Urinalysis and the plain abdominal radiograph in the diagnosis of ureteric colic von Shield, Andrew C, Chu, Kevin, Brown, Anthony FT

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Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene von Pearson, Ewan R, Boj, Sylvia F, Steele, Anna M, Barrett, Timothy, Stals, Karen, Shield, Julian P, Ellard, Sian, Ferrer, Jorge, Hattersley, Andrew T

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Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease von Lalaoui, Najoua, Boyden, Steven E., Oda, Hirotsugu, Wood, Geryl M., Stone, Deborah L., Chau, Diep, Liu, Lin, Stoffels, Monique, Kratina, Tobias, Lawlor, Kate E., Zaal, Kristien J. M., Hoffmann, Patrycja M., Etemadi, Nima, Shield-Artin, Kristy, Biben, Christine, Tsai, Wanxia Li, Blake, Mary D., Kuehn, Hye Sun, Yang, Dan, Anderton, Holly, Silke, Natasha, Wachsmuth, Laurens, Zheng, Lixin, Moura, Natalia Sampaio, Beck, David B., Gutierrez-Cruz, Gustavo, Ombrello, Amanda K., Pinto-Patarroyo, Gineth P., Kueh, Andrew J., Herold, Marco J., Hall, Cathrine, Wang, Hongying, Chae, Jae Jin, Dmitrieva, Natalia I., McKenzie, Mark, Light, Amanda, Barham, Beverly K., Jones, Anne, Romeo, Tina M., Zhou, Qing, Aksentijevich, Ivona, Mullikin, James C., Gross, Andrew J., Shum, Anthony K., Hawkins, Edwin D., Masters, Seth L., Lenardo, Michael J., Boehm, Manfred, Rosenzweig, Sergio D., Pasparakis, Manolis, Voss, Anne K., Gadina, Massimo, Kastner, Daniel L., Silke, John

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Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes von Gloyn, Anna L, Pearson, Ewan R, Antcliff, Jennifer F, Proks, Peter, Bruining, G. Jan, Slingerland, Annabelle S, Howard, Neville, Srinivasan, Shubha, Silva, José M.C.L, Molnes, Janne, Edghill, Emma L, Frayling, Timothy M, Temple, I. Karen, Mackay, Deborah, Shield, Julian P.H, Sumnik, Zdenek, van Rhijn, Adrian, Wales, Jerry K.H, Clark, Penelope, Gorman, Shaun, Aisenberg, Javier, Ellard, Sian, Njølstad, Pål R, Ashcroft, Frances M, Hattersley, Andrew T

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Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects von Ellard, Sian, Flanagan, Sarah E., Girard, Christophe A., Patch, Ann-Marie, Harries, Lorna W., Parrish, Andrew, Edghill, Emma L., Mackay, Deborah J.G., Proks, Peter, Shimomura, Kenju, Haberland, Holger, Carson, Dennis J., Shield, Julian P.H., Hattersley, Andrew T., Ashcroft, Frances M.

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Evaluating the benefit of early patient and public involvement for product development and testing with small companies von Hinton, Elanor C., Fenwick, Cameron, Hall, Martin, Bell, Mike, Hamilton‐Shield, Julian P., Gibson, Andrew

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ACE Inhibitors and Statins in Adolescents with Type 1 Diabetes von Marcovecchio, M. Loredana, Chiesa, Scott T, Bond, Simon, Daneman, Denis, Dawson, Sarah, Donaghue, Kim C, Jones, Timothy W, Mahmud, Farid H, Marshall, Sally M, Neil, H. Andrew W, Dalton, R. Neil, Deanfield, John, Dunger, David B

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Secondary Somatic Mutations Restoring RAD51C and RAD51D Associated with Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma von Kondrashova, Olga, Nguyen, Minh, Shield-Artin, Kristy, Tinker, Anna V, Teng, Nelson N H, Harrell, Maria I, Kuiper, Michael J, Ho, Gwo-Yaw, Barker, Holly, Jasin, Maria, Prakash, Rohit, Kass, Elizabeth M, Sullivan, Meghan R, Brunette, Gregory J, Bernstein, Kara A, Coleman, Robert L, Floquet, Anne, Friedlander, Michael, Kichenadasse, Ganessan, O'Malley, David M, Oza, Amit, Sun, James, Robillard, Liliane, Maloney, Lara, Bowtell, David, Giordano, Heidi, Wakefield, Matthew J, Kaufmann, Scott H, Simmons, Andrew D, Harding, Thomas C, Raponi, Mitch, McNeish, Iain A, Swisher, Elizabeth M, Lin, Kevin K, Scott, Clare L

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Developing the 134Ce and 134La pair as companion positron emission tomography diagnostic isotopes for 225Ac and 227Th radiotherapeutics von Bailey, Tyler A., Mocko, Veronika, Shield, Katherine M., An, Dahlia D., Akin, Andrew C., Birnbaum, Eva R., Brugh, Mark, Cooley, Jason C., Engle, Jonathan W., Fassbender, Michael E., Gauny, Stacey S., Lakes, Andrew L., Nortier, Francois M., O’Brien, Ellen M., Thiemann, Sara L., White, Frankie D., Vermeulen, Christiaan, Kozimor, Stosh A., Abergel, Rebecca J.

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A new strategy for vascular complications in young people with type 1 diabetes mellitus von Marcovecchio, M. Loredana, Dalton, R. Neil, Daneman, Denis, Deanfield, John, Jones, Timothy W., Neil, H. Andrew W., Dunger, David B.

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The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype von Hamilton, Alexander J, Bingham, Coralie, McDonald, Timothy J, Cook, Paul R, Caswell, Richard C, Weedon, Michael N, Oram, Richard A, Shields, Beverley M, Shepherd, Maggie, Inward, Carol D, Hamilton-Shield, Julian P, Kohlhase, Jürgen, Ellard, Sian, Hattersley, Andrew T

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Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians von Cho, Yoon Shin, Chen, Chien-Hsiun, Hu, Cheng, Long, Jirong, Hee Ong, Rick Twee, Sim, Xueling, Takeuchi, Fumihiko, Wu, Ying, Go, Min Jin, Yamauchi, Toshimasa, Chang, Yi-Cheng, Kwak, Soo Heon, Ma, Ronald C W, Yamamoto, Ken, Adair, Linda S, Aung, Tin, Cai, Qiuyin, Chang, Li-Ching, Chen, Yuan-Tsong, Gao, Yutang, Hu, Frank B, Kim, Hyung-Lae, Kim, Sangsoo, Kim, Young Jin, Lee, Jeannette Jen-Mai, Lee, Nanette R, Li, Yun, Liu, Jian Jun, Lu, Wei, Nakamura, Jiro, Nakashima, Eitaro, Ng, Daniel Peng-Keat, Tay, Wan Ting, Tsai, Fuu-Jen, Wong, Tien Yin, Yokota, Mitsuhiro, Zheng, Wei, Zhang, Rong, Wang, Congrong, So, Wing Yee, Ohnaka, Keizo, Ikegami, Hiroshi, Hara, Kazuo, Cho, Young Min, Cho, Nam H, Chang, Tien-Jyun, Bao, Yuqian, Hedman, Åsa K, Morris, Andrew P, McCarthy, Mark I, Takayanagi, Ryoichi, Park, Kyong Soo, Jia, Weiping, Chuang, Lee-Ming, Chan, Juliana C N, Maeda, Shiro, Kadowaki, Takashi, Lee, Jong-Young, Wu, Jer-Yuarn, Teo, Yik Ying, Tai, E Shyong, Shu, Xiao Ou, Mohlke, Karen L, Kato, Norihiro, Han, Bok-Ghee, Seielstad, Mark

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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or... von Edghill, Emma L, Flanagan, Sarah E, Patch, Ann-Marie, Boustred, Chris, Parrish, Andrew, Shields, Beverley, Shepherd, Maggie H, Hussain, Khalid, Kapoor, Ritika R, Malecki, Maciej, MacDonald, Michael J, Støy, Julie, Steiner, Donald F, Philipson, Louis H, Bell, Graeme I, Hattersley, Andrew T, Ellard, Sian

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The diagnosis and management of monogenic diabetes in children and adolescents von Hattersley, Andrew, Bruining, Jan, Shield, Julian, Njolstad, Pal, Donaghue, Kim C

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Renal and Cardiovascular Risk According to Tertiles of Urinary Albumin-to-Creatinine Ratio: The Adolescent Type 1 Diabetes Cardio-Renal Intervention Trial (AdDIT) von Marcovecchio, M Loredana, Chiesa, Scott T, Armitage, Jane, Daneman, Denis, Donaghue, Kim C, Jones, Timothy W, Mahmud, Farid H, Marshall, Sally M, Neil, H Andrew W, Dalton, R Neil, Deanfield, John, Dunger, David B

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Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease: A Mendelian Randomization Study von Taylor-Bateman, Victoria, Gill, Dipender, Georgakis, Marios K., Malik, Rainer, Munroe, Patricia, Traylor, Matthew

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Markers of β-Cell Failure Predict Poor Glycemic Response to GLP-1 Receptor Agonist Therapy in Type 2 Diabetes von Jones, Angus G, McDonald, Timothy J, Shields, Beverley M, Hill, Anita V, Hyde, Christopher J, Knight, Bridget A, Hattersley, Andrew T

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Age alone is not a barrier to efficacy of cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for colorectal peritoneal metastases: analysis of 1138 patients from t... von Kelly, Michael E., O’Sullivan, Niall J., Bolger, Jarlath C., Polignano, Francesco, Youssef, Haney, Renehan, Andrew, Malcomson, Lee, Alves, Sue, Cecil, Tom, Mulsow, Jürgen, Moran, Brendan, Mohamed, Faheez

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Early Surgical Therapy for Drug-Resistant Temporal Lobe Epilepsy: A Randomized Trial von Engel, Jerome, McDermott, Michael P, Wiebe, Samuel, Langfitt, John T, Stern, John M, Dewar, Sandra, Sperling, Michael R, Gardiner, Irenita, Erba, Giuseppe, Fried, Itzhak, Jacobs, Margaret, Vinters, Harry V, Mintzer, Scott, Kieburtz, Karl, Early Randomized Surgical Epilepsy Trial (ERSET) Study Group, for the

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Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations von Demirkan, Ayşe, van Duijn, Cornelia M, Ugocsai, Peter, Isaacs, Aaron, Pramstaller, Peter P, Liebisch, Gerhard, Wilson, James F, Johansson, Åsa, Rudan, Igor, Aulchenko, Yurii S, Kirichenko, Anatoly V, Janssens, A Cecile J W, Jansen, Ritsert C, Gnewuch, Carsten, Domingues, Francisco S, Pattaro, Cristian, Wild, Sarah H, Jonasson, Inger, Polasek, Ozren, Zorkoltseva, Irina V, Hofman, Albert, Karssen, Lennart C, Struchalin, Maksim, Floyd, James, Igl, Wilmar, Biloglav, Zrinka, Broer, Linda, Pfeufer, Arne, Pichler, Irene, Campbell, Susan, Zaboli, Ghazal, Kolcic, Ivana, Rivadeneira, Fernando, Huffman, Jennifer, Hastie, Nicholas D, Uitterlinden, Andre, Franke, Lude, Franklin, Christopher S, Vitart, Veronique, Nelson, Christopher P, Preuss, Michael, Bis, Joshua C, O'Donnell, Christopher J, Franceschini, Nora, Witteman, Jacqueline C M, Axenovich, Tatiana, Oostra, Ben A, Meitinger, Thomas, Hicks, Andrew A, Hayward, Caroline, Wright, Alan F, Gyllensten, Ulf, Campbell, Harry, Schmitz, Gerd

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