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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

Conference Publication

Genetic influences on life-span and its relationship to personality: a 16 year follow-up study of a sample of ageing twins

Mosing, Miriam, Medland, Sarah, McRae, Allan, Wright, Margaret and Martin, Nick G. (2011). Genetic influences on life-span and its relationship to personality: a 16 year follow-up study of a sample of ageing twins. 41st Annual Meeting of the Behaviour Genetics Association, Newport, Rhode Island, 6-9 June 2011. New York, NY, United States: Springer.

Genetic influences on life-span and its relationship to personality: a 16 year follow-up study of a sample of ageing twins

2011

Journal Article

Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder

Frank, Rene A. W., McRae, Allan F., Pocklington, Andrew J., van de Lagemaat, Louie N., Navarro, Pau, Croning, Mike D. R., Komiyama, Noboru H., Bradley, Sophie J., Challiss, R. A. John, Armstrong, J. Douglas, Finn, Robert D., Malloy, Mary P., MacLean, Alan W., Harris, Sarah E., Starr, John M., Bhaskar, Sanjeev S., Howard, Eleanor K., Hunt, Sarah E., Coffey, Alison J., Ranganath, Venkatesh, Deloukas, Panos, Rogers, Jane, Muir, Walter J., Deary, Ian J., Blackwood, Douglas H., Visscher, Peter M. and Grant, Seth G. N. (2011). Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder. PLoS One, 6 (4) e19011, e19011.1-e19011.9. doi: 10.1371/journal.pone.0019011

Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder

2010

Journal Article

No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.

Gratten, J., Wilson, A. J., McRae, A. F., Beraldi, D., Visscher, P. M., Pemberton, J. M. and Slate, J. (2010). No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.. Biology Letters, 6 (5), 678-679. doi: 10.1098/rsbl.2010.0160

No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.

2010

Journal Article

Congenital sensorineural deafness in Australian Stumpy-tail Cattle Dogs is an autosomal recessive trait that maps to CFA10

Sommerlad, Susan, McRae, Allan F., McDonald, Brenda, Johnstone, Isobel, Cuttell, Leigh, Seddon, Jennifer M. and O'Leary, Caroline A. (2010). Congenital sensorineural deafness in Australian Stumpy-tail Cattle Dogs is an autosomal recessive trait that maps to CFA10. PLoS One, 5 (10) e13364, e13364. doi: 10.1371/journal.pone.0013364

Congenital sensorineural deafness in Australian Stumpy-tail Cattle Dogs is an autosomal recessive trait that maps to CFA10

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 study of height and body mass index in Australian twin families

Liu, Jimmy Z., Medland, Sarah E., Wright, Margaret J., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Duncan, Alexis, Montgomery, Grant W., Martin, Nicholas G. and McRae, Allan F. (2010). Genome-wide association study of height and body mass index in Australian twin families. Twin Research And Human Genetics, 13 (2), 179-193. doi: 10.1375/twin.13.2.179

Genome-wide association study of height and body mass index in Australian twin families

2010

Journal Article

Horn type and horn length genes map to the same chromosomal region in Soay sheep

Johnston, S. E., Beraldi, D., McRae, A. F., Pemberton, J. M. and Slate, J. (2010). Horn type and horn length genes map to the same chromosomal region in Soay sheep. Heredity, 104 (2), 196-205. doi: 10.1038/hdy.2009.109

Horn type and horn length genes map to the same chromosomal region in Soay sheep

2010

Journal Article

Association genetics, population genomics, and conservation: Revealing the genes underlying adaptation in natural populations of plants and animals

Nichols, Krista M., Neale, David B., Gratten, Jake, Wilson, Alastair J., McRae, Allan F., Beraldi, Dario, Visscher, Peter M., Pemberton, Josephine M. and Slate, Jon (2010). Association genetics, population genomics, and conservation: Revealing the genes underlying adaptation in natural populations of plants and animals. Molecular Approaches in Natural Resource Conservation and Management, 123-168.

Association genetics, population genomics, and conservation: Revealing the genes underlying adaptation in natural populations of plants and animals

2010

Conference Publication

Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses

Medland, S. E., Nyholt, D. R., Painter, J. N., McEvoy, B. P., McRae, A. F., Montgomery, G. W. and Martin, N. G. (2010). Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses. 6th World Congress for Hair Research, Cairns, QLD, Australia, 16-19 June 2010. Oxford, United Kingdom: Wiley-Blackwell. doi: 10.1111/j.1600-0625.2010.01097.x

Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses

2009

Journal Article

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009). Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 (5), 750-755. doi: 10.1016/j.ajhg.2009.10.009

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

2009

Journal Article

Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents

E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009). Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 (11), 2359-2368. doi: 10.1007/s00125-009-1510-9

Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents

2009

Journal Article

Association Study of Common Mitochondrial Variants and Cognitive Ability

Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009). Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 (5), 504-512. doi: 10.1007/s10519-009-9276-x

Association Study of Common Mitochondrial Variants and Cognitive Ability

2009

Journal Article

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.

Matthew C. Keller, Allan F. McRae, Julie M. McGaughran, Peter M. Visscher, Nicholas G. Martin and Grant W. Montgomery (2009). Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.. American Journal of Medical Genetics. Part A, 149A (8), 1823-1826. doi: 10.1002/ajmg.a.32973

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.

2009

Journal Article

Geographical structure and differential natural selection among North European populations

Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108

Geographical structure and differential natural selection among North European populations

2009

Journal Article

Family-based genome-wide association studies

Benyamin, Beben, Visscher, Peter M. and McRae, Allan F. (2009). Family-based genome-wide association studies. Pharmacogenomics, 10 (2), 181-190. doi: 10.2217/14622416.10.2.181

Family-based genome-wide association studies

2009

Journal Article

DNA methylation profiles in monozygotic and dizygotic twins

Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286

DNA methylation profiles in monozygotic and dizygotic twins

2009

Journal Article

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

2009

Journal Article

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

Knight, Helen M., Pickard, Benjamin S., Maclean, Alan, Malloy, Mary P., Soares, Dinesh C., McRae, Allan F., Condie, Alison, White, Angela, Hawkins, William, McGhee, Kevin, van Beck, Margaret, MacIntyre, Donald J., Starr, John M., Deary, Ian J., Visscher, Peter M., Porteous, David J., Cannon, Ronald E., St Clair, David, Muir, Walter J. and Blackwood, Douglas H. R. (2009). A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression. American Journal of Human Genetics, 85 (6), 833-846. doi: 10.1016/j.ajhg.2009.11.003

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

2008

Journal Article

Divergence between human populations estimated from linkage disequilibrium

Sved, John A., McRae, Allan F. and Visscher, Peter M. (2008). Divergence between human populations estimated from linkage disequilibrium. American Journal of Human Genetics, 83 (6), 737-743. doi: 10.1016/j.ajhg.2008.10.019

Divergence between human populations estimated from linkage disequilibrium