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Results 21-30 of 32 (Search time: 0.01 seconds).
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PreviewIssue DateTitleAuthor(s)
2018BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosisMcArthur, K.; Whitehead, L.; Heddleston, J.; Li, L.; Padman, B.; Oorschot, V.; Geoghegan, N.; Chappaz, S.; Davidson, S.; Chin, H.; Lane, R.; Dramicanin, M.; Saunders, T.; Sugiana, C.; Lessene, R.; Osellame, L.; Chew, T.; Dewson, G.; Lazarou, M.; Ramm, G.; et al.
2017Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesStessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
2016Clinical and molecular analyses of Beckwith–Wiedemann syndrome: comparison between spontaneous conception and assisted reproduction techniquesTenorio, J.; Romanelli, V.; Martin-Trujillo, A.; Fernández, G.; Segovia, M.; Perandones, C.; Pérez Jurado, L.; Esteller, M.; Fraga, M.; Arias, P.; Gordo, G.; Dapía, I.; Mena, R.; Palomares, M.; Pérez de Nanclares, G.; Nevado, J.; García-Miñaur, S.; Santos-Simarro, F.; Martinez-Glez, V.; Vallespín, E.; et al.
2014Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesBras, J.; Guerreiro, R.; Darwent, L.; Parkkinen, L.; Ansorge, O.; Escott-Price, V.; Hernandez, D.G.; Nalls, M.A.; Clark, L.N.; Honig, L.S.; Marder, K.; Van Der Flier, W.M.; Lemstra, A.; Scheltens, P.; Rogaeva, E.; St George-Hyslop, P.; Londos, E.; Zetterberg, H.; Ortega-Cubero, S.; Pastor, P.; et al.
2019Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorderTrzaskowski, M.; Mehta, D.; Peyrot, W.; Hawkes, D.; Davies, D.; Howard, D.; Kemper, K.; Sidorenko, J.; Maier, R.; Ripke, S.; Mattheisen, M.; Baune, B.; Grabe, H.; Heath, A.; Jones, L.; Jones, I.; Madden, P.; McIntosh, A.; Breen, G.; Lewis, C.; et al.
2018A global cline in a colour polymorphism suggests a limited contribution of gene flow towards the recovery of a heavily exploited marine mammalHoffman, J.; Bauer, E.; Paijmans, A.; Humble, E.; Beckmann, L.; Kubetschek, C.; Christaller, F.; Kröcker, N.; Fuchs, B.; Moreras, A.; Shihlomule, Y.; Bester, M.; Cleary, A.; De Bruyn, P.; Forcada, J.; Goebel, M.; Goldsworthy, S.; Guinet, C.; Hoelzel, A.; Lydersen, C.; et al.
2012Integration of genetics into a systems model of electrocardiographic traits using humanCVD beadchipGaunt, T.; Shah, S.; Nelson, C.; Drenos, F.; Braund, P.; Adeniran, I.; Folkersen, L.; Lawlor, D.; Casas, J.; Amuzu, A.; Kivimaki, M.; Whittaker, J.; Eriksson, P.; Zhang, H.; Hancox, J.; Tomaszewski, M.; Burton, P.; Tobin, M.; Humphries, S.; Talmud, P.; et al.
2011Identification of SOX3 as an XX male sex reversal gene in mice and humansSutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
2017Neanderthal behaviour, diet, and disease inferred from ancient DNA in dental calculusWeyrich, L.; Duchene, S.; Soubrier, J.; Arriola, L.; Llamas, B.; Breen, J.; Morris, A.; Alt, K.; Caramelli, D.; Dresely, V.; Farrell, M.; Farrer, A.; Francken, M.; Gully, N.; Haak, W.; Hardy, K.; Harvati, K.; Held, P.; Holmes, E.; Kaidonis, J.; et al.
2016A method to exploit the structure of genetic ancestry space to enhance case-control studiesBodea, C.; Neale, B.; Ripke, S.; Barclay, M.; Peyrin-Biroulet, L.; Chamaillard, M.; Colombel, J.; Cottone, M.; Croft, A.; D'Incà, R.; Halfvarson, J.; Hanigan, K.; Henderson, P.; Hugot, J.; Karban, A.; Kennedy, N.; Khan, M.; Lémann, M.; Levine, A.; Massey, D.; et al.