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| | Publication Year | Title | Author(s) |
| 61 | 28-Sep-2014 | Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features. | Lessel, Davor; Vaz, Bruno; Halder, Swagata; Lockhart, Paul J; Marinovic-Terzic, Ivana; Lopez-Mosqueda, Jaime; Philipp, Melanie; Sim, Joe C H; Smith, Katherine R; Oehler, Judith; Cabrera, Elisa; Freire, Raimundo; Pope, Kate; Nahid, Amsha; Norris, Fiona; Leventer, Richard J; Delatycki, Martin B ; Barbi, Gotthold; von Ameln, Simon; Högel, Josef; Degoricija, Marina; Fertig, Regina; Burkhalter, Martin D; Hofmann, Kay; Thiele, Holger; Altmüller, Janine; Nürnberg, Gudrun; Nürnberg, Peter; Bahlo, Melanie; Martin, George M; Aalfs, Cora M; Oshima, Junko; Terzic, Janos; Amor, David John; Dikic, Ivan; Ramadan, Kristijan; Kubisch, Christian |
| 2 | 11-Aug-2014 | A study of up to 12 years of follow-up of Friedreich ataxia utilising four measurement tools. | Tai, Geneieve; Corben, Louise A; Gurrin, Lyle; Yiu, Eppie M; Churchyard, Andrew; Fahey, Michael; Hoare, Brian; Downie, Sharon; Delatycki, Martin B |
| 3 | 2-Jun-2014 | Myelin paucity of the superior cerebellar peduncle in individuals with Friedreich ataxia: an MRI magnetization transfer imaging study. | Corben, Louise A; Kashuk, Saman R; Akhlaghi, Hamed; Jamadar, Sharna; Delatycki, Martin B ; Fielding, Joanne; Johnson, Beth; Georgiou-Karistianis, Nellie; Egan, Gary F |
| 4 | 19-Apr-2014 | Saccade reprogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement. | Hocking, Darren R; Corben, Louise A; Fielding, Joanne; Cremer, Phillip D; Millist, Lynette; White, Owen B; Delatycki, Martin B |
| 5 | 3-Jan-2014 | HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia. | Delatycki, Martin B ; Tai, Geneieve; Corben, Louise A; Yiu, Eppie M; Evans-Galea, Marguerite V; Stephenson, Sarah E M; Gurrin, Lyle; Allen, Katrina J; Lynch, David; Lockhart, Paul J |
| 6 | 20-Nov-2013 | Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening. | Ioannou, Liane; Massie, John; Lewis, Sharon; Collins, Veronica; McClaren, Belinda; Delatycki, Martin B |
| 7 | 9-Oct-2013 | Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. | Wilson, Gabrielle R; Sunley, Jasmine; Smith, Katherine R; Pope, Kate; Bromhead, Catherine J; Fitzpatrick, Elizabeth; Di Rocco, Maja; van Steensel, Maurice; Coman, David J; Leventer, Richard J; Delatycki, Martin B ; Amor, David John; Bahlo, Melanie; Lockhart, Paul J |
| 8 | 12-Sep-2013 | Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research. | Ioannou, Liane; McClaren, Belinda J; Massie, John; Lewis, Sharon; Metcalfe, Sylvia A; Forrest, Laura; Delatycki, Martin B |
| 9 | 1-Feb-2012 | The ethics of screening for disease. | Delatycki, Martin B |
| 10 | 2-Aug-2010 | Ethical considerations in choosing a model for population-based cystic fibrosis carrier screening. | Modra, Lucy J ; Massie, R John; Delatycki, Martin B |
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