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2010 Journal Article Genome-wide association identifies ATOH7 as a major gene determining human optic disc sizeMacgregor, 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 |
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2010 Journal Article A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twinsPainter, 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 |
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2010 Journal Article A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposureMedland, Sarah E., Zayats,Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon,Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey and Evans, David M. (2010). A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86 (4), 519-525. doi: 10.1016/j.ajhg.2010.02.017 |
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2010 Journal Article Genome-wide association study of height and body mass index in Australian twin familiesLiu, 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 |
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2010 Journal Article Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune controlFerreira, Mar, Mangino, M, Brumme, CJ, Zhao, ZZ, Medland, SE, Wright, MJ, Nyholt, DR, Gordon, S, Campbell, M, McEvoy, BP, Henders, A, Evans, DM, Lanchbury, JS, Pereyra, F, Walker, BD, Haas, DW, Soranzo, N, Spector, TD, de Bakker, PIW, Frazer, IH, Montgomery, GW, Martin, NG and Int HIV Controllers Study (2010). Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. American Journal of Human Genetics, 86 (1), 88-92. doi: 10.1016/j.ajhg.2009.12.008 |
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2009 Journal Article Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in EuropeansMedland, 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 |
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2009 Journal Article Common variants in TMPRSS6 are associated with iron status and erythrocyte volumeBenyamin, B, Ferreira, MAR, Willemsen, G, Gordon, S, Middelberg, RPS, McEvoy, BP, Hottenga, JJ, Henders, AK, Campbell, MJ, Wallace, L, Frazer, IH, Heath, AC, de Geus, EJC, Nyholt, DR, Visscher, PM, Penninx, BW, Boomsma, DI, Martin, NG, Montgomery, GW and Whitfield, JB (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics, 41 (11), 1173-1175. doi: 10.1038/ng.456 |
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2009 Journal Article Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte VolumeFerreira, MAR, Hottenga, JJ, Warrington, NM, Medland, SE, Willemsen, G, Lawrence, RW, Gordon, S, de Geus, EJC, Henders, AK, Smit, JH, Campbell, MJ, Wallace, L, Evans, DM, Wright, MJ, Nyholt, DR, James, AL, Beilby, JP, Penninx, BW, Palmer, LJ, Frazer, IH, Montgomery, GW, Martin, NG and Boomsma, DI (2009). Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (5), 745-749. doi: 10.1016/j.ajhg.2009.10.005 |
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2009 Journal Article Rapid inexpensive genome-wide association using pooled whole bloodJamie E. Craig, Alex W. Hewitt, Amy E. McMellon, Anjali K. Henders, Lingjun Ma, Leanne Wallace, Shiwani Sharma, Kathryn P. Burdon, Peter M. Visscher, Grant W. Montgomery and Stuart MacGregor (2009). Rapid inexpensive genome-wide association using pooled whole blood. Genome Research, 19 (11), 2075-2080. doi: 10.1101/gr.094680.109 |
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2009 Journal Article Genetic linkage findings for DSM-IV nicotine withdrawal in two populationsMichele L. Pergadia, Arpana Agrawal, Anu Loukola, Grant W. Montgomery, Ulla Broms, Scott F. Saccone, Jen C. Wang, Alexandre A. Todorov, Kauko Heikkilä, Dixie J. Statham, Anjali K. Henders, Megan J. Campbell, John P. Rice, Richard D. Todd, Andrew C. Heath, Alison M. Goate, Leena Peltonen, Jaakko Kaprio, Nicholas G. Martin and Pamela A.F. Madden (2009). Genetic linkage findings for DSM-IV nicotine withdrawal in two populations. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150b (7), 950-959. doi: 10.1002/ajmg.b.30924 |
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2009 Journal Article Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin LevelsBeben 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 |
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2008 Journal Article Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypesPeters, Kirsten, Wiltshire, Steven, Henders, Anjali K., Dragovic, Milan, Badcock, Johanna C., Chandler, David, Howell, Sarah, Ellis, Chris, Bouwer, Sonja, Montgomery, Grant W., Palmer, Lyle J., Kalaydjieva, Luba and Jablensky, Assen (2008). Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B (7), 1159-1166. doi: 10.1002/ajmg.b.30741 |
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2008 Journal Article Common sequence variants on 20q11.22 confer melanoma susceptibilityBrown, K. M., MacGregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D. C., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Newton Bishop, J., Kefford, R. F. ... Hayward, N. (2008). Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 (7), 838-840. doi: 10.1038/ng.163 |
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2008 Journal Article An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics projectAgrawal, Arpana, Pergadia, Michele. L., Saccone, Scott F., Lynskey, Michael T., Wang, Jen C., Martin, Nicholas G., Statham, Dixie, Henders, Anjali, Campbell, Megan, Garcia, Robertino, Broms, Ulla, Todd, Richard D., Goate, Alison M., Rice, John, Kaprio, Jaakko, Heath, Andrew C., Montgomery, Grant W. and Madden, Pamela A. F. (2008). An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project. Archives of General Psychiatry, 65 (6), 713-722. doi: 10.1001/archpsyc.65.6.713 |
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2008 Journal Article Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arraysMacgregor, Stuart, Zhao, Zhen Zhen, Henders, Anjali, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays. Nucleic Acids Research, 36 (6) e35, 291-296. doi: 10.1093/nar/gkm1060 |
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2007 Journal Article A case of true hermaphroditism reveals an unusual mechanism of twinningSouter, Vivienne L., Parisi, Melissa A., Nyholt, Dale R., Kapur, Raj P., Henders, Anjali K., Opheim, Kent E., Gunther, Daniel F., Mitchell, Michael E., Glass, Ian A. and Montgomery, Grant W. (2007). A case of true hermaphroditism reveals an unusual mechanism of twinning. Human Genetics, 121 (2), 179-185. doi: 10.1007/s00439-006-0279-x |
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2005 Journal Article Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scanDickson, PA, Montgomery, GW, Henders, A, Campbell, MJ, Martin, NG and James, MR (2005). Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan. Nucleic Acids Research, 33 (13), 1-4. doi: 10.1093/nar/gni126 |
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2001 Journal Article Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genesHealey, S. C., Kirk, K. M., Hyland, V. J., Munns, C., Henders, A. K., Batch, J. A., Heath, A. C., Martin, N. G. and Glass, I. A. (2001). Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genes. Twin Research, 4 (1), 19-24. doi: 10.1375/twin.4.1.19 |
