A New Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Mapping to Chromosome 12q13, and Evidence for Further Genetic Heterogeneity von Reid, E., Dearlove, A.M., Rhodes, M., Rubinsztein, D.C.

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A Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Maps to Chromosome 19q13 von Reid, E., Dearlove, A.M., Osborn, O., Rogers, M.T., Rubinsztein, D.C.

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Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping von Ohadi, Mina, Lalloz, Michel R.A., Sham, Pak, Zhao, Jinghua, Dearlove, Andrew M., Shiach, Caroline, Kinsey, Sally, Rhodes, Michael, Layton, D. Mark

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Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus von Ragge, N K, Hartley, C, Dearlove, A M, Walker, J, Russell-Eggitt, I, Harris, C M

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A genome-wide family-based linkage study of coeliac disease von KING, A. L., YIANNAKOU, J. Y., BRETT, P. M., CURTIS, D., MORRIS, M.-A., DEARLOVE, A. M., RHODES, M., ROSEN-BRONSON, S., MATHEW, C., ELLIS, H. J., CICLITIRA, P. J.

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Autosomal dominant spastic paraplegia : Refined SPG8 locus and additional genetic heterogeneity von REID, E, DEARLOVE, A. M, WHITEFORD, M. L, RHODES, M, RUBINSZTEIN, D. C

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Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13 von Curtis, D, Brett, P, Dearlove, A M, McQuillin, A, Kalsi, G, Robertson, M M, Gurling, H M D

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CTLA-4/CD28 gene region is associated with genetic susceptibility to coeliac disease in UK families von King, A L, Moodie, S J, Fraser, J S, Curtis, D, Reid, E, Dearlove, A M, Ellis, H J, Ciclitira, P J

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Coeliac disease: follow-up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11 von KING, A. L., FRASER, J. S., MOODIE, S. J., CURTIS, D., DEARLOVE, A. M., ELLIS, H. J., ROSEN-BRONSON, S., CICLITIRA, P. J.

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The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate von REID, E, ESCAYG, A, DEARLOVE, A M, LEE, D D, MEISLER, M H, RUBINSZTEIN, D C

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Benign familial infantile convulsions: report of a UK family and confirmation of genetic heterogeneity von BARALLE, D, DEARLOVE, A M, BEACH, R, FFRENCH-CONSTANT, C, REID, E

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Mutation in myosin heavy chain 6 causes atrial septal defect von Ching, Yung-Hao, Ghosh, Tushar K, Cross, Steve J, Packham, Elizabeth A, Honeyman, Louise, Loughna, Siobhan, Robinson, Thelma E, Dearlove, Andrew M, Ribas, Gloria, Bonser, Andrew J, Thomas, Neil R, Scotter, Andrew J, Caves, Leo S D, Tyrrell, Graham P, Newbury-Ecob, Ruth A, Munnich, Arnold, Bonnet, Damien, Brook, J David

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Coeliac disease: follow‐up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11 von KING, A. L., FRASER, J. S., MOODIE, S. J., CURTIS, D., DEARLOVE, A. M., ELLIS, H. J., ROSEN‐BRONSON, S., CICLITIRA, P. J.

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Coeliac disease: investigation of proposed causal variants in the CTLA4 gene region von King, A. L., Moodie, S. J., Fraser, J. S., Curtis, D., Reid, E., Dearlove, A. M., Ciclitira, P. J.

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High throughput genotyping technologies von Dearlove, Andrew M

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Benign familial infantile convulsions: report of a UK family and confirmation of genetic heterogeneity von Baralle, D, Dearlove, A M, Beach, R, Ffrench-Constant, C, Reid, E

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US National Institutes of Health Prioritization of SARS-CoV-2 Variants von Turner, Sam, Alisoltani, Arghavan, Bratt, Debbie, Cohen-Lavi, Liel, Dearlove, Bethany L, Drosten, Christian, Fischer, Will M, Fouchier, Ron A M, Gonzalez-Reiche, Ana Silvia, Jaroszewski, Lukasz, Khalil, Zain, LeGresley, Eric, Johnson, Marc, Jones, Terry C, Mühlemann, Barbara, O'Connor, David, Sedova, Mayya, Shukla, Maulik, Theiler, James, Wallace, Zachary S, Yoon, Hyejin, Zhang, Yun, van Bakel, Harm, Degrace, Marciela M, Ghedin, Elodie, Godzik, Adam, Hertz, Tomer, Korber, Bette, Lemieux, Jacob, Niewiadomska, Anna M, Post, Diane J, Rolland, Morgane, Scheuermann, Richard, Smith, Derek J

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Quantifying how single dose Ad26.COV2.S vaccine efficacy depends on Spike sequence features von Magaret, Craig A., Li, Li, deCamp, Allan C., Rolland, Morgane, Juraska, Michal, Williamson, Brian D., Ludwig, James, Molitor, Cindy, Benkeser, David, Luedtke, Alex, Simpkins, Brian, Heng, Fei, Sun, Yanqing, Carpp, Lindsay N., Bai, Hongjun, Dearlove, Bethany L., Giorgi, Elena E., Jongeneelen, Mandy, Brandenburg, Boerries, McCallum, Matthew, Bowen, John E., Veesler, David, Sadoff, Jerald, Gray, Glenda E., Roels, Sanne, Vandebosch, An, Stieh, Daniel J., Le Gars, Mathieu, Vingerhoets, Johan, Grinsztejn, Beatriz, Goepfert, Paul A., de Sousa, Leonardo Paiva, Silva, Mayara Secco Torres, Casapia, Martin, Losso, Marcelo H., Little, Susan J., Gaur, Aditya, Bekker, Linda-Gail, Garrett, Nigel, Truyers, Carla, Van Dromme, Ilse, Swann, Edith, Marovich, Mary A., Follmann, Dean, Neuzil, Kathleen M., Corey, Lawrence, Greninger, Alexander L., Roychoudhury, Pavitra, Hyrien, Ollivier, Gilbert, Peter B.

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Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind, randomised, controlled, phase 2/3 trial von Folegatti, Pedro M, Bibi, Sagida, Chappell, Harry, Fedosyuk, Sofiya, Gbesemete, Diane, Kelly, Elizabeth J, Makinson, Rebecca, Rawlinson, Thomas, Ross-Russell, Amy L, Saich, Stephen, Smith, Catherine C, Tarrant, Richard, Thomas, Kelly M, Warren, Sarah C, Lambe, Teresa, Adams, Kelly, Ali, Aabidah, Allen, Lauren, Baker, Natalie, Barrett, Kelly, Bellamy, Duncan, Berg, Adam, Beveridge, Amy, Bewley, Kevin, Bijker, Else M., Boland, Elena, Bormans, Daan, Bower, Thomas, Boyd, Amy, Brenner, Tanja, Buttigieg, Karen R., Cao, Michelangelo, Chapman, David, Chelysheva, Irina, Cifuentes, Liliana, Collins, Sarah, Conlon, Christopher P., Davis, Judith, Dong, Tao, Drake, Jonathan, Fisher, Richard, Garlant, Harriet, Gavrila, Madita, Gibbons, Felicity, Gill, Hardeep, Hart, Thomas C., Hartnell, Birgit, Haskell, Louise, Hawkins, Sophia, Hermosin Herrera, Macarena, Hill, David, Hill, Jennifer, Howes, Jessica, Jackson, Susan, Joshi, Amar, Kelly, Dearbhla M., King, Lloyd D.W., Knott, Daniel, Lee, Kim Y.N., Leung, Stephanie, Liu, Shuchang, Loew, Lisa, Madhavan, Meera, Marius, Phedra, Marshall, Julia L., Martin, Jane, Moore, Maria, Morris, Susan J., O'Reilly, Peter John, Owino, Nelly, Patel, Bhumika, Patrick-Smith, Maia, Perring, James, Phillips, Daniel J., Poulton, Ian, Presland, Laura, Pulido, David, Rajapaska, Durga, Ramos Lopez, Fernando, Rollier, Christine S., Romani, Rossana, Sedik, Cynthia, Seddiqi, Samiullah, Segireddy, Rameswara R., Sharpe, Hannah R., Silva-Reyes, Laura, Smith, David J., Smith, Daniel C., Smith, Nicholas, Stockley, David, Summerton, Eloise, Szigeti, Anna, Taylor, Ursula, Tonks, Susan, Tree, Julian A., Truby, Adam, Varughese, Rachel, Woodyer, Mark, Worth, Andrew T., Yao, Xin Li

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A SARS-CoV-2 vaccine candidate would likely match all currently circulating variants von Dearlove, Bethany, Lewitus, Eric, Bai, Hongjun, Li, Yifan, Reeves, Daniel B., Joyce, M. Gordon, Scott, Paul T., Amare, Mihret F., Vasan, Sandhya, Michael, Nelson L., Modjarrad, Kayvon, Rolland, Morgane

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