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Preview	Issue Date	Title	Author(s)
	2019	Subsequent event risk in individuals with established coronary heart disease	Patel, R.S.; Tragante, V.; Schmidt, A.F.; McCubrey, R.O.; Holmes, M.V.; Howe, L.J.; Direk, K.; Åkerblom, A.; Leander, K.; Virani, S.S.; Kaminski, K.A.; Muehlschlegel, J.D.; Allayee, H.; Almgren, P.; Alver, M.; Baranova, E.V.; Behloui, H.; Boeckx, B.; Braund, P.S.; Breitling, L.P.; et al.
	2019	Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia	Gorman, 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.
	2019	Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms	Jones, S.E.; Lane, J.M.; Wood, A.R.; van Hees, V.T.; Tyrrell, J.; Beaumont, R.N.; Jeffries, A.R.; Dashti, H.S.; Hillsdon, M.; Ruth, K.S.; Tuke, M.A.; Yaghootkar, H.; Sharp, S.A.; Jie, Y.; Thompson, W.D.; Harrison, J.W.; Dawes, A.; Byrne, E.M.; Tiemeier, H.; Allebrandt, K.V.; et al.
	2019	Meta-analysis of Genomewide Association Studies reveals genetic variants for hip bone geometry	Hsu, Y.H.; Estrada, K.; Evangelou, E.; Ackert-Bicknell, C.; Akesson, K.; Beck, T.; Brown, S.J.; Capellini, T.; Carbone, L.; Cauley, J.; Cheung, C.L.; Cummings, S.R.; Czerwinski, S.; Demissie, S.; Econs, M.; Evans, D.; Farber, C.; Gautvik, K.; Harris, T.; Kammerer, C.; et al.
	2019	A reciprocal feedback between the PDZ binding kinase and androgen receptor drives prostate cancer	Warren, 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.
	2019	‘There's more to a person than what's in front of you’: nursing students’ experiences of consumer taught mental health education	Happell, B.; Waks, S.; Bocking, J.; Horgan, A.; Manning, F.; Greaney, S.; Goodwin, J.; Scholz, B.; van der Vaart, K.J.; Allon, J.; Granerud, A.; Hals, E.; Doody, R.; Russell, S.; Griffin, M.; MacGabhann, L.; Lahti, M.; Ellilä, H.; Pulli, J.; Vatula, A.; et al.
	2019	ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants	Luo, 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.
	2019	Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: an ENIGMA resource to support clinical variant classification	Parsons, M.T.; Tudini, E.; Li, H.; Hahnen, E.; Wappenschmidt, B.; Feliubadaló, L.; Aalfs, C.M.; Agata, S.; Aittomäki, K.; Alducci, E.; Alonso-Cerezo, M.C.; Arnold, N.; Auber, B.; Austin, R.; Azzollini, J.; Balmaña, J.; Barbieri, E.; Bartram, C.R.; Blanco, A.; Blümcke, B.; et al.
	2019	Chromosomal abnormalities and prognosis in NPM1-mutated acute myeloid leukemia: a pooled analysis of individual patient data from nine international cohorts	Angenendt, L.; Röllig, C.; Montesinos, P.; Martínez-Cuadrón, D.; Barragan, E.; García, R.; Botella, C.; Martínez, P.; Ravandi, F.; Kadia, T.; Kantarjian, H.M.; Cortes, J.; Juliusson, G.; Lazarevic, V.; Höglund, M.; Lehmann, S.; Recher, C.; Pigneux, A.; Bertoli, S.; Dumas, P.Y.; et al.
	2019	Suppressing fatty acid uptake has therapeutic effects in preclinical models of prostate cancer	Watt, M.J.; Clark, A.K.; Selth, L.A.; Haynes, V.R.; Lister, N.; Rebello, R.; Porter, L.H.; Niranjan, B.; Whitby, S.T.; Lo, J.; Huang, C.; Schittenhelm, R.B.; Anderson, K.E.; Furic, L.; Wijayaratne, P.R.; Matzaris, M.; Montgomery, M.K.; Papargiris, M.; Norden, S.; Febbraio, M.; et al.