Events in Early Life are Associated with Female Reproductive Ageing: A UK Biobank Study

by Ruth, Katherine S., Perry, John R. B., Henley, William E., Melzer, David, Weedon, Michael N., Murray, Anna
Published 2016

Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study

by Day, Felix R, Elks, Cathy E, Murray, Anna, Ong, Ken K, Perry, John R.B.
Published 2015

Season of birth is associated with birth weight, pubertal timing, adult body size and educational attainment: a UK Biobank study

by Day, Felix R., Forouhi, Nita G., Ong, Ken K., Perry, John R.B.
Published 2015

Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males

by Perry, John R.B., McMahon, George, Day, Felix R., Ring, Susan M, Nelson, Scott M., Lawlor, Debbie A.
Published 2016

Shared genetic aetiology of puberty timing between sexes and with health-related outcomes

by Day, Felix R., Bulik-Sullivan, Brendan, Hinds, David A., Finucane, Hilary K., Murabito, Joanne M., Tung, Joyce Y., Ong, Ken K., Perry, John R.B.
Published 2015

An Atlas of Genetic Correlations across Human Diseases and Traits

by Bulik-Sullivan, Brendan, Finucane, Hilary K, Anttila, Verneri, Gusev, Alexander, Day, Felix R., Loh, Po-Ru, Duncan, Laramie, Perry, John R.B., Patterson, Nick, Robinson, Elise B., Daly, Mark J., Price, Alkes L., Neale, Benjamin M.
Published 2015

Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk

by Marquez, Marcel, Huyvaert, Marlène, Perry, John R.B., Pearson, Richard D., Falchi, Mario, Morris, Andrew P., Vivequin, Sidonie, Lobbens, Stéphane, Yengo, Loïc, Gaget, Stefan, Pattou, Francois, Poulain-Godefroy, Odile, Charpentier, Guillaume, Carlsson, Lena M.S., Jacobson, Peter, Sjöström, Lars, Lantieri, Olivier, Heude, Barbara, Walley, Andrew, Balkau, Beverley, Marre, Michel, Froguel, Philippe, Cauchi, Stéphane
Published 2012

Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based...

by Wood, Andrew R., Perry, John R. B., Tanaka, Toshiko, Hernandez, Dena G., Zheng, Hou-Feng, Melzer, David, Gibbs, J. Raphael, Nalls, Michael A., Weedon, Michael N., Spector, Tim D., Richards, J. Brent, Bandinelli, Stefania, Ferrucci, Luigi, Singleton, Andrew B., Frayling, Timothy M.
Published 2013

Biomarkers for Type 2 Diabetes and Impaired Fasting Glucose Using a Nontargeted Metabolomics Approach

by Menni, Cristina, Fauman, Eric, Erte, Idil, Perry, John R.B., Kastenmüller, Gabi, Shin, So-Youn, Petersen, Ann-Kristin, Hyde, Craig, Psatha, Maria, Ward, Kirsten J., Yuan, Wei, Milburn, Mike, Palmer, Colin N.A., Frayling, Timothy M., Trimmer, Jeff, Bell, Jordana T., Gieger, Christian, Mohney, Rob P., Brosnan, Mary Julia, Suhre, Karsten, Soranzo, Nicole, Spector, Tim D.
Published 2013

Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study

by Østergaard, Søren D., Mukherjee, Shubhabrata, Sharp, Stephen J., Proitsi, Petroula, Lotta, Luca A., Day, Felix, Perry, John R. B., Boehme, Kevin L., Walter, Stefan, Kauwe, John S., Gibbons, Laura E., Larson, Eric B., Powell, John F., Langenberg, Claudia, Crane, Paul K., Wareham, Nicholas J., Scott, Robert A.
Published 2015

Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis

by Nead, Kevin T., Sharp, Stephen J., Thompson, Deborah J., Painter, Jodie N., Savage, David B., Semple, Robert K., Barker, Adam, Perry, John R. B., Attia, John, Dunning, Alison M., Easton, Douglas F., Holliday, Elizabeth, Lotta, Luca A., O’Mara, Tracy, McEvoy, Mark, Pharoah, Paul D. P., Scott, Rodney J., Spurdle, Amanda B., Langenberg, Claudia, Wareham, Nicholas J., Scott, Robert A.
Published 2015

Partitioning heritability by functional annotation using genome-wide association summary statistics

by Finucane, Hilary K., Bulik-Sullivan, Brendan, Gusev, Alexander, Trynka, Gosia, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle, Ripke, Stephan, Day, Felix R., Consortium, ReproGen, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R. B., Okada, Yukinori, Raychaudhuri, Soumya, Daly, Mark, Patterson, Nick, Neale, Benjamin M., Price, Alkes L.
Published 2015

Genetic Evidence for a Normal-Weight “Metabolically Obese” Phenotype Linking Insulin Resistance, Hypertension, Coronary Artery Disease, and Type 2 Diabetes

by Yaghootkar, Hanieh, Scott, Robert A., White, Charles C., Zhang, Weihua, Speliotes, Elizabeth, Munroe, Patricia B., Ehret, Georg B., Bis, Joshua C., Fox, Caroline S., Walker, Mark, Borecki, Ingrid B., Knowles, Joshua W., Yerges-Armstrong, Laura, Ohlsson, Claes, Perry, John R.B., Chambers, John C., Kooner, Jaspal S., Franceschini, Nora, Langenberg, Claudia, Hivert, Marie-France, Dastani, Zari, Richards, J. Brent, Semple, Robert K., Frayling, Timothy M.
Published 2014

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

by Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J. Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole
Published 2015

Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis

by Lotta, Luca A., Scott, Robert A., Sharp, Stephen J., Burgess, Stephen, Luan, Jian’an, Tillin, Therese, Schmidt, Amand F., Imamura, Fumiaki, Stewart, Isobel D., Perry, John R. B., Marney, Luke, Koulman, Albert, Karoly, Edward D., Forouhi, Nita G., Sjögren, Rasmus J. O., Näslund, Erik, Zierath, Juleen R., Krook, Anna, Savage, David B., Griffin, Julian L., Chaturvedi, Nishi, Hingorani, Aroon D., Khaw, Kay-Tee, Barroso, Inês, McCarthy, Mark I., O’Rahilly, Stephen, Wareham, Nicholas J., Langenberg, Claudia
Published 2016

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

by Yang, Jian, Bakshi, Andrew, Zhu, Zhihong, Hemani, Gibran, Vinkhuyzen, Anna A.E., Lee, Sang Hong, Robinson, Matthew R., Perry, John R.B., Nolte, Ilja M., van Vliet-Ostaptchouk, Jana V., Snieder, Harold, Esko, Tonu, Milani, Lili, Mägi, Reedik, Metspalu, Andres, Hamsten, Anders, Magnusson, Patrik K.E., Pedersen, Nancy L., Ingelsson, Erik, Soranzo, Nicole, Keller, Matthew C., Wray, Naomi R., Goddard, Michael E., Visscher, Peter M.
Published 2015

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

by Day, Felix R., Hinds, David A., Tung, Joyce Y., Stolk, Lisette, Styrkarsdottir, Unnur, Saxena, Richa, Bjonnes, Andrew, Broer, Linda, Dunger, David B., Halldorsson, Bjarni V., Lawlor, Debbie A., Laval, Guillaume, Mathieson, Iain, McCardle, Wendy L., Louwers, Yvonne, Meun, Cindy, Ring, Susan, Scott, Robert A., Sulem, Patrick, Uitterlinden, André G., Wareham, Nicholas J., Thorsteinsdottir, Unnur, Welt, Corrine, Stefansson, Kari, Laven, Joop S. E., Ong, Ken K., Perry, John R. B.
Published 2015

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

by Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole
Published 2014

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

by Wood, Andrew R., Tuke, Marcus A., Nalls, Mike, Hernandez, Dena, Gibbs, J. Raphael, Lin, Haoxiang, Xu, Christopher S., Li, Qibin, Shen, Juan, Jun, Goo, Almeida, Marcio, Tanaka, Toshiko, Perry, John R. B., Gaulton, Kyle, Rivas, Manny, Pearson, Richard, Curran, Joanne E., Johnson, Matthew P., Göring, Harald H. H., Duggirala, Ravindranath, Blangero, John, Mccarthy, Mark I., Bandinelli, Stefania, Murray, Anna, Weedon, Michael N., Singleton, Andrew, Melzer, David, Ferrucci, Luigi, Frayling, Timothy M
Published 2015

Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms

by Zhai, Guangju, Teumer, Alexander, Stolk, Lisette, Perry, John R. B., Vandenput, Liesbeth, Coviello, Andrea D., Koster, Annemarie, Bell, Jordana T., Bhasin, Shalender, Eriksson, Joel, Eriksson, Anna, Ernst, Florian, Ferrucci, Luigi, Frayling, Timothy M., Glass, Daniel, Grundberg, Elin, Haring, Robin, Hedman, Åsa K., Hofman, Albert, Kiel, Douglas P., Kroemer, Heyo K., Liu, Yongmei, Lunetta, Kathryn L., Maggio, Marcello, Lorentzon, Mattias, Mangino, Massimo, Melzer, David, Miljkovic, Iva, Nica, Alexandra, Penninx, Brenda W. J. H., Vasan, Ramachandran S., Rivadeneira, Fernando, Small, Kerrin S., Soranzo, Nicole, Uitterlinden, André G., Völzke, Henry, Wilson, Scott G., Xi, Li, Zhuang, Wei Vivian, Harris, Tamara B., Murabito, Joanne M., Ohlsson, Claes, Murray, Anna, de Jong, Frank H., Spector, Tim D., Wallaschofski, Henri
Published 2011