Reinforcement of sutures to close surgical incisions in frail skin von Wakeling, C P, Sandiford, A

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Height and body mass index in molecularly confirmed Silver–Russell syndrome and the long‐term effects of growth hormone treatment von 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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Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families von Callewaert, B.L, Willaert, A, Kerstjens-Frederikse, W.S, De Backer, J, Devriendt, K, Albrecht, B, Ramos-Arroyo, M.A, Doco-Fenzy, M, Hennekam, R.C.M, Pyeritz, R.E, Krogmann, O.N, Gillessen-kaesbach, G, Wakeling, E.L, Nik-zainal, S, Francannet, C, Mauran, P, Booth, C, Barrow, M, Dekens, R, Loeys, B.L, Coucke, P.J, De Paepe, A.M

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The Belle II Physics Book von Kou, E, Bishara, F, Brod, J, Buras, A J, Ciuchini, M, Deppisch, T, Godfrey, S, Haisch, U, Hirose, S, Kahlhoefer, F, Kamenik, J F, Kronfeld, A S, Logan, H, Lubicz, V, Maltman, K, Misiak, M, Nefediev, A, Nomura, D, Paz, G, Prelovsek, S, Robinson, D J, Rosiek, J, Shih, D, Tackmann, F J, Teubner, T, Virto, J, Aihara, H, Aloisio, A, Andricek, L, Anh Ky, N, Arndt, M, Aziz, T, Ban, Y, Barrett, M, Behera, P, Berger, M, de Lucia, E, Dey, S, Dong, T V, Frost, O, Gao, X, Gaz, A, Gradl, W, Heredia De La Cruz, I, Higuchi, T, Hollitt, S, Iwasaki, M, Jaegle, I, Jeon, H B, Joo, C, Kawasaki, T, Ketter, C, Kim, Y, Kinoshita, K, Krohn, J-F, Kwon, Y-J, Lacaprara, S, Lai, Y-T, Levit, D, Li, Y B, Loos, A, Müller, F, MacQueen, C, Maeda, Y, Maggiora, M, Martinez Hernandez, M, Moon, T, Nakazawa, H, Neverov, D, Nowak, G, Onuki, Y, Park, C-S, Perelló, M, Rizzuto, L, Savinov, V, Sfienti, C, Shapkin, M, Stanič, S, Strube, J F, Sumisawa, K, Summers, D, Takahashi, M, Tan, J, Taniguchi, N, Tenchini, F, Trabelsi, K, Tsuboyama, T, Uglov, T, Uno, S, Varvell, K E, Vos, M, Wehle, S, Wessel, C, Xu, X, Yamada, S, Yang, S B, Ye, H, Yeo, I, Yin, J H, Yonenaga, M

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Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders von 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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Apoptotic death in epithelial cells: cleavage of DNA to 300 and/or 50 kb fragments prior to or in the absence of internucleosomal fragmentation von Oberhammer, F., Wilson, J.W., Dive, C., Morris, I.D., Hickman, J.A., Wakeling, A.E., Walker, P.R., Sikorska, M.

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Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome von Suntharalingham, Jenifer P, Ishida, Miho, Del Valle, Ignacio, Stalman, Susanne E, Solanky, Nita, Wakeling, Emma, Moore, Gudrun E, Achermann, John C, Buonocore, Federica

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Widening the phenotypic spectrum caused by pathogenic PDX1 variants in individuals with neonatal diabetes von Jeffery, Nicola, Al Nimri, Omar, Houghton, Jayne A L, Globa, Evgenia, Wakeling, Matthew N, Flanagan, Sarah E, Hattersley, Andrew T, Patel, Kashyap Amratlal, De Franco, Elisa, Varthakavi, P K, Shaikh, A, Khadilkar, A, Khadilkar, V, Oza, C, Wolf, J, Skrabic, V, Unic, I, Alves, C, Amoli, M, Kulkarni, A, Dhivyalakshmi, J, Thiruvengadam, V, Haliloglu, B, Imane, Z, Ozdemir, A, Yildiz, M, Elbarbary, N

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Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA Associated von Johnson, Matthew B, De Franco, Elisa, Greeley, Siri Atma W, Letourneau, Lisa R, Gillespie, Kathleen M, Wakeling, Matthew N, Ellard, Sian, Flanagan, Sarah E, Patel, Kashyap A, Hattersley, Andrew T

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Phenotype and genotype in 17 patients with Goltz–Gorlin syndrome von Maas, S M, Lombardi, M P, van Essen, A J, Wakeling, E L, Castle, B, Temple, I K, Kumar, V K A, Writzl, K, Hennekam, Raoul C M

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Diagnosis and management of Silver–Russell syndrome: first international consensus statement von Wakeling, Emma L., Brioude, Frédéric, Lokulo-Sodipe, Oluwakemi, O'Connell, Susan M., Salem, Jennifer, Bliek, Jet, Canton, Ana P. M., Chrzanowska, Krystyna H., Davies, Justin H., Dias, Renuka P., Dubern, Béatrice, Elbracht, Miriam, Giabicani, Eloise, Grimberg, Adda, Grønskov, Karen, Hokken-Koelega, Anita C. S., Jorge, Alexander A., Kagami, Masayo, Linglart, Agnes, Maghnie, Mohamad, Mohnike, Klaus, Monk, David, Moore, Gudrun E., Murray, Philip G., Ogata, Tsutomu, Petit, Isabelle Oliver, Russo, Silvia, Said, Edith, Toumba, Meropi, Tümer, Zeynep, Binder, Gerhard, Eggermann, Thomas, Harbison, Madeleine D., Temple, I. Karen, Mackay, Deborah J. G., Netchine, Irène

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The Belle II Physics Book von Kou, E, Bishara, F, Brod, J, Buras, A J, Ciuchini, M, Deppisch, T, Godfrey, S, Haisch, U, Hirose, S, Kahlhoefer, F, Kamenik, J F, Kronfeld, A S, Logan, H, Lubicz, V, Maltman, K, Misiak, M, Nefediev, A, Nomura, D, Paz, G, Prelovsek, S, Robinson, D J, Rosiek, J, Shih, D, Tackmann, F J, Teubner, T, Virto, J, Aihara, H, Aloisio, A, Andricek, L, Anh Ky, N, Arndt, M, Aziz, T, Ban, Y, Barrett, M, Behera, P, Berger, M, de Lucia, E, Dey, S, Dong, T V, Frost, O, Gao, X, Gaz, A, Gradl, W, Heredia De La Cruz, I, Higuchi, T, Hollitt, S, Iwasaki, M, Jaegle, I, Jeon, H B, Joo, C, Kawasaki, T, Ketter, C, Kim, Y, Kinoshita, K, Krohn, J-F, Kwon, Y-J, Lacaprara, S, Lai, Y-T, Levit, D, Li, Y B, Loos, A, Müller, F, MacQueen, C, Maeda, Y, Maggiora, M, Martinez Hernandez, M, Moon, T, Nakazawa, H, Neverov, D, Nowak, G, Onuki, Y, Park, C-S, Perelló, M, Rizzuto, L, Savinov, V, Sfienti, C, Shapkin, M, Stanič, S, Strube, J F, Sumisawa, K, Summers, D, Takahashi, M, Tan, J, Taniguchi, N, Tenchini, F, Trabelsi, K, Tsuboyama, T, Uglov, T, Uno, S, Varvell, K E, Vos, M, Wehle, S, Wessel, C, Xu, X, Yamada, S, Yang, S B, Ye, H, Yeo, I, Yin, J H, Yonenaga, M

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Dragonfly flight. II. Velocities, accelerations and kinematics of flapping flight von Wakeling, JM, Ellington, CP

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Activation of BAD by Therapeutic Inhibition of Epidermal Growth Factor Receptor and Transactivation by Insulin-like Growth Factor Receptor von Gilmore, Andrew P., Valentijn, Anthony J., Wang, Pengbo, Ranger, Ann M., Bundred, Nigel, O'Hare, Michael J., Wakeling, Alan, Korsmeyer, Stanley J., Streuli, Charles H.

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Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling von Hanson, D, Murray, P G, Coulson, T, Sud, A, Omokanye, A, Stratta, E, Sakhinia, F, Bonshek, C, Wilson, L C, Wakeling, E, Temtamy, S A, Aglan, M, Rosser, E M, Mansour, S, Carcavilla, A, Nampoothiri, S, Khan, W I, Banerjee, I, Chandler, K E, Black, G C M, Clayton, P E

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The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders von Sidpra, Jai, Sudhakar, Sniya, Biswas, Asthik, Massey, Flavia, Turchetti, Valentina, Lau, Tracy, Cook, Edward, Alvi, Javeria Raza, Elbendary, Hasnaa M, Jewell, Jerry L, Riva, Antonella, Orsini, Alessandro, Vignoli, Aglaia, Federico, Zara, Rosenblum, Jessica, Schoonjans, An-Sofie, de Wachter, Matthias, Delgado Alvarez, Ignacio, Felipe-Rucián, Ana, Haridy, Nourelhoda A, Haider, Shahzad, Zaman, Mashaya, Banu, Selina, Anwaar, Najwa, Rahman, Fatima, Maqbool, Shazia, Yadav, Rashmi, Salpietro, Vincenzo, Maroofian, Reza, Patel, Rajan, Radhakrishnan, Rupa, Prabhu, Sanjay P, Lichtenbelt, Klaske, Stewart, Helen, Murakami, Yoshiko, Löbel, Ulrike, D'Arco, Felice, Wakeling, Emma, Jones, Wendy, Hay, Eleanor, Bhate, Sanjay, Jacques, Thomas S, Mirsky, David M, Whitehead, Matthew T, Zaki, Maha S, Sultan, Tipu, Striano, Pasquale, Jansen, Anna C, Lequin, Maarten, de Vries, Linda S, Severino, Mariasavina, Edmondson, Andrew C, Menzies, Lara, Campeau, Philippe M, Houlden, Henry, McTague, Amy, Efthymiou, Stephanie, Mankad, Kshitij

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Observation of e+e–→ωχbJ(1P) and Search for Xb→ωΥ(1S) at s near 10.75 GeV von Adachi, I., Akopov, N., Banerjee, Sw, Behera, P.  K., Bennett, J.  V., Bettarini, S., Bianchi, F., Biswas, D., Bodrov, D., Bolz, A., Bračko, M., Bussino, S., Cheema, P., De Yta-Hernandez, A., Dujany, G., Feichtinger, P., Ferber, T., Finocchiaro, G., Forti, F., Gellrich, A., Ghevondyan, G., Giordano, R., Goldenzweig, P., Granderath, S., Guilliams, J., Hara, T., Hayasaka, K., Hearty, C., Heredia de la Cruz, I., Hirata, H., Hohmann, M., Iijima, T., Ishikawa, A., Jin, Y., Joo, K.  K., Kang, K.  H., Kindo, H., Kodyš, P., Koga, T., Kojima, K., Kraetzschmar, T.  M. G., Križan, P., Krokovny, P., Kwon, Y. -J., Li, C., Lieret, K., Liu, Q.  Y., Liventsev, D., Longo, S., Lozar, A., Lyu, C., Manfredi, R., Marcello, S., Martel, L., Martini, A., Martinov, T., Massaccesi, L., Masuda, M., Maurya, S.  K., Metzner, F., Moneta, S., Nakamura, I., Ogawa, S., Oskin, P., Paladino, A., Paoloni, E., Park, S. -H., Pedlar, T.  K., Peruzzi, I., Pestotnik, R., Piilonen, L.  E., Polat, L., Praz, C., Reif, M., Robertson, S.  H., Sato, Y., Schwanda, C., Seino, Y., Shen, C.  P., Sobie, R.  J., Soffer, A., Starič, M., Stroili, R., Sue, Y., Sumihama, M., Sumisawa, K., Tanida, K., Thaller, A., Tiwary, R., Uno, K., Wang, E., Warburton, A., Welsch, M., Wessel, C., Won, E., Yang, S.  B., Yook, Y.  M., Yoshihara, K., Zhang, Y., Zhukova, V.  I.

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SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile von Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

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Search for $B^+→K^+ν\bar{ν}{$ Decays Using an Inclusive Tagging Method at Belle II von Ahlburg, P., Aihara, H., Akopov, N., Aushev, T., Baur, A., Banerjee, Sw, Becker, J., Bennett, J.  V., Biswas, D., Branchini, P., Braun, N., Bussino, S., Cecchi, C., Chang, P., Chekelian, V., Cheon, B.  G., Cremaldi, L.  M., Cunliffe, S., Dattola, F., de Marino, G., de Sangro, R., Eidelman, S., Epifanov, D., Ferlewicz, D., Fiore, S., Fulsom, B.  G., Garcia-Hernandez, M., Goldenzweig, P., Grace, P., Gradl, W., Halder, S., Hayasaka, K., Hearty, C., Hill, E.  C., Jin, Y., Junkerkalefeld, H., Kandra, J., Karyan, G., Kiesling, C., Kim, C. -H., Kim, D.  Y., Kim, Y. -K., Kodyš, P., Konno, T., Krinner, F., Kuhr, T., Kurz, S., Kwon, Y. -J., Lange, J.  S., Levit, D., Liu, Q.  Y., Marcello, S., Marinas, C., Masuda, M., Matsuda, T., Meier, F., Merola, M., Miyabayashi, K., Murphy, C., Mussa, R., Nisar, N.  K., Ozaki, H., Paoloni, E., Peruzzi, I., Piccolo, M., Piilonen, L.  E., Podesta-Lerma, P.  L. M., Podobnik, T., Popov, V., Prell, S., Prim, M.  T., Rad, N., Rizzo, G., Rizzuto, L.  B., Seddon, R.  M., Sevior, M.  E., Shiu, J. -G., Shwartz, B., Simon, F., Sobie, R.  J., Starič, M., Stottler, Z.  S., Sumisawa, K., Summers, D.  J., Svidras, H., Takahashi, M., Tamponi, U., Taniguchi, N., Torassa, E., Uchida, M., Urquijo, P., Usov, Y.  V., van Tonder, R., Wach, B., Waheed, E., Wang, M. -Z., Watanuki, S., Wiechczynski, J., Yin, J.  H., Zhou, Q.  D.

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The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders von Sidpra, Jai, Sudhakar, Sniya, Biswas, Asthik, Massey, Flavia, Turchetti, Valentina, Lau, Tracy, Cook, Edward, Alvi, Javeria Raza, Elbendary, Hasnaa M, Jewell, Jerry L, Riva, Antonella, Orsini, Alessandro, Vignoli, Aglaia, Federico, Zara, Rosenblum, Jessica, Schoonjans, An-Sofie, de Wachter, Matthias, Delgado Alvarez, Ignacio, Felipe-Rucián, Ana, Haridy, Nourelhoda A, Haider, Shahzad, Zaman, Mashaya, Banu, Selina, Anwaar, Najwa, Rahman, Fatima, Maqbool, Shazia, Yadav, Rashmi, Salpietro, Vincenzo, Maroofian, Reza, Patel, Rajan, Radhakrishnan, Rupa, Prabhu, Sanjay P, Lichtenbelt, Klaske, Stewart, Helen, Murakami, Yoshiko, Löbel, Ulrike, D'Arco, Felice, Wakeling, Emma, Jones, Wendy, Hay, Eleanor, Bhate, Sanjay, Jacques, Thomas S, Mirsky, David M, Whitehead, Matthew T, Zaki, Maha S, Sultan, Tipu, Striano, Pasquale, Jansen, Anna C, Lequin, Maarten, de Vries, Linda S, Severino, Mariasavina, Edmondson, Andrew C, Menzies, Lara, Campeau, Philippe M, Houlden, Henry, McTague, Amy, Efthymiou, Stephanie, Mankad, Kshitij

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