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Number of items: 15.

Journal Article

Boehmer, A. C., Schueller, V., Hess, T., Becker, J., Gerges, C., Anders, M., Venerito, M., Schmidt, T., Schmidt, C., Izbicki, J. R., Hoelscher, A. H., Schumacher, B., Mayershofer, R., Pech, O., Vashist, Y., Weismueller, J., Knapp, M., Moebus, S., Peters, W. H. M., Neuhaus, H., Roesch, T., Noethen, M. M., Gockel, I. and Schumacher, J. (2018). Follow-up of a CFTR association with Barrett's esophagus and esophageal adenocarcinoma. Eur. J. Hum. Genet., 26. S. 519 - 521. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Deckert, J., Weber, H., Villmann, C., Lonsdorf, T. B., Richter, J., Andreatta, M., Arias-Vasquez, A., Hommers, L., Kent, L., Schartner, C., Cichon, S., Wolf, C., Schaefer, N., von Collenberg, C. R., Wachter, B., Blum, R., Schuemann, D., Scharfenort, R., Schumacher, J., Forstner, A. J., Baumann, C., Schiele, M. A., Notzon, S., Zwanzger, P., Janzing, J. G. E., Galesloot, T., Kiemeney, L. A., Gajewska, A., Glotzbach-Schoon, E., Muehlberger, A., Alpers, G., Fydrich, T., Fehm, L., Gerlach, A. L., Kircher, T., Lang, T., Stroehle, A., Arolt, V., Wittchen, H-U, Kalisch, R., Buechel, C., Hamm, A., Noethen, M. M., Romanos, M., Domschke, K., Pauli, P. and Reif, A. (2017). GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder. Mol. Psychiatr., 22 (10). S. 1431 - 1440. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5578

Forstner, A. J., Hofmann, A., Maaser, A., Sumer, S., Khudayberdiev, S., Muehleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J., Mattheisen, M., Schumacher, J., Breuer, R., Meier, S., Herms, S., Hoffmann, P., Lacour, A., Witt, S. H., Reif, A., Mueller-Myhsok, B., Lucae, S., Maier, W., Schwarz, M., Vedder, H., Kammerer-Ciernioch, J., Pfennig, A., Bauer, M., Hautzinger, M., Moebus, S., Priebe, L., Sivalingam, S., Verhaert, A., Schulz, H., Czerski, P. M., Hauser, J., Lissowska, J., Szeszenia-Dabrowska, N., Brennan, P., McKay, J. D., Wright, A., Mitchell, P. B., Fullerton, J. M., Schofield, P. R., Montgomery, G. W., Medland, S. E., Gordon, S. D., Martin, N. G., Krasnov, V., Chuchalin, A., Babadjanova, G., Pantelejeva, G., Abramova, L. I., Tiganov, A. S., Polonikov, A., Khusnutdinova, E., Alda, M., Cruceanu, C., Rouleau, G. A., Turecki, G., Laprise, C., Rivas, F., Mayoral, F., Kogevinas, M., Grigoroiu-Serbanescu, M., Propping, P., Becker, T., Rietschel, M., Cichon, S., Schratt, G. and Noethen, M. M. (2015). Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Transl. Psychiatr., 5. LONDON: NATURE PUBLISHING GROUP. ISSN 2158-3188

Forstner, A. J., Maaser, A., Sumer, S., Khudayberdiev, S., Muehleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Herms, S., Hoffmann, P., Witt, S. H., Verhaert, A., Becker, T., Rietschel, M., Cichon, S., Schratt, G. and Noethen, M. M. (2017). Genome-wide association analysis implicates microRNAs in bipolar affective disorder. Eur. Neuropsychopharmacol., 27. S. S536 - 2. AMSTERDAM: ELSEVIER SCIENCE BV. ISSN 1873-7862

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

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

Jarick, I., Volckmar, A-L, Puetter, C., Pechlivanis, S., Nguyen, T. T., Dauvermann, M. R., Beck, S., Albayrak, Oe, Scherag, S., Gilsbach, S., Cichon, S., Hoffmann, P., Degenhardt, F., Noethen, M. M., Schreiber, S., Wichmann, H-E, Joeckel, K-H, Heinrich, J., Tiesler, C. M. T., Faraone, S. V., Walitza, S., Sinzig, J., Freitag, C., Meyer, J., Herpertz-Dahlmann, B., Lehmkuhl, G., Renner, T. J., Warnke, A., Romanos, M., Lesch, K-P, Reif, A., Schimmelmann, B. G., Hebebrand, J., Scherag, A. and Hinney, A. (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Mol. Psychiatr., 19 (1). S. 115 - 122. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5578

Koller, A. C., Strohmaier, J., Ludwig, K. U., Degenhardt, F. C., Wulff, M., Breuer, D., Winkler, L., Neukirch, F., Maaser, A., Forstner, A., Sivalingam, S., Reif, A., Ramirez, A., Maier, W., Rujescu, D., Giegling, I., Thiele, H., Nuernberg, P., Heilmann-Heimbach, S., Andlauer, T., Fischer, A., Jain, G., Kaurani, L., Klockmeier, K., Worf, K., Krumsiek, J., Wildenauer, D., Schwab, S., Rietschel, M., Noethen, M. M. and Degenhardt, F. (2018). Large family-based exome sequencing study provides new insight into schizophrenia. Eur. J. Hum. Genet., 26. S. 417 - 419. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Lacour, A., Espinosa, A., Louwersheimer, E., Heilmann, S., Hernandez, I., Wolfsgruber, S., Fernandez, V., Wagner, H., Rosende-Roca, M., Mauleon, A., Moreno-Grau, S., Vargas, L., Pijnenburg, Y. A. L., Koene, T., Rodriguez-Gomez, O., Ortega, G., Ruiz, S., Holstege, H., Sotolongo-Grau, O., Kornhuber, J., Peters, O., Froelich, L., Huell, M., Ruether, E., Wiltfang, J., Scherer, M., Riedel-Heller, S., Alegret, M., Noethen, M. M., Scheltens, P., Wagner, M., Tarraga, L., Jessen, F., Boada, M., Maier, W., van der Flier, W. M., Becker, T., Ramirez, A. and Ruiz, A. (2017). Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment. Mol. Psychiatr., 22 (1). S. 153 - 161. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5578

Ludwig, K. U., Boehmer, A. C., Bowes, J., Nikolic, M., Ishorst, N., Wyatt, N., Hammond, N., Goelz, L., Thieme, F., Spielmann, M., Aldhorae, K., Rojas-Martinez, A., Noethen, M. M., Rada-Iglesias, A., Dixon, M. J., Knapp, M. and Mangold, E. (2018). Comprehensive analyses of genome-wide data reveal novel insights into distinct etiologies of cleft lip with/without celft palate, and cleft palate only. Eur. J. Hum. Genet., 26. S. 243 - 244. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Ludwig, K. U., Boehmer, A. C., Rubini, M., Mossey, P. A., Herms, S., Nowak, S., Reutter, H., Alblas, M. A., Lippke, B., Barth, S., Paredes-Zenteno, M., Munoz-Jimenez, S. G., Ortiz-Lopez, R., Kreusch, T., Hemprich, A., Martini, M., Braumann, B., Jaeger, A., Poetzsch, B., Molloy, A., Peterlin, B., Hoffmann, P., Noethen, M. M., Rojas-Martinez, A., Knapp, M., Steegers-Theunissen, R. P. and Mangold, E. (2014). Strong Association of Variants around FOXE1 and Orofacial Clefting. J. Dent. Res., 93 (4). S. 376 - 382. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591

Maaser, A., Strohmaier, J., Ludwig, K. U., Degenhardt, F., Streit, F., Schenk, L. M., Koller, A. C., Fischer, S. B., Thiele, H., Nuernberg, P., Guzman-Parra, J., Orozco Diaz, G., Auburger, G., Albus, M., Borrmann-Hassenbach, M., Jose Gonzalez, M., Gil Flores, S., Cabaleiro Fabeiro, F. J., del Rio Noriega, F., Perez Perez, F., Haro Gonzalez, J., Rivas, F., Mayoral, F., Herms, S., Hoffmann, P., Cichon, S., Rietschel, M., Noethen, M. M. and Forstner, A. J. (2018). Exome sequencing of multiply affected bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology. Eur. J. Hum. Genet., 26. S. 373 - 375. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Marenholz, I, Esparza-Gordillo, J., Rueschendorf, F., Strachan, D. P., Spycher, B. D., Baurecht, H., Margaritte-Jeannin, P., Saeaef, A., Kerkhof, M., Ege, M., Baltic, S., Matheson, M. C., Li, J., Michel, S., Ang, W. Q., McArdle, W., Homuth, G., Bouzigon, E., Pershagen, G., Postma, D. S., Braun-Fahrlaender, C., Duffy, D. L., Marks, G. B., Robertson, C. F., Martin, N. G., James, A., Sleiman, P., Foelster-Holst, R., Lieb, W., Gieger, C., Rietschel, E., Keil, T., Noethen, M. M., Sly, P. D., Schmidt, C. O., Matanovic, A., Holt, Pg P. G., Lau, S., Kabesch, M., Weidinger, S., Hakonarson, H., Ferreira, M. A. R., Laprise, C., Freidin, M. B., Genuneit, J., Koppelman, G. H., Melen, E., Dizier, M-H, Henderson, A. J. and Lee, Y-A (2016). Genome-wide association study unravels genetic determinants of the atopic march. Allergy, 71. S. 431 - 432. HOBOKEN: WILEY-BLACKWELL. ISSN 1398-9995

Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., Treutlein, J., Degenhardt, F., Forstner, A. J., Heilmann-Heimbach, S., Dietl, L., Schwarze, C. E., Schendel, D., Strohmaier, J., Abdellaoui, A., Adolfsson, R., Air, T. M., Akil, H., Alda, M., Alliey-Rodriguez, N., Andreassen, O. A., Babadjanova, G., Bass, N. J., Bauer, M., Baune, B. T., Bellivier, F., Bergen, S., Bethell, A., Biernacka, J. M., Blackwood, D. H. R., Boks, M. P., Boomsma, D. I., Borglum, A. D., Borrmann-Hassenbach, M., Brennan, P., Budde, M., Buttenschon, H. N., Byrne, E. M., Cervantes, P., Clarke, T-K, Craddock, N., Cruceanu, C., Curtis, D., Czerski, P. M., Dannlowski, U., Davis, T., de Geus, E. J. C., Di Florio, A., Djurovic, S., Domenici, E., Edenberg, H. J., Etain, B., Fischer, S. B., Forty, L., Fraser, C., Frye, M. A., Fullerton, J. M., Gade, K., Gershon, E. S., Giegling, I., Gordon, S. D., Gordon-Smith, K., Grabe, H. J., Green, E. K., Greenwood, T. A., Grigoroiu-Serbanescu, M., Guzman-Parra, J., Hall, L. S., Hamshere, M., Hauser, J., Hautzinger, M., Heilbronner, U., Herms, S., Hitturlingappa, S., Hoffmann, P., Holmans, P., Hottenga, J-J, Jamain, S., Jones, I., Jones, L. A., Jureus, A., Kahn, R. S., Kammerer-Ciernioch, J., Kirov, G., Kittel-Schneider, S., Kloiber, S., Knott, S. V., Kogevinas, M., Landen, M., Leber, M., Leboyer, M., Li, Q. S., Lissowska, J., Lucae, S., Martin, N. G., Mayoral-Cleries, F., McElroy, S. L., McIntosh, A. M., McKay, J. D., McQuillin, A., Medland, S. E., Middeldorp, C. M., Milaneschi, Y., Mitchell, P. B., Montgomery, G. W., Morken, G., Mors, O., Muehleisen, T. W., Mueller-Myhsok, B., Myers, R. M., Nievergelt, C. M., Nurnberger, J. I., O'Donovan, M. C., Loohuis, L. M. O., Ophoff, R., Oruc, L., Owen, M. J., Paciga, S. A., Penninx, B. W. J. H., Perry, A., Pfennig, A., Potash, J. B., Preisig, M., Reif, A., Rivas, F., Rouleau, G. A., Schofield, P. R., Schulze, T. G., Schwarz, M., Scott, L., Sinnamon, G. C. B., Stahl, E. A., Strauss, J., Turecki, G., Van der Auwera, S., Vedder, H., Vincent, J. B., Willemsen, G., Witt, C. C., Wray, N. R., Xi, H. S., Tadic, A., Dahmen, N., Schott, B. H., Cichon, S., Noethen, M. M., Ripke, S., Mobascher, A., Rujescu, D., Lieb, K., Roepke, S., Schmahl, C., Bohus, M. and Rietschel, M. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Transl. Psychiatr., 7. NEW YORK: NATURE PUBLISHING GROUP. ISSN 2158-3188

Zwink, N., Choinitzki, V., Baudisch, F., Hoelscher, A., Boemers, T. M., Turial, S., Kurz, R., Heydweiller, A., Keppler, K., Mueller, A., Bagci, S., Pauly, M., Brokmeier, U., Leutner, A., Degenhardt, P., Schmiedeke, E., Maerzheuser, S., Grasshoff-Derr, S., Holland-Cunz, S., Palta, M., Schaefer, M., Ure, B. M., Lacher, M., Noethen, M. M., Schumacher, J., Jenetzky, E. and Reutter, H. (2016). Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families. Dis. Esophagus, 29 (8). S. 1032 - 1043. CARY: OXFORD UNIV PRESS INC. ISSN 1442-2050

This list was generated on Fri Oct 15 03:08:13 2021 CEST.