Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells by Bliek, Jet, Alders, Marielle, Maas, Saskia M, Oostra, Roelof-Jan, Mackay, Deborah M, van der Lip, Karin, Callaway, Johnatan L, Brooks, Alice, van 't Padje, Sandra, Westerveld, Andries, Leschot, Nico J, Mannens, Marcel MAM

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Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci by Turner, Claire Louise Susan, Mackay, Deborah M, Callaway, Jonathan L A, Docherty, Louise E, Poole, Rebecca L, Bullman, Hilary, Lever, Margaret, Castle, Bruce M, Kivuva, Emma C, Turnpenny, Peter D, Mehta, Sarju G, Mansour, Sahar, Wakeling, Emma L, Mathew, Verghese, Madden, Jackie, Davies, Justin H, Temple, I Karen

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Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome by Bliek, Jet, Verde, Gaetano, Callaway, Jonathan, Maas, Saskia M, De Crescenzo, Agostina, Sparago, Angela, Cerrato, Flavia, Russo, Silvia, Ferraiuolo, Serena, Rinaldi, Maria Michela, Fischetto, Rita, Lalatta, Faustina, Giordano, Lucio, Ferrari, Paola, Cubellis, Maria Vittoria, Larizza, Lidia, Temple, I Karen, Mannens, Marcel M A M, Mackay, Deborah J G, Riccio, Andrea

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Height and body mass index in molecularly confirmed Silver–Russell syndrome and the long‐term effects of growth hormone treatment by Lokulo‐Sodipe, Oluwakemi, Giabicani, Eloïse, Canton, Ana P. M., Ferrand, Nawfel, Child, Jenny, Wakeling, Emma L., Binder, Gerhard, Netchine, Irène, Mackay, Deborah J. G., Inskip, Hazel M., Byrne, Christopher D., Temple, I. Karen, Davies, Justin H.

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Prematurity and Genetic Testing for Neonatal Diabetes by Besser, Rachel E J, Flanagan, Sarah E, Mackay, Deborah G J, Temple, I K, Shepherd, Maggie H, Shields, Beverley M, Ellard, Sian, Hattersley, Andrew T

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Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects by 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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Phenological sensitivity to climate across taxa and trophic levels by Thackeray, Stephen J., Henrys, Peter A., Hemming, Deborah, Bell, James R., Botham, Marc S., Burthe, Sarah, Helaouet, Pierre, Johns, David G., Jones, Ian D., Leech, David I., Mackay, Eleanor B., Massimino, Dario, Atkinson, Sian, Bacon, Philip J., Brereton, Tom M., Carvalho, Laurence, Clutton-Brock, Tim H., Duck, Callan, Edwards, Martin, Elliott, J. Malcolm, Hall, Stephen J. G., Harrington, Richard, Pearce-Higgins, James W., Høye, Toke T., Kruuk, Loeske E. B., Pemberton, Josephine M., Sparks, Tim H., Thompson, Paul M., White, Ian, Winfield, Ian J., Wanless, Sarah

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Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders by Poole, Rebecca L., Docherty, Louise E., Al Sayegh, Abeer, Caliebe, Almuth, Turner, Claire, Baple, Emma, Wakeling, Emma, Harrison, Lucy, Lehmann, Anna, Temple, I. Karen, Mackay, Deborah J.G.

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Relapsing diabetes can result from moderately activating mutations in KCNJ11 by Gloyn, Anna L., Reimann, Frank, Girard, Christophe, Edghill, Emma L., Proks, Peter, Pearson, Ewan R., Temple, I. Karen, Mackay, Deborah J.G., Shield, Julian P.H., Freedenberg, Debra, Noyes, Kathryn, Ellard, Sian, Ashcroft, Frances M., Gribble, Fiona M., Hattersley, Andrew T.

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Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57 by Bak, Mads, Boonen, Susanne E, Dahl, Christina, Hahnemann, Johanne M D, Mackay, Deborah J D G, Tümer, Zeynep, Grønskov, Karen, Temple, I Karen, Guldberg, Per, Tommerup, Niels

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Persistence of adoptively transferred T cells with a kinetically engineered IL-2 receptor agonist by Parisi, Giulia, Saco, Justin D., Salazar, Felix B., Tsoi, Jennifer, Krystofinski, Paige, Puig-Saus, Cristina, Zhang, Ruixue, Zhou, Jing, Cheung-Lau, Gardenia C., Garcia, Alejandro J., Grasso, Catherine S., Tavaré, Richard, Hu-Lieskovan, Siwen, Mackay, Sean, Zalevsky, Jonathan, Bernatchez, Chantale, Diab, Adi, Wu, Anna M., Comin-Anduix, Begoña, Charych, Deborah, Ribas, Antoni

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Safety and immunogenicity of the two-dose heterologous Ad26.ZEBOV and MVA-BN-Filo Ebola vaccine regimen in children in Sierra Leone: a randomised, double-blind, controlled trial by Afolabi, Muhammed O, Swaray, Ibrahim, Foster, Julie, Luhn, Kerstin, Leigh, Bailah, Bockarie, E, James, N L, Kamara, A, Smout, E, Bangura, M S, Jalloh, H, Jalloh, A B, Kamara, I, Konteh, A, Marrah, C, Sesay, M T, Kaimbay, R M, Kain, D, Marah, W S, Tengheh, J N, Turay, A S, Fornah, A, Sesay, F, Sow, A, Swaray, E, Ade-Cole, T, Koroma, M, Sam, A, Scott, T, Sessie, T, Sunders, J-H C, Turay, S I-S, Gibson, L, Kowuor, D, Kamara, F J, Conteh, Y, Daramy, M L, Fofanah, O, Hanson, T F, Kamara, G M, Kamara, R T, Leigh, B, Greenwood, B, Deen, G F, Piot, P, Edmunds, J, Lees, S, Wilson, P, Owusu-Kyei, K, Stuart, J, Bah, O M, Swaray, I B, Kamara, M M, Gallagher, K, Cesay, M, Brown, J, Howard, K, Jendrossek, M, Offergeld, K, Van Ballaert, S, Roza, L, Liberi, T, Hafezi, H, Tuda, G O, Bangura, G, Kroma, M T, Pessima, A, Rogers, M, Foday Jr, S, Charles, M K, Lamin Karbo, M, Trye, A, Nambuchi, L, Jalloh, K F N, Jalloh, N, Kanjie, F, Kargbo, I, Sankoh, A, Williams, C T, Bangura, I, Ben-Rogers, Y, Kanawah, I, Kargbo, A T, Amara, L, Jakema, H B, Sheku, M F, Marrah, M, Moinina, E, Kalokoh, J, Hilton, T, Idriss, B, Sillah, M, Murray, T, Sannoh, M, Nyaberi, D, Vy, V, Fombah, A, Lahai, A, Yambasu, N, Bangura, M

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Safety and long-term immunogenicity of the two-dose heterologous Ad26.ZEBOV and MVA-BN-Filo Ebola vaccine regimen in adults in Sierra Leone: a combined open-label, non-randomised s... by Swaray, Ibrahim, Luhn, Kerstin, Greenwood, Brian, Leigh, Bailah, Bockarie, E, James, N L, Kamara, A, Bangura, M S, Jalloh, H, Jalloh, A B, Kamara, I, Marrah, C, Kaimbay, R M, Marah, W S, Tengheh, J N, Turay, A S, Fornah, A, Sow, A, Swaray, E, Ade-Cole, T, Koroma, M, Sam, A, Scott, T, Sessie, T, Sunders, J-H C, Turay, S I-S, Gibson, L, Kowuor, D, Kamara, F J, Conteh, Y, Daramy, M L, Fofanah, O, Hanson, T F, Kamara, G M, Kamara, R T, Leigh, B, Greenwood, B, Deen, G F, Edmunds, J, Baiden, F, Tindanbil, D, Rogers, B T, Serry-Bangura, A, Swaray, I B, Bangura, A, Kamara, M M, Suma, F B, Murray, M, Manno, D, Cox, S, Howard, N, Snowden, E, Howard, K, Melton, N, Eggo, R, Pearson, C, Van Alst, M, Gaddah, A, Lowe, B, Kohn, B, Sheriff, O, Ajala, T W, Fangawa, J, Sesay, K, Charles, M K, Heroe, P C, Egoeh, S G, Alghali, N D, Bah, A, Cole, A C, Fofanah, K, Kabba, H U, Kabba, M, Koroma, S B, Sankoh, T, Wilhem, H, Ben-Rogers, Y, Swaray, I, Kamara, K, Sheku, M F, Akhigbe, I, Chami, N P, van Roey, K, Bosompem, S, Hilton, T, Borboh, P, Saquee, T M D, Fornah, J, Edem-Hotah, J, Fatorma, T, Bangura, S, Bonnie, E, Donaldson, A, Ndingi, S, Nyallay, L, Fakaba, P J, Vincent, W, Tengbeh, A, Callaghan, M, Enria, L

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Body Composition and Metabolism in Adults With Molecularly Confirmed Silver-Russell Syndrome by Lokulo-Sodipe, Oluwakemi, Inskip, Hazel M, Byrne, Christopher D, Child, Jenny, Wakeling, Emma L, Mackay, Deborah J G, Temple, I Karen, Davies, Justin H

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Very small deletions within the NESP55 gene in pseudohypoparathyroidism type 1b by Rezwan, Faisal I, Poole, Rebecca L, Prescott, Trine, Walker, Joanna M, Karen Temple, I, Mackay, Deborah J G

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Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis by Mackay, Deborah J G, Gazdagh, Gabriella, Monk, David, Brioude, Frederic, Giabicani, Eloise, Krzyzewska, Izabela M, Kalish, Jennifer M, Maas, Saskia M, Kagami, Masayo, Beygo, Jasmin, Kahre, Tiina, Tenorio-Castano, Jair, Ambrozaitytė, Laima, Burnytė, Birutė, Cerrato, Flavia, Davies, Justin H, Ferrero, Giovanni Battista, Fjodorova, Olga, Manero-Azua, Africa, Pereda, Arrate, Russo, Silvia, Tannorella, Pierpaola, Temple, Karen I, Õunap, Katrin, Riccio, Andrea, de Nanclares, Guiomar Perez, Maher, Eamonn R, Lapunzina, Pablo, Netchine, Irène, Eggermann, Thomas, Bliek, Jet, Tümer, Zeynep

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Priority strategies to reduce socio-gendered inequities in access to person-centred osteoarthritis care: Delphi survey by Iziduh, Sharon, Abbaticchio, Angelina, Theodorlis, Madeline, Ahluwalia, Vandana, Battistella, Marisa, Borkhoff, Cornelia M, Hazlewood, Glen Stewart, Lofters, Aisha, MacKay, Crystal, Marshall, Deborah A, Gagliardi, Anna R

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The Quality and Cultural Safety of Online Osteoarthritis Information for Affected Persons and Health Care Professionals: Content Analysis by Dhakal, Smita, Merani, Shermeen, Ahluwalia, Vandana, Battistella, Marisa, Borkhoff, Cornelia M, Hazlewood, Glen Stewart, Lofters, Aisha, Marshall, Deborah A, MacKay, Crystal, Gagliardi, Anna R

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Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply by Brioude, Frédéric, Hennekam, Raoul, Bliek, Jet, Coze, Carole, Eggermann, Thomas, Ferrero, Giovanni B, Kratz, Christian, Bouc, Yves Le, Maas, Saskia M, Mackay, Deborah J G, Maher, Eamonn R, Mussa, Alessandro, Netchine, Irene

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Establishing Surrogate Kidney End Points for Lupus Nephritis Clinical Trials: Development and Validation of a Novel Approach to Predict Future Kidney Outcomes by Mackay, Meggan, Dall'Era, Maria, Fishbein, Joanna, Kalunian, Kenneth, Lesser, Martin, Sanchez‐Guerrero, Jorge, Levy, Deborah M., Silverman, Earl, Petri, Michelle, Arriens, Cristina, Lewis, Edmund J., Korbet, Stephen M., Conti, Fabrizio, Tesar, Vladimir, Hruskova, Zdenka, Borba, Eduardo F., Bonfa, Eloisa, Chan, Tak Mao, Rathi, Manish, Gupta, K. L., Jha, Vivekanand, Hasni, Sarfaraz, West, Melissa R., Solomons, Neil, Houssiau, Frederic A., Romero‐Diaz, Juanita, Mejia‐Vilet, Juan, Rovin, Brad H.

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