Recent advances in understanding the molecular genetic basis of mitochondrial disease von Thompson, Kyle, Collier, Jack J., Glasgow, Ruth I. C., Robertson, Fiona M., Pyle, Angela, Blakely, Emma L., Alston, Charlotte L., Oláhová, Monika, McFarland, Robert, Taylor, Robert W.

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Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement von Perli, Elena, Pisano, Annalinda, Glasgow, Ruth I. C., Carbo, Miriam, Hardy, Steven A., Falkous, Gavin, He, Langping, Cerbelli, Bruna, Pignataro, Maria Gemma, Zacara, Elisabetta, Re, Federica, Della Monica, Paola Lilla, Morea, Veronica, Bonnen, Penelope E., Taylor, Robert W., d’Amati, Giulia, Giordano, Carla

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Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits von Glasgow, Ruth I. C., Thompson, Kyle, Barbosa, Inês A., He, Langping, Alston, Charlotte L., Deshpande, Charu, Simpson, Michael A., Morris, Andrew A. M., Neu, Axel, Löbel, Ulrike, Hall, Julie, Prokisch, Holger, Haack, Tobias B., Hempel, Maja, McFarland, Robert, Taylor, Robert W.

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Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency von Alston, Charlotte L., Heidler, Juliana, Dibley, Marris G., Kremer, Laura S., Taylor, Lucie S., Fratter, Carl, French, Courtney E., Glasgow, Ruth I.C., Feichtinger, René G., Delon, Isabelle, Pagnamenta, Alistair T., Dolling, Helen, Lemonde, Hugh, Aiton, Neil, Bjørnstad, Alf, Henneke, Lisa, Gärtner, Jutta, Thiele, Holger, Tauchmannova, Katerina, Quaghebeur, Gerardine, Houstek, Josef, Sperl, Wolfgang, Raymond, F. Lucy, Prokisch, Holger, Mayr, Johannes A., McFarland, Robert, Poulton, Joanna, Ryan, Michael T., Wittig, Ilka, Henneke, Marco, Taylor, Robert W.

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Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype von Smith, Thomas B, Kopajtich, Robert, Demain, Leigh A M, Rea, Alessandro, Thomas, Huw B, Schiff, Manuel, Beetz, Christian, Joss, Shelagh, Conway, Gerard S, Shukla, Anju, Yeole, Mayuri, Radhakrishnan, Periyasamy, Azzouz, Hatem, Ben Chehida, Amel, Elmaleh-Bergès, Monique, Glasgow, Ruth I C, Thompson, Kyle, Oláhová, Monika, He, Langping, Jenkinson, Emma M, Jahic, Amir, Belyantseva, Inna A, Barzik, Melanie, Urquhart, Jill E, O'Sullivan, James, Williams, Simon G, Bhaskar, Sanjeev S, Carrera, Samantha, Blakes, Alexander J M, Banka, Siddharth, Yue, Wyatt W, Ellingford, Jamie M, Houlden, Henry, Munro, Kevin J, Friedman, Thomas B, Taylor, Robert W, Prokisch, Holger, O'Keefe, Raymond T, Newman, William G

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Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency von Alston, Charlotte L, Heidler, Juliana, Dibley, Marris G, Kremer, Laura S, Taylor, Lucie S, Fratter, Carl, French, Courtney E, Glasgow, Ruth IC, Feichtinger, René G, Delon, Isabelle, Pagnamenta, Alistair T, Dolling, Helen, Lemonde, Hugh, Aiton, Neil, Bjørnstad, Alf, Henneke, Lisa, Gärtner, Jutta, Thiele, Holger, Tauchmannova, Katerina, Quaghebeur, Gerardine, Houstek, Josef, Sperl, Wolfgang, Raymond, F Lucy, Prokisch, Holger, Mayr, Johannes A, McFarland, Robert, Poulton, Joanna, Ryan, Michael T, Wittig, Ilka, Henneke, Marco, Taylor, Robert W

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An Approach to a Patient With Primary Hyperparathyroidism and a Suspected Ectopic Parathyroid Adenoma von Glasgow, Clark, Lau, Eunice Y C, Aloj, Luigi, Harper, Ines, Cheow, Heok, Das, Tilak, Berman, Laurence, Powlson, Andrew S, Bashari, Waiel A, Challis, Benjamin G, Marker, Alison, Moyle, Penelope, Mohamed, Isra Ahmed, Schoenmakers, Nadia, Broomfield, Jonathan, Oddy, Sue, Moran, Carla, Gurnell, Mark, Jani, Piyush, Masterson, Liam, Fish, Brian, Casey, Ruth T

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An action plan for translating cancer survivorship research into care von Alfano, Catherine M, Smith, Tenbroeck, de Moor, Janet S, Glasgow, Russell E, Khoury, Muin J, Hawkins, Nikki A, Stein, Kevin D, Rechis, Ruth, Parry, Carla, Leach, Corinne R, Padgett, Lynne, Rowland, Julia H

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Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer von Shen, Hui, Fridley, Brooke L., Song, Honglin, Lawrenson, Kate, Cicek, Mine S., Tyrer, Jonathan, Zheng, Wei, Yang, Hannah P., Wozniak, Eva L., Ling Woo, Yin, Winterhoff, Boris, Wentzensen, Nicolas, Palmieri Weber, Rachel, Vitonis, Allison F., Vincent, Daniel, Vierkant, Robert A., Vergote, Ignace, Van Den Berg, David, Van Altena, Anne M., Thompson, Pamela J., Tessier, Daniel C., Terry, Kathryn L., Templeman, Claire, Siddiqui, Nadeem, Shu, Xiao-Ou, Severi, Gianluca, Schwaab, Ira, Salvesen, Helga B., Anne Rossing, Mary, Risch, Harvey A., Renner, Stefan P., Poole, Elizabeth M., Pike, Malcolm C., Phelan, Catherine M., Pelttari, Liisa M., Pejovic, Tanja, Ness, Roberta B., Moysich, Kirsten B., Monteiro, Alvaro N.A., Menon, Usha, Matsuo, Keitaro, Mat Adenan, Noor Azmi, Massuger, Leon F.A.G, Lurie, Galina, Lundvall, Lene, Lubiński, Jan, Lissowska, Jolanta, Levine, Douglas A., Lambrechts, Diether, Kupryjanczyk, Jolanta, Kiemeney, Lambertus A., Karlan, Beth Y., Karevan, Rod, Kalli, Kimberly R., Ji, Bu-Tian, Jakubowska, Anna, Iversen, Edwin, Høgdall, Claus K., Hoatlin, Maureen, Hillemanns, Peter, Halle, Mari K., Hall, Per, Gronwald, Jacek, Gore, Martin, Giles, Graham G., Gentry-Maharaj, Aleksandra, Fasching, Peter A., Ekici, Arif B., Edwards, Robert, Eccles, Diana, Easton, Douglas F., Doherty, Jennifer A., Despierre, Evelyn, Dansonka-Mieszkowska, Agnieszka, Cybulski, Cezary, Cramer, Daniel W., Cook, Linda S., Chen, Xiaoqing, Charbonneau, Bridget, Campbell, Ian, Butzow, Ralf, Bunker, Clareann H., Brueggmann, Doerthe, Brown, Robert, Brooks-Wilson, Angela, Brinton, Louise A., Bogdanova, Natalia, Block, Matthew S., Benjamin, Elizabeth, Beesley, Jonathan, Beckmann, Matthias W., Bandera, Elisa V., Baglietto, Laura, Armasu, Sebastian M., Liang, Dong, Lu, Karen, Hildebrandt, Michelle A.T., Sellers, Thomas A., Laird, Peter W., Leigh Pearce, Celeste

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Deregulation of MYCN, LIN28B and LET7 in a molecular subtype of aggressive high-grade serous ovarian cancers von Helland, Åslaug, Anglesio, Michael S, George, Joshy, Cowin, Prue A, Johnstone, Cameron N, House, Colin M, Sheppard, Karen E, Etemadmoghadam, Dariush, Melnyk, Nataliya, Rustgi, Anil K, Phillips, Wayne A, Johnsen, Hilde, Holm, Ruth, Kristensen, Gunnar B, Birrer, Michael J, Pearson, Richard B, Børresen-Dale, Anne-Lise, Huntsman, David G, deFazio, Anna, Creighton, Chad J, Smyth, Gordon K, Bowtell, David D L

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High levels of genomic aberrations in serous ovarian cancers are associated with better survival von Baumbusch, Lars O, Helland, Åslaug, Wang, Yun, Liestøl, Knut, Schaner, Marci E, Holm, Ruth, Etemadmoghadam, Dariush, Alsop, Kathryn, Brown, Pat, Mitchell, Gillian, Fereday, Sian, DeFazio, Anna, Bowtell, David D L, Kristensen, Gunnar B, Lingjærde, Ole Christian, Børresen-Dale, Anne-Lise

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Genetic determinants of feline leukemia virus-induced lymphoid tumors: patterns of proviral insertion and gene rearrangement von Tsatsanis, C. (University of Glasgow, Bearsden, Glasgow, Scotland.), Fulton, R, Nishigaki, K, Tsujimoto, H, Levy, L, Terry, A, Spandidos, D, Onions, D, Neil, J.C

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An Approach to a Patient With Primary Hyperparathyroidism and a Suspected Ectopic Parathyroid Adenoma von Glasgow, Clark, Lau, Eunice YC, Aloj, Luigi, Harper, Ines, Cheow, Heok, Das, Tilak, Berman, Laurence, Powlson, Andrew S, Bashari, Waiel A, Challis, Benjamin G, Marker, Alison, Moyle, Penelope, Mohamed, Isra Ahmed, Schoenmakers, Nadia, Broomfield, Jonathan, Oddy, Sue, Moran, Carla, Gurnell, Mark, Jani, Piyush, Masterson, Liam, Fish, Brian, Casey, Ruth T

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VITAMIN E ASSOCIATED WITH THE LIPOCALIN FRACTION OF HUMAN TEARS von Glasgow, Ben J., Abduragimov, Adil R., Gassymov, Oktay K., Yusifov, Taleh N., Ruth, Edward C., Faull, Kym F.

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Structural diversity and nuclear protein binding sites in the long terminal repeats of feline leukemia virus von Fulton, R. (Beatson Institute for Cancer Research, Bearsden, Glasgow, Scotland), Plumb, M, Shield, L, Neil, J.C

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Literary Supplement von Gooch, G P, Banyard, Grace, Barkeley, R, Bax, Robert N, Briggs, Asa, Catlin, George, Fausset, Hugh l'A, Hill, W Thomson, Martin, Rupert, Nicholas, H G, O'Donoghue, Florence, Smogorzewski, K M, Somervill, D C, Loveday, Martin

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Literary Supplement von MacCallum Scott, John H, Aris, Reinhold, Banyard, Grace, Cohen, Victor, Franklyn, Julian, Glasgow, George, Gooch, G P, Llewellyn, Bernard, Montmorency, A de, Norman, Sylva, Schwarz, R P, Sillery, A, Gurney Salter, Emma

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