Molecular and Population Analysis of Natural Selection on the Human Haptoglobin Duplication

nork Rodriguez, Santiago, Williams, Dylan M, Guthrie, Philip AI, McArdle, Wendy L, Smith, George Davey, Evans, David M, Gaunt, Tom R, Day, Ian NM
Argitaratua 2012

Longitudinal analysis of DNA methylation associated with birth weight and gestational age

nork Simpkin, Andrew J., Suderman, Matthew, Gaunt, Tom R., Lyttleton, Oliver, McArdle, Wendy L., Ring, Susan M., Tilling, Kate, Davey Smith, George, Relton, Caroline L.
Argitaratua izan da Hum Mol Genet (2015)

Differences in smoking associated DNA methylation patterns in South Asians and Europeans

nork Elliott, Hannah R, Tillin, Therese, McArdle, Wendy L, Ho, Karen, Duggirala, Aparna, Frayling, Tim M, Davey Smith, George, Hughes, Alun D, Chaturvedi, Nish, Relton, Caroline L
Argitaratua 2014

No Evidence of Association or Interaction between the IL4RA, IL4, and IL13 Genes in Type 1 Diabetes

nork Maier, Lisa M., Chapman, Juliet, Howson, Joanna M. M., Clayton, David G., Pask, Rebecca, Strachan, David P., McArdle, Wendy L., Twells, Rebecca C. J., Todd, John A.
Argitaratua 2005

The epigenetic clock and physical development during childhood and adolescence: longitudinal analysis from a UK birth cohort

nork Simpkin, Andrew J, Howe, Laura D, Tilling, Kate, Gaunt, Tom R, Lyttleton, Oliver, McArdle, Wendy L, Ring, Susan M, Horvath, Steve, Smith, George Davey, Relton, Caroline L
Argitaratua izan da Int J Epidemiol (2017)

DNA Methylation and BMI: Investigating Identified Methylation Sites at HIF3A in a Causal Framework

nork Richmond, Rebecca C., Sharp, Gemma C., Ward, Mary E., Fraser, Abigail, Lyttleton, Oliver, McArdle, Wendy L., Ring, Susan M., Gaunt, Tom R., Lawlor, Debbie A., Davey Smith, George, Relton, Caroline L.
Argitaratua izan da Diabetes (2016)

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

nork St Pourcain, Beate, Skuse, David H, Mandy, William P, Wang, Kai, Hakonarson, Hakon, Timpson, Nicholas J, Evans, David M, Kemp, John P, Ring, Susan M, McArdle, Wendy L, Golding, Jean, Smith, George Davey
Argitaratua 2014

Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC)

nork Richmond, Rebecca C., Simpkin, Andrew J., Woodward, Geoff, Gaunt, Tom R., Lyttleton, Oliver, McArdle, Wendy L., Ring, Susan M., Smith, Andrew D.A.C., Timpson, Nicholas J., Tilling, Kate, Davey Smith, George, Relton, Caroline L.
Argitaratua izan da Hum Mol Genet (2015)

Systematic identification of genetic influences on methylation across the human life course

nork Gaunt, Tom R., Shihab, Hashem A., Hemani, Gibran, Min, Josine L., Woodward, Geoff, Lyttleton, Oliver, Zheng, Jie, Duggirala, Aparna, McArdle, Wendy L., Ho, Karen, Ring, Susan M., Evans, David M., Davey Smith, George, Relton, Caroline L.
Argitaratua izan da Genome Biol (2016)

Common variation contributes to the genetic architecture of social communication traits

nork St Pourcain, Beate, Whitehouse, Andrew J O, Ang, Wei Q, Warrington, Nicole M, Glessner, Joseph T, Wang, Kai, Timpson, Nicholas J, Evans, David M, Kemp, John P, Ring, Susan M, McArdle, Wendy L, Golding, Jean, Hakonarson, Hakon, Pennell, Craig E, Smith, George Davey
Argitaratua 2013

Collapsed methylation quantitative trait loci analysis for low frequency and rare variants

nork Richardson, Tom G., Shihab, Hashem A., Hemani, Gibran, Zheng, Jie, Hannon, Eilis, Mill, Jonathan, Carnero-Montoro, Elena, Bell, Jordana T., Lyttleton, Oliver, McArdle, Wendy L., Ring, Susan M., Rodriguez, Santiago, Campbell, Colin, Smith, George Davey, Relton, Caroline L., Timpson, Nicholas J., Gaunt, Tom R.
Argitaratua izan da Hum Mol Genet (2016)

Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci

nork McCauley, Jacob L., Zuvich, Rebecca L., Beecham, Ashley H., De Jager, Philip L., Konidari, Ioanna, Whitehead, Patrice L., Aubin, Cristin, Ban, Maria, Pobywajlo, Susan, Briskin, Rebeccah, Romano, Susan, Aggarwal, Neelum T., Piccio, Laura, McArdle, Wendy L., Strachan, David P., Evans, Denis, Cross, Anne H., Cree, Bruce, Rioux, John D., Barcellos, Lisa F., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Hauser, Stephen L., Oksenberg, Jorge R., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L.
Argitaratua 2010

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

nork De Jager, Philip L, Jia, Xiaoming, Wang, Joanne, de Bakker, Paul I W, Ottoboni, Linda, Aggarwal, Neelum T, Piccio, Laura, Raychaudhuri, Soumya, Tran, Dong, Aubin, Cristin, Briskin, Rebeccah, Romano, Susan, Baranzini, Sergio E, McCauley, Jacob L, Pericak-Vance, Margaret A, Haines, Jonathan L, Gibson, Rachel A, Naeglin, Yvonne, Uitdehaag, Bernard, Matthews, Paul M, Kappos, Ludwig, Polman, Chris, McArdle, Wendy L, Strachan, David P, Evans, Denis, Cross, Anne H, Daly, Mark J, Compston, Alastair, Sawcer, Stephen J, Weiner, Howard L, Hauser, Stephen L, Hafler, David A, Oksenberg, Jorge R
Argitaratua 2009

Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size

nork Soranzo, Nicole, Rivadeneira, Fernando, Chinappen-Horsley, Usha, Malkina, Ida, Richards, J. Brent, Hammond, Naomi, Stolk, Lisette, Nica, Alexandra, Inouye, Michael, Hofman, Albert, Stephens, Jonathan, Wheeler, Eleanor, Arp, Pascal, Gwilliam, Rhian, Jhamai, P. Mila, Potter, Simon, Chaney, Amy, Ghori, Mohammed J. R., Ravindrarajah, Radhi, Ermakov, Sergey, Estrada, Karol, Pols, Huibert A. P., Williams, Frances M., McArdle, Wendy L., van Meurs, Joyce B., Loos, Ruth J. F., Dermitzakis, Emmanouil T., Ahmadi, Kourosh R., Hart, Deborah J., Ouwehand, Willem H., Wareham, Nicholas J., Barroso, Inês, Sandhu, Manjinder S., Strachan, David P., Livshits, Gregory, Spector, Timothy D., Uitterlinden, André G., Deloukas, Panos
Argitaratua 2009

Novel celiac disease genetic determinants related to the immune response

nork Hunt, Karen A, Zhernakova, Alexandra, Turner, Graham, Heap, Graham A.R., Franke, Lude, Bruinenberg, Marcel, Romanos, Jihane, Dinesen, Lotte C., Ryan, Anthony W, Panesar, Davinder, Gwilliam, Rhian, Takeuchi, Fumihiko, McLaren, William M, Holmes, Geoffrey KT, Howdle, Peter D, Walters, Julian RF, Sanders, David S, Playford, Raymond J, Trynka, Gosia, Mulder, Chris JJ, Mearin, M Luisa, Verbeek, Wieke HM, Trimble, Valerie, Stevens, Fiona M, O’Morain, Colm, Kennedy, Nicholas P, Kelleher, Dermot, Pennington, Daniel J, Strachan, David P, McArdle, Wendy L, Mein, Charles A, Wapenaar, Martin C, Deloukas, Panos, McGinnis, Ralph, McManus, Ross, Wijmenga, Cisca, van Heel, David A
Argitaratua 2008

Genome-wide association studies identify genetic loci for low von Willebrand factor levels

nork van Loon, Janine, Dehghan, Abbas, Weihong, Tang, Trompet, Stella, McArdle, Wendy L, Asselbergs, Folkert F W, Chen, Ming-Huei, Lopez, Lorna M, Huffman, Jennifer E, Leebeek, Frank W G, Basu, Saonli, Stott, David J, Rumley, Ann, Gansevoort, Ron T, Davies, Gail, Wilson, James J F, Witteman, Jacqueline C M, Cao, Xiting, de Craen, Anton J M, Bakker, Stephan J L, Psaty, Bruce M, Starr, John M, Hofman, Albert, Wouter Jukema, J, Deary, Ian J, Hayward, Caroline, van der Harst, Pim, Lowe, Gordon D O, Folsom, Aaron R, Strachan, David P, Smith, Nicolas, de Maat, Moniek P M, O'Donnell, Christopher
Argitaratua izan da Eur J Hum Genet (2016)

Genome-wide association studies identify genetic loci for low von Willebrand factor levels

nork van Loon, Janine, Dehghan, Abbas, Weihong, Tang, Trompet, Stella, McArdle, Wendy L, Asselbergs, Folkert W, Chen, Ming-Huei, Lopez, Lorna M, Huffman, Jennifer E, Leebeek, Frank W G, Basu, Saonli, Stott, David J, Rumley, Ann, Gansevoort, Ron T, Davies, Gail, Wilson, James J F, Witteman, Jacqueline C M, Cao, Xiting, de Craen, Anton J M, Bakker, Stephan J L, Psaty, Bruce M, Starr, John M, Hofman, Albert, Jukema, J Wouter, Deary, Ian J, Hayward, Caroline, van der Harst, Pim, Lowe, Gordon D O, Folsom, Aaron R, Strachan, David P, Smith, Nicolas, de Maat, Moniek P M, O'Donnell, Christopher
Argitaratua izan da Eur J Hum Genet (2016)

Association of Novel Genetic Loci with Circulating Fibrinogen Levels: A Genome-Wide Association Study in Six Population-Based Cohorts: Dehghan Genome-wide Association Study on Fibr...

nork Dehghan, Abbas, Yang, Qiong, Peters, Annette, Basu, Saonli, Bis, Joshua C., Rudnicka, Alicja R., Kavousi, Maryam, Chen, Ming-Huei, Baumert, Jens, Lowe, Gordon D. O, McKnight, Barbara, Tang, Weihong, de Maat, Moniek, Larson, Martin G., Eyhermendy, Susana, McArdle, Wendy L., Lumley, Thomas, Pankow, James S., Hofman, Albert, Massaro, Joseph M., Rivadeneira, Fernando, Kolz, Melanie, Taylor, Kent D., van Duijn, Cornelia M., Kathiresan, Sekar, Illig, Thomas, Aulchenko, Yurii S., Volcik, Kelly A., Johnson, Andrew D., Uitterlinden, Andre G., Tofler, Geoffrey H., Gieger, Christian, Psaty, Bruce M., Couper, David J., Boerwinkle, Eric, Koenig, Wolfgang, O'Donnell, Christopher J., Witteman, Jacqueline C., Strachan, David P., Smith, Nicholas L., Folsom, Aaron R.
Argitaratua 2009

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE Consortium

nork Smith, Nicholas L., Chen, Ming-Huei, Dehghan, Abbas, Strachan, David P., Basu, Saonli, Soranzo, Nicole, Hayward, Caroline, Rudan, Igor, Sabater-Lleal, Maria, Bis, Joshua C., de Maat, Moniek, Rumley, Ann, Kong, Xiaoxiao, Yang, Qiong, Williams, Frances M. K., Vitart, Veronique, Campbell, Harry, Mälarstig, Anders, Wiggins, Kerri L., Van Duijn, Cornelia, McArdle, Wendy L., Pankow, James S., Johnson, Andrew D., Silveira, Angela, McKnight, Barbara, Uitterlinden, Andre, Aleksic, Nena, Meigs, James B., Peters, Annette, Koenig, Wolfgang, Cushman, Mary, Kathiresan, Sekar, Rotter, Jerome I., Bovill, Edwin G., Hofman, Albert, Boerwinkle, Eric, Tofler, Geoffrey H., Peden, John F., Psaty, Bruce M., Leebeek, Frank, Folsom, Aaron R., Larson, Martin G., Spector, Timothy D., Wright, Alan F., Wilson, James F., Hamsten, Anders, Lumley, Thomas, Witteman, Jacqueline C., Tang, Weihong, O'Donnell, Christopher J.
Argitaratua 2010

Association Between Variants of PRDM1 and NDP52 and Crohn’s Disease, Based on Exome Sequencing and Functional Studies

nork Ellinghaus, David, Zhang, Hu, Zeissig, Sebastian, Lipinski, Simone, Till, Andreas, Jiang, Tao, Stade, Björn, Bromberg, Yana, Ellinghaus, Eva, Keller, Andreas, Rivas, Manuel A, Skieceviciene, Jurgita, Doncheva, Nadezhda T, Liu, Xiao, Liu, Qing, Jiang, Fuman, Forster, Michael, Mayr, Gabriele, Albrecht, Mario, Häsler, Robert, Boehm, Bernhard O, Goodall, Jane, Berzuini, Carlo R, Lee, James, Andersen, Vibeke, Vogel, Ulla, Kupcinskas, Limas, Kayser, Manfred, Krawczak, Michael, Nikolaus, Susanna, Weersma, Rinse K, Ponsioen, Cyriel Y, Sans, Miquel, Wijmenga, Cisca, Strachan, David P, McArdle, Wendy L, Vermeire, Séverine, Rutgeerts, Paul, Sanderson, Jeremy D, Mathew, Christopher G, Vatn, Morten H, Wang, Jun, Nöthen, Markus M, Duerr, Richard H, Büning, Carsten, Brand, Stephan, Glas, Jürgen, Winkelmann, Juliane, Illig, Thomas, Latiano, Anna, Annese, Vito, Halfvarson, Jonas, D’Amato, Mauro, Daly, Mark J, Nothnagel, Michael, Karlsen, Tom H, Subramani, Suresh, Rosenstiel, Philip, Schreiber, Stefan, Parkes, Miles, Franke, Andre
Argitaratua 2013