Giα and β Proteins Associate in a Complex with Cannabinoid Receptor Interacting Protein 1a (CRIP1a) von Hughes, Erin K., England, Andrew C., Leone‐Kabler, Sandra, Lowther, W. T., Howlett, Allyn C.

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Global changes in oceanic mesoscale currents over the satellite altimetry record von Martínez-Moreno, Josué, Hogg, Andrew McC, England, Matthew H., Constantinou, Navid C., Kiss, Andrew E., Morrison, Adele K.

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Comparison of in silico strategies to prioritize rare genomic variants impacting RNA splicing for the diagnosis of genomic disorders von Rowlands, Charlie, Thomas, Huw B., Lord, Jenny, Wai, Htoo A., Arno, Gavin, Beaman, Glenda, Sergouniotis, Panagiotis, Gomes-Silva, Beatriz, Campbell, Christopher, Gossan, Nicole, Hardcastle, Claire, Webb, Kevin, O’Callaghan, Christopher, Hirst, Robert A., Ramsden, Simon, Jones, Elizabeth, Clayton-Smith, Jill, Webster, Andrew R., Douglas, Andrew G. L., O’Keefe, Raymond T., Newman, William G., Baralle, Diana, Black, Graeme C. M., Ellingford, Jamie M.

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Rapid subsurface warming and circulation changes of Antarctic coastal waters by poleward shifting winds von Spence, Paul, Griffies, Stephen M., England, Matthew H., Hogg, Andrew McC, Saenko, Oleg A., Jourdain, Nicolas C.

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Weddell Sea Control of Ocean Temperature Variability on the Western Antarctic Peninsula von Morrison, Adele K., England, Matthew H., Hogg, Andrew McC, Kiss, Andrew E.

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Metamorphism and Deformation on Subduction Interfaces: 1. Physical Framework von England, Philip C., Smye, Andrew J.

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Metamorphism and Deformation on Subduction Interfaces: 2. Petrological and Tectonic Implications von Smye, Andrew J., England, Philip C.

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Clinical features and management of human monkeypox: a retrospective observational study in the UK von Adler, Hugh, Hine, Paul, Snell, Luke B, Osborne, Jane C, Rampling, Tommy, Beadsworth, Mike BJ, Dunning, Jake, Hunter, Ewan R, Jacobs, Michael, Khoo, Saye H, Porter, David, Porter, Robert J, Ratcliffe, Libuše, Schmid, Matthias L, Tunbridge, Anne J, Wingfield, Tom, Price, Nicholas M, Abouyannis, Mike, Al-Balushi, Asma, Aston, Stephen, Ball, Robert, Blanchard, Thomas J, Davies, Geraint, Gillespie, Angela, Hicks, Scott R, Hoyle, Marie-Claire, Ilozue, Chinenye, Mair, Luke, Marshall, Suzanne, Neary, Anne, Nsutebu, Emmanuel, Ryan, Hannah, Turtle, Lance, van Aartsen, Jon, Walker, Naomi F, Woolley, Stephen, Chawla, Anu, Smielewska, Anna, Benson, Cathryn, Brindley, Cheryl, Das, Urmi, Eyton-Chong, Chin K, Gnanalingham, Claire, Larru, Beatriz, McBride, Joanna, Oliver, Claire, Paul, Princy, Riordan, Andrew, Abrahamsen, Jennifer, Athan, Breda, Bhagani, Sanjay, Brown, Colin S, Carpenter, Oliver, Cropley, Ian, Hopkins, Susan, Joyce, Jessica, Lamb, Lucy, Lyons, Adrian, Mahungu, Tabitha, Mepham, Stephen, Mukwaira, Edina, Rodger, Alison, Williams, Alan, Allen, Denise, Dixon, Jill, Evans, Adam, McNicholas, Pauline, Price, D Ashley, Schwab, Uli, Ward, Margaret, Emonts, Marieke, Owens, Stephen, Douthwaite, Sam T, Goodman, Anna, MacMahon, Eithne, Nebbia, Gaia, Parsons, Joseph, Sullivan, Tadgh, Taj, Usman, van Nipsen tot Pannerden, Claire, Winslow, Helen, Zatyka, Ewa, Alozie-Otuka, Ekene, Beviz, Csaba, Ceesay, Yusupha, Gargee, Latchmin, Mitchell, Hannah, Tabios, Federico, Wigglesworth, Neil, Brooks, Tim, Dryden, Matthew, Furneaux, Jenna, Truelove, Elizabeth, Warrell, Clare E, Firth, Richard, Hobson, Gemma, Johnson, Christopher, Dewynter, Alison, Spence, Oliver, Hruby, Dennis E

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Abyssal ocean overturning slowdown and warming driven by Antarctic meltwater von Li, Qian, England, Matthew H., Hogg, Andrew McC, Rintoul, Stephen R., Morrison, Adele K.

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ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy von Mattison, Kari A, Tossing, Gilles, Mulroe, Fred, Simmons, Callum, Butler, Kameryn M, Schreiber, Alison, Alsadah, Adnan, Neilson, Derek E, Naess, Karin, Wedell, Anna, Wredenberg, Anna, Sorlin, Arthur, McCann, Emma, Burghel, George J, Menendez, Beatriz, Hoganson, George E, Botto, Lorenzo D, Filloux, Francis M, Aledo-Serrano, Ángel, Gil-Nagel, Antonio, Tatton-Brown, Katrina, Verbeek, Nienke E, van der Zwaag, Bert, Aleck, Kyrieckos A, Fazenbaker, Andrew C, Balciuniene, Jorune, Dubbs, Holly A, Marsh, Eric D, Garber, Kathryn, Ek, Jakob, Duno, Morten, Hoei-Hansen, Christina E, Deardorff, Matthew A, Raca, Gordana, Quindipan, Catherine, van Hirtum-Das, Michele, Breckpot, Jeroen, Hammer, Trine Bjørg, Møller, Rikke S, Whitney, Andrea, Douglas, Andrew G L, Kharbanda, Mira, Brunetti-Pierri, Nicola, Morleo, Manuela, Nigro, Vincenzo, May, Halie J, Tao, James X, Argilli, Emanuela, Sherr, Elliot H, Dobyns, William B, Baines, Richard A, Warwicker, Jim, Parker, J Alex, Banka, Siddharth, Campeau, Philippe M, Escayg, Andrew

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Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis von Hyder, Zerin, Calpena, Eduardo, Pei, Yang, Tooze, Rebecca S., Brittain, Helen, Twigg, Stephen R. F., Cilliers, Deirdre, Morton, Jenny E. V., McCann, Emma, Weber, Astrid, Wilson, Louise C., Douglas, Andrew G. L., McGowan, Ruth, Need, Anna, Bond, Andrew, Tavares, Ana Lisa Taylor, Thomas, Ellen R. A., Hill, Susan L., Deans, Zandra C., Boardman-Pretty, Freya, Caulfield, Mark, Scott, Richard H., Wilkie, Andrew O. M.

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A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele von Crane-Smith, Zoe, De Castro, Sandra C P, Nikolopoulou, Evanthia, Wolujewicz, Paul, Smedley, Damian, Lei, Yunping, Mather, Emma, Santos, Chloe, Hopkinson, Mark, Pitsillides, Andrew A, Finnell, Richard H, Ross, M Elisabeth, Copp, Andrew J, Greene, Nicholas D E

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Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy von Parry, David A., Martin, Carol-Anne, Greene, Philip, Marsh, Joseph A., Blyth, Moira, Cox, Helen, Donnelly, Deirdre, Greenhalgh, Lynn, Greville-Heygate, Stephanie, Harrison, Victoria, Lachlan, Katherine, McKenna, Caoimhe, Quigley, Alan J., Rea, Gillian, Robertson, Lisa, Suri, Mohnish, Jackson, Andrew P.

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Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features von Robbe, Pauline, Ridout, Kate E., Vavoulis, Dimitrios V., Dréau, Helene, Kinnersley, Ben, Denny, Nicholas, Chubb, Daniel, Appleby, Niamh, Cutts, Anthony, Cornish, Alex J., Lopez-Pascua, Laura, Clifford, Ruth, Burns, Adam, Stamatopoulos, Basile, Cabes, Maite, Alsolami, Reem, Antoniou, Pavlos, Oates, Melanie, Cavalieri, Doriane, Gibson, Jane, Prabhu, Anika V., Schwessinger, Ron, Jennings, Daisy, James, Terena, Maheswari, Uma, Duran-Ferrer, Martí, Carninci, Piero, Knight, Samantha J. L., Månsson, Robert, Hughes, Jim, Davies, James, Ross, Mark, Bentley, David, Strefford, Jonathan C., Devereux, Stephen, Pettitt, Andrew R., Hillmen, Peter, Caulfield, Mark J., Houlston, Richard S., Martín-Subero, José I., Schuh, Anna

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Diabetic Neuropathies: Update on Definitions, Diagnostic Criteria, Estimation of Severity, and Treatments von Tesfaye, Solomon, Boulton, Andrew J.M, Dyck, Peter J, Freeman, Roy, Horowitz, Michael, Kempler, Peter, Lauria, Giuseppe, Malik, Rayaz A, Spallone, Vincenza, Vinik, Aaron, Bernardi, Luciano, Valensi, Paul

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Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease von Huynh, Vinh T., Audrézet, Marie-Pierre, Sayer, John A., Ong, Albert C., Lefevre, Siriane, Le Brun, Valoris, Després, Aurore, Senum, Sarah R., Chebib, Fouad T., Barroso-Gil, Miguel, Patel, Chirag, Mallett, Andrew J., Goel, Himanshu, Mallawaarachchi, Amali C., Van Eerde, Albertien M., Ponlot, Eléonore, Kribs, Marc, Le Meur, Yannick, Harris, Peter C., Cornec-Le Gall, Emilie

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Environmental chemicals in dog testes reflect their geographical source and may be associated with altered pathology von Sumner, Rebecca N., Byers, Andrew, Zhang, Zulin, Agerholm, Jorgen S., Lindh, Lena, England, Gary C. W., Lea, Richard G.

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Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes von Le Gallo, Matthieu, O'Hara, Andrea J, Rudd, Meghan L, Urick, Mary Ellen, Hansen, Nancy F, O'Neil, Nigel J, Price, Jessica C, Zhang, Suiyuan, England, Bryant M, Godwin, Andrew K, Sgroi, Dennis C, Hieter, Philip, Mullikin, James C, Merino, Maria J, Bell, Daphne W

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SMAD6 variants in craniosynostosis: genotype and phenotype evaluation von Calpena, Eduardo, Cuellar, Araceli, Bala, Krithi, Swagemakers, Sigrid M. A., Koelling, Nils, McGowan, Simon J., Phipps, Julie M., Balasubramanian, Meena, Cunningham, Michael L., Douzgou, Sofia, Lattanzi, Wanda, Morton, Jenny E. V., Shears, Deborah, Weber, Astrid, Wilson, Louise C., Lord, Helen, Lester, Tracy, Johnson, David, Wall, Steven A., Twigg, Stephen R. F., Mathijssen, Irene M. J., Boardman-Pretty, Freya, Boyadjiev, Simeon A., Wilkie, Andrew O. M.

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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract von Münch, Johannes, Engesser, Marie, Schönauer, Ria, Hamm, J. Austin, Hartig, Christin, Hantmann, Elena, Akay, Gulsen, Pehlivan, Davut, Mitani, Tadahiro, Coban Akdemir, Zeynep, Tüysüz, Beyhan, Shirakawa, Toshihiko, Dateki, Sumito, Claus, Laura R., van Eerde, Albertien M., Smol, Thomas, Devisme, Louise, Franquet, Hélène, Attié-Bitach, Tania, Wagner, Timo, Bergmann, Carsten, Höhn, Anne Kathrin, Shril, Shirlee, Pollack, Ari, Wenger, Tara, Scott, Abbey A., Paolucci, Sarah, Buchan, Jillian, Gabriel, George C., Posey, Jennifer E., Lupski, James R., Petit, Florence, McCarthy, Andrew A., Pazour, Gregory J., Lo, Cecilia W., Popp, Bernt, Halbritter, Jan

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