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Number of items: 12.

Journal Article

Adesoji, O. and Nothnagel, M. (2020). A Simulation Study to Evaluate Existing Pleiotropy Detection Methods. Hum. Hered., 84 (4-5). S. 204 - 205. BASEL: KARGER. ISSN 1423-0062

Drichel, D., Nothnagel, M. and Becker, T. (2015). Beyond Exomes: A Nonparametric Collapsing Test for Joint Analysis of Rare Variants. Hum. Hered., 80 (3). S. 107 - 108. BASEL: KARGER. ISSN 1423-0062

Frye, B., Gaede, K. I., Saltini, C., Rossman, M. D., Monos, D. S., Rosenman, K. D., Schuler, C. R., Weston, A., Wegner, R., Noth, R., Zissel, G., Schreiber, S., Nothnagel, M. and Muller-Quernheim, J. (2020). Analysis of Single Nucleotide Polymorphisms in Sarcoidosis and Chronic Beryllium Disease. Am. J. Respir. Crit. Care Med., 201. NEW YORK: AMER THORACIC SOC. ISSN 1535-4970

Heilmann-Heimbach, S., Herold, C., Hochfeld, L. M., Hillmer, A. M., Nyholt, D. R., Hecker, J., Javed, A., Chew, E. G. Y., Pechlivanis, S., Drichel, D., Heng, X., del Rosario, R. C. H., Fier, H. L., Paus, R., Ruedi, R., Galesloot, T. E., Moebus, S., Anhalt, T., Prabhakar, S., Li, R., Kanoni, S., Papanikolaou, G., Papanikolaou, G., Kutalik, Z., Deloukas, P., Philpott, M. P., Waeber, G., Spector, T. D., Vollenweider, P., Kiemeney, L. A. L. M., Dedoussis, G., Richards, J. B., Nothnagel, M., Martin, N. G., Becker, T., Hinds, D. A. and Noethen, M. M. (2018). GWAS meta-analysis yields novel insights into the biology of male-pattern baldness. Eur. J. Hum. Genet., 26. S. 761 - 763. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Hoelzel, S., Ishorst, N., Greve, C., Degenhardt, F., Drichel, D., Maj, C., Nothnagel, M., Hehir-Kwa, J. Y., Veltman, J. A., Kruse, T., Reutter, H., Nowak, S., Carels, C., van Rooij, I., Ludwig, K. U. and Mangold, E. (2020). Nonsyndromic orofacial clefts - Identifying putative causative genes by CNV analysis of whole exome sequencing data. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 839 - 840. LONDON: SPRINGERNATURE. ISSN 1476-5438

Katsara, M-A, Nothnagel, M., Branicki, W., Pospiech, E., Kayser, M., Walsh, S. and Hysi, P. (2020). Incorporating and Validating the Impact of Priors on DNA Prediction of External Visible Characteristics. Hum. Hered., 84 (4-5). S. 212 - 213. BASEL: KARGER. ISSN 1423-0062

Koch, M., Freitag-Wolf, S., Schlesinger, S., Borggrefe, J., Hov, J. R., Jensen, M. K., Pick, J., Markus, M. R. P., Hoepfner, T., Jacobs, G., Siegert, S., Artati, A., Kastenmueller, G., Roemisch-Margl, W., Adamski, J., Illig, T., Nothnagel, M., Karlsen, T. H., Schreiber, S., Franke, A., Krawczak, M., Noethlings, U. and Lieb, W. (2017). Serum metabolomic profiling highlights pathways associated with liver fat content in a general population sample. Eur. J. Clin. Nutr., 71 (8). S. 995 - 1002. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5640

Neupert, L. -M., May, P., Kobow, K., Nothnagel, M., Nuernberg, P., Freiman, T., Harter, P., Klein, K. M., Weber, Y., Bluemcke, I. and Lal, D. (2017). DISCOVERY AND PATHOGENICITY ASSESSMENT OF NEUROPATHOLOGY-ASSOCIATED GENE VARIANTS. Epilepsia, 58. S. S174 - 1. HOBOKEN: WILEY. ISSN 1528-1167

Siegert, S., Roewer, L. and Nothnagel, M. (2015). Equivocation-Based Y-STR Marker Selection at the Population Level. Hum. Hered., 80 (3). S. 120 - 121. BASEL: KARGER. ISSN 1423-0062

Siegert, S., Roewer, L. and Nothnagel, M. (2015). Shannon Equivocation for Forensic Y-STR Marker Selection. Hum. Hered., 79 (1). S. 45 - 46. BASEL: KARGER. ISSN 1423-0062

Syrbe, S., Hedrich, U., Riesch, E., Djemie, T., Mueller, S., Moller, R. S., Maher, B., Hernandez-Hernandez, L., Synofzik, M., Caglayan, H., Arslan, M., Serratosa, J., Nothnagel, M., May, P., Krause, R., Loeffler, H., Detert, K., Dorn, T., Vogt, H., Kraemer, G., Schoels, L., Mullis, P., Linnankivi, T., Lehesjoki, A. -E., Sterbova, K., Craiu, D., Hoffman-Zacharska, D., Korff, C., Weber, Y., Steinlin, M., Gallati, S., Bertsche, A., Bernhard, M., Merkenschlager, A., Kiess, W., Gonzalez, M., Zuechner, S., Palotie, A., Suls, A., De Jonghe, P., Helbig, I., Biskup, S., Wolff, M., Maljevic, S., Schuele, R., Sisodiya, S., Weckhuysen, S., Lerche, H. and Lemke, J. (2015). DE NOVO LOSS- OR GAIN-OF-FUNCTION MUTATIONS IN KCNA2 CAUSE EPILEPTIC ENCEPHALOPATHY. Epilepsia, 56. S. 77 - 78. HOBOKEN: WILEY-BLACKWELL. ISSN 1528-1167

Syrbe, S., Hedrich, U., Riesch, E., Djemie, T., Mueller, S., Moller, R. S., Maher, B., Hernandez-Hernandez, L., Synofzik, M., Caglayan, H., Arslan, M., Serratosa, J., Nothnagel, M., May, P., Krause, R., Loeffler, H., Detert, K., Dorn, T., Vogt, H., Kraemer, G., Schoels, L., Mullis, P., Linnankivi, T., Lehesjoki, A. -E., Sterbova, K., Craiu, D., Hoffman-Zacharska, D., Korff, C., Weber, Y., Steinlin, M., Gallati, S., Bertsche, A., Bernhard, M., Merkenschlager, A., Kiess, W., Gonzalez, M., Zuechner, S., Palotie, A., Suls, A., De Jonghe, P., Helbig, I., Biskup, S., Wolff, M., Maljevic, S., Schuele, R., Sisodiya, S., Weckhuysen, S., Lerche, H. and Lemke, J. (2015). DE NOVO LOSS- OR GAIN-OF-FUNCTION MUTATIONS IN KCNA2 CAUSE EPILEPTIC ENCEPHALOPATHY. Epilepsia, 56. S. 77 - 78. HOBOKEN: WILEY-BLACKWELL. ISSN 1528-1167

This list was generated on Sun May 16 01:29:46 2021 CEST.