Neuregulin 3 ( ) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition von Morar, B, Dragović, M, Waters, F A V, Chandler, D, Kalaydjieva, L, Jablensky, A

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A newly discovered founder population: the Roma/Gypsies von Kalaydjieva, Luba, Morar, Bharti, Chaix, Raphaelle, Tang, Hua

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KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment von Almeida, O. P., Schwab, S. G., Lautenschlager, N. T., Morar, B., Greenop, K. R., Flicker, L., Wildenauer, D.

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Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia von Jablensky, A., Morar, B., Wiltshire, S., Carter, K., Dragovic, M., Badcock, J. C., Chandler, D., Peters, K., Kalaydjieva, L.

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Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia von Jablensky, A, Angelicheva, D, Donohoe, G J, Cruickshank, M, Azmanov, D N, Morris, D W, McRae, A, Weickert, C S, Carter, K W, Chandler, D, Alexandrov, B, Usheva, A, Morar, B, Verbrugghe, P L, Filipovska, A, Rackham, O, Bishop, A R, Rasmussen, K Ø, Dragovic, M, Cooper, M, Phillips, M, Badcock, J, Bramon-Bosch, E, Almeida, O P, Flicker, L, Gill, M, Corvin, A, MacGregor, S, Kalaydjieva, L

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Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia von Morar, B., Schwab, S.G., Albus, M., Maier, W., Lerer, B., Wildenauer, D.B.

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Origins and Divergence of the Roma (Gypsies) von Gresham, David, Morar, Bharti, Underhill, Peter A., Passarino, Giuseppe, Lin, Alice A., Wise, Cheryl, Angelicheva, Dora, Calafell, Francesc, Oefner, Peter J., Shen, Peidong, Tournev, Ivailo, de Pablo, Rosario, Kuĉinskas, Vaidutis, Perez-Lezaun, Anna, Marushiakova, Elena, Popov, Vesselin, Kalaydjieva, Luba

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Vlax Roma history: what do coalescent-based methods tell us? von CHAIX, R, AUSTERLITZ, F, MORAR, B, KALAYDJIEVA, L, HEYER, E

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Genetic substructure in South African Bantu-speakers: Evidence from autosomal DNA and Y-chromosome studies von Lane, A.B., Soodyall, H., Arndt, S., Ratshikhopha, M.E., Jonker, E., Freeman, C., Young, L., Morar, B., Toffie, L.

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The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time von Zhivotovsky, Lev A., Underhill, Peter A., Cinnioğlu, Cengiz, Kayser, Manfred, Morar, Bharti, Kivisild, Toomas, Scozzari, Rosaria, Cruciani, Fulvio, Destro-Bisol, Giovanni, Spedini, Gabriella, Chambers, Geoffrey K., Herrera, Rene J., Yong, Kiau Kiun, Gresham, David, Tournev, Ivailo, Feldman, Marcus W., Kalaydjieva, Luba

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Mutation History of the Roma/Gypsies von Morar, Bharti, Gresham, David, Angelicheva, Dora, Tournev, Ivailo, Gooding, Rebecca, Guergueltcheva, Velina, Schmidt, Carolin, Abicht, Angela, Lochmüller, Hanns, Tordai, Attila, Kalmár, Lajos, Nagy, Melinda, Karcagi, Veronika, Jeanpierre, Marc, Herczegfalvi, Agnes, Beeson, David, Venkataraman, Viswanathan, Warwick Carter, Kim, Reeve, Jeff, de Pablo, Rosario, Kučinskas, Vaidutis, Kalaydjieva, Luba

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BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain von Cabrera-Serrano, M., Rivas-Infante, E., Mavillard, F., Morar, B., Comas, D., Carvajal, A., Avila, R., Muelas, N., Olive, M., Diaz, J., Verges, E., Romero, N., Laporte, J., Vilchez, J., Laing, N., Kalaydjieva, L., Paradas, C.

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P.258 - BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain von Cabrera-Serrano, M., Rivas-Infante, E., Mavillard, F., Morar, B., Comas, D., Carvajal, A., Avila, R., Muelas, N., Olive, M., Diaz, J., Verges, E., Romero, N., Laporte, J., Vilchez, J., Laing, N., Kalaydjieva, L., Paradas, C.

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Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome von Kremensky, Ivo, Guerguelcheva, Velina, Swoboda, Kathryn, Baas, Frank, Kwa, Marcel, Gooding, Rebecca, Marns, Lorna, Ambrugger, Petra, Steglich, Christina, Bürger, Joachim, von Moers, Arpad, Müllner-Eidenböck, Andrea, Neumann, Luitgard, Yong, Kiau Kiun, Merlini, Luciano, Lochmüller, Hanns, Varon, Raymonda, Risch, Neil, Walter, Maggie, Morar, Bharti, Tournev, Ivailo, Kalaydjieva, Luba, Angelicheva, Dora, Tang, Hua, Reinhold, Anke, Thomas, P K

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LONGEVITY KLOTHO GENE POLYMORPHISM AND THE RISK OF DEMENTIA IN OLDER MEN von Flicker, L., Morar, B., Hankey, G., Yeap, B., Golledge, J., Jablensky, A., Almeida, O.

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A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus von KIDD, K. K, MORAR, B, YONG SUK NAM, GRANDY, D. K, JENKINS, T, KIDD, J. R, CASTIGLIONE, C. M, HONGYU ZHAO, PAKSTIS, A. J, SPEED, W. C, BONNE-TAMIR, B, LU, R.-B, GOLDMAN, D, CHAEYOUNG LEE

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Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease von Hunter, Michael, Bernard, Rafaëlle, Freitas, Elizabeth, Boyer, Amandine, Morar, Bharti, Martins, Ian J., Tournev, Ivailo, Jordanova, Albena, Guergelcheva, Velina, Ishpekova, Boryana, Kremensky, Ivo, Nicholson, Garth, Schlotter, Beate, Lochmüller, Hanns, Voit, Thomas, Colomer, Jaume, Thomas, P.K., Levy, Nicolas, Kalaydjieva, Luba

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Genealogy and genes: tracing the founding fathers of Tristan da Cunha von SOODYALL, Himla, NEBEL, Almut, MORAR, Bharti, JENKINS, Trefor

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Y-chromosomal evidence for a strong reduction in male population size of Yakuts von Pakendorf, Brigitte, Morar, Bharti, Tarskaia, Larissa A, Kayser, Manfred, Soodyall, Himla, Rodewald, Alexander, Stoneking, Mark

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The molecular characterization of Gaucher disease in South Africa von Morar, B., Lane, A.B.

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