Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.
Nature Genetics
Hysi, Pirro G PG; Cheng, Ching-Yu CY; Springelkamp, Henriët H; Macgregor, Stuart S; Bailey, Jessica N Cooke JNC; Wojciechowski, Robert R; Vitart, Veronique V; Nag, Abhishek A; Hewitt, Alex W AW; Höhn, René R; Venturini, Cristina C; Mirshahi, Alireza A; Ramdas, Wishal D WD; Thorleifsson, Gudmar G; Vithana, Eranga E; Khor, Chiea-Chuen CC; Stefansson, Arni B AB; Liao, Jiemin J; Haines, Jonathan L JL; Amin, Najaf N; Wang, Ya Xing YX; Wild, Philipp S PS; Ozel, Ayse B AB; Li, Jun Z JZ; Fleck, Brian W BW; Zeller, Tanja T; Staffieri, Sandra E SE; Teo, Yik-Ying YY; Cuellar-Partida, Gabriel G; Luo, Xiaoyan X; Allingham, R Rand RR; Richards, Julia E JE; Senft, Andrea A; Karssen, Lennart C LC; Zheng, Yingfeng Y; Bellenguez, Céline C; Xu, Liang L; Iglesias, Adriana I AI; Wilson, James F JF; Kang, Jae H JH; van Leeuwen, Elisabeth M EM; Jonsson, Vesteinn V; Thorsteinsdottir, Unnur U; Despriet, Dominiek D G DDG; Ennis, Sarah S; Moroi, Sayoko E SE; Martin, Nicholas G NG; Jansonius, Nomdo M NM; Yazar, Seyhan S; Tai, E-Shyong ES; Amouyel, Philippe P; Kirwan, James J; van Koolwijk, Leonieke M E LME; Hauser, Michael A MA; Jonasson, Fridbert F; Leo, Paul P; Loomis, Stephanie J SJ; Fogarty, Rhys R; Rivadeneira, Fernando F; Kearns, Lisa L; Lackner, Karl J KJ; de Jong, Paulus T V M PTVM; Simpson, Claire L CL; Pennell, Craig E CE; Oostra, Ben A BA; Uitterlinden, André G AG; Saw, Seang-Mei SM; Lotery, Andrew J AJ; Bailey-Wilson, Joan E JE; Hofman, Albert A; Vingerling, Johannes R JR; Maubaret, Cécilia C; Pfeiffer, Norbert N; Wolfs, Roger C W RCW; Lemij, Hans G HG; Young, Terri L TL; Pasquale, Louis R LR; Delcourt, Cécile C; Spector, Timothy D TD; Klaver, Caroline C W CCW; Small, Kerrin S KS; Burdon, Kathryn P KP; Stefansson, Kari K; Wong, Tien-Yin TY; , ; , ; , ; Viswanathan, Ananth A; Mackey, David A DA; Craig, Jamie E JE; Wiggs, Janey L JL; van Duijn, Cornelia M CM; Hammond, Christopher J CJ; Aung, Tin T
PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals.
Addiction Biology
Nelson, Elliot C EC; Heath, Andrew C AC; Lynskey, Michael T MT; Agrawal, Arpana A; Henders, Anjali K AK; Bowdler, Lisa M LM; Todorov, Alexandre A AA; Madden, Pamela A F PA; Moore, Elizabeth E; Degenhardt, Louisa L; Martin, Nicholas G NG; Montgomery, Grant W GW
SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE