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2020
Hoelzel, S., Ishorst, N., Greve, C., Degenhardt, F., Drichel, D., Maj, C., Nothnagel, M. 
ORCID: 0000-0001-8305-7114, 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
2018
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. ORCID: 0000-0001-8305-7114, 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
2017
Hoebel, A. K., Drichel, D., van de Vorst, M., Boehmer, A. C., Sivalingam, S., Ishorst, N., Klamt, J., Goelz, L., Alblas, M., Maaser, A., Keppler, K., Zink, A. M., Dixon, M. J., Dixon, J., Hemprich, A., Kruse, T., Graf, I., Dunsche, A., Schmidt, G., Daratsianos, N., Nowak, S., Aldhorae, K. A., Noethen, M. M., Knapp, M., Thiele, H., Gilissen, C., Reutter, H., Hoischen, A., Mangold, E. and Ludwig, K. U. (2017). Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing. J. Dent. Res., 96 (11). S. 1314 - 1322. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591
2016
Mobascher, A., Diaz-Lacava, A., Wagner, M., Gallinat, J., Wienker, T. F., Drichel, D., Becker, T., Steffens, M., Dahmen, N., Gruender, G., Thuerauf, N., Kiefer, F., Kornhuber, J., Toliat, M. R., Thiele, H., Nuernberg, P., Steinlein, O. and Winterer, G. (2016). Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample. PLoS One, 11 (4). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203
2015
Drichel, D., Nothnagel, M. ORCID: 0000-0001-8305-7114 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