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Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi et al (show 64 more authors) , Watson, Nathaniel F, Melville, Scott A, Del Greco, Fabiola M, Byrne, Enda M, Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S, Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A, Zgaga, Lina, Mihailov, Evelin, Stone, Katie L, Campbell, Harry, Brouwer, Rutger Ww, Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D, Campbell, Susan, Borovecki, Fran, Luik, Annemarie I, Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E, van den Hout, Mirjam CGN, Cummings, Steven R, Aulchenko, Yuru S, Gehrman, Philip R, Uitterlinden, Andre G, Wichmann, Heinz-Erich, Muller-Nurasyid, Martina, Fehrmann, Rudolf SN, Montgomery, Grant W, Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A, Wright, Alan F, Vink, Jacqueline M, Wilson, James F, Pramstaller, Peter P, Hicks, Andrew A, Polasek, Ozren, Punjabi, Naresh M, Redline, Susan, Psaty, Bruce M, Heath, Andrew C, Merrow, Martha, Tranah, Gregory J, Gottlieb, Daniel J, Boomsma, Dorret I, Martin, Nicholas G, Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred FJ, Penninx, Brenda W, Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till and van Duijn, Cornelia M (2016) Genetic variants in <i>RBFOX3</i> are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). pp. 1488-1495.

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Stanton, Chloe M, Borooah, Shyamanga, Drake, Camilla, Marsh, Joseph A, Campbell, Susan, Lennon, Alan, Soares, Dinesh C, Vallabh, Neeru A ORCID: 0000-0002-0109-4112, Sahni, Jayashree, Cideciyan, Artur V et al (show 5 more authors) , Dhillon, Baljean, Vitart, Veronique, Jacobson, Samuel G, Wright, Alan F and Hayward, Caroline (2017) Novel pathogenic mutations in <i>C1QTNF5</i> support a dominant negative disease mechanism in late-onset retinal degeneration. SCIENTIFIC REPORTS, 7 (1). 12147-.