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Results 21-30 of 36 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2014Refining analyses of copy number variation identifies specific genes associated with developmental delayCoe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.
2012A genome-wide association meta-analysis identifies new childhood obesity lociBradfield, J.; Taal, H.; Timpson, N.; Scherag, A.; Lecoeur, C.; Warrington, N.; Hypponen, E.; Holst, C.; Valcarcel, B.; Thiering, E.; Salem, R.; Schumacher, F.; Cousminer, D.; Sleiman, P.; Jianhua, Z.; Berkowitz, R.; Vimaleswaran, K.; Ivonne, J.; Pennell, C.; Evans, D.; et al.
2023CRISPR screens identify gene targets at breast cancer risk lociTuano, N.K.; Beesley, J.; Manning, M.; Shi, W.; Perlaza-Jimenez, L.; Malaver-Ortega, L.F.; Paynter, J.M.; Black, D.; Civitarese, A.; McCue, K.; Hatzipantelis, A.; Hillman, K.; Kaufmann, S.; Sivakumaran, H.; Polo, J.M.; Reddel, R.R.; Band, V.; French, J.D.; Edwards, S.L.; Powell, D.R.; et al.
2010Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesElks, C.; Perry, J.; Sulem, P.; Chasman, D.; Franceschini, N.; He, C.; Lunetta, K.; Visser, J.; Byrne, E.; Cousminer, D.; Gudbjartsson, D.; Esko, T.; Feenstra, B.; Hottenga, J.; Koller, D.; Kutalik, Z.; Lin, P.; Mangino, M.; Marongiu, M.; McArdle, P.; et al.
2010Hundreds of variants clustered in genomic loci and biological pathways affect human heightAllen, H.; Estrada, K.; Lettre, G.; Berndt, S.; Weedon, M.; Rivadeneira, F.; Willer, C.; Jackson, A.; Vedantam, S.; Raychaudhuri, S.; Ferreira, T.; Wood, A.; Weyant, R.; Segre, A.; Speliotes, E.; Wheeler, E.; Soranzo, N.; Park, J.-H.; Yang, J.; Gudbjartsson, D.; et al.
2011A genome-wide significant linkage for severe depression on chromosome 3: the depression network studyBreen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
2007Genome wide association study identifies novel breat cancer susceptibility lociEaston, D.; Pooley, K.; Pharoah, P.; Thompson, D.; Ballinger, D.; Struewing, J.; Morrison, J.; Field, H.; Luben, R.; Wareham, N.; Ahmed, S.; Healey, C.; Bowman, R.; Luccarini, C.; Conroy, D.; Shah, M.; Munday, H.; Jordan, C.; Perkins, B.; West, J.; et al.
2007Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control studyCavalleri, G.; Weale, M.; Shianna, K.; Singh, R.; Lynch, J.; Grinton, B.; Szoeke, C.; Murphy, K.; Kinirons, P.; O'Rourke, D.; Ge, D.; Depondt, C.; Claeys, K.; Pandolfo, M.; Gumbs, C.; Walley, N.; McNamara, J.; Mulley, J.; Linney, K.; Sheffield, L.; et al.
2011Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Burdon, K.; MacGregor, S.; Hewitt, A.; Sharma, S.; Chidlow, G.; Mills, R.; Danoy, P.; Casson, R.; Viswanathan, A.; Liu, J.; Landers, J.; Henders, A.; Wood, J.; Souzeau, E.; Crawford, A.; Leo, P.; Wang, J.; Rochtchina, E.; Nyholt, D.; Martin, N.; et al.
2011Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaHahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al.

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