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Visscher, Peter M., Wray, Naomi R., Zhang, Qian, Sklar, Pamela, McCarthy, Mark I., Brown, Matthew A. and Yang, Jian (2017) 10 years of GWAS discovery: biology, function, and translation. American Journal of Human Genetics, 101 1: 5-22. doi:10.1016/j.ajhg.2017.06.005     157 Cited 171 times in Scopus171 247
Sovio, Ulla, Mook-Kanamori, Dennis O., Warrington, Nicole M., Lawrence, Robert, Briollais, Laurent, Palmer, Colin N. A., Cecil, Joanne, Sandling, Johanna K., Syvanen, Ann-Christin, Kaakinen, Marika, Beilin, Lawrie J., Millwood, Iona Y., Bennett, Amanda J., Laitinen, Jaana, Pouta, Anneli, Molitor, John, Smith, George Davey, Ben-Shlomo, Yoav, Jaddoe, Vincent W. V., Palmer, Lyle J., Pennell, Craig E., Cole, Tim J., McCarthy, Mark I., Jarvelin, Marjo-Riitta and Timpson, Nicholas J. (2011) Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: The complex nature of genetic association through growth and development. PLoS Genetics, 7 2: e1001307.1-e1001307.13. doi:10.1371/journal.pgen.1001307     99 Cited 105 times in Scopus105 9
Barker, Adam, Sharp, Stephen J., Timpson, Nicholas J., Bouatia-Naji, Nabila, Warrington, Nicole M., Kanoni, Stavroula, Beilin, Lawrence J., Brage, Soren, Deloukas, Panos, Evans, David M., Grontved, Anders, Hassanali, Neelam, Lawlor, Deborah A., Lecoeur, Cecile, Loos, Ruth J.F., Lye, Stephen J., McCarthy, Mark I., Mori, Trevor A., Ndiaye, Ndeye Coumba, Newnham, John P., Ntalla, Ioanna, Pennell, Craig E., St Pourcain, Beate, Prokopenko, Inga, Ring, Susan M., Sattar, Naveed, Visvikis-Siest, Sophie, Dedoussis, George V., Palmer, Lyle J., Froguel, Philippe, Smith, George Davey, Ekelund, Ulf, Wareham, Nicholas J. and Langenberg, Claudia (2011) Association of genetic loci with glucose levels in childhood and adolescence: A meta-analysis of over 6,000 children. Diabetes, 60 6: 1805-1812. doi:10.2337/db10-1575     58 Cited 60 times in Scopus60 3
Ikram, M. Arfan, Fornage, Myriam, Smith, Albert V., Seshadri, Sudha, Schmidt, Reinhold, Debette, Stephanie, Vrooman, Henri A., Sigurdsson, S., Ropele, Sigurdur, Taal, H. Rob, Mook-Kanamori, Dennis O., Coker, Laura H., Longstreth, W. T., Niessen, Wiro J., Destefano, Anita L., Beiser, Alexa, Zijdenbos, Alex P., Struchalin, Maksim, Jack,Clifford R., Rivadeneira, Fernando, Uitterlinden, Andre G., Knopman, David S., Hartikainen, Anna-Liisa, Pennell, Craig E., Thiering, Elisabeth, Steegers, Eric A. P., Hakonarson, Hakon, Heinrich, Joachim, Palmer, Lyle J., Jarvelin, Marjo-Riitta, Mccarthy, Mark I., Grant, Struan F. A., St Pourcain, Beate, Timpson, Nicholas J., Smith, George D., Sovio, Ulla, Nalls, Mike A., Au, Rhoda, Hofman, Albert, Gudnason, Haukur, Van Der Lugt, Aad, Harris, Tamara B., Meeks, William M., Vernooij, Meike W., Van Buchem, Mark A., Catellier, Diane, Jaddoe, Vincent W. V., Gudnason, Vilmundur, Windham, B. Gwen, Wolf, Philip A., Van Duijn, Cornelia M., Mosley, Thomas H., Schmidt, Helena, Launer, Lenore J., Breteler, Monique M. B., Decarli, Charles, Early Growth Genetics (EGG) Consortium, Coin, Lachlan, Middeldorp, Christel and . (2012) Common variants at 6q22 and 17q21 are associated with intracranial volume. Nature Genetics, 44 5: 539-544. doi:10.1038/ng.2245     69 Cited 69 times in Scopus69 33
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     218 Cited 259 times in Scopus259 2
Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012) Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 4: 369-375. doi:10.1038/ng.2213     309 Cited 311 times in Scopus311 22
Field, Yair, Boyle, Evan A., Telis, Natalie, Gao, Ziyue, Gaulton, Kyle J., Golan, David, Yengo, Loic, Rocheleau, Ghislain, Froguel, Philippe, McCarthy, Mark I. and Pritchard, Jonathan K. (2016) Detection of human adaptation during the past 2000 years. Science, 354 6313: 1-10. doi:10.1126/science.aag0776     52 Cited 57 times in Scopus57 230
Liu, Fan, Wollstein, Andreas, Hysi, Pirro G., Ankra-Badu, Georgina A., Spector, Timothy D., Park, Daniel, Zhu, Gu, Larsson, Mats, Duffy, David L., Montgomery, Grant W., Mackey, David A., Walsh, Susan, Lao, Oscar, Hofman, Albert, Rivadeneira, Fernando, Vingerling, Johannes R., Uitterlinden, Andrew G., Martin, Nicholas G., Hammond, Christopher J. and Kayser, Manfred (2010) Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genetics, 6 5: e1000934-1-e1000934-15. doi:10.1371/journal.pgen.1000934     85 Cited 99 times in Scopus99 28
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     13 Cited 13 times in Scopus13 15
Elliott, Katherine S., Zeggini, Eleftheria, McCarthy, Mark I., Gudmundsson, Julius, Sulem, Patrick, Stacey, Simon N., Thorlacius, Steinunn, Amundadottir, Laufey, Gronberg, Henrik, Xu, Jianfeng, Gaborieau, Valerie, Eeles, Rosalind A., Neal, David E., Donovan, Jenny L., Hamdy, Freddie C., Muir, Kenneth, Hwang, Shih-Jen, Spitz, Margaret R., Zanke, Brent, Carvajal-Carmona, Luis, Brown, Kevin M., Hayward, Nicholas K., Macgregor, Stuart, Tomlinson, Ian P. M., Lemire, Mathieu, Amos, Christopher I., Murabito, Joanne M., Isaacs, William B., Easton, Douglas F., Brennan, Paul, Barkardottir, Rosa B., Gudbjartsson, Daniel F., Rafnar, Thorunn, Hunter, David J., Chanock, Stephen J., Stefansson, Kari and Ioannidis, John P. A. (2010) Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies. PLoS One, 5 5: e10858-e10864. doi:10.1371/journal.pone.0010858   2 21 Cited 21 times in Scopus21 3
Visscher, Peter M., Brown, Matthew .A, McCarthy, Mark I. and Yang, Jian (2012) Five years of GWAS discovery. American Journal of Human Genetics, 90 1: 7-24. doi:10.1016/j.ajhg.2011.11.029     1033 Cited 1091 times in Scopus1091 117
Corbin, Laura J., Tan, Vanessa Y., Hughes, David A., Wade, Kaitlin H., Paul, Dirk S., Tansey, Katherine E., Butcher, Frances, Dudbridge, Frank, Howson, Joanna M., Jallow, Momodou W., John, Catherine, Kingston, Nathalie, Lindgren, Cecilia M., O'Donavan, Michael, O'Rahilly, Stephen, Owen, Michael J., Palmer, Colin N. A., Pearson, Ewan R., Scott, Robert A., van Heel, David A., Whittaker, John, Frayling, Tim, Tobin, Martin D., Wain, Louise V., Smith, George Davey, Evans, David M., Karpe, Fredrik, McCarthy, Mark I., Danesh, John, Franks, Paul W. and Timpson, Nicholas J. (2018) Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference. Nature Communications, 9 1: 711. doi:10.1038/s41467-018-03109-y     2 Cited 2 times in Scopus2 27
Ikram, M. Kamran, Sim, Xueling, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B., Cheung, Ning, Liew, Gerald, Mitchell, Paul, Uitterlinden, Andrew G., Rivadeneira, Fernando, Hofman, Albert, de Jong, Paulus T. V. M., van Kuijn, Cornelia M., Kao, Linda, Cheng, Ching-Yu, Smith, Albert Vernon, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Jonasson, Fridbert, Eiriksdottir, Gudny, Aspelund, Thor, Global BPgen Consortium, Harris, Tamara B., Launer, Lenore J., Taylor, Kent D., Li, Xiaohui, Iyengar, Sudha K., Xi, Quansheng, Sivakumaran, Theru A., Mackey, David A., MacGregor, Stuart, Martin, Nicholas G., Young, Terri L., Bis, Josh C., Wiggins, Kerri L., Heckbert, Susan R., Hammond, Christopher J., Andrew, Toby, Fahy, Samantha, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Islam, F. M. Amirul, Rotter, Jerome I., McAuley, Annie K., Boerwinkle, Eric, Tai, E. Shyong, Gudnason, Vilmundur, Siscovick, David S., Vingerling, Johannes R. and Wong, Tien Y. (2010) Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genetics, 6 10: 1-12. doi:10.1371/journal.pgen.1001184     76 Cited 81 times in Scopus81 4
Sovio, Ulla, Bennett, Amanda J., Millwood, Iona Y., Molitor, John, O'Reilly, Paul F., Timpson, Nicholas J., Kaakinen, Marika, Laitinen, Jaana, Haukka, Jari, Pillas, Demetris, Tzoulaki, Ioanna, Molitor, Jassy, Hoggart, Clive, Coin, Lachlan J. M., Whittaker, John, Pouta, Anneli, Hartikainen, Anna-Liisa, Freimer, Nelson B., Widen, Elisabeth, Peltonen, Leena, Elliott, Paul, Mccarthy, Mark I. and Jarvelin, Marjo-Riitta (2009) Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966. PLoS Genetics, 5 3: e1000409.1-e1000409.8. doi:10.1371/journal.pgen.1000409     78 Cited 88 times in Scopus88 12
Tyrrell, Jessica, Richmond, Rebecca C., Palmer, Tom M., Feenstra, Bjarke, Rangarajan, Janani, Metrustry, Sarah, Cavadino, Alana, Paternoster, Lavinia, Armstrong, Loren L., De Silva, N. Maneka G., Wood, Andrew R., Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Bradfield, Jonathan P., Kreiner-Moller, Eskil, Huikari, Ville, Painter, Jodie N., Hottenga, Jouke-Jan, Allard, Catherine, Berry, Diane J., Bouchard, Luigi, Das, Shikta, Evans, David M., Hakonarson, Hakon, Hayes, M. Geoffrey, Heikkinen, Jani, Hofman, Albert, Knight, Bridget, Lind, Penelope A., McCarthy, Mark I., McMahon, George, Medland, Sarah E., Melbye, Mads, Morris, Andrew P., Nodzenski, Michael, Reichetzeder, Christoph, Ring, Susan M., Sebert, Sylvain, Sengpiel, Verena, Sorensen, Thorkild I. A., Willemsen, Gonneke, de Geus, Eco J. C., Martin, Nicholas G., Spector, Tim D., Power, Christine, Jarvelin, Marjo-Riitta, Bisgaard, Hans, Grant, Struan F. A., Nohr, Ellen A., Jaddoe, Vincent W., Jacobsson, Bo, Murray, Jeffrey C., Hocher, Berthold, Hattersley, Andrew T., Scholtens, Denise M., Smith, George Davey, Hivert, Marie-France, Felix, Janine F., Hypponen, Elina, Lowe, William L., Jr., Frayling, Timothy M., Lawlor, Debbie A. and Freathy, Rachel M. (2016) Genetic evidence for causal relationships between maternal obesity-related traits and birth weight. Journal of the American Medical Association, 315 11: 1129-1140. doi:10.1001/jama.2016.1975     57 Cited 65 times in Scopus65 420
Elliott, Paul, Chambers, John C., Zhang, Weihua, Clarke, Robert, Hopewell, Jemma C., Peden, John F., Erdmann, Jeanette, Braund, Peter, Engert, James C., Bennett, Derrick, Coin, Lachlan, Ashby, Deborah, Tzoulaki, Ioanna, Brown, Ian J., Mt-Isa, Shahrul, McCarthy, Mark I., Peltonen, Leena, Freimer, Nelson B., Farrall, Martin, Ruokonen, Aimo, Hamsten, Anders, Lim, Noha, Froguel, Philippe, Waterworth, Dawn M., Vollenweider, Peter, Waeber, Gerard, Jarvelin, Marjo-Riitta, Mooser, Vincent, Scott, James, Hall, Alistair S., Schunkert, Heribert, Anand, Sonia S., Collins, Rory, Samani, Nilesh J., Watkins, Hugh and Kooner, Jaspal S. (2009) Genetic loci associated with C-reactive protein levels and risk of coronary heart disease. JAMA: The Journal of the American Medical Association, 302 1: 37-48. doi:10.1001/jama.2009.954     370 Cited 399 times in Scopus399 22
Speliotes, Elizabeth K., Yerges-Armstrong, Laura M., Wu, Jun, Hernaez, Ruben, Kim, Lauren J., Palmer, Cameron D., Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E., Launer, Lenore J., Nalls, Michael A., Clark, Jeanne M., Mitchell, Braxton D., Shuldiner, Alan R., Butler, Johannah L., Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M., O'Donnell, Christopher J., Sahani, Dushyant V., Salomaa, Veikko, Schadt, Eric E., Schwartz, Stephen M., Siscovick, David S., NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F., Carr, J. Jeffrey, Feitosa, Mary F., Harris, Tamara B., Fox, Caroline S., Smith, Albert V., Kao, W. H. Linda, Hirschhorn, Joel N., Borecki, Ingrid B., GOLD Consortium, Martin, Nicholas G., Montgomery, Grant W., Yang, Jian and Coin, Lachlan (2011) Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genetics, 7 3: e1001324.1-e1001324.14. doi:10.1371/journal.pgen.1001324     363 Cited 411 times in Scopus411 2
Sabatti, Chiara, Service, Susan K., Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G., Zaitlen, Noah A., Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I., Daly, Mark J., Jarvelin, Marjo-Riitta, Freimer, Nelson B. and Peltonen, Leena (2009) Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nature Genetics, 41 1: 35-46. doi:10.1038/ng.271     463 Cited 442 times in Scopus442 21
Meyre, David, Delplanque, Jerome, Chevre, Jean-Claude, Lecoeur, Cecile, Lobbens, Stephane, Gallina, Sophie, Durand, Emmanuelle, Vatin, Vincent, Degraeve, Franck, Proenca, Christine, Gaget, Stefan, Korner, Antje, Kovacs, Peter, Kiess, Wieland, Tichet, Jean, Marre, Michel, Hartikainen, Anna-Liisa, Horber, Fritz, Potoczna, Natascha, Hercberg, Serge, Levy-Marchal, Claire, Pattou, Francois, Heude, Barbara, Tauber, Maithe´, McCarthy, Mark I., Blakemore, Alexandra I. F., Montpetit, Alexandre, Polychronakos, Constantin, Weill, Jacques, Coin, Lachlan J. M., Asher, Julian, Elliott, Paul, Jarvelin, Marjo-Riitta, Visvikis-Siest, Sophie, Balkau, Beverley, Sladek, Rob, Balding, David, Walley, Andrew, Dina, Christian and Froguel, Philippe (2009) Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nature Genetics, 41 2: 157-159. doi:10.1038/ng.301     406 Cited 424 times in Scopus424 17
Pillas, Demetris, Hoggart, Clive J., Evans, David M., O'Reilly, Paul F., Sipila, Kirsi, Lahdesmaki, Raija, Millwood, Iona Y., Kaakinen, Marika., Netuveli, Gopalakrishnan, Blane, David, Charoen, Pimphen, Sovio, Ulla, Pouta, Anneli, Freimer, Nelson, Hartikainen, Anna-Lisa., Laitinen, Jaana, Vaara, Sarianna, Glaser, Beate, Crawford, Peter, Timpson, Nicholas J., Ring, Susan M., Deng, Guohong, Zhang, Weihua, McCarthy, Mark I., Deloukas, Panos, Peltonen, Leena, Elliott, Paul, Coin, Lachlan J. M., Smith, George D. and Jarvelin, Marjo-Riita (2010) Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. PLoS Genetics, 6 2: e1000856.1-e1000856.7. doi:10.1371/journal.pgen.1000856     40 Cited 43 times in Scopus43 17
Yang, Jian, Weedon, Michael N., Purcell, Shaun, Lettre, Guillaume, Estrada, Karol, Willer, Cristen J., Smith, Albert V., Ingelsson, Erik, O'Connell, Jeffrey R., Mangino, Massimo, Maegi, Reedik, Madden, Pamela A., Heath, Andrew C., Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Frayling, Timothy M., Hirschhorn, Joel N., McCarthy, Mark I., Goddard, Michael E. and Visscher, Peter M. (2011) Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics, 19 7: 807-812. doi:10.1038/ejhg.2011.39     177 Cited 185 times in Scopus185 2
Zhou, Kaixin, Donnelly, Lousie, Yang, Jian, Li, Miaoxin, Deshmukh, Harshal, Van Zuydam, Natalie, Ahlqvist, Emma, Spencer, Chris C., Groop, Leif, Morris, Andrew D., Colhoun, Helen M., Sham, Pak C., McCarthy, Mark I., Palmer, Colin N. A. and Pearson, Ewan R. (2014) Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis. The Lancet Diabetes and Endocrinology, 2 6: 481-487. doi:10.1016/S2213-8587(14)70050-6     42 Cited 48 times in Scopus48 10
Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O'Donovan, Michael C., Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S., Dale, Anders M., International Consortium for Blood Pressure GWAS and Mowry, Bryan (2013) Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. American Journal of Human Genetics, 92 2: 197-209. doi:10.1016/j.ajhg.2013.01.001     147 Cited 156 times in Scopus156 27
Travers, Mary E., Mackay, Deborah J. G., Dekker Nitert, Marloes, Morris, Andrew P., Lindgren, Cecilia M., Berry, Andrew, Johnson, Paul R., Hanley, Neil, Groop, Leif C., McCarthy, Mark I. and Gloyn, Anna L. (2013) Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets. Diabetes, 62 3: 987-992. doi:10.2337/db12-0819     54 Cited 58 times in Scopus58 2
Loh, Nellie Y., Neville, Matt J., Marinou, Kyriakoula, Hardcastle, Sarah A., Fielding, Barbara A., Duncan, Emma L., McCarthy, Mark I., Tobias, Jonathan H., Gregson, Celia L., Karpe, Fredrik and Christodoulides, Constantinos (2015) LRP5 regulates human body fat distribution by modulating adipose progenitor biology in a dose- and depot-specific fashion. Cell Metabolism, 21 2: 262-272. doi:10.1016/j.cmet.2015.01.009     26 Cited 24 times in Scopus24 7
Beaumont, Robin N., Warrington, Nicole M., Horikoshi, Momoko, Day, Felix R., Ong, Ken K., McCarthy, Mark I., Perry, John R. B., Freathy, Rachel M. and Evans, David M. (2018). Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic disease. In: 27th Annual Meeting of the International-Genetic-Epidemiology-Society (IGES), San Diego, Ca, United States, (688-688). Oct 14-16, 2018.     0
Kolz, Melanie, Johnson, Toby, Sanna, Serena, Teumer, Alexander, Vitart, Veronique, Perola, Markus, Mangino, Massimo, Albrecht, Eva, Wallace, Chris, Farrall, Martin, Johansson, Åsa, Nyholt, Dale R., Aulchenko, Yurii, Beckmann, Jacques S., Bergmann, Sven, Bochud, Murielle, Brown, Morris, Campbell, Harry, Connell, John, Dominiczak, Anna, Homuth, Georg, Lamina, Claudia, McCarthy, Mark I., Meitinger, Thomas, Mooser, Vincent, Munroe, Patricia, Nauck, Matthias, Peden, John, Prokisch, Holger, Salo, Perttu, Salomaa, Veikko, Samani, Nilesh J., Schlessinger, David, Uda, Manuela, Völker, Uwe, Waeber, Gérard, Waterworth, Dawn, Wang-Sattler, Rui, Wright, Alan F., Adamski, Jerzy, Whitfield, John B., Gyllensten, Ulf, Wilson, James F., Rudan, Igor, Pramstaller, Peter, Watkins, Hugh, Doering, Angela, Wichmann, H.-Erich, Spector, Tim D., Peltonen, Leena, Völzke, Henry, Nagaraja, Ramaiah, Vollenweider, Peter, Caulfield, Mark, Illig, Thomas and Gieger, Christian (2009) Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genetics, 5 6: . doi:10.1371/journal.pgen.1000504     Cited 395 times in Scopus395 7
Ng, Susanna S., Souza-Fonseca-Guimaraes, Fernando, Rivera, Fabian de Labastida, Amante, Fiona H., Kumar, Rajiv, Gao, Yulong, Sheel, Meru, Beattie, Lynette, de Oca, Marcela Montes, Guillerey, Camille, Edwards, Chelsea L., Faleiro, Rebecca J., Frame, Teija, Bunn, Patrick T., Vivier, Eric, Godfrey, Dale I., Pellicci, Daniel G., Lopez, J. Alejandro, Andrews, Katherine T., Huntington, Nicholas D., Smyth, Mark J., McCarthy, James and Engwerda, Christian R. (2018) Rapid loss of group 1 innate lymphoid cells during blood stage Plasmodium infection. Clinical and Translational Immunology, 7 1: e1003. doi:10.1002/cti2.1003     1 Cited 1 times in Scopus1 3
Bonnefond, Amelie, Clement, Nathalie, Fawcett, Katherine, Yengo, Loic, Vaillant, Emmanuel, Guillaume, Jean-Luc, Dechaume, Aurelie, Payne, Felicity, Roussel, Ronan, Czernichow, Sebastien, Hercberg, Serge, Hadjadj, Samy, Balkau, Beverley, Marre, Michel, Lantieri, Olivier, Langenberg, Claudia, Bouatia-Naji, Nabila, Charpentier, Guillaume, Vaxillaire, Martine, Rocheleau, Ghislain, Wareham, Nicholas J., Sladek, Robert, McCarthy, Mark I., Dina, Christian, Barroso, Ines, Jockers, Ralf and Froguel, Philippe (2012) Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nature Genetics, 44 3: 297-301. doi:10.1038/ng.1053     188 Cited 195 times in Scopus195 16