The use of frozen pooled citrated normal plasma as a daily control for determinations of plasma prothrombin time von ELLERBROOK, L D, RAMSDEN, D L, RHEES, M C, BROWN, D V

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Wheat straw availability for bioenergy in England von Townsend, T.J., Sparkes, D.L., Ramsden, S.J., Glithero, N.J., Wilson, P.

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Subretinal Visual Implant Alpha IMS – Clinical trial interim report von Stingl, Katarina, Bartz-Schmidt, Karl Ulrich, Besch, Dorothea, Chee, Caroline K., Cottriall, Charles L., Gekeler, Florian, Groppe, Markus, Jackson, Timothy L., MacLaren, Robert E., Koitschev, Assen, Kusnyerik, Akos, Neffendorf, James, Nemeth, Janos, Naeem, Mohamed Adheem Naser, Peters, Tobias, Ramsden, James D., Sachs, Helmut, Simpson, Andrew, Singh, Mandeep S., Wilhelm, Barbara, Wong, David, Zrenner, Eberhart

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Assessment of the Electronic Retinal Implant Alpha AMS in Restoring Vision to Blind Patients with End-Stage Retinitis Pigmentosa von Edwards, Thomas L., Cottriall, Charles L., Xue, Kanmin, Simunovic, Matthew P., Ramsden, James D., Zrenner, Eberhart, MacLaren, Robert E.

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Interim Results of a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherited Retinal Degenerations von Stingl, Katarina, Schippert, Ruth, Bartz-Schmidt, Karl U, Besch, Dorothea, Cottriall, Charles L, Edwards, Thomas L, Gekeler, Florian, Greppmaier, Udo, Kiel, Katja, Koitschev, Assen, Kühlewein, Laura, MacLaren, Robert E, Ramsden, James D, Roider, Johann, Rothermel, Albrecht, Sachs, Helmut, Schröder, Greta S, Tode, Jan, Troelenberg, Nicole, Zrenner, Eberhart

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CD4+ T Follicular Helper Cells in Human Tonsils and Blood Are Clonally Convergent but Divergent from Non-Tfh CD4+ Cells von Brenna, Elena, Davydov, Alexey N., Ladell, Kristin, McLaren, James E., Bonaiuti, Paolo, Metsger, Maria, Ramsden, James D., Gilbert, Sarah C., Lambe, Teresa, Price, David A., Campion, Suzanne L., Chudakov, Dmitriy M., Borrow, Persephone, McMichael, Andrew J.

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Where, when and why brain activation differs for bilinguals and monolinguals during picture naming and reading aloud von Parker Jones, Oiwi, Green, David W, Grogan, Alice, Pliatsikas, Christos, Filippopolitis, Konstantinos, Ali, Nilufa, Lee, Hwee Ling, Ramsden, Sue, Gazarian, Karine, Prejawa, Susan, Seghier, Mohamed L, Price, Cathy J

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligat... von Evans, D Gareth R, Ramsden, R T, Shenton, A, Gokhale, C, Bowers, N L, Huson, S M, Pichert, G, Wallace, A

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Elevated stearoyl-CoA desaturase 1 activity is associated with alcohol-associated liver disease von Klepp, T.D., Sloan, M.E., Soundararajan, Soundarya, Ramsden, C.E., Cinar, R., Schwandt, M.L., Diazgranados, N., Vatsalya, V., Ramchandani, V.A.

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Quantifying fossil fuel methane emissions using observations of atmospheric ethane and an uncertain emission ratio von Ramsden, Alice E, Ganesan, Anita L, Western, Luke M, Rigby, Matthew, Manning, Alistair J, Foulds, Amy, France, James L, Barker, Patrick, Levy, Peter, Say, Daniel, Wisher, Adam, Arnold, Tim, Rennick, Chris, Stanley, Kieran M, Young, Dickon, O'Doherty, Simon

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Inflammasome-independent role of AIM2 in suppressing colon tumorigenesis via DNA-PK and Akt von Wilson, Justin E, Petrucelli, Alex S, Chen, Liang, Koblansky, A Alicia, Truax, Agnieszka D, Oyama, Yoshitaka, Rogers, Arlin B, Brickey, W June, Wang, Yuli, Schneider, Monika, Mühlbauer, Marcus, Chou, Wei-Chun, Barker, Brianne R, Jobin, Christian, Allbritton, Nancy L, Ramsden, Dale A, Davis, Beckley K, Ting, Jenny P Y

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Recommendations for clinical interpretation of variants found in non-coding regions of the genome von Ellingford, Jamie M, Ahn, Joo Wook, Bagnall, Richard D, Baralle, Diana, Barton, Stephanie, Campbell, Chris, Downes, Kate, Ellard, Sian, Duff-Farrier, Celia, FitzPatrick, David R, Greally, John M, Ingles, Jodie, Krishnan, Neesha, Lord, Jenny, Martin, Hilary C, Newman, William G, O'Donnell-Luria, Anne, Ramsden, Simon C, Rehm, Heidi L, Richardson, Ebony, Singer-Berk, Moriel, Taylor, Jenny C, Williams, Maggie, Wood, Jordan C, Wright, Caroline F, Harrison, Steven M, Whiffin, Nicola

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A Gradient of Template Dependence Defines Distinct Biological Roles for Family X Polymerases in Nonhomologous End Joining von Nick McElhinny, Stephanie A., Havener, Jody M., Garcia-Diaz, Miguel, Juárez, Raquel, Bebenek, Katarzyna, Kee, Barbara L., Blanco, Luis, Kunkel, Thomas A., Ramsden, Dale A.

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Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal Disease von Taylor, Rachel L., PhD, Parry, Neil R.A., PhD, Barton, Stephanie J., BSc, Campbell, Christopher, BSc, Delaney, Claire M., MSc, Ellingford, Jamie M., MRes, Hall, Georgina, MSc, Hardcastle, Claire, BSc, Morarji, Jiten, MSc, BMBS, Nichol, Elisabeth J., DBO, Williams, Lindsi C., DBO, Douzgou, Sofia, PhD, MD, Clayton-Smith, Jill, MD(Res), FRCP, Ramsden, Simon C., PhD, FRCPath, Sharma, Vinod, FRCOphth, Biswas, Susmito, FRCOphth, Lloyd, I. Chris, FRCOphth, Ashworth, Jane L., PhD, FRCOphth, Black, Graeme C., DPhil, FRCOphth, Sergouniotis, Panagiotis I., PhD, FEBO

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Fatty acids in cardiovascular health and disease: A comprehensive update von Baum, Seth J., MD, FNLA, Kris-Etherton, Penny M., PhD, RD, Willett, Walter C., MD, DrPH, Lichtenstein, Alice H., DSc, Rudel, Lawrence L., PhD, Maki, Kevin C., PhD, Whelan, Jay, PhD, MPH, Ramsden, Christopher E., MD, USPHS, Block, Robert C., MD, MPH

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The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2 von Baser, M E, Kuramoto, L, Woods, R, Joe, H, Friedman, J M, Wallace, A J, Ramsden, R T, Olschwang, S, Bijlsma, E, Kalamarides, M, Papi, L, Kato, R, Carroll, J, Lázaro, C, Joncourt, F, Parry, D M, Rouleau, G A, Evans, D G R

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Human catechol- O-methyltransferase down-regulation by estradiol von Jiang, H, Xie, T, Ramsden, D.B, Ho, S.L

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Clinical utility of genetic testing in 201 preschool children with inherited eye disorders von Lenassi, Eva, Clayton-Smith, Jill, Douzgou, Sofia, Ramsden, Simon C., Ingram, Stuart, Hall, Georgina, Hardcastle, Claire L., Fletcher, Tracy A., Taylor, Rachel L., Ellingford, Jamie M., Newman, William D., Fenerty, Cecilia, Sharma, Vinod, Lloyd, I. Chris, Biswas, Susmito, Ashworth, Jane L., Black, Graeme C., Sergouniotis, Panagiotis I.

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Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease von Jiman, Omamah A, Taylor, Rachel L, Lenassi, Eva, Smith, Jill Clayton, Douzgou, Sofia, Ellingford, Jamie M, Barton, Stephanie, Hardcastle, Claire, Fletcher, Tracy, Campbell, Christopher, Ashworth, Jane, Biswas, Susmito, Ramsden, Simon C, Manson, Forbes D, Black, Graeme C

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