Clinical Chemistry of Congenic Mice with Quantitative Trait Loci for Predicted Responses to Trypanosoma congolense Infection by Rathkolb, Birgit, Noyes, Harry A, Brass, Andy, Dark, Paul, Fuchs, Helmut, Gailus-Durner, Valérie, Gibson, John, de Angelis, Martin Hrabé, Ogugo, Moses, Iraqi, Fuad, Kemp, Steve J, Naessens, Jan, Pope, Mathew E, Wolf, Eckhard, Agaba, Morris

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Integrating climate change induced flood risk into future population projections by Shu, Evelyn G., Porter, Jeremy R., Hauer, Mathew E., Sandoval Olascoaga, Sebastian, Gourevitch, Jesse, Wilson, Bradley, Pope, Mariah, Melecio-Vazquez, David, Kearns, Edward

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An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14 by Rafehi, Haloom, Read, Justin, Szmulewicz, David J, Davies, Kayli C, Snell, Penny, Fearnley, Liam G, Scott, Liam, Thomsen, Mirja, Gillies, Greta, Pope, Kate, Bennett, Mark F, Munro, Jacob E, Ngo, Kathie J, Chen, Luke, Wallis, Mathew J, Butler, Ernest G, Kumar, Kishore R, Wu, Kathy Hc, Tomlinson, Susan E, Tisch, Stephen, Malhotra, Abhishek, Lee-Archer, Matthew, Dolzhenko, Egor, Eberle, Michael A, Roberts, Leslie J, Fogel, Brent L, Brüggemann, Norbert, Lohmann, Katja, Delatycki, Martin B, Bahlo, Melanie, Lockhart, Paul J

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Ambient Particulate Air Pollution, Heart Rate Variability, and Blood Markers of Inflammation in a Panel of Elderly Subjects by Pope, C. Arden, Hansen, Matthew L., Long, Russell W., Nielsen, Karen R., Eatough, Norman L., Wilson, William E., Eatough, Delbert J.

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An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 by Rafehi, Haloom, Read, Justin, Szmulewicz, David J., Davies, Kayli C., Snell, Penny, Fearnley, Liam G., Scott, Liam, Thomsen, Mirja, Gillies, Greta, Pope, Kate, Bennett, Mark F., Munro, Jacob E., Ngo, Kathie J., Chen, Luke, Wallis, Mathew J., Butler, Ernest G., Kumar, Kishore R., Wu, Kathy HC, Tomlinson, Susan E., Tisch, Stephen, Malhotra, Abhishek, Lee-Archer, Matthew, Dolzhenko, Egor, Eberle, Michael A., Roberts, Leslie J., Fogel, Brent L., Brüggemann, Norbert, Lohmann, Katja, Delatycki, Martin B., Bahlo, Melanie, Lockhart, Paul J.

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Close Observation of Hydraulic Fracturing at EGS Collab Experiment 1: Fracture Trajectory, Microseismic Interpretations, and the Role of Natural Fractures by Fu, Pengcheng, Schoenball, Martin, Ajo‐Franklin, Jonathan B., Chai, Chengping, Maceira, Monica, Morris, Joseph P., Wu, Hui, Knox, Hunter, Schwering, Paul C., White, Mark D., Burghardt, Jeffrey A., Strickland, Christopher E., Johnson, Timothy C., Vermeul, Vince R., Sprinkle, Parker, Roberts, Benjamin, Ulrich, Craig, Guglielmi, Yves, Cook, Paul J., Dobson, Patrick F., Wood, Todd, Frash, Luke P., Huang, Lianjie, Ingraham, Mathew D., Pope, Joseph S., Smith, Megan M., Neupane, Ghanashyam, Doe, Thomas W., Roggenthen, William M., Horne, Roland, Singh, Ankush, Zoback, Mark D., Wang, Herb, Condon, Kate, Ghassemi, Ahmad, Chen, Hao, McClure, Mark W., Vandine, George, Blankenship, Douglas, Kneafsey, Timothy J.

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An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 by Rafehi, Haloom, Read, Justin, Szmulewicz, David J., Davies, Kayli C., Snell, Penny, Fearnley, Liam G., Scott, Liam, Thomsen, Mirja, Gillies, Greta, Pope, Kate, Bennett, Mark F., Munro, Jacob E., Ngo, Kathie J., Chen, Luke, Wallis, Mathew J., Butler, Ernest G., Kumar, Kishore R., Wu, Kathy HC, Tomlinson, Susan E., Tisch, Stephen, Malhotra, Abhishek, Lee-Archer, Matthew, Dolzhenko, Egor, Eberle, Michael A., Roberts, Leslie J., Fogel, Brent L., Brüggemann, Norbert, Lohmann, Katja, Delatycki, Martin B., Bahlo, Melanie, Lockhart, Paul J.

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A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship by Austin, Rachel, Brown, Jaye S., Madelli, Evanthia O., Das, Debjani, Soka, Magdalena, Blue, Gillian M., Atherton, John J., Quinn, Michael C.J., Poplawski, Nicola K., Weintraub, Robert G., De Fazio, Paul, Thompson, Tina, Macciocca, Ivan, Ingles, Jodie, McGaughran, Julie, McLean, Alison, Smyth, Renee, Fatkin, Diane, McNamara, James, Medi, Caroline, Al-Shinnag, Mohammad, Metke, Alejandro, Sy, Raymond, Atherton, John J., Finlay, Keri, Milnes, Di, Austin, Rachel, Milward, Michael, Bagnall, Richard D., Giannoulatou, Eleni, Morrish, Ansley, Taylor, Shelby, Barnett, Chris, Blue, Gillian M., Mountain, Helen, Thompson, Tina, Bodek, Simon, Boggs, Kirsten, Ng, Chai-Ann, Trainer, Alison, Bogwitz, Michael, Haas, Mathilda, Trivedi, Gunjan, Boughtwood, Tiffany, Martinez, Noelia Nunez, Hayward, Janette, Vandenberg, Jamie, Brown, Jaye, Herrera, Carmen, Verma, Kunal, Richardson, Rob Bryson, Hill, Adam, Pachter, Nicholas, Vidgen, Miranda, Patel, Chirag, Vohra, Jitendra, Burns, Charlotte, Perrin, Mark, Cao, Michelle, Horton, Ari E., Perry, Matthew, Howting, Denise, Pflaumer, Andreas, Weintraub, Robert G., Ingles, Jodie, Phillips, Peta, Wilson, Meredith, Chalinor, Heather, Phuong, Thuan, Winlaw, David, Chang, Yuchen, Jackson, Matilda, Worgan, Lisa, Charitou, Theosodia, Jane-Pantaleo, Sarah, Chong, Belinda, Johnson, Renee, Quinn, Michael C.J., Collins, Felicity, Quinn, Michael, Rajagopalan, Sulekha, Cox, Kathy, Kummerfeld, Sarah, Das, Debjani, Davis, Jason, Rogers, Jonathan, Lunke, Sebastian, Sandaradura, Sarah, Dobbins, Julia, Mansour, Julia, Sherburn, Isabella, Dunwoodie, Sally L., Dwyer, Nathan, Mathew, Jacob, Singer, Emma, Elbracht-Leong, Stefanie, Mattiske, Tessa, Smerdon, Carla, Elliott, David, McGaughran, Julie

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Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2 by Sykes, B, Ogilvie, D, Wordsworth, P, Wallis, G, Mathew, C, Beighton, P, Nicholls, A, Pope, F M, Thompson, E, Tsipouras, P

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Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COLIA1 and COLIA2 by Sykes, B, Ogilvie, D, Wordsworth, P, Wallis, G, Mathew, C, Beighton, P, Nicholls, A, Pope, F M, Steinmann, B

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