Acute Exposure to Circularly Polarized 50-Hz Magnetic Fields of 200–300 μT Does Not Affect the Pattern of Melatonin Secretion in Young Men von Warman, G. R., Tripp, H., Warman, V. L., Arendt, J.

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Circadian neuroendocrine physiology and electromagnetic field studies: Precautions and complexities von R. Warman, G., M. Tripp, H., L. Warman, V., Arendt, J.

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Phase advancing human circadian rhythms with short wavelength light von Warman, Victoria L., Dijk, Derk-Jan, Warman, Guy R., Arendt, Josephine, Skene, Debra J.

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Acute exposure to circularly polarized 50-Hz magnetic fields of 200-300 microT does not affect the pattern of melatonin secretion in young men von Warman, G R, Tripp, H, Warman, V L, Arendt, J

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Nosology of genetic skeletal disorders: 2023 revision von Unger, Sheila, Ferreira, Carlos R., Mortier, Geert R., Ali, Houda, Bertola, Débora R., Calder, Alistair, Cohn, Daniel H., Cormier‐Daire, Valerie, Girisha, Katta M., Hall, Christine, Krakow, Deborah, Makitie, Outi, Mundlos, Stefan, Nishimura, Gen, Robertson, Stephen P., Savarirayan, Ravi, Sillence, David, Simon, Marleen, Sutton, V. Reid, Warman, Matthew L., Superti‐Furga, Andrea

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Decreased BMD and Limb Deformities in Mice Carrying Mutations in Both Lrp5 and Lrp6 von Holmen, Sheri L, Giambernardi, Troy A, Zylstra, Cassandra R, Buckner‐Berghuis, Bree D, Resau, James H, Hess, J Fred, Glatt, Vaida, Bouxsein, Mary L, Ai, Minrong, Warman, Matthew L, Williams, Bart O

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The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth von Rhee, David K, Marcelino, Jose, Baker, MacArthur, Gong, Yaoqin, Smits, Patrick, Lefebvre, Véronique, Jay, Gregory D, Stewart, Matthew, Wang, Hongwei, Warman, Matthew L, Carpten, John D

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Lymphatic and Other Vascular Malformative/Overgrowth Disorders Are Caused by Somatic Mutations in PIK3CA von Luks, Valerie L., BS, Kamitaki, Nolan, Vivero, Matthew P., BA, Uller, Wibke, MD, Rab, Rashed, BA, Bovée, Judith V.M.G., MD, PhD, Rialon, Kristy L., MD, Guevara, Carlos J., MD, Alomari, Ahmad I., MD, Greene, Arin K., MD, MMSc, Fishman, Steven J., MD, Kozakewich, Harry P.W., MD, Maclellan, Reid A., MD, MMSc, Mulliken, John B., MD, Rahbar, Reza, MD, Spencer, Samantha A., MD, Trenor, Cameron C., MD, Upton, Joseph, MD, Zurakowski, David, PhD, Perkins, Jonathan A., DO, Kirsh, Andrew, PhD, Bennett, James T., MD, PhD, Dobyns, William B., MD, Kurek, Kyle C., MD, MMSc, Warman, Matthew L., MD, McCarroll, Steven A., PhD, Murillo, Rudy, MD

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Providing foraging resources for bumblebees in intensively farmed landscapes von Pywell, R.F., Warman, E.A., Carvell, C., Sparks, T.H., Dicks, L.V., Bennett, D., Wright, A., Critchley, C.N.R., Sherwood, A.

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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care von Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza-Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.

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Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia von Hul, Els Van, Warman, Matthew L, Al-Alami, Jamil, Roudier, Jean, Bahabri, Sultan A, Hurvitz, Jennifer R, Pauli, Richard M, El-Shanti, Hatem, Rezai-Delui, Hossien, Van Hul, Wim, Suwairi, Wafaa M, Legius, Eric, Holderbaum, Daniel, Herd, J. Kenneth, Superti-Furga, Andrea, Le Merrer, Martine

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CACP , encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome von Trent, Jeffrey M, Warman, Matthew L, Marcelino, Jose, Carpten, John D, Suwairi, Wafaa M, Gutierrez, Orlando M, Schwartz, Stuart, Robbins, Christiane, Sood, Raman, Makalowska, Izabela, Baxevanis, Andy, Johnstone, Brian, Laxer, Ronald M, Zemel, Lawrence, Kim, Chong Ae, Herd, J. Kenneth, Ihle, Johannes, Williams, Cal, Johnson, Mark, Raman, Vidya, Alonso, Luís Garcia, Brunoni, Decio, Gerstein, Amy, Papadopoulos, Nickolas, Bahabri, Sultan A

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The clinical spectrum of SMA‐PME and in vitro normalization of its cellular ceramide profile von Lee, Michelle M., McDowell, Graeme S. V., De Vivo, Darryl C., Friedman, Daniel, Berkovic, Samuel F., Spanou, Maria, Dinopoulos, Argirios, Grand, Katheryn, Sanchez‐Lara, Pedro A., Allen‐Sharpley, Michelle, Warman‐Chardon, Jodi, Solyom, Alexander, Levade, Thierry, Schuchman, Edward H., Bennett, Steffany A. L., Dyment, David A., Pearson, Toni S.

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Identification of 2‑Aryl-Quinolone Inhibitors of Cytochrome bd and Chemical Validation of Combination Strategies for Respiratory Inhibitors against Mycobacterium tuberculosis von Jeffreys, Laura N., Ardrey, Alison, Hafiz, Taghreed A., Dyer, Lauri-Anne, Warman, Ashley J., Mosallam, Nada, Nixon, Gemma L., Fisher, Nicholas E., Hong, W. David, Leung, Suet C., Aljayyoussi, Ghaith, Bibby, Jaclyn, Almeida, Deepak V., Converse, Paul J., Fotouhi, Nader, Berry, Neil G., Nuermberger, Eric L., Upton, Anna M., O’Neill, Paul M., Ward, Stephen A., Biagini, Giancarlo A.

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Dexmedetomidine hemodynamics in children after cardiac surgery von POTTS, AMANDA L., ANDERSON, BRIAN J., HOLFORD, NICK H.G., VU, THUY C., WARMAN, GUY R.

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Laparoscopic or open abdominal surgery with thoracotomy for patients with oesophageal cancer: ROMIO randomized clinical trial von Akhtar, K, Alkhaffaf, B, Ariyarathenam, A, Avery, K, Barham, P, Bateman, A, Beard, C, Berrisford, R, Blazeby, JM, Blencowe, N, Boddy, A, Bowrey, D, Bracey, T, Brierley, RC, Briton, K, Byrne, J, Catton, J, Chaparala, R, Clark, SK, Clarke, T, Cooke, J, Couper, G, Culliford, L, Dawson, H, Deans, C, Donovan, JL, Ekblad, C, Elliott, J, Exon, D, Falk, S, Farooq, N, Garfield, K, Gaunt, DM, Gill, F, Goldin, R, Gravani, A, Hayes, S, Heys, R, Hindmarsh, C, Hollinghurst, S, Hollowood, A, Houlihan, R, Howes, B, Howie, L, Humphreys, L, Hutton, D, Jarvis, R, Jepson, M, Kandiyali, R, Kaur, S, Kelly, J, King, A, Kirwin, J, Krysztopik, R, Lamb, P, Lang, A, Lee, V, Maitland, S, Mapstone, N, Melia, G, Metcalfe, C, Melhado, R, Moure-Fernandez, A, Nair, B, Nicklin, J, Noble, F, Noble, SM, O'Connell, A, Palmer, S, Parsons, S, Pursnani, K, Rea, N, Reed, F, Rice, C, Richards, C, Rogers, C, Sanders, G, Save, V, Schiller, M, Schranz, R, Shetty, V, Shirkey, B, Singleton, J, Skipworth, R, Smith, J, Streets, C, Titcomb, D, Turner, P, Ubhi, S, Underwood, T, Vohra, R, Ward, EM, Warman, R, Welch, N, Wheatley, T, Wickens, RA, Wilkerson, P, Williams, R, Wilmshurst, N, Wong, NACS

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Nosology of genetic skeletal disorders: 2023 revision von Unger, Sheila, Ferreira, Carlos R, Mortier, Geert R, Ali, Houda, Bertola, Debora R, Calder, Alistair, Cohn, Daniel H, Cormier-Daire, Valerie, Girisha, Katta M, Hall, Christine, Krakow, Deborah, Makitie, Outi, Mundlos, Stefan, Nishimura, Gen, Robertson, Stephen P, Savarirayan, Ravi, Sillence, David, Simon, Marleen, Sutton, V. Reid, Warman, Matthew L, Superti-Furga, Andrea

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Nosology of genetic skeletal disorders: 2023 revision von Unger, Sheila, Ferreira, Carlos R, Mortier, Geert R, Ali, Houda, Bertola, Débora R, Calder, Alistair, Cohn, Daniel H, Cormier-Daire, Valerie, Girisha, Katta M, Hall, Christine, Krakow, Deborah, Makitie, Outi, Mundlos, Stefan, Nishimura, Gen, Robertson, Stephen P, Savarirayan, Ravi, Sillence, David, Simon, Marleen, Sutton, V Reid, Warman, Matthew L, Superti-Furga, Andrea

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Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome von Bowen, Margot E, Boyden, Eric D, Holm, Ingrid A, Campos-Xavier, Belinda, Bonafé, Luisa, Superti-Furga, Andrea, Ikegawa, Shiro, Cormier-Daire, Valerie, Bovée, Judith V, Pansuriya, Twinkal C, de Sousa, Sérgio B, Savarirayan, Ravi, Andreucci, Elena, Vikkula, Miikka, Garavelli, Livia, Pottinger, Caroline, Ogino, Toshihiko, Sakai, Akinori, Regazzoni, Bianca M, Wuyts, Wim, Sangiorgi, Luca, Pedrini, Elena, Zhu, Mei, Kozakewich, Harry P, Kasser, James R, Seidman, Jon G, Kurek, Kyle C, Warman, Matthew L

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Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux von Bartels, Cynthia F., Bükülmez, Hülya, Padayatti, Pius, Rhee, David K., van Ravenswaaij-Arts, Conny, Pauli, Richard M., Mundlos, Stefan, Chitayat, David, Shih, Ling-Yu, Al-Gazali, Lihadh I., Kant, Sarina, Cole, Trevor, Morton, Jenny, Cormier-Daire, Valérie, Faivre, Laurence, Lees, Melissa, Kirk, Jeremy, Mortier, Geert R., Leroy, Jules, Zabel, Bernhard, Kim, Chong Ae, Crow, Yanick, Braverman, Nancy E., van den Akker, Focco, Warman, Matthew L.

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