Fluoroquinolone and Macrolide Resistance-Associated Mutations in Mycoplasma genitalium von Tagg, Kaitlin A, Jeoffreys, Neisha J, Couldwell, Deborah L, Donald, Jennifer A, Gilbert, Gwendolyn L

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Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26 von McAuley, Erica Z, Scimone, Anna, Tiwari, Yash, Agahi, Giti, Mowry, Bryan J, Holliday, Elizabeth G, Donald, Jennifer A, Weickert, Cynthia Shannon, Mitchell, Phillip B, Schofield, Peter R, Fullerton, Janice M

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Common patterns in 558 diagnostic radiology errors von Donald, Jennifer J, Barnard, Stuart A

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Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy: A Genome-Wide Analysis von CHIU, Christine, BAGNALL, Richard D, INGLES, Jodie, YEATES, Laura, KENNERSON, Marina, DONALD, Jennifer A, JORMAKKA, Mika, LIND, Joanne M, SEMSARIAN, Christopher

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Utility of FDG PET‐CT in CT Stage IA non‐small cell lung cancer: The New Zealand Te Whatu Ora Northern region experience von Kelly, Richard J, Anderson, Graeme D, Joshi, Budresh S, Donald, Jennifer J

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Predicting outcomes following cognitive behaviour therapy in child anxiety disorders: the influence of genetic, demographic and clinical information von Hudson, Jennifer L., Lester, Kathryn J., Lewis, Cathryn M., Tropeano, Maria, Creswell, Cathy, Collier, David A., Cooper, Peter, Lyneham, Heidi J., Morris, Talia, Rapee, Ronald M., Roberts, Susanna, Donald, Jennifer A., Eley, Thalia C.

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Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease von Roscioli, Tony, Cliffe, Simon T, Bloch, Donald B, Bell, Christopher G, Mullan, Glenda, Taylor, Peter J, Sarris, Maria, Wang, Joanne, Donald, Jennifer A, Kirk, Edwin P, Ziegler, John B, Salzer, Ulrich, McDonald, George B, Wong, Melanie, Lindeman, Robert, Buckley, Michael F

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Two-Dimensional Genome Scan Identifies Multiple Genetic Interactions in Bipolar Affective Disorder von Fullerton, Janice M, Donald, Jennifer A, Mitchell, Philip B, Schofield, Peter R

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A Novel Approach to the Assessment of Variations in the Human Platelet Count von Buckley, Michael F., James, John W., Brown, Dianne E., Whyte, Gordon S., Dean, Mark G., Chesterman, Colin N., Donald, Jennifer A.

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Low genetic variation in cold tolerance linked to species distributions in butterflies von Davis, Jonathan M. P, van Heerwaarden, Belinda, Sgrò, Carla M, Donald, Jennifer A, Kemp, Darrell J

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Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy von Chiu, Christine, BSc, Bagnall, Richard D., PhD, Ingles, Jodie, BBioMedSc, Yeates, Laura, BSc, Kennerson, Marina, PhD, Donald, Jennifer A., PhD, Jormakka, Mika, PhD, Lind, Joanne M., PhD, Semsarian, Christopher, MBBS, PhD

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Randomized controlled trial of Gastrografin in adhesive small bowel obstruction von Burge, Jonathan, Abbas, Saleh M., Roadley, Graeme, Donald, Jennifer, Connolly, Andrew, Bissett, Ian P., Hill, Andrew G.

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Patent Foramen Ovale Closure or Antiplatelet Therapy for Cryptogenic Stroke von Søndergaard, Lars, Kasner, Scott E, Rhodes, John F, Andersen, Grethe, Iversen, Helle K, Nielsen-Kudsk, Jens E, Settergren, Magnus, Sjöstrand, Christina, Roine, Risto O, Hildick-Smith, David, Spence, J. David, Thomassen, Lars

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Association between the serotonin 2A receptor gene and bipolar affective disorder in an Australian cohort von McAuley, Erica Z, Fullerton, Janice M, Blair, Ian P, Donald, Jennifer A, Mitchell, Philip B, Schofield, Peter R

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Genome screen of 15 Australian bipolar affective disorder pedigrees supports previously identified loci for bipolar susceptibility genes von Fullerton, Janice M, Liu, Zhixin, Badenhop, Renee F, Scimone, Anna, Blair, Ian P, Van Herten, Mary, Donald, Jennifer A, Mitchell, Philip B, Schofield, Peter R

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Genome-wide Linkage Analysis Identifies α-Actinin-2 as a Causative Gene in Familial Hypertrophic Cardiomyopathy von Chiu, Christine, Lind, Joanne M, Bagnall, Richard D, Ingles, Jodie, Yeates, Laura, Kennerson, Marina, Jormakka, Mika, Donald, Jennifer A, Semsarian, Christopher

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The 10q24-linked split hand/split foot syndrome (SHFM3): Narrowing of the critical region and confirmation of the clinical phenotype von Roscioli, Tony, Taylor, Peter J., Bohlken, Andrew, Donald, Jennifer A., Masel, John, Glass, Ian A., Buckley, Michael F.

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Association analysis of transcripts from the bipolar susceptibility locus on chromosome 4q35, exclusion of a pathogenic role for eight positional candidate genes von Blair, Ian P., Badenhop, Renee F., Scimone, Anna, Moses, Melissa J., Kerr, Nicholas P., Donald, Jennifer A., Mitchell, Philip B., Schofield, Peter R.

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Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35 von Badenhop, Renee F., Moses, Melissa J., Scimone, Anna, Adams, Linda J., Kwok, John B.J., Jones, Anne-Marie, Davison, Gail, Evans, Mary R., Kirkby, Kenneth C., Hewitt, Jane E., Donald, Jennifer A., Mitchell, Philip B., Schofield, Peter R.

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Nonleg Venous Thrombosis in Critically Ill Adults: A Nested Prospective Cohort Study von Lamontagne, Francois, McIntyre, Lauralyn, Dodek, Peter, Heels-Ansdell, Diane, Meade, Maureen, Pemberton, Julia, Skrobik, Yoanna, Seppelt, Ian, Vlahakis, Nicholas E, Muscedere, John, Reece, Graham, Ostermann, Marlies, Padayachee, Soundrie, Alhashemi, Jamal, Walsh, Michael, Lewis, Bradley, Schiff, David, Moody, Alan, Zytaruk, Nicole, LeBlanc, Martine, Cook, Deborah J

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