Reverse Feeding Suppresses the Activity of the GH Axis in Rats and Induces a Preobesogenic State von Glad, Camilla A.-M, Kitchen, Edward E. J, Russ, Gemma C, Harris, Sophie M, Davies, Jeffrey S, Gevers, Evelien F, Gabrielsson, Britt G, Wells, Timothy

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DNA methylation of blood cells is associated with prevalent type 2 diabetes in a meta-analysis of four European cohorts von Juvinao-Quintero, Diana L, Marioni, Riccardo E, Ochoa-Rosales, Carolina, Russ, Tom C, Deary, Ian J, van Meurs, Joyce B J, Voortman, Trudy, Hivert, Marie-France, Sharp, Gemma C, Relton, Caroline L, Elliott, Hannah R

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Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement von LaFlamme, Christy W., Rastin, Cassandra, Sengupta, Soham, Pennington, Helen E., Russ-Hall, Sophie J., Schneider, Amy L., Bonkowski, Emily S., Almanza Fuerte, Edith P., Allan, Talia J., Zalusky, Miranda Perez-Galey, Goffena, Joy, Gibson, Sophia B., Nyaga, Denis M., Lieffering, Nico, Hebbar, Malavika, Walker, Emily V., Darnell, Daniel, Olsen, Scott R., Kolekar, Pandurang, Djekidel, Mohamed Nadhir, Rosikiewicz, Wojciech, McConkey, Haley, Kerkhof, Jennifer, Levy, Michael A., Relator, Raissa, Lev, Dorit, Lerman-Sagie, Tally, Park, Kristen L., Alders, Marielle, Cappuccio, Gerarda, Chatron, Nicolas, Demain, Leigh, Genevieve, David, Lesca, Gaetan, Roscioli, Tony, Sanlaville, Damien, Tedder, Matthew L., Gupta, Sachin, Jones, Elizabeth A., Weisz-Hubshman, Monika, Ketkar, Shamika, Dai, Hongzheng, Worley, Kim C., Rosenfeld, Jill A., Chao, Hsiao-Tuan, Neale, Geoffrey, Carvill, Gemma L., Wang, Zhaoming, Berkovic, Samuel F., Sadleir, Lynette G., Miller, Danny E., Scheffer, Ingrid E., Sadikovic, Bekim, Mefford, Heather C.

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 von Paul, Maimuna S., Michener, Sydney L., Pan, Hongling, Chan, Hiuling, Pfliger, Jessica M., Rosenfeld, Jill A., Lerma, Vanesa C., Tran, Alyssa, Longley, Megan A., Lewis, Richard A., Weisz-Hubshman, Monika, Bekheirnia, Mir Reza, Bekheirnia, Nasim, Massingham, Lauren, Zech, Michael, Wagner, Matias, Engels, Hartmut, Cremer, Kirsten, Mangold, Elisabeth, Peters, Sophia, Trautmann, Jessica, Perne, Claudia, Mester, Jessica L., Guillen Sacoto, Maria J., Person, Richard, McDonnell, Pamela P., Cohen, Stacey R., Lusk, Laina, Cohen, Ana S.A., Le Pichon, Jean-Baptiste, Pastinen, Tomi, Zhou, Dihong, Engleman, Kendra, Racine, Caroline, Faivre, Laurence, Moutton, Sébastien, Denommé-Pichon, Anne-Sophie, Koh, Hyun Yong, Poduri, Annapurna, Bolton, Jeffrey, Knopp, Cordula, Julia Suh, Dong Sun, Maier, Andrea, Toosi, Mehran Beiraghi, Karimiani, Ehsan Ghayoor, Maroofian, Reza, Schaefer, Gerald Bradley, Ramakumaran, Vijayalakshmi, Vasudevan, Pradeep, Banos-Pinero, Benito, Pagnamenta, Alistair T., Prasad, Chitra, Osmond, Matthew, Schuhmann, Sarah, Vasileiou, Georgia, Russ-Hall, Sophie, Scheffer, Ingrid E., Carvill, Gemma L., Mefford, Heather, Bacino, Carlos A., Lee, Brendan H., Chao (趙孝端), Hsiao-Tuan

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A comparison of blood and brain‐derived ageing and inflammation‐related DNA methylation signatures and their association with microglial burdens von Stevenson, Anna J., McCartney, Daniel L., Gadd, Danni A., Shireby, Gemma, Hillary, Robert F., King, Declan, Tzioras, Makis, Wrobel, Nicola, McCafferty, Sarah, Murphy, Lee, McColl, Barry W., Redmond, Paul, Taylor, Adele M., Harris, Sarah E., Russ, Tom C., McIntosh, Andrew M., Mill, Jonathan, Smith, Colin, Deary, Ian J., Cox, Simon R., Marioni, Riccardo E., Spires‐Jones, Tara L.

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 von Paul, Maimuna S., Michener, Sydney L., Pan, Hongling, Chan, Hiuling, Pfliger, Jessica M., Rosenfeld, Jill A., Lerma, Vanesa C., Tran, Alyssa, Longley, Megan A., Lewis, Richard A., Weisz-Hubshman, Monika, Bekheirnia, Mir Reza, Bekheirnia, Nasim, Massingham, Lauren, Zech, Michael, Wagner, Matias, Engels, Hartmut, Cremer, Kirsten, Mangold, Elisabeth, Peters, Sophia, Trautmann, Jessica, Perne, Claudia, Mester, Jessica L., Guillen Sacoto, Maria J., Person, Richard, McDonnell, Pamela P., Cohen, Stacey R., Lusk, Laina, Cohen, Ana S.A., Le Pichon, Jean-Baptiste, Pastinen, Tomi, Zhou, Dihong, Engleman, Kendra, Racine, Caroline, Faivre, Laurence, Moutton, Sébastien, Denommé-Pichon, Anne-Sophie, Koh, Hyun Yong, Poduri, Annapurna, Bolton, Jeffrey, Knopp, Cordula, Julia Suh, Dong Sun, Maier, Andrea, Toosi, Mehran Beiraghi, Karimiani, Ehsan Ghayoor, Maroofian, Reza, Schaefer, Gerald Bradley, Ramakumaran, Vijayalakshmi, Vasudevan, Pradeep, Banos-Pinero, Benito, Pagnamenta, Alistair T., Prasad, Chitra, Osmond, Matthew, Schuhmann, Sarah, Vasileiou, Georgia, Russ-Hall, Sophie, Scheffer, Ingrid E., Carvill, Gemma L., Mefford, Heather, Bacino, Carlos A., Lee, Brendan H., Chao, Hsiao-Tuan

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Nutrition in CAPD: Serum bicarbonate and the ubiquitin-proteasome system in muscle von Pickering, Warren P., Price, S. Russ, Bircher, Gemma, Marinovic, Anne C., Mitch, William E., Walls, John

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DNA methylation of blood cells is associated with prevalent type 2 diabetes in a meta-analysis of four European cohorts von Juvinao-Quintero, Diana L, Marioni, Riccardo E, Ochoa-Rosales, Carolina, Russ, Tom C, Deary, Ian J, van Meurs, Joyce BJ, Voortman, Trudy, Hivert, Marie-France, Sharp, Gemma C, Relton, Caroline L, Elliott, Hannah R

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