Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome von Hinds, Heather L., Ashley, Claude T., Sutcliffe, James S., Nelson, David L., Warren, Stephen T., Housman, David E., Schalling, Martin

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Essential Function of α-Calcium/Calmodulin-Dependent Protein Kinase II in Neurotransmitter Release at a Glutamatergic Central Synapse von Hinds, Heather L., Goussakov, Ivan, Nakazawa, Kazu, Tonegawa, Susumu, Bolshakov, Vadim Y.

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Clonal analysis of human tumors with M27β, a highly informative polymorphic X chromosomal probe von FEY, M. F, PETER, H.-J, HINDS, H. L, ZIMMERMANN, A, LIECHTI-GALLATI, S, GERBER, H, STUDER, H, TOBLER, A

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CA1 long-term potentiation is diminished but present in hippocampal slices from alpha-CaMKII mutant mice von Hinds, H L, Tonegawa, S, Malinow, R

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Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif von Hinds, Heather L., Hendriks, Rudolf W., Craig, Ian W., Chen, Zheng-Yi

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Currents in Contemporary Ethics: Pediatric Obesity: Ethical Dilemmas in Treatment and Prevention von Hinds, Heather L.

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Magnetic Trapping and Coherent Control of Laser-Cooled Molecules von Williams, H J, Caldwell, L, Fitch, N J, Truppe, S, Rodewald, J, Hinds, E A, Sauer, B E, Tarbutt, M R

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Novel associations for hypothyroidism include known autoimmune risk loci von Eriksson, Nicholas, Tung, Joyce Y, Kiefer, Amy K, Hinds, David A, Francke, Uta, Mountain, Joanna L, Do, Chuong B

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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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Molecules cooled below the Doppler limit von Truppe, S., Williams, H. J., Hambach, M., Caldwell, L., Fitch, N. J., Hinds, E. A., Sauer, B. E., Tarbutt, M. R.

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Characteristics of a magneto-optical trap of molecules von Williams, H J, Truppe, S, Hambach, M, Caldwell, L, Fitch, N J, Hinds, E A, Sauer, B E, Tarbutt, M R

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Identification of 15 genetic loci associated with risk of major depression in individuals of European descent von Hyde, Craig L, Nagle, Michael W, Tian, Chao, Chen, Xing, Paciga, Sara A, Wendland, Jens R, Tung, Joyce Y, Hinds, David A, Perlis, Roy H, Winslow, Ashley R

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Coherent characterisation of a single molecule in a photonic black box von Boissier, Sebastien, Schofield, Ross C., Jin, Lin, Ovvyan, Anna, Nur, Salahuddin, Koppens, Frank H. L., Toninelli, Costanza, Pernice, Wolfram H. P., Major, Kyle D., Hinds, E. A., Clark, Alex S.

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Retraction Note: PPARδ binding to heme oxygenase 1 promoter prevents angiotensin II-induced adipocyte dysfunction in Goldblatt hypertensive rats von Sodhi, K., Puri, N., Kim, D. H., Hinds, T. D., Stechschulte, L. A., Favero, G., Rodella, L., Shapiro, J. I., Jude, D., Abraham, N. G.

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Effects of in utero delta-9-tetrahydrocannabinol (THC) exposure on fetal and infant musculoskeletal development in a preclinical nonhuman primate model von Moellmer, Samantha A, Hagen, Olivia L, Farhang, Parsa A, Duke, Victoria R, Fallon, Meghan E, Hinds, Monica T, McCarty, Owen J T, Lo, Jamie O, Nakayama, Karina H

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Genetic Associations with Gestational Duration and Spontaneous Preterm Birth von Zhang, Ge, Feenstra, Bjarke, Bacelis, Jonas, Liu, Xueping, Muglia, Lisa M, Juodakis, Julius, Miller, Daniel E, Litterman, Nadia, Jiang, Pan-Pan, Russell, Laura, Hinds, David A, Hu, Youna, Weirauch, Matthew T, Chen, Xiaoting, Chavan, Arun R, Wagner, Günter P, Pavličev, Mihaela, Nnamani, Mauris C, Maziarz, Jamie, Karjalainen, Minna K, Rämet, Mika, Sengpiel, Verena, Geller, Frank, Boyd, Heather A, Palotie, Aarno, Momany, Allison, Bedell, Bruce, Ryckman, Kelli K, Huusko, Johanna M, Forney, Carmy R, Kottyan, Leah C, Hallman, Mikko, Teramo, Kari, Nohr, Ellen A, Davey Smith, George, Melbye, Mads, Jacobsson, Bo, Muglia, Louis J

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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N., Lee, James J., Kong, Augustine, Yengo, Loic, Cesarini, David, Turley, Patrick, Visscher, Peter M., Beauchamp, Jonathan P., Benjamin, Daniel J., Young, Alexander I.

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Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways von Jansen, Philip R., Watanabe, Kyoko, Stringer, Sven, Skene, Nathan, Bryois, Julien, Hammerschlag, Anke R., de Leeuw, Christiaan A., Benjamins, Jeroen S., Muñoz-Manchado, Ana B., Nagel, Mats, Savage, Jeanne E., Tiemeier, Henning, White, Tonya, Tung, Joyce Y., Hinds, David A., Vacic, Vladimir, Wang, Xin, Sullivan, Patrick F., van der Sluis, Sophie, Polderman, Tinca J. C., Smit, August B., Hjerling-Leffler, Jens, Van Someren, Eus J. W., Posthuma, Danielle

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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways von Nagel, Mats, Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, de Leeuw, Christiaan A., Bryois, Julien, Savage, Jeanne E., Hammerschlag, Anke R., Skene, Nathan G., Muñoz-Manchado, Ana B., White, Tonya, Tiemeier, Henning, Linnarsson, Sten, Hjerling-Leffler, Jens, Polderman, Tinca J. C., Sullivan, Patrick F., van der Sluis, Sophie, Posthuma, Danielle

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Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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