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2007 Journal Article Intergenerational transmission of childhood conduct problems: a children of twins studyD'Onofrio, Brian M., Slutske, Wendy S., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2007). Intergenerational transmission of childhood conduct problems: a children of twins study. Archives of General Psychiatry, 64 (7), 820-829. doi: 10.1001/archpsyc.64.7.820 |
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2007 Journal Article Evidence of genetic effects on blood lead concentrationWhitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Montgomery, Grant W., Ferreira, Manuel A. R., Duffy, David L., Neale, Michael C., Heijmans, Bas T., Heath, Andrew C. and Martin, Nicholas G. (2007). Evidence of genetic effects on blood lead concentration. Environmental Health Perspectives, 115 (8), 1224-1230. doi: 10.1289/ehp.8847 |
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2007 Journal Article Variants in EMX2 and PTEN do not contribute to risk of endometriosisTreloar, S. A., Zhao, Z. Z., Le, L., Zondervan, K. T., Martin, N. G., Kennedy, S., Nyholt, D. R. and Montgomery, G. W. (2007). Variants in EMX2 and PTEN do not contribute to risk of endometriosis. Molecular Human Reproduction, 13 (8), 587-594. doi: 10.1093/molehr/gam023 |
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2007 Journal Article Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian lociPerola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick G., Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R., Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Karre, Kyvik, Kirsten Ohm, Sorensen, Thorkild I., Pedersen, Nancy L., Magnusson, Patrik K., Spector, Tim D., Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno, Peltonen, Leena and GenomEUtwin Project (2007). Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097 |
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2007 Journal Article Heritability of NEO PI-R extraversion facets and their relationship with IQPincombe, Jennifer L., Luciano, Michelle, Martin, Nicholas G. and Wright, Margaret J. (2007). Heritability of NEO PI-R extraversion facets and their relationship with IQ. Twin Research and Human Genetics, 10 (3), 462-469. doi: 10.1375/twin.10.3.462 |
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2007 Journal Article Spousal concordance for alcohol dependence: evidence for assortative mating or spousal interaction effects?Grant, J. D., Heath, A. C., Bucholz, K. K., Madden, P. A., Agrawal, A., Statham, D. J. and Martin, N. G. (2007). Spousal concordance for alcohol dependence: evidence for assortative mating or spousal interaction effects?. Alcoholism: Clinical & Experimental Research, 31 (5), 717-728. doi: 10.1111/j.1530-0277.2007.00356.x |
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2007 Journal Article The Genetics of Voting: an Australian Twin StudyHatemi, P. K., Medland, S. E., Morley, K. I., Heath, A. C. and Martin, N. G. (2007). The Genetics of Voting: an Australian Twin Study. Behavior Genetics, 37 (3) 435, 435-448. doi: 10.1007/s10519-006-9138-8 |
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2007 Journal Article Common and specific genetic influences on EEG power bands delta, theta, alpha, and betaZietsch, Brendan P., Hansen, Jonathan L., Hansell, Narelle K, Geffen, Gina M., Martin, Nicholas G. and Wright, Margaret J. (2007). Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta. Biological Psychology, 75 (2), 154-164. doi: 10.1016/j.biopsycho.2007.01.004 |
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2007 Journal Article Cohort Trends in Prevalence and Spousal Concordance for SmokingKuo, P. H., Wood, P., Morley, K. I., Madden, P., Martin, N. G. and Heath, A. C. (2007). Cohort Trends in Prevalence and Spousal Concordance for Smoking. Drug & Alcohol Dependence, 88 (2-3), 122-129. doi: 10.1016/j.drugalcdep.2006.09.021 |
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2007 Journal Article Height and 2D : 4D within and between ethnic groups: Reply to Hurd and van Anders (2007)Loehlin, John C., McFadden, Dennis, Medland, Sarah E. and Martin, Nicholas G. (2007). Height and 2D : 4D within and between ethnic groups: Reply to Hurd and van Anders (2007). Archives of Sexual Behavior, 36 (2), 143-143. doi: 10.1007/s10508-006-9153-0 |
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2007 Journal Article Effect of the BDNF V166M polymorphism on working memory in healthy adolescentsHansell, N. K., James, M. R., Duffy, D. L., Birley, A. J., Luciano, M., Geffen, G. M., Wright, M. J., Montgomery, G. W. and Martin, N. G. (2007). Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes, Brain and Behavior, 6 (3), 260-268. doi: 10.1111/j.1601-183X.2006.00254.x |
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2007 Journal Article Anxiety and comorbid measures associated with PLXNA2Wray, Naomi R., James, Michael R., Mah, Steven P., Nelson, Matthew, Andrews, Gavin, Sullivan, Patrick F., Montgomery, Grant W., Birley, Andrew J., Braun, Andreas and Martin, Nicholas G. (2007). Anxiety and comorbid measures associated with PLXNA2. Archives of General Psychiatry, 64 (3), 318-326. doi: 10.1001/archpsyc.64.3.318 |
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2007 Journal Article Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell linesMcRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007). Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics, 16 (4), 364-373. doi: 10.1093/hmg/ddl456 |
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2007 Journal Article Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17Bates, Timothy C., Luciano, Michelle, Castles, Anne, Coltheart, Max, Wright, Margaret J. and Martin, Nicholas G. (2007). Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. European Journal of Human Genetics, 15 (2), 194-203. doi: 10.1038/sj.ejhg.5201739 |
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2007 Journal Article Prevalence of premature ovarian failure in monozygotic and dizygotic twinsGosden, R. G., Treloar, S. A., Martin, N. G., Cherkas, L. F., Spector, T. D., Faddy, M. J. and Silber, S. J. (2007). Prevalence of premature ovarian failure in monozygotic and dizygotic twins. Human Reproduction, 22 (2), 610-615. doi: 10.1093/humrep/del382 |
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2007 Journal Article A longitudinal genetic study of plasma lipids in adolescent twinsMiddelberg, Rita P. S., Martin, Nicholas G. and Whitfield, John B. (2007). A longitudinal genetic study of plasma lipids in adolescent twins. Twin Research & Human Genetics, 10 (1), 127-135. doi: 10.1375/twin.10.1.127 |
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2007 Journal Article The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligenceMekel-Bobrov, Nitzan, Posthuma, Danielle, Gilbert, Sandra L., Lind, Penelope, Gosso, M. Florencia, Luciano, Michelle, Harris, Sarah E., Bates, Timothy C., Polderman, Tinca J., Whalley, Lawrence J., Fox, Helen, Starr, John M., Evans, Patrick D., Montgomery, Grant W., Fernandes, Croydon, Heutink, Peter, Martin, Nicholas G., Boomsma, Dorret I., Deary, Ian J., Wright, Margaret J., de Geus, Eco J. and Lahn, Bruce T. (2007). The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence. Human Molecular Genetics, 16 (6), 600-608. doi: 10.1093/hmg/ddl487 |
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2007 Journal Article A behavior genetic investigation of adolescent motherhood and offspring mental health problemsHarden, K. P., Lynch, S. K., Turkheimer, E., Emery, R. E., D'Onofrio, B. M., Slutske, W. S., Waldron, M. D., Statham, D. J. and Martin, N. G. (2007). A behavior genetic investigation of adolescent motherhood and offspring mental health problems. Journal of Abnormal Psychology, 116 (4), 667-683. doi: 10.1037/0021-843X.116.4.667 |
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2007 Journal Article Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twinsLuciano, M, Hine, E., Wright, M. J., Duffy, D. L., MacMillan, J. and Martins, N. G. (2007). Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 144B (1), 95-100. doi: 10.1002/ajmg.b.30413 |
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2007 Journal Article Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15Zondervan, K. T., Treloar, S. A., Lin, J., Weeks, D. E., Nyholt, D. R., Mangion, J., MacKay, I. J., Cardon, L. R., Martin, N. G., Kennedy, S. H. and Montgomery, G. W. (2007). Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15. Human Reproduction, 22 (3), 717-728. doi: 10.1093/humrep/del446 |
