检索结果 - Müller-Myhsok, B

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

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

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

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