Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts von Muglia, P, Tozzi, F, Galwey, N W, Francks, C, Upmanyu, R, Kong, X Q, Antoniades, A, Domenici, E, Perry, J, Rothen, S, Vandeleur, C L, Mooser, V, Waeber, G, Vollenweider, P, Preisig, M, Lucae, S, Müller-Myhsok, B, Holsboer, F, Middleton, L T, Roses, A D

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Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score--the CoLaus Study von Lin, X, Song, K, Lim, N, Yuan, X, Johnson, T, Abderrahmani, A, Vollenweider, P, Stirnadel, H, Sundseth, S. S, Lai, E, Burns, D. K, Middleton, L. T, Roses, A. D, Matthews, P. M, Waeber, G, Cardon, L, Waterworth, D. M, Mooser, V

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Family history of depression is associated with younger age of onset in patients with recurrent depression von Tozzi, F., Prokopenko, I., Perry, J. D., Kennedy, J. L., McCarthy, A. D., Holsboer, F., Berrettini, W., Middleton, L. T., Chilcoat, H. D., Muglia, P.

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PINK1 mutations and parkinsonism von ISHIHARA-PAUL, L, HULIHAN, M. M, ZOUARI, M, SASSI, S. B, YAHMED, S. B, EL EUCH-FAYECHE, G, MATTHEWS, P. M, MIDDLETON, L. T, GIBSON, R. A, HENTATI, F, FARRER, M. J, KACHERGUS, J, UPMANYU, R, WARREN, L, AMOURI, R, ELANGO, R, PRINJHA, R. K, SOTO, A, KEFI, M

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Young‐onset type 2 diabetes and younger current age: increased susceptibility to retinopathy in contrast to other complications von Middleton, T. L., Constantino, M. I., Molyneaux, L., D'Souza, M., Twigg, S. M., Wu, T., Yue, D. K., Zoungas, S., Wong, J.

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Vitamin B12 and Folate Status in Cognitively Healthy Older Adults and Associations with Cognitive Performance von Nalder, L., Zheng, B., Chiandet, G., Middleton, L. T., de Jager, Celeste A.

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Cortical Lewy bodies and Aβ burden are associated with prevalence and timing of dementia in Lewy body diseases von Ruffmann, C., Calboli, F. C. F., Bravi, I., Gveric, D., Curry, L. K., de Smith, A., Pavlou, S., Buxton, J. L., Blakemore, A. I. F., Takousis, P., Molloy, S., Piccini, P., Dexter, D. T., Roncaroli, F., Gentleman, S. M., Middleton, L. T.

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Novel Blood-Based Biomarkers and Disease Modifying Therapies for Alzheimer’s Disease. Are We Ready for the New Era? von Korologou-Linden, Roxanna, Kalsi, J., Kafetsouli, D., Olawale, A., Wingfield, D., Mummery, D., Hayhoe, B., Robinson, O., Majeed, A., Middleton, L. T.

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Lower Incidence of Dementia Following Cancer Diagnoses: Evidence from a Large Cohort and Mendelian Randomization Study von Bassil, Darina T., Zheng, Bang, Su, B., Kafetsouli, D., Udeh-Momoh, C., Tzoulaki, I., Ahmadi-Abhari, S., Muller, D. C., Riboli, Elio, Middleton, L. T.

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Associations of Cardiovascular and Non-Cardiovascular Comorbidities with Dementia Risk in Patients with Diabetes: Results from a Large UK Cohort Study von Zheng, B., Su, B., Udeh-Momoh, C., Price, G., Tzoulaki, I., Vamos, E. P., Majeed, A., Riboli, E., Ahmadi-Abhari, S., Middleton, Lefkos T.

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At a Glance: An Update on Neuroimaging and Retinal Imaging in Alzheimer’s Disease and Related Research von Ford, J., Kafetsouli, D., Wilson, H., Udeh-Momoh, C., Politis, M., AhmadiAbhari, S., Rabiner, I., Middleton, Lefkos T.

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Editorial: Dementia Prevention: A Global Challenge in Urgent Need of Solutions von Price, G, Udeh-Momoh, C, Kivipelto, M, Middleton, L T

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Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V von Antonellis, Anthony, Ellsworth, Rachel E., Sambuughin, Nyamkhishig, Puls, Imke, Abel, Annette, Lee-Lin, Shih-Queen, Jordanova, Albena, Kremensky, Ivo, Christodoulou, Kyproula, Middleton, Lefkos T., Sivakumar, Kumaraswamy, Ionasescu, Victor, Funalot, Benoit, Vance, Jeffery M., Goldfarb, Lev G., Fischbeck, Kenneth H., Green, Eric D.

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Pharmacogenetics and disease genetics of complex diseases von Schmith, V D, Campbell, D A, Sehgal, S, Anderson, W H, Burns, D K, Middleton, L T, Roses, A D

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Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p von Christodoulou, Kyproula, Kyriakides, Theodoros, Hristova, Anna H., Georgiou, Domna-Maria, Kalaydjieva, Ljuba, Yshpekova, Borjana, Ivanova, Tatjana, L.Weber, James, T.Middleton, Lefkos

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Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity von Othmane, Kamel Ben, Middleton, Lefkos T., Loprest, Lorraine J., Wilkinson, Kenneth M., Lennon, Felicia, Rozear, Marvin P., Stajich, Jeffrey U., Gaskell, Perry C., Roses, Allen D., Pericak-Vance, Margaret A., Vance, Jeffery M.

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Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease von VAN DER WALT, J. M, MARTIN, E. R, PAHWA, R, STERN, M. B, COLCHER, A, HINER, B. C, JANKOVIC, J, ONDO, W. G, ALLEN, F. H, GOETZ, C. G, SMALL, G. W, MASTAGLIA, F, SCOTT, W. K, ROSES, A. D, STAJICH, J. M, BOOZE, M. W, FUJIWARA, K, GIBSON, R. A, MIDDLETON, L. T, SCOTT, B. L, PERICAK-VANCE, M. A, VANCE, J. M, ZHANG, F, NANCE, M. A, WATTS, R. L, HUBBLE, J. P, HAINES, J. L, KOLLER, W. C, LYONS, K

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Editorial: Dietary Cholesterol and Dementia Risk von Middleton, L T, Riboli, E

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Congenital myasthenic syndromes 34th ENMC international workshop, 10–11 June 1995 von Middleton, L.T.

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Dietary Cholesterol and Dementia Risk von Middleton, Lefkos T., Riboli, E.

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