI, Eleftheria, FRAYLING, Timothy M, MCCARTHY, Mark I, WEEDON, Michael N, RANDALL, Joshua, OUWEHAND, Willem H, STRACHAN, David P, RAYNER, N. William, WALKER, Mark, HITMAN, Graham A, DONEY, Alex S. F

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An Obesity-Associated FTO Gene Variant and Increased Energy Intake in Children von Cecil, Joanne E, Tavendale, Roger, Watt, Peter, Hetherington, Marion M, Palmer, Colin N.A

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Matrix metalloproteinase-12 is a therapeutic target for asthma in children and young adults von Mukhopadhyay, Somnath, FRCPCH, MD, PhD, Sypek, Joseph, PhD, Tavendale, Roger, PhD, Gartner, Ulrike, PhD, Winter, John, FRCP, Li, Wei, PhD, Page, Karen, PhD, Fleming, Margaret, PhD, Brady, Jeff, PhD, O'Toole, Margot, PhD, Macgregor, Donald F., FRCPCH, Goldman, Samuel, PhD, Tam, Steve, PhD, Abraham, William, MD, Williams, Cara, PhD, Miller, Douglas K., PhD, Palmer, Colin N.A., PhD

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Neutrophil extracellular traps are associated with disease severity and microbiota diversity in patients with chronic obstructive pulmonary disease von Dicker, Alison J., PhD, Crichton, Megan L., MFM, Pumphrey, Eleanor G, Cassidy, Andrew J., PhD, Suarez-Cuartin, Guillermo, MD, Sibila, Oriol, MD, Furrie, Elizabeth, PhD, Fong, Christopher J, Ibrahim, Wasyla, Brady, Gill, BSc, Einarsson, Gisli G., PhD, Elborn, J. Stuart, MD, Schembri, Stuart, MD, Marshall, Sara E., PhD, Palmer, Colin N.A., PhD, Chalmers, James D., PhD

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Systematic review and meta-analysis of genetic risk factors for neuropathic pain von Veluchamy, Abirami, Hébert, Harry L., Meng, Weihua, Palmer, Colin N.A., Smith, Blair H.

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Biomarkers of rapid chronic kidney disease progression in type 2 diabetes von Looker, Helen C., Colombo, Marco, Hess, Sibylle, Brosnan, Mary J., Farran, Bassam, Dalton, R. Neil, Wong, Max C., Turner, Charles, Palmer, Colin N.A., Nogoceke, Everson, Groop, Leif, Salomaa, Veikko, Dunger, David B., Agakov, Felix, McKeigue, Paul M., Colhoun, Helen M.

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Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT von Soto-Pedre, Enrique, Newey, Paul J, Srinivasan, Sundararajan, Siddiqui, Moneeza K, Palmer, Colin N A, Leese, Graham P

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Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity von Frayling, Timothy M, Timpson, Nicholas J, Weedon, Michael N, Zeggini, Eleftheria, Freathy, Rachel M, Lindgren, Cecilia M, Perry, John R.B, Elliott, Katherine S, Lango, Hana, Rayner, Nigel W, Shields, Beverley, Harries, Lorna W, Barrett, Jeffrey C, Ellard, Sian, Groves, Christopher J, Knight, Bridget, Patch, Ann-Marie, Ness, Andrew R, Ebrahim, Shah, Lawlor, Debbie A, Ring, Susan M, Ben-Shlomo, Yoav, Jarvelin, Marjo-Riitta, Sovio, Ulla, Bennett, Amanda J, Melzer, David, Ferrucci, Luigi, Loos, Ruth J.F, Barroso, Inês, Wareham, Nicholas J, Karpe, Fredrik, Owen, Katharine R, Cardon, Lon R, Walker, Mark, Hitman, Graham A, Palmer, Colin N.A, Doney, Alex S.F, Morris, Andrew D, Smith, George Davey, Hattersley, Andrew T, McCarthy, Mark I

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Elevated circulating amyloid concentrations in obesity and diabetes promote vascular dysfunction von Meakin, Paul J., Coull, Bethany M., Tuharska, Zofia, McCaffery, Christopher, Akoumianakis, Ioannis, Antoniades, Charalambos, Brown, Jane, Griffin, Kathryn J., Platt, Fiona, Ozber, Claire H., Yuldasheva, Nadira Y., Makava, Natallia, Skromna, Anna, Prescott, Alan, McNeilly, Alison D., Siddiqui, Moneeza, Palmer, Colin N. A., Khan, Faisel, Ashford, Michael L. J.

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Filaggrin variants confer susceptibility to asthma von McLean, W. H. Irwin, PhD, DSc, Palmer, Colin N.A., PhD, Henderson, John, MD, Kabesch, Michael, MD, Weidinger, Stephan, MD, Irvine, Alan D., MD

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Childhood obesity in relation to poor asthma control and exacerbation: a meta-analysis von Ahmadizar, Fariba, Vijverberg, Susanne J H, Arets, Hubertus G M, de Boer, Anthonius, Lang, Jason E, Kattan, Meyer, Palmer, Colin N A, Mukhopadhyay, Somnath, Turner, Steve, Maitland-van der Zee, Anke H

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Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy von Brown, Sara J., MD, Asai, Yuka, MD, Cordell, Heather J., DPhil, Campbell, Linda E., MSc, Zhao, Yiwei, MD, PhD, Liao, Haihui, MD, PhD, Northstone, Kate, PhD, Henderson, John, MD, Alizadehfar, Reza, MD, Ben-Shoshan, Moshe, MD, Morgan, Kenneth, PhD, Roberts, Graham, DM, Masthoff, Laury J.N., MD, Pasmans, Suzanne G.M.A., MD, PhD, van den Akker, Peter C., MD, Wijmenga, Cisca, PhD, Hourihane, Jonathan O’B., PhD, Palmer, Colin N.A., PhD, Lack, Gideon, PhD, Clarke, Ann, MD, MSc, Hull, Peter R., MD, PhD, Irvine, Alan D., MD, McLean, W. H. Irwin, PhD, DSc

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SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout von Wright, Alan F, Vitart, Veronique, Rudan, Igor, Hayward, Caroline, Gray, Nicola K, Floyd, James, Palmer, Colin NA, Knott, Sara A, Kolcic, Ivana, Polasek, Ozren, Graessler, Juergen, Wilson, James F, Marinaki, Anthony, Riches, Philip L, Shu, Xinhua, Janicijevic, Branka, Smolej-Narancic, Nina, Gorgoni, Barbara, Morgan, Joanne, Campbell, Susan, Biloglav, Zrinka, Barac-Lauc, Lovorka, Pericic, Marijana, Klaric, Irena Martinovic, Zgaga, Lina, Skaric-Juric, Tatjana, Wild, Sarah H, Richardson, William A, Hohenstein, Peter, Kimber, Charley H, Tenesa, Albert, Donnelly, Louise A, Fairbanks, Lynette D, Aringer, Martin, McKeigue, Paul M, Ralston, Stuart H, Morris, Andrew D, Rudan, Pavao, Hastie, Nicholas D, Campbell, Harry

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The burden of disease associated with filaggrin mutations: A population-based, longitudinal birth cohort study von Henderson, John, MD, Northstone, Kate, MSc, Lee, Simon P., MSc, Liao, Haihui, MD, Zhao, Yiwei, MD, Pembrey, Marcus, MD, Mukhopadhyay, Somnath, MD, Smith, George Davey, MD, DSc, Palmer, Colin N.A., PhD, McLean, W. H. Irwin, PhD, DSc, Irvine, Alan D., MD

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Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects von Saunders, Sean P., PhD, Goh, Christabelle S.M., BSc, Brown, Sara J., MD, Palmer, Colin N.A., PhD, Porter, Rebecca M., PhD, Cole, Christian, PhD, Campbell, Linda E., MSc, Gierlinski, Marek, PhD, Barton, Geoffrey J., PhD, Schneider, Georg, PhD, Balmain, Allan, PhD, Prescott, Alan R., PhD, Weidinger, Stephan, MD, PhD, Baurecht, Hansjörg, PhD, Kabesch, Michael, MD, Gieger, Christian, PhD, Lee, Young-Ae, MD, Tavendale, Roger, PhD, Mukhopadhyay, Somnath, MD, Turner, Stephen W., MD, Madhok, Vishnu B., MD, Sullivan, Frank M., MD, Relton, Caroline, PhD, Burn, John, MD, Meggitt, Simon, MD, Smith, Catherine H., MD, Allen, Michael A., PhD, Barker, Jonathan N.W. N., MD, Reynolds, Nick J., MD, Cordell, Heather J., DPhil, Irvine, Alan D., MD, McLean, W.H. Irwin, DSc, Sandilands, Aileen, PhD, Fallon, Padraic G., PhD

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Clinical and Genetic Determinants of Progression of Type 2 Diabetes: A DIRECT Study von KAIXIN ZHOU, DONNELLY, Louise A, MORRIS, Andrew D, FRANKS, Paul W, JENNISON, Chris, PALMER, Colin N. A, PEARSON, Ewan R

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