Skip to menu Skip to content Skip to footer

2011

Journal Article

Transferrin saturation and mortality

Benyamin, Beben, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Transferrin saturation and mortality. Clinical Chemistry, 57 (6), 921-923. doi: 10.1373/clinchem.2011.162784

Transferrin saturation and mortality

2011

Journal Article

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011)

Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stephane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011). Proceedings of the National Academy of Sciences of the United States of America, 108 (22), 9316-9316. doi: 10.1073/pnas.1106917108

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011)

2011

Journal Article

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2011). Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. The Journal of Neuroscience, 31 (18), 6764-6770. doi: 10.1523/JNEUROSCI.5794-10.2011

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

2011

Journal Article

Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior

Meier, Madeline H., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2011). Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior. Journal of Abnormal Psychology, 120 (2), 377-388. doi: 10.1037/a0022303

Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior

2011

Journal Article

Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating

Zietsch, Brendan P., Verweij, Karin J. H., Heath, Andrew C. and Martin, Nicholas G. (2011). Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating. The American Naturalist, 177 (5), 605-616. doi: 10.1086/659629

Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating

2011

Journal Article

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stéphane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America, 108 (17), 7119-7124. doi: 10.1073/pnas.1017288108

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

2011

Journal Article

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Obstetrical and Gynecological Survey, 66 (4), 214-216. doi: 10.1097/OGX.0b013e318210cea1

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

2011

Journal Article

Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]

Loehlin, John C. and Martin, Nicholas G. (2011). Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]. Journal of Research in Personality, 45 (2), 258-258. doi: 10.1016/j.jrp.2011.02.010

Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]

2011

Journal Article

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

Ferreira, Manuel A. R., McRae, Allan F., Medland, Sarah E., Nyholt, Dale R., Gordon, Scott D., Wright, Margaret J., Henders, Anjali K., Madden, Pamela A., Visscher, Peter M., Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Duffy, David L. and Martin, Nicholas G. (2011). Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. European Journal of Human Genetics, 19 (4), 458-464. doi: 10.1038/ejhg.2010.191

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

2011

Journal Article

Does teenage childbearing reduce investment in human capital?

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2011). Does teenage childbearing reduce investment in human capital?. Journal of Population Economics, 24 (2), 701-730. doi: 10.1007/s00148-009-0270-7

Does teenage childbearing reduce investment in human capital?

2011

Journal Article

The politics of mate choice

Alford, John R., Hatemi, Peter K., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2011). The politics of mate choice. The Journal of Politics, 73 (2), 362-379. doi: 10.1017/S0022381611000016

The politics of mate choice

2011

Journal Article

Alcoholic marriage: later start, sooner end

Waldron, Mary, Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Alcoholic marriage: later start, sooner end. Alcoholism: Clinical and Experimental Research, 35 (4), 632-642. doi: 10.1111/j.1530-0277.2010.01381.x

Alcoholic marriage: later start, sooner end

2011

Journal Article

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Aexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics, 88 (3), 372-381. doi: 10.1016/j.ajhg.2011.01.017

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

2011

Journal Article

Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

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. ... 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, e1001324.1-e1001324.14. doi: 10.1371/journal.pgen.1001324

Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

2011

Journal Article

Whole genome association scan for genetic polymorphisms influencing information processing speed

Luciano, Michelle, Hansell, Narelle K., Lahti, Jari, Davies, Gail, Medland, Sarah E., Raikkonen, Katri, Tenesa, Albert, Widen, Elisabeth, McGhee, Kevin A., Palotie, Aarno, Liewald, David, Porteous, David J., Starr, John M., Montgomery, Grant W., Martin, Nicholas G., Eriksson, Johan G., Wright, Margaret J. and Deary, Ian J. (2011). Whole genome association scan for genetic polymorphisms influencing information processing speed. Biological Psychology, 86 (3), 193-202. doi: 10.1016/j.biopsycho.2010.11.008

Whole genome association scan for genetic polymorphisms influencing information processing speed

2011

Journal Article

BDNF gene effects on brain circuitry replicated in 455 twins

Chiang, M. C., Barysheva, M., Toga, A. W., Medland, S. E., Hansel, N. K., James, M. R., McMahon, K. L., de Zubicaray, G. I., Martin, N. G., Wright, M. J. and Thompson, P. M. (2011). BDNF gene effects on brain circuitry replicated in 455 twins. NeuroImage, 55 (2), 448-454. doi: 10.1016/j.neuroimage.2010.12.053

BDNF gene effects on brain circuitry replicated in 455 twins

2011

Journal Article

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)

Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011). American Journal of Human Genetics, 88 (3), 396-396. doi: 10.1016/j.ajhg.2011.03.001

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)

2011

Journal Article

The contribution of genes to cortical thickness and volume

Joshi, A.A., Lepore, N., Joshi, S.H., Lee, A.D., Barysheva, M., Stein, J.L., McMahon, K.L., Johnson, K., de Zubicaray, G.I., Martin, N.G., Wright, M.J., Toga, A.W. and Thompson, P.M. (2011). The contribution of genes to cortical thickness and volume. NeuroReport, 22 (3), 101-105. doi: 10.1097/WNR.0b013e3283424c84

The contribution of genes to cortical thickness and volume

2011

Journal Article

Fast and slow spindle involvement in the consolidation of a new motor sequence

Barakat, M., Doyon, J., Debas, K., Vandewalle, G., Morin, A., Poirier, G., Martin, N., Lafortune, M., Karni, A., Ungerleider, L. G., Benali, H. and Carrier, J. (2011). Fast and slow spindle involvement in the consolidation of a new motor sequence. Behavioural Brain Research, 217 (1), 117-121. doi: 10.1016/j.bbr.2010.10.019

Fast and slow spindle involvement in the consolidation of a new motor sequence

2011

Journal Article

The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease

Fahy, Samantha J., Sun, Cong, Zhu, Gu, Healey, Paul R., Spector, Tim D., Martin, Nicolas G., Mitchell, Paul, Wong, Tien Y., Mackey, David A., Hammond, Christopher J. and Andrew, Toby (2011). The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease. Investigative Ophthalmology & Visual Science, 52 (2), 975-981. doi: 10.1167/iovs.10-5927

The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease