Search Results - Müller-Myhsok, B

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

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Reply to Lin by 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. by Abel, L, Müller-Myhsok, B

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

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Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function by 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. by 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. by 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 by 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 by 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. by 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. by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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