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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
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
Zhao, Zhen Zhen, Nyholt, Dale R., James, Michael R., Mayne, Renee, Treloar, Susan A. and Montgomery, Grant W. (2005) A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs. Twin Research and Human Genetics, 8 4: 353-361. doi:10.1375/1832427054936718 130   9 Cited 10 times in Scopus10 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
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
Surakka, Ida, Whitfield, John B., Perola, Markus, Visscher, Peter M., Montgomery, Grant W., Falchi, Mario, Willemsen, Gonneke, de Geus, Eco J. C., Magnusson, Patrik K. E., Christensen, Kaare, Sorensen, Thorild I. A., Pietilainen, Kirsi H., Rantanen, Taina, Silander, Kaisa, Widen, Elisabeth, Muilu, Juhu, Rahman, Iffat, Liljedahl, Ulrika, Syvanen, Ann-Christine, Palotie, Aarno, Kaprio, Jaakko, Kyvik, Kirsten O., Pedersen, Nancy L., Boomsma, Dorret I., Spector, Tim, Martin, Nicolas G., Ripatti, Samuli and Peltonen, Leena (2012) A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Research and Human Genetics, 15 6: 691-699. doi:10.1017/thg.2012.63 83   5 Cited 4 times in Scopus4 1
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
Randall, Louise M., Kenangalem, Enny, Lampah, Daniel A., Tjitra, Emiliana, Mwaikambo, Esther D., Handojo, Tjandra, Piera, Kim A., Zhao, Zhen Zhen, Rivera, Fabian de Labastida, Zhou, Yonghong, McSweeney, Karli M., Le, Lien, Amante, Fiona H., Haque, Ashraful, Stanley, Amanda C., Woodberry, Tonia, Salwati, Ervi, Granger, Donald L., Hobbs, Maurine R., Price, Ric N., Weinberg, J. Brice, Montgomery, Grant W., Anstey, Nicholas M. and Engwerda, Christian R. (2010) Age-related susceptibility to severe malaria associated with galectin-2 in highland Papuans. Journal of Infectious Diseases, 202 1: 117-124. doi:10.1086/653125 76   5 Cited 5 times in Scopus5 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
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
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
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
Lee, 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 38   6 Cited 5 times in Scopus5 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, Marjolein J Peters, Michael Preuss, Samuli Ripatti, Fernando Rivadeneira, Camilla Sandholt, Laura J Scott, Nicholas J Timpson, Jonathan P Tyrer, Sophie van Wingerden, Richard M Watanabe, Charles C White, Fredrik Wiklund, Christina Barlassina, Daniel I Chasman, Matthew N Cooper, John-Olov Jansson, Robert W Lawrence, Niina Pellikka, Inga Prokopenko, Jianxin Shi, Elisabeth Thiering, Helene Alavere, Maria T S Alibrandi, Peter Almgren, Alice M Arnold, Thor Aspelund, Larry D Atwood, Beverley Balkau, Anthony J Balmforth, Amanda J Bennett, Yoav Ben-Shlomo, Richard N Bergman, Sven Bergmann, Heike Biebermann, Alexandra I F Blakemore, Tanja Boes, Lori L Bonnycastle, Stefan R Bornstein, Morris J Brown, Thomas A Buchanan, Fabio Busonero, Harry Campbell, Francesco P Cappuccio, Christine Cavalcanti-Proenca, Yii-Der Ida Chen, Chih-Mei Chen, Peter S Chines, Robert Clarke, Lachlan Coin, John Connell, Ian N M Day, Martin den Heijer, Jubao Duan, Shah Ebrahim, Paul Elliott, Roberto Elosua, Gudny Eiriksdottir, Michael R Erdos, Johan G Eriksson, Maurizio F Facheris, Stephan B Felix, Pamela Fischer-Posovszky, Aaron R Folsom, Nele Friedrich, Nelson B Freimer, Mao Fu, Stefan Gaget, Pablo V Gejman, Eco J C Geus, Christian Gieger, Anette P Gjesing, Anuj Goel, Philippe Goyette, Harald Grallert, Jurgen Grassler, Danielle M Greenawalt, Christopher J Groves, Vilmundur Gudnason, Candace Guiducci, Anna-Liisa Hartikainen, Neelam Hassanali, Alistair S Hall, Aki S Havulinna, Caroline Hayward, Andrew C Heath, Christian Hengstenberg, Andrew A Hicks, Anke Hinney, Albert Hofman, Georg Homuth, Jennie Hui, Wilmar Igl, Carlos Iribarren, Bo Isomaa, Kevin B Jacobs, Ivonne Jarick, Elizabeth Jewell, Ulrich John, Torben Jorgensen, Pekka Jousilahti, Antti Jula, Marika Kaakinen, Eero Kajantie, Lee M Kaplan, Sekar Kathiresan, Johannes Kettunen, Leena Kinnunen, Joshua W Knowles, Ivana Kolcic, Inke R Konig, Seppo Koskinen, Peter Kovacs, Johanna Kuusisto, Peter Kraft, Kirsti Kvaloy, Jaana Laitinen, Olivier Lantieri, Chiara Lanzani, Lenore J Launer, Cecile Lecoeur, Terho Lehtimaki, Guillaume Lettre, Jianjun Liu, Marja-Liisa Lokki, Mattias Lorentzon, Robert N Luben, Barbara Ludwig, The MAGIC (Meta-Analyses of Glucose and Insulin-Related Traits Consortium) investigators, Paolo Manunta, Diana Marek, Michel Marre, Martin, Nicholas G., Wendy L McArdle, Anne McCarthy, Barbara McKnight, Thomas Meitinger, Olle Melander, David Meyre, Kristian Midthjell, Montgomery, Grant W., Mario A Morken, Andrew P Morris, Rosanda Mulic, Julius S Ngwa, Mari Nelis, Matt J Neville, Nyholt, Dale R., Christopher J O'Donnell, Stephen O'Rahilly, Ken K Ong, Ben Oostra, Guillaume Pare, Alex N Parker, Markus Perola, Irene Pichler, Kirsi H Pietilainen, Carl G P Platou, Ozren Polasek, Anneli Pouta, Suzanne Rafelt, Olli Raitakari, Nigel W Rayner, Martin Ridderstrale, Winfried Rief, Aimo Ruokonen, Neil R Robertson, Peter Rzehak, Veikko Salomaa, Alan R Sanders, Manjinder S Sandhu, Serena Sanna, Jouko Saramies, Markku J Savolainen, Susann Scherag, Sabine Schipf, Stefan Schreiber, Heribert Schunkeret, Kaisa Silander, Juha Sinisalo, David S Siscovick, Jan H Smit, Nicole Soranzo, Ulla Sovio, Jonathan Sephens, Ida Surakka, Amy J Swift, Mari-Liis Tammesoo, Jean-Claude Tardif, Maris Teder-Laving, Tanya M Teslovich, John R Thompson, Brian Thomson, Anke Tonjes, Tiinamaija Tuomi, Joyce B J van Meurs, Gert-Jan van Ommen, Vincent Vatin, Jorma Viikari, Sophie Visvikis-Siest, Veronique Vitart, Carla I G Vogel, Benjamin F Voight, Lindsay L Waite, Henri Wallaschofski, G Bragi Walters, Elisabeth Widen, Susanna Wiegand, Sarah H Wild, Gonneke Willemsen, Daniel R Witte, Jacqueline C Witteman, Jianfeng Xu, Qunyuan Zhang, Lina Zgaga, Andreas Ziegler, Paavo Zitting, John P Beilby, I Sadaf Farooqi, Johannes Hebebrand, Heikki V Huikuri, Alan L James, Mika Kahonen, Douglas F Levinson, Fabio Macciardi, Markku S Nieminen, Claes Ohlsson, Lyle J Palmer, Paul M Ridker, Michael Stumvoll, Jacques S Beckmann, Heiner Boeing, Eric 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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 32   0 Cited 35 times in Scopus35 0
Treloar, Susan A., Zhao, Zhen Zhen, Armitage, Trudi, Duffy, David L., Wicks, Jacqueline, O'Connor, Daniel T., Martin, Nicholas G. and Montgomery, Grant W. (2005) Association between polymorphisms in the progesterone receptor gene and endometriosis. Molecular Human Reproduction, 11 9: 641-647. doi:10.1093/molehr/gah221 101 100 21 Cited 23 times in Scopus23 0
Fernández-Rhodes, Lindsay, Demerath, Ellen W., Cousminer, Diana L., Tao, Ran, Dreyfus, Jill G., Esko, Tõnu, Smith, Albert V., Gudnason, Vilmundur, Harris, Tamara B., Launer, Lenore, McArdle, Patrick F., Yerges-Armstrong, Laura M., Elks, Cathy E., Strachan, David P., Kutalik, Zoltán, Vollenweider, Peter, Feenstra, Bjarke, Boyd, Heather A., Metspalu, Andres, Mihailov, Evelin, Broer, Linda, Zillikens, M. Carola, Oostra, Ben, van Duijn, Cornelia M., Lunetta, Kathryn L., Perry, John R. B., Murray, Anna, Koller, Daniel L., Lai, Dongbing, Corre, Tanguy, Toniolo, Daniela, Albrecht, Eva, Stöckl, Doris, Grallert, Harald, Gieger, Christian, Hayward, Caroline, Polasek, Ozren, Rudan, Igor, Wilson, James F., He, Chunyan, Kraft, Peter, Hu, Frank B., Hunter, David J., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Byrne, Enda M., Martin, Nicholas G., Montgomery, Grant W., Warrington, Nicole M., Pennell, Craig E., Stolk, Lisette, Visser, Jenny A., Hofman, Albert, Uitterlinden, André G., Rivadeneira, Fernando, Lin, Peng, Fisher, Sherri L., Bierut, Laura J., Crisponi, Laura, Porcu, Eleonora, Mangino, Massimo, Zhai, Guangju, Spector, Tim D., Buring, Julie E., Rose, Lynda M., Ridker, Paul M., Poole, Charles, Hirschhorn, Joel N., Murabito, Joanne M., Chasman, Daniel I., Widen, Elisabeth, North, Kari E., Ong, Ken K. and Franceschini, Nora (2013) Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. American Journal of Epidemiology, 178 3: 451-460. doi:10.1093/aje/kws473 56   6 Cited 5 times in Scopus5 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., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014) Association of OPRD1 polymorphisms with heroin dependence in a large case-control series. Addiction Biology, 19 1: 111-121. doi:10.1111/j.1369-1600.2012.00445.x 13   7 Cited 3 times in Scopus3 1
Birley, Andrew J., James, Michael R., Dickson, Peter A., Montgomery, Grant W., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2008) Association of the gastric alcohol dehydrogenase gene Adh7 with variation in alcohol metabolism. Human Molecular Genetics, 17 2: 179-189. doi:10.1093/hmg/ddm295 107   21 Cited 22 times in Scopus22 0
Wray, Naomi R., James, Michael R., Handoko, Herlina Y., Dumenil, Troy, Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008) Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression. Psychiatric Genetics, 18 5: 219-225. doi:10.1097/YPG.0b013e3283050aee 5   12 Cited 13 times in Scopus13 0
Wray, Naomi, James, Michael R., Dumenil, Troy, Handoko, Herlina Y., Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008) Association study of candidate variants of COMT with neuroticism, anxiety and depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B 7: 1314-1318. doi:10.1002/ajmg.b.30744 6   28 Cited 29 times in Scopus29 0
Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A. R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006) Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Plos Genetics, 2 3: 316-325. doi:10.1371/journal.pgen.0020041 130 26 177 Cited 146 times in Scopus146 61
Fowler, Elizabeth V., Doecke, James, Simms, Lisa A., Zhao, Zhen Zhen, Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Florin, Timothy H., Montgomery, Grant W., Cavanaugh, Juleen A. and Radford-Smith, Graham L. (2008) ATG16L1 T300A shows strong associations with disease subgroups in a large Australian IBD population: Further support for significant disease heterogeneity. The American Journal of Gastroenterology, 103 10: 2519-2526. doi:10.1111/j.1572-0241.2008.02023.x 98   33 Cited 40 times in Scopus40 0
Medland, 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 98   36 Cited 42 times in Scopus42 1
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.2010.06.009 120 3 216 Cited 214 times in Scopus214 9
James, Michael R., Roth, Richard B., Shi, Michael M., Kammerer, Stefan, Nelson, Matthew R., Stark, Mitchell S., Dumenil, Troy, Montgomery, Grant W., Hayward, Nicholas K., Martin, Nicholas G., Braun, Andreas and Duffy, David L. (2005) BRAF Polymorphisms and Risk of Melanocytic Neoplasia. Journal of Investigative Dermatology, 125 6: 1252-1258. doi:10.1111/j.0022-202X.2005.23937.x 50   16 Cited 17 times in Scopus17 0
Jahanshad, Neda, Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Whitfield, John B., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2012) Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Proceedings of the National Academy of Sciences of USA, 109 14: E851-E859. doi:10.1073/pnas.1105543109 98 1 32 Cited 34 times in Scopus34 17
Valle, Anne, OConnor, Daniel T., Taylor, Palmer, Zhu, Gu, Montgomery, Grant W., Slagboom, P. Eline, Martin, Nicholas G. and Whitfield, John B. (2006) Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity. Clinical Chemistry, 52 6: 1014-1020. doi:10.1373/clinchem.2005.065052 94   34 Cited 37 times in Scopus37 0
Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Changes in Anatomical Brain Connectivity Between Ages 12 and 30: A HARDI Study of 484 Adolescents and Adults. In: 2012 9th IEEE International Symposium on Biomedical Imaging : From Nano to Macro : proceedings. 9th IEEE International Symposium on Biomedical Imaging, Barcelona, Spain, (904-907). 2-5 May 2012. doi:10.1109/ISBI.2012.6235695 97 15 0 Cited 0 times in Scopus0 0
Martin, Nicolas W., Benyamin, Beben, Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011) Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50 1: 55-62.e4. doi:10.1016/j.jaac.2010.10.010 52 1 7 Cited 8 times in Scopus8 9
Perola, 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 101   98 Cited 31 times in Scopus31 0
van Koolwijk, Leonieke M. E., Ramdas, Wishal D., Ikram, M. Kamran, Jansonius, Nomdo M., Pasutto, Francesca, Hysi, Pirro G., Macgregor, Stuart, Janssen, Sarah F., Hewitt, Alex W., Viswanathan, Ananth C., ten Brink, Jacoline B., Hosseini, S. Mohsen, Amin, Najaf, Despriet, Dominiek D. G., Willemse-Assink, Jacqueline J. M., Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S., Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y., Gramer, Eugen, Welge-Luessen, Ulrich, Montgomery, Grant W., Carbonaro, Francis, Young, Terri L., The DCCT/EDIC Research Group, Bellenguez, Celine, McGuffin, Peter, Foster, Paul J., Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y., Czudowska, Monika A., Hofman, Albert, Uitterlinden, Andre G., Wolfs, Roger C. W., de Jong, Paulus T. V. M., Oostra, Ben A., Paterson, Andrew D., Wellcome Trust Case Control Consortium 2, Mackey, David A., Bergen, Arthur A. B., Reis, Andre, Hammond, Christopher J., Vingerling, Johannes R., Lemij, Hans G., Klaver, Caroline C. W., van Duijn, Cornelia M. and Brown, Matthew A. (2012) Common genetic determinants of intraocular pressure and primary open-angle glaucoma. PLoS Genetics, 8 5: e1002611.1-e1002611.13. doi:10.1371/journal.pgen.1002611 57   38 Cited 35 times in Scopus35 2
Nyholt, Dale R., Gillespie, Nathan G., Merikangas, Kathleen R., Treloar, Susan A., Martin, Nicholas G. and Montgomery, Grant W. (2009) Common genetic influences underlie comorbidity of migraine and endometriosis. Genetic Epidemiology, 33 2: 105-113. doi:10.1002/gepi.20361 47   13 Cited 14 times in Scopus14 0
Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010) Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 5: e1000947.1-e1000947.10. doi:10.1371/journal.pgen.1000947 80   47 Cited 51 times in Scopus51 3

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