Na-ion mobility in layered Na2FePO4F and olivine Na[Fe,Mn]PO4 von Tripathi, R., Wood, S. M., Islam, M. S., Nazar, L. F.

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Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis von Rudd, E, Bryceson, Y T, Zheng, C, Edner, J, Wood, S M, Ramme, K, Gavhed, S, Gürgey, A, Hellebostad, M, Bechensteen, A G, Ljunggren, H-G, Fadeel, B, Nordenskjöld, M, Henter, J-I

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Accidental underdosing of intrathecal diamorphine von Wood, M. S., Oakes, N. D., Roberts, M., Grassmann, C.

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The educational value of using cumulative sum charts von Smith, S. E., Tallentire, V. R., Spiller, J., Wood, S. M., Cameron, H. S.

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Trends in sexually transmitted infection screening during COVID-19 and missed cases among adolescents von Bonett, S., Teixeira da Silva, D., Lazar, N., Makeneni, S., Wood, S.M.

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The epitheliome: agent-based modelling of the social behaviour of cells von Walker, D.C., Southgate, J., Hill, G., Holcombe, M., Hose, D.R., Wood, S.M., Mac Neil, S., Smallwood, R.H.

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S., Nicholson, James C., Burke, G. A. Amos, Behjati, Sam, Murray, Matthew J., Hook, Catherine E., Tarpey, Patrick

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Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing von Macken, William L., Falabella, Micol, McKittrick, Caroline, Pizzamiglio, Chiara, Ellmers, Rebecca, Eggleton, Kelly, Woodward, Cathy E., Patel, Yogen, Labrum, Robyn, Phadke, Rahul, Reilly, Mary M., DeVile, Catherine, Sarkozy, Anna, Footitt, Emma, Davison, James, Rahman, Shamima, Houlden, Henry, Bugiardini, Enrico, Quinlivan, Rosaline, Hanna, Michael G., Vandrovcova, Jana, Pitceathly, Robert D. S.

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Wavelength Tuning of the Photonic Band Gap of an Achiral Nematic Liquid Crystal Filled into a Chiral Polymer Scaffold von Wood, S. M, Fells, J. A. J, Elston, S. J, Morris, S. M

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Assessing the digenic model in rare disorders using population sequencing data von Moreno-Ruiz, Nerea, Lao, Oscar, Aróstegui, Juan Ignacio, Laayouni, Hafid, Casals, Ferran

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Targeting de novo loss-of-function variants in constrained disease genes improves diagnostic rates in the 100,000 Genomes Project von Seaby, Eleanor G., Thomas, N. Simon, Webb, Amy, Brittain, Helen, Taylor Tavares, Ana Lisa, Baralle, Diana, Rehm, Heidi L., O’Donnell-Luria, Anne, Ennis, Sarah

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A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project) von Leggatt, Gary, Cheng, Guo, Narain, Sumit, Briseño-Roa, Luis, Annereau, Jean-Philippe, Gast, Christine, Gilbert, Rodney D., Ennis, Sarah

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Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome von Gibson, Joel T., Sadeghi-Alavijeh, Omid, Gale, Daniel P., Rothe, Hansjörg, Savige, Judy

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Mutation-Attention (MuAt): deep representation learning of somatic mutations for tumour typing and subtyping von Sanjaya, Prima, Maljanen, Katri, Katainen, Riku, Waszak, Sebastian M, Aaltonen, Lauri A, Stegle, Oliver, Korbel, Jan O, Pitkänen, Esa

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Attitudinal survey of adverse drug reaction reporting by medical practitioners in the United Kingdom [see comments] von Belton, KJ, Lewis, SC, Payne, S, Rawlins, MD, Wood, SM

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A novel likely pathogenic CLCN5 variant in Dent’s disease von Hayward, S, Norton, J, Bownass, L, Platt, C, Ambrose, J. C, Arumugam, P, Bevers, R, Bleda, M, Boardman-Pretty, F, Boustred, C. R, Brittain, H, Brown, M. A, Caulfield, M. J, Chan, G. C, Giess, A, Griffin, J. N, Hamblin, A, Henderson, S, Hubbard, T. J. P, Jackson, R, Jones, L. J, Kasperaviciute, D, Kayikci, M, Kousathanas, A, Lahnstein, L, Lakey, A, Leigh, S. E. A, Leong, I. U. S, Lopez, F. J, Maleady-Crowe, F, McEntagart, M, Minneci, F, Mitchell, J, Moutsianas, L, Mueller, M, Murugaesu, N, Need, A. C, O'Donovan, P, Odhams, C. A, Patch, C, Perez-Gil, D, Pereira, M. B, Pullinger, J, Rahim, T, Rendon, A, Rogers, T, Savage, K, Sawant, K, Scott, R. H, Siddiq, A, Sieghart, A, Smith, S. C, Sosinsky, A, Stuckey, A, Tanguy, M, Taylor Tavares, A. L, Thomas, E. R. A, Thompson, S. R, Tucci, A, Welland, M. J, Williams, E, Witkowska, K, Wood, S. M, Zarowiecki, M

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Use of nonprescription topical steroids: patients' experiences von Rogers, P.J., Wood, S.M., Garrett, E.L., Krykant, S.P., Haddington, N.J., Hayhurst, J., Player, G.R.H.

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A comparison of the post‐marketing safety of four selective serotonin re‐uptake inhibitors including the investigation of symptoms occurring on withdrawal von PRICE, JOHN S., WALLER, PATRICK C., WOOD, SUSAN M., MACKAY, ANGUS V. P.

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Oxidative stress in humans during work at moderate altitude von CHAO, W.-H, ASKEW, E. W, ROBERTS, D. E, WOOD, S. M, PERKINS, J. B

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Application of ensemble clustering and survival tree analysis for identifying prognostic clinicogenomic features in patients with colorectal cancer from the 100,000 Genomes Project von Wei, Yuguo, Papachristou, Nikolaos, Mueller, Stefanie, Chang, Wai Hoong, Lai, Alvina G

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