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Results 21-30 of 333 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2019Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionGuo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
2018Protocol for the Lactoferrin Infant Feeding Trial (LIFT): a randomised trial of adding lactoferrin to the feeds of very-low birthweight babies prior to hospital dischargeMartin, A.; Ghadge, A.; Manzoni, P.; Lui, K.; Brown, R.; Tarnow-Mordi, W.; Lu, K.; Simes, J.; Hague, W.; Osborn, D.; Deshpande, G.; Kochar, A.; Lewis, T.; Watkins, A.; Pritchard, M.; Schofield, D.; Mohamed, A.L.; Soll, R.; Darlow, B.; Isaacs, D.; et al.
2018Paritaprevir, ritonavir, ombitasvir, and dasabuvir with and without ribavirin in people with HCV genotype 1 and recent injecting drug use or receiving opioid substitution therapyGrebely, J.; Conway, B.; Cunningham, E.B.; Fraser, C.; Moriggia, A.; Gane, E.; Stedman, C.; Cooper, C.; Castro, E.; Schmid, P.; Petoumenos, K.; Hajarizadeh, B.; Marks, P.; Erratt, A.; Dalgard, O.; Lacombe, K.; Feld, J.J.; Bruneau, J.; Daulouede, J.P.; Powis, J.; et al.
2019Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant dataPatel, R.S.; Schmidt, A.F.; Tragante, V.; McCubrey, R.O.; Holmes, M.; Howe, L.J.; Direk, K.; Akerblom, A.; Leander, K.; Virani, S.S.; Kaminski, K.A.; Muehlschlegel, J.D.; Dube, M.-P.; Allayee, H.; Almgren, P.; Alver, M.; Baranova, E.; Behlouli, H.; Boeckx, B.; Braund, P.S.; et al.
2019Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesiaGorman, K.M.; Meyer, E.; Grozeva, D.; Spinelli, E.; McTague, A.; Sanchis-Juan, A.; Carss, K.J.; Bryant, E.; Reich, A.; Schneider, A.L.; Pressler, R.M.; Simpson, M.A.; Debelle, G.D.; Wassmer, E.; Morton, J.; Sieciechowicz, D.; Jan-Kamsteeg, E.; Paciorkowski, A.R.; King, M.D.; Cross, J.H.; et al.
2017Developing consensus-based priority outcome domains for trials in kidney transplantation: a multinational Delphi Survey with patients, caregivers, and health professionalsSautenet, B.; Tong, A.; Manera, K.; Chapman, J.; Warrens, A.; Rosenbloom, D.; Wong, G.; Gill, J.; Budde, K.; Rostaing, L.; Marson, L.; Josephson, M.; Reese, P.; Pruett, T.; Hanson, C.; O'Donoghue, D.; Tam-Tham, H.; Halimi, J.; Shen, J.; Kanellis, J.; et al.
2019A reciprocal feedback between the PDZ binding kinase and androgen receptor drives prostate cancerWarren, A.; Massie, C.; Watt, K.; Luko, K.; Orafidiya, F.; Selth, L.; Mohammed, H.; Chohan, B.; Menon, S.; Baridi, A.; Zhao, W.; Escriu, C.; Pungsrinont, T.; D Santos, C.; Yang, X.; Taylor, C.; Qureshi, A.; Zecchini, V.; Shaw, G.; Dehm, S.; et al.
2019An essential role for α4A-tubulin in platelet biogenesisStrassel, C.; Magiera, M.M.; Dupuis, A.; Batzenschlager, M.; Hovasse, A.; Pleines, I.; Guéguen, P.; Eckly, A.; Moog, S.; Mallo, L.; Kimmerlin, Q.; Chappaz, S.; Strub, J.-M.; Kathiresan, N.; de la Salle, H.; Van Dorsselaer, A.; Ferec, C.; Py, J.-Y.; Gachet, C.; Schaeffer-Reiss, C.; et al.
2018A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersZhang, M.; Ferrari, R.; Tartaglia, M.C.; Keith, J.; Surace, E.I.; Wolf, U.; Sato, C.; Grinberg, M.; Liang, Y.; Xi, Z.; Dupont, K.; McGoldrick, P.; Weichert, A.; McKeever, P.M.; Schneider, R.; McCorkindale, M.D.; Manzoni, C.; Rademakers, R.; Graff-Radford, N.R.; Dickson, D.W.; et al.
2019ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variantsLuo, X.; Feurstein, S.; Mohan, S.; Porter, C.C.; Jackson, S.A.; Keel, S.; Chicka, M.; Brown, A.L.; Kesserwan, C.; Agarwal, A.; Luo, M.; Li, Z.; Ross, J.E.; Baliakas, P.; Pineda-Alvarez, D.; DiNardo, C.D.; Bertuch, A.A.; Mehta, N.; Vulliamy, T.; Wang, Y.; et al.

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