|
2011 Journal Article Genome-wide association study identifies a locus at 7p15.2 associated with endometriosisPainter, 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 |
|
2011 Journal Article Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platformsVinkhuyzen, A. A. E., Dumenil, T., Ryan, L., Gordon, S. D., Henders, A. K., Madden, P. A. F., Heath, A. C., Montgomery, G. W., Martin, N. G. and Wray, N. R. (2011). Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms. Molecular Psychiatry, 16 (11), 1073-1075. doi: 10.1038/mp.2011.68 |
|
2011 Journal Article A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking familiesPergadia, Michele L., Glowinski, Anne L., Wray, Naomi, Agrawal, Arpana, Saccone, Scott F., Loukola, Anu, Broms, Ulla, Koronen, Tellervo, Penninx, Brenda W. J. H., Grant, Julia D., Nelson, Elliot C., Henders, Anjali K., Schrage, Andrew J., Chou, Yi-Ling, Keskitalo-Vuokko, Kaisu, Zhu, Qin, Gordon, Scott D., Vink, Jacqueline M., de Geus, Eco J. C., MacGregor, Stuart, Liu, Jimmy Z., Willemsen, Gonneke, Medland, Sarah E., Boomsma, Dorret I., Montgomery, Grant W., Rice, John P., Goate, Alison M., Heath, Andrew, C, Martin, Nicholas G. and Madden, Pamela A. F. (2011). A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families. American Journal Psychiatry, 168 (8), 848-852. doi: 10.1176/appi.ajp.2011.10091319 |
|
2011 Journal Article Genome-wide association study identifies a locus at 7p15.2 associated with endometriosisPainter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731 |
|
2010 Journal Article A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studiesLee, Sang Hong, Nyholt, Dale R., Macgregor, Stuart, Henders, Anjali K., Zondervan, Krina T., Montgomery, Grant W. and Visscher, Peter M. (2010). A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies. Genetic Epidemiology, 34 (8), 854-862. doi: 10.1002/gepi.20541 |
|
2010 Journal Article The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12Reed, Danielle R., Zhu, Gu, Breslin, Paul A. S., Duke, Fujiko F., Henders, Anjali K., Campbell, Megan J., Montgomery, Grant W., Medland, Sarah E., Martin, Nicholas G. and Wright, Margaret J. (2010). The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. Human Molecular Genetics, 19 (21) ddq324, 4278-4285. doi: 10.1093/hmg/ddq324 |
|
2010 Journal Article A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personalityVerweij, Kjh, Zietsch, BP, Medland, SE, Gordon, SD, Benyamin, B, Nyholt, DR, McEvoy, BP, Sullivan, PF, Heath, AC, Madden, PAF, Henders, AK, Montgomery, GW, Martin, NG and Wray, NR (2010). A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personality. Biological Psychology, 85 (2), 306-317. doi: 10.1016/j.biopsycho.2010.07.018 |
|
2010 Journal Article Common SNPs explain a large proportion of the heritability for human heightYang, 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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
