Mid-term outcomes after total hip arthroplasty in 106 Crowe II/III hips: different hip center positions by Jia, Cheng-Qi, Pan, Hong-Fa, Wu, Yu-Jie, You, Yong-Gang, Cao, Shi-Qi, Zhang, Xue-Song

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A biomimetic gradient porous cage with a micro-structure for enhancing mechanical properties and accelerating osseointegration in spinal fusion by Jia, Cheng-Qi, Zhang, Zhen, Cao, Shi-Qi, Wang, Tian-Jiao, Yu, Hai-Chao, Wang, Wen-Xiang, Guo, Bo-Min, Qiu, Xiong-Ying, You, Yong-Gang, Hu, Fan-Qi, Zhao, Jun, Zhang, Xue-Song

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Reduced microbiome alpha diversity in young patients with ADHD by Prehn-Kristensen, Alexander, Zimmermann, Alexandra, Tittmann, Lukas, Lieb, Wolfgang, Schreiber, Stefan, Baving, Lioba, Fischer, Annegret

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Assessing genetic architecture and signatures of selection of dual purpose Gir cattle populations using genomic information by Maiorano, Amanda Marchi, Lourenco, Daniela Lino, Tsuruta, Shogo, Ospina, Alejandra Maria Toro, Stafuzza, Nedenia Bonvino, Masuda, Yutaka, Filho, Anibal Eugenio Vercesi, Cyrillo, Joslaine Noely Dos Santos Goncalves, Curi, Rogério Abdallah, Silva, Josineudson Augusto Ii de Vasconcelos

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Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease by Escott-Price, Valentina, Harold, Denise, Jones, Lesley, Gerrish, Amy, Vedernikov, Alexey, DeStefano, Anita L, Ibrahim-Verbaas, Carla A, Bis, Joshua C, Grenier-Boley, Benjamin, Russo, Giancarlo, Smith, Albert V, Chouraki, Vincent, Thomas, Charlene, Zelenika, Diana, Kamatani, Yoichiro, Lin, Chiao-Feng, Dunstan, Melanie L, Vronskaya, Maria, Ruiz, Agustin, Bihoreau, Marie-Thérèse, Reitz, Christiane, Pasquier, Florence, Hollingworth, Paul, Hanon, Olivier, Fitzpatrick, Annette L, Becker, Tim, Gudnason, Vilmundur, Amin, Najaf, De Jager, Philip L, Johnston, Janet A, Evans, Denis, Hernández, Isabel, Goate, Alison M, Fiévet, Nathalie, Kamboh, M Ilyas, Keller, Lina, McGuinness, Bernadette, Wallon, David, Love, Seth, Gallacher, John, George-Hyslop, Peter St, Lleo, Alberto, Bayer, Anthony, Tsuang, Debby W, Yu, Lei, Spalletta, Gianfranco, Proitsi, Petra, Sorbi, Sandro, Garcia, Florentino Sanchez, Fox, Nick C, Naranjo, Maria Candida Deniz, Bosco, Paolo, Clarke, Robert, Brayne, Carol, Bonuccelli, Ubaldo, Mancuso, Michelangelo, Moebus, Susanne, Zompo, Maria Del, Maier, Wolfgang, Panza, Francesco, Caffarra, Paolo, Perry, William, Mayhaus, Manuel, Lannfelt, Lars, Pichler, Sabrina, Carrasquillo, Minerva M, Alvarez, Victoria, Valladares, Otto, Hamilton-Nelson, Kara L, Pastor, Pau, Owen, Michael J, Faber, Kelley M, Jonsson, Palmi V, O'Donovan, Michael C, Cantwell, Laura B, Blacker, Deborah, Mead, Simon, Mosley, Jr, Thomas H, de Bruijn, Renee F A G, Passmore, Peter, Brice, Alexis, Morgan, Kevin, Foroud, Tatiana M, Kukull, Walter A, Hannequin, Didier, Powell, John F, Nalls, Michael A, Ritchie, Karen, Kauwe, John S K, Riemenschneider, Matthias, Boada, Mercè, Martin, Eden R, Rujescu, Dan, Tzourio, Christophe, Hofman, Albert, Graff, Caroline, Launer, Lenore J, Van Broeckhoven, Christine, van Duijn, Cornelia M, Seshadri, Sudha

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Replication of association between schizophrenia and chromosome 6p21-6p22.1 polymorphisms in Chinese Han population by Zhang, Yang, Lu, Tianlan, Yan, Hao, Ruan, Yanyan, Wang, Lifang, Zhang, Dai, Yue, Weihua, Lu, Lin

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A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes by Taira, Makiko, Imamura, Minako, Takahashi, Atsushi, Kamatani, Yoichiro, Yamauchi, Toshimasa, Araki, Shin-Ichi, Tanaka, Nobue, van Zuydam, Natalie R, Ahlqvist, Emma, Toyoda, Masao, Umezono, Tomoya, Kawai, Koichi, Imanishi, Masahito, Watada, Hirotaka, Suzuki, Daisuke, Maegawa, Hiroshi, Babazono, Tetsuya, Kaku, Kohei, Kawamori, Ryuzo, Groop, Leif C, McCarthy, Mark I, Kadowaki, Takashi, Maeda, Shiro

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Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants by Winsvold, Bendik S, Bettella, Francesco, Witoelar, Aree, Anttila, Verneri, Gormley, Padhraig, Kurth, Tobias, Terwindt, Gisela M, Freilinger, Tobias M, Frei, Oleksander, Shadrin, Alexey, Wang, Yunpeng, Dale, Anders M, van den Maagdenberg, Arn M J M, Chasman, Daniel I, Nyholt, Dale R, Palotie, Aarno, Andreassen, Ole A, Zwart, John-Anker

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Genome-wide analysis of attention deficit hyperactivity disorder in Norway by Zayats, Tetyana, Athanasiu, Lavinia, Sonderby, Ida, Djurovic, Srdjan, Westlye, Lars T, Tamnes, Christian K, Fladby, Tormod, Aase, Heidi, Zeiner, Pål, Reichborn-Kjennerud, Ted, Knappskog, Per M, Knudsen, Gun Peggy, Andreassen, Ole A, Johansson, Stefan, Haavik, Jan

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Mitochondrial Biomarkers Reflect Semen Quality: Results from the MARCHS Study in Chongqing, China by Zhang, Guowei, Wang, Zhi, Ling, Xi, Zou, Peng, Yang, Huan, Chen, Qing, Zhou, Niya, Sun, Lei, Gao, Jianfang, Zhou, Ziyuan, Cao, Jia, Ao, Lin

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Dopamine genetic risk score predicts depressive symptoms in healthy adults and adults with depression by Pearson-Fuhrhop, Kristin M, Dunn, Erin C, Mortero, Sarah, Devan, William J, Falcone, Guido J, Lee, Phil, Holmes, Avram J, Hollinshead, Marisa O, Roffman, Joshua L, Smoller, Jordan W, Rosand, Jonathan, Cramer, Steven C

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Common genetic variation in the human FNDC5 locus, encoding the novel muscle-derived 'browning' factor irisin, determines insulin sensitivity by Staiger, Harald, Böhm, Anja, Scheler, Mika, Berti, Lucia, Machann, Jürgen, Schick, Fritz, Machicao, Fausto, Fritsche, Andreas, Stefan, Norbert, Weigert, Cora, Krook, Anna, Häring, Hans-Ulrich, de Angelis, Martin Hrabě

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Blood Transcriptomic Markers in Patients with Late-Onset Major Depressive Disorder by Miyata, Shigeo, Kurachi, Masashi, Okano, Yoshiko, Sakurai, Noriko, Kobayashi, Ayumi, Harada, Kenichiro, Yamagata, Hirotaka, Matsuo, Koji, Takahashi, Keisuke, Narita, Kosuke, Fukuda, Masato, Ishizaki, Yasuki, Mikuni, Masahiko

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Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium by Wong, Yee-Ling, Hysi, Pirro, Cheung, Gemmy, Tedja, Milly, Hoang, Quan V, Tompson, Stuart W J, Whisenhunt, Kristina N, Verhoeven, Virginie, Zhao, Wanting, Hess, Moritz, Wong, Chee-Wai, Kifley, Annette, Hosoda, Yoshikatsu, Haarman, Annechien E G, Hopf, Susanne, Laspas, Panagiotis, Sensaki, Sonoko, Sim, Xueling, Miyake, Masahiro, Tsujikawa, Akitaka, Lamoureux, Ecosse, Ohno-Matsui, Kyoko, Nickels, Stefan, Mitchell, Paul, Wong, Tien-Yin, Wang, Jie Jin, Hammond, Christopher J, Barathi, Veluchamy A, Cheng, Ching-Yu, Yamashiro, Kenji, Young, Terri L, Klaver, Caroline C W, Saw, Seang-Mei

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Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population by Sakono, Takuto, Meguro, Akira, Takeuchi, Masaki, Yamane, Takahiro, Teshigawara, Takeshi, Kitaichi, Nobuyoshi, Horie, Yukihiro, Namba, Kenichi, Ohno, Shigeaki, Nakao, Kumiko, Sakamoto, Taiji, Sakai, Tsutomu, Nakano, Tadashi, Keino, Hiroshi, Okada, Annabelle A, Takeda, Atsunobu, Ito, Takako, Mashimo, Hisashi, Ohguro, Nobuyuki, Oono, Shinichirou, Enaida, Hiroshi, Okinami, Satoshi, Horita, Nobuyuki, Ota, Masao, Mizuki, Nobuhisa

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Vertical and horizontal genetic connectivity in Chromis verater, an endemic damselfish found on shallow and mesophotic reefs in the Hawaiian Archipelago and adjacent Johnston Atoll by Tenggardjaja, Kimberly A, Bowen, Brian W, Bernardi, Giacomo

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Plasma volume, cell volume, total blood volume and F factor in the tree shrew by Xia, Wei, Huang, Zong-jian, Guo, Zhao-liang, Feng, Yi-wei, Zhang, Chao-yin, He, Guang-yao, Tang, An-zhou

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Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study by de Vries, Paul S, Sabater-Lleal, Maria, Chasman, Daniel I, Trompet, Stella, Ahluwalia, Tarunveer S, Teumer, Alexander, Kleber, Marcus E, Chen, Ming-Huei, Wang, Jie Jin, Attia, John R, Marioni, Riccardo E, Steri, Maristella, Weng, Lu-Chen, Pool, Rene, Grossmann, Vera, Brody, Jennifer A, Venturini, Cristina, Tanaka, Toshiko, Rose, Lynda M, Oldmeadow, Christopher, Mazur, Johanna, Basu, Saonli, Frånberg, Mattias, Yang, Qiong, Ligthart, Symen, Hottenga, Jouke J, Rumley, Ann, Mulas, Antonella, de Craen, Anton J M, Grotevendt, Anne, Taylor, Kent D, Delgado, Graciela E, Kifley, Annette, Lopez, Lorna M, Berentzen, Tina L, Mangino, Massimo, Bandinelli, Stefania, Morrison, Alanna C, Hamsten, Anders, Tofler, Geoffrey, de Maat, Moniek P M, Draisma, Harmen H M, Lowe, Gordon D, Zoledziewska, Magdalena, Sattar, Naveed, Lackner, Karl J, Völker, Uwe, McKnight, Barbara, Huang, Jie, Holliday, Elizabeth G, McEvoy, Mark A, Starr, John M, Hysi, Pirro G, Hernandez, Dena G, Guan, Weihua, Rivadeneira, Fernando, McArdle, Wendy L, Slagboom, P Eline, Zeller, Tanja, Psaty, Bruce M, Uitterlinden, André G, de Geus, Eco J C, Stott, David J, Binder, Harald, Hofman, Albert, Franco, Oscar H, Rotter, Jerome I, Ferrucci, Luigi, Spector, Tim D, Deary, Ian J, März, Winfried, Greinacher, Andreas, Wild, Philipp S, Cucca, Francesco, Boomsma, Dorret I, Watkins, Hugh, Tang, Weihong, Ridker, Paul M, Jukema, Jan W, Scott, Rodney J, Mitchell, Paul, Hansen, Torben, O'Donnell, Christopher J, Smith, Nicholas L, Strachan, David P, Dehghan, Abbas

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Cranio-morphometric and aDNA corroboration of the Austronesian dispersal model in ancient Island Southeast Asia: Support from Gua Harimau, Indonesia by Matsumura, Hirofumi, Shinoda, Ken-Ichi, Shimanjuntak, Truman, Oktaviana, Adhi Agus, Noerwidi, Sofwan, Octavianus Sofian, Harry, Prastiningtyas, Dyah, Nguyen, Lan Cuong, Kakuda, Tsuneo, Kanzawa-Kiriyama, Hideaki, Adachi, Noboru, Hung, Hsiao-Chun, Fan, Xuechun, Wu, Xiujie, Willis, Anna, Oxenham, Marc F

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Examining the role of common and rare mitochondrial variants in schizophrenia by Gonçalves, Vanessa F, Giamberardino, Stephanie N, Crowley, James J, Vawter, Marquis P, Saxena, Richa, Bulik, Cynthia M, Yilmaz, Zeynep, Hultman, Christina M, Sklar, Pamela, Kennedy, James L, Sullivan, Patrick F, Knight, Jo

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