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PreviewIssue DateTitleAuthor(s)
2020The EMT modulator SNAI1 contributes to AML pathogenesis via its interaction with LSD1Carmichael, C.L.; Wang, J.; Nguyen, T.; Kolawole, O.; Benyoucef, A.; De Mazière, C.; Milne, A.R.; Samuel, S.; Gillinder, K.; Hediyeh-Zadeh, S.; Vo, A.N.Q.; Huang, Y.; Knezevic, K.; McInnes, W.R.L.; Shields, B.J.; Mitchell, H.; Ritchie, M.E.; Lammens, T.; Lintermans, B.; Van Vlierberghe, P.; et al.
2020Septum resection in women with a septate uterus: a cohort studyRikken, J.F.; Verhorstert, K.W.; Emanuel, M.H.; Kuchenbecker, W.K.; Jansen, F.W.; Torrenga, B.; Schols, W.A.; Verhoeve, H.R.; Hoek, A.; Clark, T.J.; Stephenson, M.; Mol, B.W.; Van der Veen, F.; Van Wely, M.; Goddijn, M.; Bongers, M.Y.; van der Steeg, J.W.; Janssen, I.A.H.; Kapiteijn, K.; Torrance, H.L.; et al.; 35th Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology (ESHRE) as punlished in Human reproduction (24 Jun 2019 - 26 Jun 2019 : Vienna, AUSTRIA)
2020Evaluation of DNA methylation episignatures for diagnosis and phenotype correlations in 42 mendelian neurodevelopmental disordersAref-Eshghi, E.; Kerkhof, J.; Pedro, V.P.; Barat-Houari, M.; Ruiz-Pallares, N.; Andrau, J.C.; Lacombe, D.; Van-Gils, J.; Fergelot, P.; Dubourg, C.; Cormier-Daire, V.; Rondeau, S.; Lecoquierre, F.; Saugier-Veber, P.; Nicolas, G.; Lesca, G.; Chatron, N.; Sanlaville, D.; Vitobello, A.; Faivre, L.; et al.
2020Genetic history from the Middle Neolithic to present on the Mediterranean island of SardiniaMarcus, J.H.; Posth, C.; Ringbauer, H.; Lai, L.; Skeates, R.; Sidore, C.; Beckett, J.; Furtwängler, A.; Olivieri, A.; Chiang, C.W.K.; Al-Asadi, H.; Dey, K.; Joseph, T.A.; Liu, C.-C.; Der Sarkissian, C.; Radzevičiūtė, R.; Michel, M.; Gradoli, M.G.; Marongiu, P.; Rubino, S.; et al.
2020ENIGMA MDD: seven years of global neuroimaging studies of major depression through worldwide data sharingSchmaal, L.; Pozzi, E.; C Ho, T.; van Velzen, L.S.; Veer, I.M.; Opel, N.; Van Someren, E.J.W.; Han, L.K.M.; Aftanas, L.; Aleman, A.; Baune, B.T.; Berger, K.; Blanken, T.F.; Capitão, L.; Couvy-Duchesne, B.; R Cullen, K.; Dannlowski, U.; Davey, C.; Erwin-Grabner, T.; Evans, J.; et al.
2020RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLBrown, A.L.; Arts, P.; Carmichael, C.L.; Babic, M.; Dobbins, J.; Chong, C.-E.; Schreiber, A.W.; Feng, J.; Phillips, K.; Wang, P.P.S.; Ha, T.; Homan, C.C.; King-Smith, S.L.; Rawlings, L.; Vakulin, C.; Dubowsky, A.; Burdett, J.; Moore, S.; McKavanagh, G.; Henry, D.; et al.
2020An investigation of antihypertensive class, dementia, and cognitive declinePeters, R.; Yasar, S.; Anderson, C.S.; Andrews, S.; Antikainen, R.; Arima, H.; Beckett, N.; Beer, J.C.; Bertens, A.S.; Booth, A.; van Boxtel, M.; Brayne, C.; Brodaty, H.; Carlson, M.C.; Chalmers, J.; Corrada, M.; DeKosky, S.; Derby, C.; Dixon, R.A.; Forette, F.; et al.
2020The genetic architecture of the human cerebral cortexGrasby, K.L.; Jahanshad, N.; Painter, J.N.; Colodro-Conde, L.; Bralten, J.; Hibar, D.P.; Lind, P.A.; Pizzagalli, F.; Ching, C.R.K.; McMahon, M.A.B.; Shatokhina, N.; Zsembik, L.C.P.; Thomopoulos, S.I.; Zhu, A.H.; Strike, L.T.; Agartz, I.; Alhusaini, S.; Almeida, M.A.A.; Alnæs, D.; Amlien, I.K.; et al.
2021ELOVL5 is a critical and targetable fatty acid elongase in prostate cancerCentenera, M.M.; Scott, J.S.; Machiels, J.; Nassar, Z.D.; Miller, D.C.; Zininos, I.; Dehairs, J.; Burvenich, I.J.G.; Zadra, G.; Chetta, P.; Bango, C.; Evergren, E.; Ryan, N.K.; Gillis, J.L.; Mah, C.Y.; Tieu, T.; Hanson, A.R.; Carelli, R.; Bloch, K.; Panagopoulos, V.; et al.
2021Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")Kirk, E.P.; Ong, R.; Boggs, K.; Hardy, T.; Righetti, S.; Ben, K.; Roscioli, T.; Amor, D.J.; Bakshi, M.; Chung, C.W.T.; Colley, A.; Jamieson, R.; Liebelt, J.; Ma, A.; Pachter, N.; Rajagopalan, S.; Ravine, A.; Wilson, M.; Caruana, J.; Casella, R.; et al.