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2010

Journal Article

Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings

Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2010). Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings. NeuroImage, 52 (2), 455-469. doi: 10.1016/j.neuroimage.2010.04.236

Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings

2010

Journal Article

Major depression and the metabolic syndrome

Foley, Debra L., Morley, Katherine I., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2010). Major depression and the metabolic syndrome. Twin Research and Human Genetics, 13 (4), 347-358. doi: 10.1375/twin.13.4.347

Major depression and the metabolic syndrome

2010

Journal Article

Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins

Mosing, Miriam A., Pedersen, Nancy L., Martin, Nicholas G. and Wright, Margaret J. (2010). Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins. Twin Research And Human Genetics, 13 (4), 322-329. doi: 10.1375/twin.13.4.322

Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins

2010

Journal Article

Genetic covariance structure of the four main features of borderline personality disorder

Distel, Marijn A., Willemsen, Gonneke, Ligthart, Lannie, Derom, Catherine A., Martin, Nicholas G., Neale, Michael C., Trull, Timothy J. and Boomsma, Dorret I. (2010). Genetic covariance structure of the four main features of borderline personality disorder. Journal of Personality Disorders, 24 (4), 427-444. doi: 10.1521/pedi.2010.24.4.427

Genetic covariance structure of the four main features of borderline personality disorder

2010

Journal Article

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD

Saccone, Nancy L., Culverhouse, Robert C., Schwantes-An, Tae-Hwi, Cannon, Dale S., Chen, Xiangning, Cichon, Sven, Giegling, Ina, Han, Shizhong, Han, Younghun, Keskitalo-Vuokko, Kaisu, Kong, Xiangyang, Landi, Maria Teresa, Ma, Jennie Z., Short, Susan E., Stephens, Sarah H., Stevens, Victoria L., Sun, Lingwei, Wang, Yufei, Wenzlaff, Angela S., Aggen, Steven H., Breslau, Naomi, Broderick, Peter, Chatterjee, Nilanjan, Chen, Jingchun, Heath, Andrew C., Heliovaara, Markku, Hoft, Nicole R., Hunter, David J., Jensen, Majken K. ... Bierut, Laura J. (2010). Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD. PLoS Genetics, 6 (8) e1001053, 1-16. doi: 10.1371/journal.pgen.1001053

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD

2010

Journal Article

Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling

Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2010). Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling. Twin Research And Human Genetics, 13 (4), 330-339. doi: 10.1375/twin.13.4.330

Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling

2010

Journal Article

A versatile gene-based test for genome-wide association studies

Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010). A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 (1), 139-145. doi: 10.1016/j.ajhg.2010.06.009

A versatile gene-based test for genome-wide association studies

2010

Journal Article

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J. and Mackey, David A. (2010). Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics, 19 (13) ddq144, 2716-2724. doi: 10.1093/hmg/ddq144

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

2010

Journal Article

Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs

Hatemi, Peter K., Hibbing, John R., Medland, Sarah E., Keller, Matthew C., Alford, John R., Smith, Kevin B., Martin, Nicholas G. and Eaves, Lindon J. (2010). Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs. American Journal of Political Science, 54 (3), 798-814. doi: 10.1111/j.1540-5907.2010.00461.x

Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs

2010

Journal Article

IRF4 variants have age-specific effects on nevus count and predispose to melanoma

Duffy, David L., Iles, Mark M., Glass, Dan, Zhu, Gu, Barrett, Jennifer H., Hoiom, Veronica, Zhao, Zhen Z., Sturm, Richard A., Soranzo, Nicole, Hammond, Chris, Kvaskoff, Marina, Whiteman, David C., Mangino, Massimo, Hansson, Johan, Newton-Bishop, Julia A., Bataille, Veronique, Hayward, Nicholas K., Martin, Nicholas G., Bishop, D. Timothy, Spector, Timothy D. and Montgomery, Grant W. (2010). IRF4 variants have age-specific effects on nevus count and predispose to melanoma. American Journal of Human Genetics, 87 (1), 6-16. doi: 10.1016/j.ajhg.2010.05.017

IRF4 variants have age-specific effects on nevus count and predispose to melanoma

2010

Journal Article

Common SNPs explain a large proportion of the heritability for human height

Yang, Jian, Benyamin, Beben, McEvoy, Brian P., Gordon, Scott, Henders, Anjali K., Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Goddard, Michael E. and Visscher, Peter M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42 (7), 565-569. doi: 10.1038/ng.608

Common SNPs explain a large proportion of the heritability for human height

2010

Journal Article

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

Painter, Jodie N., Willemsen, Gonneke, Nyholt, Dale, Hoekstra, Chantal, Duffy, David L., Henders, Anjali K., Wallace, Leanne, Healey, Sue, Cannon-Albright, Lisa A., Skolnick, Mark, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2010). A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction, 25 (6), 1569-1580. doi: 10.1093/humrep/deq084

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

2010

Journal Article

Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2010). Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes. Environmental Health Perspectives, 118 (6), 776-782. doi: 10.1289/ehp.0901541

Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

2010

Journal Article

A genetic basis for social trust?

Sturgis, Patrick, Read, Sanna, Hatemi, Peter K., Zhu, Gu, Trull, Tim, Wright, Margaret J. and Martin, Nicholas G. (2010). A genetic basis for social trust?. Political Behavior, 32 (2), 205-230. doi: 10.1007/s11109-009-9101-5

A genetic basis for social trust?

2010

Journal Article

Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

Lind, Penelope A., Luciano, Michelle, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2010). Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18 (6), 668-673. doi: 10.1038/ejhg.2009.237

Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

2010

Journal Article

Genetic and environmental influences on disordered gambling in men and women

Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2010). Genetic and environmental influences on disordered gambling in men and women. Archives of General Psychiatry, 67 (6), 624-630. doi: 10.1001/archgenpsychiatry.2010.51

Genetic and environmental influences on disordered gambling in men and women

2010

Journal Article

The reliability and validity of the family history method for assessing pathological gambling and gambling involvement

Ellingson, Jarrod M., Slutske, Wendy S. and Martin, Nicholas G. (2010). The reliability and validity of the family history method for assessing pathological gambling and gambling involvement. Psychology of Addictive Behaviors, 24 (2), 292-299. doi: 10.1037/a0018126

The reliability and validity of the family history method for assessing pathological gambling and gambling involvement

2010

Journal Article

Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010). Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 (5) e1000947, e1000947.1-e1000947.10. doi: 10.1371/journal.pgen.1000947

Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

2010

Journal Article

Digital quantification of human eye color highlights genetic association of three new loci

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, e1000934-1-e1000934-15. doi: 10.1371/journal.pgen.1000934

Digital quantification of human eye color highlights genetic association of three new loci

2010

Journal Article

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

Thorgeirsson, Thorgeir E., Gudbjartsson, Daniel F., Surakka, Ida, Vink, Jacqueline M., Amin, Najaf, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Esko, Tōnu, Walter, Stefan, Gieger, Christian, Rawal, Rajesh, Mangino, Massimo, Prokopenko, Inga, Mägi, Reedik, Keskitalo, Kaisu, Gudjonsdottir, Iris H., Gretarsdottir, Solveig, Stefansson, Hreinn, Thompson, John R., Aulchenko, Yurii S., Nelis, Mari, Aben, Katja K., den Heijer, Martin, Dirksen, Asger, Ashraf, Haseem, Soranzo, Nicole, Valdes, Ana M., Steves, Claire ... Stefansson, Kari (2010). Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, 42 (5), 448-454. doi: 10.1038/ng.573

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior