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Pergadia, 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 15   16 Cited 18 times in Scopus18 18
Brant, Angela M., Boomsma, Dorret I., Corley, Robin P., DeFries, John C., Haworth, Clare M. A., Hewitt, John K., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J. and Wright, Margaret J. (2010). Ability and heritability: Investigating the continuous effect of IQ score on IQ etiology in multiple samples. In: Behavior Genetics Association 40th Annual Meeting Abstracts. The 40th Annual Behavior Genetic Association Meeting, Seoul, Korea, (788-788). 2- 5 June 2010. doi:10.1007/s10519-010-9392-7 317   0 0
Heath, Andrew C., Knopik, Valerie S., Madden, Pamela A., Neuman, Rosalind J., Lynskey, Michael J., Slutske, Wendy S., Jacob, Theodore and Martin, Nicholas G. (2003) Accuracy of Mothers' Retrospective Reports of Smoking During Pregnancy: Comparison with Twin Sister Informant Ratings. Twin Research, 6 4: 297-301. doi:10.1375/136905203322296656 128   28 Cited 30 times in Scopus30 0
Roussotte, Florence F., Jahanshad, Neda, Hibar, Derrek P., Sowell, Elizabeth R., Kohannim, Omid, Barysheva, Marina, Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Jack Jr, Clifford R., Weiner, Michael W., Thompson, Paul M. and ADNI (2014) A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations. Human Brain Mapping, 35 4: 1226-1236. doi:10.1002/hbm.22247 111 5 3 Cited 1 times in Scopus1 1
Sachdev, Perminder S., Lammel, Andrea, Trollor, Julian N., Lee, Teresa, Wright, Margaret J., Ames, David, Wen, Wei, Martin, Nicholas G., Brodaty, Henry, Schofield, Peter R. and OATS Research Team (2009) A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study. Twin Research and Human Genetics, 12 6: 573-582. doi:10.1375/twin.12.6.573 174   14 Cited 15 times in Scopus15 0
Whitfield, John B., OBrien, Martin E., Nightingale, Brian N., Zhu, Gu, Heath, Andrew C. and Martin, Nicholas G. (2003) ADH genotype does not modify the effects of alcohol on high-density lipoprotein. Alcoholism-clinical And Experimental Research, 27 3: 509-514. doi:10.1097/01.ALC.0000057940.57330.70 91   20 Cited 22 times in Scopus22 0
D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. and Martin, Nicholas G. (2005) A genetically informed study of marital instability and its association with offspring psychopathology. Journal of Abnormal Psychology, 114 4: 570-586. doi:10.1037/0021-843X.114.4.570 49   64 Cited 70 times in Scopus70 20
Lynch, Stacy K., Turkheimer, Eric, D'Onofrio, Brian M., Mendle, Jane, Emery, Robert E., Slutske, Wendy S. and Martin, Nicholas G. (2006) A genetically informed study of the association between harsh punishment and offspring behavioral problems. Journal of Family Psychology, 20 2: 190-198. doi:10.1037/0893-3200.20.2.190 93   34 Cited 38 times in Scopus38 1
Donofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. and Martin, Nicholas G. (2006) A genetically informed study of the processes underlying the association between parental marital instability and offspring adjustment. Developmental Psychology, 42 3: 486-499. doi:10.1037/0012-1649.42.3.486 51   49 Cited 57 times in Scopus57 17
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/s11109-009-9101-5 112 3 29 Cited 35 times in Scopus35 0
Luciano, Michelle, Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B., Smith, Glen A. and Martin, Nicholas G. (2004) A genetic investigation of the covariation among Inspection Time, Choice Reaction Time, and IQ subtest scores. Behavior Genetics, 34 1: 41-50. doi:10.1023/B:BEGE.0000009475.35287.9d 86   42 Cited 42 times in Scopus42 0
Shekar, Sri Niranjan, Duffy, David L., Montgomery, Grant W. and Martin, Nicholas G. (2006) A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31. Journal of Investigative Dermatology, 126 2: 277-282. doi:10.1038/sj.jid.5700067 73   1 Cited 1 times in Scopus1 0
Hatemi, Peter K., Gillespie, Nathan A., Eaves, Lindon J., Maher, Brion S., Webb, Bradley T., Heath, Andrew C., Medland, Sarah E., Smyth, David C., Beeby, Harry N., Gordon, Scott D., Montgomery, Grant W., Zhu, Ghu, Byrne, Enda M. and Martin, Nicholas G. (2011) A genome-wide analysis of liberal and conservative political attitudes. Journal of Politics, 73 1: 271-285. doi:10.1017/S0022381610001015 111 3 27 Cited 30 times in Scopus30 53
Hysi, Pirro G., Young, Terri L., Mackey, David A., Andrew, Toby, Fernandez-Medarde, Alberto, Solouki, Abbas M., Hewitt, Alex W., Macgregor, Stuart, Vingerling, Johannes R., Li, Yi-Ju, Ikram, M. Kamran, Fai, Lee Yiu, Sham, Pak C., Manyes, Lara, Porteros, Angel, Lopes, Margarida C., Carbonaro, Francis, Fahy, Samantha J., Martin, Nicholas G., van Diujn, Cornelia M., Spector, Timothy D., Rahi, Jugnoo S., Santos, Eugenio, Klaver, Caroline C. W. and Hammond, Christopher J. (2010) A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nature Genetics, 42 10: 902-905. doi:10.1038/ng.664 128   93 Cited 101 times in Scopus101 25
Liu, Fan, van der Lijn, Fedde, Schurmann, Claudia, Zhu, Gu, Chakravarty, M. Mallar, Hysi, Pirro G., Wollstein, Andreas, Lao, Oscar, de Bruijne, Marleen, Ikram, M. Arfan, van der Lugt, Aad, Rivadeneira, Fernando, Uitterlinden, Andre G., Hofman, Albert, Niessen, Wiro J., Homuth, Georg, de Zubicaray, Greig, McMahon, Katie L., Thompson, Paul M., Daboul, Amro, Puls, Ralf, Hegenscheid, Katrin, Bevan, Liisa, Pausova, Zdenka, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J., Wicking, Carol A., Boehringer, Stefan, Spector, Timothy D., Paus, Tomas, Martin, Nicholas G., Biffar, Reiner and Kayser, Manfred for the International Visible Trait Genetics (VisiGen) Consortium (2012) A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans. PLoS Genetics, 8 9: e1002932.1-e1002932.13. doi:10.1371/journal.pgen.1002932 69   48 Cited 50 times in Scopus50 111
Byrne, Enda M., Johnson, Julie, McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Gehrman, Philip R., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Chenevix-Trench, Georgia and Martin, Nicholas G. (2012) A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Sleep, 35 7: 967-975. doi:10.5665/sleep.1962 112 1 6 Cited 6 times in Scopus6 12
Lind, Penelope A., Macgregor, Stuart, Vink, Jacqueline M., Pergadia, Michele L., Hansell, Narelle K., de Moor, Marleen H. M., Smit, August B., Hottenga, Jouke-Jan, Richter, Melinda M., Heath, Andrew C., Martin, Nicholas G., Willemsen, Gonneke, de Geus, Eco J. C., Vogelzangs,Nicole, Penninx, Brenda W., Whitfield, John B., Montgomery, Grant W., Boomsma, Dorret I. and Madden, Pamela A. F. (2010) A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Research And Human Genetics, 13 1: 10-29. doi:10.1375/twin.13.1.10 101   48 Cited 53 times in Scopus53 0
Mosing, Miriam A., Verweij, Karin J. H., Medland, Sarah E., Painter, Jodie, Gordon, Scott D., Heath, Andrew C., Madden, Pamela A., Montgomery, Grant W. and Martin, Nicholas G. (2010) A genome-wide association study of self-rated health. Twin Research and Human Genetics, 13 4: 398-403. doi:10.1375/twin.13.4.398 106   2 Cited 3 times in Scopus3 0
Byrne, Enda M., Gehrman, Philip R., Medland, Sarah E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Hickie, Ian B., Van Duijn, Cornelia M., Henders, Anjali K., Montgomery, Grant W., Martin, Nicholas G., Wray, Naomi R. and The Chronogen Consortium (2013) A genome-wide association study of sleep habits and insomnia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162 5: 439-451. doi:10.1002/ajmg.b.32168 59 53 7 Cited 6 times in Scopus6 3
Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M. and Montgomery, Grant W. (2008) A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism., 93 10: 3965-3970. doi:10.1210/jc.2007-2568 109   28 Cited 27 times in Scopus27 0
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 111   7 Cited 10 times in Scopus10 0
Zhu, Gu, Montgomery, Grant W., James, Michael R., Trent, Jeff M., Hayward, Nicholas K., Martin, Nicholas G. and Duffy, David L. (2007) A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics, 15 1: 94-102. doi:10.1038/sj.ejhg.5201729 102   45 Cited 47 times in Scopus47 0
Luciano, Michelle, Lind, Penelope A., Duffy, David L., Castles, Anne, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2007) A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biological Psychiatry, 62 7: 811-817. doi:10.1016/j.biopsych.2007.03.007 84   53 Cited 53 times in Scopus53 3
Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas G. (2006) A linkage study of academic skills defined by the Queensland Core Skills Test. Behavior Genetics, 36 1: 56-64. doi:10.1007/s10519-005-9013-z 219   14 Cited 12 times in Scopus12 0
Antoniou, Antonis C., Wang, Xianshu, Fredericksen, Zachary S., McGuffog, Lesley, Tarrell, Robert, Sinilnikova, Olga M., Healey, Sue, Morrison, Jonathan, Kartsonaki,Christiana, Lesnick, Timothy, Ghoussaini, Maya, Barrowdale, Daniel, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Eccles, Diana, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Chu, Carol, Douglas, Fiona, Paterson, Joan, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Mazoyer, Sylvie, Giraud, Sophie, Lasset, Christine, Remenieras, Audrey, Caron, Olivier, Hardouin, Agnes, Berthet, Pascaline, Hogervorst, Frans B. L., Rookus, Matti A., Jager, Agnes, van den Ouweland, Ans, Hoogerbrugge, Nicoline, van der Luijt, Rob B., Meijers-Heijboer, Rob B., Gomez Garcia, Encarna B., Devilee, Peter, Vreeswijk, Maaike P. G., Lubinski, Jan, Jakubowska, Anna, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Gorski, Bohdan, Cybulski, Cezary, Spurdle, Amanda B., Holland, Helene, Goldgar, David E., John, Esther M., Hopper, John L., Southey, Melissa, Buys,Saundra S., Daly,Mary B., Terry, Mary-Beth, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Preisler-Adams, Sabine, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy, Blum, Joanne L., Piedmonte, Marion, Rodriguez, Gustavo C., Wakeley, Katie, Boggess, John F., Basil, Jack, Blank, Stephanie V., Friedman, Eitan, Kaufman, Bella, Laitman, Yael, Milgrom, Roni, Andrulism, Irene L., Glendon, Gord, Ozcelik, Hilmi, Kirchhoff, Tomas, Vijai, Joseph, Gaudet, Mia M., Altshuler, David, Guiducci, Candace, Loman, Niklas, Harbst, Katja, Rantala, Johanna, Ehrencrona, Hans, Gerdes, Anne-Marie, Thomassen, Mads, Sunde, Lone, Peterlongo, Paolo, Manoukian, Siranoush, Bonanni, Bernardo, Viel, Alessandra, Radice, Paolo, Caldes, Trinidad, de la Hoya, Miguel, Singer, Christian F., Fink-Retter, Anneliese, Greene,Mark H., L. Mai, Phuong, Loud, Jennifer T., Guidugli, Lucia, Lindor, Noralane M., Hansen, Thomas V. O., Nielsen, Finn C., Blanco, Ignacio, Lazaro,Conxi, Garber, Judy, Ramus, Susan J., Gayther, Simon A., Phelan, Catherine, Narod, Stephen, Szabo, Csilla I ., Benitez, Javier, Osorio, Ana, Nevanlinna,Heli, Heikkinen, Tuomas, Caligo, Maria A., Beattie,Mary S., Hamann,Ute, Godwin, Andrew K., Montagna, Marco, Casella, Cinzie, Neuhausen, Susan L., Karlan, Beth Y., Tung, Nadine, Toland, Amanda E ., Weitzel, Jeffrey, Olopade, Olofunmilayo, Simard, Jacques, Soucy, Penny, Rubinstein, Wendy S., Arason, Adalgeir, Rennert, Gad, Martin, Nicholas G., Montgomery, Grant W., Chang-Claude,Jenny, Flesch-Janys, Dieter, Brauch, Hiltrud, Severi, Gianluca, Baglietto, Laura, Cox, Angela, Cross, Simon S., Miron, Penelope, Gerty, Sue M, Tapper, William, Yannoukakos, Drakoulis, Fountzilas, George, Fasching, Peter A., Beckmann, Matthias W., dos Santos Silva, Isabel, Peto, Julian, Lambrechts, Diether, Paridaens, Robert, Rudiger, Thomas, Forsti, Asta, Winqvist, Robert, Pylkas, Katri, Diasio, Robert B., Lee, Adam M., Eckel-Passow, Jeanette, Vachon, Celine, Blows, Fiona, Driver, Kristy, Dunning, Alison, Pharoah, Paul P. D., Offit, Kenneth, Pankratz, V. Shane, Hakonarson, Hakon, Chenevix-Trench, Georgia, Easton,Douglas F., Couch, Fergus J., EMBRACE, GEMO Study Collaborators, HEBON, kConFab, SWE-BRCA, MOD SQUAD, GENICA, Brown, Melissa, Cummings, Margaret and Lakhani, Sunil (2010) A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population. Nature Genetics, 42 10: 885-892. doi:10.1038/ng.669 233 5 132 Cited 130 times in Scopus130 24
Middelberg, 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.10.1.127 112   10 Cited 11 times in Scopus11 0
Middelberg, Rita P. S., Medland, Sarah E., Martin, Nicholas G. and Whitfield, John B. (2007) A longitudinal genetic study of uric Acid and liver enzymes in adolescent twins. Twin Research and Human Genetics, 10 5: 757-764. doi:10.1375/twin.10.5.757 167   8 Cited 9 times in Scopus9 0
Dennis, Emily L., Jahanshad, Neda, Rudie, Jeffrey D., Brown, Jesse A., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant, Martin, Nicholas G., Wright, Margaret J., Bookheimer, Susan Y., Dapretto, Mirella, Toga, Arthur W. and Thompson, Paul M. (2012) Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2. Brain Connectivity, 1 6: 447-460. doi:10.1089/brain.2011.0064 86 3 4
Hibar, Derrek P., Jahanshad, Neda, Stein, Jason L., Kohannim, Omid, Toga, Arthur W., Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012) Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Twin Research and Human Genetics, 15 3: 286-295. doi:10.1017/thg.2012.15 93   6 Cited 5 times in Scopus5 0
Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Wray, Naomi, Byrne, Enda M., Martin, Nicholas G., Gordon, Scott D., Henders, Anjali K., Montgomery, Grant M. and Nyholt, Dale R. (2013) A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18 4: 497-511. doi:10.1038/mp.2012.21 225   27 Cited 94 times in Scopus94 48
Evangelou, Evangelos, Kerkhos, Hanneke J., Styrkarsdottir, Unnur, Ntzani, Evangelia E., Bos, Steffan D., Esko, Tonu, Evans, Daniel S., Metrustry, Sarah, Panoutsopoulou, Kalliope, Ramos, Yolande F. M., Thorleifsson, Gudmar, Tsilides, Konstantinos K., arcOGEN Consortium, Arden, Nigel, Aslam, Nadim, Bellamy, Nicholas, Birrell, Fraser, Blanco, Francisco J., Carr, Andrew, Chapman, Kay, Day-Williams, Aaron G., Deloukas, Panos, Doherty, Michael, Engstrom, Gunnar, Helgadottir, Hafdis T., Hoffman, Albert, Ingvarsson, Thorvaldur, Jonsson, Helgi, Keis, Aime, Keurentjes, J. Christiaan, Kloppenburg, Margreet, Lind, Penelope A., McCaskie, Andrew, Martin, Nicholas G., Milani, Lili, Montgomery, Grant W., Nelissen, Rob G. H. H., Nevitt, Michael C., Nilsson, Peter M., Ollier, William E. R., Parimi, Netta, Rai, Ashok, Ralston, Stuart H., Reed, Mike R., Riancho, Jose A., Rivadeneira, Fernando, Rodriquez-Fontenla, Christina, Southam, Lorraine, Thorsteinsdottir, Unnar, Tsezou, Aspasia, Wallis, Gillian A., Wilkinson, J. Mark, Gonzales, Antonio, Lane, Nancy E., Lohmander, L. Stefan, Loughlin, John, Metspalu, Andres, Uitterlinden, Andre G., Jonsdottir, Ingileif, Steffansson, Karl, Slagboom, P. Eline, Zeggini, Eleftheria, Meulenbelt, Ingrid, Ioannidis, John P. A., Spector, Tim D., van Meurs, Joyce B. J. and Valdes, Anna M. (2013) A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Annals of the Rheumatic Diseases, Online First 1-7. doi:10.1136/annrheumdis-2012-203114 78   Cited 6 times in Scopus6 8
Do, Kim-Anh, Aitken, Joanne F., Green, Adele C and Martin, Nicholas G. (2004) Analysis of Melanoma Onset: Assessing Familial Aggregation by Using Estimating Equations and Fitting Variance Components via Bayesian Random Effects Models. Twin Research, 7 1: 98-113. doi:10.1375/13690520460741480 76   7 Cited 7 times in Scopus7 0
Siskind, Victor, Whiteman, David C., Aitken, Joanne F., Martin, Nicholas G. and Green, Adele C. (2005) An analysis of risk factors for cutaneous melanoma by anatomical site (Australia). Cancer Causes and Control, 16 3: 193-199. doi:10.1007/s10552-004-4325-5 42   21 Cited 22 times in Scopus22 0
Treloar, Susan A., Cooper, Desmond W., Brennecke, Shaun P., Grehan, Madonna M. and Martin, Nicholas G. (2001) An Australian twin study of the genetic basis of preeclampsia and eclampsia. American Journal of Obstetrics And Gynecology, 184 3: 374-381. doi:10.1067/mob.2001.109400 118   33 Cited 42 times in Scopus42 0
Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Saccone, Nancy L., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2013) ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. JAMA Psychiatry, 70 3: 325-333. doi:10.1001/jamapsychiatry.2013.282 73 3 8 Cited 7 times in Scopus7 1
Hemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014) Another explanation for apparent epistasis Reply. Nature, 514 7520: E5-E6. doi:10.1038/nature13692 9   0 Cited 0 times in Scopus0 12
Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Whiteman, David C., Pharoah, Paul D., Easton, Douglas F., Dunning, Alison M., Newton-Bishop, Julia A., Montgomery, Grant W., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Tsao, Hensin, Trent, Jeffrey M., Fisher, David E., Hayward, Nicholas K. and Brown, Kevin M. (2011) A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 7375: 99-103. doi:10.1038/nature10630 159 3 101 Cited 109 times in Scopus109 11
Wray, 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.64.3.318 103   26 Cited 31 times in Scopus31 3
Morley, Katherine I., Medland, Sarah E., Ferreira, Manuel A. R., Lynskey, Michael T., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2006) A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families. Behavior Genetics, 36 1: 87-99. doi:10.1007/s10519-005-9004-0 128   21 Cited 21 times in Scopus21 0
Byrne, Edna M., Carrillo-Roa, Tania, Penninx, Brenda W. J. H., Sallis, Hannah M., Viktorin, Alexander, Chapman, Brett, Henders, Anjali K., Pergadia, Michele L., Heath, Andrew C., Madden, Pamela A. F., Sullivan, Patrick F., Boschloo, Lynn, van Grootheest, Gerard, McMahon, George, Lawlor, Debbie A., Landen, Mikael, Lichtenstein, Paul, Magnusson, Patrik K. E., Evans, David M., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G., Meltzer-Brody, Samantha and Wray, Naomi R. (2014) Applying polygenic risk scores to postpartum depression. Archives of Women's Mental Health, 17 6: 519-528. doi:10.1007/s00737-014-0428-5 31   0 Cited 1 times in Scopus1 7
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 48 2 6 Cited 5 times in Scopus5 0
Ferreira, Manuel A. R., Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2006) A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits. European Journal of Human Genetics, 14 8: 953-962. doi:10.1038/sj.ejhg.5201646 59   7 Cited 7 times in Scopus7 0
Sturm, Richard A., Duffy, David L., Zhao, Zhen Zhen, Leite, Fabio P.N., Stark, Mitchell S., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2008) A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour. The American Journal of Human Genetics, 82 2: 424-431. doi:10.1016/j.ajhg.2007.11.005 85   132 Cited 137 times in Scopus137 16
Aoude, Lauren G., Xu, Mai, Zhao, Zhen Zhen, Kovacs, Michael, Palmer, Jane M., Johansson, Peter, Symmons, Judith, Trent, Jeffrey M., Martin, Nicholas G., Montgomery, Grant W., Brown, Kevin M. and Hayward, Nicholas K. (2014) Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One, 9 6: e100683-e100683. doi:10.1371/journal.pone.0100683 24   1 Cited 0 times in Scopus0 2
Elizabeth K Speliotes, Cristen J Willer, Sonja I Berndt, Keri L Monda, Gudmar Thorleifsson, Anne U Jackson, Hana Lango Allen, Cecilia M Lindgren, Jian'an Luan, Reedik Magi, Joshua C Randall, Sailaja Vedantam, Thomas W Winkler, Lu Qi, Tsegaselassie Workalemahu, Iris M Heid, Valgerdur Steinthorsdottir, Heather M Stringham, Michael N Weedon, Eleanor Wheeler, Andrew R Wood, Teresa Ferreira, Robert J Weyant, Ayellet V Segre, Karol Estrada, Liming Liang, James Nemesh, Ju-Hyun Park, Stefan Gustafsson, Tuomas O Kilpelainen, Jian Yang, Nabila Bouatia-Naji, Tonu Esko, Mary F Feitosa, Zoltan Kutalik, Massimo Mangino, Soumya Raychaudhuri, Andre Scherag, Albert Vernon Smith, Ryan Welch, Jing Hua Zhao, Katja K Aben, Devin M Absher, Najaf Amin, Anna L Dixon, Eva Fisher, Nicole L Glazer, Michael E Goddard, Nancy L Heard-Costa, Volker Hoesel, Jouke-Jan Hottenga, Asa Johansson, Toby Johnson, Shamika Ketkar, Claudia Lamina, Shengxu Li, Miriam F Moffatt, Richard h Myers, Narisu Narisu, John R B Perry, 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