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Results 71-80 of 88 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2008Estimating the ancestral recombinations graph (ARG) as compatible networks of SNP patternsParida, L.; Mele, M.; Calafell, F.; Bertranpetit, J.; Schurr, T.; Santos, F.; Quintana-Murci, L.; Comas, D.; Tyler-Smith, C.; Zalloua, P.; Balanovska, E.; Balanovsky, O.; Behar, D.; Mitchell, R.; Jin, L.; Soodyall, H.; Pitchappan, R.; Cooper, A.; Royyuru, A.; Rosset, S.; et al.; Cooper, Alan
2007A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyCavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.
2015A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adultsPerez-Andreu, V.; Roberts, K.; Xu, H.; Smith, C.; Zhang, H.; Yang, W.; Harvey, R.; Payne-Turner, D.; Devidas, M.; Cheng, I.; Carroll, W.; Heerema, N.; Carroll, A.; Raetz, E.; Gastier-Foster, J.; Marcucci, G.; Bloomfield, C.; Mrozek, K.; Kohlschmidt, J.; Stock, W.; et al.
2018Genome-wide association study of intraocular pressure uncovers new pathways to glaucomaMacGregor, S.; Ong, J.; An, J.; Han, X.; Zhou, T.; Siggs, O.; Law, M.; Souzeau, E.; Sharma, S.; Lynn, D.; Beesley, J.; Sheldrick, B.; Mills, R.; Landers, J.; Ruddle, J.; Graham, S.; Healey, P.; White, A.; Casson, R.; Best, S.; et al.
2010Genome-wide pharmacogenetics of antidepressant response in the GENDEP projectUher, R.; Perroud, N.; Ng, M.; Hauser, J.; Henigsberg, N.; Maier, W.; Mors, O.; Placentino, A.; Rietschel, M.; Souery, D.; Zagar, T.; Czerski, P.; Jerman, B.; Larsen, E.; Schulze, T.; Zobel, A.; Cohen-Woods, S.; Pirlo, K.; Butler, A.; Muglia, P.; et al.
2011Genomewide association scan of suicidal thoughts and behaviour in major depressionSchosser, A.; Butler, A.; Ising, M.; Perroud, N.; Uher, R.; Ng, M.; Cohen-Woods, S.; Craddock, N.; Owen, M.; Korszun, A.; Jones, L.; Jones, I.; Gill, M.; Rice, J.; Maier, W.; Mors, O.; Rietschel, M.; Lucae, S.; Binder, E.; Preisig, M.; et al.; Domschke, K.
2008The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4610 cases amongst 18637 participantsLawlor, D.; Harbord, R.; Timpson, N.; Lowe, G.; Rumley, A.; Gaunt, T.; Baker, I.; Yarnell, J.; Kivimaki, M.; Kumari, M.; Norman, P.; Jamrozik, K.; Hankey, G.; Almeida, O.; Flicker, L.; Warrington, N.; Marmot, M.; Ben-Shlomo, Y.; Palmer, L.; Day, I.; et al.; Keavney, B.

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