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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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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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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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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FOLLOW-UP LINKAGE STUDY OF COELIAC DISEASE: FURTHER EVIDENCE FOR THE EXISTENCE OF A SUSCEPTIBILITY LOCUS ON CHROMOSOME 11p11 von King, A.L, Fraser, J.S, Moodie, S.J, Cu, Dearlove, A.M, Ellis, H.J, Rosen-Bronson, S, Ciclitira, P.J

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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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