Výsledky vyhledávání - Müller-Myhsok, B

Rapid Simulation of P Values for Product Methods and Multiple-Testing Adjustment in Association Studies Autor Seaman, S. R., Müller-Myhsok, B.

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Reply to Lin Autor Seaman, S. R., Müller-Myhsok, B.

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Robustness and power of the maximum-likelihood-binomial and maximum-likelihood-score methods, in multipoint linkage analysis of affected-sibship data. Autor Abel, L, Müller-Myhsok, B

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Maximum-likelihood expression of the transmission/disequilibrium test and power considerations. Autor Abel, L, Müller-Myhsok, B

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Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function Autor Brattig, N W, Timmann, C, Abraha, R S, Lepping, B, Müller-Myhsok, B, Horstmann, R D

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De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling. Autor Wirth, B, Schmidt, T, Hahnen, E, Rudnik-Schöneborn, S, Krawczak, M, Müller-Myhsok, B, Schönling, J, Zerres, K

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Evidence for linkage of spelling disability to chromosome 15. Autor Schulte-Körne, G, Grimm, T, Nöthen, M M, Müller-Myhsok, B, Cichon, S, Vogt, I R, Propping, P, Remschmidt, H

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Should phenotype of previous preterm birth influence management of women with short cervix in subsequent pregnancy? Comparison of vaginal progesterone and Arabin pessary Autor Care, A., Muller‐Myhsok, B., Olearo, E., Todros, T., Caradeux, J., Goya, M., Palacio, M., Carreras, E., Alfirevic, Z.

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Discriminating metastasised from non-metastasised seminoma based on transcriptional changes in primary tumours using NGS Autor Ruf, C G, Schmelz, H-U, Port, M, Wagner, W, Matthies, C, Müller-Myhsok, B, Meineke, V, Abend, M

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The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease. Autor Gasser, T, Müller-Myhsok, B, Supala, A, Zimmer, E, Wieditz, G, Wszolek, Z K, Vieregge, P, Bonifati, V, Oertel, W H

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Further evidence suggesting the presence of a locus, on human chromosome 5q31-q33, influencing the intensity of infection with Schistosoma mansoni. Autor Müller-Myhsok, B, Stelma, F F, Guissé-Sow, F, Muntau, B, Thye, T, Burchard, G D, Gryseels, B, Horstmann, R D

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Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling Autor Becker, J, Czamara, D, Hoffmann, P, Landerl, K, Blomert, L, Brandeis, D, Vaessen, A, Maurer, U, Moll, K, Ludwig, K U, Müller-Myhsok, B, Nöthen, M M, Schulte-Körne, G, Schumacher, J

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The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations Autor Sharma, M, Mueller, J C, Zimprich, A, Lichtner, P, Hofer, A, Leitner, P, Maass, S, Berg, D, Dürr, A, Bonifati, V, De Michele, G, Oostra, B, Brice, A, Wood, N W, Muller‐Myhsok, B, Gasser, T

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Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1 Autor Meier, S, Mattheisen, M, Vassos, E, Strohmaier, J, Treutlein, J, Josef, F, Breuer, R, Degenhardt, F, Mühleisen, T W, Müller-Myhsok, B, Steffens, M, Schmael, C, McMahon, F J, Nöthen, M M, Cichon, S, Schulze, T G, Rietschel, M

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease Autor Török, H-P, Glas, J, Tonenchi, L, Lohse, P, Müller-Myhsok, B, Limbersky, O, Neugebauer, C, Schnitzler, F, Seiderer, J, Tillack, C, Brand, S, Brünnler, G, Jagiello, P, Epplen, J T, Griga, T, Klein, W, Schiemann, U, Folwaczny, M, Ochsenkühn, T, Folwaczny, C

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Replication of restless legs syndrome loci in three European populations Autor Kemlink, D, Polo, O, Frauscher, B, Gschliesser, V, Högl, B, Poewe, W, Vodicka, P, Vavrova, J, Sonka, K, Nevsimalova, S, Schormair, B, Lichtner, P, Silander, K, Peltonen, L, Gieger, C, Wichmann, H E, Zimprich, A, Roeske, D, Müller-Myhsok, B, Meitinger, T, Winkelmann, J

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A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults Autor Ludwig, K U, Sämann, P, Alexander, M, Becker, J, Bruder, J, Moll, K, Spieler, D, Czisch, M, Warnke, A, Docherty, S J, Davis, O S P, Plomin, R, Nöthen, M M, Landerl, K, Müller-Myhsok, B, Hoffmann, P, Schumacher, J, Schulte-Körne, G, Czamara, D

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Genetic risk prediction and neurobiological understanding of alcoholism Autor Levey, D F, Le-Niculescu, H, Frank, J, Ayalew, M, Jain, N, Kirlin, B, Learman, R, Winiger, E, Rodd, Z, Shekhar, A, Schork, N, Kiefe, F, Wodarz, N, Müller-Myhsok, B, Dahmen, N, Nöthen, M, Sherva, R, Farrer, L, Smith, A H, Kranzler, H R, Rietschel, M, Gelernter, J, Niculescu, A B

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Genetic risk prediction and neurobiological understanding of alcoholism Autor Levey, D F, Le-Niculescu, H, Frank, J, Ayalew, M, Jain, N, Kirlin, B, Learman, R, Winiger, E, Rodd, Z, Shekhar, A, Schork, N, Kiefe, F, Wodarz, N, Müller-Myhsok, B, Dahmen, N, Nöthen, M, Sherva, R, Farrer, L, Smith, A H, Kranzler, H R, Rietschel, M, Gelernter, J, Niculescu, A B

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Replication and meta-analysis of TMEM132D gene variants in panic disorder Autor Erhardt, A, Akula, N, Schumacher, J, Czamara, D, Karbalai, N, Müller-Myhsok, B, Mors, O, Borglum, A, Kristensen, A S, Woldbye, D P D, Koefoed, P, Eriksson, E, Maron, E, Metspalu, A, Nurnberger, J, Philibert, R A, Kennedy, J, Domschke, K, Reif, A, Deckert, J, Otowa, T, Kawamura, Y, Kaiya, H, Okazaki, Y, Tanii, H, Tokunaga, K, Sasaki, T, Ioannidis, J P A, McMahon, F J, Binder, E B

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